MXPA00003895A - Hair composition containing a polycondensate comprising at least a polyurethane and/or polyurea unit and a polyol - Google Patents
Hair composition containing a polycondensate comprising at least a polyurethane and/or polyurea unit and a polyolInfo
- Publication number
- MXPA00003895A MXPA00003895A MXPA/A/2000/003895A MXPA00003895A MXPA00003895A MX PA00003895 A MXPA00003895 A MX PA00003895A MX PA00003895 A MXPA00003895 A MX PA00003895A MX PA00003895 A MXPA00003895 A MX PA00003895A
- Authority
- MX
- Mexico
- Prior art keywords
- composition according
- diisocyanate
- composition
- polycondensate
- polyol
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 73
- 150000003077 polyols Chemical class 0.000 title claims abstract description 19
- 229920005862 polyol Polymers 0.000 title claims abstract description 18
- 229920002396 Polyurea Polymers 0.000 title claims abstract description 12
- 229920003226 polyurethane urea Polymers 0.000 title claims abstract description 11
- 239000003380 propellant Substances 0.000 claims abstract description 11
- 229920000642 polymer Polymers 0.000 claims abstract description 10
- 239000000443 aerosol Substances 0.000 claims abstract description 9
- 239000003960 organic solvent Substances 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims description 24
- 150000002009 diols Chemical class 0.000 claims description 17
- -1 polyethylsiloxanes Polymers 0.000 claims description 16
- 229920000728 polyester Polymers 0.000 claims description 12
- 239000007789 gas Substances 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 229920001296 polysiloxane Polymers 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 229920000570 polyether Polymers 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 150000004985 diamines Chemical class 0.000 claims description 5
- 150000002430 hydrocarbons Chemical group 0.000 claims description 5
- 238000007493 shaping process Methods 0.000 claims description 5
- 210000001736 Capillaries Anatomy 0.000 claims description 4
- RRAMGCGOFNQTLD-UHFFFAOYSA-N Hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 4
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- CZZYITDELCSZES-UHFFFAOYSA-N Diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims description 3
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N Isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 3
- 229920001228 Polyisocyanate Polymers 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000005056 polyisocyanate Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 claims description 2
- CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 claims description 2
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N Toluene diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 2
- 229940029983 VITAMINS Drugs 0.000 claims description 2
- 229940021016 Vitamin IV solution additives Drugs 0.000 claims description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N [N-]=C=O Chemical compound [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims description 2
- 239000003213 antiperspirant Substances 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 239000000490 cosmetic additive Substances 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 125000005442 diisocyanate group Chemical group 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims description 2
- 239000002304 perfume Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 229920000023 polynucleotide Polymers 0.000 claims description 2
- 239000002157 polynucleotide Substances 0.000 claims description 2
- 102000004169 proteins and genes Human genes 0.000 claims description 2
- 108090000623 proteins and genes Proteins 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 239000011782 vitamin Substances 0.000 claims description 2
- 235000013343 vitamin Nutrition 0.000 claims description 2
- 229930003231 vitamins Natural products 0.000 claims description 2
- 150000004676 glycans Polymers 0.000 claims 2
- 229920001282 polysaccharide Polymers 0.000 claims 2
- 239000005017 polysaccharide Substances 0.000 claims 2
- 150000004804 polysaccharides Polymers 0.000 claims 2
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 claims 1
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 claims 1
- JIABEENURMZTTI-UHFFFAOYSA-N 1-isocyanato-2-[(2-isocyanatophenyl)methyl]benzene Chemical compound O=C=NC1=CC=CC=C1CC1=CC=CC=C1N=C=O JIABEENURMZTTI-UHFFFAOYSA-N 0.000 claims 1
- IWZLPYQUOBUNBF-UHFFFAOYSA-N [N-]=C=O.CC1=CC(=O)CC(C)(C)C1 Chemical compound [N-]=C=O.CC1=CC(=O)CC(C)(C)C1 IWZLPYQUOBUNBF-UHFFFAOYSA-N 0.000 claims 1
- 230000000875 corresponding Effects 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims 1
- 230000000887 hydrating Effects 0.000 claims 1
- 229920000831 ionic polymer Polymers 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 229920005903 polyol mixture Polymers 0.000 claims 1
- 230000003252 repetitive Effects 0.000 claims 1
- 238000005303 weighing Methods 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-Butanediol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 8
- 239000002537 cosmetic Substances 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- SLCVBVWXLSEKPL-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 3
