FR3131208A1 - Cosmetic composition comprising a polyhydroxyalkanoate copolymer with an (un)saturated hydrocarbon chain, and at least one polyurethane latex - Google Patents

Abstract

Title: Cosmetic composition comprising a polyhydroxyalkanoate copolymer with an (un)saturated hydrocarbon chain, and at least one polyurethane latex The present invention relates to a cosmetic composition C1 comprising a) at least one polyhydroxyalkanoate copolymer with (un)saturated hydrocarbon groups, b) at at least one polyurethane latex, c) optionally at least one fatty substance, d) optionally at least one surfactant and e) water as well as a process for treating keratin materials using such a composition.

Description

Cosmetic composition comprising a polyhydroxyalkanoate copolymer with an (un)saturated hydrocarbon chain, and at least one polyurethane latex

The present invention relates to a cosmetic composition C1 comprising a) at least one polyhydroxyalkanoate copolymer with (un)saturated hydrocarbon groups, b) at least one polyurethane latex, c) optionally at least one fatty substance, d) optionally at least one surfactant and e) water as well as a process for treating keratin materials using such a composition.

It is known to use film-forming polymers in cosmetics which can be transported in organic media such as hydrocarbon oils. Polymers are used in particular as a film-forming agent in makeup products such as mascaras, eyeliners, eye shadows or lipsticks.

Document FR-A-2964663 describes a cosmetic composition comprising pigments coated with a C ₃ -C ₂₁ polyhydroxyalkanoate such as poly(hydroxybutyrate-co-hydroxyvalerate).

Document WO 2011/154508 describes a cosmetic composition comprising a 4-carboxy-2-pyrolidinone ester derivative and a film-forming polymer which may be a polyhydroxyalkanoate such as polyhydroxybutyrate, polyhydroxyvalerate and polyhydroxybutyrate-co-polyhydroxyvalerate.

Document US-A-2015/274972 describes a cosmetic composition comprising a cosmetic composition comprising a thermoplastic resin, such as a polyhydroxyalkanoate, in aqueous dispersion and a silicone elastomer.

Document US2011/0015279 describes the use of polyurethane latex (PUR) in skin care. Document EP1970391 describes the use of PUR latex to increase adhesion to the hair and its shaping properties. Document WO2020074490 describes the use of PUR latex as a film-forming agent in the field of cosmetics and document WO2021198051 describes these derivatives in makeup applications. None of these documents describes the association of PUR latex with polyhydroxyalkanoates. They do not talk about the technical problem of resistance to friction or the potential improvement in adhesion to the substrate in a fatty medium.

Most polyhydroxyalkanoate copolymers are polymers resulting from the polycondensation of largely identical repeating polymer units and originating from the same carbon source or substrate. These documents do not describe the cosmetic use of copolymers resulting from polycondensation from a substrate or ^1st source of aliphatic carbon, and at least a ^2nd substrate different from the first comprising one or more hydrocarbon groups (in) saturated with polyurethane latexes. A need therefore exists to have a composition comprising hydrophilic or lipophilic polyhydroxyalkanoate copolymers soluble in the fatty phase. This makes it possible to obtain a film on keratin materials having good cosmetic properties, in particular good resistance to oils and sebum, as well as being able to play on shine or dullness, which is easy to apply, non-sticky and flexible enough to be comfortable after application to keratin materials.

The applicant has discovered that polyhydroxyalkanoate copolymers with particular grafted or functionalized hydrocarbon groups, as defined below, can be easily used in fatty media, thus making it possible to obtain homogeneous compositions. The composition has good stability, particularly after storage for one month at room temperature (25°C). The composition, particularly after its application to keratin materials, makes it possible to obtain a film having good cosmetic properties, in particular good resistance to oils and sebum, as well as a matte or shiny appearance.

However, in many conditions of use of flame-forming materials on keratin materials such as in makeup or coloring applications for example, it is desirable to have, in addition to good resistance to water and particularly food oils such as olive oil, very good resistance to friction of deposits of film-forming materials both to avoid transfer, for example to clothing, and to maintain a homogeneous appearance of the deposits. If the friction resistance is insufficient, deposits can be obtained which quickly become very unsightly for consumers, particularly if these deposits are colored as in makeup applications such as lipsticks, foundations or mascaras. In hair applications, the lack of resistance to friction is also very problematic in all coloring applications because they cause transfer to clothing and create an unsightly appearance of the keratin fibers.
There is therefore a real need to obtain deposits of film-forming materials which are resistant to oils, particularly food oils, resistant to water and have very good resistance to friction. Furthermore, for cosmetic use, it is necessary that the shine or dullness conform to consumer expectations depending on the expected use. Thus, for a gloss, we will look for a high shine while for a foundation we will look for the most natural appearance possible. In the hair field, a shine may be sought which must nevertheless remain within an acceptable range, too high a shine may be unsightly and too much dullness may be a hindrance to use. It is therefore important to be able to modulate the shine and/or dullness, for example by using specific adjuvants when possible or by using mixtures of film-forming polymers whose properties in terms of shine and dullness can be complementary. We can thus, for example, associate with a compound considered too matte in an application another shiny compound so that the combination of the two is of shine or dullness consistent with the intended application.

This problem is solved by the use of compositions C1 described below, these compositions making it possible to significantly improve the friction resistance of the polyhydroxyalkanoate (PHA) copolymer(s). Furthermore, the C1 compositions according to the invention make it possible to obtain, after deposition, a film on keratin materials having good cosmetic properties, in particular good resistance to oils and sebum, good resistance to water as well as being able to play on shine or dullness. The deposits obtained are non-sticky and flexible, therefore comfortable after application to keratin materials.

• R ¹ représente une chaine hydrocarbonée, non cyclique saturée ou insaturée, linéaire ou ramifiée, ou cyclique saturée ou insaturée, aromatique ou non aromatique, comprenant de 5 à 28 atomes de carbones ; de préférence la chaine hydrocarbonée est choisie parmi i) (C₅-C₂₈)alkyle, linéaire ou ramifié, ii) (C₅-C₂₈)alkényle, linéaire ou ramifié, iii) (C₅-C₂₈)alkynyle, linéaire ou ramifié, de préférence le groupe hydrocarboné est linéaire ;

ladite chaine hydrocarbonée étant :

• éventuellement substituée par un ou plusieurs atomes ou groupes choisis parmi : a) halogène tels que chlore ou brome, b) hydroxy, c) thiol, d) (di)(C₁-C₄)(alkyl)amino, e) (thio)carboxy, f) (thio)carboxamide –C(O)-N(R_a)₂ou –C(S)-N(R_a)₂, g) cyano, h) iso(thio)cyanate, i) (hétéro)aryle tel que phényl ou furyl, et j) (hétéro)cycloalkyle tel que anhydride, époxyde ou dithiolane, k) actif cosmétique ; l) R-X avecRreprésentant un groupe choisi parmi α) cycloalkyle tel que cyclohexyle, β) hétérocycloalkyle tel que sucre de préférence monosaccharide tel que glucose, γ) (hétéro)aryle tel que phényle, δ) actif cosmétique, m) thiosulfate et X représentant a’) O, S, N(R_a) ou Si(R_b)(R_c), b’) S(O)_r, ou (thio)carbonyle, c’) ou les associations de a’) avec b’) tels que (thio)ester, (thio)amide, (thio)urée, sulfonamide ;R _a représentant un atome d’hydrogène, ou un groupe (C₁-C₄)alkyle, ou aryl(C₁-C₄)alkyle tel que benzyle, de préférence R_areprésente un atome d’hydrogène ;R _b etR _c , identiques ou différents, représentent un groupe (C₁-C₄)alkyle ou (C₁-C₄)alkoxy particulièrement un seul substituant ; de préférence choisi parmi b) halogène, et j) tel que epoxide ; et/ou
• éventuellement interrompue par un ou plusieurs a’) hétéroatomes tels que O, S, N(R_a), et Si(R_b)(R_c), b’) S(O)_r, (thio)carbonyle, c’) ou les associations de a’) avec b’) tels que (thio)ester, (thio)amide, (thio)urée, sulfonamide avecrvalant 1 ou 2,R _a étant tel que défini précédemment, de préférenceR _a représente un atome d’hydrogène,R _b etR _c , étant tels que définis précédemment ; et

b) un ou plusieurs latex de polyuréthane;et
c) éventuellement un ou plusieurs corps gras ; de préférence liquides à 25 °C et à pression atmosphérique ; et
d) éventuellement un ou plusieurs tensioactifs ; et
e) de l’eau,
de préférence la composition C1 comprend c) un ou plusieurs corps gras et d) un ou plusieurs tensioactifs et e) de l’eau.Thus the main object of the present invention is a composition C1 comprising:
a) one or more polyhydroxyalkanoate (PHA) copolymer(s) which contains, preferably consisting of, several repeating units chosen from the following units (A) , as well as their optical, geometric isomers, their acid salts or basic, organic or mineral, and their solvates such as hydrates:
-[-O-CH(R ¹ )-CH ₂ -C(O)-]- unit (A)
polymeric units (A) in which:

• R ¹ represents a hydrocarbon chain, non-cyclic saturated or unsaturated, linear or branched, or cyclic saturated or unsaturated, aromatic or non-aromatic, comprising from 5 to 28 carbon atoms; preferably the hydrocarbon chain is chosen from i) (C ₅ -C ₂₈ ) alkyl, linear or branched, ii) (C ₅ -C ₂₈ ) alkenyl, linear or branched, iii) (C ₅ -C ₂₈ ) alkynyl, linear or branched, preferably the hydrocarbon group is linear;

said hydrocarbon chain being:

• optionally substituted by one or more atoms or groups chosen from: a) halogen such as chlorine or bromine, b) hydroxy, c) thiol, d) (di)(C ₁ -C ₄ )(alkyl)amino, e) (thio )carboxy, f) (thio)carboxamide –C(O)-N(R _a ) ₂ or –C(S)-N(R _a ) ₂ , g) cyano, h) iso(thio)cyanate, i) ( hetero)aryl such as phenyl or furyl, and j) (hetero)cycloalkyl such as anhydride, epoxide or dithiolane, k) cosmetic active ingredient; l) RX with R representing a group chosen from α) cycloalkyl such as cyclohexyl, β) heterocycloalkyl such as sugar preferably monosaccharide such as glucose, γ) (hetero)aryl such as phenyl, δ) cosmetic active ingredient, m) thiosulfate and representing a') O, S, N(R _a ) or Si(R _b )(R _c ), b') S(O) _r , or (thio)carbonyl, c') or the associations of a') with b') such as (thio)ester, (thio)amide, (thio)urea, sulfonamide; R _a representing a hydrogen atom, or a (C ₁ -C ₄ )alkyl group, or aryl (C ₁ -C ₄ )alkyl such as benzyl, preferably R _a represents a hydrogen atom; R _b and R _c , identical or different, represent a (C ₁ -C ₄ ) alkyl or (C ₁ -C ₄ ) alkoxy group, particularly a single substituent; preferably chosen from b) halogen, and j) such as epoxide; and or
• optionally interrupted by one or more a') heteroatoms such as O, S, N(R _a ), and Si(R _b )(R _c ), b') S(O) _r , (thio)carbonyl, c') or the associations of a') with b') such as (thio)ester, (thio)amide, (thio)urea, sulfonamide with r being 1 or 2, R _a being as defined above, preferably R _a represents a hydrogen atom, R _b and R _c , being as defined above; And

b) one or more polyurethane latexes ; And
c) possibly one or more fatty substances; preferably liquid at 25°C and atmospheric pressure; And
d) optionally one or more surfactants; And
e) water,
preferably composition C1 comprises c) one or more fatty substances and d) one or more surfactants and e) water.

Another subject of the invention is the use in cosmetics of a composition C1 comprising a) one or more PHA copolymer(s) as defined above, b) one or more polyurethane latexes as defined above, c) optionally one or more fatty substances as defined above, d) one or more surfactants and d) water, preferably comprising c) a or more fatty substances and d) one or more surfactants and e) water.

Another object of the invention is a process for treating keratin materials, preferably α) keratin fibers, in particular human fibers such as hair, or β) human skin, in particular lips, using a) one or more PHA copolymer(s) as defined above, b) one or more polyurethane latexes as defined above, optionally c) one or more fatty substances as defined( s) previously, optionally d) one or more surfactants and d) water preferably using a) and b) and c) and d) and e).

More particularly, the subject of the invention is a cosmetic, non-therapeutic process for treating keratin materials, comprising the application to the keratin materials of a composition C1 as defined above. The treatment process is in particular a process of care or makeup of keratin materials.

For the purposes of the present invention, and unless otherwise indicated:

By “ polyurethane latex ” is meant an aqueous dispersion of polyurethane polymer as defined above; the terms “polyurethane polymer(s) latex ” and polyurethane latex ” are equivalent;

• Par «(hétéro)aryle» on entend les groupes aryle ou hétéroaryle ;
• Par «(hétéro)cycloalkyle» on entend les groupes cycloalkyle ou hétérocycloalkyle;
• Les radicaux «aryle» ou «hétéroaryle» ou la partie aryle ou hétéroaryle d’un radical peuvent être substitués par au moins un substituant porté par un atome de carbone, choisi parmi :

• un radical alkyle en C₁-C₆, de préférence en C₁-C₄;
• un atome d’halogène tel que chlore, fluor ou brome ;
• un groupement hydroxy ;
• un radical alcoxy en C₁-C₂; un radical (poly)-hydroxyalcoxy en C₂-C₄;
• un radical amino ;
• un radical amino substitué par un ou deux radicaux alkyle, identiques ou différents, en C₁-C₆, C₁-C₆, de préférence en C₁-C₄;
• un radical acylamino (-NR-COR’) dans lequel le radical R est un atome d’hydrogène,
• un radical alkyle en C₁-C₄et le radical R’ est un radical alkyle en C₁-C₄; un radical carbamoyle ((R)₂N-CO-) dans lequel les radicaux R, identiques ou non, représentent un atome d’hydrogène, un radical alkyle en C₁-C₄;
• un radical alkylsulfonylamino (R’SO₂-NR-) dans lequel le radical R représente un atome d’hydrogène, un radical alkyle en C₁-C₄et le radical R’ représente un radical alkyle en C₁-C₄, un radical phényle ;
• un radical aminosulfonyle ((R)₂N-SO₂-) dans lequel les radicaux R, identiques ou non, représentent un atome d’hydrogène, un radical alkyle en C₁-C₄;
• un radical carboxylique sous forme acide ou salifiée (de préférence avec un métal alcalin ou un ammonium, substitué ou non) ;
• un groupement cyano (CN) ;
• un groupement polyhalogéno(C₁-C₄)alkyle, préférentiellement le trifluorométhyle (CF₃) ;

• la partie cyclique ou hétérocyclique d’un radical non aromatique peut être substituée par au moins un substituant porté par un atome de carbone choisi parmi les groupements :

• hydroxy,
• alcoxy en C₁-C₄, (poly)hydroxyalcoxy en C₂-C₄,
• alkylcarbonylamino ((RCO-NR’-) dans lequel le radical R’ est un atome d’hydrogène, un radical alkyle en C₁-C₄et le radical R est un radical alkyle en C₁-C₂, amino substitué par un ou deux groupements alkyle identiques ou différents en C₁-C₄;
• alkylcarbonyloxy ((RCO-O-) dans lequel le radical R est un radical alkyle en C₁-C₄, amino substitué par un ou deux groupements alkyle identiques ou différents en C₁-C₄;
• alkcoxycarbonyle ((RO-CO-) dans lequel le radical R est un radical alkyle en C₁-C₄, amino substitué par un ou deux groupements alkyle identiques ou différents en C₁-C₄;

• un radical cyclique, hétérocyclique, ou une partie non aromatique d’un radical aryle ou hétéroaryle, peut également être substitué par un ou plusieurs groupements oxo ;
• une chaîne hydrocarbonée est insaturée lorsqu’elle comporte une ou plusieurs liaisons doubles et/ou une ou plusieurs liaisons triples ;
• un radical «aryle» représente un groupement mono ou polycyclique hydrocarboné, condensé ou non, comprenant de 6 à 22 atomes de carbones, et dont au moins un cycle est aromatique ; préférentiellement le radical aryle est un phényle, biphényle, naphtyle, indényle, anthracényle, ou tétrahydronaphtyle ;
• un radical «hétéroaryle» représente un groupement mono ou polycyclique, condensé ou non, comprenant de 5 à 22 chaînons, de 1 à 6 hétéroatomes choisis parmi l’atome d’azote, d’oxygène, de soufre et de sélénium, et dont au moins un cycle est aromatique ; préférentiellement un radical hétéroaryle est choisis parmi acridinyle, benzimidazolyle, benzobistriazolyle, benzopyrazolyle, benzopyridazinyle, benzoquinolyle, benzothiazolyle, benzotriazolyle, benzoxazolyle, pyridinyle, tetrazolyle, dihydrothiazolyle, imidazopyridinyle, imidazolyle, indolyle, isoquinolyle, naphthoimidazolyle, naphthooxazolyle, naphthopyrazolyle, oxadiazolyle, oxazolyle, oxazolopyridyle, phénazinyle, phénooxazolyle, pyrazinyle, pyrazolyle, pyrilyle, pyrazoyltriazyle, pyridyle, pyridinoimidazolyle, pyrrolyle, quinolyle, tétrazolyle, thiadiazolyle, thiazolyle, thiazolopyridinyle, thiazoylimidazolyle, thiopyrylyle, triazolyle, xanthylyle;
• un radical «cyclique» ou «cycloalkyle» est un radical hydrocarboné cyclique non aromatique, mono ou polycyclique, condensé ou non, contenant de 5 à 22 atomes de carbone, pouvant comporter de 1 à plusieurs insaturations, de préférence le cycloalkyle est un groupe cyclohexyle ;
• un radical «hétérocyclique» ou «hétérocycloalkyle» est un radical cyclique non aromatique mono ou polycyclique, condensé ou non, contenant de 3 à 9 chaînons, comportant de 1 à 4 hétéroatomes choisis parmi l’atome d’azote, d’oxygène, de soufre et de sélénium, de préférence l’hétérocycloalkyle est choisi parmi epoxyde, pipérazinyl, pipéridinyl, morpholinyl, dithiolane ;
• un radical «alkyle» est un radical hydrocarboné saturé, linéaire ou ramifié, en particulier en en C₁-C₆, de préférence en C₁-C₄;
• un radical «alkényle» est un radical hydrocarboné insaturé, linéaire ou ramifié, comprenant une ou plusieurs doubles liaisons, conjuguées ou non ;
• un radical «alkynyle» est un radical hydrocarboné insaturé, linéaire ou ramifié, comprenant une ou plusieurs triples liaisons, conjuguées ou non ;
• un radical «alkoxy» est un radical alkyl-oxy pour lequel le radical alkyle est un radical hydrocarboné, linéaire ou ramifié, en C₁-C₆préférentiellement en C₁-C₄;
• un radical «sucre», est un radical monosaccharide, ou polysaccharide, et leurs dérivés de sucre O-protégés tels que les esters de sucres et d'acides (C₁-C₆)alkylcarboxyliques comme l’acide acétique, les sucres à groupe(s) amine et dérivés (C₁-C₄)alkylés, tels que les dérivés méthylés comme le méthylglucose. On peut citer comme radical sucre : le sucrose (ou saccharose), le glucose, le galactose, le ribose, le fucose, le maltose, le fructose, le mannose, l'arabinose, le xylose, le lactose ;
• par «monosaccharide», on entend un sucre mono-osidique comprenant au moins 5 atomes de carbone de formule C_x(H₂O)_x, avec x un entier supérieur ou égal à 5, de préférence x est supérieur ou égal à 6, en particulier x est compris inclusivement entre 5 et 7, de préférence x = 6, ils peuvent être de configuration D ou L, et d’anomère alpha ou béta, ainsi que leurs sels et leurs solvates tels que les hydrates ;
• par «polysaccharide», on entend un sucre poly-osidique qui est un polymère constitué de plusieurs oses liés entre eux par des liaisons O-osidiques lesdits polymères étant constitués d’unités monosaccharides (également appelées mono-osidiques) telles que définies précédemment lesdites unités monosaccharidique comprenant au moins 5 atomes de carbone, de préférence 6, particulièrement les unités mono-osidiques sont reliées entre elles en 1,4 ou 1,6 en anomère α (alpha) ou β(beta), chaque unité osidique pouvant être de configuration L ou D, ainsi que ses sels et ses solvates tels que les hydrates desdits monosaccharides ; il s’agit plus particulièrement de polymères formés d'un certain nombre d'oses (ou monosaccharides) ayant pour formule générale : -[C_x(H₂O)_y)]_w- ou -[(CH₂O)_x]_w-, avec x un entier supérieur ou égal à 5, de préférence x est supérieur ou égal à 6, en particulier x est compris inclusivement entre 5 et 7, de préférence x = 6, et y un entier qui représente x - 1, et w est un entier supérieur ou égal à 2, particulièrement compris inclusivement entre 3 et 3000, plus particulièrement entre 5 et 2500, préférentiellement entre 10 et 2300, particulièrement compris inclusivement entre 15 et 1000, plus particulièrement entre 20 et 500, préférentiellement entre 25 et 200 ;
• par « sucre à groupe(s) amine », on entend que le radical sucre est substitué par un ou plusieurs groupe(s) amino NR₁R₂i.e. au moins un des groupes hydroxy d’au moins une unité osidique du radical sucre est remplacé par un groupe NR₁R₂, avec R₁et R₂, identiques ou différents, représentant i) un atome d’hydrogène, ii) un groupe (C₁-C₆)alkyle, iii) un groupe aryle tel que phényle, iv) un groupe aryl(C₁-C₄)alkyle tel que benzyle, vii) –C(Y)-(Y’)_f-R’₁avec Y et Y’, identiques ou différents, représentant un atome d’oxygène, de soufre ou N(R’₂), de préférence oxygène, f = 0 ou 1, de préférence 0 ; et R’₁et R’₂représentant i) à vi) de R₁et R₂définis précédemment, et en particulier R’₁désignant un groupe (C₁-C₆)alkyle tel que méthyle. De préférence R₁et/ou R₂représentent un atome d’hydrogène, ou un groupe (C₁-C₄)alkylcarbonyle tel que acétyle et plus préférentiellement R₁représente un atome d’hydrogène et R₂représente un groupe (C₁-C₄)alkylcarbonyle tel que acétyle.
• par «sel d'acide organique ou minéral», on entend plus particulièrement les sels d’acide organique ou minéral en particulier choisis parmi un sel dérivé i) d’acide chlorhydrique HCl, ii) d'acide bromhydrique HBr, iii) d'acide sulfurique H₂SO₄, iv) d'acides alkylsulfoniques : Alk-S(O)₂OH tels que d'acide méthylsulfonique et d’acide éthylsulfonique ; v) d'acides arylsulfoniques : Ar-S(O)₂OH tel que d'acide benzène sulfonique et d’acide toluène sulfonique ; vi) d’acides alkoxysulfiniques : Alk-O-S(O)OH tels que d'acide méthoxysulfinique et d'acide éthoxysulfinique ; vii) d’acides aryloxysulfiniques tels que d'acide toluèneoxysulfinique et d'acide phénoxysulfinique ; viii) d'acide phosphorique H₃PO₄; ix) d'acide triflique CF₃SO₃H et x) d'acide tétrafluoroborique HBF₄; xi) d’acides organiques carboxyliques R°-C(O)-OH (I’z) formule (I’z) dans laquelle R° représente un groupe (hétéro)aryle tel que phényle, (hétéro)aryl(C₁-C₄)alkyle tel que benzyle, ou (C₁-C₁₀)alkyle ledit groupe alkyle étant éventuellement substitué de préférence par un ou plusieurs groupes hydroxy, radicaux amino, ou carboxy, R° désignant de préférence un groupe (C₁-C₆)alkyle éventuellement substitué par 1, 2 ou 3 groupes hydroxy, ou carboxy plus préférentiellement les acides de formule (I’z) monocarboxyliques sont choisis parmi choisis parmi l’acide acétique l’acide glycolique, l'acide lactique, et leurs mélanges, et plus particulièrement parmi l’acide acétique et l’acide lactique ; et les acides polycarboxyliques sont choisis parmi l’acide tartrique, l'acide succinique, l’acide fumarique, l’acide citrique et leurs mélanges ; et xii) les acides aminés comportant plus de radicaux acides carboxyliques que de groupes amino tels que l’acide gamma-carboxyglutamique, l’acide aspartique, l’acide glutamique, en particulier l’acide gamma-carboxyglutamique ;
• un «contre-ion anionique» est un anion ou un groupement anionique associé à la charge cationique; plus particulièrement le contre-ion anionique est choisi parmi i) les halogénures tels que le chlorure, le bromure ; ii) les nitrates ; iii) les sulfonates parmi lesquels les C₁-C₆alkylsulfonates : Alk-S(O)₂O^-tels que le méthylsulfonate ou mésylate et l’éthylsulfonate ; iv) les arylsulfonates : Ar-S(O)₂O^-tel que le benzènesulfonate et le toluènesulfonate ou tosylate ; v) le citrate ; vi) le succinate ; vii) le tartrate ; viii) le lactate ; ix) les alkylsulfates : Alk-O-S(O)O^-tels que le méthylsulfate et l’éthylsulfate ; x) les arylsulfates : Ar-O-S(O)O^-tels que le benzènesulfate et le toluènesulfate ; xi) les alcoxysulfates : Alk-O-S(O)₂O^-tel que le méthoxy sulfate et l’éthoxysulfate ; xii) les aryloxysulfates : Ar-O-S(O)₂O^-, xiii) le phosphate ; xiv) l'acétate ; xv) le triflate ; et xvi) les borates tels que le tétrafluoroborate.
• Les «solvates» représentent les hydrates ainsi que l’association avec des alcools linéaires ou ramifiés en C₁-C₄linéaire ou ramifié tels que l’éthanol, l’isopropanol, le n-propanol ;
• par «chromophore» on entend un radical issu d’un composé incolore ou coloré capable d’absorber dans le rayonnement UV et/ou visible à une longueur d’onde λ_abscomprise entre 250 et 800 nm ; De préférence le chromophore est coloré i.e. qu’il absorbe les longueur d’onde dans le visible i.e. de préférence entre 400 et 800 nm. De préférence les chromophores apparaissent colorés à l’ œil; particulièrement entre 400 et 700 nm (Ullmann’s Encyclopedia, 2005, Wiley-VcH, Verlag « Dyes, General Survey », § 2.1 Basic Principle of Color) ;
• par «chromophore fluorescent» on entend un chromophore qui est en outre capable de réémettre dans le domaine du visible à une longueur d’onde d’émission λ_émcomprise entre 400 et 800 nm, et supérieure à la longueur d’onde d’absorption. De préférence avec un déplacement de Stoke i.e. différence entre la longueur d’onde d’absorption maximale et la longueur d’onde d’émission est d’au moins 10 nm. De préférence chromophores fluorescents sont issus de colorants fluorescents capables d’absorber dans le visible λ_absi.e. à une longueur d’onde comprise entre 400 et 800 nm et de réémettre dans le visible λ_émcomprise entre 400 et 800 nm. Plus préférentiellement les chromophores fluorescents sont capables d’absorber à une λ_abscomprise entre 420 nm et 550 nm et de réémettre dans le visible à une λ_émcomprise entre 470 et 600 nm.
• par «chromophored’azurant»,on entend un chromophore issu de composé d’azurant optique ou d’«Optical brighteners, optical brightening agents (OBAs) »ou de« fluorescent brightening agents (FBAs) »,ou de« fluorescent whitening agents (FWAs) » i.e.qui absorbe dans le rayonnement UV i.e. à une longueur d’onde λ_abscomprise entre entre 250 et 350 nm de longueur d'onde et réémet ensuite cette énergie par fluorescence dans le visible à une longueur d’onde d’émission λ_émcomprise entre 400 et 600 nm, soit les longueurs d'onde entre le bleu-violet et le bleu-vert avec un maximum dans le bleu. Les chromophores d’azurant optique sont donc incolore à l’œil.
• Par «filtre UV-A» on entend un chromophore issu de composé qui filtre (ou absorbe) les rayons ultraviolets UV-A à une longueur d’onde comprise entre 320 et 400 nm. On peut distinguer les filtres UV-A courts (absorbant les rayons à une longueur d’onde comprise entre 320 et 340 nm), les filtres UV-A longs (absorbant les rayons à une longueur d’onde entre 340 et 400 nm).

Par « filtre UV-B » on entend un chromophore issu de composé qui filtre (ou absorbe) les rayons ultraviolets UV-B à une longueur d’onde comprise entre 280 et 320 nm.De plus, sauf indication contraire, les bornes délimitant l'étendue d'une plage de valeurs sont comprises dans cette plage de valeurs.By "Cosmetic active ingredient»: we mean the radical of an organic or organosilicon compound that can be integrated into a cosmetic composition to provide an effect on keratin materials, whether this effect is immediate or provided by repeated applications. As examples of cosmetic active ingredients, we can cite colored or non-colored, fluorescent or non-fluorescent chromophores such as those from optical brighteners, or chromophores from UVA and/or UVB filters, anti-aging active ingredients or intended for provide a benefit to the skin such as active ingredients having an action on the barrier function, deodorant active ingredients different from mineral particles, antiperspirant active ingredients different from mineral particles, desquamating active ingredients, antioxidant active ingredients, moisturizing active ingredients, sebum regulating active ingredients , active ingredients intended to limit the shine of the skin, active ingredients intended to combat the effects of pollution, antimicrobial or bactericidal active ingredients, anti-dandruff active ingredients, and perfumes.

• By “ (hetero)aryl ” we mean the aryl or heteroaryl groups;
• By “ (hetero)cycloalkyl ” is meant cycloalkyl or heterocycloalkyl groups;
• The “ aryl ” or “ heteroaryl ” radicals or the aryl or heteroaryl part of a radical can be substituted by at least one substituent carried by a carbon atom, chosen from:

• a C ₁ -C ₆ alkyl radical, preferably C ₁ -C ₄ ;
• a halogen atom such as chlorine, fluorine or bromine;
• a hydroxy group;
• a C ₁ -C ₂ alkoxy radical; a (poly)-hydroxyalkoxy C ₂ -C ₄ radical;
• an amino radical;
• an amino radical substituted by one or two alkyl radicals, identical or different, in C ₁ -C ₆ , C ₁ -C ₆ , preferably in C ₁ -C ₄ ;
• an acylamino radical (-NR-COR') in which the radical R is a hydrogen atom,
• a C ₁ -C ₄ alkyl radical and the radical R' is a C ₁ -C ₄ alkyl radical; a carbamoyl radical ((R) ₂ N-CO-) in which the R radicals, identical or not, represent a hydrogen atom, a C ₁ -C ₄ alkyl radical;
• an alkylsulfonylamino radical (R'SO ₂ -NR-) in which the radical R represents a hydrogen atom, a C ₁ -C ₄ alkyl radical and the radical R' represents a C ₁ -C ₄ alkyl radical, a phenyl radical;
• an aminosulfonyl radical ((R) ₂ N-SO ₂ -) in which the R radicals, identical or not, represent a hydrogen atom, a C ₁ -C ₄ alkyl radical;
• a carboxylic radical in acidic or salified form (preferably with an alkali metal or an ammonium, substituted or not);
• a cyano group (CN);
• a polyhalo(C ₁ -C ₄ ) alkyl group, preferably trifluoromethyl (CF ₃ );

• the cyclic or heterocyclic part of a non-aromatic radical can be substituted by at least one substituent carried by a carbon atom chosen from the groups:

• hydroxy,
• C ₁ -C ₄ alkoxy, (poly)hydroxyC ₂ -C ₄ alkoxy,
• alkylcarbonylamino ((RCO-NR'-) in which the radical R' is a hydrogen atom, a C ₁ -C ₄ alkyl radical and the radical R is a C ₁ -C ₂ alkyl radical, amino substituted by a or two identical or different C ₁ -C ₄ alkyl groups;
• alkylcarbonyloxy ((RCO-O-) in which the radical R is a C ₁ -C ₄ alkyl radical, amino substituted by one or two identical or different C ₁ -C ₄ alkyl groups;
• alkkoxycarbonyl ((RO-CO-) in which the radical R is a C ₁ -C ₄ alkyl radical, amino substituted by one or two identical or different C ₁ -C ₄ alkyl groups;

• a cyclic, heterocyclic radical, or a non-aromatic part of an aryl or heteroaryl radical, can also be substituted by one or more oxo groups;
• a hydrocarbon chain is unsaturated when it contains one or more double bonds and/or one or more triple bonds;
• an “ aryl ” radical represents a mono or polycyclic hydrocarbon group, condensed or not, comprising from 6 to 22 carbon atoms, and of which at least one cycle is aromatic; preferably the aryl radical is phenyl, biphenyl, naphthyl, indenyl, anthracenyl, or tetrahydronaphthyl;
• a “ heteroaryl ” radical represents a mono or polycyclic group, condensed or not, comprising from 5 to 22 members, from 1 to 6 heteroatoms chosen from nitrogen, oxygen, sulfur and selenium atoms, and of which at least the less aromatic a ring is; preferably a heteroaryl radical is chosen from acridinyl, benzimidazolyl, benzobistriazolyl, benzopyrazolyl, benzopyridazinyl, benzoquinolyl, benzothiazolyl, benzotriazolyl, benzoxazolyl, pyridinyl, tetrazolyl, dihydrothiazolyl, imidazopyridinyl, imidazolyl, indolyl, isoquinolyl, naphthoimidazolyl, naphthooxazolyl, naphthopyrazolyl, oxadiazolyl, oxazolyl, oxazolopyridyl , phenazinyl, phenooxazolyl, pyrazinyl, pyrazolyl, pyrilyl, pyrazoyltriazyl, pyridyl, pyridinoimidazolyl, pyrrolyl, quinolyl, tetrazolyl, thiadiazolyl, thiazolyl, thiazolopyridinyl, thiazoylimidazolyl, thiopyrylyl, triazolyl, xanthylyl ;
• a “ cyclic ” or “ cycloalkyl ” radical is a non-aromatic cyclic hydrocarbon radical, mono or polycyclic, condensed or not, containing from 5 to 22 carbon atoms, which may contain from 1 to several unsaturations, preferably the cycloalkyl is a cyclohexyl group ;
• a “ heterocyclic ” or “ heterocycloalkyl ” radical is a non-aromatic mono or polycyclic cyclic radical, condensed or not, containing from 3 to 9 members, comprising from 1 to 4 heteroatoms chosen from the atom of nitrogen, oxygen, sulfur and selenium, preferably the heterocycloalkyl is chosen from epoxide, piperazinyl, piperidinyl, morpholinyl, dithiolane;
• an “ alkyl ” radical is a saturated hydrocarbon radical, linear or branched, in particular in C ₁ -C ₆ , preferably in C ₁ -C ₄ ;
• an “ alkenyl ” radical is an unsaturated hydrocarbon radical, linear or branched, comprising one or more double bonds, conjugated or not;
• an “ alkynyl ” radical is an unsaturated hydrocarbon radical, linear or branched, comprising one or more triple bonds, conjugated or not;
• an “ alkoxy ” radical is an alkyl-oxy radical for which the alkyl radical is a hydrocarbon radical, linear or branched, in C ₁ -C ₆ , preferably in C ₁ -C ₄ ;
• a “ sugar ” radical, is a monosaccharide radical, or polysaccharide, and their O-protected sugar derivatives such as esters of sugars and (C ₁ -C ₆ ) alkylcarboxylic acids such as acetic acid, sugars with (s) amine and (C ₁ -C ₄ ) alkylated derivatives, such as methylated derivatives such as methylglucose. We can cite as sugar radical: sucrose (or sucrose), glucose, galactose, ribose, fucose, maltose, fructose, mannose, arabinose, xylose, lactose;
• by “ monosaccharide ” is meant a monosaccharide sugar comprising at least 5 carbon atoms of formula C _x (H ₂ O) _x , with x an integer greater than or equal to 5, preferably x is greater than or equal to 6, in particular x is inclusively between 5 and 7, preferably x = 6, they can be of D or L configuration, and of alpha or beta anomer, as well as their salts and their solvates such as hydrates;
• by “ polysaccharide ” is meant a polysaccharide sugar which is a polymer consisting of several oses linked together by O-saccharide bonds, said polymers being made up of monosaccharide units (also called monosaccharides) as defined above, said units monosaccharide comprising at least 5 carbon atoms, preferably 6, particularly the monosaccharide units are linked together at 1.4 or 1.6 in an α (alpha) or β(beta) anomer, each saccharide unit being able to be of L or D configuration, as well as its salts and solvates such as the hydrates of said monosaccharides; these are more particularly polymers formed from a certain number of oses (or monosaccharides) having the general formula: -[C _x (H ₂ O) _y )] _w - or -[(CH ₂ O) _x ] _w -, with x an integer greater than or equal to 5, preferably x is greater than or equal to 6, in particular x is inclusively between 5 and 7, preferably x = 6, and y an integer which represents x - 1, and w is an integer greater than or equal to 2, particularly included inclusively between 3 and 3000, more particularly between 5 and 2500, preferably between 10 and 2300, particularly included inclusively between 15 and 1000, more particularly between 20 and 500, preferably between 25 and 200;
• by “sugar with amine group(s)”, it is meant that the sugar radical is substituted by one or more amino group(s) NR ₁ R ₂ ie at least one of the hydroxy groups of at least one sugar unit of the sugar radical is replaced by an NR ₁ R ₂ group, with R ₁ and R ₂ , identical or different, representing i) a hydrogen atom, ii) a (C ₁ -C ₆ ) alkyl group, iii) an aryl group such as phenyl , iv) an aryl(C ₁ -C ₄ )alkyl group such as benzyl, vii) –C(Y)-(Y') _f -R' ₁ with Y and Y', identical or different, representing an atom of oxygen, sulfur or N(R' ₂ ), preferably oxygen, f = 0 or 1, preferably 0; and R' ₁ and R' ₂ representing i) to vi) of R ₁ and R ₂ defined previously, and in particular R' ₁ designating a (C ₁ -C ₆ ) alkyl group such as methyl. Preferably R ₁ and/or R ₂ represent a hydrogen atom, or a (C ₁ -C ₄ ) alkylcarbonyl group such as acetyl and more preferably R ₁ represents a hydrogen atom and R ₂ represents a (C ₁ -C ₄ )alkylcarbonyl such as acetyl.
• by “ organic or mineral acid salt ”, we mean more particularly the salts of organic or mineral acid in particular chosen from a salt derived from i) hydrochloric acid HCl, ii) hydrobromic acid HBr, iii) sulfuric acid H ₂ SO ₄ , iv) alkylsulfonic acids: Alk-S(O) ₂ OH such as methylsulfonic acid and ethylsulfonic acid; v) arylsulfonic acids: Ar-S(O) ₂ OH such as benzene sulfonic acid and toluene sulfonic acid; vi) alkoxysulfinic acids: Alk-OS(O)OH such as methoxysulfinic acid and ethoxysulfinic acid; vii) aryloxysulfinic acids such as tolueneoxysulfinic acid and phenoxysulfinic acid; viii) phosphoric acid H ₃ PO ₄ ; ix) triflic acid CF ₃ SO ₃ H and x) tetrafluoroboric acid HBF ₄ ; xi) organic carboxylic acids R°-C(O)-OH (I'z) formula (I'z) in which R° represents a (hetero)aryl group such as phenyl, (hetero)aryl(C ₁ - C ₄ )alkyl such as benzyl, or (C ₁ -C ₁₀ )alkyl said alkyl group being optionally substituted preferably by one or more hydroxy groups, amino radicals, or carboxy, R° preferably designating a group (C ₁ -C ₆ ) alkyl optionally substituted by 1, 2 or 3 hydroxy, or carboxy groups, more preferably the monocarboxylic acids of formula (I'z) are chosen from acetic acid, glycolic acid, lactic acid, and mixtures thereof , and more particularly among acetic acid and lactic acid; and the polycarboxylic acids are chosen from tartaric acid, succinic acid, fumaric acid, citric acid and mixtures thereof; and xii) amino acids containing more carboxylic acid radicals than amino groups such as gamma-carboxyglutamic acid, aspartic acid, glutamic acid, in particular gamma-carboxyglutamic acid;
• A "anionic counterion» is an anion or an anionic group associated with the cationic charge; more particularly the anionic counterion is chosen from i) halides such as chloride, bromide; ii) nitrates; iii) sulfonates including C₁-VS₆alkylsulfonates: Alk-S(O)₂O^-such as methylsulfonate or mesylate and ethylsulfonate; iv) arylsulfonates: Ar-S(O)₂O^-such as benzenesulfonate and toluenesulfonate or tosylate; v) citrate; vi) succinate; vii) tartrate; viii) lactate; ix) alkyl sulfates: Alk-O-S(O)O^-such as methyl sulfate and ethyl sulfate; x) arylsulfates: Ar-O-S(O)O^-such as benzenesulfate and toluenesulfate; xi) alkoxy sulfates: Alk-O-S(O)₂O^-such as methoxy sulfate and ethoxy sulfate; xii) aryloxy sulfates: Ar-O-S(O)₂O^-, xiii) phosphate; xiv) acetate; xv) triflate; and xvi) borates such as tetrafluoroborate.
• The “ solvates ” represent the hydrates as well as the association with linear or branched linear or branched C ₁ -C ₄ alcohols such as ethanol, isopropanol, n-propanol;
• by “ chromophore ” is meant a radical originating from a colorless or colored compound capable of absorbing UV and/or visible radiation at a wavelength λ _abs of between 250 and 800 nm; Preferably the chromophore is colored ie it absorbs wavelengths in the visible ie preferably between 400 and 800 nm. Preferably the chromophores appear colored to the eye; particularly between 400 and 700 nm ( Ullmann's Encyclopedia , 2005, Wiley-VcH, Verlag “Dyes, General Survey”, § 2.1 Basic Principle of Color);
• by “ fluorescent chromophore ” we mean a chromophore which is also capable of re-emitting in the visible range at an emission wavelength λ _em between 400 and 800 nm, and greater than the absorption wavelength . Preferably with a Stoke shift the difference between the maximum absorption wavelength and the emission wavelength is at least 10 nm. Preferably fluorescent chromophores come from fluorescent dyes capable of absorbing in the visible λ _abs ie at a wavelength between 400 and 800 nm and re-emitting in the visible λ _em between 400 and 800 nm. More preferably, the fluorescent chromophores are capable of absorbing at a λ _abs between 420 nm and 550 nm and re-emitting in the visible at a λ _em between 470 and 600 nm.
• by “ brightener chromophore ” is meant a chromophore derived from an optical brightener compound or “ Optical brighteners, optical brightening agents (OBAs)” or “fluorescent brightening agents (FBAs)”, or “fluorescent whitening agents (FWAs) » ie which absorbs UV radiation ie at a wavelength λ _abs between 250 and 350 nm wavelength and then re-emits this energy by fluorescence in the visible at a wavelength of emission λ _em between 400 and 600 nm, i.e. the wavelengths between blue-violet and blue-green with a maximum in the blue. Optical brightener chromophores are therefore colorless to the eye.
• By “ UV-A filter ” we mean a chromophore derived from a compound which filters (or absorbs) UV-A ultraviolet rays at a wavelength between 320 and 400 nm. We can distinguish between short UV-A filters (absorbing rays at a wavelength between 320 and 340 nm), and long UV-A filters (absorbing rays at a wavelength between 340 and 400 nm).

