Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
  • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
  • C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
  • C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
  • C07C217/08—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to an acyclic carbon atom
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
  • A61K8/41—Amines
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/002—Preparations for repairing the hair, e.g. hair cure
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
  • C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
  • C07C211/02—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
  • C07C211/09—Diamines
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
  • C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
  • C07C211/20—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic unsaturated carbon skeleton
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
  • C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
  • C07C211/20—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an acyclic unsaturated carbon skeleton
  • C07C211/21—Monoamines
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
  • C07C57/18—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon triple bonds as unsaturation
  • C07C57/20—Propiolic acid
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
  • C07C59/235—Saturated compounds containing more than one carboxyl group
  • C07C59/305—Saturated compounds containing more than one carboxyl group containing ether groups, groups, groups, or groups
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
  • A61K2800/10—General cosmetic use

Definitions

• the present disclosure relates to salts and cosmetic preparations thereof and their use as hair care products. Further disclosed is a method for treatment of keratin materials, such as hair.
• Background of the Disclosure Human hair has a highly organized but complex structure. It is composed of the hair follicle, which is embedded in the skin, and hair shaft, which extends out of the skin. Hair is typically composed of two or three layers. The outermost layer is the cuticle, the middle layer is the cortex and in some cases there is a central medulla region that is made of packed cells and/or hollow spaces.
• a large part of the mass of the human hair is composed of fibrous structures called macrofibrils, each one consists of microfibrils held together by matrix pro- teins.
• Human hair consists of 65–95 wt% proteins, predominantly keratin which is a fi- brous, helicoidal protein particularly rich in the amino acid cysteine, whose thiol groups may form disulfide crosslinks adding rigidity and resistance to the entire hair structure.
• treatments for hair such as bleaching, dyeing, straightening and perma- nent waving, during which hair may become overprocessed or damaged due to the chem- icals needed to effect the change desired.
• some known hair straightening processes consist of treatment with alkaline straightener.
• the high pH (9.0–14.0) causes the hair to swell, which allows the alkaline agent to penetrate into the hair fibers, where it reacts with keratin and causes breaking and rearranging of the disulfide bridges present in keratin, allowing hair to be stretched.
• physical treatments such as frequent and/or high heat or environmental exposure may produce changes in hair texture and lead to further often permanent damage.
• P25822PC00 04.04.2023 2/44 Summary of the Disclosure It would be highly desirable to be able to avoid, minimize, alleviate or repair any such dam- age that occurs during those hair treatment processes and in particular to restore disulfide bridges to regain and improve hair quality, strength and texture. It is an object of the present disclosure to advance the state of the art of hair repair. It is a further object of the present disclosure to provide salts and preparations for use as hair care products, which are preferably able to crosslink thiol moieties.
• the thiol moieties to be crosslinked may, for example, have been formed by cleavage of disulfide bridges as a result of physical or chemical hair treatments.
• thiol-reactive crosslinking agents which are capable of cross- linking thiol moieties, thus emulating disulfide bridges.
• the thiol moieties to be crosslinked may, for example, result from prior cleavage of disulfide bridges, e.g. as a result of physical or chemical hair treatments.
• the thiol-reactive crosslink- ing agents disclosed herein effectively enable restoration of disulfide bridges.
• the diallylammonium group is a moiety of formula d1 or d2 wherein, for each occurrence independently, R 4 is selected from H, linear or branched C1-6 alkyl.
• the present disclosure is directed towards a salt of formula III wherein M is selected from O, S and NR 6 , wherein R 6 is selected from H, linear or branched C 1-6 alkyl; R 5 is, for each occurrence independently, selected from H, linear or branched C 1-6 alkyl; m and n are independently selected from 1, 2 and 3; x and y are independently selected from 0, 1 and 2.
• R 5 is H and M is O.
• m and n are independently selected from 2 or 3.
• m and n are both selected from 2 or 3.
• the present disclosure is directed towards a salt of formula IV wherein M is selected from O, S and NR 6 , wherein R 6 is selected from H, linear or branched C1-6 alkyl; P25822PC00 04.04.2023 6/44 R 4 is, for each occurrence independently, selected from H, linear or branched C1-6 alkyl; m and n are independently selected from 1, 2 and 3; x and y are independently selected from 0, 1 and 2.