- 229940117969 NEOPENTYL GLYCOL Drugs 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N acetic acid ethyl ester Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 239000011528 polyamide (building material) Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-N propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- PCIBVZXUNDZWRL-UHFFFAOYSA-L 2-hydroxyethyl phosphate Chemical compound OCCOP([O-])([O-])=O PCIBVZXUNDZWRL-UHFFFAOYSA-L 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N Adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N Diphenylmethane p,p'-diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N Isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N Methyl acetate Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N Phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920001451 Polypropylene glycol Polymers 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000001414 amino alcohols Chemical class 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 230000005591 charge neutralization Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N ethanolamine Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 230000001264 neutralization Effects 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 230000000576 supplementary Effects 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N 1,2-ethanediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 229940035437 1,3-propanediol Drugs 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N 1-propanol Substances CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- UHAMPPWFPNXLIU-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)pentanoic acid Chemical compound CCCC(CO)(CO)C(O)=O UHAMPPWFPNXLIU-UHFFFAOYSA-N 0.000 description 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N 3-aminopropanol Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 3-hydroxy-2-(hydroxymethyl)-2-methylpropanoic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N Hexamethylenediamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N Isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 1
- 235000001484 Trigonella foenum graecum Nutrition 0.000 description 1
- 240000005216 Trigonella foenum-graecum Species 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 230000002378 acidificating Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000000240 adjuvant Effects 0.000 description 1
- 230000001476 alcoholic Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 230000003113 alkalizing Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbamate Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 230000001143 conditioned Effects 0.000 description 1
- 230000003750 conditioning Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000001808 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N fumaric acid Chemical compound OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000003020 moisturizing Effects 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
Abstract
The invention concerns hair compositions in the form of an aerosol and comprising, in a cosmetically acceptable medium, a multiple sequence polymer comprising at least a polyurethane and/or polyurea unit, at least a polyol, an organic solvent and a propellant. The invention also concerns a hair styling or hair dressing method using said compositions and their use for making hair care products for hairdressing or hairstyling.
Description
"CAPILLARY COMPOSITION CONTAINING A POLYCONDENSATE COMPRISING AT LEAST ONE POLYURETHANE AND / OR POLYUREA UNIT AND A POLYOL". DESCRIPTION OF THE INVENTION The invention relates to hair compositions prepared in the form of an aerosol and comprising, in a cosmetically acceptable medium, a multi-sequence polymer comprising at least one polyurethane and / or polyurea unit, at least one polyol, an organic solvent and a propellant gas. The invention also relates to a method for shaping or maintaining the hairstyle comprising the embodiment of e; compositions as well as their use for the manufacture of hair products, in order to obtain a maintenance or a conformation of the hairstyle. The fixation of the hairstyle is an important element of the hair that consists in maintaining the shape already made or in cushion forming the hair and in fixing them simultaneously. The hair products for shaping and / or the most widespread styling on the cosmetics market are spray compositions essentially constituted by a solution that is most often alcoholic or aqueous and by one or more materials, generally polymer resins, whose function is to form welds between the hair, also called fixative materials, mixed with various co-mestic adjuvants.This solution can be conditioned, for example, in an appropriate aerosol container placed under pressure with the help of REF .: 119515 The quality of the spray obtained by means of an aerosol device, that is to say, essentially the distribution of the droplets in the space at the exit of the nozzle, depends - strongly on the chemical constitution of the composition used. a very particular interest for the formulation of cosmetic compositions that provide a quality of spray c every time more satisfying. The compositions intended for fixing and / or for maintaining the hairstyle sometimes have the disadvantage of altering the cosmetic properties of the hair. Thus, the hair can become rough and lose its natural balance. Therefore combing compositions are sought which fix and / or maintain the hairstyle well by providing good cosmetic properties. It is known from DE 195 41 326 styling compositions distributed from an aerosol device containing, in a hydroalcoholic medium, a polymer of unit-polyurethane as a fixing polymer, and a propellant. These compositions, which