By “UV-B filter” we mean a chromophore derived from a compound which filters (or absorbs) UV-B ultraviolet rays at a wavelength between 280 and 320 nm. In addition, unless otherwise indicated, the limits delimiting the The extent of a range of values are included in this range of values.

a) The PHA copolymer(s)

The composition C1 or C'1 of the invention comprises as first ingredient a) one or more PHA copolymer(s) which contain, or preferably consist of, at least two different polymeric units repeating units (A) as defined previously.

According to a particular embodiment of the invention, the composition according to the invention C1' comprises as first ingredient a) one or more PHA copolymer(s) which contains, or preferably consists of, at least two polymeric units different repeats chosen from units (A) and (B) as defined previously.

• R ¹ représente une chaine hydrocarbonée, non cyclique saturée ou insaturée, linéaire ou ramifiée, ou cyclique saturée ou insaturée aromatique ou non aromatique, comprenant de 5 à 28 atomes de carbones, particulièrement une chaine hydrocarbonée choisie parmi i) (C₅-C₂₈)alkyle, linéaire ou ramifié, ii) (C₅-C₂₈)alkényle, linéaire ou ramifié, iii) (C₅-C₂₈)alkynyle, linéaire ou ramifié, de préférence le groupe hydrocarboné est linéaire ;

ladite chaine hydrocarbonée étant :

• éventuellement substituée par un ou plusieurs atomes ou groupes choisis parmi : a) halogène tels que chlore ou brome, b) hydroxy, c) thiol, d) (di)(C₁-C₄)(alkyl)amino, e) (thio)carboxy, f) (thio)carboxamide –C(O)-N(R_a)₂ou –C(S)-N(R_a)₂, g) cyano, h) iso(thio)cyanate, i) (hétéro)aryle tel que phényl ou furyl, et j) (hétéro)cycloalkyle tel que anhydride, époxyde ou dithiolane, k) actif cosmétique ; l) R-X avecRreprésentant un groupe choisi parmi α) cycloalkyle tel que cyclohexyle, β) hétérocycloalkyle tel que sucre de préférence monosaccharide tel que glucose, γ) (hétéro)aryle tel que phényle, δ) actif cosmétique, m) thiosulfate et X représentant a’) O, S, N(R_a) ou Si(R_b)(R_c), b’) S(O)_r, ou (thio)carbonyle, c’) ou les associations de a’) avec b’) tels que (thio)ester, (thio)amide, (thio)urée, sulfonamide ;R _a représentant un atome d’hydrogène, ou un groupe (C₁-C₄)alkyle, ou aryl(C₁-C₄)alkyle tel que benzyle, de préférence R_areprésente un atome d’hydrogène ;R _b etR _c , identiques ou différents, représentent un groupe (C₁-C₄)alkyle ou (C₁-C₄)alkoxy particulièrement un seul substituant ; de préférence choisi parmi b) halogène, et j) tel que epoxide ; et/ou
• éventuellement interrompue par un ou plusieurs a’) hétéroatomes tels que O, S, N(R_a), et Si(R_b)(R_c), b’) S(O)_r, (thio)carbonyle, c’) ou les associations de a’) avec b’) tels que (thio)ester, (thio)amide, (thio)urée, sulfonamide avecrvalant 1 ou 2,R _a étant tel que défini précédemment, de préférenceR _a représente un atome d’hydrogène,R _b etR _c , étant tels que définis précédemment ;
• R ² représente un groupe hydrocarboné, cyclique ou non cyclique, linéaire ou ramifiée, saturé ou insaturé, comprenant de 3 à 30 atomes de carbone éventuellement substituée par un ou plusieurs atomes ou groupes a) à m) et/ou éventuellement intérrompu par un ou plusieurs hétéroatomes ou groupes a’) à c’) tels que défini pour R¹; en particulier choisi parmi (C₃-C₂₈)alkyle, linéaire ou ramifié, et (C₃-C₂₈)alkényle linéaire ou ramifié, en particulier un groupe hydrocarboné linéaire, plus particulièrement (C₄-C₂₀)alkyle ou (C₄-C₂₀)alkényle, de préférence le groupe hydrocarboné possède un nombre de carbone correspondant au nombre d’atomes de carbone du radicalR ¹ auquel on retranche au moins un atome de carbone, de préférence correspondant au nombre d’atomes de carbone du radicalR ¹ auquel on retranche deux atomes de carbone ; et

b) un ou plusieurs latex de polyuréthane(s) tel(s) que défini(s) précédemment et
c) éventuellement un ou plusieurs corps gras ; de préférence liquides à 25 °C et à pression atmosphérique ; et
d) éventuellement un ou plusieurs tensioactifs ; et
d) de l’eau,
de préférence la composition C1 comprend c) un ou plusieurs corps gras et d) un ou plusieurs tensioactifs et e) de l’eau.Preferably the composition C1 of the invention is a composition C1', preferably cosmetic comprising a):
a) one or more polyhydroxyalkanoate (PHA) copolymer(s) which contains, and preferably consists of, at least two different repeating polymeric units chosen from the units(HAS)And(B)following, as well as their optical and geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates:
-[-O-CH(R¹)-CH₂-C(O)-]- unit(HAS)
-[-O-CH(R²)-CH₂-C(O)-]- unit(B)
polymeric units(HAS)And(B)in which :

• R ¹ represents a hydrocarbon chain, non-cyclic saturated or unsaturated, linear or branched, or cyclic saturated or unsaturated aromatic or non-aromatic, comprising from 5 to 28 carbon atoms, particularly a hydrocarbon chain chosen from i) (C ₅ -C ₂₈ )alkyl, linear or branched, ii) (C ₅ -C ₂₈ )alkenyl, linear or branched, iii) (C ₅ -C ₂₈ )alkynyl, linear or branched, preferably the hydrocarbon group is linear;

said hydrocarbon chain being:

• optionally substituted by one or more atoms or groups chosen from: a) halogen such as chlorine or bromine, b) hydroxy, c) thiol, d) (di)(C ₁ -C ₄ )(alkyl)amino, e) (thio )carboxy, f) (thio)carboxamide –C(O)-N(R _a ) ₂ or –C(S)-N(R _a ) ₂ , g) cyano, h) iso(thio)cyanate, i) ( hetero)aryl such as phenyl or furyl, and j) (hetero)cycloalkyl such as anhydride, epoxide or dithiolane, k) cosmetic active ingredient; l) RX with R representing a group chosen from α) cycloalkyl such as cyclohexyl, β) heterocycloalkyl such as sugar preferably monosaccharide such as glucose, γ) (hetero)aryl such as phenyl, δ) cosmetic active ingredient, m) thiosulfate and representing a') O, S, N(R _a ) or Si(R _b )(R _c ), b') S(O) _r , or (thio)carbonyl, c') or the associations of a') with b') such as (thio)ester, (thio)amide, (thio)urea, sulfonamide; R _a representing a hydrogen atom, or a (C ₁ -C ₄ )alkyl group, or aryl (C ₁ -C ₄ )alkyl such as benzyl, preferably R _a represents a hydrogen atom; R _b and R _c , identical or different, represent a (C ₁ -C ₄ ) alkyl or (C ₁ -C ₄ ) alkoxy group, particularly a single substituent; preferably chosen from b) halogen, and j) such as epoxide; and or
• optionally interrupted by one or more a') heteroatoms such as O, S, N(R _a ), and Si(R _b )(R _c ), b') S(O) _r , (thio)carbonyl, c') or the associations of a') with b') such as (thio)ester, (thio)amide, (thio)urea, sulfonamide with r being 1 or 2, R _a being as defined above, preferably R _a represents a hydrogen atom, R _b and R _c , being as defined above;
• R ² represents a hydrocarbon group, cyclic or non-cyclic, linear or branched, saturated or unsaturated, comprising from 3 to 30 carbon atoms optionally substituted by one or more atoms or groups a) to m) and/or optionally interrupted by one or more heteroatoms or groups a') to c') as defined for R¹; in particular chosen from (C₃-VS₂₈)alkyl, linear or branched, and (C₃-VS₂₈) linear or branched alkenyl, in particular a linear hydrocarbon group, more particularly (C₄-VS₂₀)alkyl or (C₄-VS₂₀)alkenyl, preferably the hydrocarbon group has a carbon number corresponding to the number of carbon atoms of the radicalR ¹ from which at least one carbon atom is subtracted, preferably corresponding to the number of carbon atoms of the radicalR ¹ from which two carbon atoms are subtracted; And

b) one or more polyurethane latex(s) as defined(s) above and
c) possibly one or more fatty substances; preferably liquid at 25°C and atmospheric pressure; And
d) optionally one or more surfactants; And
d) water,
preferably composition C1 comprises c) one or more fatty substances and d) one or more surfactants and e) water.

By “ co-polymer ” we mean that said polymer comes from the polycondensation of repeating polymer units different from each other, ie said polymer comes from the polycondensation of repeating polymer units (A) with (B) it being understood that the units polymers (A) are different from the polymeric units (B) said copolymer can be obtained from a single saturated or unsaturated aliphatic carbon source optionally substituted and/or interrupted, preferably unsubstituted uninterrupted, or from several sources of carbon, in particular at least one of which is uninterrupted unsubstituted saturated aliphatic and the other carbon source(s) being saturated or unsaturated aliphatic optionally substituted in particular by a halogen atom such as bromine, or by a cyano group, a bunte salt, a dithiolane radical, a carboxy etc.

According to one embodiment, the copolymer according to the invention comes from a single carbon source, preferably a single saturated or unsaturated aliphatic carbon source optionally substituted and/or interrupted, preferably unsubstituted uninterrupted

According to one embodiment, the copolymer according to the invention comes from several carbon sources, preferably from 2 to 10 carbon sources, more preferably 2 to 5 carbon sources, even more preferably 2 carbon sources.

According to one embodiment, the copolymer according to the invention comes from several carbon sources and at least one is saturated aliphatic.

According to a particular embodiment of the invention, the PHA copolymer(s) preferably comprise consist(s) of two different repeating polymeric units chosen from the units (A) as defined previously, the units (B) such asR ² represents a hydrocarbon group, cyclic or non-cyclic, linear or branched, saturated or unsaturated, comprising from 3 to 30 carbon atoms; in particular chosen from (C₃-VS₂₈)alkyl, linear or branched, and (C₃-VS₂₈) linear or branched alkenyl, in particular a linear hydrocarbon group, more particularly (C₄-VS₂₀)alkyl or (C₄-VS₂₀)alkenyl, preferably the hydrocarbon group has a carbon number corresponding to the number of carbon atoms of the radicalR ¹ from which at least one carbon atom is subtracted, preferably corresponding to the number of carbon atoms of the radicalR ¹ from which two carbon atoms are subtracted.

More particularly, the PHA copolymer(s) according to the invention comprise the repeating unit of formula (I), as well as their optical, geometric isomers, their organic or mineral acid or base salts, and their solvates such as hydrates:

• R ¹ etR ² sont tels que défini précédemment ;
• metnsont des entiers supérieurs ou égal à 1, de préférence la somme n + m est compris inclusivement entre 450 et 1400,

de préférence m > n lorsqueR ¹ etR ² représentent un groupe alkyle non substitué et non intérrompu – plus préférentiellement lorsque R¹et R²sont alkyle linéaire alors R¹est un groupe alkyle en C₅-C₁₃; et R²représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 2 atomes de carbone tel qu’un groupe alkyle en C₃-C₁₁; et
de préférence m < n lorsqueR ¹ représente un groupe alkyle substitué et/ou intérrompu, alkényle éventuellement substitué et/ou intérrompu ou alkynyle éventuellement substitué et/ou intérrompu, etR ² représente un groupe alkyle.[Chem. 1]:
Formula (I) in which:

• R ¹ and R ² are as defined previously;
• m and n are integers greater than or equal to 1, preferably the sum n + m is inclusively between 450 and 1400,

preferably m > n when R ¹ and R ² represent an unsubstituted and uninterrupted alkyl group – more preferably when R ¹ and R ² are linear alkyl then R ¹ is a C ₅ -C ₁₃ alkyl group; and R ² represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which 2 carbon atoms are subtracted such as a C ₃ -C ₁₁ alkyl group; And
preferably m < n when R ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or interrupted alkenyl or optionally substituted and/or interrupted alkynyl, and R ² represents an alkyl group.

• R ¹ , etR ² sont tels que définis précédemment ;
• R ³ représente un groupe hydrocarboné, cyclique ou non cyclique, linéaire ou ramifiée, saturé ou insaturé, comprenant de 1 à 30 atomes de carbone éventuellement substitué par un ou plusieurs atomes ou groupes a) à m) et/ou éventuellement intérrompu par un ou plusieurs hétéroatomes ou groupes a’) à c’) tels que défini pour R¹; en particulier représente un groupe hydrocarboné choisi parmi (C₁-C₂₈)alkyle, linéaire ou ramifié, et (C₂-C₂₈)alkényle linéaire ou ramifié, en particulier un groupe hydrocarboné linéaire, plus particulièrement (C₄-C₂₀)alkényle, de préférence le groupe hydrocarboné possède un nombre de carbone correspondant au nombre d’atomes de carbone du radical R¹, ou alors correspondant au nombre d’atomes de carbone du radical R¹auquel on retranche au moins trois atomes de carbone, de préférence correspondant au nombre d’atomes de carbone du radical R¹auquel on retranche quatre atomes de carbone ; et

étant entendu que :

• (A)est différent de(B)et(C),(B)est différent de(A)et(C),et(C)est différent de(A)et(B); et
• de préférence lorsqueR ¹ ,R ² etR ² représentent un groupe alkyle non substitué et non intérrompu le pourcentage molaire en unité(A)est supérieur au pourcentage molaire en unité(B),et supérieur au pourcentage molaire en unité(C)– plus préférrentiellement lorsque R¹, R²et R³sont alkyle linéaire, alors R¹est un groupe alkyle en C₅-C₁₃; et R²représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 2 atomes de carbone, et R³représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 4 atomes de carbone,et
• de préférence lorsqueR ¹ représente un groupe alkyle substitué et/ou intérrompu, alkényle éventuellement substitué et/ou éventuellement intérrompu ou alkynyle éventuellement substitué et/ou éventuellement intérrompu, alors le pourcentage molaire en unité(A)est inférieur au pourcentage molaire en unité(B)et au pourcentage molaire en unité(C)notamment si R²représente un groupe alkyle et/ou R³représentent un groupe alkyle.

According to a particular embodiment, the PHA copolymer(s) of composition a) contain three different repeating polymeric units(HAS),(B)And(VS), preferably consists of 3 different polymer units(HAS),(B)And(VS)following, as well as their optical and geometric isomers and their solvates such as hydrates:
-[-O-CH(R¹)-CH₂-C(O)-]- unit(HAS)
-[-O-CH(R²)-CH₂-C(O)-]- unit(B)
-[-O-CH(R³)-CH₂-C(O)-]- unit(VS)
polymeric units(HAS),(B)And(VS)in which :

• R ¹ , and R ² are as defined previously;
• R ³ represents a hydrocarbon group, cyclic or non-cyclic, linear or branched, saturated or unsaturated, comprising from 1 to 30 carbon atoms optionally substituted by one or more atoms or groups a) to m) and/or optionally interrupted by one or several heteroatoms or groups a') to c') as defined for R ¹ ; in particular represents a hydrocarbon group chosen from (C ₁ -C ₂₈ ) alkyl, linear or branched, and (C ₂ -C ₂₈ ) linear or branched alkenyl, in particular a linear hydrocarbon group, more particularly (C ₄ -C ₂₀ ) alkenyl, preferably the hydrocarbon group has a number of carbons corresponding to the number of carbon atoms of the radical R ¹ , or corresponding to the number of carbon atoms of the radical R ¹ from which at least three carbon atoms are subtracted, preference corresponding to the number of carbon atoms of the radical R ¹ from which four carbon atoms are subtracted; And

Being heard that :

• (A) is different from (B) and (C) , (B) is different from (A) and (C), and (C) is different from (A) and (B) ; And
• preferably when R ¹ , R ² and R ² represent an unsubstituted and uninterrupted alkyl group, the mole percentage in units (A) is greater than the molar percentage in units (B), and greater than the molar percentage in units (C) – more preferably when R ¹ , R ² and R ³ are linear alkyl, then R ¹ is a C ₅ -C ₁₃ alkyl group; and R ² represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which 2 carbon atoms are subtracted, and R ³ represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which we subtract 4 carbon atoms , and
• preferably whenR ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group, then the molar percentage in unit(HAS)is less than the mole percentage in unit(B)and the mole percentage in unit(VS)especially if R²represents an alkyl group and/or R³represent an alkyl group.

According to a particular embodiment of the invention, the PHA copolymer(s) comprise the repeating unit of formula (II), as well as their optical, geometric isomers, their acid or base, organic or mineral salts, and their solvates. such as hydrates:

• R ¹ ,R ² etR ³ , sont tels que défini précédemment ;
• m,netp,sont des entiers supérieurs ou égal à 1, de préférence la somme n + m + p est compris inclusivement entre 450 et 1400 ; et

• de préférence m > n + p lorsqueR ¹ ,R ² etR ³ représentent un groupe alkyle non substitué et non intérrompu - plus préférentiellement lorsque R¹, R²et R³sont alkyle linéaire, alors R¹est un groupe alkyle en C₅-C₁₃; et R²représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustraite 2 atomes de carbone tel qu’un groupe alkyle en C₃-C₁₁, et R³représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustraite 4 atomes de carbone tel qu’un groupe alkyle en C₁-C₉; et
• de préférence m < n + p lorsqueR ¹ représente un groupe alkyle substitué et/ou intérrompu, alkényle éventuellement substitué et/ou éventuellement intérrompu ou alkynyle éventuellement substitué et/ou éventuellement intérrompu, etR ² etR ³ représentent un groupe alkyle.

[Chem. 2]:
Formula (II) in which:

• R ¹ , R ² and R ³ are as defined above;
• m , n and p, are integers greater than or equal to 1, preferably the sum n + m + p is inclusively between 450 and 1400; And

• preferably m > n + p when R ¹ , R ² and R ³ represent an unsubstituted and uninterrupted alkyl group - more preferably when R ¹ , R ² and R ³ are linear alkyl, then R ¹ is a C alkyl group ₅ -C ₁₃ ; and R ² represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which 2 carbon atoms are subtracted such as a C ₃ -C ₁₁ alkyl group, and R ³ represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which 4 carbon atoms are subtracted such as a C ₁ -C ₉ alkyl group; And
• preferably m < n + p when R ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl, and R ² and R ³ represent an alkyl group.

• R ¹ ,R ² etR ³ sont tels que définis précédemment ;
• R ⁴ représente un groupe hydrocarboné, cyclique ou non cyclique, linéaire ou ramifié, saturé comprenant de 3 à 30 atomes de carbone éventuellement substituée par un ou plusieurs atomes ou groupes a) à m) et/ou éventuellement intérrompu par un ou plusieurs hétéroatomes ou groupes a’) à c’) tels que défini pour R¹; en particulier représente un groupe hydrocarboné choisi parmi (C₄-C₂₈)alkyle, linéaire ou ramifié éventuellement substitué par un ou plusieurs atomes ou groupes a) à m) et/ou intérrompu par un ou plusiuers hétéroatomes ou groupes a’) à c’) tels que défini pour R¹; et

étant entendu que :

• (A)est différent de(B),(C)et(D),(B)est différent de(A),(C)et(D),et(C)est différent de(A),(B)et(D); et(D)est différent de(A),(B)et(C); et
• de préférence lorsqueR ¹ ,R ² ,R ³ etR ⁴ représentent un groupe alkyle non substitué et non intérrompu le pourcentage molaire en unité(A)est supérieur au pourcentage molaire en unité(B),supérieur au pourcentage molaire en unité(C),et supérieur au pourcentage molaire en unité(D) -plus préférentiellement lorsque R¹, R², R³et R⁴sont alkyle linéaire, alors R¹est un groupe alkyle en C₅-C₁₃; et R²représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 2 atomes de carbone tel qu’un groupe alkyle en C₃-C₁₁, R³représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 4 atomes de carbone tel qu’un groupe alkyle en C₁-C₉, et R⁴représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 6 atomes de carbone,et
• de préférence lorsqueR ¹ représente un groupe alkyle substitué et/ou intérrompu, alkényle éventuellement substitué et/ou éventuellement intérrompu ou alkynyle éventuellement substitué et/ou éventuellement intérrompu, alors le pourcentage molaire en unité(A)est inférieur au pourcentage molaire en unité(B),est inférieur au pourcentage molaire en unité(B),et est inférieur au pourcentage molaire en unité(C),notamment siR ² représente un groupe alkyle et/ouR ³ représentent un groupe alkyle, etR ⁴ représente un groupe alkyle éventuellement substitué et/ou éventuellement intérrompu, alkényle éventuellement substitué et/ou éventuellement intérrompu ou alkynyle éventuellement substitué et/ou éventuellement intérrompu.

According to a particular embodiment, the PHA copolymer(s) of composition a) contain four different repeating polymeric units(HAS),(B),(VS), And(D)preferably consists of 4 different polymer units(HAS),(B),(VS), And(D), following, as well as their optical, geometric isomers and their acid or base, organic or mineral salts, as well as their solvates such as hydrates:
-[-O-CH(R¹)-CH₂-C(O)-]- unit(HAS)
-[-O-CH(R²)-CH₂-C(O)-]- unit(B)
-[-O-CH(R³)-CH₂-C(O)-]- unit(VS)
-[-O-CH(R⁴)-CH₂-C(O)-]- unit(D)
polymeric units(HAS),(B),(VS)And(D)in which :

• R ¹ ,R ² AndR ³ are as defined above;
• R ⁴ represents a hydrocarbon group, cyclic or non-cyclic, linear or branched, saturated comprising from 3 to 30 carbon atoms optionally substituted by one or more atoms or groups a) to m) and/or optionally interrupted by one or more heteroatoms or groups a') to c') as defined for R ¹ ; in particular represents a hydrocarbon group chosen from (C ₄ -C ₂₈ ) alkyl, linear or branched optionally substituted by one or more atoms or groups a) to m) and/or interrupted by one or more heteroatoms or groups a') to c ') as defined for R ¹ ; And

Being heard that :

• (A) is different from (B) , (C) and (D) , (B) is different from (A) , (C) and (D), and (C) is different from (A) , (B) and D) ; and (D) is different from (A) , (B) and (C) ; And
• preferably when R ¹ , R ² , R ³ and R ⁴ represent an unsubstituted and uninterrupted alkyl group, the mole percentage in units (A) is greater than the molar percentage in units (B), greater than the molar percentage in units (C ), and greater than the molar percentage in units (D) - more preferably when R ¹ , R ² , R ³ and R ⁴ are linear alkyl, then R ¹ is a C ₅ -C ₁₃ alkyl group; and R ² represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which 2 carbon atoms are subtracted such as a C ₃ -C ₁₁ alkyl group, R ³ represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which 4 carbon atoms are subtracted such as a C ₁ -C ₉ alkyl group, and R ⁴ represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which we subtract 6 carbon atoms , and
• preferably whenR ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group, then the molar percentage in unit(HAS)is less than the mole percentage in unit(B),is less than the mole percentage in unit(B),and is less than the mole percentage in unit(VS),especially ifR ² represents an alkyl group and/orR ³ represent an alkyl group, andR ⁴ represents an optionally substituted and/or optionally interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group.

According to a particular embodiment of the invention, the PHA copolymer(s) comprise the repeating unit of formula (III), as well as their optical, geometric isomers, their acid or base, organic or mineral salts, and their solvates. such as hydrates:

• R ¹ ,R ² ,R ³ , etR ⁴ sont tels que défini précédemment ;
• m,n, p,etvsont des entiers supérieurs ou égal à 1,

• de préférence la somme n + m + p + v est compris inclusivement entre 450 et 1400 ; et
• de préférence lorsqueR ¹ ,R ² ,R ³ etR ⁴ représentent un groupe alkyle non substitué et non intérrompu alors m > n + p + q-plus préférrentiellement lorsque R¹, R², R³et R⁴sont alkyle linéaire, alors R¹est un groupe alkyle en C₅-C₁₃; et R²représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 2 atomes de carbone, R³représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 4 atomes de carbone, et R⁴représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 6 atomes de carbone ; et
• de préférence lorsqueR ¹ représente un groupe alkyle substitué et/ou intérrompu, alkényle éventuellement substitué et/ou éventuellement intérrompu ou alkynyle éventuellement substitué et/ou éventuellement intérrompu, etR ² etR ³ représentent un groupe alkyle, etR ⁴ représente un groupe un groupe alkyle substitué et/ou intérrompu, alkényle éventuellement substitué et/ou éventuellement intérrompu ou alkynyle éventuellement substitué et/ou éventuellement intérrompu alors n > m + v ; plus préférentiellement n + p > m + v .

[Chem. 3]:

Formula(III)in which :

• R ¹ , R ² , R ³ , and R ⁴ are as defined above;
• m , n, p, and v are integers greater than or equal to 1,

• preferably the sum n + m + p + v is inclusively between 450 and 1400; And
• preferably when R ¹ , R ² , R ³ and R ⁴ represent an unsubstituted and uninterrupted alkyl group then m > n + p + q - more preferably when R ¹ , R ² , R ³ and R ⁴ are linear alkyl, then R ¹ is a C ₅ -C ₁₃ alkyl group; and R ² represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ to which 2 carbon atoms are subtracted, R ³ represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ to which 4 carbon atoms are subtracted, and R ⁴ represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which 6 carbon atoms are subtracted; And
• preferably whenR ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group, andR ² AndR ³ represent an alkyl group, andR ⁴ represents a group a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group then n > m + v; more preferably n + p > m + v.

• R ¹ ,R ² ,R ³ etR ⁴ sont tels que définis précédemment ; et
• R ⁵ représente un groupe hydrocarboné, cyclique ou non cyclique, linéaire ou ramifiée, saturé comprenant de 3 à 30 atomes de carbone éventuellement substituée par un ou plusieurs atomes ou groupes a) à m) et/ou éventuellement intérrompu par un ou plusiuers hétéroatomes ou groupes a’) à c’) tels que défini pour R¹; en particulier représente un groupe hydrocarboné choisi parmi (C₄-C₂₈)alkyle, linéaire ou ramifié éventuellement substituée par un ou plusieurs atomes ou groupes a) à m) et/ou intérrompu par un ou plusieurs hétéroatomes ou groupes a’) à c’) tels que défini pour R¹, de préférence le groupe hydrocarboné possède un nombre de carbone correspondant au nombre d’atomes de carbone du radical R⁴auquel on retranche au moins un atome de carbone, de préférence correspondant au nombre d’atomes de carbone du radical R⁴auquel on retranche au moins 2 atomes de carbone, de préférence auquel on retranche 2 atomes de carbone ;

étant entendu que :

• (A)est différent de(B),(C), (D)et(E);(B)est différent de(A),(C), (D)et(E),et(C)est différent de(A),(B), (D)et(E);(D)est différent de(A),(B), (C)et(E); et(E)est différent de(A),(B), (C)et(D); et
• de préférence lorsqueR ¹ ,R ² ,R ³ ,R ⁴ etR ⁵ représentent un groupe alkyle non substitué et non intérrompu le pourcentage molaire en unité(A)est supérieur au pourcentage molaire en unité(B),supérieur au pourcentage molaire en unité(C),et supérieur au pourcentage molaire en unité(D),supérieur au pourcentage molaire en unité(E) -plus préférentiellement lorsque R¹, R², R³, R⁴et R⁵sont alkyle linéaire, alors R¹est un groupe alkyle en C₅-C₁₃; et R²représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 2 atomes de carbone, R³représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 4 atomes de carbone, R⁴représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 6 atomes de carbone, et R⁵représente un groupe alkyle linéaire avec un nombre de carbone correspondant au nombre de carbone de R¹auquel on soustrait 8 atomes de carbone,et
• de préférence lorsqueR ¹ représente un groupe alkyle substitué et/ou intérrompu, alkényle éventuellement substitué et/ou éventuellement intérrompu ou alkynyle éventuellement substitué et/ou éventuellement intérrompu, alors le pourcentage molaire en unité(A)est inférieur au pourcentage molaire en unité(B),et est inférieur au pourcentage molaire en unité(C),notamment siR ² représente un groupe alkyle et/ouR ³ représente un groupe alkyle, etR ⁴ etR ⁵ représentent un groupe alkyle substitué et/ou intérrompu, alkényle éventuellement substitué et/ou éventuellement intérrompu ou alkynyle éventuellement substitué et/ou éventuellement intérrompu.

According to one embodiment more particularly the PHA copolymer(s) of composition a) contain five different repeating polymeric units(HAS),(B),(VS),(D), And(E)preferably consists of 5 different polymer units(HAS),(B),(VS),(D), And(E)following, as well as their optical, geometric isomers and their acid or base, organic or mineral salts, as well as their solvates such as hydrates:
-[-O-CH(R¹)-CH₂-C(O)-]- unit(HAS)
-[-O-CH(R²)-CH₂-C(O)-]- unit(B)
-[-O-CH(R³)-CH₂-C(O)-]- unit(VS)
-[-O-CH(R⁴)-CH₂-C(O)-]- unit(D)
-[-O-CH(R⁵)-CH₂-C(O)-]- unit(E)
polymeric units(HAS),(B),(C), (D)And(E)in which :

• R ¹ ,R ² ,R ³ AndR ⁴ are as defined above; And
• R ⁵ represents a hydrocarbon group, cyclic or non-cyclic, linear or branched, saturated comprising from 3 to 30 carbon atoms optionally substituted by one or more atoms or groups a) to m) and/or optionally interrupted by one or more heteroatoms or groups a') to c') as defined for R ¹ ; in particular represents a hydrocarbon group chosen from (C ₄ -C ₂₈ ) alkyl, linear or branched optionally substituted by one or more atoms or groups a) to m) and/or interrupted by one or more heteroatoms or groups a') to c ') as defined for R ¹ , preferably the hydrocarbon group has a number of carbons corresponding to the number of carbon atoms of the radical R ⁴ from which at least one carbon atom is subtracted, preferably corresponding to the number of atoms of carbon of the radical R ⁴ from which at least 2 carbon atoms are removed, preferably from which 2 carbon atoms are removed;

Being heard that :

• (A) is different from (B) , (C), (D) and (E) ; (B) is different from (A) , (C), (D) and (E), and (C) is different from (A) , (B), (D) and (E) ; (D) is different from (A) , (B), (C) and (E) ; and (E) is different from (A) , (B), (C) and (D) ; And
• preferably whenR ¹ ,R ² ,R ³ ,R ⁴ AndR ⁵ represent an unsubstituted and uninterrupted alkyl group the molar percentage in unit(HAS)is greater than the mole percentage in units(B),greater than the mole percentage in unit(VS),and greater than the mole percentage in unit(D),greater than the mole percentage in unit(E) -more preferentially when R¹,R²,R³, R⁴and R⁵are linear alkyl, then R¹is a C alkyl group₅-VS₁₃; and R²represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 2 carbon atoms, R³represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 4 carbon atoms, R⁴represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 6 carbon atoms, and R⁵represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 8 carbon atoms,And
• preferably whenR ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group, then the molar percentage in unit(HAS)is less than the mole percentage in unit(B),and is less than the mole percentage in unit(VS),especially ifR ² represents an alkyl group and/orR ³ represents an alkyl group, andR ⁴ AndR ⁵ represent a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group.

According to a particular embodiment of the invention, the PHA copolymer(s) comprise the repeating unit of formula (IV), as well as their optical, geometric isomers, their acid or base, organic or mineral salts, and their solvates. such as hydrates:

• R ¹ ,R ² ,R ³ ,R ⁴ etR ⁵ sont tels que définis précédemment ;
• m,n, p, vetzsont des entiers supérieurs ou égal à 1, de préférence la somme n + m + p + v + z est compris inclusivement entre 450 et 1400 ; et

• de préférence lorsqueR ¹ ,R ² ,R ³ ,R ⁴ etR ⁵ représentent un groupe alkyle non substitué et non intérrompu alors m > n + p + v + z ;
• de préférence lorsqueR ¹ représente un groupe alkyle substitué et/ou intérrompu ; alkényle éventuellement substitué et/ou éventuellement intérrompu ; ou alkynyle éventuellement substitué et/ou éventuellement intérrompu,R ² etR ³ représentent un groupe alkyle et les groupesR ⁴ etR ⁵ représentent un groupe alkyle substitué et/ou intérrompu ; alkényle éventuellement substitué et/ou éventuellement intérrompu ; ou alkynyle éventuellement substitué et/ou éventuellement intérrompu, alors n > m + v + z; plus préférentiellement n + p > m + v + z .

[Chem. 4]:

Formula(IV)in which :

• R ¹ , R ² , R ³ , R ⁴ and R ⁵ are as defined above;
• m , n, p, v and z are integers greater than or equal to 1, preferably the sum n + m + p + v + z is inclusively between 450 and 1400; And

• preferably when R ¹ , R ² , R ³ , R ⁴ and R ⁵ represent an unsubstituted and uninterrupted alkyl group then m > n + p + v + z;
• preferably whenR ¹ represents a substituted and/or interrupted alkyl group; optionally substituted and/or optionally interrupted alkenyl; or optionally substituted and/or optionally interrupted alkynyl,R ² AndR ³ represent an alkyl group and the groupsR ⁴ AndR ⁵ represent a substituted and/or interrupted alkyl group; optionally substituted and/or optionally interrupted alkenyl; or optionally substituted and/or optionally interrupted alkynyl, then n > m + v + z; more preferably n + p > m + v + z.

Preferably R ¹ represents a hydrocarbon (C ₅ -C ₂₈ ) alkyl chain, linear or branched, preferably linear. According to one embodiment of the composition according to the invention, the PHA copolymer(s) are such that the radical R ¹ is an alkyl group comprising 5 to 14, preferably between 6 and 12 carbon atoms, more preferably between 7 and 10 carbon atoms such as n-pentyl, n-hexyl, n-octyl, or n-nonyl.

According to a particular embodiment of the invention, the hydrocarbon chain R ¹ is not substituted. According to a particular embodiment of the invention the hydrocarbon chain R ¹ is not interrupted.

According to another embodiment, the hydrocarbon chain of the radical R ¹ of the invention is 1) either substituted, 2) either interrupted, 3) either substituted and interrupted.

According to a particular embodiment of the invention, the PHA copolymer(s) are such that R ¹ represents a hydrocarbon chain, in particular an alkyl group as defined above, which is interrupted by one or more (preferably one) selected atoms or groups among O, S, N(R _a ), carbonyl, or their associations such as ester, amide, urea, with R _a being as defined above, preferably R _a represents a hydrogen atom; preferably R ¹ represents an alkyl group which is interrupted by one or more atoms chosen from O, S, more preferably by an O atom, or S in particular S. Particularly the radical R ¹ when it represents an interrupted hydrocarbon chain, in particular alkyl , is in C ₇ -C ₂₀ , more particularly in C ₈ -C ₁₈ , even more particularly in C ₉ -C ₁₆ . Preferably said interrupted hydrocarbon chain, in particular alkyl, is linear.

According to another embodiment of the invention, the PHA copolymer(s) are such that R ¹ represents a hydrocarbon chain, in particular an alkyl group as defined above, substituted by one or more (preferably one) atoms or groups chosen from: a) to k) as defined previously. Preferably said hydrocarbon chain is substituted by a single atom or group chosen from: a) to k) as defined previously.

According to a particular embodiment of the invention, the PHA copolymer(s) are such that R ¹ represents a hydrocarbon chain, in particular an alkyl group as defined above, which is substituted by one or more (preferably one) groups chosen from a ) halogen such as chlorine or bromine, b) hydroxy, c) thiol, d) (di)(C ₁ -C ₄ )(alkyl)amino and preferably amino, e) carboxy, i) (hetero)cycloalkyl such as anhydride , dithiolane or epoxy, j) cosmetic active chosen from colored or non-colored, fluorescent or non-fluorescent chromophores such as optical brighteners, UV filters, h) (hetero)aryl such as phenyl or furyl, k) RX with R representing a selected group among α) cycloalkyl such as cyclohexyl, β) heterocycloalkyl such as sugar radical preferably monosaccharide such as glucosyl, γ) (hetero)aryl such as phenyl, δ) cosmetic active as defined above m) thiosulfate and X representing a') O , S, N(R _a ), b') carbonyl, c') or their associations of a') with b') such as ester, amide, urea; R _a representing a hydrogen atom, a (C ₁ -C ₄ )alkyl group, or aryl (C ₁ -C ₄ )alkyl such as benzyl, preferably R _a represents a hydrogen atom.

Even more preferably the PHA copolymer(s) are such that R ¹ represents a hydrocarbon chain, in particular an alkyl group as defined above, which is substituted by one or more (preferably one) group(s) chosen from a) halogen such as chlorine or bromine, b) hydroxy, d) (di)(C ₁ -C ₄ )(alkyl)amino preferably amino, e) carboxy, i) (hetero)cycloalkyl such as epoxide, h) (hetero)aryl such as phenyl or furyl, k) RX with R representing a group chosen from α) cycloalkyl such as cyclohexyl, β) heterocycloalkyl such as sugar radical preferably monosaccharide such as glucosyl, γ) (hetero)aryl such as phenyl, and X representing a' ) O, S, N(R _a ) preferably S; R _a representing a hydrogen atom, a (C ₁ -C ₄ ) alkyl group, preferably R _a represents a hydrogen atom.

According to one embodiment, said substituted hydrocarbon chain, in particular alkyl, is linear.

According to another embodiment, said substituted hydrocarbon chain, in particular alkyl, is branched. According to another particular embodiment of the invention, the hydrocarbon chain of the radical R ¹ of the invention is substituted and interrupted.

• substituée par un ou plusieurs (de préférence un) groupes choisis parmi a) halogène tels que chlore ou brome,b) hydroxy, c) thiol, d) (di)(C₁-C₄)(alkyl)amino de préférence amino, e) carboxy, i) (hétéro)cycloalkyle tel que anhydride, dithiolane ou époxyde, j) actif cosmétique choisi parmi les chromophores colorés ou non, fluorescents ou non tels que les azurants optiques, filtres UV, h) (hétéro)aryle tel que phényl ou furyl, k) R-X avecRreprésentant un groupe choisi parmi α) cycloalkyle tel que cyclohexyle, β) hétérocycloalkyle tel que sucre de préférence monosaccharide tel que glucose, γ) (hétéro)aryle tel que phényle, δ) actif cosmétique tel que défini précédemment et X représentant a’) O, S, N(R_a), b’) carbonyle, c’) ou leurs associations de a’) avec b’) tels que ester, amide, urée ;R _a représentant un atome d’hydrogène, un groupe (C₁-C₄)alkyle, ou aryl(C₁-C₄)alkyle tel que benzyle, de préférence R_areprésente un atome d’hydrogène ; et
• interrompue par un ou plusieurs (de préférence un) atomes ou groupes choisis parmi O, S, N(R_a), carbonyle, ou leurs associations telles que ester, amide, urée, avecR _a étant tel que défini précédemment, de préférence R_areprésente un atome d’hydrogène; de préférence un groupe alkyle qui est interrompu par un ou plusieurs atomes choisis parmi O, S, plus préférentiellement par un atome O, ou S notamment S. Particulièrement le radicalR ¹ lorsqu’il représente une chaine hydrocarbonée interrompue, notamment alkyle, est en C₇-C₂₀, plus particulièrement en C₈-C₁₈, encore plus particulièrement en C₉-C₁₆.