• R 4 is H and M is O.
• m and n are independently selected from 1 and 2.
• m is equal to n.
• m is equal to n and x is equal to y. In some embodiments of a salt of formula II, III or IV, m is equal to n and x is different from y. In a second aspect, the disclosure is directed to a cosmetic preparation comprising at least one salt according to any of the embodiments described herein.
• the cosmetic preparation further com- prises at least one cosmetic additive selected from the group consisting of surfactants, oil components, emulsifiers, pearlescent waxes, consistency-enhancing agents, thickeners, superfatting agents, stabilizers, polymers, silicone compounds, fats, waxes, lecithins, phospholipids, UV light protection factors, humectants, biogenic agents, antioxidants, de- odorants, antiperspirants, antidandruff agents, film-forming agents, swelling agents, in- sect repellents, self-tanning agents, tyrosine inhibitors (depigmentation agents), hy- drotropes, solubilizers, preservatives, perfumed oils and dyes, as well as mixtures thereof.
• at least one cosmetic additive selected from the group consisting of surfactants, oil components, emulsifiers, pearlescent waxes, consistency-enhancing agents, thickeners, superfatting agents, stabilizers, polymers, silicone compounds, fats,
• the cosmetic preparation further comprises a carrier, preferably a carrier selected from water, C(2-6)-alcohols, C(1-10)polyols, as well as oil components.
• a carrier preferably a carrier selected from water, C(2-6)-alcohols, C(1-10)polyols, as well as oil components.
• the disclosure is directed to a salt, a composition or a cosmetic preparation according to any of the embodiments described herein, for use as hair care products.
• the disclosure is directed to the use of salts according to any of the em- bodiments described herein, for the production of cosmetic preparations, preferably hair care products.
• the disclosure is directed to a method for treatment of keratin materials, such as hair, the method comprising applying to the keratin materials a salt or a cosmetic preparation according any of the embodiments described herein.
• the salts and cosmetic preparations disclosed herein are suitable for cosmetic use, in par- ticular for the protection of healthy hair or the amelioration of damaged hair.
• restoration of disulfide bridges refers to a process by which two thiol moieties are linked together (it is understood that the term “disulfde bridges” refers to two thiol moieties being linked using the salts of the invention and not directly linked –S-S-bonds).
• the thiol moieties may, for example, be part of keratin protein.
• the process of linking the thiol moieties together may involve reaction of each thiol with an electrophilic moiety in the crosslinking agent.
• the thiol-reactive crosslinking agents dis- closed herein typically react with two thiol moieties to form a crosslinking unit which links the two thiol moieties together.
• salt of the disclosure refers to salts represented by formulae I-IV and any of the specific examples disclosed herein. It is understood that “independently of each other” means that when a group is occurring more than one time in any salt, its definition on each occurrence is independent from any other occurrence.
• a dashed line or a solid line without attachment depicts the site of attachment of a residue (i.e. a partial formula).
• the two or more CH2 groups shall be replaced such that the alkyl chain does not contain peroxide groups.
• groups defined herein such as L, which are selected such that directly adjacent heteroatoms, e.g. -O-O- or -NH- NH-, are avoided.
• diallylammonium group refers to a positively charged nitrogen atom that is co- valently bonded to four substituents, wherein at least two of the four substituents are allyl substituents.
• diallylammonium group refers to a positively charged nitrogen atom that is covalently bonded to four substituents, wherein two of the four substituents are allyl substituents and the other two substituents are not allyl substit- uents.
• the terms "C1-14 alkyl”, “C1-12 alkyl”, “C1-11 alkyl” and “C1-6 alkyl” refer to a fully saturated branched or unbranched hydrocarbon moiety having the indicated number of carbon at- oms.
• C 1-14 alkyl include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, n-pentyl, iso-pentyl, neopen- tyl, n-hexyl, iso-hexyl, neohexyl, heptyl, octyl, nonyl, decyl, dodecyl, etc.
• C1-6 alkyl include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n- butyl, sec-butyl, iso-butyl, tert-butyl, n-pentyl, iso-pentyl, neopentyl, n-hexyl, iso-hexyl or neohexyl.