are satisfactory already in terms of fixation - of the hairstyle, can nevertheless be improved as regards particularly the cosmetic properties that the COJIs themselves give to the hair by offering an optimum spray quality. Surprisingly and unexpectedly, the Firm has requested you, against all expectations, that by associating certain particular conditioning agents with a polycommodity containing at least one polyurethane and / or polyurea unit, it is possible to comply with the aforementioned requirements . The subject of the invention is a capillary composition intended to be applied from an aerosol device comprising, in a cosmetically acceptable medium, in a relative proportion by weight relative to the total weight of the composition. (i) from 0.1 to 20% of a polycondensate comprising at least one polyurethane and / or polyurea sequence. (ii) from 7.5 to 70% of an organic solvent; (iii) from 15 to 85% of a propellant gas, characterized in that the composition further comprises from 0.01 to 20% of at least one polyol or of a mixture thereof, the ratio being by weight of the propellant gas with respect to the organic solvent greater than or equal to 1.75. For the purposes of the present invention, the term "polyol" means a C 2 to C 4 compound of the linear, branched or cyclic, saturated or unsaturated aliphatic hydrocarbon type., which has at least two hydroxyl functions in the alkyl chain, as well as the polyether polymers of these alkyl polyhydroxy compounds. Another object of the invention relates to a method of shaping or maintaining the hairstyle that comprises the embodiment of this composition. Another object of the invention also relates to the use of this composition for the manufacture of hair compositions, in order to obtain a maintenance or conformation of the hairstyle. The polycondensates comprising at least one polyurethane and / or polyurea sequence particularly considered by the present invention are those described in EP 0 751 162, EP 0 637 600, FR 2 743 297 and EP 06 48 455 -whose Solid signature is Holder, as well as EP 0 656.021 or W0 94/03510 of the Basf Company or EP 0619 111 of the National Starch Company. The polycondensates used according to the invention can be soluble in the cosmetically acceptable medium, paricularly after neutralization by an organic or mineral base, or even form a dispersion in this medium. The dispersion can then comprise at least 0.05% of surfactant allowing the dispersion and the dispersion adjustment of the polycondensate. According to the invention, any type of surfactant may be used in the said dispersion, but preferably a non-ionic surfactant. The average particle size of the polycondensate in the dispersion is preferably between 0.1 and 1 micron. By way of example, the polycondensate may be formed by a block arrangement, this arrangement being obtained -particularly from: (1) at least one compound containing two or more than two active hydrogen atoms per molecule; (2) at least one diol or a mixture of diols containing acidic radicals or their salts; (3) at least one di- or polyisocyanate. Advantageously, the compounds (1) are chosen from -the group comprising the diols, the diamines, the polyesters, the polyetherols or their mixture. The compounds (1) which are preferred are polyethers and linear polypropylene glycols, in particular those which are obtained by reacting ethylene oxide or propylene oxide with water or diethylene or dipropyl glycol in the presence of sodium hydroxide as catalyst. These polyglycols generally have a molecular weight of between about 600 and 20,000. Other preferred organic compounds are those having mercapto, amino, carboxyl or hydroxyl groups. Among these, polyhydroxy compounds, such as polyether diols, polyester diols, polyalkyl diols, polyamide diols, polyamide diols, poly (alkylen ether) diols, polythioethers, are more particularly cited. diols and -the polycarbonate diols. Preferred polyether diols are, for example, the condensation products of ethylene oxide, propylene oxide or tetrahydrofuran, their copolymerization or condensation products, grafted or in blocks, such as mixtures of condensates of ethylene oxide and propylene, and the olefin polymerization products, at high pressure, with the alkylene oxide condensates. Suitable polyethers are prepared, for example, by condensation of alkylene oxides and polyhydric alcohols, such as ethylene glycol, 1,2-propylenglycol and 1,4-butanediol. Polyester diols, polyester amides, polyamide diols are preferably saturated and are obtained, for example, from the reaction of saturated or unsaturated polycarboxylic acids with polyhydric alcohols, diamines or polyamines. To prepare these compounds, for example, adipic acid, succinic acid, phthalic acid, terephthalic acid and maleic acid can be used. Suitable polyhydric alcohols for preparing the polyesters include, for example, ethylene glycol, 1,2-propylenolyl, 1,4-butanediol, neopentyl glycol, and hexane diol. It is also possible to use aminoalcohols, for example ethanolamine. The diamines suitable for preparing the polyester amides are ethylenediamine and hexamethylenediamine. Suitable polyacetals can be prepared, for example, from 1,4-butanediol or hexanediol and formaldehyde. Suitable polyethioethers can be prepared, for example, by condensation reaction between thioglycols either alone or in combination with other glycols such as ethylene glycol, 1,2-propylene glycol or with other polyhydroxy compounds.