According to a particular embodiment of the invention, the hydrocarbon chain (in particular an alkyl group as defined above) of the radical R ¹ of the invention is:

• substituted by one or more (preferably one) groups chosen from a) halogen such as chlorine or bromine, b) hydroxy, c) thiol, d) (di)(C ₁ -C ₄ )(alkyl)amino, preferably amino, e) carboxy, i) (hetero)cycloalkyl such as anhydride, dithiolane or epoxide, j) cosmetic active chosen from colored or uncolored, fluorescent or non-fluorescent chromophores such as optical brighteners, UV filters, h) (hetero)aryl such as phenyl or furyl, k) RX with R representing a group chosen from α) cycloalkyl such as cyclohexyl, β) heterocycloalkyl such as sugar preferably monosaccharide such as glucose, γ) (hetero)aryl such as phenyl, δ) cosmetic active such as defined previously _and R _a representing a hydrogen atom, a (C ₁ -C ₄ )alkyl group, or aryl (C ₁ -C ₄ )alkyl such as benzyl, preferably R _a represents a hydrogen atom; And
• interrupted by one or more (preferably one) atoms or groups chosen from O, S, N(R _a ), carbonyl, or their associations such as ester, amide, urea, with R _a being as defined above, preferably R _a represents a hydrogen atom; preferably an alkyl group which is interrupted by one or more atoms chosen from O, S, more preferably by an O, or S atom in particular S. Particularly the radical R ¹ when it represents an interrupted hydrocarbon chain, in particular alkyl, is in C ₇ -C ₂₀ , more particularly in C ₈ -C ₁₈ , even more particularly in C ₉ -C ₁₆ .

• substituée par un ou plusieurs (de préférence un) groupes choisis parmi a) halogène tels que chlore ou brome,b) hydroxy, d) (di)(C₁-C₄)(alkyl)amino de préférence amino, e) carboxy, i) (hétéro)cycloalkyle tel que époxyde, h) (hétéro)aryle tel que phényl ou furyl, k) R-X avecRreprésentant un groupe choisi parmi α) cycloalkyle tel que cyclohexyle, β) hétérocycloalkyle tel que sucre de préférence monosaccharide tel que glucose, γ) (hétéro)aryle tel que phényle, et X représentant a’) O, S, N(R_a) de préférence S ;R _a représentant un atome d’hydrogène, un groupe (C₁-C₄)alkyle, de préférence R_areprésente un atome d’hydrogène; et
• interrompue par un ou plusieurs (de préférence un) atomes ou groupes choisis parmi O, S, N(R_a), carbonyle, ou leurs associations telles que ester, amide, urée, avecR _a étant tel que défini précédemment, de préférence R_areprésente un atome d’hydrogène; de préférence un groupe alkyle qui est interrompu par un ou plusieurs atomes choisis parmi O, S, plus préférentiellement par un atome O, ou S notamment S. Particulièrement le radicalR ¹ lorsqu’il représente une chaine hydrocarbonée interrompue, notamment alkyle, est en C₇-C₂₀, plus particulièrement en C₈-C₁₈, encore plus particulièrement en C₉-C₁₆.

According to a preferred embodiment of the invention, the hydrocarbon chain (in particular an alkyl group as defined above) of the radical R ¹ of the invention is:

• substituted by one or more (preferably one) groups chosen from a) halogen such as chlorine or bromine, b) hydroxy, d) (di)(C ₁ -C ₄ )(alkyl)amino preferably amino, e) carboxy, i) (hetero)cycloalkyl such as epoxide, h) (hetero)aryl such as phenyl or furyl, k) RX with R representing a group chosen from α) cycloalkyl such as cyclohexyl, β) heterocycloalkyl such as sugar preferably monosaccharide such as glucose, γ) (hetero)aryl such as phenyl, and X representing a') O, S, N(R _a ) preferably S; R _a representing a hydrogen atom, a (C ₁ -C ₄ )alkyl group, preferably R _a representing a hydrogen atom; And
• interrupted by one or more (preferably one) atoms or groups chosen from O, S, N(R _a ), carbonyl, or their associations such as ester, amide, urea, with R _a being as defined above, preferably R _a represents a hydrogen atom; preferably an alkyl group which is interrupted by one or more atoms chosen from O, S, more preferably by an O atom, or S in particular S. Particularly the radical R ¹ when it represents an interrupted hydrocarbon chain, in particular alkyl, is in C ₇ -C ₂₀ , more particularly in C ₈ -C ₁₈ , even more particularly in C ₉ -C ₁₆ .

Preferably said substituted and interrupted hydrocarbon chain is in particular alkyl, and preferably is linear.

More preferably when said hydrocarbon chain R ¹ is substituted, it is substituted at the end of the chain on the opposite side of the carbon atom which carries said radical R ¹ .

According to one embodiment of the invention said hydrocarbon chain R ¹ is of the following formula –(CH ₂ ) _r -X-(ALK) _u -G with X being as defined above, in particular representing O, S, N( R _a ), preferably S, ALK represents a (C ₁ -C ₁₀ ) alkylene chain, linear or branched, preferably linear, more particularly (C ₁ -C ₈ ) alkylene, r represents an integer inclusively between 6 and 11 , preferably between 7 and 10 such as 8; u is 0 or 1; and G represents a hydrogen atom, or a group chosen from hydroxy, carboxy, (di)(C ₁ -C ₄ )(alkyl)amino, (hetero)aryl in particular aryl such as phenyl, cycloalkyl such as cyclohexyl, or sugar, in particular a monosaccharide optionally protected by one or more groups such as acyl, preferably Suc

[Chem. 4]:

According to another particular embodiment of the invention, the PHA copolymer(s) are such that R ¹ represents (C ₃ -C ₃₀ ) alkyl substituted by one or more halogen atoms such as fluorine, chlorine, or bromine. More particularly (C ₄ -C ₂₀ ) alkyl, even more particularly (C ₅ -C ₁₃ ) alkyl, linear, substituted by a halogen atom such as bromine. Preferably the halogen atom is substituted at the end of said alkyl group. More preferably R ¹ represents 1-halo-5-yl such as 1-bromo-5-yl.

According to another particular embodiment of the invention, the PHA copolymer(s) are such that R ¹ represents a (C ₃ -C ₃₀ ) alkyl group substituted by one or more or groups chosen from a) cyano, more particularly represents a group ( C ₃ -C ₁₃ )alkyl, preferably linear, substituted by a g)cyano group, such as 1-cyano-3-propyl.

According to another particular embodiment of the invention, the PHA copolymer(s) are such that R ¹ represents a group vii) (hetero)aryl(C ₁ -C ₂ )alkyl, more particularly aryl aryl(C ₁ -C ₂ )alkyl , preferably phenylethyl.

According to another particular embodiment of the invention, the PHA copolymer(s) are such that R ¹ represents a (C ₅ -C ₂₈ ) alkyl group substituted by one or more or groups chosen from c) (hetero)cycloalkyl. More particularly R ¹ represents a (C ₅ -C ₁₃ ) alkyl group, preferably linear, substituted by a heterocycloalkyl group such as epoxide or dithiolane, preferably epoxide.

In particular the PHA copolymer(s) are such that R ² is chosen from (C ₁ -C ₂₈ ) alkyl, linear or branched, and (C ₂ -C ₂₈ ) linear or branched alkenyl, in particular a linear hydrocarbon group, more particularly (C ₃ -C ₂₀ ) alkyl or (C ₃ -C ₂₀ ) alkenyl, preferably (C ₃ -C ₂₀ ) linear or branched and more particularly linear alkyl.

In particular the PHA copolymer(s) are such that R ² is chosen from (C ₁ -C ₂₈ ) alkyl, linear or branched, and (C ₂ -C ₂₈ ) linear or branched alkenyl, in particular a linear hydrocarbon group, more particularly (C ₃ -C ₂₀ ) alkyl or (C ₃ -C ₂₀ ) alkenyl, preferably the hydrocarbon group has a carbon number corresponding to the number of carbon atoms of the radical R ¹ from which at least one carbon atom is subtracted, preferably corresponding to the number of carbon atoms of the radical R ¹ from which two carbon atoms are subtracted;

According to one embodiment of the invention, the PHA copolymer(s) are such that the radical R ² is a (C ₃ -C ₈ ) alkyl group, linear or branched, preferably linear, particularly in (C ₃ -C ₆ )alkyl, preferably (C ₄ -C ₆ )alkyl such as n -pentyl or n -hexyl.

According to another embodiment of the composition according to the invention, the PHA copolymer(s) comprise a radical R ² (C ₃ -C ₈ ) branched alkyl, particularly in (C ₄ -C ₆ ) alkyl, preferably in (C ₄ -C ₅ ) branched alkyl such as isobutyl.

According to another embodiment of the composition according to the invention, the PHA copolymer(s) of the invention comprise the units (A) having an alkyl radical R ¹ as defined above, the units (B) as defined above and the units (C) having a linear or branched (C ₆ -C ₂₀ )alkenyl radical, particularly (C ₇ -C ₁₄ )alkenyl, more particularly (C ₈ -C ₁₀ )alkenyl, preferably linear and comprising a single unsaturation in end of chain, in particular –[CR ⁴ (R ⁵ )] _q -C(R ⁶ )=C(R ⁷ )-R ⁸ with R ⁴ , R ⁵ , R ⁶ , R ⁷ and R ⁸ , identical or different , representing a hydrogen atom or a (C ₁ -C ₄ ) alkyl group such as methyl, preferably a hydrogen atom and q represents an integer inclusively between 2 and 20, preferably between 3 and 10, more preferably between 4 and 8 such as 6, such as –[CH ₂ ] _q -CH=CH ₂ and q represents an integer inclusively between 3 and 8, preferably between 4 and 6, such as 5.

According to one embodiment of the composition according to the invention, the PHA copolymer(s) comprise units (A) having an alkyl radical R ¹ comprising between 8 and 16 carbon atoms substituted by one or more (preferably one) selected groups among hydroxy, (di)(C ₁ -C ₄ )(alkyl)amino, carboxy, and RX- as defined above, preferably RS- with R representing a cycloalkyl group such as cyclohexyl, heterocycloalkyl such as sugar or preferably monosaccharide such as glucose, optionally substituted aryl(C ₁ -C ₄ )alkyl such as (C ₁ -C ₄ )(alkyl)benzyl or phenylethyl, or heteroaryl(C ₁ -C ₄ )alkyl such as furylmethyl,

According to one embodiment of the composition according to the invention, the copolymer(s) comprise units (B) having an R ² (C ₁ -C ₈ ) alkyl radical, linear or branched, preferably linear, particularly in (C ₂ -C ₆ ) alkyl, preferably (C ₄ -C ₅ ) alkyl such as pentyl.

According to another embodiment of the composition according to the invention, the PHA copolymer(s) comprise units (A) having an alkyl radical R ¹ as defined above, units (B) as defined above and (C) having a linear or branched (C ₆ -C ₂₀ )alkenyl radical, particularly (C ₇ -C ₁₄ )alkenyl, more particularly (C ₈ -C ₁₀ )alkenyl, preferably linear and comprising a single unsaturation at the end of the chain such as – [CH ₂ ] _p -CH=CH ₂ and p represents an integer inclusively between 3 and 8, preferably between 4 and 6, such as 5.

According to a particular embodiment of the invention in the PHA copolymer(s), the unit (A) comprises a hydrocarbon chain as defined previously, in particular ii), said unit (A) being present preferably in a molar percentage ranging from 0.1 to 99%, more preferably a molar percentage ranging from 0.5 and 50%, even more preferably a molar percentage ranging from 1 and 40%, even better a molar percentage ranging from 2 and 30%, a percentage molar ranging from 5 and 20%.

According to a more particular embodiment of the invention in the PHA copolymer(s), the unit (A) is preferably present in a molar percentage ranging from 0.5 to 99%.

According to one embodiment, when R ¹ represents a (C ₃ -C ₃₀ ) alkyl group, the unit (A) is preferably present in a molar percentage ranging from 0.5% to 99%, more preferably 50% to 99%, more particularly from 60 to 99% and even more preferably from 70 to 99%. According to this embodiment, the unit (B) is preferably present in a molar percentage ranging from 2 to 40%; and the unit (C) is preferably present in a molar percentage ranging from 0.5 to 20% relative to all of the units (A) , (B) and (C) .

According to another embodiment when R ¹ represents hydrocarbon chain chosen from i) (C ₅ -C ₂₈ ) alkyl, linear or branched, ii) (C ₅ -C ₂₈ ) alkenyl, linear or branched, iii) (C ₅ - C ₂₈ ) alkynyl, linear or branched, preferably the hydrocarbon group is linear, said hydrocarbon chain being substituted by one or more atoms or groups a) to m) and/or interrupted by one or more heteroatoms or groups a') to c' ) as defined for R ¹ ; in particular represents a hydrocarbon group chosen from (C ₄ -C ₂₈ ) alkyl, linear or branched optionally substituted by one or more atoms or groups a) to m) and/or interrupted by one or more heteroatoms or groups a') to c ') as defined previously, the unit (A) is preferably present in a molar percentage ranging from 0.5% to 99%, more preferably a molar percentage ranging from 1% and 50%, even more preferably a molar percentage ranging from 5% and 40%, even better a molar percentage ranging from 10% and 30%; the unit (B) is present in a molar percentage ranging from 1% to 99.5%, preferably from 1 to 90%, more preferably from 2 to 70%, most particularly from 2% to 40%; and the unit (C) is present in a molar percentage ranging from 0.5% to 20% relative to all of the units (A) , (B) and (C) . Advantageously, the PHA copolymer(s) of the invention comprise from 2% to 10% by mole of unit (B) ; and from 0.5% to 7% by mole of unit (C) , more advantageously the copolymer comprises from 5% to 35% by mole of unit (B) ; and from 0.5% to 7% by mole of unit (C) .

• l’unité(A)comprend une chaine hydrocarbonée substituée par un ou plusieurs atomes ou groupes a) à m) et/ou intérrompue par un ou plusieurs hétéroatomes ou groupes a’) à c’) telle que définie précédemment, ladite unité(A)étant présente en un pourcentage molaire allant de 0,1 à 99 %, préférentiellement un pourcentage molaire allant de 0,5 et 50 %, plus préférentiellement un pourcentage molaire allant de 1 et 40 %, encore plus préférentiellement un pourcentage molaire allant de 2 et 30 %, mieux un pourcentage molaire allant de 5 et 20 % ; encore mieux un pourcentage molaire allant de 10 et 30 % en mole d’unité(A); et
• l’unité(B)est présente en un pourcentage molaire allant de 1 à 40 % ; préférentiellement un pourcentage molaire de 2 à 10 %, plus préférentiellement un pourcentage molaire de 5 à 35 % en mole d’unité(B); et/ou
• l’unité(C)est présente en un pourcentage molaire allant de 0,5 à 20 %, préférentiellement un pourcentage molaire de 1 à 7 %, plus préférentiellement de 0,5 à 7 % en mole d’unité(C).

According to a more particular embodiment of the invention, the PHA copolymer(s) are such as in the PHA copolymer(s) a):

• the unit (A) comprises a hydrocarbon chain substituted by one or more atoms or groups a) to m) and/or interrupted by one or more heteroatoms or groups a') to c') as defined previously, said unit (A) ) being present in a molar percentage ranging from 0.1 to 99%, preferably a molar percentage ranging from 0.5 and 50%, more preferably a molar percentage ranging from 1 and 40%, even more preferably a molar percentage ranging from 2 and 30%, better a molar percentage ranging from 5 and 20%; even better a mole percentage ranging from 10 and 30% by mole of unit (A) ; And
• the unit (B) is present in a molar percentage ranging from 1 to 40%; preferably a mole percentage of 2 to 10%, more preferably a mole percentage of 5 to 35 mole % of unit (B) ; and or
• the unit (C) is present in a mole percentage ranging from 0.5 to 20%, preferably a mole percentage of 1 to 7%, more preferably from 0.5 to 7 mole % of unit (C) .

Preferably when R ¹ of unit (A) is an uninterrupted unsubstituted saturated hydrocarbon chain said unit (A) is present in a molar percentage greater than 30%, more particularly greater than 50%, more preferably greater than 60% preferably between 60 and 90%.

The values of the molar percentages of the units (A), (B) and (C) of the PHA copolymer(s) are calculated relative to the total number of moles of (A) + (B) if the copolymer(s) do not include additional unit (C), otherwise if the copolymer(s) of the invention contain 3 different units (A), (B) and (C) then the mole percentage is calculated in relation to the total number of moles (A) + (B) + (C); otherwise if the copolymer(s) of the invention contain 4 different units (A), (B), (C) and (D) then the mole percentage is calculated in relation to the total number of moles (A) + (B) + (C) + (D); otherwise if the copolymer(s) of the invention contain 5 different units (A), (B), (C), (D) and (E) then the mole percentage is calculated in relation to the total number of moles (A) + (B) + (C) + (D) + (E).

According to one form of the invention, the PHA copolymer(s) of the invention comprise the repeating units(HAS)following, as well as their optical and geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates: R ¹ A1 -ALK ₁ -S-ALK ₂ -COOH A2 -ALK ₁ -S-ALK ₂ -H A3 -ALK ₁ -S-ALK ₂ -OH A4 -ALK ₁ -S-ALK ₂ -NH ₂ AT 5 -ALK ₁ -S-Cycl' A6 -ALK ₁ -S-CH ₂ -Fur A7 -ALK ₁ -S-Suc AT 8 -ALK ₁ -S-ALK ₂ -Ar A9 -ALK ₁ -Hal A10 -ALK ₁ -CN A11 -ALK ₁ -CH=CRrRw AT 12 -ALK ₂ -H ALK₁represents a divalent hydrocarbon radical in C₁-VS₂₀linear or branched, preferably C₁-VS₁₀linear or branched, more preferably linear;
ALK₂represent a divalent hydrocarbon radical in C₁-VS₂₀linear or branched, preferably C₁-VS₁₂linear or branched;
Rr and Rw independently designate a hydrogen atom or an alkyl radical (C₁-VS₄such as methyl, preferably Rr and Rw are identical;
Hal represents a halogen atom such as bromine;
Ar: represents a (hetero)aryl group such as phenyl;
Cycl': represents a cycloalkyl group such as cyclohexyl or heterocycloalkyl such as dithiolane or epoxide, preferably epoxide;
Fur: represents a furyl group, preferably 2-furyl;
Suc: represents a sugar group, in particular a monosaccharide possibly protected by one or more groups such as acyl, in particular acetyl.
Particularly the stereochemistry of carbon atoms carrying R radicals¹is of configuration (R).

According to one form of the invention, the PHA copolymer(s) of the invention comprise the repeating units(B)of formula (A12), as well as their optical, geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates, it being understood that(B)is different from(HAS).

Preferably the PHA copolymer(s) of the invention comprise the following repeating units, as well as their optical, geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates:

[Chem. 5]:

m and n are as defined above, Hal represents a halogen atom such as bromine and t represents an integer between 1 and 10, preferably between 3 and 8 such as 6.
Ar: represents a (hetero)aryl group such as phenyl;
Ar': represents a (C ₁ -C ₄ )alkyl(hetero)aryl group such as t-Butylphenyl, preferably 4- t -butylphenyl;
Cycl: represents a cyclohexyl group;
Fur: represents a furyl group, preferably 2-furyl;
Suc: represents a sugar group, in particular a monosaccharide optionally protected by one or more groups such as acyl, preferably Suc represents:
[Chem. 6]:
Particularly the stereochemistry of the carbon atoms carrying the radicals R ¹ , and R ² is the same configuration (R) or (S), preferably configuration (R).

More particularly the stereochemistry of the carbon atoms carrying the radicals R ¹ , R ² and R ³ is the same configuration (R) or (S), preferably of configuration (R). More particularly the stereochemistry of the carbon atoms carrying the radicals R ¹ , R ² , R ³ , and R ⁴ is the same configuration (R) or (S), preferably of configuration (R).

More particularly the stereochemistry of the carbon atoms carrying the radicals R ¹ , R ² , R ³ , R ⁴ , and R ⁵ is the same configuration (R) or (S), preferably of configuration (R).

More preferably, the PHA copolymer(s) have the following formula, as well as their optical isomers, their organic or mineral acid or base salts, and their solvates such as hydrates:

[Chem. 7]:

M, n, Hal, t, Ar, Ar', Cycl, Fur, and Suc are as defined above for compounds (1) to (14).

Preferably the PHA(s) a) of the invention are chosen from compounds (15), (16) and (17) in particular (16).

More particularly, the PHA(s) a) of the invention are chosen from compounds (15'), (16') and (17') in particular (16').

Preferably the PHA(s) a) of the invention are chosen from compounds (25), (26), (31) and (32) in particular (26).

The PHA copolymer(s) of the invention preferably have a number average molecular weight ranging from 50,000 to 150,000.

The molecular weight can be measured in particular by steric exclusion chromatography. One method is described below in the examples.

The PHA copolymer(s) are particularly present in the composition according to the invention in a content ranging from 0.1 to 65% by weight, relative to the total weight of the composition, preferably ranging from 0.1 to 60% by weight. .
Method of preparation of the PHA copolymer(s):

The methods for preparing the PHA copolymer(s) of the invention are known to those skilled in the art. We can in particular cite the use of microbial strains producing “ functionalizable ” PHA.

By “ functionalizable ” we mean that the PHA copolymer(s) comprises a hydrocarbon chain comprising one or more atoms or groups capable of reacting chemically with another reagent – also called “reactive atoms or reactive groups ” – to lead to a covalent bond Σ with said reagent. The reagent is for example a compound comprising at least one nucleophilic group and said functionalized hydrocarbon chain comprises at least one electrophilic or nucleophobic atom or group, the nucleophilic group(s) reacting with the electrophilic group(s) to graft covalently onto the reagent. The nucleophilic reagent can also react with one or more unsaturations of the alkylenyl group(s) to also lead to grafting by covalent bond of the hydrocarbon chain functionalized by said reagent. The addition reaction can also be radical, a Markovnikov or anti-Markovnikov type addition, a nucleophilic or electrophilic substitution. The addition or condensation reactions can be carried out by radical means or not, using catalysts or not, enzymes or not, heat preferably at a temperature less than or equal to 100°C or without the addition of heat, under pressure greater than 1 atm or not, under inert atmosphere or not, or under oxygen or not.

By “ nucleophile ” we mean any atom or electron-donating group by inductive effect +I and/or mesomer +M. As an electron donor group, we can cite hydroxy, thiol and amino groups.

By “ electrophile ” we mean any atom or group which is electroattractant by inductive effect –I and/or by mesomeric effect –M. As an electroattractor we can cite.

The microorganisms producing PHAs of the invention, in particular with a hydrocarbon chain, can be naturally produced by the Bacterial kingdom such as Cyanobacteria of the order Nostocales (e.g. Nostoc muscorum, Synechocystis and Synechococcus ) but mainly among Proteobacteria, for example in the class of:
- beta - Proteobacteria , of the order Burkholderiales ( Cupriavidus negator synonym Rasltonia eutropha )
- alpha - Proteobacteria , of the order Rhodobacteriales (marine and photosynthetic Rhodobacter capsulatus )
- gamma-Proteobacteria , of the order Pseudomonaes of the family Moraxellaceae (Acinetobacter Junii)

Among the microorganisms of the Bacterial kingdom, the genera Azotobacter, Hydrogenomomas, or Chromatium are the most representative of PHA-producing organisms.

The organisms naturally producing PHAs with a hydrocarbon chain in particular in C ₃ -C ₅ are in particular the Proteobacteria , such as gamma-Proteobacteria , and more particularly of the order of Pseudomonas of the Pseudomonas family such as Pseudomonas resinovorans , Pseudomonas putida , Pseudomonas fluorescens , Pseudomonas aeruginosa , Pseudomonas citronellolis , Pseudomonas mendocina , Pseudomonas chlororaphis and preferably Pseudomonas putida GPo1 and Pseudomonas putida KT2440 , preferably Pseudomonas putida and in particular Pseudomonas putida GPo1 and Pseudomonas putida KT2440.

Some organisms can also naturally produce PHAs without belonging to the order Pseudomonales such as Commamonas testosteroni which belongs to the class of beta-Proteobacteria of the order Burkholderiales of the family Comamonadaceae .

The PHA-producing microorganism according to the invention can also be a recombinant strain if a PHA 3-oxidation synthase metabolic pathway is present. The 3-oxidation PHA synthase metabolic pathway is mainly represented by four classes of EC enzymes: 2.3.1 B2; EC: 2.3.1 B3 EC: 2.3.1 B4 and EC: 2.3.1 B5.

The recombinant strain can be from the Bacteria kingdom such as Escherichia coli , or from the Plantae kingdom such as Chlorella pyrenoidosa ( International Journal of Biological Macromolecules , 116, 552-562 “Influence of nitrogen on growth, biomass composition, production, and properties of polyhydroxyalkanoates (PHAs) by microalgae") or from the kingdom Fungi ex Saccaromyces cerevisiae or Yarrowia lipotyca: Applied Microbiology and Biotechnology 91 , 1327–1340 (2011) "Engineering polyhydroxyalkanoate content and monomer composition in the oleaginous yeast Yarrowia lipolytica by modifying the ß-oxidation multifunctional proteins”).

It is also possible to use genetically modified microorganisms, which can allow for example the increase in PHA production, and/or to increase the oxygen consumption capacity, and/or to decrease autolysis and/or to modify the ratio of monomers.

It is known that for PHAs, a large part of the total production cost is allocated to the culture medium and mainly to the substrate/carbon source. Thus we can use genetically modified microorganisms using less nutrient (carbon source) for their growth, for example photo-autotrophic by nature, ie using light and CO ₂ as the main source of energy.

The copolymer can be obtained in a known manner by biosynthesis, for example with microorganisms belonging to the genus Pseudomonas, such as Pseudomonas resinovorans, Pseudomonas putida, Pseudomonas fluorescens, Pseudomonas aeruginosa, Pseudomonas citronellolis, Pseudomonas mendocina, Pseudomonas chlororaphis and preferably Pseudomonas putida; and with a carbon source which may be a C ₂ -C ₂₀ carboxylic acid, preferably C ₆ -C ₁₈ , such as acetic acid, propionic acid, butyric acid, hexanoic acid , heptanoic acid, octanoic acid, nonanoic acid, dodecanoic acid; an alkenoic acid such as undecylenic acid, a saccharide such as fructose, maltose, lactose, xylose, arabinose, etc. ) ; an n -alkane such as hexane, octane, dodecane; an n -alcohol such as methanol, ethanol, octanol, glycerol; methane, carbon dioxide.

The biosynthesis can optionally be carried out in the presence of an inhibitor of the β-oxidation pathway such as acrylic acid, methacrylic acid, propionic acid, cinnamic acid, salicylic acid, pentenoic acid. , 2-butynoic acid, 2-octynoic acid, phenylpropionic acid, and preferably acrylic acid.

According to one embodiment, the process for preparing PHAs of the invention uses microbial cells producing PHAs by genetically modified microorganisms (GMO). Genetic modification may increase PHA production, increase oxygen uptake capacity, increase resistance to solvent toxicity, decrease autolysis, alter the ratio of PHA co-monomers, and/or any combination of these -this. In some of these embodiments, changing the ratio of unit co-monomers (A) increases the amount of predominant monomer vs (B) of the PHA of the invention obtained. In another embodiment, the PHA-producing microbial cells reproduce naturally.

As an example of a microbial strain producing genetically modified functionalizable PHA or comprising a reactive group, we can cite Pseudomonas entomophila LAC23 ( Biomacromolecules . 2014 Jun 9;15(6):2310-9. doi: 10.1021/bm500669s)

It is also possible to use genetically modified microorganisms producing phenylvaleric co 3-Hydroxydodecanoic copolymers ( Sci China Life Sci , Shen R, et al.,. 57 No.1, (2014) with a strain such as Pseudomonas entomophila LAC23 .

Nutrients such as water-soluble salts based on nitrogen, phosphorus, sulfur, magnesium, sodium, potassium and iron can also be used for biosynthesis.

Known suitable conditions of temperature, pH, dissolved oxygen (DO) can be used for the cultivation of microorganisms.

The microorganisms can be cultivated according to any known cultivation method, such as in a bioreactor in continuous, batch mode, in fed or non-fed mode.

The biosynthesis of the polymers used according to the invention is described in particular in the article “Biosynthesis and Properties of Medium-Chain-Length Polyhydroxyalkanoates with Enriched Content of the Dominant Monomer”, Xun Juan et al; Biomacromolecules 2012, 13, 2926−2932 and in application WO 2011/069244.

The microbial strains producing functionalizable PHA or comprising a reactive group as defined above, are for example of the Pseudomonas genus such as P. cichorii YN2 , P. citronellolis , P. jessenii, and more generally by species of Pseudomonas putida such as Pseudomonas putida GPo1 (synonymous with Pseudomonas oleovorans), P. putida KT2442, P. putida KT2440 , P. putida KCTC 2407, P. putida BM01 and in particular P. putida KT2440.

The source(s) of carbon:

One way to access the PHAs of the invention is to introduce one or more organic compounds into the culture medium, this or these organic compounds represent one or more carbon sources preferably chosen from alkanes, alkenes, alcohols. , carboxylic acids and their mixture.

In one embodiment, the organic compound(s) will preferably be chosen from alcohols, carboxylic acids and their mixture.

1. Source de carbone par un ou plusieurs composés organiques introduit dans le milieu :

Selon un mode de réalisation particulier de l’invention, le ou les composés organiques sont choisis parmi les alcools, en particulier les (C₅-C₂₀)alcanols, et/ou acides carboxyliques, en particulier les acides (C₅-C₂₀)alcanoïques éventuellement substitués et/ou interrompus, notamment les acides (C₅-C₂₀)alcanoïques tels que les acides (C₇-C₁₁)alcanoïques comme l’acide nonanoïque ou acide pélargonique et/ou les acides (C₅-C₂₀)alcènoïques, notamment les acides (C₅-C₂₀)alcènoïques tels que les acides (C₇-C₁₁)alcènoïques comme l’acide undécylènique , et leurs mélanges.The carbon source(s) can be classified into 2 categories:

1. Source of carbon by one or more organic compounds introduced into the environment:

According to a particular embodiment of the invention, the organic compound(s) are chosen from alcohols, in particular (C ₅ -C ₂₀ ) alkanols, and/or carboxylic acids, in particular (C ₅ -C ₂₀ ) acids. )alkanoic acids optionally substituted and/or interrupted, in particular (C ₅ -C ₂₀ )alkanoic acids such as (C ₇ -C ₁₁ )alkanoic acids such as nonanoic acid or pelargonic acid and/or (C ₅ -C) acids ₂₀ ) alkenoic acids, in particular (C ₅ -C ₂₀ ) alkenoic acids such as (C ₇ -C ₁₁ ) alkenoic acids such as undecylenic acid, and mixtures thereof.

• groupe A, le composé organique peut aider à la croissance de la souche productrice et aide à la production de PHA structurellement lié au composé organique.
• groupe B, le composé organique peut aider à la croissance de la souche mais ne participe pas à la production de PHA structurellement lié au composé organique.
• groupe C : le composé organique ne participe pas à la croissance de la souche.

The carbon source(s) can be classified into 3 groups according to their destination:

• group A, the organic compound can aid in the growth of the producing strain and aids in the production of PHA structurally related to the organic compound.
• group B, the organic compound can help the growth of the strain but does not participate in the production of PHA structurally linked to the organic compound.
• group C: the organic compound does not participate in the growth of the strain.

Such microbiological processes are known to those skilled in the art, particularly in the scientific literature. We can cite: International Journal of Biological Macromolecules 28 , 23–29 (2000); The Journal of Microbiology , 45 , No. 2, 87-97, (2007).

According to a variant, the integration of the substrate which is structurally linked to the reactive atom(s) or to the reactive group(s) of the PHA(s) of the invention is introduced directly into the medium as a unique carbon source in a suitable medium for microbial growth. (Example: group A for P.putida GPo1 : alkenoic acid in particular terminals).

According to another variant, the integration of the substrate which is structurally linked to the reactive atom(s) in particular halogen or to the reactive group(s) of the PHA(s) of the invention is introduced into the medium as a carbon source. with a second carbon source as a co-substrate that is also structurally linked to the PHA in a medium suitable for microbial growth. (Example: group B for P.putida GPo1 : preferably terminal haloalkanoic acids such as terminal Bromo-alkanoic acids).

According to yet another variant, the integration of the substrate which is structurally linked to the reactive atom(s) in particular halogen or to the reactive group(s) of the PHA(s) of the invention can be introduced directly into the medium as carbon source with a second co-substrate carbon source that is also structurally related to the PHA(s) and a third co-substrate carbon source that is not structurally related to the PHA(s) in a suitable medium for microbial growth. (Example: group C glucose or sucrose).

In one embodiment, the inhibitor of the beta oxidation pathway is acrylic acid, 2-butynoic acid, 2-octynoic acid, phenylpropionic acid, propionic acid, trans-acid cinnamic acid, salicylic acid, methacrylic acid, 4-pentenoic acid or 3-mercaptopropionic acid, preferably acrylic acid.

In one embodiment of the first aspect, the functionalized fatty acid is a functionalized hexanoic acid, functionalized heptanoic acid, functionalized octanoic acid, functionalized nonanoic acid, functionalized decanoic acid, functionalized undecanoic acid, functionalized dodecanoic acid or functionalized tetradecanoic acid.

• pour une fonctionnalisation du ou des PHA avec un groupe alkyl ramifié ou branché : voir par ex.Applied and Environmental Microbiology,.60, No.9, 3245-325 (1994) ;
• pour une fonctionnalisation du ou des PHA avec un groupe alkyl linéaire comprenant un motif terminal en cyclohexyl : voir par ex. doi.org/10.1016/S0141-8130(01)00144-1 ;
• pour une fonctionnalisation du ou des PHA avec un groupe alkyl insaturé de préférence terminal voir par ex. doi.org/10.1021/bm8005616) ;
• pour une fonctionnalisation du ou des PHA avec un groupe alkyl linéaire comprenant un halogène de préférence en terminaison de la chaine hydrocarbonée (doi.org/10.1021/ma00033a002) ;
• pour une fonctionnalisation du ou des PHA avec un groupe (hétéro)aromatique alkyle par exemple phényl, benzoyl, phénoxy, voir par ex.J.Microbiol. Biotechnol, 11, 3,435-442 (2001) ;
• pour une fonctionnalisation du ou des PHA avec un groupe alkyl linéaire comprenant un hétéroatome notamment en terminaison de chaine hydrocarbonée, voir par ex. DOI 10.1007/s00253-011-3099-4 ;
• pour une fonctionnalisation du ou des PHA avec un groupe alkyl linéaire comprenant une fonction cyano notamment en terminaison de chaine hydrocarbonée, voir par ex. .org/10.1111/j.1574-6968.1992.tb05839.x ;
• pour une fonctionnalisation du ou des PHA avec un groupe alkyl linéaire comprenant une fonction époxy notamment en terminaison de chaine hydrocarbonée, voir par ex. doi.org/10.1016/S1381-5148(97)00024-2 ;

La revueInternational Microbiology16:1-15 (2013) doi:10.2436/20.1501.01.175) mentionne également la majorité des PHA natifs fonctionnalisés.The functionalization can be introduced by an organic compound chosen from the precursors of the alcohol and/or carboxylic acid category, in particular:

• for functionalization of the PHA(s) with a branched or branched alkyl group: see e.g. Applied and Environmental Microbiology, . 60 , No.9, 3245-325 (1994);
• for functionalization of the PHA(s) with a linear alkyl group comprising a terminal cyclohexyl unit: see e.g. doi.org/10.1016/S0141-8130(01)00144-1;
• for functionalization of the PHA(s) with a preferably terminal unsaturated alkyl group see e.g. doi.org/10.1021/bm8005616);
• for functionalization of the PHA(s) with a linear alkyl group comprising a halogen preferably at the end of the hydrocarbon chain (doi.org/10.1021/ma00033a002);
• for functionalization of the PHA(s) with a (hetero)aromatic alkyl group, for example phenyl, benzoyl, phenoxy, see e.g. J. Microbiol. Biotechnol, 11 , 3,435-442 (2001);
• for functionalization of the PHA(s) with a linear alkyl group comprising a heteroatom in particular at the end of the hydrocarbon chain, see e.g. DOI 10.1007/s00253-011-3099-4;
• for functionalization of the PHA(s) with a linear alkyl group comprising a cyano function in particular at the end of the hydrocarbon chain, see e.g. .org/10.1111/j.1574-6968.1992.tb05839.x;
• for functionalization of the PHA(s) with a linear alkyl group comprising an epoxy function in particular at the end of the hydrocarbon chain, see e.g. doi.org/10.1016/S1381-5148(97)00024-2;

The journal International Microbiology 16:1-15 (2013) doi:10.2436/20.1501.01.175) also mentions the majority of functionalized native PHAs.

In a particular embodiment of the invention, the group A fatty acid is chosen from 11-undecenoic acid, 10-epoxyundecanoic acid, 5-phenyl valeric acid, citronellol, and acid 5-cyanopentanoic.

In a particular embodiment of the invention, the group A fatty acid is chosen from halogenooctanoic acids such as 8-bromooctanoic acid.

1. Source de carbone en présence d’inhibiteur d’oxydation introduit dans le milieu :

In a particular embodiment of the invention, the carbon source of group C is a monosaccharide, preferably glucose.

1. Source of carbon in the presence of an oxidation inhibitor introduced into the environment:

Another aspect of the invention is the use of microbial strains producing PHA, in a medium suitable for microbial growth, said medium comprising: a substrate which is structurally linked to the PHA(s); at least one carbon source that is not structurally related to the PHA(s); and at least one inhibitor of the oxidation pathway, in particular beta oxidation. This allows the growth of microbial cells to occur in said medium, the microbial cells synthesize the PHA polymer(s) of the invention; preferably copolymer having particularly more than 95% identical unit, which has a co-monomer ratio of unit (A) and unit (B) which differs from that obtained in the absence of the inhibitor of the pathway. beta oxidation.

The diagram below illustrates by way of example the functionalization of PHA copolymers according to the invention from PHA copolymer with an unsaturated hydrocarbon chain according to the following diagram 1:

• R ² ,m, etnsont tels que définis précédemment ;
• Yreprésente un groupe choisi parmi Hal tel que chlore ou brome, hydroxy, thiol, (di)(C₁-C₄)(alkyl)amino, R-X avecRreprésentant un groupe choisi parmi α) cycloalkyle tel que cyclohexyle, β) hétérocycloalkyle tel que sucre de préférence monosaccharide tel que glucose, γ) (hétéro)aryle tel que phényle ; δ) actif cosmétique tel que défini précédemment ; ε) (C₁-C₂₀)alkyle, (C₂-C₂₀)alkényle, (C₂-C₂₀)alkynyle ; et X représentant a’) O, S, N(R_a) ou Si(R_b)(R_c) ou e) (C₁-C₂₀)alkyle, linéaire ou ramifié, avec R_a, R_bet R_ctels que définis précédemment;
• q’représente un entier compris inclusivement entre 2 et 20, de préférence entre 3 et 10, plus préférentiellement entre 4 et 8 tel que 6, mieux entre 3 et 8, de préférence entre 4 et 6, tel que 5.

[Chem. 8]:
Diagram 1 in which:

• R ² , m , and n are as defined previously;
• Y represents a group chosen from Hal such as chlorine or bromine, hydroxy, thiol, (di)(C ₁ -C ₄ )(alkyl)amino, RX with R representing a group chosen from α) cycloalkyl such as cyclohexyl, β) heterocycloalkyl such as sugar, preferably monosaccharide such as glucose, γ) (hetero)aryl such as phenyl; δ) cosmetic active ingredient as defined previously; ε) (C ₁ -C ₂₀ )alkyl, (C ₂ -C ₂₀ )alkenyl, (C ₂ -C ₂₀ )alkynyl; _{and _ _ _ _ _ _ _} as defined previously;
• q' represents an integer inclusively between 2 and 20, preferably between 3 and 10, more preferably between 4 and 8 such as 6, better still between 3 and 8, preferably between 4 and 6, such as 5.