• the charge may, for example, be 2+, +, – or 2–. 2+ refers to two positive charges, i.e. the respective ion is doubly positively charged.
• 2– refers to two negative charges, i.e. the respec- tive ion is doubly negatively charged.
• a charge typically refers to an ion, which may be an entire chemical moiety or fragment or entity.
• the charge of an ion refers to the overall charge of that ion, which may be calculated by adding all positive and negative charges comprised in the ion.
• an ion comprising an ammonium group and two car- boxylate groups would have an overall charge of –.
• the charge of an ion may be delocal- ized over more than one atom.
• the charge may also be localized on a small number of atoms, such as one atom.
• q is +. In some embodiments of a salt of for- mula I, q is –. In some embodiments of a salt of formula I, p is 2+. In some embodiments of a salt of formula I, p is +. In some embodiments of a salt of formula I, p is 2–. In some embodiments of a salt of formula I, p is –. In some embodiments of a salt of formula I, g is 1. In some embodiments of a salt of for- mula I, g is 2. In some embodiments of a salt of formula I, q is +, p is – and g is 1.
• q is +, p is 2– and g is 2.
• P25822PC00 04.04.2023 12/44 q is –, p is + and g is 1.
• q is –, p is 2+ and g is 2.
• G is selected from R 5 -C ⁇ C-CO2 – and a diallylammonium group, wherein R 5 is independently selected from H, linear or branched C1-6 alkyl.
• q is + and G is a diallylammonium group.
• p is – and g is 1.
• q is – and G is R 5 -C ⁇ C- CO2 – , wherein R 5 is independently selected from H, linear or branched C1-6 alkyl.
• p is 2+ and g is 2.
• L is straight-chain C 1-10 alkyl, wherein one or more CH 2 groups are independently replaced by -(CH 2 -O-CH 2 )-, -(CH 2 - CH2-O)-, -(O-CH2-CH2)- or -O-.
• p is + or 2+ and A is NR 2 3 + , wherein R 2 is, for each occurrence independently, selected from H, linear or branched C1-6 alkyl.
• p is – or 2– and A is CO2 – .
• E is se- lected from NR 3 2, NR 3 3 + , CO2H, CO2 – , wherein, for each occurrence independently, R 3 is selected from H, linear or branched C1-6 alkyl.
• q is +. In some embodiments of a salt of formula II, q is –. In some embodiments of a salt of formula II, p is 2+. In some embodiments of a salt of formula II, p is +. In some embodiments of a salt of formula II, p is 2–. In some embodi- ments of a salt of formula II, p is –. In some embodiments of a salt of formula II, g is 1. In some embodiments of a salt of for- mula II, g is 2. P25822PC00 04.04.2023 18/44 In some embodiments of a salt of formula II, q is +, p is – and g is 1.
• q is +, p is 2– and g is 2. In some embodiments of a salt of formula II, q is –, p is + and g is 1. In some embodiments of a salt of formula II, q is –, p is 2+ and g is 2.
• p is – and g is 1.
• q is – and G is R 5 -C ⁇ C- CO2 – , wherein R 5 is independently selected from H, linear or branched C1-6 alkyl.
• p is 2+ and g is 2.
• m and n are both selected from 1, 2 and 3. In some embodiments of a salt of formula II, m and n are 1. In some embodiments of a salt of formula II, m and n are 2. In some embodiments of a salt of formula II, m and n are 3. In some embodiments of a salt of formula II, x and y are both selected from 0, 1 and 2. In some embodiments of a salt of formula II, x and y are both 0. In some embodiments of a salt of formula II, x and y are both 1. In some embodiments of a salt of formula II, x and y are both 2. In some embodiments of a salt of formula II, x is 0 and y is 1.
• p is + or 2+ and A is NR 2 3 + , wherein R 2 is, for each occurrence independently, selected from H, linear or branched C 1-6 alkyl.
• R 2 is, for each occurrence independently, selected from H, linear or branched C1-6 alkyl.
• p is – or 2– and A is CO 2 – .
• E is selected from NR 3 2 , NR 3 3 + , CO 2 H, CO 2 – , wherein, for each occurrence independently, R 3 is selected from H, linear or branched C1-6 alkyl.