Polyhydroxy compounds which already contain urea or urethane groups, natural polyols, which can be modified for a longer time, for example, castor oil and carbohydrates can also be used. More preferably, the compound of group (1) is a -poliesterol, particularly a polyester diol formed by the reaction of at least one (di) polyol (1 a) and by at least one acid (1b). The (di) -pol i ol (1) is in particular chosen from -the group comprising neopentyl glycol, 1,4-butanediol, -hexanediol, ethylene glycol, diethylene glycol, propylene glycol, buty lengl icol, the neopenti lgl icol and (di) -pol ietilen-glycol. The acid (1b) is in particular chosen from the group comprising phthalic acid, isophthalic acid, -adipic acid and (poly i) -lactic acid. As the compound (2), it is particularly possible to use a hydroxycarboxylic acid such as dimethylol propanoic acid (DMPA) or a 2, 2-hydroxymethyl carboxylic acid 1. In general, the compound (2) is useful as coupling block. As copolymers (2), those which comprise at least one poly- (alpha- (alpha-hydroxycarboxylic acid) are preferred.) Particularly preferred compounds (2) according to the invention are those selected from the group consisting of 2.2. -di- (hydroxymethyl) acetic acid, 2,2-dihydroxymethi-1 propionic acid, 2,2-dihydroxymethi-1-butyric acid, 2,2-dihydroxymethyl-1-pentanoic acid, di- or polyisocyanate (3) to be chosen in particular from the group comprising hexamethylene diisocyanate, isophorone diisocyanate (IDPI), toluylene diisocyanate, diphenylmethane 4,4'-diisocyanate (DPMD) and dicyclohexy-limetane 4,4'-diisocyanate (DCMD) , methi len-di-p-pheni 1 diisocyanate * -methylene-bis (4-cyclohexy-1-isocyanate), isophorone diisocyanate, toluene diisocyanate, 1,5-naphthalene diisocyanate, -4,4 ' -difeni lmetano diisocianato, the 2,2 '-dimeti 1-4,4' -dife-nilmethane diisocianato, the 1,3-phenylene diisocyanate, the 1, 4-fe nileno d isocyanate, mixtures of 2,4- and 2,6-toluene diis cyanate, 2,2 '-dichloro-4,4'-diisocyanate diphenylmethane, -2,4-dibromo-1,5-diisocyanate naphthalene, 1,4-diisocyanate butane, 1,6-hexane diisocyanate, 1,4-cyclohexane diisocyanate. The polycondensate can be formed with the aid of a supplementary com-ponent (4) which serves in general to lengthen the polycondensate chain. These compounds (4) can be selected from the group comprising, in particular, saturated or unsaturated glycols, such as ethylene glycol, diethylene glycol, neopentyl glycol, triethylglycol, aminoalcohols such as ethanolamine, propanolamine, butane-lamellar, heterocyclic, aromatic, cycloaliphatic, and aliphatic primary amines, diamines, carboxylic acids such as aliphatic, aromatic, heterocyclic carboxylic acids with oxalic, succiramic, glutaric, adipic, sebacic, te-reftalic, the aminocarboxylic acids. The (4) -preferred compounds are the aliphatic diols. The polycondensates according to the invention can also be formed from supplementary compounds (5) with a silicone structure such as polysiloxanes, polyalkyl siloxanes or polyalkyl loxanes, particularly polystyrene, polyesters, polyesters, and polymers. if loxanes and the polyphenols 1 s_i_ loxanes, which eventually comprise hydrocarbon chains -grafted on the silicon atoms. According to an advantageous embodiment of the combinations according to the invention, the polymer polyurethane and / or polyurea sequences have a repeating unit of ba that corresponds to the general formula I given below: - X - B - X - CO - NH - R - NH - CO - (I) in which: X represents 0 and / or NH, - B is a divalent hydrocarbon radical, this radical being substituted or not, and R is a divalent radical selected from the alkylene radicals of aromatic type, aliphatic of C, to C2Q, cycloal ifatic of C1 to C2Q, these radicals being substituted or not. Preferably, radical B is a radical of C. a ^ and is a carrier of a group that has one or more func- tion ( es) carboxy 1 ica (s) and / or one of the sulfonic functions, the indicated carboxylic and / or sulphonic futions being found in free form or partially or totally neutralized by a mineral or organic base. The radical R is advantageously chosen from the radicals which correspond to the following formulas:
CH2. -?