Other reactions can be carried out from double or triple unsaturations such as Michael additions, Diels-Alder additions, radical additions, catalytic hydrogenation reactions (in particular with Pd, Ni) or not, hydrogenation reactions. halogenation in particular with bromine, hydration, controlled or uncontrolled oxidation, and reactions on electrophiles as shown schematically below:

• une chaine hydrocarbonée R¹linéaire ou ramifiée saturée, substituée et/ou intérrompue par des atomes ou groupes tels que définis précédemment pour R¹, comprenant au total entre 5 et 30 atomes de carbone, de préférence entre 6 et 20 atomes de carbone plus particulièrement entre 7 et 11 carbone et
• une chaine hydrocarbonée R²représentant un radical (C₃-C₂₀)alkényle linéaire ou ramifié, particulièrement (C₅-C₁₄)alkényle, plus particulièrement (C₇-C₁₀)alkényle, de préférence linéaire et comprenant une seule insaturation en bout de chaine, en particulier –[CR⁴(R⁵)]_q-C(R⁶)=C(R⁷)-R⁸avec R⁴, R⁵, R⁶, R⁷et R⁸, identiques ou différents, représentant un atome d’hydrogène ou un groupe (C₁-C₄)alkyle tel que méthyle, de préférence un atome d’hydrogène et q représente un entier compris inclusivement entre 2 et 20, de préférence entre 3 et 10, plus préférentiellement entre 4 et 8 tel que 6, tel que –[CH₂]_q-CH=CH₂et q représente un entier compris inclusivement entre 3 et 8, de préférence entre 4 et 6, tel que 5 ,

ladite chaine R²comprenant entre 1 et 99 %, préférentiellement entre 2 à 50% et encore plus préférentiellement entre 3 et 40% d’insaturations, et encore plus particulièrement entre 3 et 30 % d’insaturation, mieux entre 5 et 20% d’insaturations. Selon ce mode particulier de l’invention dans lequel les copolymères PHA comprenent des insaturations, ces insaturations peuvent être modifiés chimiquement :
A) par des réactions d’addition, telles que des additions radicalaires, additions de Michael, additions électrophiles, réaction de Diels-Alder, d’halogénation, d’hydratation, d’hydrogénation, et de préférence d’hydrothiolation avec des particules, des composés chimiques ou des polymères.According to a particular embodiment of the invention, the PHA copolymers comprise

• a saturated linear or branched hydrocarbon chain R ¹ , substituted and/or interrupted by atoms or groups as defined above for R ¹ , comprising in total between 5 and 30 carbon atoms, preferably between 6 and 20 carbon atoms more particularly between 7 and 11 carbon and
• a hydrocarbon chain R ² representing a linear or branched (C ₃ -C ₂₀ )alkenyl radical, particularly (C ₅ -C ₁₄ )alkenyl, more particularly (C ₇ -C ₁₀ )alkenyl, preferably linear and comprising a single unsaturation in end of chain, in particular –[CR ⁴ (R ⁵ )] _q -C(R ⁶ )=C(R ⁷ )-R ⁸ with R ⁴ , R ⁵ , R ⁶ , R ⁷ and R ⁸ , identical or different , representing a hydrogen atom or a (C ₁ -C ₄ ) alkyl group such as methyl, preferably a hydrogen atom and q represents an integer inclusively between 2 and 20, preferably between 3 and 10, more preferably between 4 and 8 such as 6, such as –[CH ₂ ] _q -CH=CH ₂ and q represents an integer inclusively between 3 and 8, preferably between 4 and 6, such as 5,

said R ² chain comprising between 1 and 99%, preferably between 2 to 50% and even more preferably between 3 and 40% unsaturations, and even more particularly between 3 and 30% unsaturation, better still between 5 and 20% d unsaturations. According to this particular mode of the invention in which the PHA copolymers comprise unsaturations, these unsaturations can be chemically modified:
A) by addition reactions, such as radical additions, Michael additions, electrophilic additions, Diels-Alder reaction, halogenation, hydration, hydrogenation, and preferably hydrothiolation with particles, chemical compounds or polymers.

• Les alcanethiols linéaires, ramifiés, cycliques ou aromatiques comportant 1 à 14 atomes de carbone, tel que méthane-, éthane-, propane-, pentane-, cyclopentane-, hexane-, cyclohexane-, heptane-, octane, phénylethane-, 4-tert-butylphénylmethane-, 2-furanmethane-thiol, de préférence hexane-, cyclohexane-, heptane-, octane, phénylethane-, 4-tert-butylphénylmethane-, 2-furanmethane-thiol ;
• Les organosiloxanes portant une fonction thiol, tels que le (3-mercaptopropyl)trimethoxysilane, le (3-Mercaptopropyl)methyldimethoxysilane, le 2-(Triethoxysilyl)ethanethiol, le mercaptopropyl-isobutyl-POSS ;
• Les Huiles silicones thiolées notamment celle décrites dans le document DOI : 10.1016/j.actbio.2015.01.020) ;
• Les oligomères ou polymères thiolés portant une fonction réactive, tel qu’une amine, un alcool, un acide, un halogène, un thiol, un époxyde, un nitrile, un isocyanate, un hétéroatome, de préférence la cysteine, la cystéamine, la N-acetylcysteamine, 2-Mercaptoethanol, 1-Mercapto-2-propanol, 8-Mercapto-1-octanol, l’acide thiolactique, l’acide thioglycolique, l’acide mercapto-3-propionique, l’acide 11-mercaptoundecanoique, le polyéthylene glycol dithiol, le 3-Mercaptopropionitrile, le 1,3-Propanedithiol, le4-Cyano-1-butanethiol, le 3-Chloro-1-propanethiol, le 1-Thio-β-D-glucose tetraacetate ; et
• Les thiols pouvant être obtenus à partir de la réduction de disulfide, tel que le phenyldisulfide, le furfuryl disulfide.

Particularly, the hydrothiolation reactions can be carried out in the presence of a thermal initiator, an oxidation-reduction (redox) initiator or a photochemical initiator and an organic compound carrying a sulfhydryl group, in particular chosen from:

• Linear, branched, cyclic or aromatic alkanethiols containing 1 to 14 carbon atoms, such as methane-, ethane-, propane-, pentane-, cyclopentane-, hexane-, cyclohexane-, heptane-, octane, phenylethane-, 4- tert-butylphenylmethane-, 2-furanmethane-thiol, preferably hexane-, cyclohexane-, heptane-, octane, phenylethane-, 4-tert-butylphenylmethane-, 2-furanmethane-thiol;
• Organosiloxanes carrying a thiol function, such as (3-mercaptopropyl)trimethoxysilane, (3-Mercaptopropyl)methyldimethoxysilane, 2-(Triethoxysilyl)ethanethiol, mercaptopropyl-isobutyl-POSS;
• Thiolated silicone oils, in particular those described in the document DOI: 10.1016/j.actbio.2015.01.020);
• Thiolated oligomers or polymers carrying a reactive function, such as an amine, an alcohol, an acid, a halogen, a thiol, an epoxide, a nitrile, an isocyanate, a heteroatom, preferably cysteine, cysteamine, N -acetylcysteamine, 2-Mercaptoethanol, 1-Mercapto-2-propanol, 8-Mercapto-1-octanol, thiolactic acid, thioglycolic acid, mercapto-3-propionic acid, 11-mercaptoundecanoic acid, polyethylene glycol dithiol, 3-Mercaptopropionitrile, 1,3-Propanedithiol, 4-Cyano-1-butanethiol, 3-Chloro-1-propanethiol, 1-Thio-β-D-glucose tetraacetate; And
• Thiols obtainable from the reduction of disulfide, such as phenyldisulfide, furfuryl disulfide.

As an initiator, we can cite for example: tert-butyl peroxy-2-ethylhexanoate, cumin perpivalate, tert-butyl peroxylaurate, benzoyl peroxide, lauroyl peroxide, octanoyl peroxide, di-tert-peroxide butyl, tert-butylcumyl peroxide, dicumyl peroxide, 2,2'-azobis isobutyronitrile, 2,2'-azobis(2-methylbutyronitrile), 2,2'-azobis(2,4-dimethylvaleronitrile), 2,2' -azobis(4-methoxy-2,4-dimethylvaleronitrile), 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane, 1,1-bis(tert-butylperoxy)cyclohexane, 1,4-bis (tert-butylperoxycarbonyl)cyclohexane, 2,2-bis(tert-butylperoxy)octane, 4,4-bis(tert-butylperoxy)valerate of n-butyl, 2,2-bis(tert-butylperoxy)butane, 1,3 -bis(tert-butylperoxyisopropyl)benzene, 2,5-dimethyl-2,5-di(tert-butylperoxy)hexane, 2,5-dimethyl-2,5-di(benzoylperoxy)hexane, di-tert-diperoxy isophthalate butyl, 2,2-bis(4,4-di-tert-butylperoxycyclohexyl)propane, di-tert-butyl peroxy-α-methylsuccinate, di-tert-butyl peroxydimethylglutarate, di-tert-butyl peroxyhexahydroterephthalate, di-tert-butyl peroxyazelate di-tert-butyl, 2,5-dimethyl-2,5-di(tertbutylperoxy)hexane, diethylene glycol bis(tert-butylperoxycarbonate), di-tert-butyl peroxytrimethyladipate, tris(tertbutylperoxy) triazine, vinyltris(tert-butylperoxy )silane phenothiazine, tetracene, perylene, anthracene, diphenyl-9-10-anthracene, thioxanthone, benzophenone, acetophenone, xanthone, fluorenone, anthraquinone, 9, 10-dimethylanthracene, 2-ethyl-9, 10-dimethyloxyanthracene, 2, 6- dimethyl- naphthalene, 2, 5-diphenyl-1-34-oxadiazole, xanthopinacol, 1, 2-benzanthracene, 9-nitro-anthracene. Each of these primers can be used alone or in combination with others.

The chemical reactions mentioned above are known to those skilled in the art. We can cite in particular the following documents: Synthesis and preparation of PHAs modified with polyethylene glycol dithiol: 10.1021/acs.biomac.9b00479; Biomacromolecules , 19 , 3536–3548 (2018); Synthesis and preparation of PHAs modified with mercaptohexanol: 10.1021/acs.biomac.8b01257; Biomacromolecules , 20 , 2, 645–652 (2019); Synthesis and preparation of PHAs modified with Hydroxy-, Cinnamic Acid-, Sulfate-, and Zosteric Acid: 10.1021/bm049962e; Biomacromolecules , 5 , 4, 1452–1456 (2004); Radical addition of methyl methacrylate to a PHOUn: 10.1002/1521-3935(20010701)202:11<2281::AID-MACP2281>3.0.CO;2-9; Macromolecular Chemistry and Physics, vol. 202, 11 , 2281-2286 (2001); Synthesis and preparation of PHAs modified with a polysilsesquioxane (POSS): 10.1016/j.polymer.2005.04.020; Polymer Vol. 46, 14 , 5025-5031 (2005); Grafting of thio-beta-glucose on unsaturated side chains: 1022-1336/99/0202–0091$17.50+.50/0; Macromol. Rapid Commun., 20 , 91–94 (1999)
And or
B) by oxidation reactions controlled or not, for example with permanganates of concentrated or diluted alkaline agent, or ozonolysis, oxidation in the presence of a reducing agent, and make it possible to obtain new materials having in terminal position side chains of hydroxy, epoxide or carboxy groups.

The chemical reactions mentioned above are known to those skilled in the art. We can cite in particular the following documents: 10.1021/bm049337; Biomacromolecules , vol. 6, 2 , 891–896 (2005); 10.1016/S0032-3861(99)00347-X; Polymer , vol. 41, 5 , 1703-1709 (2000); 10.1021/ma9714528 and 10.1016/S1381-5148(97)00024-2; Macromolecules , 23, 15, 3705–3707 (1990); 10.1016/S0032-3861(01)00692-9; Polymer , vol 43, 4 , 1095-1101 (2002); 10.1016/S0032-3861(99)00347-X; Polymer, vol 41, 5 , 1703-1709 (2000); and 10.1021/bm025728h ; Biomacromolecules , vol 4, 2 , 193–195 (2003).

Example of functionalization of PHA copolymers according to the invention from PHA copolymer with a hydrocarbon chain with an epoxy group according to the following diagram 2:

[Chem. 9]:

Scheme 2 in which Y, m, n, q’, and R2 are as defined in scheme 1.

The epoxidized structure can be obtained by conventional method known to those skilled in the art, whether by biotechnological processes, or by chemical means such as the oxidation of unsaturation as mentioned previously. The peroxide group(s) can react with carboxylic acids, maleic anhydrides, amines, alcohols, thiols, isocyanates, all of these reagents comprising at least one C ₁ -C ₂₀ hydrocarbon chain, linear or branched, cyclic or acyclic, saturated or unsaturated, or carried by an oligomer or polymer in particular amino (poly)saccharides such as compounds derived from chitosan and (poly)sil(ox)anes; 3-glycidyloxypropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-(trimethoxysilyl)propylcarbamic acid, diethanolamine, 3-mercapto-1-propanesulfonate of alkali or alkaline earth salts such as sodium. the water.

• Préparation de PHA portant des charges à partir de diéthanolamine : 10.1021/bm8005616,Biomacromolecules, vol 9,8, 2091–2096 (2008) ;
• Préparation de PHA portant des charges à partir de 3-mercapto-1-propanesulfonate de sodium : 10.1021/acs.biomac.9b00870Biomacromolecules, vol 20, 9, 3324–3332 (2019);
• Préparation de PHA comportant un motif époxyde natif: 10.1016/S1381-5148(97)00024-2) ;Reactive and Functional Polymers,vol 34,1, , 65-77 (1997)

We can cite in particular the following documents:

• Preparation of charged PHA from diethanolamine: 10.1021/bm8005616, Biomacromolecules , vol 9, 8 , 2091–2096 (2008);
• Preparation of charged PHA from sodium 3-mercapto-1-propanesulfonate: 10.1021/acs.biomac.9b00870 Biomacromolecules , vol 20, 9, 3324–3332 (2019);
• Preparation of PHA comprising a native epoxy unit: 10.1016/S1381-5148(97)00024-2); Reactive and Functional Polymers, vol 34, 1 , 65-77 (1997)

Example of functionalization of PHA copolymers according to the invention from PHA copolymer with a hydrocarbon chain with a nucleofuge group according to the following diagram 3:

[Chem. 10]:

Scheme 3 in which Y, m, n, q', and R ² are as defined in scheme 1. M corresponds to a nucleofuge group, organic or inorganic, which can be substituted by a nucleophilic group, preferably said nucleophile is a heteroatom electron donor by +I and/or +M effect such as O, S, or N. Preferably the nucleofuge M is chosen from halogen atoms such as Br, and mesylate, tosylate or triflate groups. This is a reaction known to those skilled in the art. We can cite for example the following document 10.1016/j.ijbiomac.2016.11.118, International Journal of Biological Macromolecules , vol 95, 796-808 (2017).

Example of functionalization of PHA copolymers according to the invention from PHA copolymer with a hydrocarbon chain with a cyano group according to the following diagram 4:

[Chem. 11]:
:

Scheme 4 in which Y, m, n, q', Y and R ² are as defined in scheme 1.

In a first step i) the PHA copolymer with a side chain with a cyano or nitrile group reacts with an organoalkaline or organomagnesium compound Y-MgHal, Y-Li, or Y-Na, followed by hydrolysis to lead to the PHA copolymer with a side chain with group Y grafted with a ketone function. The ketone function can be changed to thioketone by thionation for example with S8 in the presence of amine, or with Lawesson's reagent. The latter after total reduction ii) (for example by Clemensen reduction) leads to the PHA copolymer with a side chain with a Y group grafted with an alkylene group. Or the latter can be reduced in a gentle manner iii) by a conventional reducer to lead to the PHA copolymer with a side chain with a Y group grafted with a hydroxyalkylene group. The cyano group of the starting PHA copolymer can react with water after hydration v) to lead to the amide derivative, after hydrolysis iv) to the carboxy derivative. The cyano group of the starting PHA copolymer can also after reduction vi) lead to the amine derivative or the ketone derivative. The PHA copolymers with a nitrile-functional hydrocarbon side chain are prepared by conventional methods known to those skilled in the art. We can for example cite the document: 10.1016/0378-1097(92)90311-B, FEMS Microbiology Letters , vol. 103, 2-4 , 207-214 (1992).

Example of functionalization of PHA copolymers according to the invention from PHA copolymer with a hydrocarbon chain at the end of the chain according to the following diagram 5:

[Chem. 12]:

Scheme 5 in which R ¹ , R ² , m, n and Y are as defined above, and R' ¹ represents a hydrocarbon chain chosen from i) (C ₁ -C ₂₀ ) alkyl, linear or branched, ii) (C ₂ -C ₂₀ )alkenyl, linear or branched, iii) (C ₂ -C ₂₀ )alkynyl, linear or branched, iii) preferably the hydrocarbon group is linear; said hydrocarbon chain being substituted by one or more atoms or groups chosen from: a) halogen such as chlorine or bromine, b) hydroxy, c) thiol, d) (di)(C ₁ -C ₄ )(alkyl)amino, e ) (thio)carboxy, f) (thio)carboxamide –C(O)-N(R _a ) ₂ or –C(S)-N(R _a ) ₂ , f) cyano, g) iso(thio)cyanate, h) (hetero)aryl such as phenyl or furyl, and i) (hetero)cycloalkyl such as anhydride, or epoxide, j) cosmetic active chosen from colored or uncolored, fluorescent or non-fluorescent chromophores such as those from optical brighteners, or chromophores from UVA and/or UVB filters, anti-aging active ingredients.

• Préparation d’oligomères de PHAs par dégradation thermique : 10.1021/bm0156274 ;Biomacromolecules, vol 3,1, 219–224 (2002) ;
• Préparation d’oligomères de PHAs par transestérification : 10.1021/ma011420r,Macromolecules, vol 35,3, 684–689 (2002) ;
• Préparation d’oligomères de PHAs par hydrolyse : 10.1016/0032-3861(94)90590-8Polymer vol 35, 19, 4156-4162 (1994) ;
• Préparation d’oligomères de PHAs par méthanolyse : 10.1021/bm060981t,Biomacromolecules, vol 8,4, 1255–1265 (2007) ;

These grafts at the end of the chain are known on PHA polymers by those skilled in the art. For example, we can cite the following documents:

• Preparation of PHAs oligomers by thermal degradation: 10.1021/bm0156274; Biomacromolecules , vol 3, 1 , 219–224 (2002);
• Preparation of PHA oligomers by transesterification: 10.1021/ma011420r, Macromolecules , vol 35, 3 , 684–689 (2002);
• Preparation of PHA oligomers by hydrolysis: 10.1016/0032-3861(94)90590-8Polymer vol 35, 19, 4156-4162 (1994);
• Preparation of PHA oligomers by methanolysis: 10.1021/bm060981t, Biomacromolecules , vol 8, 4 , 1255–1265 (2007);

• Synthèse et caractérisation de PHA greffé avec de l’acide ascorbique : 10.1016/j.ijbiomac.2018.11.052 ;International journal of biological macromolecules, vol 123: 7 (2019) ;
• Préparation de copolymères PHB-b-PHO par polycondensation avec du divinyl adipate catalysée par une lipase : 10.1021/bm9011634,Biomacromolecules, vol 10,12, 3176–3181 (2009) ;
• Synthèse de copolymères PHB-b-PHO couplés par une jonction diisocyanate : 10.1021/ma012223v ;Macromolecules, vol 35,13, 4946–4950 (2002) ;
• Préparation d’oligomères de PHO sur du chitosan par condensation entre l’extrémité acide carboxylique du PHO et les fonctions amines du chitosan : 10.1002/app.24276 ;Journal of Applied Polymer Science, vol 103,1, (2006);
• Transestérification des PHAs par l’alcool propargylique afin de produire des oligomères de PHAs modifiables par chimie « click » : 10.1016/j.reactfunctpolym.2011.12.005 ;Reactive and Functional Polymers ,vol 72, 2, , 160-167 (2012) ;
• Préparation de copolymère PHO-b-PCL : 10.1002/mabi.200400104 ;Macromolecular Bioscience, vol 4,11(2004) ;
• Préparation de copolymère PHO-b-PEG : 10.1002/macp.201000562 ;Macromolecular Chemistry and Physics; vol 212, 3, (2010) ;
• Epoxydation d’insaturation en bout de chaine et greffage d’acide en bout de chaine : 10.14314/polimery.2017.317 ;Polimery, vol 62,4, 317-322 (2017) ;
• Greffage de motif organosiloxane en bout de chaine sur PHA : 10.1016/j.reactfunctpolym.2014.09.008 ;Reactive and Functional Polymers,vol 84, 53-59 (2014).

We can also cite other methods known to those skilled in the art:

• Synthesis and characterization of PHA grafted with ascorbic acid: 10.1016/j.ijbiomac.2018.11.052; International journal of biological macromolecules , vol 123: 7 (2019);
• Preparation of PHB-b-PHO copolymers by lipase-catalyzed polycondensation with divinyl adipate: 10.1021/bm9011634, Biomacromolecules , vol 10, 12 , 3176–3181 (2009);
• Synthesis of PHB-b-PHO copolymers coupled by a diisocyanate junction: 10.1021/ma012223v; Macromolecules , vol 35, 13 , 4946–4950 (2002);
• Preparation of PHO oligomers on chitosan by condensation between the carboxylic acid end of PHO and the amine functions of chitosan: 10.1002/app.24276; Journal of Applied Polymer Science , vol 103, 1 , (2006);
• Transesterification of PHAs with propargyl alcohol in order to produce PHA oligomers that can be modified by “click” chemistry: 10.1016/j.reactfunctpolym.2011.12.005; Reactive and Functional Polymers , vol 72, 2, 160-167 (2012);
• Preparation of PHO-b-PCL copolymer: 10.1002/mabi.200400104; Macromolecular Bioscience , vol 4, 11 (2004);
• Preparation of PHO-b-PEG copolymer: 10.1002/macp.201000562; Macromolecular Chemistry and Physics ; vol 212, 3, (2010);
• Epoxidation of unsaturation at the end of the chain and acid grafting at the end of the chain: 10.14314/polimery.2017.317; Polimery , vol 62, 4 , 317-322 (2017);
• Grafting of organosiloxane motif at the end of the chain on PHA: 10.1016/j.reactfunctpolym.2014.09.008; Reactive and Functional Polymers, vol 84, 53-59 (2014).

All of the grafted PHA copolymers of the invention described previously, according to diagram 6:

[Chem. 13]:

Scheme 6 in which R' ¹ , R ² , m, n and Y are as defined previously, and
X ' represents an atom or reactive group likely to react with an atom or electrophilic group E or nucleophilic nucleophilic to create a convincing bond σ if x' is an electrophilic or nucleofuge group so it can react with a reagent r ' ¹ - naked, if X' is a Nu nucleophilic group so it can react with R' ¹ - E to create a covalent bond Σ;

As an example, the covalent bonds or Σ bonding group that can be generated are listed in the table below from the condensation of electrophiles with nucleophiles:

[Painting. 1]:

It is also possible, from a PHA functionalized in the side chain, to carry out grafting at the end of the chain in a second step as described in diagram 7. The converse is also true, where grafting at the end of the chain is possible in a first step, then the functionalization of functionalizable pendant side chain is carried out in a second step.

[Chem. 14]:
Scheme 7 in which R' ¹ , R ² , m, n and Y are as defined previously, and

• Synthèse et préparation de PHAs modifiés par thiol-ène, puis réaction sur nouvelle fonction greffée : 10.1021/ma0304426 ;Macromolecules, vol 37,2, 385–389 (2004) ;
• Greffage de PEG et de PLA sur de PHAs fonctionnalisés avec des acides : 10.1002/marc.200900803 et 10.1002/mabi.200390033 ;
• Synthèse et préparation de PHAs modifiés avec du polyéthylène glycol dithiol : 10.1021/acs.biomac.9b00479.

All these chemical reactions are known to those skilled in the art. For example, we can cite the following documents:

• Synthesis and preparation of PHAs modified by thiol-ene, then reaction on new grafted function: 10.1021/ma0304426; Macromolecules , vol 37, 2 , 385–389 (2004);
• Grafting of PEG and PLA onto PHAs functionalized with acids: 10.1002/marc.200900803 and 10.1002/mabi.200390033;
• Synthesis and preparation of PHAs modified with polyethylene glycol dithiol: 10.1021/acs.biomac.9b00479.

b) the polyurethane latex(es)

The composition C1 or C1' of the invention comprises one or more polyurethane latexes

By “polyurethane” or “polyurethane” is meant a urethane polymer, i.e. an organic polymer comprising the repeat function -N(R)-C(O)-O-.

• B₁₁) un polyester polyol issu de la réaction de :
  • au moins un polyol B₁₁₁) avec
  • au moins un acide polycarboxylique B₁₁₂) et
  • éventuellement B₁₁₃) au moins un monoacide carboxylique ;
• B₁₂) un diol ; et
• le mélange de B₁₁) et B₁₂) ; et

B₂) d’au moins un polyisocyanate, de préférence un diisocyanate, en particulier aliphatique ou cycloaliphatique et ses mélanges ; et
B₃) d’au moins un monomère hydrophile choisi parmi :

• B₃₁) les composés porteurs d’une fonction acide, notamment carboxylique, ou d’une fonction basique, notamment amine primaire, secondaire ou tertiaire, et comprenant en outre au moins une fonction hydroxyle, de préférence au moins deux fonctions hydroxyles, en particulier deux fonctions hydroxyles tel que l’acide 2,2-bis(hydroxyméthyl)propionique et
• B₃₂) les composés diaminés de formuleH ₂ N-R ₅ -NH ₂ (X)dans laquelleR ₅ représente un radical alkylène substitué par un ou plusieurs groupes ioniques ou potentiellement ioniques ; et

B₄) éventuellement d’au moins un composé aminé qui n’est pas substitué par un ou plusieurs groupes ioniques ou potentiellement ioniques.The polyurethane latex(es) of the invention is(are) capable of being obtained from:
B ₁ ) of at least one polyol chosen from:

• B ₁₁ ) a polyester polyol resulting from the reaction of:
  • at least one polyol B ₁₁₁ ) with
  • at least one polycarboxylic acid B ₁₁₂ ) and
  • optionally B ₁₁₃ ) at least one monocarboxylic acid;
• B ₁₂ ) a diol; And
• the mixture of B ₁₁ ) and B ₁₂ ); And

B ₂ ) of at least one polyisocyanate, preferably a diisocyanate, in particular aliphatic or cycloaliphatic and its mixtures; And
B ₃ ) of at least one hydrophilic monomer chosen from:

• B ₃₁ ) compounds carrying an acid function, in particular carboxylic, or a basic function, in particular primary, secondary or tertiary amine, and further comprising at least one hydroxyl function, preferably at least two hydroxyl functions, in particular two hydroxyl functions such as 2,2-bis(hydroxymethyl)propionic acid and
• B ₃₂ ) diamine compounds of formula H ₂ NR ₅ -NH ₂ (X) in which R ₅ represents an alkylene radical substituted by one or more ionic or potentially ionic groups; And

B ₄ ) optionally of at least one amino compound which is not substituted by one or more ionic or potentially ionic groups.

• B₁₁) au moins un polyester polyol issu de la réaction de :
  • au moins un polyol B₁₁₁) tel que le néopentylglycol, l’hexanediol , le butanediol avec
  • au moins un acide polycarboxylique B₁₁₂) comme l’acide adipique, l’acide succinique et éventuellement B₁₁₃) au moins un monoacide carboxylique de préférence l’acide abiétique ou la colophane ; et/ou B₁₂) au moins un diol; et leur mélange ; et

B₂) d’au moins un polyisocyanate, de préférence au moins un diisocyanate, en particulier aliphatique ou cycloaliphatique comme l’isocyanate de 3-isocyanatométhyle-3,5,5-triméthylcyclohexane (diisocyanate d'isophorone ou IPDI), le bis-(4-isocyanatocyclohexyl)-méthane hexamethylène diisocyanate et leur mélange ; et
B₃) d’au moins un monomère hydrophile choisi parmi B₃₁) les composés porteurs d’une fonction acide, par exemple une fonction carboxylique, ou d’une fonction basique, par exemple une fonction amine primaire, secondaire ou tertiaire, et comprenant en outre au moins une fonction hydroxyle, de préférence au moins deux fonctions hydroxyles, en particulier deux fonctions hydroxyles tel que l’acide 2,2-bis(hydroxyméthyl)propionique et/ou B₃₂) au moins un composé diaminé de formuleH ₂ N-R ₅ -NH ₂ (X)dans laquelleR ₅ représente un radical alkylène substitué par un ou plusieurs groupes ioniques ou potentiellement ioniques tel que carboxy; et
B₄) éventuellement au moins au moins un composé aminé qui n’est pas substitué par un ou plusieurs groupes ioniques ou potentiellement ioniques.
B ₁₁ ) Polyester Polyol More particularly, the polyurethane latex(es) of the invention is(are) capable of being obtained from:
B ₁ ) of at least one polyol chosen from:

• B ₁₁ ) at least one polyester polyol resulting from the reaction of:
  • at least one polyol B ₁₁₁ ) such as neopentyl glycol, hexanediol, butanediol with
  • at least one polycarboxylic acid B ₁₁₂ ) such as adipic acid, succinic acid and optionally B ₁₁₃ ) at least one monocarboxylic acid, preferably abietic acid or rosin; and/or B ₁₂ ) at least one diol; and their mixture; And

B ₂ ) of at least one polyisocyanate, preferably at least one diisocyanate, in particular aliphatic or cycloaliphatic such as 3-isocyanatomethyl-3,5,5-trimethylcyclohexane isocyanate (isophorone diisocyanate or IPDI), bis- (4-isocyanatocyclohexyl)-methane hexamethylene diisocyanate and their mixture; And
B ₃ ) of at least one hydrophilic monomer chosen from B ₃₁ ) compounds carrying an acid function, for example a carboxylic function, or a basic function, for example a primary, secondary or tertiary amine function, and comprising in addition at least one hydroxyl function, preferably at least two hydroxyl functions, in particular two hydroxyl functions such as 2,2-bis(hydroxymethyl)propionic acid and/or B ₃₂ ) at least one diamine compound of formula H ₂ NR ₅ -NH ₂ (X) in which R ₅ represents an alkylene radical substituted by one or more ionic or potentially ionic groups such as carboxy; And
B ₄ ) optionally at least at least one amino compound which is not substituted by one or more ionic or potentially ionic groups.
B ₁₁ ) Polyester Polyol

According to one form of the invention, the polyurethane polymer of latex b) is prepared from at least one polyester polyol B ₁₁ ) resulting from the reaction of at least one polyol B ₁₁₁ ) with at least one polycarboxylic acid B ₁₁₂ ) and optionally B ₁₁₃ ) at least one monocarboxylic acid; and/or B ₁₂ ) at least one diol.
B ₁₁₁ ) Polyol

According to one form of the invention, the polyester polyol B ₁₁ ) is obtained from at least one polyol B ₁₁₁ ) component. The polyol B ₁₁₁ ) preferably comprises from 2 to 6 hydroxyl groups (-OH), in particular two, three or four hydroxyl groups.

According to one form of the invention, the polyester polyols B ₁₁ ) are dihydroxylated polyesters resulting from the reaction of at least one dihydroxylated organic compound (diol) with at least one polycarboxylic acid.

According to a particular embodiment, the polyol B ₁₁₁ ) is an organic compound comprising a hydrocarbon chain, linear or branched, acyclic or (poly)cyclic, saturated or unsaturated, aromatic or not, comprising from 3 to 18 carbon atoms, in particularly from 4 to 12 carbon atoms, or even from 5 to 10 carbon atoms; and from 2 to 6 hydroxyl groups, said hydrocarbon chain being optionally interrupted by one or more oxygen atoms, in particular which may have ether functions.

As examples of such polyols B ₁₁₁ ), we can cite, without this list being exhaustive, i) oses such as pentoses such as ribose, arabinose, xylose, lyxose, ribulose, xylulose or hexoses such as allose, altrose, galactose, glucose, idose, mannose, talose, fructose, sorbose or even deoxyhexoses such as fucose or rhamnose; ii) triols such as glycerol, iii) tetraols such as pentaerythritol (tetramethylolmethane), erythritol, diglycerol, iv) pentols such as xylitol, v) hexols such as sorbitol and mannitol, or also dipentaerythritol or triglycerol, and their mixtures.

According to a particular embodiment, the polyol B ₁₁₁ ) is a diol of formula (I) HO-ALK-OH (I) in which ALK represents a C ₁ -C ₁₈ alkylene group, in particular C ₁ -C ₈ , linear or branched. The polyol B ₁₁₁ ) is then a (C ₁ -C ₈ ) alkane diol. As examples of (C ₁ -C ₈ ) alkane diols, we can cite without this list being exhaustive, ethylene glycol, butylene glycol, 1,2-propanediol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 1,6-hexanediol, neopentyl glycol.

According to a particular embodiment, the polyol B ₁₁₁ ) is an alkane diol whose alkylene chain is interrupted by one or more oxygen atoms such as, for example, diethylene glycol, triethylene glycol, polyethylene glycol,

According to a particular embodiment, polyol B ₁₁₁ ) is an alkane diol whose alkylene chain is interrupted by one or more ester groups such as for example hydroxypivalic acid neopentyl glycol ester.

According to one embodiment, the polyol B ₁₁₁ ) may be an oligomer derived from one or more diols of formula (I) above with a weight average molecular mass of between 200 and 4,000 g.mol ^-1 , in particular between 300 and 3,000 g.mol ^-1 . By way of example, the compound of formula (I) is such that ALK represents a (C ₁ -C ₆ ) alkylene group, the oligomer then being a poly(C ₁ -C ₆ ) alkane diol. Mention may in particular be made of polypropane diol (also known under the name polypropylene glycol) with a weight average molecular mass of between 300 and 3,000 g.mol ^-1 , or polyethylene glycol with a weight average molecular mass of between 300 and 3 000 g.mol ^-1 .

Among the dihydroxylated compounds B ₁₁₁ ) which can be used according to the present invention, mention may in particular be made of compounds having two hydroxy groups and a number molecular weight of approximately 700 to approximately 16,000, and preferably of approximately 750 to approximately 5000. A as an example of dihydroxy compounds having a high molecular weight, mention may be made of polyol polyethers, polyhydroxylated polycarbonates, polyhydroxylated polyacetates, polyhydroxylated polyacrylates, polyhydroxylated amide polyesters, polyhydroxylated polyalkadienes, polyhydroxylated polythioethers and mixtures thereof . Preferably, the hydroxylated compounds are chosen from polyol polyethers, polyhydroxylated polycarbonates and mixtures thereof.

According to another particular embodiment, the polyol B ₁₁₁ ) can be chosen from organic polyols chosen from:
- triols, such as glycerol;
- tetraols, such as pentaerythritol (tetramethylolmethane), erythritol, diglycerol;
- pentols such as xylitol;
- hexols such as sorbitol and mannitol, or even dipentaerythritol or triglycerol; and their mixtures.

According to a particular embodiment, the polyol B ₁₁₁ ) comprises at least one compound chosen from glycerol, pentaerythritol and/or sorbitol. In particular, the polyol B ₁₁₁ ) can be chosen from glycerol, pentaerythritol, sorbitol and their mixtures, more preferably glycerol.

According to another particular embodiment, the polyol B ₁₁₁ ) comprises at least one diol of formula (I) .

According to another embodiment, the polyol B ₁₁₁ ) is a mixture of at least one diol of formula (I) and at least one diol such as a polyether.
B ₁₁₂ ) Polyacid

According to one form of the invention, the polyurethane polymer of latex b) is prepared from at least one polyester polyol B ₁₁ ) resulting from the reaction of at least one polyol B ₁₁₁ ) as described previously with at least one polycarboxylic acid B ₁₁₂ ) also called in the rest of the text "polyacid", and possibly B ₁₁₃ ) at least one monocarboxylic acid.

Said polyacid B ₁₁₂ ) may be acyclic or (poly)cyclic, saturated or unsaturated, aromatic or not, linear or branched, and comprises at least two -C(O)OH carboxyl groups, in particular two to four -C(O) groups. )OH and more particularly two -C(O)OH groups.

It is understood that the polyester polyol B ₁₁ ) can be prepared from a single polyacid or a mixture of at least two polyacids. In the rest of the text, unless otherwise indicated, the term "polyacid" or "polycarboxylic acid" means a single polyacid compound or a mixture of several polyacid compounds.

Said polycarboxylic acid B ₁₁₂ ) may be more particularly chosen from linear, branched and/or cyclic, saturated or unsaturated, or even aromatic polycarboxylic acids, comprising from 2 to 54 carbon atoms, in particular from 2 to 40 and more particularly from 3 to 36 carbon atoms, said acid comprising at least two carboxyl groups -C(O)OH, in particular from 2 to 4 carboxyl groups.

In particular, polycarboxylic acid B ₁₁₂ ) can contain two carboxyl groups; we then speak of dicarboxylic acid or diacid.

According to a particular embodiment, said polycarboxylic acid B ₁₁₂ ) can be chosen from polycarboxylic acids, in particular dicarboxylic acids, having a molecular molar mass MM less than or equal to 200 g.mol ^-1 . In particular, said polycarboxylic acid B ₁₁₂ ) can be chosen from oxalic acid, succinic acid, adipic acid, and their mixtures, as well as their optical, geometric isomers, their salts of organic or mineral bases, and their solvates such as hydrates.

According to another particular embodiment of the invention, the polycarboxylic acid B ₁₁₂ ) used to form the polyester polyol B ₁₁ ) can be chosen from acids, in particular diacids, with a molecular molar mass MM greater than 200 g .mol ^-1 . In particular, the polycarboxylic acid B ₁₁₂ ) can be chosen from fatty acids (also called polyfatty acids), in particular dicarboxylic fatty acids (also called difatty acids), and in particular from fatty acid dimers.

By the expression "fatty acid" is meant a carboxylic acid comprising at least one aliphatic chain, linear or branched, preferably linear, saturated or unsaturated, which may contain at least one carbocycle, in particular one or two carbocycle(s). , in particular of the mono or polycyclic cycloalkyl type, for example cyclohexyl or decalinyl ( cis or trans decalinyl). The fatty acids are C ₈ to C ₃₈ acids, in particular C ₈ to C ₃₆ , in particular C ₁₀ to C ₃₄ , it being understood that the number of carbons characterizing a fatty acid takes into consideration the aliphatic chain of the fatty acid and the carbon atom(s) of said carboxyl group(s). Preferably, the number of carbon atoms of the fatty acid is even.

The dicarboxylic fatty acids can be chosen from the compounds of formula (II) below, as well as their organic or mineral base salts, and their solvates such as hydrates: HO-C(O)-ALK'-C(O)- OH (II) in which ALK' represents an aliphatic chain as defined above for the fatty acid, preferably C ₁₆ to C ₃₆ , in particular C ₃₂ to C ₃₆ , in particular C ₃₄ .

Examples of dicarboxylic fatty acids include sebacic acid and fatty acid dimers. The expression “fatty acid dimer” refers to the dimerization product of mono- or poly-unsaturated fatty acids.

Thus, in a particular embodiment, the polyacid component B ₁₁₂ ) comprises at least, or even is formed, a diacid of fatty acid dimer type.

The fatty acids from which fatty acid dimers can be prepared can be more particularly chosen from oleic acid, linoleic acid, palmitoleic acid, linolenic acid, eleostearic acid and their mixtures.

The polyacid B ₁₁₂ ) may be a dimer of C ₁₈ to C ₃₈ fatty acids, in particular C ₃₄ to C ₃₈ and more particularly C ₃₆ .

In particular, the fatty acid dimer may be a diacid of formula (II) mentioned above, in which ALK' represents an aliphatic chain, preferably in C ₁₆ to C ₃₆ , in particular in C ₃₂ to C ₃₆ , in particular in C ₃₄ , incorporating at least one carbocycle group, preferably one or two carbocycle(s), and more preferably a central carbocycle group, in particular of the mono or polycyclic cycloalkyl type, in particular cyclohexyl or decalinyl, in particular cyclohexyl.

In a particular embodiment, the polycarboxylic acid B ₁₁₂ ) can be a diacid of fatty acid dimer type, containing a cycloalkyl group, in particular cyclohexyl, connected to the -C(O)-OH groups via alkylene chains in C ₂ to C ₁₀ , in particular in C ₄ to C ₈ , in particular in C ₆ , said cycloalkyl group having in particular pendant alkyl groups in C ₄ to C ₁₂ , in particular in C ₇ to C ₉ , in particular in _C8 .

In particular, the fatty acid dimer can be formed from C ₁₆ to C ₂₀ fatty acids, in particular C ₁₈ , for example from oleic acid and/or linoleic acid.

Fatty acid dimers may be commercially available. As examples, we can cite the fatty acid dimers marketed by the company Croda under the references Pripol ^® , in particular Pripol ^® 1009, of cosmetic grade, of the following structure:

in which n is an integer between 6 and 8.

According to a particular embodiment, the polyacid component B ₁₁₂ ) may comprise, or even consist of, diacid(s) of fatty acid dimer type, for example Pripol ^® 1009.

According to another embodiment, the polyacid component B ₁₁₂ ) may comprise, or even consist of, diacid(s) having a molecular molar mass MM less than or equal to 200 g.mol ^-1 , in particular chosen from oxalic acid , succinic acid, adipic acid, and mixtures thereof.
B ₁₁₃ ) Monoacid

According to one form of the invention, the polyurethane polymer of latex b) is prepared from at least one polyester polyol B ₁₁ ) resulting from the reaction of at least one polyol B ₁₁₁ ) as described previously with at least one polycarboxylic acid B ₁₁₂ ) as described above, and at least one monocarboxylic acid B ₁₁₃ ).

The monocarboxylic acid is also called a monocarboxylic acid, or “monoacid”, that is to say comprising a single carboxyl group -C(O)-OH.

The monocarboxylic acids B ₁₁₃ ) considered are more particularly acyclic or (poly)cyclic monocarboxylic acids, saturated or unsaturated, aromatic or not, linear or branched, comprising from 6 to 32 carbon atoms, in particular from 8 to 28 carbon atoms. and more particularly from 10 to 20 carbon atoms.

It is understood that the polyester polyol B ₁₁ ) can be prepared from a single monoacid B ₁₁₃ ) or from a mixture of at least two monoacids B ₁₁₃ ). In the remainder of the text, unless otherwise indicated, the term “monoacid” or “monocarboxylic acid” B ₁₁₃ ) means a single monoacid compound or a mixture of several monoacid compounds.

According to a particular embodiment, said monocarboxylic acid B ₁₁₃ ) is non-aromatic, saturated or unsaturated, linear or branched, cyclic or not, and comprises from 6 to 32 carbon atoms, in particular from 8 to 30 carbon atoms and more particularly from 10 to 28 carbon atoms, preferably from 12 to 26 carbon atoms, more preferably from 16 to 24 carbon atoms, even more preferably from 18 to 22 carbon atoms.

Preferably, said monoacid component B ₁₁₃ ) is biosourced, in particular of plant origin.

When the monoacid B ₁₁₃ ) used is of natural origin, it may in particular consist of mixtures comprising saturated acids and unsaturated acids with conjugated and/or non-conjugated unsaturations.