• the diallylammonium group is a moiety of formula d1 or d2 wherein, for each occurrence independently, R 4 is selected from H, linear or branched C1-6 alkyl. In some embodiments of any of the salts disclosed herein, the diallylammonium group is of formula d1 or d2, wherein R 4 is H. In some embodiments of any of the salts disclosed herein, the diallylammonium group is a moiety of formula d1. In some embodiments of any of the salts disclosed herein, the dial- lylammonium group is a moiety of formula d2.
• the salt of the invention is of formula III P25822PC00 04.04.2023 23/44 wherein M is selected from O, S and NR 6 , wherein R 6 is selected from H, linear or branched C1-6 alkyl; R 5 is, for each occurrence independently, selected from H, linear or branched C 1-6 alkyl; m and n are independently selected from 1, 2 and 3; x and y are independently selected from 0, 1 and 2.
• M is O.
• M is S.
• M is NR 6 , wherein R 6 is selected from H, linear or branched C1-6 alkyl.
• R 5 is H.
• R 5 linear or branched C 1-6 alkyl.
• x and y are independently selected from 0 and 1.
• x and y are selected from 0, 1 and 2.
• x and y are selected from 0 and 1.
• x and y are 0.
• x and y are 1. In some embodiments of a salt of formula III, x is 0 and y is 1. In some embodiments of a salt of formula III, m and n are independently selected from 2 and 3. In some embodiments of a salt of formula III, m and n are selected from 1, 2 and 3. In some embodiments of a salt of formula III, m and n are selected from 2 and 3. In some embodiments of a salt of formula III, m and n are 2. In some embodiments of a salt of formula III, m and n are 3. In some embodiments of a salt of formula III, m and n are 2 and x and y are 0.
• m and n are 3 and x and y are 1. In some embodiments of a salt of formula III, m and n are 2, x is 0 and y is 1. In some embodiments of a salt of formula III, m and n are 3, x is 0 and y is 1. In some embodiments of a salt of formula III, M is O, m and n are 2 and x and y are 0. In some embodiments of a salt of formula III, M is O, m and n are 3 and x and y are 1. In some embodiments of a salt of formula III, M is O, m and n are 2, x is 0 and y is 1.
• M is O, m and n are 3, x is 0 and y is 1.
• the salt of the invention is of formula IV P25822PC00 04.04.2023 25/44 wherein M is selected from O, S and NR 6 , wherein R 6 is selected from H, linear or branched C1-6 alkyl; R 4 is, for each occurrence independently, selected from H, linear or branched C 1-6 alkyl; m and n are independently selected from 1, 2 and 3; x and y are independently selected from 0, 1 and 2.
• M is O.
• M is S.
• M is NR 6 , wherein R 6 is selected from H, linear or branched C 1-6 alkyl.
• R 4 is H for each occurrence.
• R 4 linear or branched C1-6 alkyl for each occurrence, such as methyl, ethyl or n-propyl, particularly methyl.
• m and n are independently selected from 1 and 2.
• m and n are selected from 1, 2 and 3.
• m and n are selected from 1 and 2.
• m and n are 1. In some embodiments of a salt of formula IV, m and n are 2. In some embodiments of a salt of formula IV, x and y are independently selected from 0 and 1. In some embodiments of a salt of formula IV, x and y are selected from 0, 1 and 2. P25822PC00 04.04.2023 26/44 In some embodiments of a salt of formula IV, x and y are selected from 0 and 1. In some embodiments of a salt of formula IV, x and y are 0. In some embodiments of a salt of for- mula IV, x and y are 1. In some embodiments of a salt of formula IV, x is 0 and y is 1.
• m and n are 1 and x and y are 1. In some embodiments of a salt of formula IV, m and n are 1 and x and y are 0. In some embodi- ments of a salt of formula IV, m and n are 2 and x and y are 1. In some embodiments of a salt of formula IV, M is O, m and n are 1 and x and y are 1. In some embodiments of a salt of formula IV, M is O, m and n are 1 and x and y are 0. In some embodiments of a salt of formula IV, M is O, m and n are 2 and x and y are 1. In further specific embodiments, the disclosure is directed to the specific examples dis- closed in Table 1.