in which b is an integer between 0 and 3, and c an integer between 1 and 20, preferably between 2 and 12. In particular, the radical R is chosen from the radicals hexamethylene, 4, 4 -bifeni lenoethane, 2,4- and / or 2,6-tolyl, 1,5-naphthyl, p-phenylene, 4,4bis-methyl cyclohexyl and the divalent radical derived from isophorone. The polycondensate used according to the invention comprising at least one polyurethane and / or polyurea sequence can advantageously also comprise at least one polysiloxane sequence whose base repeating unit corresponds, for example, to the general formula II given below:
X - P - X CO NH - R NH - CO - (ID
in which: - P is a polynucleotide segment, - X represents 0 and / or NH, and - R is a divalent radical selected from alkylane radicals of the aromatic, aliphatic type of C. to C2Q, syrah these radicals substituted or not. Advantageously, the poly isi loxái ico P segment responds to the general formula III given below:
A A i (Yes O) Si - y (III) i? TO
wherein: - radicals A, which may be identical or different, are selected from, on the one hand, monovalent hydrocarbon radicals of C, C2Q exempt or substantially free of ethylenic saturation and, on the other hand, aromatic radicals, Y represents a bivalent hydrocarbon radical, and - z represents an integer, selected in such a way that the average molecular weight of the polysiloxane segment is between 300 and 10,000. In general, the bivalent radical Y is chosen from the alkylene radicals of the formula - (CH2) -, in which a represents an integer which may be between 1 and 10. The radicals A can be chosen from alkyl radicals, in particular the methyl, ethyl, propyl, and ss propyl radicals, butyl, pentyl, hexyl, octyl, decyl, dodecyl and 0-tadecyl, the cycloalkyl radicals, in particular the radical-cyclohexyl, the aryl radicals, particularly phenyl and naphthyl, the radicals ar ilalkyl, particularly benzyl and feni. lethyl, as well as the tolyl and xylyl radicals. The composition according to the invention comprises, in relative proportion by weight relative to the total weight of the composition between 0.1 and 20% of the polycondensate comprising at least one polyurethane and / or polyurea sequence, more advantageously between 1 and 15%, and more advantageously still between 2 and 8% of this polycondensate. It is used between 7.5 and 70% of the organic solvent, more advantageously between 10 and 50%, and more advantageously still between 10 and 25% in relative proportion in weight with respect to the total weight of the solvent. the composition. According to the invention, the organic solvent is particularly chosen from the group comprising the lower alcohols of C. to C. such as ethanol, isopropanol, acetone, methyl ethyl ketone, methyl acetate, acetate of butyl, ethyl acetate, dimethoxyethane, diethoxyethane and mixtures thereof. Preferably, ethanol is used. According to an advantageous embodiment of the composition according to the invention, it comprises in relative proportion by weight relative to the total weight of the composition, between 25 and 60% of the propellant gas, and even more advantageously between the 30 and 50%. According to the invention, it is preferably used as the propellant gas, a gas soluble or not in the composition such as dimethyl ether, fluorinated or non-fluorinated hydrocarbons, the usual liquefied gases or a mixture of these propellant gases. Even more advantageously, dimethylether is used. The relative proportion by weight, relative to the total weight of the composition in polyol or in mixture of polyols is between 0.01 and 20%, more advantageously between 0.01 and 10%, and more advantageously still between 0.05 and 5%. The polyols used according to the invention can be chosen in particular from the polyols of C2 to C1? as well as polyalkylene glycols such as more particularly polyethylene glycols and polypropylene glycols. Preferably, it is used