According to a particular embodiment, said monocarboxylic acid B ₁₁₃ ) is a fatty acid, saturated or unsaturated, preferably biosourced.

According to a first particular embodiment, said monoacid B ₁₁₃ ) is a monocarboxylic acid comprising an aliphatic chain, linear or branched, preferably linear, saturated or unsaturated, comprising more than 10 carbon atoms, in particular more than 14 carbon atoms , in particular from 14 to 30 carbon atoms, in particular from 14 to 26 carbon atoms and more particularly from 16 to 22 carbon atoms, even more preferably from 18 to 20 carbon atoms.

As examples, a monoacid B ₁₁₃ ) can be chosen from isostearic acid (branched saturated at C ₁₈ ), stearic acid (linear saturated at C ₁₈ ), linoleic acid (linear polyunsaturated at C ₁₈ ) , arachidic acid (linear saturated in C ₂₀ ), behenic acid (linear saturated in C ₂₂ ) and their mixtures, as well as their geometric isomers, their salts of organic or mineral bases.

According to another particular embodiment, said monoacid B ₁₁₃ ) is a (poly)cyclic monocarboxylic acid, preferably polycyclic, comprising in particular a fused mono, bicyclic, or tricyclic carbocycle, saturated and/or unsaturated, preferably unsaturated, in particular non-aromatic, and comprising from 5 to 20 carbon atoms, said carbocycle being optionally substituted by one or more (C ₁ -C ₄ ) alkyl groups such as methyl. In particular, said monoacid B ₁₁₃ ) comprises a polycyclic carbocycle, in particular a tricyclic fused at C ₈ -C ₁₄ , preferably unsaturated and non-aromatic, such as a partially hydrogenated phenantrenyl group, in particular a decahydrophenantrenyl group.

It may in particular be abietic acid or one of its optical isomers, its salts of organic or mineral bases, and their solvates, such as hydrates. In particular, abietic acid can be derived from natural rosin.

According to another particular embodiment, said monoacid B ₁₁₃ ) can be rosin.

Rosin is a mixture comprising mainly organic acids called rosin acids of which abietic acid is the main constituent.
According to a particular embodiment, said monoacid B ₁₁₃ ) may comprise at least abietic acid or rosin. In particular, the monoacid B ₁₁₃ ) can be abietic acid or rosin.
B ₁₂ ) Diols

According to one embodiment, the composition C1 or C1' of the invention comprises one or more polyurethane polymer latexes b) obtained from B ₁ ) at least one polyol chosen from B ₁₂ ) at least one diol.

According to one embodiment, the diol B ₁₂ ) is a “low molecular weight diol”, having a molecular weight of approximately 62 to 700, and preferably of 62 to 200. These diols may comprise aliphatic, alicyclic or aromatic. Preferably, they only include aliphatic groups.

Preferably, B ₁₂ ) represents a low molecular weight diol, having more than 20 carbon atoms, more preferably chosen from ethylene glycol, diethylene glycol, propane 1,2-diol, propane 1,3-diol , butane 1,4-diol, butylene 1,3-glycol, neopentyl glycol, buthyl-ethyl-propane diol, cyclohexane diol, 1,4-cyclohexane dimethanol, hexane 1,6-diol, bisphenol A (2,2-bis(4-hydroxyphenyl)propane), hydrogenated bisphenol A (2,2-bis(4-hydroxycyclohexyl)propane), and mixtures thereof.

Low molecular weight diols may optionally include ionic or potentially ionic groups. Examples of low molecular weight diols containing ionic or potentially ionic groups are described in particular in US patent 3,412,054. Such compounds are preferably chosen from dimethylol butanoic acid, dimethylol propionic acid, polycaprolactone diols containing a carboxyl group and mixtures thereof.

If lower molecular weight diols containing ionic or potentially ionic groups are used, they are preferably used in an amount such that less than 0.30 meq of C(O)-OH per gram of polyurethane in the polyurethane dispersion are present.

According to another embodiment, the diol B ₁₂ ) is a compound having two hydroxy groups and a number molecular weight of approximately 700 to approximately 16,000, and preferably of approximately 750 to approximately 5000. By way of example of dihydroxy compounds having a high molecular weight, mention may be made of polyol polyethers, polyhydroxylated polycarbonates, polyhydroxylated polyacetates, polyhydroxylated polyacrylates, polyhydroxylated amide polyesters, polyhydroxylated polyalkadienes, polyhydroxylated polythioethers and mixtures thereof. Preferably, the hydroxylated compounds are chosen from polyol polyethers, polyhydroxylated polycarbonates and mixtures thereof. In particular, polyalkylene glycols can be used, such as polyethylene, polypropylene and/or polybutylene glycols.
B2) Polyisocyanate

As indicated previously, a polyurethane of latex b) is obtained from at least one polyisocyanate B ₂ ).

It is understood that the polyurethane of latex b) can be prepared from a single polyisocyanate or a mixture of at least two distinct polyisocyanates. In the remainder of the text, unless otherwise indicated, the term "polyisocyanate" B ₂ ) means a single polyisocyanate compound or a mixture of several polyisocyanates.

The polyisocyanates B ₂ ) used according to the invention can be aliphatic, cycloaliphatic or aromatic polyisocyanates capable of allowing the formation of polyurethanes.

In particular, the polyisocyanates B ₂ ) can be chosen from diisocyanates and triisocyanates, and more particularly diisocyanates.

The polyisocyanates which can be used according to the present invention are in particular chosen from organic diisocyanates having a molecular weight of approximately 112 to 1000, and preferably of approximately 140 to 400.

According to one form of the invention, the polyisocyanates B ₂ ) are chosen from diisocyanates and more particularly from those represented by the general formula R ₂ (NCO) ₂ , in which R ₂ represents a divalent aliphatic hydrocarbon group having from 4 to 18 carbon atoms, a divalent cycloaliphatic hydrocarbon group having 5 to 15 carbon atoms, a divalent araliphatic hydrocarbon group having 7 to 15 carbon atoms or a divalent aromatic hydrocarbon group having 6 to 15 carbon atoms. Preferably, R ₂ represents an organic diisocyanate. As an example of organic diisocyanates, one can in particular choose tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, dodecamethylene diisocyanate, 1,3-diisocyanatocyclohexane, 1,4-diisocyanatocyclohexane, isocyanate of 3-isocyanatomethyl-3,5,5-trimethylcyclohexane (isophorone diisocyanate or IPDI), bis-(4-isocyanatocyclohexyl)-methane, 1,3-bis(isocyanatomethyl)-cyclohexane, 1,4-bis( isocyanatomethyl)-cyclohexane, bis-(4-isocyanato-3-methyl-cyclohexyl)-methane, isomers of toluene diisocyanate (TDI) such as toluene 2,4-diisocyanate, toluene 2,6-diisocyanate and mixtures thereof, hydrogenated toluene diisocyanate, 4,4'-diphenylmethane diisocyanate and mixtures with its isomers 2,4-diphenylmethane diisocyanate and optionally 2,2'-diphenylmethane diisocyanate, naphthalene 1,5-diisocyanate , and their mixtures. Preferably, the diisocyanates are aliphatic and cycloaliphatic diisocyanates, and are more preferably chosen from 1,6-hexamethylene diisocyanate, 3-isocyanatomethyl-3,5,5-trimethylcyclohexane isocyanate and mixtures thereof.

According to another form of the invention, the diisocyanates B ₂ ) can be more particularly chosen from the compounds of formula (III) following O=C=NRN=C=O with R representing a divalent hydrocarbon group, linear or branched, acyclic or (poly)cyclic, saturated or unsaturated, aromatic or not, comprising from 2 to 20 carbon atoms, in particular from 3 to 18 carbon atoms, in particular from 5 to 16 carbon atoms and more particularly from 6 to 14 carbon atoms carbon.

The diisocyanates may more particularly be of the aforementioned formula (III) , in which R represents a divalent aliphatic hydrocarbon group having from 4 to 18 carbon atoms, a divalent cycloaliphatic hydrocarbon group having from 5 to 15 carbon atoms, a divalent araliphatic hydrocarbon group having from 7 to 15 carbon atoms or a divalent aromatic hydrocarbon group having from 6 to 15 carbon atoms.

The diisocyanate(s) B2) which can be used for the preparation of a latex polyurethane b) according to the invention are advantageously chosen from tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, dodecamethylene diisocyanate, 1,3-diisocyanatocyclohexane, 1,4-diisocyanatocyclohexane, 3-isocyanatomethyl-3,5,5-trimethylcyclohexane isocyanate (isophorone diisocyanate or IPDI), bis-(4-isocyanatocyclohexyl)-methane, 1 ,3-bis(isocyanatomethyl)-cyclohexane, 1,4-bis(isocyanatomethyl)-cyclohexane, bis-(4-isocyanato-3-methyl-cyclohexyl)-methane, isomers of toluene diisocyanate (TDI) such as toluene 2,4-diisocyanate, toluene 2,6-diisocyanate and mixtures thereof, hydrogenated toluene diisocyanate, diphenylmethane 4,4'-diisocyanate and mixtures with its isomers diphenylmethane 2,4-diisocyanate and optionally Diphenylmethane 2,2'-diisocyanate, naphthalene 1,5-diisocyanate, and mixtures thereof. Preferably, the diisocyanate(s) are chosen from aliphatic and cycloaliphatic diisocyanates.

More particularly, a single polyisocyanate is used, in particular a single diisocyanate. In particular, the polyisocyanate B ₂ ) can be 3-isocyanatomethyl-3,5,5-trimethylcyclohexane isocyanate, also called isophorone diisocyanate (IPDI) or the isomers bis (4,4'-isocyanatocyclohexyl) methanes, l hexamethylene diisocyanate.

Said polyisocyanate(s) B ₂ ), for example isophorone diisocyanate, can be used to form the polyurethane of latex b).
B ₃ ) Hydrophilic monomers

The composition C1 or C1' of the invention comprises one or more latexes of polyurethane polymers obtained from B ₃ ) at least one hydrophilic monomer chosen from B ₃₁ ) compounds carrying an acid function, for example a function carboxylic, or a basic function, for example a primary, secondary or tertiary amine function, and further comprising at least one hydroxyl function, preferably at least two hydroxyl functions, in particular two hydroxyl functions such as acid 2, 2-bis(hydroxymethyl)propionic or B ₃₂ ) at least one diamine compound of formula H ₂ NR ₅ -NH ₂ (X) in which R ₅ represents an alkylene radical substituted by one or more ionic or potentially ionic groups;

Said hydrophilic compound, integrated at the level of a polyurethane latex polymer b) advantageously allows stabilization of the polymer thus formed in aqueous dispersion (latex), without requiring the addition of surfactant.
B31) Compounds carrying an acid, or basic, and hydroxyl function

According to one form of the invention, the composition C1 or C1' comprises one or more latexes of polyurethane polymers b) obtained from B ₃ ) at least one hydrophilic monomer chosen from B ₃₁ ) compounds carrying a function acid or a basic function and further comprising at least one hydroxyl function.

These hydrophilic compounds B ₃₁ ) may be compounds carrying an acid function, for example a carboxylic function, or a basic function, for example a primary, secondary or tertiary amine function, and further comprising at least one hydroxyl function. , preferably at least two hydroxyl functions, in particular two hydroxyl functions.

A polyurethane latex polymer b) can be obtained from a single hydrophilic monomer B ₃₁ ) or from a mixture of at least two hydrophilic monomers B ₃₁ ). Preferably, it uses a single hydrophilic monomer.

The acid functions (respectively basic) of the hydrophilic monomers B ₃₁ ) can optionally be neutralized, partially or totally, by a base (respectively an acid), preferably organic.

Said hydrophilic compound(s) B ₃₁ ) used in the preparation of a polyurethane latex polymer b) can be more particularly chosen from:
the compounds of formula (IV) R''-C(O)-OH in which R'' represents a linear or branched, saturated or unsaturated, C ₁ to C ₁₀ alkyl group, substituted by one or more hydroxyl groups.

Preferably, R'' represents a branched, saturated C ₁ to C ₈ alkyl group, in particular C ₁ to C ₆ , substituted by one or more hydroxyl groups, in particular by 1 to 4 hydroxyl groups, in particular by at least two hydroxyl groups, in particular by 2 to 4 hydroxyl groups, for example by two hydroxyl groups. As an example of a compound of formula (IV) , mention may be made of 2,2-bis(hydroxymethyl)propionic acid (DMPA);
Said hydrophilic compound(s) B ₃₁ ) used in the preparation of a polyurethane latex polymer b) can also be chosen from the compounds of formula (V) R ₁ R ₂ R ₃ N in which R ₁ , R ₂ and R ₃ represent, independently of each other, an alkyl chain, linear or branched, saturated or unsaturated, C ₁ to C ₁₀ , optionally substituted by one or more hydroxyl groups, or a hydrogen atom, it being understood that at least one of R ₁ , R ₂ and R ₃ is other than a hydrogen atom and carries at least one hydroxyl group. As examples of a compound of formula (V) , mention may be made of N-methyldiethanolamine or N-tertbutyldiethanolamine.

According to a first variant embodiment, the hydrophilic monomer(s) B ₃₁ ) used in the composition of a polyurethane polymer latex b) are of formula (IV) mentioned above. In the context of this variant, said hydrophilic monomer(s) may be more particularly of formula (IV) in which R'' represents a branched alkyl chain, saturated at C ₁ to C ₁₀ , in particular at C ₁ to C ₈ and more particularly in C ₁ to C ₆ , substituted by one or more hydroxyl groups.

According to one embodiment, a single hydrophilic monomer of formula (IV) above, in particular as defined above, is used in the composition of a polyurethane polymer latex b). In particular, it may be 2,2-bis(hydroxymethyl)propionic acid (DMPA).

According to another alternative embodiment, the hydrophilic monomer(s) B ₃₁ ) used in the composition of a polyurethane latex polymer b) are of the aforementioned formula (V). In the context of this variant, said hydrophilic monomer(s) may be more particularly of formula (V) , in which R ₁ , R ₂ and R ₃ represent, independently of each other, an alkyl chain, linear or branched, saturated or unsaturated, C ₁ to C ₁₀ , optionally substituted by one or more hydroxyl groups, or a hydrogen atom, provided that at least one of R ₁ , R ₂ and R ₃ is different from an atom d hydrogen and carries at least one hydroxyl group.

According to one embodiment, a single hydrophilic monomer B ₃₁ ) of formula (V) above, in particular as defined above, is used in the composition of an alkyd-polyurethane polymer b). In particular, it may be N-methyldiethanolamine or N-tertbutyldiethanolamine.

A polyurethane latex polymer b) obtained from at least one additional hydrophilic monomer is advantageously neutralized, totally or partially, by addition of a base or an acid (neutralization agent), depending on the nature of the functions (acids or basic) of the hydrophilic monomer(s) used in the composition of the polyurethane polymer. It is up to those skilled in the art to adjust the quantity of neutralization agent to be introduced into the reaction medium to obtain the desired neutralization.

In particular, a neutralization percentage of a polyurethane polymer as described above may be greater than or equal to 70%, in particular between 70 and 100%. The neutralization percentage represents the percentage of acidic functions (respectively basic) of the polyurethane polymer neutralized (in salt form). It can be evaluated in relation to the quantity of neutralizing agent added.

Thus, the hydrophilic monomer B ₃₁ ) can be chosen from the compounds of formula (IV) and (V) mentioned above in which the acid or basic functions are preferably neutralized, totally or partially, by addition of a base or a acidic, preferably organic.

In particular, in a polyurethane polymer of latex b) obtained from at least one additional hydrophilic monomer of formula (IV) above, the acid functions of the monomeric units can be in neutralized form, totally or partially, by an organic base or mineral, preferably organic, in particular chosen from primary, secondary or tertiary amines, which may or may not contain substituents, for example hydroxyl groups, such as for example amino-2-methyl-2-propanol, and salified forms of these.

According to a particular embodiment, a polyurethane of latex b), obtained from at least one additional hydrophilic monomer of formula (IV) mentioned above, can be neutralized by a tertiary amine such as diisopropylethylamine.

Other bases can also be used, such as potash, soda or ammonia.

In a polyurethane polymer of latex b) obtained from at least one additional hydrophilic monomer of formula (V) above, the amine functions of the monomeric units can advantageously be in neutralized form, totally or partially, by an organic or mineral acid, preferably organic. As examples, mention may be made of hydrochloric acid, acetic acid or tartaric acid.

According to a particular embodiment, the polyurethane of latex b) is prepared from at least one hydrophilic monomer, in particular from a single hydrophilic monomer, of formula (IV) above, and more particularly 2,2 acid -bis(hydroxymethyl)propionic acid (DMPA), the acid functions being advantageously, totally or partially, neutralized, preferably by an organic base, in particular by a tertiary amine such as diisopropylethylamine.
B32) Diamines H ₂ NR ₅ -NH ₂ (X),

According to one form of the invention, the composition C1 comprises one or more latexes of polyurethane polymers b) obtained from B ₃₂ ) at least one diamine compound of formula H ₂ NR ₅ -NH ₂ (X) in which R ₅ represents an alkylene radical substituted by one or more ionic or potentially ionic groups;

The diamines of formula (X) correspond to the compounds of general formula H ₂ NR ₅ -NH ₂ in which R ₅ represents an alkylene radical substituted by one or more ionic or potentially ionic groups. Such compounds preferably have one ionic or potentially ionic group and two groups capable of reacting with isocyanate groups. Such compounds may optionally comprise two groups reactive with isocyanate groups and an ionic group or capable of forming an ionic group.

The ionic or potentially ionic group may preferably be chosen from ternary or quaternary ammonium groups or groups convertible into such groups, a carboxyl group, a carboxylate group, a sulfonic acid group and a sulfonate group. The conversion, at least partial, of the convertible groups into salts of ternary or quaternary ammonium groups can take place before or during mixing with water.

According to a preferred form of the invention, the ionic group designates a sulfonic acid group partially or totally neutralized by a preferably mineral base such as sodium hydroxide.

The diamines of formula (X) are preferably chosen from diaminosulfonates, such as for example the sodium salt of N-(2-aminoethyl)-2-aminoethanesulfonic acid (AAS), the sodium salt of the acid N-(2-aminoethyl)-2-aminopropionic acid, and mixtures thereof.

According to a preferred form of the invention, when diamines B ₃₂ ) are used in the preparation of polyurethane latex polymers b), amines B ₄ ) are also used.
B4) amino compound unsubstituted by ionic group(s)

According to one embodiment, the polyurethane polymer of latex b) is obtained from B ₄ ) at least one amino compound which is not substituted by one or more ionic or potentially ionic groups.

According to one embodiment, said amino compound not substituted by an ionic or potentially ionic group is a diamine compound.

According to one embodiment, the diamine compound not substituted by an ionic or potentially ionic group is a compound of formula (XI) H ₂ NR ₄ -NH ₂ in which R ₄ represents an alkylene or alkylene oxide radical which n is not substituted by one or more ionic or potentially ionic groups.

Formula diamines (XII)are preferably chosen from alkylene diamines, such as hydrazine, ethylenediamine, 1,2-propylenediamine, 1,3-propylenediamine, 1,4-butylenediamine, 1,6-diamino hexane, piperazine ; alkylene oxide diamines, such as 3-{2-[2-(3-aminopropoxy)ethoxy]-ethoxy}propylamine (also called dipropylamine diethylene glycol or DPA-DEG available from Tomah Products, Milton, Wis.) , 2-methyl-1,5-pentanediamine (Dytec A from DuPont), hexane diamine, isophorone diamine, 4,4-methylenedi- (cyclohexylamine), ether amines of the DPA series available from Tomah Products, Milton, Wis., such as dipropylamine propylene glycol, dipropylamine dipropylene glycol, dipropylamine tripropylene glycol, dipropylamine poly(propylene glycol), dipropylamine ethylene glycol, dipropylamine poly(ethylene glycol), dipropylamine 1,3-propane diol, dipropylamine 2-methyl-1,3-propane diol, dipropylamine 1,4-butane diol, dipropylamine 1,3-butane diol, dipropylamine 1,6-hexane diol and dipropylamine cyclohexane-1,4-dimethanol; and their mixtures.

Amino compounds B ₄ ) can also designate 1,isophoronediamine, mixtures of 2, 2,4- and 2,4,4-trimethylhexamethylenediamine, 2-methylpentamethylenediamine, diethylenetriamine, 4,4-diaminodicyclohexylmethane, hydrazine hydrate and/or dimethylethylenediamine.

According to one embodiment, the amine compound B ₄ ) designates a compound comprising a primary and/or secondary amine and a hydroxyl group such as diethanolamine, 3-amino-1-methylaminopropane, 3-amino-1-ethylaminopropane, 3-amino-1-cyclohexylaminopropane, 3-amino-1-methylaminobutane, alkanolamines such as N-aminoethylethanolamine, ethanolamine, 3-aminopropanol, neopentanolamine.

According to one embodiment, the amino compound B ₄ ) designates methylamine, ethylamine, propylamine, butylamine, octylamine, laurylamine, stearylamine, isononyloxypropylamine, dimethylamine, diethylamine,

Dipropylamine, di-butylamine, N-methylaminopropylamine, diethyl (methyl)aminopropylamine, morpholine, piperidine,

According to a particular embodiment, the amino compound B ₄ ) is chosen from 1,2-ethylenediamine, bis (4-aminocyclohexyl) methane, 1,4-diaminobutane, isophoronediamine, ethanolamine, diethanolamine and diethylenetriamine.

According to a preferred form of the invention, when diamines B ₄ ) are used in the preparation of polyurethane latex polymers b), amines B ₃₂ ) as described above are also used.

According to one embodiment, when one or more amines B ₄ ) are used, these preferably comprise one or more amines of formula ( XI ).

According to a particular embodiment, when one or more amines B ₄ ) are used in the preparation of the polyurethane latex polymer b), the amine(s) B ₄ ) preferably comprise one or more diamines preferably of formula ( XI) , said polyurethane polymer also being derived from the use of one or more hydrophilic compounds B ₃₂ ).

According to a first variant, the polyurethane latex polymer b) is formed from:
B₁₁) from 50 to 95% by weight, in particular from 60 to 90% by weight, in particular from 70 to 85% by weight, in particular from 75 to 80% by weight, of a polyester polyol B₁₁) as defined previously, said polyester polyol being for example formed from at least:
B₁₁₁) glycerol; B₁₁₂) of a C fatty acid dimer₁₈to C₃₈, especially in C₃₄to C₃₈and more particularly in C₃₆, for example that marketed by the company Croda, under the reference Pripol^®1009, cosmetic grade; and B₁₁₃) abietic acid or rosin ;
B₂) from 5 to 50% by weight, in particular from 5 to 40% by weight, in particular from 10 to 30% by weight and more particularly from 15 to 20% by weight, of at least one polyisocyanate, in particular as defined previously, in particular of a diisocyanate such as isophorone diisocyanate; and, B₃₁) from 2 to 15% by weight, in particular from 3 to 10% by weight and more particularly from 3 to 5% by weight, of at least one hydrophilic monomer as defined above, in particular of a single hydrophilic monomer such as defined previously; the acidic or basic functions of said hydrophilic monomer being advantageously, totally or partially, neutralized; said hydrophilic monomer being for example 2,2-bis(hydroxymethyl)propionic acid (DMPA) with the acid functions being advantageously, totally or partially, neutralized, preferably by an organic base, in particular by a tertiary amine such as diisopropylethylamine; the mass percentages being defined in relation to the total weight of the components of the polyurethane latex polymer b).

Preferably, the polyurethane latex polymer b) does not comprise any monomeric unit other than those derived from the aforementioned components B ₁₁ ), B ₂ ), B ₃₁ ). In other words, according to a particular embodiment, the sum of the mass contents of components B ₁₁ ), B ₂ ), B ₃₁ ), is equal to 100%.

According to a second variant, the latex polyurethanes b) are formed from B ₁₂ ) at least one diol, B ₁₁ ) optionally at least one polyester polyol (in particular polyester polyol by reaction between hexandiol/neopentyl glycol and adipic acid ), B ₂ ) at least one polyisocyanate, B ₃₂ ) and B ₄ ) at least one hydrophilic monomer (such as sodium N-(2-aminoethyl)-2-aminoethane sulfonate) and at least one amine compound.

• au moins un prépolymère de formule(VI)suivante :

More particularly, the polyurethane(s) present in the aqueous dispersions b) usable in the present invention come from the reaction of:

• at least one prepolymer of formula (VI) below:

(VI)

• au moins un extendeur de chaîne selon la formuleH ₂ N-R ₄ -NH ₂ (VII), dans laquelle R₄représente un radical alkylène ou d’oxyde d’alkylène qui n’est pas substitué par un ou plusieurs groupes ioniques ou potentiellement ioniques ; et
• au moins un extendeur de chaîne selon la formuleH ₂ N-R ₅ -NH ₂ (VIII), dans laquelle R₅représente un radical alkylène substitué par un ou plusieurs groupes ioniques ou potentiellement ioniques.

Formula(VI)in which,
-R ₁ represents a bivalent radical of a dihydroxy compound,
-R ₂ represents a radical of an aliphatic or cycloaliphatic polyisocyanate,
-R ₃ represents a radical of a low molecular weight diol, optionally substituted by one or more ionic groups,
-notrepresents an integer ranging from 1 to 5, and
-mis greater than 1;

• at least one chain extender according to the formula H ₂ NR ₄ -NH ₂ (VII) , in which R ₄ represents an alkylene or alkylene oxide radical which is not substituted by one or more ionic or potentially ionic groups ; And
• at least one chain extender according to the formula H ₂ NR ₅ -NH ₂ (VIII) , in which R ₅ represents an alkylene radical substituted by one or more ionic or potentially ionic groups.

Among the dihydroxy compounds which can be used according to the present invention, mention may in particular be made of compounds having two hydroxy groups and a number molecular weight of approximately 700 to approximately 16,000, and preferably of approximately 750 to approximately 5,000. example of dihydroxy compounds having a high molecular weight, mention may be made of polyol polyesters, polyol polyethers, polyhydroxylated polycarbonates, polyhydroxylated polyacetates, polyhydroxylated polyacrylates, polyhydroxylated amide polyesters, polyhydroxylated polyalkadienes, polyhydroxylated polythioethers and their mixtures. Preferably, the hydroxylated compounds are chosen from polyol polyesters, polyol polyethers, polyhydroxylated polycarbonates and mixtures thereof.

The polyisocyanates B ₂ ) which can be used according to the present invention are chosen in particular from organic diisocyanates having a molecular weight of approximately 112 to 1000, and preferably of approximately 140 to 400.

Preferably, the polyisocyanates are chosen from diisocyanates and more particularly from those represented by the general formula (VIII) R ₂ (N=C=O) ₂ , in which R ₂ represents a divalent aliphatic hydrocarbon group having from 4 to 18 atoms carbon, a divalent cycloaliphatic hydrocarbon group having 5 to 15 carbon atoms, a divalent araliphatic hydrocarbon group having 7 to 15 carbon atoms or a divalent aromatic hydrocarbon group having 6 to 15 carbon atoms.

Preferably, (VI) represents an organic diisocyanate. As an example of organic diisocyanates, one can in particular choose tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, dodecamethylene diisocyanate, 1,3-diisocyanatocyclohexane, 1,4-diisocyanatocyclohexane, isocyanate of 3-isocyanatomethyl-3,5,5-trimethylcyclohexane (isophorone diisocyanate or IPDI), bis-(4-isocyanatocyclohexyl)-methane, 1,3-bis(isocyanatomethyl)-cyclohexane, 1,4-bis( isocyanatomethyl)-cyclohexane, bis-(4-isocyanato-3-methyl-cyclohexyl)-methane, isomers of toluene diisocyanate (TDI) such as toluene 2,4-diisocyanate, toluene 2,6-diisocyanate and mixtures thereof, hydrogenated toluene diisocyanate, 4,4'-diphenylmethane diisocyanate and mixtures with its isomers 2,4-diphenylmethane diisocyanate and optionally 2,2'-diphenylmethane diisocyanate, naphthalene 1,5-diisocyanate , and their mixtures.

Preferably, the diisocyanates (VI) are aliphatic and cycloaliphatic diisocyanates, and are more preferably chosen from 1,6-hexamethylene diisocyanate, 3-isocyanatomethyl-3,5,5-trimethylcyclohexane isocyanate and mixtures thereof.

By “low molecular weight diol” is meant, according to the present invention, a diol having a molecular weight of approximately 62 to 700, and preferably of 62 to 200. These diols may comprise aliphatic, alicyclic or aromatic groups. Preferably, they only include aliphatic groups.

Preferably, B ₁₂ ) represents a low molecular weight diol, having more than 20 carbon atoms, more preferably chosen from ethylene glycol, diethylene glycol, propane 1,2-diol, propane 1,3-diol , butane 1,4-diol, butylene 1,3-glycol, neopentyl glycol, buthyl-ethyl-propane diol, cyclohexane diol, 1,4-cyclohexane dimethanol, hexane 1,6-diol, bisphenol A (2,2-bis(4-hydroxyphenyl)propane), hydrogenated bisphenol A (2,2-bis(4-hydroxycyclohexyl)propane), and mixtures thereof.

Low molecular weight diols may optionally include ionic or potentially ionic groups. Examples of low molecular weight diols containing ionic or potentially ionic groups are described in particular in US patent 3,412,054. Such compounds are preferably chosen from dimethylol butanoic acid, dimethylol propionic acid, polycaprolactone diols containing a carboxyl group and mixtures thereof.

If lower molecular weight diols containing ionic or potentially ionic groups are used, they are preferably used in an amount such that less than 0.30 meq C(O)OH per gram of polyurethane in the polyurethane dispersion is present. .

The prepolymer is elongated using two families of chain extenders. The first family of chain extenders corresponds to compounds of general formula H ₂ NR ₄ -NH ₂ (VII), in which R ₄ represents an alkylene or alkylene oxide radical which is not substituted by one or more ionic or potentially ionic groups.

The chain extenders of formula (VII) are preferably chosen from alkylene diamines, such as hydrazine, ethylenediamine, propylenediamine, 1,4-butylenediamine, piperazine; alkylene oxide diamines, such as 3-{2-[2-(3-aminopropoxy)ethoxy]-ethoxy}propylamine (also called dipropylamine diethylene glycol or DPA-DEG available from Tomah Products, Milton, Wis.) , 2-methyl-1,5-pentanediamine (Dytec A from DuPont), hexane diamine, isophorone diamine, 4,4-methylenedi- (cyclohexylamine), ether amines of the DPA series available from Tomah Products, Milton, Wis., such as dipropylamine propylene glycol, dipropylamine dipropylene glycol, dipropylamine tripropylene glycol, dipropylamine poly(propylene glycol), dipropylamine ethylene glycol, dipropylamine poly(ethylene glycol), dipropylamine 1,3-propane diol, dipropylamine 2-methyl-1,3-propane diol, dipropylamine 1,4-butane diol, dipropylamine 1,3-butane diol, dipropylamine 1,6-hexane diol and dipropylamine cyclohexane-1,4-dimethanol; and their mixtures.

The second family of chain extenders corresponds to compounds of general formula H ₂ NR ₅ -NH ₂ (VIII), in which R5 represents an alkylene radical substituted by one or more ionic or potentially ionic groups. Such compounds preferably have one ionic or potentially ionic group and two groups capable of reacting with isocyanate groups. Such compounds may optionally comprise two groups reactive with isocyanate groups and an ionic group or capable of forming an ionic group.

The ionic or potentially ionic group may preferably be chosen from ternary or quaternary ammonium groups or groups convertible into such groups, a carboxyl group, a carboxylate group, a sulfonic acid group and a sulfonate group. The conversion, at least partial, of the convertible groups into salts of ternary or quaternary ammonium groups can take place before or during mixing with water.

The chain extenders of formula (VIII) are preferably chosen from diaminosulfonates, such as for example the sodium salt of N-(2-aminoethyl)-2-aminoethanesulfonic acid (AAS), the sodium salt of N-(2-aminoethyl)-2-aminopropionic acid, and mixtures thereof.

The polyurethane usable according to the present invention may optionally also comprise compounds which are respectively located at the ends of the chains and terminate said chains (chain terminators). Such compounds are described in particular in U.S. patents 7,445,770 and/or U.S. 7,452,770.

Preferably, the aqueous dispersion of polyurethane particles has a viscosity of less than 2000 mPa.s at 23°C, more preferably less than 1500, and better still less than 1000. Even more preferably, the aqueous dispersion of polyurethane has a glass transition temperature less than 0°C.

Also preferably, the aqueous polyurethane dispersion b) has a solids content (or active material, or dry matter) based on the weight of the dispersion of 20% to 60% by weight, more preferably from 25% to 55% by weight. % by weight and better still from 30% to 50% by weight. By this we mean that the polyurethane content (dry matter) of the aqueous dispersion is preferably 20% to 60% by weight, more preferably 25% to 55% by weight and better still 30% to 50% by weight. , relative to the total weight of the dispersion.

Also preferably, the aqueous dispersion of polyurethane particles b) has a glass transition temperature (Tg) equal to or lower than -25°C, preferably lower than -35°C, and more preferably lower than -40°C. .

The polyurethane particles can have an average diameter of up to about 1000 nm, for example from about 50 nm to about 800 nm, better still from about 100 nm to about 500 nm. These particle sizes can be measured with a laser particle size analyzer (e.g. Brookhaven BI90).

As a non-limiting example of aqueous polyurethane dispersions, we can cite those sold under the name Baycusan® by Covestro such as, for example, Baycusan® C1000 (INCI name: polyurethane-34), Baycusan® C1001 (INCI name: polyurethane-34), Baycusan® C1003 (INCI name: polyurethane-32), Baycusan® C1004 (INCI name: polyurethane-35) and Baycusan® C1008 (INCI name: polyurethane-48).

• B₂) au moins un polyisocyanate aliphatique, araliphatique et/ou cycloaliphatique de préférence choisi parmi HDI, IPDI, H12-MDI et leur mélange ;
• au moins un polyol de masse molaire moyenne en nombre Mn > 330 et
• < 6000 g/mol, de préférence > 350 et < 5000 g/mol, de préférence B₁₁) au moins un polyester polyol issu de préférence d’au moins un diacide choisi parmi l’acide succinique, l’acide adipique et d’au moins un diol choisi parmi le 1, 6 hexanediol, le 1,4-butanediol et /ou d’au moins le neopentyl glycol, et B₁₂) au moins un polyéther polyol ;
• éventuellement au moins un compose aminé B₄) comportant au moins deux groupes amino telle que l’éthylènediamine, pouvant réagir avec des fonctions isocyanates,
• éventuellement au moins un monomère hydrophile B₃) choisi parmi les composés B₃₂) tels que décrits précédemment, en particulier choisis parmi les composés substitués par un groupe ionique acide tel que l’acide 2- (2-aminoéthylamino) éthanesulfonique ou ses sels tels que ses sels de sodium ;
• éventuellement au moins un alcool comprenant au moins deux fonctions hydroxy B₁₂) et de masse molaire > 62 et < 399 g/mol,
• e)_ éventuellement au moins un composé dont une function est réactive vis-à-vis des isocyanates,

According to a third variant, the polyurethane latex polymer comes from:

• B ₂ ) at least one aliphatic, araliphatic and/or cycloaliphatic polyisocyanate preferably chosen from HDI, IPDI, H12-MDI and their mixture;
• at least one polyol with a number average molar mass Mn > 330 and
• < 6000 g/mol, preferably > 350 and < 5000 g/mol, preferably B ₁₁ ) at least one polyester polyol preferably derived from at least one diacid chosen from succinic acid, adipic acid and at least one diol chosen from 1,6 hexanediol, 1,4-butanediol and/or at least neopentyl glycol, and B ₁₂ ) at least one polyether polyol;
• optionally at least one amino compound B ₄ ) comprising at least two amino groups such as ethylenediamine, capable of reacting with isocyanate functions,
• optionally at least one hydrophilic monomer B ₃ ) chosen from compounds B ₃₂ ) as described above, in particular chosen from compounds substituted by an ionic acid group such as 2-(2-aminoethylamino)ethanesulfonic acid or its salts such as its sodium salts;
• optionally at least one alcohol comprising at least two hydroxy functions B ₁₂ ) and of molar mass > 62 and < 399 g/mol,
• e)_ optionally at least one compound whose function is reactive with respect to isocyanates,

As a non-limiting example of aqueous polyurethane dispersions, we can cite those sold under the name Baycusan® by Covestro such as, for example, Baycusan® eco E1000 (INCI name: polyurethane-93), Baycusan® eco E1001 (name INCI: polyurethane-99).

Particularly the polyurethane latex b) of the invention is(are) chosen from the polyurethanes with the following INCI names: polyurethane-32, polyurethane-32, polyurethane-34, polyurethane-35, polyurethane-48, polyurethane-93 , and polyurethane-99 and their mixtures.

According to one embodiment, the total quantity of the aqueous dispersion(s) of polyurethane particles b) present in the composition C1 or C1' according to the invention, is preferably between 0.01% to 60% by weight, plus preferably from 0.1% to 55% by weight, and better still from 0.2% to 50% by weight, relative to the total weight of the composition.

According to one embodiment, the total quantity of polyurethane (dry matter), present in the composition C1 or C1' according to the invention, is between 0.01% and 30% by weight, more preferably from 0.05% to 28% by weight, and better still from 0.1% to 25% by weight, relative to the total weight of the composition.
c) Fatty substances

According to a particular embodiment of the invention, the composition further comprises one or more fatty substances.

By “ fatty substance ” is meant an organic compound insoluble in water at ordinary room temperature (25°C) and at atmospheric pressure (760 mm Hg) (solubility less than 5% and preferably 1% again). more preferably at 0.1%). They have in their structure at least one hydrocarbon chain comprising at least 6 carbon atoms or a chain of at least two siloxane groups. In addition, fatty substances are generally soluble in organic solvents under the same temperature and pressure conditions, such as for example chloroform, ethanol, benzene, petroleum jelly or decamethyl cyclopentasiloxane.

The fatty substance(s) of the invention are of natural or synthetic origin, preferably natural, more preferably of plant origin. They are different from fatty acids because salified fatty acids constitute soaps that are generally soluble in aqueous media.

According to a particular embodiment of the invention, the composition comprises one or more fatty substances which are non-liquid at 25°C and at atmospheric pressure.
The wax(es)

According to a particular embodiment, the composition of the invention comprises one or more waxes.

By “ wax ” we mean a lipophilic compound, solid at room temperature (25°C), with a reversible solid/liquid state change, having a melting point greater than or equal to 30°C and up to 200°C. and in particular up to 120°C.

In particular, the wax(es) suitable for the invention may have a melting point greater than or equal to 45°C, and in particular greater than or equal to 55°C.

The composition according to the invention preferably comprises a wax content(s) ranging from 0.5% to 30% by weight relative to the total weight of the composition, in particular from 1 to 20%, more particularly from 2 to 15 %.

According to a particular form of the invention, the composition of the invention is solid, in particular anhydrous. It can then be in the form of a stick, polyethylene micro-waxes will be used in the form of crystallites with a form factor of at least 2 having a melting point ranging from 70 to 110°C and preferably 70 to 100°C. C, in order to reduce or even eliminate the presence of strata in the solid composition. These needle-shaped crystallites and in particular their dimensions can be characterized visually according to the following method.
The pasty compound(s)

According to a particular embodiment, the composition of the invention comprises one or more pasty compounds .

By “ pasty compound ” within the meaning of the present invention, is meant a lipophilic fatty compound with a reversible solid/liquid state change, presenting in the solid state an anisotropic crystalline organization, and comprising at a temperature of 23°C a fraction liquid and a solid fraction.

Preferably the composition contains one or more fatty substances c) which are hydrocarbon fatty substances which are liquid at 25°C and atmospheric pressure.

The liquid hydrocarbon fatty substance(s) are in particular chosen from hydrocarbons and C ₆ -C ₁₆ or with more than 16 carbon atoms up to 60 carbon atoms, preferably between C ₆ and C ₁₆ , and in particular alkanes , oils of animal origin, oils of vegetable origin, glycerides or fluorinated oils of synthetic origin, fatty alcohols, fatty acid and/or fatty alcohol esters, silicones. Particularly the liquid fatty substance(s) are chosen from non-silicone oils.

It is recalled that within the meaning of the invention, alcohols, esters and fatty acids more particularly present one or more hydrocarbon group(s), linear or branched, saturated or unsaturated. (s), comprising 6 to 60 carbon atoms, optionally substituted, in particular by one or more OH hydroxyl group(s) (in particular from 1 to 4 hydroxyl group(s). If they are unsaturated, these compounds can comprise one to three unsaturation(s), preferably 1 to 3 carbon-carbon double bonds, conjugated or not.

Concerning C alkanes₆-VS₁₆, the latter are linear or branched, possibly cyclic, preferably the fatty substance(s) c) of the invention are chosen from alkanes, linear or branched, in C₈-VS₁₄, more preferably in C₉-VS₁₃Again more preferably in C₉-VS₁₂. By way of example, we can cite hexane, decane, undecane, dodecane, tridecane, isoparaffins such as isohexadecane, isodecane or isododecane. Linear or branched hydrocarbons of more than 16 carbon atoms can be chosen from paraffin oils, vaseline oil, polydecenes, hydrogenated polyisobutene such as Parléam®.

Among the hydrocarbon liquid fatty substances c) having an overall solubility parameter according to the HANSEN solubility space less than or equal to 20 (MPa) ^1/2 , we can cite oils, which can be chosen from natural or synthetic oils , hydrocarbons, optionally fluorinated, optionally branched, alone or in a mixture.