• the salts of the disclosure may contain one or more asymmetric centers in the molecule.
• a salt without designation of the stereochemistry is to be understood to include all the optical isomers (e.g., diastereomers, enantiomers, etc.) in pure or substantially pure form, as well as mixtures thereof (e.g. a racemic mixture, or an enantiomerically enriched mixture). It is well known in the art how to prepare such optically active forms (e.g.
• the salts may be isotopically-labeled compounds, for example, compounds including var- ious isotopes of hydrogen, carbon, nitrogen, oxygen.
• the disclosed salts may exist in tau- tomeric forms and mixtures and separate individual tautomers are contemplated. In addi- tion, some salts may exhibit polymorphism.
• the salts of the disclosure may exist in solid, i.e.
• crystalline e.g., polymorphs, i.e., different crystalline structures that have the same chemical composition but differ in packing, geo- metrical arrangement
• noncrystalline form optionally as solvates
• liquid form In the solid state, it may exist in, or as a mixture thereof.
• solvent molecules are incorporated into the crystalline lattice during crystallization.
• the formation of solvates may include non-aqueous solvents such as, but not limited to, ethanol, isopropanol, DMSO, acetic acid, ethanolamine, or ethyl acetate, or aqueous solvents such as water (also called “hydrates”).
• the disclosure also provides methods of preparation of the salts of for- mula I-IV of the disclosure.
• the disclosure further provides a cosmetic preparation comprising an effective amount of one or more of the salts of the disclosure and one or more pharma- ceutically acceptable carriers and/or excipients (also referred to as diluents).
• the excipients P25822PC00 04.04.2023 29/44 are acceptable in the sense of being compatible with the other ingredients of the formula- tion and not deleterious to the recipient thereof.
• the term "effective amount” as used herein refers to the amount of a salt (as such or in form of a cosmetic preparation) of the present disclosure which is effective for producing the desired effect of hair repair.
• the pH of the cosmetic preparation is 3.5-6, particularly 4-5 at 20 °C.
• the pH may, for example, be adjusted using lactic acid, citric acid and the like.
• the concentration of the salt disclosed herein will be between 0.01% and 5% by weight of the cosmetic preparation, such as 2%-4% by weight.
• the concentration of the salt disclosed herein is 50-130 mmol per liter of the cosmetic preparation, particularly 80-100 mmol per liter.
• the cosmetic preparation comprises a solubilizer.
• the concentration of the solubilizer may, for example, be 5%-20% by weight of the cosmetic preparation, particularly 10%-20%, e.g.15%-20%.
• the cosmetic preparation comprises phenoxyethanol at a concen- tration of 0.1%-1.7% by weight of the cosmetic preparation, particularly 0.7%-1.1%, e.g. 0.9%.
• the cosmetic preparation comprises ethylhexylglycerin at a concen- tration of 0.01%-0.2% by weight of the cosmetic preparation, particularly 0.08%-0.12%, e.g.0.1%.
• pharmaceutically-acceptable carrier means a pharmaceuti- cally-acceptable material, composition or vehicle, such as a liquid or solid filler, diluent, excipient, manufacturing aid (e.g., lubricant, talc magnesium, calcium or zinc stearate, or steric acid), or solvent encapsulating material, involved in carrying or transporting the sub- ject salt or compound from one organ, or portion of the body, to another organ, or portion of the body.
• manufacturing aid e.g., lubricant, talc magnesium, calcium or zinc stearate, or steric acid
• solvent encapsulating material involved in carrying or transporting the sub- ject salt or compound from one organ, or portion of the body, to another organ, or portion of the body.
• Each carrier must be “acceptable” in the sense of being compatible with the other ingredients of the formulation and not injurious to the person being treated.