as polyol, a derivative of alkane polyhydroxy side of C2 to Cg, Advantageously, it is chosen-a compound of C- to C ?, and more particularly still glycine, propylene glycol or 1, 3- propane diol The compositions according to the invention can on the other hand contain conventional cosmetic additives selected in particular from fatty substances, thickening agents, softeners, anti-foam agents, moisturizing agents, antiperspirant agents, alkalizing agents, dyes , pigments, perfumes, advisors valants, surfactants, hydrocarbon polymers-two, volatile silicones or not, proteins and vitamins. - - There is a very particular interest in the realization of cosmetic compositions according to the invention for which the amount of volatile organic compounds expelled is getting smaller and smaller. In particular, it may be advantageous to associate at least one other anionic, cationic, nonionic or amphoteric fixing polymer to the polyurethane of the invention. The invention may be better understood with the aid of the non-limiting example which follows and which constitutes an advantageous embodiment of the compositions according to the invention. Example: The capillary composition according to the invention given below was performed. Polycondensate polyester lactic acid / ethylene glycol P (MIS-EG) - dimethylol propane acid (DMPA) - isoformone and socianate 4 g - Glycerol 0.07 g Ethanol 15 g Dimethylether 35 g - 2-amino-2-methy1-1-propanol. ..cs neutralization Demineralized water csp 100 g
It is noted that in relation to this date, the best method known to the applicant to carry out the aforementioned invention, is that which is clear from the present description of the invention.
Claims (21)
- R E I V I N D I C A C I O N S
- Having described the invention as above, the content of the following claims is claimed as property: 1.- Capillary composition intended to be applied from an aerosol device comprising, in a cosmetically acceptable medium, in a relative proportion by weight in relation to the total weight of the composition: (i) from 0.1 to 20% of a polycondensate comprising at least one polyurethane and / or polyurea sequence. (ii) from 7.5 to 70% of an organic solvent, (iii) from 15 to 85% of a propellant gas, characterized in that the composition further comprises - a 0.01 at 20% of at least one polyol or of a mixture of esters, the weight ratio of the propellant gas to the organic solvent being greater than or equal to 1.75. 2. Composition according to claim 1, characterized in that the polycondensate is formed by a block arrangement obtained from: (1) at least one compound containing two or more active two hydrogen atoms per molecule; (2) at leastundiol or a mixture of diols containing acid radicals or their salts; (3) at least one di- or polyisocyanate.
- 3. - Composition according to claim 2, characterized in that the compounds - are chosen from the group comprising diols, diamines, polyesteroles, polyetherols or their mixture.
- 4. Composition according to rei indication 2, characterized by the fact that the compound t-?:? it is a carboxyp acid with 2,2-hydroxymethyl.
- 5. Composition according to claim 2, characterized in that the compound (3) is chosen from the group comprising the hexamethylene diisocyanate, the isophorone isocyanate, the tolui lendi isocyanate, the diphenylmethane 4,4'-di - isocyanate and 4,4'-dicyclohexy-limetane-di-isocyanate, methylene-di-phenyl-diisocyanate, methylene-bis (4-cyclohexy-1-isocyanate), isophorone diisocyanate, toluene diisocyanate, , 5-naphthalene diisocyanate, 4,4 '-difeni 1 -methane diisocyanate, -2,2' -dimeti 1-4,4 '-difeni lmethane diisocyanate, 1,3-phenylene-diisocyanate, 1,4-phenylene diisocyanate, mixtures of -2,4- and 2,6-toluene diisocyanate, 2,2'-dichloro-4,4'-diisocyanate diphenylmethane, 2,4-dibromo-l, 5-di-isocyanate naphthaleno, 1,4-diisocyanatobutane, 1,6-hexane diisocyanate, 1,4-cyclohexane diisocyanate.