According to a very advantageous embodiment, the composition of the invention comprises one or more fatty substances which are (are) one or more hydrocarbon oil(s). The oil(s) may be volatile or non-volatile.

According to a preferred embodiment of the invention, the fatty substance(s) c) are hydrocarbon oils, linear or branched, which are volatile, in particular chosen from undecane, decane, dodecane, isododecane, tridecane, and their mixture of different, volatile oils preferably comprising isododecane in the mixture, or a mixture of undecane and tridecane

According to another particular embodiment, the liquid fatty substance(s) c) are a mixture of a volatile hydrocarbon oil and a non-volatile hydrocarbon oil, the mixture of which preferably comprises dodecane or isododecane as volatile oil.

Particularly the fatty substance(s) c) of the invention are a mixture of C ₉ -C ₁₂ alkanes, preferably of natural origin, whose chains comprise from 9 to 12 carbon atoms, preferably linear or branched, in C ₉ -C ₁₂ . This mixture is notably known under the name INCI C ₉ -C ₁₂ ALKANE, CAS 68608-12-8, VEGELIGHT SILK® marketed by BioSynthIs. This biodegradable, volatile oil blend obtained from coconut oil (viscosity is 0.9-1.1 cSt (40°C) and a flash point at 65°C)
According to one embodiment, composition C1 contains only liquid oils at 25°C and atmospheric pressure.
According to another embodiment, composition C1 contains at least 80% of liquid oils at 25°C and atmospheric pressure hydrocarbons, preferably volatile, more preferably chosen from isodecane, decane, Cetiol UT®, VEGELIGHT SILK® .
According to another embodiment, composition C1 may comprise volatile and non-volatile oils, in particular in a volatile oil/non-volatile oil proportion greater than or equal to 4.
According to another embodiment, composition C1 contains from 0 to 10% of silicone oils, preferably from 0 to 5% of silicone oils.

As volatile silicone oils, mention may be made of linear or cyclic volatile silicone oils, in particular those having a viscosity less than or equal to 8 centistokes (cSt) (8 x 10 ^-6 m ² /s), and having, in particular, 2 to 10 silicon atoms, and in particular, from 2 to 7 silicon atoms, these silicones optionally comprising alkyl or alkoxy groups having 1 to 10 carbon atoms. As volatile silicone oil which can be used in the invention, mention may be made, in particular, of dimethicones of viscosity 5 and 6 cSt, octamethyl cyclotetrasiloxane, decamethyl cyclopentasiloxane, dodecamethyl cyclohexasiloxane, heptamethyl hexyltrisiloxane, heptamethyloctyl trisiloxane, hexamethyl disiloxane, octamethyl trisiloxane, decamethyl tetrasiloxane, dodecamethyl pentasiloxane, and mixtures thereof.

As non-volatile silicone oils, mention may be made of non-volatile, linear or cyclic polydimethylsiloxanes (PDMS); polydimethylsiloxanes comprising alkyl, alkoxy and/or phenyl groups, during or at the end of a silicone chain, groups having from 2 to 24 carbon atoms; phenyl silicones such as phenyl trimethicones, phenyl dimethicones, phenyl trimethylsiloxy diphenyl siloxanes, diphenyl dimethicones, diphenyl methyldiphenyl trisiloxanes, 2-phenyl ethyl trimethyl-siloxysilicates and pentaphenylated silicone oils.

The hydrocarbon oil can be chosen from:
* hydrocarbon oils having 8 to 14 carbon atoms, and in particular:
- C-branched alkanes₈-VS₁₄like C isoalkanes₈-VS₁₄of petroleum origin (also called isoparaffins) such as isododecane (also called 2,2,4,4,6-pentamethylheptane), isodecane, and for example oils sold under the trade names Isopars' or Permetyls ,
- linear alkanes, for example such as n-dodecane (C12) and n-tetradecane (C14) sold by Sasol respectively under the references PARAFOL 12-97 and PARAFOL 14-97,as well as their mixtures, the undecane-tridecane mixture, the mixtures of n-undecane (C11) and n-tridecane (C13) obtained in Examples 1 and 2 of application WO 2008/155059 from the Cognis Company, and their mixtures as well as the mixtures ofnot-undecane (C11) andnot-tridecane (C13) Cetiol Ultimate® from BASF.
* short-chain esters (having 3 to 8 carbon atoms in total) such as ethyl acetate, methyl acetate, propyl acetate, n-butyl acetate
* hydrocarbon oils of plant origin such as triglycerides consisting of esters of fatty acids and glycerol whose fatty acids can have varied chain lengths from C₄to C₂₄, the latter being able to be linear or branched, saturated or unsaturated; these oils are in particular triglycerides of heptanoic acid or octanoic acid, or even wheat germ, sunflower, grape seed, sesame, corn, apricot, castor, shea, avocado, olive, soy, sweet almond, palm, rapeseed, cotton, hazelnut, macadamia, jojoba, alfalfa, poppy, pumpkin, sesame, squash, rapeseed, blackcurrant, evening primrose, millet, barley, quinoa, rye, safflower, cancholy, passionflower, muscat rose, coconut; shea butter; or even the triglycerides of caprylic/capric acids such as those sold by the company Stéarineries Dubois or those sold under the names Miglyol 810^®, 812^®and 818^®by the company Dynamit Nobel,
* synthetic ethers having 10 to 40 carbon atoms;
* linear or branched hydrocarbons, of mineral or synthetic origin such as petroleum jelly, polydecenes, hydrogenated polyisobutene such as Parleam ®, squalane, paraffin oils, and their mixtures,
* esters like formula R oils¹C(O)-O-R² in which R¹represents the remainder of a linear or branched fatty acid containing 1 to 40 carbon atoms and R² represents a particularly branched hydrocarbon chain containing from 1 to 40 carbon atoms provided that R¹+R² or  10, such as for example Purcellin oil (cetostearyl octanoate), isopropyl myristate, isopropyl palmitate, C alcohol benzoates₁₂to C₁₅, hexyl laurate, diisopropyl adipate, isononyl isononanoate, 2-ethyl-hexyl palmitate, isostearyl isostearate, 2-hexyl-decyl laurate, 2- octyl-decyl, 2-octyl-dodecyl myristate, heptanoates, octanoates, decanoates or ricinoleates of alcohols or polyalcohols such as propylene glycol dioctanoate; hydroxylated esters such as isostearyl lactate, di-isostearyl malate, 2-octyl-dodecyl lactate; polyol esters and pentaerythritol esters, more preferably linear or branched C fatty acid esters₈-VS₁₀and C fatty alcohol₁₂-VS₁₈linear or branched alone or in mixture with alkanes resulting from the hydrogenation / complete reduction of fatty acids from Cocos Nucifera (Coconut) oil, particularly dodecane or mixtures of cococaprylate / caprate with dodecane, we can cite those with the INCI name coconut alkanes (and) Coco-caprylate / caprate marketed under the name VEGELIGHT 1212LC® by Grant Industries.
* fatty alcohols that are liquid at room temperature with a branched and/or unsaturated carbon chain having 12 to 26 carbon atoms such as octyl dodecanol, isostearyl alcohol, oleic alcohol, 2-hexyldecanol, 2-butyloctanol, and 2-undecylpentadecanol.

In particular, the composition comprises at least one liquid hydrocarbon fatty substance c) chosen from:
- vegetable oils formed by esters of fatty acids and polyols, in particular triglycerides, such as sunflower, sesame or rapeseed oil, macadamia oil, soybean oil, sweet almond oil, calophyllum, palm, grape seeds, corn, arara, cotton, apricot, avocado, jojoba, olive, coconut or cereal sprouts;
- linear, branched or cyclic esters, having more than 6 carbon atoms, in particular 6 to 30 carbon atoms; and in particular isononyl isononanoate;
and more particularly the esters of formula R ^d -C(O)-OR ^e in which R ^d represents the remainder of a higher fatty acid comprising from 7 to 19 carbon atoms and R ^e represents a hydrocarbon chain comprising from 3 to 20 carbon atoms, such as palmitates, adipates, myristates and benzoates, including diisopropyl adipate and isopropyl myristate; more preferably the esters of formula R ^d -C(O)-OR ^e in which R ^d represents the remainder of a higher fatty acid comprising from 8 to 10 carbon atoms and R ^e represents a hydrocarbon chain comprising from 12 to 18 atoms of carbon ;
- hydrocarbons and in particular linear, branched and/or cyclic alkanes, volatile or non-volatile, such as C ₅ -C ₆₀ isoparaffins, possibly volatile such as undecane, dodecane, isododecane, tridecane Parléam ( hydrogenated polyisobutene), isohexadecane, cyclohexane, or 'ISOPARs', and their mixture; or alkanes resulting from the hydrogenation / complete reduction of mixtures of fatty acids from Cocos Nucifera (Coconut) oil such as dodecane, the mixture of C ₉ -C ₁₂ alkanes, whose chains comprise from 9 to 12 carbon atoms, preferably linear or branched alkanes, C ₉ -C ₁₂ in particular including dodecane or paraffin oils, petroleum jelly, or hydrogenated polyisobutylene;
- ethers having 6 to 30 carbon atoms;
- ketones having 6 to 30 carbon atoms;
- aliphatic fatty monoalcohols having 6 to 30 carbon atoms, the hydrocarbon chain not comprising a substitution group, such as oleic alcohol, decanol, dodecanol, octadecanol, octyldodecanol and linoleic alcohol;
- polyols having 6 to 30 carbon atoms, such as hexylene glycol; And
- their mixtures, such as mixtures of linear or branched C ₈ -C ₁₀ fatty acid esters and C ₁₂ -C ₁₈ fatty alcohol and alkanes resulting from the hydrogenation / complete reduction of mixtures of fatty acids from Cocos Nucifera (Coconut) oil, in particular dodecane, such as mixtures of cococaprylate/caprate and dodecane, we can cite those with the name INCI coconut alkanes (and) Coco-caprylate/caprate marketed under the name of VEGELIGHT 1212LC® by Grant Industries; or mixtures of C ₉ -C ₁₂ alkanes, the chains of which comprise from 9 to 12 carbon atoms, preferably linear or branched alkanes, in C ₉ -C ₁₂ in particular including dodecane, we can cite the mixture oil named INCI C9-12 ALKANE, VEGELIGHT SILK® marketed by BioSynthIs.

Preferably, the composition of the invention comprises at least one liquid hydrocarbon fatty substance c) chosen from:
- vegetable oils formed by esters of fatty acids and polyols, in particular triglycerides,
- esters of formula R ^d -C(O)-OR ^e in which R ^d represents the remainder of a higher fatty acid comprising 7 to 19 carbon atoms and R ^e represents a hydrocarbon chain comprising 3 to 20 carbon atoms , more preferably the esters of formula R ^d -C(O)-OR ^e in which R ^d represents the remainder of a higher fatty acid comprising from 8 to 10 carbon atoms and R ^e represents a hydrocarbon chain comprising from 12 to 18 carbon atoms;
- linear or branched C ₈ -C ₆₀ alkanes, volatile or non-volatile such as isododecane and alkanes resulting from the hydrogenation / complete reduction of mixtures of fatty acids from Cocos Nucifera oil (Coconut ) in particular dodecane;
- cyclic, non-aromatic, C ₅ -C ₁₂ alkanes; volatile or non-volatile;
- ethers having 7 to 30 carbon atoms;
- ketones having 8 to 30 carbon atoms;
- aliphatic fatty monoalcohols having 12 to 30 carbon atoms, the hydrocarbon chain not comprising a substitution group, and
- their mixtures.

Advantageously, the fatty substance(s) c) of the invention, in particular liquid ones, are non-polar, i.e. formed only of carbon and hydrogen atoms.

The liquid hydrocarbon fatty substance(s) are preferably chosen from hydrocarbon oils having 8 to 14 carbon atoms, in particular volatile ones, more particularly non-polar oils, described above.

Preferably the fatty substance(s) c) of the invention, in particular liquids, are chosen from alkanes such as dodecane, decane, isododecane, fatty alcohols such as octyldodecanol, esters such as isononanoate isononyl, Coco-caprylate/caprate and their mixtures, more preferably alkanes.

More particularly the fatty substance(s) c) of the invention, in particular liquid, are chosen from C alkanes₆-VS₁₆, linear or branched, preferably in C₈-VS₁₄, more preferably in C₉-VS₁₃Again more preferably in C₉-VS_12,and even more preferably the alkanes are volatile. More particularly the liquid fatty substance(s) iii) of the invention are volatile and chosen from undecane, decane, dodecane, isododecane, tridecane, and their mixture comprising in particular dodecane, isododecane or a mixture undecane and tridecane.

Preferably, the fatty substance(s) c) of the invention, in particular liquids, are isododecane.

According to another advantageous embodiment of the invention, the fatty substance(s) c) of the invention, in particular liquid(s), is(are) a mixture of non-volatile oil(s) and oil(s). ) volatile(s) preferably the mixture comprises isododecane, undecane, dodecane, isododecane, tridecane, more preferably isododecane as volatile oil. As a volatile and non-volatile oil mixture, mention may be made of the mixture of isododecane and isononyl isononanoate or the mixture of isododecane and isononyl isononanoate.

More preferably when the fatty substance(s) are a mixture of volatile and non-volatile oil, the quantity of volatile oil is greater than the quantity of non-volatile oil

In particular in the mixture the non-volatile oil is a phenyl silicone oil preferably chosen from pentaphenylated silicone oils.

Advantageously, the composition comprises one or more fatty substances, in particular liquids at 25 ° C and at atmospheric pressure, preferably one or more oils, in a content ranging from 2 to 99.9% by weight, relative to the total weight of the composition, preferably ranging from 5 to 90% by weight, preferably ranging from 10 to 80% by weight, preferably ranging from 20 to 80% by weight.

According to a preferred embodiment of the invention, the composition C1 or C1' according to the invention comprises c) one or more fatty substances, in particular liquids at 25°C and at atmospheric pressure, e) water and d) a or more several surfactants.
Surfactants

According to a particular embodiment of the invention the composition further comprises d) one or more surfactant(s) preferably non-ionic(s), ionic(s) or mixtures thereof.

According to another particular embodiment of the invention, the composition does not include a surfactant.

By “ surfactant ” we mean a compound which modifies the surface tension between two surfaces. The surfactant(s) d) are amphiphilic molecules, which have two parts of different polarity, one lipophilic (which retains fat) which is nonpolar, the other hydrophilic (miscible or soluble in water) is polar. The lipophilic part is generally a fatty chain, and the other water-miscible part is polar and/or protic.

By “ ionic ” we mean anionic, cationic, amphoteric, or zwitterionic.

By “ fatty chain ” is meant a hydrocarbon chain comprising more than 6 atoms, preferably between 6 to 30 carbon atoms, preferably from 8 to 24 carbon atoms, linear or branched, saturated or not.

According to a first particular embodiment, the composition of the invention contains d) at least one non-ionic, silicone or non-silicone surfactant.

Among the nonionic surfactants according to the invention, we can cite, alone or mixtures, fatty alcohols, alpha-diols, alkylphenols, these 3 types of compounds being polyethoxylated, polypropoxylated and/or polyglycerolated, and having a fatty chain comprising for example 8 with 22 carbon atoms, the number of ethylene oxide or propylene oxide groups which can range in particular from 2 to 50 and the number of glycerol groups which can range in particular from 2 to 30. Mention may also be made of ethylene oxide copolymers. ethylene and propylene, condensates of ethylene and propylene oxide on fatty alcohols; polyethoxylated fatty amides preferably having from 2 to 30 moles of ethylene oxide, polyglycerolated fatty amides comprising on average 1 to 5 glycerol groups and in particular 1.5 to 4; oxyethylenated sorbitan fatty acid esters having from 2 to 30 moles of ethylene oxide; fatty acid esters of sucrose, fatty acid esters of polyethylene glycol, alkylpolyglycosides, N-alkylglucamine derivatives, amine oxides such as (C ₁₀ -C ₁₄ ) alkylamine oxides or oxides of N-acylaminopropylmorpholine.

More particularly, the surfactant or surfactants of the invention are chosen from nonionic surfactants in particular chosen from: i) (poly)ethoxylated fatty alcohols; ii) (poly)glycerolated fatty alcohols; and iii) alkylpolyglycosides (APG).

• R’ ₁ représente un radical alkyle et/ou alcényle linéaire ou ramifié comportant environ de 8 à 24 atomes de carbone, un radical alkylphényle dont le radical alkyle linéaire ou ramifié comporte de 8 à 24 atomes de carbone ;
• R’ ₂ représente un radical alkylène comportant environ de 2 à 4 atomes de carbone ;
• G’représente un motif sucre comportant de 5 à 6 atomes de carbone ;
• t'désigne un entier compris inclusivement entre 0 et 10, de préférence entre 0 et 4, de préférence entre 0 et 4 ; et
• v’désigne un entier compris inclusivement 1 et 15.

With regard to alkylpolyglycosides, these compounds are well known and can be more particularly represented by the formulaR' ₁ GOLD' ₂ O) _you (G') _v' in which :

• R' ₁ represents a linear or branched alkyl and/or alkenyl radical comprising approximately 8 to 24 carbon atoms, an alkylphenyl radical whose linear or branched alkyl radical comprises 8 to 24 carbon atoms;
• R' ₂ represents an alkylene radical comprising approximately 2 to 4 carbon atoms;
• G' represents a sugar unit comprising 5 to 6 carbon atoms;
• t' designates an integer inclusively between 0 and 10, preferably between 0 and 4, preferably between 0 and 4; And
• v' designates an integer inclusive of 1 and 15.

Preferred alkylpolyglycosides according to the present invention are compounds of formula(V)in whichR ₁ denotes more particularly a saturated or unsaturated, linear or branched alkyl radical comprising from 8 to 18 carbon atoms, t' denotes a value ranging from 0 to 3 and even more particularly equal to 0,G'may refer to glucose, fructose or galactose, preferably glucose. The degree of polymerization, i.e. the value ofv'in the formula(V), can range from 1 to 15, preferably from 1 to 4. The average degree of polymerization is more particularly between 1 and 2 and even more preferably from 1.1 to 1.5.

The glycosidic bonds between the sugar units are of type 1-6 or 1-4 and preferably 1-4.

The (poly)ethoxylated fatty alcohols suitable for implementing the invention are more particularly chosen from alcohols comprising from 8 to 30 carbon atoms, and preferably from 12 to 22 carbon atoms.

(Poly)ethoxylated fatty alcohols more particularly have one or more hydrocarbon groups, linear or branched, saturated or unsaturated, comprising 8 to 30 carbon atoms, optionally substituted, in particular by one or more hydroxyl groups (in particular 1 to 4). . If they are unsaturated, these compounds can include one to three carbon-carbon double bonds, conjugated or not.

(Poly)ethoxylated fatty alcohols are more particularly fatty alcohols containing 8 to 22 carbon atoms and oxyethylenated with 1 to 30 moles of ethylene oxide (1 to 30 EO). Among them, we can more particularly mention lauryl alcohol 2 EO, lauryl alcohol 3 EO, decyl alcohol 3 EO, decyl alcohol 5 EO and oleic alcohol 20 EO.

Mixtures of these (poly)oxyethylenated fatty alcohols can also be used.

Preferably, the nonionic surfactants are chosen from (C ₆ -C ₂₄ ) alkyl (poly) glycosides, and more particularly (C ₈ -C ₁₈ ) alkyl (poly) glycosides, esters of C _{8 -} fatty acids. C ₃₀ ethoxylated sorbitan, polyethoxylated C ₈ -C ₃₀ fatty alcohols, polyoxyethylenated C ₈ -C ₃₀ fatty acid esters, these compounds preferably having 2 to 150 moles of ethylene oxide, and mixtures thereof .

Among the non-ionic surfactants, C ₆ -C ₂₄ alkyl polyglucosides and (poly) ethoxylated fatty alcohols are preferably used and C ₈ -C ₁₆ alkyl polyglucosides are more particularly used.

The total quantity of nonionic surfactants preferably ranges from 0.01% to 60% by weight relative to the total weight of the composition, preferably from 0.5% to 30% by weight, and more particularly from 2 to 10% by weight. weight relative to the total weight of the composition of the invention.

According to a particular embodiment of the invention, the composition comprises one or more ionic surfactants.

According to a particular embodiment of the invention, the composition comprises one or more cationic surfactants. They are advantageously chosen from salts of primary, secondary or tertiary fatty amines, optionally polyoxyalkylenated; quaternary ammonium salts, and mixtures thereof.

As quaternary ammonium salts, mention may in particular be made of quaternary ammonium salts of formula R ₈ R ₉ R ₁₀ R ₁₁ N ⁺ , Q ^- in which the groups R ₈ to R ₁₁ , identical or different, represent an aliphatic group linear or branched, comprising from 1 to 30 carbon atoms, or an aromatic group such as aryl or alkylaryl, at least one of the groups R ₈ to R ₁₁ comprising from 8 to 30 carbon atoms, preferably from 12 to 24 carbon atoms; linear or branched aliphatic groups which may contain heteroatoms such as in particular oxygen, nitrogen, sulfur, these heteroatoms being non-adjacent and halogens; and Q ^- is an anionic counterion chosen in particular from i) halides such as bromides, chlorides, iodides, fluorides, ii) phosphates, iii) acetates, iv) lactates, v) alkyl (C ₁ -C ₄ ) sulfates, vi ) alkyl(C ₁ -C ₄ )sulfonates and vii) alkyl(C ₁ -C ₄ )aryl sulfonates.

Mention may in particular be made of halides, in particular chlorides, of tetraalkylammonium such as dialkyldimethylammonium or alkyltrimethylammonium chlorides in which the alkyl group contains from 12 to 22 carbon atoms, in particular from 14 to 20 carbon atoms such as chlorides of behenyltrimethylammonium, distearyldimethylammonium, cetyltrimethylammonium (cetrimonium chloride), benzyldimethylstearylammonium. Mention may also be made of halides, and in particular chlorides, of palmitylamidopropyltrimethylammonium or stearamidopropyldimethyl-(myristylacetate)-ammonium; in particular the product marketed under the name CERAPHYL ^® 70 by the company VAN DYK.

The anionic counterion Q ^- is preferably a halide, preferably chloride, bromide or iodide, an alkyl(C ₁ -C ₄ ) sulfate, an alkyl(C ₁ -C ₄ ) sulfonate or an alkyl(C ₁ -C ₄₎ )aryl-sulfonate, a methanesulfonate, a phosphate, a nitrate, a tosylate, an anion derived from an organic acid such as an acetate or a lactate or any other anion compatible with ester-functional ammonium. The anionic counterion Q ^- is more particularly a chloride, a methyl sulfate or an ethyl sulfate.

The composition according to the invention may contain, for example, a mixture of quaternary ammonium mono-, di- and triester salts with a majority by weight of diester salts. It is also possible to use the ammonium salts containing at least one ester function described in patents US-A-4874554 and US-A-4137180. It is also possible to use behenoylhydroxypropyltrimethylammonium chloride, for example, offered by the company KAO under the name Quartamin BTC 131.

Preferably, ammonium salts containing at least one ester function contain two ester functions.

Preferably, the surfactant(s) are cationic and are chosen from cetyltrimethylammonium, behenyltrimethylammonium, dipalmitoylethylhydroxyethylmethylammonium salts and mixtures thereof; and more particularly among behenyltrimethylammonium chloride or methosulfate, cetyltrimethylammonium chloride or methosulfate, dipalmitoylethylhydroxyethylmethylammonium chloride or methosulfate and mixtures thereof.

More preferably, the cationic surfactant(s) according to the invention are chosen from alkyltrimethylammonium salts whose alkyl group contains from 12 to 22 carbon atoms, more preferably from 14 to 20 carbon atoms and more particularly behenyltrimethylammonium salts. , cetrimonium salts and in particular cetyltrimethylammonium chloride, behenyltrimethylammonium chloride or their mixtures in all proportions.

According to another particular embodiment of the invention, the composition comprises one or more anionic surfactants.

We hear by "anionic surfactant», a surfactant comprising only anionic groups as ionic or ionizable groups. These groups anionic are preferably chosen from the groups –C(O)OH, –C(O)O^-, -SO₃H, -S(O)₂O^-, -OS(O)₂OH, -OS(O)₂O^-, -P(O)OH₂, -P(O)₂O^-, -P(O)O₂ ^-, -P(OH)₂, =P(O)OH, -P(OH)O^-, =P(O)O^-, =POH, =PO^-, the anionic parts comprising a cationic counterion such as those coming from an alkali metal, an alkaline earth metal, or an amine or an ammonium.

As examples of anionic surfactants which can be used in the composition according to the invention, mention may be made of alkyl sulfates, alkyl ether sulfates, alkylamidoethersulfates, alkylaryl polyethersulfates, monoglyceride sulfates, alkylsulfonates, alkylamidesulfonates, alkylarylsulfonates, alpha-olefin-sulfonates, paraffin-sulfonates, alkylsulfosuccinates, alkyl ethersulfosuccinates, alkylamide-sulfosuccinates, alkylsulfo-acetates, acylsarcosinates, acylglutamates, alkylsulfosuccinamates, acylisethionates and N-acyltaurates, salts of monoesters of alkyl and polyglycoside polycarboxylic acids, acyllactylates, salts of D-galactoside uronic acids, salts of alkyl ether carboxylic acids, salts of alkyl aryl ether carboxylic acids, salts of alkyl acids amidoether-carboxylic acids, and the corresponding non-salified forms of all these compounds, the alkyl and acyl groups of all these compounds having from 6 to 24 carbon atoms and the aryl group denoting a phenyl group.

These compounds can be oxyethylenated and then preferably contain from 1 to 50 ethylene oxide units.

Among the anionic surfactants, it is preferred to use alkyl (C ₆ -C ₂₄ ) sulfates, alkyl (C ₆ -C ₂₄ ) ether sulfates comprising from 2 to 50 ethylene oxide units, in particular in the form of alkali metal salts, ammonium, amino alcohols, and alkaline earth metals, or a mixture of these compounds.

In particular, it is preferred to use alkyl (C ₁₂ -C ₂₀ ) sulfates, alkyl (C ₁₂ -C ₂₀ ) ether sulfates comprising from 2 to 20 ethylene oxide units, in particular in the form of alkali metal salts, ammonium , amino alcohols, and alkaline earth metals, or a mixture of these compounds. Better yet, we prefer to use sodium lauryl ether sulfate, particularly those with 2.2 moles of ethylene oxide. More preferably alkyl (C ₁₂ -C ₂₀ ) sulfates such as alkali metal lauryl sulfate such as sodium.

According to a particular embodiment of the invention, the composition comprises one or more amphoteric or zwitterionic surfactants. Amphoteric surfactants are in particular derivatives of secondary or tertiary aliphatic amines, optionally quaternized, in which the aliphatic group is a linear or branched chain comprising from 8 to 22 carbon atoms, said amine derivatives containing at least one anionic group such as, for example, a carboxylate, sulfonate, sulfate, phosphate or phosphonate group. Mention may be made in particular of alkyl(C ₈ -C ₂₀ )betaines, sulphobetaines, alkyl(C ₈ -C ₂₀ )amidoalkyl(C ₃ -C ₈ )betaines and alkyl(C ₈ -C ₂₀ )-amidalkyl( C ₆ -C ₈ )sulfobetaines.

Among the amphoteric or zwitterionic surfactants cited above, alkyl(C ₈ -C ₂₀ )betaines such as cocobetaine, alkyl(C ₈ -C ₂₀ )amidoalkyl(C ₃ -C ₈ )betaines such as as cocamidopropyl betaine, and mixtures thereof. More preferably, the amphoteric or zwitterionic surfactant(s) are chosen from cocamidopropyl betaine and cocobetaine.

According to a particular embodiment of the invention, the surfactant(s) have a high HLB i.e. greater than 10, preferably greater than 15.

According to another particular embodiment of the invention, the surfactant(s) have an HLB or low i.e. less than or equal to 10, more preferably between 1 and 6.

By "HLB» or Hydrophilic-Lipophilic Balance we mean a hydrophilic/lipophilic balance value, according to the definition of WC Griffin (Classification of Surface-Active Agents by HLB,Journal of the Society of Cosmetic Chemists 1, 311 (1949). It is possible to calculate the HLB using the classic JT Davies method (Davies JT,A quantitative kinetic theory of emulsion type, I. Physical chemistry of the emulsifying agent, Gas/Liquid and Liquid/Liquid Interface. Proceedings of the International Congress of Surface Activity (1957): 426-438).

• les N-lauroyl sarcosinates de métaux alcalins ou alcalino terreux tel que sodium
• les laureth sulfates de métaux alcalins ou alcalino terreux tel que sodium
• les halogénures de béhényl triméthylammonium de préférence chlorure
• les halogénures de de cetrimonium de préférence chlorure
• les dodécyl sulfates de métaux alcalins ou alcalino terreux tels que sodium
• les N-cocoyle glycinates de métaux alcalins ou alcalino terreux tels que sodium

et le ou les tensio-actifs non ioniques sont choisis parmi :

• les alcools lauriques polyoxyéthylénés 4 OE et/ou 23 OE (laureth-23 et/ou laureth-4)
• le monopalmitate de sorbitane polyoxyéthyléné (20OE) et
• le polyglycéryl-4-isostéarate (PG4-isostérarate).

Plus préférentiellement le PG4-isostérarate.Preferably the surfactant(s) of the invention are chosen from:

• N-lauroyl sarcosinates of alkali or alkaline earth metals such as sodium
• laureth sulfates of alkali or alkaline earth metals such as sodium
• behenyl trimethylammonium halides preferably chloride
• cetrimonium halides preferably chloride
• dodecyl sulfates of alkali or alkaline earth metals such as sodium
• N-cocoyl glycinates of alkali or alkaline earth metals such as sodium

and the nonionic surfactant(s) are chosen from:

• polyoxyethylenated lauryl alcohols 4 EO and/or 23 EO (laureth-23 and/or laureth-4)
• polyoxyethylenated sorbitan monopalmitate (20OE) and
• polyglyceryl-4-isostearate (PG4-isostearate).

More preferably PG4-isosterarate.

According to a particular embodiment of the invention, the surfactant(s) are a mixture of nonionic surfactants in ratios such that the HLB of the mixture is a high HLB, preferably the nonionic surfactants are chosen from polyglyceryl- 4 isostearate, polyoxyethylenated lauryl alcohols 4 EO and/or 23 EO (laureth-23 and/or laureth-4) and polyoxyethylenated sorbitan monopalmitate (20OE)

Preferably, the surfactant(s) included in the composition of the invention is a single type of surfactant, preferably non-ionic.

By non-ionic surfactant is preferably meant LAURETH-23, LAURETH-4, oxyethylene sorbitan monopalmitate (20 EO), polyglyceryl-4 –isostearate.

As an example of high HLB non-ionic surfactants, we can cite for example: oxyethylene sorbitan monopalmitate (20OE), Laureth-23.

Preferably the surfactants of the invention are non-ionic and of low HLB, for example laureth-4, polyglyceryl-4-isostearate, more preferably PG4-isosterarate.

According to another preferred embodiment of the invention, the composition comprises one or more silicone surfactants.

The composition according to the invention may comprise one or more silicone surfactants. Silicone surfactants can be water-soluble, spontaneously water-dispersible or water-insoluble. Preferably, they are water-soluble or spontaneously water-dispersible.

Preferably the silicone surfactants are oxyalkylenated, preferably oxyethylenated.

The composition may include silicone surfactants. The silicone surfactants can be chosen from the following compounds of formulas (Id), (IId), (IIId), (IVd) and (Vd) :

[Chem. 17]:

[Chem. 18]:

• R ₁ , identique ou différent, représente un radical alkyle, linéaire ou ramifié, en C₁-C₃₀, ou un radical phényle ;
• R ₃ etR ₄ , identiques ou différents, désignent un radical alkyle, linéaire ou ramifié, en C₁-C₁₂, de préférence un radical méthyle ;
• R ₂ , identique ou différent, représente un groupement –(CH₂)c-O-(C₂H₄O)a’-(C₆H₆O)b’-R₅ou bien –(CH₂)c-O-(C₄H₈O)a’-R₅dans lesquels a’ varie de 0 à 50 ; b’ varie de 0 à 50 et a’+b’ est supérieur ou égal à 1; c varie de 0 à 4 ; et
• R ₅ , identique ou différent, est choisi parmi un atome d'hydrogène, un groupe alkyle linéaire ou ramifié, comportant de 1 à 12 atomes de carbone; un groupe alcoxy linéaire ou ramifié, comportant de 1 à 6 atomes de carbone; un groupe acyle linéaire ou ramifié, comportant de 2 à 12 atomes de carbone; un groupe hydroxyle, un groupe -SO₃M, un groupe -O-C(O)-R₆ou -C(O)O-R₆, un groupe aminoalcoxy en C₁-C₆éventuellement substitué sur l'amine par un ou deux radicaux alkyle en C1-C4, éventuellement porteurs d’au moins un groupement hydroxyle; un groupe aminoacyle en C₂-C₆éventuellement substitué sur l'amine par un ou deux radicaux alkyle en C₁-C₄, éventuellement porteurs d’au moins un groupement hydroxyle; un groupe -NHCH₂CH₂COOM, un groupe -N(CH₂CH₂COOM)₂; un groupe aminoalkyle en C₁-C₁₂, éventuellement substitué sur l'amine et sur la chaîne alkyle par un ou deux radicaux alkyle en C₁-C₄, éventuellement porteurs d’au moins un groupement hydroxyle, un groupe carboxyacyle en C₁-C₃₀, un groupe phosphono éventuellement substitué par un ou deux groupes aminoalkyle en C₁-C₁₂substitués, un groupe -CO(CH₂)dCOOM, un groupe -OCO-CHR₇(CH₂)dCOOM, un groupe -NHCO(CH₂)dOH, un groupe ammonium -NH₃Y ; dans lesquels M, identique ou différent, désigne un atome d'hydrogène, ou un contre ion cationique tel que un métal alcalin ou alcalino terreux comme Na, K, Li, NH₄ou une amine organique ; R6 désigne un groupe alkyle, linéaire ou ramifié, en C₁-C₃₀; R₇désigne un atome d'hydrogène ou un groupe SO₃M; d varie de 1 à 10; et Y représente un contre ion anionique tel qu'un halogénure (chlorure, bromure), un sulfate, ou un carboxylate (acétate, lactate, citrate);
• m varie de 0 à 20 ; m' varie de 1 à 20 ; n varie de 0 à 500 ; p varie de 1 à 50 ;
• q varie de 0 à 20 ; w varie de 1 à 100 ;
• a varie de 0 à 50 ; b varie de 0 à 50; et a+b est supérieur ou égal à 1, dans la formule (IVb).

[Chem. 19]:

[Chem. 20]:

[Chem. 21]:
Formulas(ID)has(Vd)in which :

• R ₁ , identical or different, represents a linear or branched C ₁ -C ₃₀ alkyl radical, or a phenyl radical;
• R ₃ and R ₄ , identical or different, designate a linear or branched C ₁ -C ₁₂ alkyl radical, preferably a methyl radical;
• R ₂ , identical or different, represents a group –(CH ₂ )cO-(C ₂ H ₄ O)a'-(C ₆ H ₆ O)b'-R ₅ or –(CH ₂ )cO-(C ₄ H ₈ O)a'-R ₅ in which a' varies from 0 to 50; b' varies from 0 to 50 and a'+b' is greater than or equal to 1; c varies from 0 to 4; And
• R ₅ , identical or different, is chosen from a hydrogen atom, a linear or branched alkyl group, comprising from 1 to 12 carbon atoms; a linear or branched alkoxy group, containing 1 to 6 carbon atoms; a linear or branched acyl group, containing 2 to 12 carbon atoms; a hydroxyl group, a -SO group₃M, a group -O-C(O)-R₆Or -C(O)O-R₆, a C-aminoalkoxy group₁-VS₆optionally substituted on the amine by one or two C1-C4 alkyl radicals, optionally carrying at least one hydroxyl group; a C aminoacyl group₂-VS₆optionally substituted on the amine by one or two C alkyl radicals₁-VS₄, optionally carrying at least one hydroxyl group; a group -NHCH₂CH₂COOM, a group -N(CH₂CH₂COOM)₂; a C aminoalkyl group₁-VS₁₂, optionally substituted on the amine and on the alkyl chain by one or two C alkyl radicals₁-VS₄, optionally carrying at least one hydroxyl group, a C carboxyacyl group₁-VS₃₀, a phosphono group optionally substituted by one or two C aminoalkyl groups₁-VS₁₂substituted, a group -CO(CH₂)dCOOM, an -OCO-CHR group₇(CH₂)dCOOM, a group -NHCO(CH₂)dOH, an ammonium group -NH₃Y; in which M, identical or different, designates a hydrogen atom, or a cationic counterion such as an alkali or alkaline earth metal such as Na, K, Li, NH₄or an organic amine; R6 denotes an alkyl group, linear or branched, in C₁-VS₃₀; R₇denotes a hydrogen atom or an SO group₃M; d ranges from 1 to 10; and Y represents an anionic counterion such as a halide (chloride, bromide), a sulfate, or a carboxylate (acetate, lactate, citrate);
• m varies from 0 to 20; m' varies from 1 to 20; n varies from 0 to 500; p varies from 1 to 50;
• q varies from 0 to 20; w varies from 1 to 100;
• a varies from 0 to 50; b ranges from 0 to 50; and a+b is greater than or equal to 1, in formula (IVb).

We can in particular cite the silicone surfactants sold under the trade names FLUID DC193 and DC5225C by the company DOW CORNING, SILWET® L 77 by the company OSI and MAZIL ® 756 by the company MAZER PPG.

Preferably, the silicone surfactant is a mixture of silicones comprising hydrophilic grafts. It is preferably constituted by a mixture of oxyethylenated (EO) oxypropylenated (OP) polydimethylsiloxane (18 EO/18 OP), cyclopentadimethylsiloxane and water (10/88/2) such as the product marketed under the name Dow Corning 5225C Aid formulation by the DOW CORNING company.

According to a preferred embodiment of the invention, the surfactant(s) are siliconized, optionally poly alkoxylated, in particular polyglycerolated (PEG) and/or are mixed with one or more nonionic surfactants, in particular poly alkoxylated surfactants, such as polyglycerolated polyethylene glycol (PEG) or polypropylene. glycol (PPG).

The composition according to the invention may comprise silicone surfactants in an amount ranging from 0.01% to 30% by weight, in particular from 0.1% to 20% by weight, particularly between 1% and 10% by weight, better still between 2% and 6% by weight relative to the total weight of the composition.

1. les alcools gras,
2. les alpha-diols,
3. les alkylphénols,

ces 3 types composés étant poly(C₁-C₆)alkoxylé (polyéthoxylés, polypropoxylés et/ou polyglycérolés), et ayant une chaîne grasse comportant par exemple 8 à 22 atomes de carbone, le nombre de groupements oxyde d'éthylène ou oxyde de propylène pouvant aller notamment de 2 à 50 et le nombre de groupements glycérol pouvant aller notamment de 2 à 30 ; notamment

• les esters d'acides gras en C₈-C₃₀d’alcool d’alcool gras en C₈à C₂₂polyéthoxylés, polypropoxylés, polyglycérolés et/ou polyéthylèneglycol tel que le PG4-isostéarate, et
• les alkylpolyglycosides (APG),

1. les tensioactifs siliconés éventuellement polyalkoxylés notamment polyglycérolés (PG) et/ou en mélange avec un ou plusieurs tensioactifs non ioniques notamment poly alkoxylés tels que polyglycérolés (PEG), tel que PEG-siliconé comme le polymethylcetyl dimethyl methylsiloxane oxyethylene, ou le mélange CETYL PEG / PPG-10 / 1 DIMETHICONE.

More particularly, the composition of the invention comprises d) one or more surfactants, in particular non-ionic, siliconized or not, preferably chosen from:

1. fatty alcohols,
2. alpha-diols,
3. alkylphenols,

these 3 types of compounds being poly(C ₁ -C ₆ )alkoxylated (polyethoxylated, polypropoxylated and/or polyglycerolated), and having a fatty chain comprising for example 8 to 22 carbon atoms, the number of ethylene oxide or carbon oxide groups propylene which can range in particular from 2 to 50 and the number of glycerol groups which can range in particular from 2 to 30; notably

• C ₈ -C ₃₀ fatty acid esters of polyethoxylated, polypropoxylated, polyglycerolated and/or polyethylene glycol C ₈ to C ₂₂ fatty alcohol alcohols such as PG4-isostearate, and
• alkylpolyglycosides (APG),

1. silicone surfactants optionally polyalkoxylated, in particular polyglycerolated (PG) and/or mixed with one or more nonionic surfactants, in particular polyalkoxylated surfactants such as polyglycerolated (PEG), such as PEG-silicone like polymethylcetyl dimethyl methylsiloxane oxyethylene, or the mixture CETYL PEG / PPG-10 / 1 DIMETHICONE.

We can cite PEG-silicone such as polymethylcetyl dimethyl methylsiloxane oxyethylene, or the CETYL PEG / PPG-10 / 1 DIMETHICONE mixture sold for example by the company EVONIK GOLDSCHMIDT under the name ABIL EM 90.

The surfactant(s) represent(s) in total particularly from 0.01% to 30% by weight relative to the total weight of the composition, preferably from 0.5% to 15% by weight and even more preferably from 1 % to 10% by weight, better between 1% and 5% by weight of the composition.

Some water

According to a particular embodiment of the invention, the composition C1 comprises e) water.