• materials which can serve as pharmaceutically-acceptable carriers include: (1) sugars, such as lactose, glucose and sucrose; (2) starches, such as corn starch and potato starch; (3) cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cel- lulose and cellulose acetate; (4) powdered tragacanth; (5) malt; (6) gelatin; (7) talc; (8) excipients, such as cocoa butter and suppository waxes; (9) oils, such as peanut oil, cot- tonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; (10) glycols, such as propylene glycol; (11) polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; (12) esters, such as ethyl oleate and ethyl laurate; (13) agar; (14) buffering agents, such as magnesium hydro
• compositions may contain further components conventional in cosmetic preparations, e.g. wetting agents, emulsifiers and lubricants, such as sodium lauryl sulfate and magne- sium stearate, as well as coloring agents, release agents, coating agents, sweetening, fla- voring and perfuming agents, preservatives and antioxidants, pH modifiers, bulking agents, and further active agents.
• wetting agents e.g. wetting agents, emulsifiers and lubricants, such as sodium lauryl sulfate and magne- sium stearate
• coloring agents e.g. coloring agents, release agents, coating agents, sweetening, fla- voring and perfuming agents, preservatives and antioxidants, pH modifiers, bulking agents, and further active agents.
• antioxidants examples include: P25822PC00 04.04.2023 31/44 (1) water soluble antioxidants, such as ascorbic acid, cysteine hydrochloride, sodium bi- sulfate, sodium metabisulfite, sodium sulfite and the like; (2) oil-soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, alpha-tocopherol, and the like; and (3) metal chelating agents, such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phos- phoric acid, and the like.
• water soluble antioxidants such as ascorbic acid, cysteine hydrochloride, sodium bi- sulfate, sodium metabisulfite, sodium sulfite and the like
• oil-soluble antioxidants such as ascorbyl palmitate, butylated
• compositions may be prepared by any method known in the art, for example, by bringing into association the active ingredient with one or more carriers and/or excipients.
• Different compositions and examples of carriers and/or excipients are well known to the skilled person and are described in detail in, e.g., Remington: The Science and Practice of Pharmacy. Pharmaceutical Press, 2013; Rowe, Sheskey, Quinn: Handbook of Pharmaceu- tical Excipients. Pharmaceutical Press, 2009.
• Excipients that may be used in the prepara- tion of the cosmetic preparations may include one or more of buffers, stabilizing agents, surfactants, wetting agents, lubricating agents, emulsifiers, suspending agents, preserva- tives, antioxidants, opaquing agents, glidants, processing aids, colorants, sweeteners, per- fuming agents, flavoring agents, diluents and other known additives to provide a compo- sition or preparation suitable for an administration of choice.
• the cosmetic preparations of the disclosure may be in any suitable form. In some embodi- ments, such suitable forms include but are not limited to liquids, e.g.
• low to moderate vis- cosity liquids such as lotions, milks, mousses, sprays, gels, creams, ointments, pastes and the like.
• Suitable excipients such as those listed above, are included or excluded from the skin formulation depending on the form of use of the formulation (e.g., lotion, gel, oint- ment, or cream).
• P25822PC00 04.04.2023 32/44 Liquid forms of the salts of the disclosure include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs.
• the liquid forms may contain inert diluents commonly used in the art, such as, for example, water or other solvents, solubilizing agents and emulsifiers, such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propyl- ene glycol, 1,3-butylene glycol, oils (in particular, cottonseed, groundnut, corn, germ, ol- ive, castor and sesame oils), glycerol, tetrahydrofuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof.
• inert diluents commonly used in the art, such as, for example, water or other solvents, solubilizing agents and emulsifiers, such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate
• a salt may con- tain suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, benton- ite, agar-agar and tragacanth, and mixtures thereof.
• a salt or compound may be mixed under sterile conditions with a pharmaceutically-acceptable carrier, and with any preservatives, buffers, or propellants which may be required.
• Such ointments, pastes, creams and gels may contain, in addition to a salt of the disclosure, excipients, such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.
• excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.
• a salt of the disclosure may contain excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances.
• Sprays can additionally contain customary propellants, such as chlorofluorohydrocarbons and volatile unsubstituted hydrocarbons, such as butane and propane.
• the cosmetic preparations are hair care products, which includes products in form of a shampoo, a conditioner, a hair mask, a hair rinse, hair spray, hair foam, hair mousse, hair gel, hair tonic, and the like. It is understood that all contemplated compositions and preparations must be stable under the conditions of manufacture and storage, and preserved against the contaminating ac- tion of microorganisms, such as bacteria and fungi.