- 6. Composition according to claim 2, characterized in that the polycondensate is formed in part from at least one additional compound having a silicone structure and chosen from the group comprising the poly siloxanes, the polysaccharides, and the polysaccharide. lsoxanos or polyalkyl loxanes, particularly polyethylsiloxanes, polyesters, loxanes and polyesters, which optionally comprise hydrocarbon chains grafted to the silicon atoms.
- 7. Composition according to claim 1, characterized in that the polyurethane and / or polyurea sequences of the polycondensate have a repeating base unit corresponding to the general formula I1 given below: - X X '- CO NH - R NH CO (I1) wherein: - X 'represents 0 and / or NH, - B is a bivalent hydrocarbon radical, this radical being substituted or not, and - R is a divalent radical selected from alkylene radicals of the aromatic, aliphatic type of C. a C? n, cyclo-aliphatic C1 to C20 > these radicals being substituted or not.
- 8. Composition according to claim 7, characterized in that B is a hydrocarbon radical bivalejí
- 9. - Composition according to claim 7, characterized in that the radical R is chosen from the "group comprising the hexamethylene, 4,4'-bifeni-lentomene-2,4- and / or 2,6-tol radicals Ilene, 1, 5-naphthylene, p-phenylene, 4,4-bis-methylene cyclohexyl and the divalent radical derived from the ison 3 10. Composition according to claim 1, characterized in that the polycondensate has a unit repetitive base that responds to the formula (II1):
- - X X '- CO NH - R - NH CO (II') in which: - P is a polynucleotide segment, - X 'represents 0 and / or NH, and - R is a divalent radical selected from the alkylene radicals of the aromatic, aliphatic type of C,. a C? r), C-Cloaliphatic C to C20, these radicals being substituted or not.
- 11. Composition according to any one of the preceding claims, characterized in that the composition comprises, in relative proportion by weight, between-1 and 15% of the polycondensate, and more advantageously between 2 and 8%. .
- 12. Composition according to any one of the preceding claims, characterized in that the composition comprises between 10 and 50% of the organic solvent, and more advantageously between 10 and 25%.
- 13. Composition according to any one of the preceding claims, characterized in that the propellant gas is present in a relative concentration by weight - comprised between 25 and 60%, and more advantageously between 30 and 50%.
- 14. Composition according to any one of the preceding claims, characterized in that the relative proportion by weight, relative to the total weight of the composition, in polyol or in polyol mixture is between 0, 01 and 10, and more advantageously still between 0.05 and 5%.
- 15. Composition according to any one of the preceding claims, characterized in that the polyol chosen from the group comprising the compounds of C2 to C *, - of the linear, branched or cyclic, saturated or unsaturated aliphatic hydrocarbon type, which it has at least two hydroxyl functions in the alkyl chain and the polyether polymers of these alkyl polyhydroxy compounds.
- 16. The composition according to claim 15, characterized in that the polyol is an alkane-polyhydroxy derivative side of C2 to C12, preferably of C2 to Cß, and more preferably of C3 to Cg.
- 17. Composition according to any one of the preceding claims, characterized in that it contains in addition to the conventional cosmetic additives selected from the group comprising the fatty substances, the weighing agents, the softeners, the anti-foam agents , hydrating agents, antiperspirant agents, alkalinizing agents, dyes, pigments, perfumes, advisers, surfactants, hydrocarbon polymers-two, volatile silicones or not, particularly anionic silicones, polyols , proteins and vitamins.
- 18. Composition according to any one of the preceding claims, characterized in that the composition also contains at least one additional fixing polymer -selected from the group comprising the non-ionic, cationic, anionic and amphoteric non-ionic polymers. .
- 19. An aerosol device consisting of a container containing an aerosol composition according to any one of the preceding claims in a suitable container, as well as a means for distributing the composition.
- 20. Procedure for shaping or maintaining the hairstyle, characterized in that it comprises making a composition according to any of the rei indications 1 to 17.
- 21.- Use of a composition according to any one of claims 1 to 17, for the manufacture of hair products, with a view to obtaining a maintenance or shaping of the hairstyle.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR98/10782 | 1998-08-27 |
Publications (1)
Publication Number | Publication Date |
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MXPA00003895A true MXPA00003895A (en) | 2001-06-26 |
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