According to a particular embodiment, the composition C1 or C1' contains e) water, d) optionally one or more surfactants as defined previously and c) less than 10% by weight of fatty substances relative to the total weight of the composition, preferably less than 5% by weight of fatty substances, more preferably less than 2% by weight of fatty substances and even more preferably said composition C1 is free of fatty substances c).
The water suitable for the invention may be tap water, distilled water, spring water, floral water, such as cornflower water and/or mineral water such as VITTEL water, LUCAS water or LA ROCHE POSAY water and/or thermal water.

According to one embodiment, the composition C1or C1' of the invention comprises e) water and at least one fatty substance c), in particular in a ratio between the mass of water and the mass of fatty substance c) lower to 1, preferably less than 0.9, more preferably less than 0.9 such as between 0.5 and 0.8.

According to another preferred embodiment of the invention, the composition C1 or C1' comprises mainly by weight water vs. the quantity of fat.
Form of composition:

According to one embodiment of the invention the composition comprises an aqueous phase. The composition is in particular formulated in aqueous lotions or in water-in-oil, oil-in-water emulsions, or in multiple emulsions (triple oil-in-water-in-oil or water-in-oil-in-water emulsion ( such emulsions are known and described for example by C. FOX in “ Cosmetics and Toiletries ” - November 1986 - Vol 101 - pages 101-112).

According to a particular embodiment of the invention the composition is a direct emulsion i.e. oil in water or Oil in water O/W type. The quantity of oil by weight is preferably less than 40% in the inverse emulsion, preferably less than or equal to 35%, more particularly less than or equal to 30% by weight relative to the total weight of the composition.

More particularly in the direct emulsion the quantity of water is greater than or equal to 40% by weight relative to the total weight of the composition, more particularly greater than or equal to 45%, preferably greater than or equal to 50%.

According to another particular embodiment of the invention, the composition of the invention is an inverse emulsion i.e. water in oil or water in oil W/O type. The quantity of oil by weight is preferably greater than 30% in the inverse emulsion, preferably greater than 40%, more preferably greater than or equal to 45% by weight relative to the total weight of the composition. More particularly in the inverse emulsion the quantity of water is less than 40% by weight relative to the total weight of the composition, preferably less than or equal to 35% by weight.

The composition according to the invention preferably has a pH ranging from 3 to 9 depending on the support chosen.

According to a particular embodiment of the invention, the pH of the composition(s) is neutral or even slightly acidic. Preferably the pH of the composition is between 6 and 7. The pH of these compositions can be adjusted to the desired value using acidifying or alkalizing agents usually used in cosmetics or even using conventional buffer systems.

By “ alkalizing agent ” or “ base ” is meant an agent making it possible to increase the pH of the composition in which it is found. The alkalizing agent is a Bronsted, Lowry or Lewis base. It can be mineral or organic. Particularly said agent is chosen from a) ammonia, b) (bi)carbonate, c) alkanolamines such as mono-, di- and triethanolamines as well as their derivatives d) oxyethylenated and/or oxypropylenated ethylenediamines, e) organic amines, f) mineral or organic hydroxides, g) alkali metal silicates such as sodium metasilicates, h) amino acids with basic preferences such as arginine, lysine, ornithine, citruline and hystidine, and i) the compounds of formula (F) following:

• West un radical divalent alkylène en C₁-C₆éventuellement substitué par un ou plusieurs groupements hydroxyle ou un radical alkyle en C₁-C₆, et/ou éventuellement interrompu par un ou plusieurs hétéroatomes tel que O, ou NR_u;
• R _x ,R _y ,R _z ,R _t , etR _u , identiques ou différents, représentent un atome d'hydrogène, un radical alkyle en C₁-C₆ou hydroxyalkyle en C₁-C₆, aminoalkyle en C₁-C₆.

[Chem. 22]:
Formula (F) in which:

• W is a divalent C ₁ -C ₆ alkylene radical optionally substituted by one or more hydroxyl groups or a C ₁ -C ₆ alkyl radical, and/or optionally interrupted by one or more heteroatoms such as O, or NR _u ;
• R _x , R _y , R _z , R _t , and R _u , identical or different, represent a hydrogen atom, a C ₁ -C ₆ alkyl or C ₁ -C ₆ hydroxyalkyl radical, C ₁ -aminoalkyl _C6 .

Mention may be made, as an example of amines of formula (F) , of 1,3 diaminopropane, 1,3 diamino 2-propanol, spermine and spermidine.

By “ alkanolamine ” is meant an organic amine comprising a primary, secondary or tertiary amine function, and one or more linear or branched C ₁ -C ₈ alkyl groups carrying one or more hydroxyl radicals.

Among the mineral or organic hydroxides, mention may be made of those chosen from a) the hydroxides of an alkali metal, b) the hydroxides of an alkaline earth metal, such as sodium or potassium hydroxides, c) the hydroxides of a transition metal, d) lanthanide or actinide hydroxides, quaternary ammonium hydroxides and guanidinium hydroxide. Mineral or organic hydroxides a) and b) being preferred.

Among the acidifying agents of the compositions used in the invention, mention may be made, by way of example, of mineral or organic acids such as hydrochloric acid, orthophosphoric acid, sulfuric acid, carboxylic acids such as hydrochloric acid. acetic acid, tartaric acid, citric acid, lactic acid, sulfonic acids.

The alkalizing agents and the acidifying agents as defined above preferably represent from 0.001% to 20% by weight of the weight of the composition containing them. More particularly from 0.005% to 8% by weight of the composition.

According to a particular embodiment of the invention, the composition comprises a quantity of water less than or equal to 10% by weight relative to the total weight of the composition.

Advantageously, the composition according to the invention comprises a physiologically acceptable medium. In particular the composition is a cosmetic composition.

By physiologically acceptable medium, we mean an environment compatible with the keratin materials of human beings, such as for example skin, lips, nails, eyelashes, eyebrows, hair.

By cosmetic composition is meant a composition compatible with keratin materials, which has a pleasant color, odor and feel, and which does not generate unacceptable discomfort (tingling, tightness, etc.), likely to deter the consumer.

By keratin materials, we mean the skin (body, face, eye area, scalp), hair, eyelashes, eyebrows, body hair, nails, lips.

The composition C1 according to the invention may comprise one or more cosmetic additives chosen from perfumes, preservatives, fillers, coloring agents, UV filters, oils other than fatty substances c), moisturizers, vitamins, ceramides , antioxidants, anti-free radical agents, polymers other than a), thickeners, trace elements, softeners, sequestrants, anti-hair loss agents, anti-dandruff agents, propellants. Particularly the composition according to the invention further comprises one or more coloring agents chosen from pigments, direct dyes and mixtures thereof, preferably pigments; more preferably the pigment(s) of the invention are chosen from carbon black, iron oxides in particular black and micas coated with iron oxide, triarylmethane pigments in particular blue and violet such as BLUE 1 LAKE, pigments azo, particularly red ones such as D&C RED 7 alkali metal salt of lithol red such as the calcium salt of lithol red B, even more preferably red iron oxides.

Advantageously, the composition according to the invention is a makeup composition, in particular a composition for lip makeup, mascara, eyeliner, eye shadow, foundation.
Additional Solvents
According to a particular embodiment of the invention, the composition comprises one or more preferably polar and/or protic solvents different from water. Preferably these polar and/or protic solvents are chosen from monoalcohols having from 2 to 6 atoms of carbon such as ethanol, propanol, n-butanol, isopropanol, isobutanol, tert-butanol, pentanol, hexanol, preferably n-butanol or ethanol, even more preferably ethanol
According to one embodiment, the composition of the invention comprises one or more additional solvents, preferably chosen from monoalcohols having 2 to 6 carbon atoms such as ethanol, propanol, n-butanol, isopropanol, isobutanol, tert-butanol, pentanol, hexanol, preferably n-butanol or ethanol, even more preferably ethanol, in an amount less than 70%, more preferably less than 20%, again more preferably less than 10%, more particularly less than 8% relative to the total weight of fatty substances c) and water e).
The additives

The composition according to the invention may further comprise one or more fillers, in particular in a content ranging from 0.01% to 30% by weight, relative to the total weight of the composition, preferably ranging from 0.01%. at 20% by weight. By fillers, we must understand particles of any shape, colorless or white, mineral or synthetic, insoluble in the medium of the composition whatever the temperature at which the composition is manufactured. These fillers are used in particular to modify the rheology or texture of the composition.

The composition according to the invention can be in the form of an aqueous composition, a water-in-oil emulsion or an oil-in-water emulsion,

According to a particular form of the invention, composition C1 comprises a) one or more polyhydroxyalkanoate (PHA) copolymer(s) as defined above; and b) one or more polyurethane polymer latexes; and c) one or more fatty substances, preferably liquid at 25°C and atmospheric pressure; and f) optionally one or more polar and/or protic solvents chosen from monoalcohols having 2 to 6 carbon atoms such as ethanol, propanol, n-butanol, isopropanol, isobutanol, tertio- butanol, pentanol, hexanol, preferably n-butanol or ethanol, even more preferably ethanol.

The invention is illustrated in more detail in the following examples. Quantities are indicated in weight percentage.

Examples

The PHAs presented in the different examples were prepared in 3-liter chemostats and/or 5-liter Fernbachs flasks depending on the use of an inhibitor of the β-oxidation pathway or not. The isolation of PHAs is similar for all the examples obtained.

During a first step, the microorganism generates PHAs which are stored in intracellular granules whose proportion varies depending on the conditions applied such as the temperature or the nature of the culture medium. The generation of PHAs granules can be associated with the growth of the microorganism or not depending on the nature of the microorganisms. During the second step, the biomass containing the PHAs is isolated, i.e. separated from the fermentation medium, then dried. PHAs are extracted from the biomass before being purified if necessary.

A mixture of saturated and unsaturated carbon sources is, for certain examples, necessary for the stability of the PHA obtained.

Example 1:R side chain PHA ¹ representing a 10% linear unsaturated n-octalenyl group and R ² representing an n-pentyl group

[Chem. 23]:

The process for synthesizing the compound of Example 1 is adapted from the article: Fed-batch production of unsaturated medium-chain-length polyhydroxyalkanoates with controlled composition by Pseudomonas putida KT2440 , Z. Sun, JA Ramsay, M. Guay, BA Ramsay, Applied Microbiological Biotechnology, 82. 657–662. 2009.

The microorganism used is Pseudomonas putida KT2440 ATCC® 47054™. The culture mode is carried out in axenic conditions in discontinuous growth supplied with a maintenance solution containing a mixture of carbon sources at a rate of µ=0.15h ^-1 in a 3L chemostat containing 2.5L of culture medium.

The system is ventilated with an air flow of 0.5 vvm for a dissolved oxygen (DO) setpoint at 30% of saturation. The pH is regulated with a 15% ammonia solution. The temperature of the fermentation medium is regulated at 30°C.

Setting up the fed batch growth fermentation mode:

The fermentation medium is regulated in temperature, dissolved oxygen pressure and pH (not shown) See in the appendix.

The production process is carried out using three distinct culture media. The first culture medium defined MC1 “inoculum” is used for the preparation of the preculture. The second defined culture medium MC2 “bach” is used for the unfed batch growth of the microorganism with the primary carbon sources in the Fernbachs flasks. The third culture medium defined MC3 “maintenance” is used for batch feeding, or maintenance, of the fermentation with the carbon sources of interest at a flow rate calibrated according to the growth of the microorganism.

The composition of Nutrient Broth in mass percentage is 37.5% beef extract and 62.5% peptone. Reference 233000 DIFCO™.

100 mL of preculture are prepared by suspending a cryotube containing 1 mL of the strain with 100 mL “inoculum” culture media at pH adjusted to 6.8 with 2N NaOH in a 250 mL Fernbach flask then incubate at 30°C at 150 rpm for 24 hours. 1.9L of MC2 “BATCH” culture medium placed in a 3L chemostat previously sterilized are inoculated at OD=0.1 with the 100 mL of preculture. After 4 hours at 30°C at 850 rpm.

At the end of the introduction, the biomass is isolated by centrifugation then washed three times with water. The biomass is dried by freeze-drying before being extracted with ethyl acetate for 24 hours. The suspension is clarified by filtration on a GF/A filter (Wattman®). The filtrate, composed of PHA in solution in ethyl acetate, is concentrated by evaporation then dried under high vacuum at 40°C to constant mass.

PHA can optionally be purified by solubilization and successive precipitation in an ethyl acetate/Ethanol 70% methanol system for example.

PHA was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure.

Preparation of example 1’:PHA copolymer with R side chain ¹ representing a 5% unsaturated n-octalenyl group and R ² representing an n-hexyl group
[Chem. 24]:
The copolymer of Example 1’ (5% unsaturation and R chain²representing n-hexyl) was prepared according to the procedure described for Example 1, with the same composition of the microelement solution as that described in Example 1 and with the following culture medium compositions: Ingredients
in grams per liter MC1
“ inoculum ” MC2
“ batch ” MC3 “ maintenance ” (NH ₄ ) ₂ SO ₄ 4.7 4.7 Na ₂ HPO ₄ ; 7H ₂ W 12 9 KH ₂ PO ₄ 2.7 2.03 MgSO ₄ ; 7H ₂ W 0.8 1.03 Nutrient Broth 3 / Nonanoic acid / 0.95 950 Undecylene acid 0.05 50 Microelements Solution / 10 NaOH 2N QSP pH=6.8 milliQ water QSP 1000 g The PHA copolymer of Example 1' has been fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure, with an unsaturation rate of 5%.
Example 1'': CopolymerR side chain PHA ¹ representing a 10% linear unsaturated n-octalenyl group and R ² representing an n-hexyl group
The copolymer of example 1’’ (with 10% unsaturation and R chain²representing n-hexyl) was prepared according to the procedure described for Example 1, with the same composition of the microelement solution as that described in Example 1 and with the following culture medium compositions: Ingredients
In grams per liter MC1
“ inoculum ” MC2
“ batch ” MC3 “ maintenance ” (NH ₄ ) ₂ SO ₄ 4.7 4.7 / Na ₂ HPO ₄ ; 7H ₂ W 12 9 / KH ₂ PO ₄ 2.7 2.03 / MgSO ₄ ; 7H ₂ W 0.8 1.03 / Nutrient Broth 3 / / Nonanoic acid / 0.90 900 Undecylene acid / 0.1 100 Microelements Solution / 10 / NaOH 2N QSP pH=6.8 milliQ water QSP 1000 g PHA was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure.
Example 1''':PHA copolymer with R side chain ¹ representing a 30% linear unsaturated n-octalenyl group and R ² representing an n-pentyl group
The copolymer of example 1’’’ (with 30% unsaturation and R chain²representing n-pentyl) was prepared according to the procedure described for Example 1, with the same composition of the microelement solution as that described in Example 1 and with the following culture medium compositions: Ingredients
In grams per liter MC1
“ inoculum ” MC2
“ batch ” MC3 “ maintenance ” (NH ₄ ) ₂ SO ₄ 4.7 4.7 / Na ₂ HPO ₄ ; 7H ₂ W 12 9 / KH ₂ PO ₄ 2.7 2.03 / MgSO ₄ ; 7H ₂ W 0.8 1.03 / Nutrient Broth 3 / / Octanoic acid / 0.70 700 Undecylene acid / 0.3 300 Microelements Solution / 10 / NaOH 2N QSP pH=6.8 milliQ water QSP 1000 g The PHA copolymer was fully characterized by spectroscopic and spectrometric methods and conforms to the expected chemical structure.
Example 2: Poly(3-HydroxyOctanoate-co-Undecenoate) 10% unsaturations grafted at 100% with thiolactic acid (Compound of Example 1 grafted with TLA thiolactic acid):

[Chem. 25]:

1 g of compound of Example 1 and 150 mg of thiolactic acid were dissolved in 20 mL of ethyl acetate at room temperature with stirring. 20 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365 nm (reference) and with stirring for at least 10 minutes.

20 mL of the reaction medium was then precipitated in a 200 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 2 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure.
Example 3 : Poly(3-HydroxyOctanoate-co-Undecenoate) 10% unsaturations grafted at 100% with octanethiol (Compound from Example 1 grafted with n-octanthiol)

[Chem. 26]:

0.5 g of compound of Example 1 and 125 mg of octanethiol were dissolved in 10 mL of ethyl acetate at room temperature with stirring. 15 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365 nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 100 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 3 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure.
Example 4 : Poly(3-HydroxyOctanoate-co-Undecenoate) 10% unsaturations grafted at 75% with 8-mercapto-1-octanol (Compound from Example 1 grafted with 8-mercapto-1-octanol)

[Chem. 27]:

50 mg of compound of Example 1 and 10 mg of 8-mercapto-1-octanol were dissolved in 5 mL of ethyl acetate at room temperature with stirring. 2 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365 nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 50 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 4 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. Grafting at 75% or 7.5% function in total.
Example 5 : Poly(3-HydroxyOctanoate-co-Undecenoate) 10% unsaturations grafted at 32% with cysteamine (Compound from Example 1 grafted with cysteamine)

[Chem. 28]:

0.5 g of compound of Example 1 and 54 mg of cysteamine were solubilized in a mixture of 10 mL of dichloromethane and 2 mL of ethanol at room temperature with stirring. 10 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365 nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 100 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 5 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. Grafting at 32% or 3.2% function in total.
Example 6 : Poly(3-HydroxyOctanoate-co-Undecenoate) 10% unsaturations grafted at 73% with cyclohexanethiol (CHT) (Compound from Example 1 grafted CHT)

[Chem. 29]:

100 mg of compound of Example 1 and 26 mg of cyclohexanethiol were dissolved in 5 mL of dichloromethane at room temperature with stirring. 5 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365 nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 50 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 6 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. Grafting at 73% or 7.3% function in total.
Example 7: Poly(3-HydroxyOctanoate-co-Undecenoate) 10% unsaturations grafted at 66% with 2-furanmethanethiol (FT) (Compound from Example 1 grafted FT)

[Chem. 30] :

100 mg of compound of Example 1 and 26 mg of 2-furanmethanethiol were dissolved in 5 mL of dichloromethane at room temperature with stirring. 5 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365 nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 50 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 7 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. Grafting at 66% or 6.6% function in total.
Example 8: Poly(3-HydroxyOctanoate-co-Undecenoate) 10% unsaturations grafted at 70% with 1-Thio-β-D-glucose tetraacetate (Compound from Example 1 grafted TGT)

[Chem. 31]:

100 mg of compound of Example 1 and 26 mg of 1-Thio-β-D-glucose tetraacetate were dissolved in 5 mL of dichloromethane at room temperature with stirring. 5 mg of 2,2-dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365 nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 50 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 8 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. Grafting at 70% or 7% function in total.
Example 9: Poly(3-HydroxyOctanoate-co-Undecenoate) 10% unsaturations grafted at 50% with 2-phenylethanthiol (PT) (Compound of Example 1 grafted PT)

[Chem. 32]:

100 mg of compound of Example 1 and 26 mg of 2-phenylethanthiol were dissolved in 5 mL of dichloromethane at room temperature with stirring. 5 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365 nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 50 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 9 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. Grafting at 50% or 5% function in total.
Example 10: Poly(3-HydroxyOctanoate-co-Undecenoate) 10% unsaturations grafted at 64% with 4-tert-Butylbenzyl mercaptan (TBM) (Compound from Example 1 grafted TBM)

[Chem. 33]:

100 mg of compound of Example 1 and 26 mg of 4-tert-Butylbenzyl mercaptan were dissolved in 5 mL of dichloromethane at room temperature with stirring. 5 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 50 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 10 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. Grafting at 64% or 6.4% function in total.
Example 11: Poly(3-HydroxyNonanoate-co-Undecenoate) with 10% unsaturations grafted at 100% with thiolactic acid

[Chem. 34]:

0.1 g of compound of Example 1'' and 15 mg of thiolactic acid were dissolved in 5 mL of chloroform at room temperature with stirring. 5 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 50 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 11 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. 100% grafting.
Example 12: Poly(3-HydroxyNonanoate-co-Undecenoate) 5% unsaturations grafted at 100% with octanethiol

[Chem. 35]:

1 g of PHA copolymer from Example 1' and 150 mg of octanethiol were dissolved in 15 mL of ethyl acetate at room temperature with stirring. 20 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 500 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The grafted PHA of Example 12 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. 100% grafting.
Example 13: Poly(3-HydroxyNonanoate-co-Undecenoate) 5% unsaturations epoxidized at 100%

[Chem. 36]:

20 g of PHA copolymer from Example 1' are dissolved in 80 mL of anhydrous dichloromethane. A suspension of 1.9 g of m-CPBA 77% is prepared with 20 mL of anhydrous dichloromethane and added to the mixture with stirring, at room temperature for at least 120 hours.

The reaction medium was then precipitated in a 500 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The PHA of Example 13 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. 100% epoxidation.
Example 14: Poly(3-HydroxyNonanoate-co-Undecenoate) 10% unsaturations epoxidized at 100%
[Chem. 37]

10 g of PHA copolymer from Example 1'' (unsaturation rate of 10)% are dissolved in 40 mL of anhydrous dichloromethane. A suspension of 1.9 g of m-CPBA 77% is prepared with 10 mL of anhydrous dichloromethane and added to the mixture with stirring, at room temperature for at least 120 hours.

The reaction medium was then precipitated in a 500 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The PHA of Example 14 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. 100% epoxidation.
Example 15: Poly(3-HydroxyOctanoate-co-Undecenoate) 30% unsaturations epoxidized at 100%

10 g of PHA copolymer from Example 1” (unsaturation rate of 30%) are dissolved in 40 mL of anhydrous dichloromethane. A suspension of 6.2 g of m-CPBA 77% is prepared with 10 mL of anhydrous dichloromethane and added to the mixture with stirring, at room temperature for at least 120 hours.

The reaction medium was then precipitated in a 250 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The PHA of Example 15 was fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure. 100% epoxidation.
Example 16: Poly(3-HydroxyNonanoate-co-Undecenoate) 5% unsaturations grafted at 100% with 4-tert-Butylbenzyl mercaptan (TBM) (Compound from Example 1' grafted TBM)

[Chem. 39]:

2 g of PHA copolymer from Example 1' and 300 mg of 4-tert-butylbenzylmercaptan were dissolved in 25 mL of ethyl acetate at room temperature with stirring. 25 mg of 2,2-Dimethoxy-2-Phenylacetophenone (IRGACURE 651) was added to the mixture. The medium was then irradiated under a 100W UV lamp at 365nm (reference) and with stirring for at least 10 minutes.

The reaction medium was then precipitated in a 500 mL mixture of ethanol/water 70/30 vv. A viscous white precipitate was obtained. This step can be repeated. The product thus obtained is dissolved in a minimum of ethyl acetate, poured onto a Teflon plate, then dried under dynamic vacuum at 40°C, to obtain a homogeneous film.

The PHA of Example 16 was fully characterized by spectroscopic and spectrometric methods and conforms to the expected chemical structure. 100% grafting.
Example 17 : PHA copolymer with side chain R ¹ representing an isohexylenyl group and R ² representing an isobutyl group

[Chem. 40]:
The process for obtaining Example 17 is an adaptation of Applied and Environmental Microbiology , Vol 60, No. 9. 3245-3254 (1994) “Polyester Biosynthesis Characteristics of Pseudomonas citronellolis Grown on Various Carbon Sources, Including 3-Methyl- Branched Substrate”. MUN HWAN CHOI and SUNG CHUL YOON. The microorganism used is Pseudomonas citronellolis ATCC® 13674™. The culture mode is carried out under axenic conditions in non-fed discontinuous culture in 5L Fernbachs flasks (Corning® ref. 431685) containing 2 of culture medium, shaken at 110rpm at 30°C in an orbital incubator (diameter of the 'orbit of 2.5cm).
The production process is carried out using two distinct culture media. The first culture medium defined MC1 “inoculum” is used for the preparation of the preculture. The second culture medium defined MC2 “bach” is used for the growth in unfed batch culture of the microorganism with the carbon source of interest in the Fernbachs flasks.

The composition of Nutrient Broth in mass percentage is 37.5% beef extract and 62.5% peptone. Reference 233000 DIFCO™ BD.
The composition of the yeast extract in mass percentage is 100% autolyzate of the yeast Saccharomyces cerevisiae. Reference 210933 DIFCO™ BD.

100 mL of preculture are prepared by suspending a cryotube containing 1 mL of the strain with 100 mL “inoculum” culture media at pH adjusted to 6.8 with 2N NaOH in a 250 mL Fernbach then incubate at 30 °C at 150 rpm for 24 hours. 1.9L of MC2 “BATCH” culture medium placed in a previously sterilized 5L Fernbach are inoculated at OD=0.1 with 100mL of inoculum.
After 70 hours at 30°C at 110rpm, the biomass dried by freeze-drying before being extracted with dichloromethane for 24 hours. The suspension is clarified by filtration on a GF/A filter (Wattman®). The filtrate, composed of PHA in solution in dichloromethane, is concentrated by evaporation then dried under high vacuum at 40°C to constant mass.
The PHA can optionally be purified by solubilization and successive precipitation such as a dichloromethane methanol system for example.
The PHA copolymer of Example 3 has been fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure with: 68 mole % of unit (A) including R¹=isohexylenyland 32 mole % of unit (B) of which R²=isobutyl.
Example 18 :Copolymer of R side chain PHA ¹ representing an isohexyl group and R ² representing an isobutyl group

[Chem. 41]:
Example 18 is obtained by hydrogenation of the PHA copolymer of Example 17 via an H-Cube Midi® continuous hydrogenator from ThalesNanotechnology.
A solution of 2 g (8.83 millimoles) of PHA from Example 17 is prepared with a mixture composed of 100 ml of ethyl acetate (SIGMA ALDRICH – CAS: 141-78-6) and 100 ml of methanol ( SIGMA ALDRICH – CAS: 67-56-1) is introduced at a flow rate of 3 ml per minute into a hydrogenation cartridge containing the 5% palladium on carbon catalyst (MidiCard ref DHS 2141; Thalesnano technology) maintained at 100° C under a pressure of 80 bars in the presence of hydrogen within the ThalesNanotechnology H-Cube Midi® system. The reduction of the double bond is followed by NMR. After 6 consecutive reduction cycles, the solution is concentrated by evaporation then dried under vacuum to constant mass.
The PHA can optionally be purified by solubilization and successive precipitation such as a dichloromethane methanol system for example.
The PHA copolymer of Example 18 was entirely characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure with: 68 mole % of unit (A) of which R ¹ = isohexyl and 32 mole % of unit ( B) of which R ² = isobutyl

Example 19:

A polymer was prepared using the microorganism Pseudomonas putida KT2440 ATCC 47054™, octanoic acid.
The culture method was carried out under axenic batch conditions in 5 L Fernbachs flasks (Corning® ref. 431685) containing 2 L of culture medium, shaken at 110 rpm at 30°C in an orbital incubator ( orbit diameter of 2.5 cm).
The synthesis process was carried out using two distinct culture media. The first defined culture medium MC1 “inoculum” was used for the preparation of the inoculum. The second culture medium defined MC2 “batch” was used for the unfed batch growth of the microorganism with octanoic acid in Fernbach flasks.
The composition in grams per liter of the two media is described in Table 8 below:

(2) The composition of the microelement solution in grams per liter is described in Table 9 below:

100 ml of inoculum were prepared by suspending a cryotube containing 1 ml of the strain with 100 ml “inoculum” culture media at pH adjusted to 6.8 with 2N NaOH in a 250 ml Fernbach flask then incubated at 30°C at 150 rpm for 24 hours. 1.9 l of MC2 “BATCH” culture medium placed in a previously sterilized 5 l Fernbach flask were inoculated at OD = 0.1 with 100 ml of inoculum. After 70 hours at 30°C at 110 rpm, the biomass was dried by freeze-drying before being extracted with dichloromethane for 24 hours. The suspension was clarified by filtration on a GF/A filter (Wattman®); the filtrate, containing the copolymer in solution in dichloromethane, was concentrated by evaporation then dried under high vacuum at 40°C to constant mass. The crude polyhydroxyalkanoate was purified by precipitation of a solution of the latter in solution in 10 times its weight of dichloromethane, in 10 volumes of cold methanol solution. The solid obtained was dried under high vacuum at 40 °C to constant mass.
The molecular weight of the polyhydroxyalkanoate obtained was characterized by size exclusion chromatography, refractive index detection
■ Eluent: THF
■ Analytical flow rate: 1 mL/min
■ Injection: 100 μL
■ Columns: 1 Agilent PLGel Mixed-D 5μm column; 300 x 7.5mm; 1 Agilent PLGel Mixed-C 5μm column; 300 x 7.5mm; 1 Agilent Oligopore column; 300 x 7.5mm
■ at room temperature (25°C)
■ Detection: Waters 2487 Dual Absorbance Detector, Waters 2414 Refractive
■ Index Detector
■ Integrator: refractive index at 45°C and 64mV
■ Empower (GPC Module Relative/conventional molar mass)
■ Empower injection duration 40 min
■ Standards: High mass polystyrene / EasiVial PS-H 4 mL from Agilent Technology Part No. PL2010-0200
The analysis makes it possible to measure the weight average molecular weight (Mw in g/mole), the number average molecular weight (Mn in g/mole), the polydispersity index Ip (Mw/Mn) and the degree of polymerization DPn.
The monomeric composition of the polyhydroxyalkanoate obtained was defined by gas chromatography equipped with a flame ionization detector.
Identification is carried out via the injection of commercial standards and the monomeric composition was determined by methanolysis and sylylation treatment.
To determine the monomeric composition, 7 mg of the polyhydroxyalkanoate polymer was dissolved in 1.5 mL of chloroform and was methanolyzed in the presence of 1.5 mL of a solution of MeOH/HCl (17/2, v/v) at 100°C for 4 hours. The organic phase was then washed with 1 mL of water then dried over MgSO4. Sylilation of the methyl esters formed was carried out by adding 100 μL of BSTFA (N,Obis(trimethylsilyl)trifluoroacetamide) and 100 μL of pyridine to the methylated sample. The solution was heated to 70°C for 1 hour then evaporated to dryness. The sample is then dissolved in 600 μL of dichloromethane and analyzed by chromatography under the following conditions:
■ Hewlett Packard 6890 Series device
■ ZB-5 HT stationary phase column from Phenomenex (length: 30 m, diameter: 0.25 mm)
■ Temperature: isothermal 60°C to 300°C in 6 min (heating rate: 10°C/min)
■ Gas: Helium; flow rate: 0.8 ml/min
■ Injector: Temperature: 250°C; 50ml/min
■ Flame ionization detector; Temperature: 300°C
■ Injection: Volume 1 µl
A copolymer was thus obtained containing 91% by weight of poly (hydroxy-3-octanoate), 6% by weight of poly (hydroxy-3-hexanoate) and 3% by weight of poly (hydroxy-3-butanoate).
■ Mn = 68,100 g/mol
■ Mw = 149,100 g/mol
■ Ip = 2.2
■ DPn = 531
Example 20:
A polymer was prepared using the microorganism Pseudomonas putida KT2440 ATCC® 47054™, octanoic acid and acrylic acid.
The culture mode was carried out in continuous axenic conditions at a dilution of D=0.25h-1 in a 3 L chemostat containing 1.1 L of culture medium. The system was aerated with air at a flow of 3 vvm (vvm = volume of air per volume of fermentation medium per minute) for a dissolved oxygen (DO) setpoint at 30% of saturation.
The production process was carried out using three distinct culture media. The first undefined culture medium (MC1) was used for the preparation of the inoculum. The second defined culture medium (MC2) was used for non-fed batch growth of the microorganism in the fermenter. The third defined culture medium (MC3) was used to feed, or maintain, the continuous fermentation containing octanoic acid and acrylic acid (inhibitor of the β-oxidation pathway).
The MC1 and MC2 media are identical to those described in Example 1. The composition in grams per liter of the MC3 medium is described in Table 10 below:

100 mL of inoculum was prepared by suspending a cryotube containing 1 mL of the strain with 100 mL of Nutrient Broth at pH adjusted to 7.0 with 2N NaOH in a 250 mL Fernbach flask and then incubated at 30° C at 150 rpm for 24 hours.
The fermenter containing 1 liter of MC2 culture medium at 30°C was inoculated at an optical density of 0.1 at 630 nm (OD630=0.1). The system was maintained at 30°C with stirring at 700 +/-200 rpm and regulated in cascade with oxygenation for approximately 16 h or until the microorganism could reach its growth plateau.
The feeding of the fermenter with the MC3 medium was initiated when the microorganism reached its growth plateau, the withdrawal was carried out in order to keep the mass of initial fermentation medium. Once the equilibrium state was reached in continuous culture, a fraction of the withdrawal was centrifuged in order to separate the biomass from the fermentation medium. The biomass was dried by freeze-drying, then extracted with dichloromethane for 24 h. The suspension obtained was clarified by filtration on a GF/A filter (Wattman®). The filtrate obtained, comprising the copolymer in solution in dichloromethane, was concentrated by evaporation then dried under high vacuum at 40°C to constant mass. The crude polyhydroxyalkanoate was purified by precipitation of a solution of the latter in solution in 10 times its weight of dichloromethane, in 10 volumes of cold methanol solution. The solid obtained was dried under high vacuum at 40°C to constant mass.
A copolymer was thus obtained comprising 96% by weight of poly (hydroxy-3-octanoate), 3% by weight of poly (hydroxy-3-hexanoate) and 1% by weight of poly (hydroxy-3-butanoate).
■ Mn = 67,900 g/mol:
■ Mw = 142,000 g/mol:
■ Ip = 2.1:
■ DPn = 611
Example 21: PHA copolymer with R side chain¹representing a groupnot-hexyl and R²representing a groupnot-butyl

[Chem. 42]:


A polymer was prepared using the microorganism Pseudomonas putida KT2440 ATCC® 47054™, nonanoic acid and acrylic acid.
The culture mode is carried out in continuous axenic conditions at a dilution of D=0.25h-1 in a 3L chemostat containing 1.1L of culture medium. The system is aerated with air at a flow rate of 1 vvm for a dissolved oxygen (DO) setpoint at 30% of saturation.
The production process is carried out using three distinct culture media. The first culture medium (MC1) is used for the preparation of the inoculum. The second culture medium (MC2) is used for batch growth of the microorganism in the fermenter. The third culture medium (MC3) is used for feeding, or maintaining, the continuous fermentation containing the carbon source of interest and the inhibitor of the β-oxidation pathway (acrylic acid). The composition in grams per liter of the three media MC1, MC2 and MC3 is described in Table 11 below: The composition of Nutrient Broth in mass percentage is 37.5% beef extract and 62.5% peptone. Reference 233000 DIFCO™.
The composition of the microelement solution in grams per liter is described in Table 15 below. 100 mL of inoculum are prepared by suspending a cryotube containing 1 mL at OD=10 of the strain with 100 mL of MC1 “inoculum” at pH previously adjusted to 7.0 with 2N NaOH in a 500 mL Fernbach then incubate at 30° C at 150rpm for 24 hours.
The 3L fermenter containing 1 liter of MC2 “batch” culture medium at 30°C is inoculated at an optical density of 0.1 at 600nm (OD600=0.1). The system is maintained at 30°C with stirring at 700rpm +/-200rpm regulated in cascade with oxygenation for approximately 16 hours and/or until the microorganism can reach its growth plateau.
The fermenter is fed with “continuous” MC3 media once the microorganism has reached its growth plateau, and withdrawal is carried out in order to maintain the mass of initial fermentation medium. Once the equilibrium state is reached in continuous culture, a fraction of the withdrawal is centrifuged in order to separate the biomass from the fermentation medium. The biomass is dried by freeze-drying before being extracted with dichloromethane for 24 hours. The suspension is clarified by filtration on a GF/A filter (Wattman®). The filtrate composed of PHA in solution in dichloromethane is concentrated by evaporation then dried under high vacuum at 40°C to constant mass.
The molecular weight of the polyhydroxyalkanoate obtained was characterized by size exclusion chromatography, refractive index detection
■ Eluent: THF
■ Analytical flow rate: 1 mL/min
■ Injection: 100 μL
■ Columns: 1 Agilent PLGel Mixed-D 5μm column; 300 x 7.5mm; 1 Agilent PLGel Mixed-C 5μm column; 300 x 7.5mm; 1 Agilent Oligopore column; 300 x 7.5mm
■ at room temperature (25°C)
■ Detection: Waters 2487 Dual Absorbance Detector, Waters 2414 Refractive
■ Index Detector
■ Integrator: refractive index at 45°C and 64mV
■ Empower (GPC Module Relative/conventional molar mass)
■ Empower injection duration 40 min
■ Standards: High mass polystyrene / EasiVial PS-H 4 mL from Agilent Technology Part No. PL2010-0200
The analysis makes it possible to measure the weight average molecular weight (Mw in g/mole), the number average molecular weight (Mn in g/mole), the polydispersity index Ip (Mw/Mn) and the degree of polymerization DPn.
The monomeric composition of the polyhydroxyalkanoate obtained was defined by gas chromatography equipped with a flame ionization detector.
Identification is carried out via the injection of commercial standards and the monomeric composition was determined by methanolysis and sylylation treatment.
To determine the monomeric composition, 7 mg of the polyhydroxyalkanoate polymer was dissolved in 1.5 mL of chloroform and was methanolyzed in the presence of 1.5 mL of a solution of MeOH/HCl (17/2, v/v) at 100°C for 4 hours. The organic phase was then washed with 1 mL of water then dried over MgSO₄. Sylilation of the methyl esters formed was carried out by adding 100 μL of BSTFA (N,Obis(trimethylsilyl)trifluoroacetamide) and 100 μL of pyridine to the methylated sample. The solution was heated to 70°C for 1 hour then evaporated to dryness. The sample is then dissolved in 600 μL of dichloromethane and analyzed by chromatography under the following conditions:
■ Hewlett Packard 6890 Series device
■ ZB-5 HT stationary phase column from Phenomenex (length: 30 m, diameter: 0.25 mm)
■ Temperature: isothermal 60°C to 300°C in 6 min (heating rate: 10°C/min)
■ Gas: Helium; flow rate: 0.8 ml/min
■ Injector: Temperature: 250°C; 50ml/min
■ Flame ionization detector; Temperature: 300°C
■ Injection: Volume 1 µl
A copolymer was thus obtained comprising 86% by weight of poly(hydroxy-3-nonanoate), 9% by weight of poly(hydroxy-3-heptanoate and 5% by weight of poly(hydroxy-3-pentanoate)
■ Mn = 65,900 g/mol
■ Mw = 143,600 g/mol
■ Ip = 2.2
■ DPn = 531

Example 22:

A polymer was prepared according to the procedure of Example 19 using nonanoic acid (instead of octanoic acid) and without acrylic acid.
A copolymer was thus obtained comprising 68% by weight of poly(hydroxy-3-nonanoate), 27% by weight of poly(hydroxy-3-heptanoate) and 5% by weight of poly(hydroxy-3-pentanoate).
■ Mn = 55,800 g/mol
■ Mw = 124,500 g/mol
■ Ip = 2.2
■ DPn = 469

Example 23:

A polymer was prepared according to the procedure of Example 19 using dodecanoic acid (instead of octanoic acid).
A copolymer was obtained comprising 44% by weight of poly(hydroxy-3-dodecanoate) and 38% by weight of poly(hydroxy-3-decanoate), and 18% by weight of poly(hydroxy-3-octanoate).
■ Mn = 67,400 g/mol
■ Mw = 129,800 g/mol
■ Ip = 1.9
■ DPn = 484
Example 24 : PHA copolymer with side chain R ¹ representing an n -pentyl group and R ² representing an n-propyl group

[Chem. 43]:
The process for obtaining Example 24 is an adaptation of the article Biomacromolecules 2012, 13, 2926−2932: “Biosynthesis and Properties of Medium-Chain-Length Polyhydroxyalkanoates with Enriched Content of the Dominant Monomer”
The microorganism used is Pseudomonas putida ATCC® 47054™
The culture mode is carried out in continuous axenic conditions at a dilution of D = 0.25h ^-1 in a 3L chemostat containing 1.1L of culture medium.
The system is aerated with air at a flow rate of 3 vvm for a dissolved oxygen (DO) setpoint at 30% of saturation.
Assembly :

See
The production process is carried out using three distinct culture media
The first undefined culture medium (MC1) is used for the preparation of the inoculum.
The second defined culture medium (MC2) is used for batch growth of the microorganism in the fermenter.
The third defined culture medium (MC3) is used for feeding, or maintaining, the continuous fermentation containing the carbon source of interest and the inhibitor of the β-oxidation pathway.
The composition in grams per liter of the three media is described in Table 16. Composition in grams per liter of culture media for inoculum and maintenance.