• the amounts of a salt of the disclosure in the cosmetic preparations of the disclosure may be adjusted in order to obtain an amount of a salt of the disclosure which is effective to achieve the desired cosmetic response for a particular person, composition, and mode of administration, without being deleterious to the person.
• the chosen amount will depend upon a variety of factors including the nature of the particular salt of the present disclosure used, the route of administration, the time of administration, the duration of the treatment, other compounds, salts and/or materials used in combination with the particular salt, the age, sex, weight, condition, general health and prior medical history of the person being treated, and like factors well known in the medical arts.
• a suitable amount of a salt of the disclosure will be that amount of the salt, which is the lowest amount effective to produce a desired effect.
• the amount of cos- metic preparation applied per treatment may, for example, be 1g – 10 g.
• the amount of cosmetic preparation applied per treatment may, for example, be 1 g – 10 g.
• the amount of cosmetic preparation applied per treatment may, for example, be 0.1 g – 7 g. P25822PC00 04.04.2023 34/44 All of the salts, compositions, preparations and/or methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclo- sure.
• the active agent is hereinafter labelled “Olaplex active agent”.
• Example 1 Synthesis of Olaplex active agent The active agent “Olaplex active agent”, which was used as a reference compound in ex- ample 8, has the following structure: It was synthesized by reacting 2 equivalents of the corresponding acid with 1 equivalent of the corresponding diamine. P25822PC00 04.04.2023 35/44
• Example 2 Synthesis of salt 15 (SPC-TB-0015) (a) SPC-TB-0015 To a solution of 2,2'-oxybis(ethan-1-amine) (100 mg, 1.0 eq, 0.96 mmol) in DCM (1.92 mL) was added propiolic acid (134 mg, 2.0 eq., 1.92 mmol).
• Example 4 Synthesis of salt 17 (SPC-TB-0017) P25822PC00 04.04.2023 36/44 (a) SPC-TB-0017 To a solution of 2,2'-((oxybis(ethane-2,1-diyl))bis(oxy))diacetic acid (5.000 g, 1 Eq, 22.50 mmol) dissolved in MeCN (24.46 ml) was added diallylamine (2.186 g, 2.78 mL, 1 Eq, 22.50 mmol) slowly at rt. The solution is stirred at rt for 2h. The solvent was removed under reduced pressure to afford the resulting salt (7.179 g, 22.48 mmol, 99.90 %) as a yellow oil.
• Example 6 Synthesis of salt 19 (SPC-TB-0019) (a) SPC-TB-0019 P25822PC00 04.04.2023 37/44 To a solution of 3,3'-((oxybis(ethane-2,1-diyl))bis(oxy))dipropionic acid (400 mg, 1.0 eq, 1.60 mmol) in DCM (16.0 mL) was added diallylamine (311 mg, 2.0 eq., 3.20 mmol). After 2h of reaction time the solvent was concentrated to obtain the resulting salt as col- orless oil (580 mg, quant.).
• Example 7 Synthesis of salt 20 (SPC-TB-0020)
• SPC-TB-0020 To a solution of 2,2'-(ethane-1,2-diylbis(oxy))bis(ethan-1-amine) (5.00 g, 1.00 Eq, 34.0 mmol) in DCM (14.0 mL) at 0°C was added propiolic acid (4.20 mL, 2.00 Eq, 67.0 mmol) in DCM (14.0 mL) precooled to 0°C. Caution: very exothermic reaction, add very slowly. The reaction mixture was stirred at 0°C for 15 min and allowed to warm to rt for 1h. It was concentrated under reduced pressure to produce an orange oil (quant yield).
• the tests were performed at ambient temperature of 30°C under stirring with small mag- netic stirrers in LC-MS vials or small glass vials. The reactions were performed under normal atmosphere. The reactions were monitored by LC-MS.
• the reaction scale was between 4 P25822PC00 04.04.2023 38/44 and 10 mg of tested compound.
• the ratio be- tween cysteine reagent the respective mono-adduct (mono) and bis-adduct (bis) as shown in the following schemes were compared.
• the tested compounds show improved reactivity with the cysteine derivative compared to the Olaplex active agent. Results * conversion was assessed after dilution of the reaction mixture with MeCN.

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