The composition of Nutrient Broth in mass percentage is 37.5% beef extract and 62.5% peptone. Reference 233000 DIFCO™.
The composition of the microelement solution in grams per liter is described in Table 17 composition in grams per liter of the microelement solution

100 mL of inoculum are prepared by suspending a cryotube containing 1 mL of the strain with 100 mL of Nutrient Broth at pH adjusted to 7.0 with 2N NaOH in a 250 mL Fernbach then incubating at 30°C at 150 rpm for 24 hours.
The fermenter containing 1 liter of MC2 culture medium at 30°C is inoculated at an optical density of 0.1 at 630nm (OD630=0.1). The system is maintained at 30°C with stirring at 700rpm +/-200rpm regulated in cascade with oxygenation for approximately 16 hours and or until the microorganism can reach its growth plateau.
The fermenter is fed with the MC3 medium once the microorganism has reached its growth plateau, the withdrawal is carried out in order to keep the mass of initial fermentation medium. Once the equilibrium state is reached in continuous culture, a fraction of the withdrawal is centrifuged in order to separate the biomass from the fermentation medium. The biomass is dried by freeze-drying before being extracted with dichloromethane for 24 hours. The suspension is clarified by filtration on a GF/A filter (Wattman®). The filtrate, composed of PHA in solution in dichloromethane, is concentrated by evaporation then dried under high vacuum at 40°C to constant mass.
The PHA can optionally be purified by solubilization and successive precipitation such as a dichloromethane methanol system for example.
The PHA copolymer of Example 24 was fully characterized by spectrometric and spectroscopic methods. By gas chromatography equipped with an FID detector it appears that the copolymer contains 96% of radical R¹= n-pentyl and 4% radical R²= n-propyl.
Example 25: R side chain PHA ¹ representing a 5% linear 8-bromo-n-octanoyl group and R ² representing an n-hexyl group

[Chem. 44]:

The process for synthesizing the compound of Example 1 is adapted from the article: Fed-batch production of unsaturated medium-chain-length polyhydroxyalkanoates with controlled composition by Pseudomonas putida KT2440 , Z. Sun, JA Ramsay, M. Guay, BA Ramsay, Applied Microbiological Biotechnology, 82. 657–662. 2009.

The microorganism used is Pseudomonas putida KT2440 ATCC® 47054™. The culture mode is carried out in axenic conditions in discontinuous growth supplied with a maintenance solution containing a mixture of carbon sources at a rate of µ=0.15h-1 in a 3L chemostat containing 2.5L of culture medium.

The system is ventilated with an air flow of 0.5 vvm for a dissolved oxygen (DO) setpoint at 30% of saturation. The pH is regulated with a solution composed of ammonia and glucose at 15% and 40% final mass respectively. The temperature of the fermentation medium is regulated at 30°C.

Setting up the fed batch growth fermentation mode:
The fermentation medium is regulated in temperature-dissolved oxygen pressure and pH (not shown).

The production process is carried out using three distinct culture media. The first culture medium defined MC1 “inoculum” is used for the preparation of the preculture. The second defined culture medium MC2 “bach” is used for the unfed batch growth of the microorganism with the primary carbon sources in the Fernbachs flasks. The third culture medium defined MC3 “maintenance” is used for batch feeding, or maintenance, of the fermentation with the carbon sources of interest at a flow rate calibrated according to the growth of the microorganism.

[Table 15]:

The composition of Nutrient Broth in mass percentage is 37.5% beef extract and 62.5% peptone. Reference 233000 DIFCO™.
[Painting. 19]:

100 mL of preculture are prepared by suspending a cryotube containing 1 mL of the strain with 100 mL “inoculum” culture media at pH adjusted to 6.8 with 2N NaOH in a 250 mL Fernbach flask then incubate at 30°C at 150 rpm for 24 hours. 1.9 L of MC2 “BATCH” culture medium placed in a 3L chemostat previously sterilized are inoculated at OD = 0.1 with the 100 mL of preculture. After 4 hours at 30°C at 850 rpm, the introduction of maintenance is carried out by applying the flow rate defined by equation 1.

At the end of the introduction, the biomass is isolated by centrifugation then washed three times with water. The biomass is dried by freeze-drying before being extracted with ethyl acetate for 24 hours. The suspension is clarified by filtration on a GF/A filter (Wattman®). The filtrate, composed of PHA in solution in ethyl acetate, is concentrated by evaporation then dried under high vacuum at 40°C to constant mass.

PHA can optionally be purified by solubilization and successive precipitation in an ethyl acetate/Ethanol 70% methanol system for example.

PHA has been fully characterized by spectroscopic and spectrometric method and conforms to the expected chemical structure: 95 mole % of unit (B) of which R²= n-hexyl (71%) and n-butyl (24%) and 5 molar % of unit (A) of which R1 = 8-bromo-n-octanyl (5.9%) and 6-bromo-n-hexyl (0.2%).
.
Examples 26 to 32: Compositions of association examples and evaluation.
Preparation of compositions:
The compositions described in Tables 20 and 21 below were prepared according to the following protocol:
The fatty phase A was produced by mixing all the ingredients of phase A using a SpeedMixer DAC 150 from the company Speedmixer.^TMfor 5 minutes at 3500 rpm.
In parallel, aqueous phase B was also produced by mixing all the ingredients of phase B using a speedmixer for 5 minutes at 3500 rpm.
Once formed, the two phases were mixed using a speedmixer for 5 minutes at 3500 rpm.
We thus obtained stable emulsions Evaluations of the compositions:
Each composition 26 to 32 is deposited on a Byko Chart Lenata contrast card using a film puller and left to dry for 24 hours at 25°C and 45% relative humidity. The final thickness of the deposit is 30µm.
Water resistance was evaluated according to the following protocol:
On the 30µm dry deposit, the sensitivity to water is evaluated after depositing 20µl of water on the surface of the deposit. The evaluations are made after 1 hour of contact between the water and the deposit. The level of water sensitivity is assessed as follows: Sensitivity level Appearance of the deposit 1- solubilized the deposit is solubilized and the support visible 2- sticky the deposit is present but sticky to the finger 3- marked the deposit is present and after wiping the drop of water,
the imprint of the drop is visible 4 - unsolubilized the deposit remained intact after wiping off the drop of water Wear resistance was evaluated according to the following protocol:
On the 30µm dry deposit, a hydrophilic steel ball is used as a wiper. The load or normal force applied is 1N, the movement speed is 50 mm.s^-1. On each film, tracks are defined on which the wiper makes multiple passes.
In the case of wear measurements, permanent contact is maintained during the back and forth movements of the ball on the deposit. The number of passages increases for each track. Wear resistance is quantified as corresponding to the minimum number of passes to completely wear out the deposit.
In the case of this study the number of passages per track are respectively 10, 30, 50,100, 200 and 300 passages.
Each measurement was the subject of 5 replies.
Wear resistance test results will be quantified as described in the table below: Wear resistance Ratings 0-10 ball passes -- 10-30 ball passes - 30-50 ball passes +

Claims (23)

Composition, in particular cosmetic, comprising:
a) one or more polyhydroxyalkanoate (PHA) copolymer(s) which contains, and preferably consists of, several repeating units chosen from the units(HAS)following, as well as their optical and geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates:
-[-O-CH(R¹)-CH₂-C(O)-]- unit(HAS)
polymeric units(HAS)in which :

• R ¹ represents a hydrocarbon chain, non-cyclic saturated or unsaturated, linear or branched, or cyclic saturated or unsaturated, aromatic or non-aromatic, comprising from 5 to 28 carbon atoms; preferably the hydrocarbon chain is chosen from i) (C ₅ -C ₂₈ ) alkyl, linear or branched, ii) (C ₅ -C ₂₈ ) alkenyl, linear or branched, iii) (C ₅ -C ₂₈ ) alkynyl, linear or branched, preferably the hydrocarbon group is linear;

said hydrocarbon chain being:

• optionally substituted by one or more atoms or groups chosen from: a) halogen such as chlorine or bromine, b) hydroxy, c) thiol, d) (di)(C ₁ -C ₄ )(alkyl)amino, e) (thio )carboxy, f) (thio)carboxamide –C(O)-N(R _a ) ₂ or –C(S)-N(R _a ) ₂ , g) cyano, h) iso(thio)cyanate, i) ( hetero)aryl such as phenyl or furyl, and j) (hetero)cycloalkyl such as anhydride, epoxide or dithiolane, k) cosmetic active ingredient; l) RX with R representing a group chosen from α) cycloalkyl such as cyclohexyl, β) heterocycloalkyl such as sugar preferably monosaccharide such as glucose, γ) (hetero)aryl such as phenyl, δ) cosmetic active ingredient, m) thiosulfate and representing a') O, S, N(R _a ) or Si(R _b )(R _c ), b') S(O) _r , or (thio)carbonyl, c') or the associations of a') with b') such as (thio)ester, (thio)amide, (thio)urea, sulfonamide; R _a representing a hydrogen atom, or a (C ₁ -C ₄ )alkyl group, or aryl (C ₁ -C ₄ )alkyl such as benzyl, preferably R _a represents a hydrogen atom; R _b and R _c , identical or different, represent a (C ₁ -C ₄ ) alkyl or (C ₁ -C ₄ ) alkoxy group, particularly a single substituent; preferably chosen from b) halogen, and j) such as epoxide; and or
• optionally interrupted by one or more a') heteroatoms such as O, S, N(R _a ), and Si(R _b )(R _c ), b') S(O) _r , (thio)carbonyl, c') or the associations of a') with b') such as (thio)ester, (thio)amide, (thio)urea, sulfonamide with r being 1 or 2, R _a being as defined above, preferably R _a represents a hydrogen atom, R _b and R _c , being as defined above; And

b) one or more polyurethane latexes;And
c) possibly one or more fatty substances; preferably liquid at 25°C and atmospheric pressure; And
d) optionally one or more surfactants; And
e) water,
preferably composition C1 comprises c) one or more fatty substances and d) one or more surfactants and e) water. Composition C1’, according to the preceding claim, comprising:
a) one or more polyhydroxyalkanoate (PHA) copolymer(s) which contains, and preferably consists of, at least two different repeating polymeric units chosen from the units(HAS)And(B)following, as well as their optical and geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates:
-[-O-CH(R¹)-CH₂-C(O)-]- unit(HAS)
-[-O-CH(R²)-CH₂-C(O)-]- unit(B)
polymeric units(HAS)And(B)in which :

• R ¹ is as defined in the preceding claim; and or

• optionally interrupted by one or more a') heteroatoms such as O, S, N(R _a ), and Si(R _b )(R _c ), b') S(O) _r , (thio)carbonyl, c') or the associations of a') with b') such as (thio)ester, (thio)amide, (thio)urea, sulfonamide with r being 1 or 2, R _a being as defined above, preferably R _a represents a hydrogen atom, R _b and R _c , being as defined above;
• R ² represents a hydrocarbon group, cyclic or non-cyclic, linear or branched, saturated or unsaturated, comprising from 3 to 30 carbon atoms optionally substituted by one or more atoms or groups a) to m) and/or optionally interrupted by one or more heteroatoms or groups a') to c') as defined for R¹; in particular chosen from (C₃-VS₂₈)alkyl, linear or branched, and (C₃-VS₂₈) linear or branched alkenyl, in particular a linear hydrocarbon group, more particularly (C₄-VS₂₀)alkyl or (C₄-VS₂₀)alkenyl, preferably the hydrocarbon group has a carbon number corresponding to the number of carbon atoms of the radicalR ¹ from which at least one carbon atom is subtracted, preferably corresponding to the number of carbon atoms of the radicalR ¹ from which two carbon atoms are subtracted; And

b) one or more polyurethane latexes;And
c) possibly one or more fatty substances; preferably liquid at 25°C and atmospheric pressure; And
d) optionally one or more surfactants; And
e) water,
Being heard that :

• (A) is different from (B) and
• preferably composition C1' comprises c) one or more fatty substances and d) one or more surfactants and e) water.

Composition C1 or C1' according to claim 1 or 2, in which the PHA copolymer(s) a) contains the repeating unit of formula (I), as well as their optical, geometric isomers, their acid salts or basic, organic or mineral, and their solvates such as hydrates:
(I)
Formula(I)in which :

• R ¹ and R ² are as defined in claim 1;
• m and n are integers greater than or equal to 1, preferably the sum n + m is inclusively between 450 and 1400;

preferably m > n whenR ¹ AndR ² represent an unsubstituted and uninterrupted alkyl group – more preferably when R¹and R²are linear alkyl then R¹is a C alkyl group₅-VS₁₃; and R²represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 2 carbon atoms; And
preferably m < n whenR ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or interrupted alkenyl or optionally substituted and/or interrupted alkynyl group, andR ² represents an alkyl group. Composition C1 or C1' according to claim 1, in which the PHA copolymer(s) a) contains three different repeating polymeric units(HAS),(B)And(VS), preferably consisting of 3 different polymeric units(HAS),(B)And(VS), following, as well as their optical and geometric isomers and their solvates such as hydrates:
-[-O-CH(R¹)-CH₂-C(O)-]- unit(HAS)
-[-O-CH(R²)-CH₂-C(O)-]- unit(B)
-[-O-CH(R³)-CH₂-C(O)-]- unit(VS)
polymeric units(HAS),(B)And(VS)in which :

• R ¹ , and R ² are as defined in claim 1 or 2;
• R ³ represents a hydrocarbon group, cyclic or non-cyclic, linear or branched, saturated or unsaturated, comprising from 1 to 30 carbon atoms optionally substituted by one or more atoms or groups a) to m) and/or optionally interrupted by one or several heteroatoms or groups a') to c') as defined for R ¹ in claim 1 or 2; in particular represents a hydrocarbon group chosen from (C ₁ -C ₂₈ ) alkyl, linear or branched, and (C ₂ -C ₂₈ ) linear or branched alkenyl, in particular a linear hydrocarbon group, more particularly (C ₄ -C ₂₀ ) alkenyl, preferably the hydrocarbon group has a number of carbons corresponding to the number of carbon atoms of the radical R ¹ , or corresponding to the number of carbon atoms of the radical R ¹ from which at least three carbon atoms are subtracted, preference corresponding to the number of carbon atoms of the radical R ¹ from which four carbon atoms are subtracted; And

Being heard that :

• (A) is different from (B) and (C) , (B) is different from (A) and (C), and (C) is different from (A) and (B) ; And

preferably whenR ¹ ,R ² AndR ² represent an unsubstituted and uninterrupted alkyl group the molar percentage in unit(HAS)is greater than the mole percentage in units(B),and greater than the mole percentage in unit(VS)– more preferentially when R¹,R²and R³are linear alkyl, then R¹is a C alkyl group₅-VS₁₃; and R²represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 2 carbon atoms, and R³represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 4 carbon atoms,And
preferably whenR ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group, then the molar percentage in unit(HAS)is less than the mole percentage in unit(B)and the mole percentage in unit(VS)especially if R²represents an alkyl group and/or R³represent an alkyl group;
more preferably the PHA copolymer(s) a) contains the repeating unit of formula(II),as well as their optical and geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates:
(II)
Formula(II)in which :

• R ¹ , R ² and R ³ are as defined above;
• m , n and p, are integers greater than or equal to 1, preferably the sum n + m + p is inclusively between 450 and 1400;

preferably m > n + p whenR ¹ ,R ² AndR ³ represent an unsubstituted and uninterrupted alkyl group - more preferably when R¹,R²and R³are linear alkyl, then R¹is a C alkyl group₅-VS₁₃; and R²represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 2 carbon atoms, and R³represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 4 carbon atoms; And
preferably m < n + p whenR ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group, andR ² AndR ³ represent an alkyl group. Composition C1 or C1' according to any one of the preceding claims, in which the PHA copolymer(s) a) contains four different repeating polymeric units(HAS),(B),(VS), And(D)preferably consists of 4 different polymer units(HAS),(B),(VS), And(D), following, as well as their optical, geometric isomers and their acid or base, organic or mineral salts, as well as their solvates such as hydrates:
-[-O-CH(R¹)-CH₂-C(O)-]- unit(HAS)
-[-O-CH(R²)-CH₂-C(O)-]- unit(B)
-[-O-CH(R³)-CH₂-C(O)-]- unit(VS)
-[-O-CH(R⁴)-CH₂-C(O)-]- unit(D)
polymeric units(HAS),(B),(VS)And(D)in which :

• R ¹ ,R ² AndR ³ are as defined in any one of claims 1 to 4;
• R ⁴ represents a hydrocarbon group, cyclic or non-cyclic, linear or branched, saturated comprising from 3 to 30 carbon atoms optionally substituted by one or more atoms or groups a) to m) and/or optionally interrupted by one or more heteroatoms or groups a') to c') as defined for R ¹ in any one of the preceding claims; in particular represents a hydrocarbon group chosen from (C ₄ -C ₂₈ ) alkyl, linear or branched optionally substituted by one or more atoms or groups a) to m) and/or interrupted by one or more heteroatoms or groups a') to c ') as defined for R ¹ as defined previously; And

Being heard that :

• (A) is different from (B) , (C) and (D) , (B) is different from (A) , (C) and (D), and (C) is different from (A) , (B) and D) ; and (D) is different from (A) , (B) and (C) ;
• preferably when R ¹ , R ² , R ³ and R ⁴ represent an unsubstituted and uninterrupted alkyl group, the mole percentage in units (A) is greater than the molar percentage in units (B), greater than the molar percentage in units (C ), and greater than the molar percentage in units (D) - more preferably when R ¹ , R ² , R ³ and R ⁴ are linear alkyl, then R ¹ is a C ₅ -C ₁₃ alkyl group; and R ² represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which 2 carbon atoms are subtracted, R ³ represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ to which 4 carbon atoms are subtracted, and R ⁴ represents a linear alkyl group with a carbon number corresponding to the carbon number of R ¹ from which 6 carbon atoms are subtracted , and
• preferably whenR ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group, then the molar percentage in unit(HAS)is less than the mole percentage in unit(B),is less than the mole percentage in unit(B),and is less than the mole percentage in unit(VS),especially ifR ² represents an alkyl group and/orR ³ represent an alkyl group, andR ⁴ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group;

more preferably the PHA copolymer(s) comprise the repeating unit of formula(III),as well as their optical and geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates:
(III)
Formula(III)in which :

• R ¹ , R ² , R ³ , and R ⁴ are as defined above;
• m , n, p, and v are integers greater than or equal to 1, preferably the sum n + m + p + v is inclusively between 450 and 1400;

preferably whenR ¹ ,R ² ,R ³ AndR ⁴ represent an unsubstituted and uninterrupted alkyl group then m > n + p + q-more preferentially when R¹,R²,R³and R⁴are linear alkyl, then R¹is a C alkyl group₅-VS₁₃; and R²represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 2 carbon atoms, R³represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 4 carbon atoms, and R⁴represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 6 carbon atoms; And
preferably whenR ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group, andR ² AndR ³ represent an alkyl group, andR ⁴ represents a group a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group then n > m + v; more preferably n + p > m + v. Composition C1 or C1' according to any one of the preceding claims, in which the PHA copolymer(s) a) contains five different repeating polymeric units(HAS),(B),(VS),(D), And(E)preferably consists of 5 different polymer units(HAS),(B),(VS),(D), And(E)following, as well as their optical, geometric isomers and their acid or base, organic or mineral salts, as well as their solvates such as hydrates:
-[-O-CH(R¹)-CH₂-C(O)-]- unit(HAS)
-[-O-CH(R²)-CH₂-C(O)-]- unit(B)
-[-O-CH(R³)-CH₂-C(O)-]- unit(VS)
-[-O-CH(R⁴)-CH₂-C(O)-]- unit(D)
-[-O-CH(R⁵)-CH₂-C(O)-]- unit(E)
polymeric units(HAS),(B),(C), (D)And(E)in which :

• R ¹ ,R ² ,R ³ AndR ³ are as defined in any one of the preceding claims; And
• R ⁵ represents a hydrocarbon group, cyclic or non-cyclic, linear or branched, saturated comprising from 3 to 30 carbon atoms optionally substituted by one or more atoms or groups a) to m) and/or optionally interrupted by one or more heteroatoms or groups a') to c') as defined for R ¹ ; in particular represents a hydrocarbon group chosen from (C ₄ -C ₂₈ ) alkyl, linear or branched, substituted by one or more atoms or groups a) to l) and/or interrupted by one or more heteroatoms or groups a') to c ') as defined for R ¹ ; preferably the hydrocarbon group has a number of carbons corresponding to the number of carbon atoms of the radical R ⁴ from which at least one carbon atom is subtracted, preferably corresponding to the number of atoms of carbon of the radical R ⁴ from which at least 2 carbon atoms are removed, preferably from which 2 carbon atoms are removed;

Being heard that :

• (A) is different from (B) , (C), (D) and (E) ; (B) is different from (A) , (C), (D) and (E), and (C) is different from (A) , (B), (D) and (E) ; (D) is different from (A) , (B), (C) and (E) ; and (E) is different from (A) , (B), (C) and (D);
• preferably whenR ¹ ,R ² ,R ³ ,R ⁴ AndR ⁵ represent an unsubstituted and uninterrupted alkyl group the molar percentage in unit(HAS)is greater than the mole percentage in units(B),greater than the mole percentage in unit(VS),and greater than the mole percentage in unit(D),greater than the mole percentage in unit(E) -more preferentially when R¹,R²,R³, R⁴and R⁵are linear alkyl, then R¹is a C alkyl group₅-VS₁₃; and R²represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 2 carbon atoms, R³represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 4 carbon atoms, R⁴represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 6 carbon atoms, and R⁵represents a linear alkyl group with a carbon number corresponding to the carbon number of R¹from which we subtract 8 carbon atoms,And
• preferably whenR ¹ represents a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group, then the molar percentage in unit(HAS)is less than the mole percentage in unit(B),is less than the mole percentage in unit(B),and is less than the mole percentage in unit(VS),especially ifR ² represents an alkyl group and/orR ³ represent an alkyl group, andR ⁴ AndR ⁵ represent a substituted and/or interrupted alkyl group, optionally substituted and/or optionally interrupted alkenyl or optionally substituted and/or optionally interrupted alkynyl group;

more preferably the PHA copolymer(s) comprise the repeating unit of formula(IV),as well as their optical and geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates:
(IV)
Formula(IV)in which :

• R ¹ , R ² , R ³ , R ⁴ and R ⁵ are as defined above;
• m , n, p, v and z are integers greater than or equal to 1, preferably the sum n + m + p + v + z is inclusively between 450 and 1400;
• preferably when R ¹ , R ² , R ³ , R ⁴ and R ⁵ represent an unsubstituted and uninterrupted alkyl group then m > n + p + v + z;
• preferably whenR ¹ represents a substituted and/or interrupted alkyl group; optionally substituted and/or optionally interrupted alkenyl; or optionally substituted and/or optionally interrupted alkynyl,R ² AndR ³ represent an alkyl group and the groupsR ⁴ AndR ⁵ represent a substituted and/or interrupted alkyl group; optionally substituted and/or optionally interrupted alkenyl; or optionally substituted and/or optionally interrupted alkynyl, then n > m + v + z; more preferably n + p > m + v + z.

Composition C1 or C1' according to any one of the preceding claims, in which R ¹ represents a hydrocarbon (C ₅ -C ₂₈ ) alkyl chain, linear or branched, preferably linear, more particularly R ¹ is an alkyl group substituted by one or more atoms or groups a) to k), said alkyl group comprising 5 to 12, preferably between 6 and 10 carbon atoms, more preferably between 7 and 9 carbon atoms such as n-octyl; preferably R ¹ represents a hydrocarbon chain, substituted by one or more (preferably one) groups chosen from b) hydroxy, c) thiol, d) (di)(C ₁ -C ₄ )(alkyl)amino, preferably amino, e) carboxy, i) (hetero)cycloalkyl such as anhydride, or epoxide, j) cosmetic active chosen from colored or uncolored, fluorescent or non-fluorescent chromophores such as optical brighteners, UV filters, h) (hetero)aryl such as phenyl or furyl, k) RX with R representing a group chosen from α) cycloalkyl such as cyclohexyl, β) heterocycloalkyl such as sugar preferably monosaccharide such as glucose, γ) (hetero)aryl such as phenyl, δ) cosmetic active as defined previously _and R _a representing a hydrogen atom, a (C ₁ -C ₄ )alkyl group, or aryl (C ₁ -C ₄ )alkyl such as benzyl, preferably R _a represents a hydrogen atom;
even more preferably the PHA copolymer(s) are such that R ¹ represents a hydrocarbon chain, in particular an alkyl group as defined above, which is substituted by one or more (preferably one) groups chosen from a) halogen such as chlorine or bromine , b) hydroxy, d) (di)(C ₁ -C ₄ )(alkyl)amino preferably amino, e) carboxy, i) (hetero)cycloalkyl such as epoxide, h) (hetero)aryl such as phenyl or furyl , k) RX with R representing a group chosen from α) cycloalkyl such as cyclohexyl, β) heterocycloalkyl such as sugar preferably monosaccharide such as glucose, γ) (hetero)aryl such as phenyl, and X representing a') O, S , N(R _a ) preferably S; R _a representing a hydrogen atom, a (C ₁ -C ₄ ) alkyl group, preferably R _a represents a hydrogen atom;
better said hydrocarbon chain R ¹ is substituted at the end of the chain on the opposite side of the carbon atom which carries said radical R ¹ . Composition C1 or C1' according to any one of the preceding claims, in which R ¹ represents a hydrocarbon chain, in particular alkyl, in particular C ₇ -C ₂₀ , more particularly C ₈ -C ₁₈ , even more particularly C ₉ -C ₁₆ , which is interrupted by one or more (preferably one) atoms or groups chosen from O, S, N(R _a ), carbonyl, or their associations such as ester, amide, urea, with R _a being as defined in the preceding claims, preferably R _a represents a hydrogen atom; preferably an alkyl group which is interrupted by one or more atoms chosen from O, S, more preferably by an O, or S atom, in particular S; preferably said interrupted hydrocarbon chain, in particular alkyl, is linear. Composition C1 or C1' according to any one of the preceding claims, in which R ¹ is of the following formula –(CH ₂ ) _r -X-(ALK) _u -G with X being as defined above, in particular representing O, S, N(R _a ), preferably S, ALK represents a (C ₁ -C ₁₀ ) alkylene chain, linear or branched, preferably linear, more particularly (C ₁ -C ₈ ) alkylene, r represents an integer inclusively between 6 and 11, preferably between 7 and 10 such as 8; u is 0 or 1; and G represents a hydrogen atom, or a group chosen from hydroxy, carboxy, (di)(C ₁ -C ₄ )(alkyl)amino, (hetero)aryl in particular aryl such as phenyl, cycloalkyl such as cyclohexyl, or sugar, in particular a monosaccharide optionally protected by one or more groups such as acyl, preferably Suc represents with R ^e representing a group R ^f -C(O)-, with R ^f representing a (C ₁ -C ₄ ) alkyl group such as methyl. Preferably when u is 0, G represents a cycloalkyl group such as cyclohexyl, or sugar as defined above. According to another advantageous variant when u is 1, G represents a hydrogen atom, or a group chosen from hydroxy, carboxy, (di)(C ₁ -C ₄ )(alkyl)amino, (hetero)aryl in particular aryl such than phenyl. Composition C1 or C1' according to any one of the preceding claims, in which the PHA copolymer(s) a) comprise a radical R ² chosen from (C ₁ -C ₂₈ ) alkyl, linear or branched, and (C ₂ -C ₂₈ ) alkenyl linear or branched, in particular a linear hydrocarbon group; particularly (C ₃ -C ₂₀ ) alkyl or (C ₃ -C ₂₀ ) alkenyl, preferably the hydrocarbon group has a carbon number corresponding to the number of carbon atoms of the radical R ¹ from which at least one carbon atom is subtracted , preferably corresponding to the number of carbon atoms of the radical R ¹ from which at least two carbon atoms are subtracted. Composition C1 or C1' according to any one of the preceding claims, in which the PHA copolymer(s) a) comprise a radical R ² is a (C ₁ -C ₈ ) alkyl group, linear or branched, preferably linear, particularly in (C ₂ -C ₆ )alkyl, preferably (C ₄ -C ₆ )alkyl such as n-pentyl or n-hexyl; or R ² is a (C ₃ -C ₈ ) branched alkyl group, particularly (C ₄ -C ₆ ) alkyl, preferably branched (C ₄ -C ₅ ) alkyl such as isobutyl. Composition C1 or C1' according to any one of claims 1, 3, 4 to 11, in which the PHA copolymer(s) are such that, when R ¹ represents a (C ₃ -C ₃₀ ) alkyl group, the unit (A) is preferably present in a molar percentage ranging from 0.5% to 99%, more preferably from 50% to 99%, more particularly from 60% to 99% and even more preferably from 70% to 99%. According to this embodiment, the unit (B) is preferably present in a molar percentage ranging from 2 to 40%; and the unit (C) is preferably present in a molar percentage ranging from 0.5 to 20% relative to all of the units (A) , (B) and (C) . Composition C1 or C1' according to any one of claims 1, 3, 4 to 11, in which the PHA copolymer(s) a) are such that whenR ¹ represents hydrocarbon chain chosen from i) (C₅-VS₂₈)alkyl, linear or branched, ii) (C₅-VS₂₈)alkenyl, linear or branched, iii) (C₅-VS₂₈)alkynyl, linear or branched, preferably the hydrocarbon group is linear said hydrocarbon chain being substituted by one or more atoms or groups a) to m) and/or interrupted by one or more heteroatoms or groups a') to c') such as defined for R¹; in particular represents a hydrocarbon group chosen from (C₄-VS₂₈) alkyl, linear or branched optionally substituted by one or more atoms or groups a) to m) and/or interrupted by one or more heteroatoms or groups a’) to c’) as defined above,

• the unit (A) is present in a molar percentage ranging from 0.1 to 99%, preferably a molar percentage ranging from 0.5 and 50%, more preferably a molar percentage ranging from 1 and 40%, even more preferably a molar percentage ranging from 2 and 30%, better a molar percentage ranging from 5 and 20%; even better a mole percentage ranging from 10 and 30% by mole of unit (A) ; And
• the unit (B) is present in a molar percentage ranging from 1% to 99.5%, preferably from 1% to 90%, more preferably from 2% to 70%, most particularly from a molar percentage of 2 to 10 %,; And
• the unit (C) is present in a molar percentage ranging from 0.5 to 20%, relative to all of the units (A) , (B) and (C) ; advantageously, the PHA copolymer(s) of the invention comprise from 2% to 10% by mole of unit (B) ; and from 0.5% to 7% by mole of unit (C) , more advantageously the copolymer comprises from 5% to 35% by mole of unit (B) ; and from 0.5% to 7% in mole of unit (C) ..

Composition C1 or C1' according to any one of the preceding claims, in which the PHA copolymer(s) which comprise the repeating units(HAS)following, as well as their optical and geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates: (HAS) R ¹ A1 -ALK ₁ -S-ALK ₂ -COOH A2 -ALK ₁ -S-ALK ₂ -H A3 -ALK ₁ -S-ALK ₂ -OH A4 -ALK ₁ -S-ALK ₂ -NH ₂ AT 5 -ALK ₁ -S-Cycl' A6 -ALK ₁ -S-CH ₂ -Fur A7 -ALK ₁ -S-Suc AT 8 -ALK ₁ -S-ALK ₂ -Ar A9 -ALK ₁ -Hal A10 -ALK ₁ -CN A11 -ALK ₁ -CH=CR _r R _w AT 12 -ALK ₂ -H Repeater unit A1 to A12 in which:
-ALK₁represents a divalent hydrocarbon radical in C₁-VS₂₀linear or branched, preferably C₁-VS₁₀linear or branched, more preferably linear;
-ALK₂represent a divalent hydrocarbon radical in C₁-VS₂₀linear or branched, preferably C₁-VS₁₂linear or branched;
- Rr and Rw independently designate a hydrogen atom or an alkyl radical (C₁-VS₄such as methyl, preferably Rr and Rw are identical;
- Hal represents a halogen atom such as bromine;
- Ar: represents a (hetero)aryl group such as phenyl;
- Cycl': represents a cycloalkyl group such as cyclohexyl or heterocycloalkyl such as dithiolane or epoxide, preferably epoxide;
- Fur: represents a furyl group, preferably 2-furyl;
- Suc: represents a sugar group, in particular a monosaccharide possibly protected by one or more groups such as acyl, in particular acetyl.
Particularly the stereochemistry of carbon atoms carrying R radicals¹is of configuration (R). Composition C1 or C1' according to any one of the preceding claims, in which the PHA copolymer(s) a) comprise the following repeating units as well as their optical, geometric isomers, their acid or base, organic or mineral salts, and their solvates such as hydrates:


m and n are as defined above, Hal represents a halogen atom such as bromine and t represents an integer between 1 and 10, preferably between 3 and 8 such as 6.
Ar: represents a (hetero)aryl group such as phenyl;
Ar': represents a (C ₁ -C ₄ )alkyl(hetero)aryl group such as t-Butylphenyl, preferably 4- t -butylphenyl;
Cycl: represents a cyclohexyl group;
Fur: represents a furyl group, preferably 2-furyl;
Suc: represents a sugar group, in particular a monosaccharide optionally protected by one or more groups such as acyl, preferably Suc represents:

more preferably the PHA copolymer(s) have the following formula, as well as their optical isomers, their organic or mineral acid or base salts, and their solvates such as hydrates:

M, n, Hal, t, Ar, Ar', Cycl, Fur, and Suc are as defined above for compounds (1) to (14).

s


preferably the PHA(s) a) of the invention are chosen from compounds (15), (16) and (17) in particular (16); more particularly the PHA(s) a) of the invention are chosen from compounds (15'), (16') and (17') in particular (16'); more preferably the PHA(s) a) of the invention are chosen from compounds (25), (26), (31) and (32) in particular (26). Composition C1 or C1' according to any one of the preceding claims, in which b) the polyurethane latex(es) is(are) capable of being obtained from:
B₁) of at least one polyol chosen from:

• B ₁₁ ) a polyester polyol resulting from the reaction of:
  • at least one polyol B ₁₁₁ ) with
  • at least one polycarboxylic acid B ₁₁₂ ) and
  • optionally B ₁₁₃ ) at least one monocarboxylic acid;
• B ₁₂ ) a diol; And
• the mixture of B ₁₁ ) and B ₁₂ ); And

B₂) at least one polyisocyanate, preferably a diisocyanate, in particular aliphatic or cycloaliphatic and its mixtures; And
B₃) of at least one hydrophilic monomer chosen from:

• B ₃₁ ) compounds carrying an acid function, in particular carboxylic, or a basic function, in particular primary, secondary or tertiary amine, and further comprising at least one hydroxyl function, preferably at least two hydroxyl functions, in particular two hydroxyl functions such as 2,2-bis(hydroxymethyl)propionic acid and
• B ₃₂ ) diamine compounds of formula H ₂ NR ₅ -NH ₂ (X) in which R ₅ represents an alkylene radical substituted by one or more ionic or potentially ionic groups; And

B₄) optionally at least one amino compound which is not substituted by one or more ionic or potentially ionic groups;
more particularly the polyurethane latex(es) b) is(are) capable of being obtained from:
B₁) of at least one polyol chosen from:

• B ₁₁ ) at least one polyester polyol resulting from the reaction of:
  • at least one polyol B ₁₁₁ ) such as neopentyl glycol, hexanediol, butanediol with
  • at least one polycarboxylic acid B ₁₁₂ ) such as adipic acid, succinic acid and optionally B ₁₁₃ ) at least one monocarboxylic acid, preferably abietic acid or rosin; and/or B ₁₂ ) at least one diol; and their mixture; And

B₂) of at least one polyisocyanate, preferably at least one diisocyanate, in particular aliphatic or cycloaliphatic such as 3-isocyanatomethyl-3,5,5-trimethylcyclohexane isocyanate (isophorone diisocyanate or IPDI), bis-(4 -isocyanatocyclohexyl)-methane hexamethylene diisocyanate and their mixture; And
B₃) of at least one hydrophilic monomer chosen from B₃₁) compounds carrying an acid function, for example a carboxylic function, or a basic function, for example a primary, secondary or tertiary amine function, and further comprising at least one hydroxyl function, preferably at least two functions hydroxyls, in particular two hydroxyl functions such as 2,2-bis(hydroxymethyl)propionic acid and/or B₃₂) at least one diamine compound of formulaH ₂ NR ₅ -NH ₂ (X)in whichR ₅ represents an alkylene radical substituted by one or more ionic or potentially ionic groups such as carboxy; And
B₄) optionally at least at least one amino compound which is not substituted by one or more ionic or potentially ionic groups. Composition C1 or C1' according to any one of the preceding claims, in which b) the polyurethane latex(es) b) is(are) chosen from the following polyurethanes with the following INCI names: polyurethane-32, polyurethane-32, polyurethane-34, polyurethane-35, polyurethane-48, polyurethane-93, and polyurethane-99 and mixtures thereof. Composition C1 or C1' according to any one of the preceding claims, in which:
the total quantity of polyurethane latex(es) b) in dry matter, present in composition C1 or C1', is between 0.01% and 30% by weight, more preferably from 0.05% to 28% by weight, and better still from 0.1% to 25% by weight, relative to the total weight of the composition. Composition C1 or C1' according to any one of the preceding claims, which comprises c) one or more fatty substances, preferably liquid at 20°C and at atmospheric pressure, particularly chosen from:
■ hydrocarbons, particularly alkanes, oils of animal origin,
■ oils of vegetable origin,
■ glycerides or fluorinated oils of synthetic origin,
■ fatty alcohols,
■ fatty acid and/or fatty alcohol esters,
■ non-silicone waxes, silicones; And
■ their mixtures;
in particular the hydrocarbon liquid fatty substance(s) are hydrocarbon oils, preferably volatile or are a mixture of different volatile oils, preferably chosen; the volatile oil(s) are chosen from alkanes, linear or branched, in C₈-VS₁₄, more preferably in C₉-VS₁₃Again more preferably in C₉-VS₁₂more particularly chosen from undecane, dodecane, tridecane, and isododecane; or a mixture of different oils, preferably volatile including isododecane in the mixture, or a mixture of undecane and tridecane. Composition C1 or C1' according to any one of the preceding claims, which comprises c) one or more fatty substances, preferably liquid at 20°C and at atmospheric pressure, particularly chosen from:
- vegetable oils formed by esters of fatty acids and polyols, in particular triglycerides, such as sunflower, sesame or rapeseed oil, macadamia oil, soybean oil, sweet almond oil, calophyllum, palm, grape seeds, corn, arara, cotton, apricot, avocado, jojoba, olive or cereal sprouts;
- linear, branched or cyclic esters, having more than 6 carbon atoms, in particular 6 to 30 carbon atoms; and in particular isononyl isononanoate;
and more particularly the esters of formula R^d-C(O)-O-R^ein which R^drepresents the remainder of a higher fatty acid containing 7 to 19 carbon atoms and R^erepresents a hydrocarbon chain comprising 3 to 20 carbon atoms, such as palmitates, adipates, myristates and benzoates, in particular diisopropyl adipate and isopropyl myristate; more preferably the esters of formula R^d-C(O)-O-R^ein which R^drepresents the remainder of a higher fatty acid containing 8 to 10 carbon atoms and R^erepresents a hydrocarbon chain comprising 12 to 18 carbon atoms;
- hydrocarbons and in particular linear, branched and/or cyclic alkanes, volatile or non-volatile, such as C isoparaffins₅-VS₆₀, possibly volatile such as isododecane, Parléam (hydrogenated polyisobutene), isohexadecane, cyclohexane, or 'ISOPARs' and their mixture; or alkanes resulting from the complete hydrogenation/reduction of mixtures of fatty acids from Cocos Nucifera (Coconut) oil such as dodecane; or the mixture of C alkanes₉-VS₁₂, whose chains comprise from 9 to 12 carbon atoms, preferably linear or branched alkanes, in C₉-VS₁₂in particular including dodecane; or paraffin oils, petroleum jelly, or hydrogenated polyisobutylene;
- ethers having 6 to 30 carbon atoms;
- ketones having 6 to 30 carbon atoms;
- aliphatic fatty monoalcohols having 6 to 30 carbon atoms, the hydrocarbon chain not comprising a substitution group, such as oleic alcohol, decanol, dodecanol, octadecanol, octyldodecanol and linoleic alcohol;
- polyols having 6 to 30 carbon atoms, such as hexylene glycol; And
- their mixtures such as mixtures of linear or branched C fatty acid esters₈-VS₁₀and C fatty alcohol₁₂-VS₁₈and alkanes from the complete hydrogenation/reduction of mixtures of fatty acids from Cocos Nucifera (Coconut) oil, in particular dodecane such as mixtures of cococaprylate/caprate and dodecane; or mixtures of C alkanes₉-VS₁₂, whose chains comprise from 9 to 12 carbon atoms, preferably linear or branched alkanes, in C₉-VS₁₂in particular comprising dodecane; preferably the hydrocarbon liquid fatty substance(s) iii) is(are) chosen from C alkanes₆-VS₁₆, linear or branched, preferably in C₈-VS₁₄, more preferably in C₉-VS₁₃Again more preferably in C₉-VS_12,and even more preferably the alkanes are volatile and chosen from undecane, dodecane, isododecane, tridecane, and their mixture comprising in particular dodecane, isododecane or a mixture of undecane and tridecane;
or the liquid fatty substance(s) iii) is(are) a mixture of non-volatile oil(s) and volatile oil(s) in particular comprising isododecane as volatile oil, undecane, dodecane, isododecane, and/or tridecane, more preferably isododecane; as a volatile and non-volatile oil mixture, we can cite the mixture of isododecane and isononyl isononanoate; and more preferably when the fatty substance(s) are a mixture of volatile and non-volatile oil, the quantity of volatile oil is greater than the quantity of non-volatile oil. Composition according to any one of the preceding claims, which further comprises one or more coloring agents chosen from pigments, direct dyes and mixtures thereof, preferably pigments; more preferably the pigment(s) of the invention are chosen from carbon black, iron oxides in particular black and micas coated with iron oxide, triarylmethane pigments in particular blue and violet such as BLUE 1 LAKE, pigments azo, particularly red ones such as D&C RED 7 alkali metal salt of lithol red such as the calcium salt of lithol red B, even more preferably red iron oxides. Process for treating keratin materials, preferably α) keratin fibers, in particular human fibers such as hair, or β) human skin, in particular of the lips, by application of the composition as defined in any one of the preceding claims. Cosmetic use of the composition according to any one of claims 1 to 21.