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WO2023123196A1 - Composition d'huiles pour le soin des matières kératiniques - Google Patents

Composition d'huiles pour le soin des matières kératiniques Download PDF

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Publication number
WO2023123196A1
WO2023123196A1 PCT/CN2021/143017 CN2021143017W WO2023123196A1 WO 2023123196 A1 WO2023123196 A1 WO 2023123196A1 CN 2021143017 W CN2021143017 W CN 2021143017W WO 2023123196 A1 WO2023123196 A1 WO 2023123196A1
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Prior art keywords
composition
component
oils
composition according
oil
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Ceased
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PCT/CN2021/143017
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English (en)
Inventor
Lili Yang
Lingchao KONG
Wi Soon CHIA
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LOreal SA
Original Assignee
LOreal SA
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Priority to PCT/CN2021/143017 priority Critical patent/WO2023123196A1/fr
Priority to CN202180105325.4A priority patent/CN118488827A/zh
Priority to FR2201191A priority patent/FR3131533B1/fr
Publication of WO2023123196A1 publication Critical patent/WO2023123196A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • 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
    • A61K8/31—Hydrocarbons
    • 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
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37—Esters of carboxylic acids
    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
    • A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
    • 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
    • A61Q5/12—Preparations containing hair conditioners
    • 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
    • A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/30—Characterized by the absence of a particular group of ingredients
    • A61K2800/31—Anhydrous

Definitions

  • the present invention relates to a composition of various oils for caring for keratin material, in particular the hair.
  • the present invention also relates to a use of at least two specific oils.
  • Keratin materials are present widely on surface of human bodies, e.g., skin, scalp and hair. Many people have for a long time sought to fresh the body surface, so as to feel comfortable in daily life and work. Amongst others, the feeling of sticky/greasy, in particular that from hair, is particularly concerned by many people. Accordingly, various products are developed to deal with the sticky or greasy feeling of person.
  • the scalp and hair are particularly readily to suffer from grease.
  • Various formulations have been developed for the sticky or greasy feeling, including those provided in a separate form, e.g., lotion, spray and the like, and those incorporated into conventional products for hair and/or for scalp, e.g., shampoo, leave-on and/or rinse-off conditioner/oil.
  • keratin material in particular the hair is cleansed and treated with many cosmetic regiments to improve the sticky or greasy feeling, e.g., by shampoo.
  • These various regiments can remove the hair’s natural oils and impart structural damage to the hair.
  • shampoos are often formulated with anionic surfactants that primarily clean as opposed to condition the hair.
  • Anionic surfactants are highly effective for removing dirt, pollution, build-up, etc., from the hair, but they also remove sebum, a naturally occurring oily or waxy matter that automatically lubricates hair.
  • Conditioner compositions are used to improve or return to the hair its natural luster, shine, smoothness, and softness, for example, after shampooing the hair and/or after subjecting the hair to a chemical treatment.
  • Conditioner compositions are often applied as cream-like emulsions, or lotions, and typically include one or more cationic compound, in form of either rinse-off or leave-on product.
  • Other hair-care products may also be procued into a leave-on product. As being present on hair for a long time, the requirement on a leave-on product may particularly focus on the achievement of the desired function thereof without affecting adversely the hair.
  • An object of the present invention is to provide a composition for caring for keratin material, in particular the hair, which can deliver instant and long lasting shine with light sensory.
  • Another object of the present invention is to provide a composition for caring for keratin material, in particular the hair, which will not adversely bring stickiness and greasiness feeling.
  • the inventors have discovered surprisingly that when specific non-volatile oil and specific volatile oil are used in a combination, the objects above can be satisfied.
  • the non-volatile oil may comprise silicone, e.g., ⁇ , ⁇ -aminosilicone, preferably ⁇ , ⁇ -amino (C1-C6) alkyl silicone, especially one having a viscosity of 500-50000 mPa/s, preferably 10000-15000mPa/s.
  • the non-volatile silicone according to the present invention is free of phenyl group.
  • the non-volatile oil may also comprise hydrocarbon-based oil chosen from synthetic esters.
  • the volatile oil can comprise or be selected from the group consisting of volatile silicone and C8-C16 isoparaffin.
  • the volatile silicone can comprise C6-C10 alkyl methicone, e.g., caprylyl methicone.
  • the C8-C16 isoparaffin is preferably a C8-C14 isoparaffin.
  • the present invention provides a composition of oils for caring for keratin material, in particular the hair, comprising the components of:
  • the component A) may be:
  • A1 a synthetic ester of formula R 1 COOR 2 , selected from the group consisting of monoesters of a saturated branched C6-C10 monocarboxylic acid with a saturated branched C6-C10 alcohol.
  • the component B) may be:
  • At least two volatile oils selected from the group consisting of components B1) oil volatile silicone and B2) C8-C16 isoparaffin.
  • the component B1) may be a C6-C10 alkyl methicone, e.g., caprylyl methicone.
  • composition of oils of the invention may comprise the components of:
  • A) at least one non-volatile oil comprising component A1) a synthetic ester of formula R 1 COOR 2 , selected from the group consisting of monoesters of a saturated branched C6-C10 monocarboxylic acid with a saturated branched C6-C10 alcohol; and
  • the component B1) may be present in an amount of 10 wt%or more, preferably 15 wt%or more, relative to the total weight of the composition of oils.
  • the component B2) may be present in an amount of 40 wt%or more, preferably 50 wt%or more, relative to the total weight of the composition of oils.
  • composition of the present invention can be in the form of oil gel or oil balm.
  • a further object of the present invention is to provide use of a combination of components A1) , B1) and B2) according to the present invention to be used on human body, especially on keratin material, e.g., on hair.
  • the present invention relates to a non-therapeutic method for caring for keratin material, in particular the hair, comprising applying the composition according to the first aspect of the present invention to the skin, in particular the hair.
  • the “keratin material” according to the present invention is the skin, hair, scalp, eyelashes, eyebrows, bodily hair, nails, lips or mucous membranes.
  • the keratin material according to the present invention is hair.
  • oil means a water-immiscible non-aqueous compound that is liquid at room temperature (25°C) and atmospheric pressure (760 mmHg) .
  • silicon oil means an oil containing at least one silicon atom, and in particular containing Si-O groups.
  • volatile oil means any non-aqueous medium that is capable of evaporating on contact with the skin or the lips in less than one hour, at room temperature and atmospheric pressure.
  • the volatile oil is a cosmetic volatile oil, which is liquid at room temperature. More specifically, a volatile oil has an evaporation rate of between 0.01 and 200 mg/cm 2 /min, limits inclusive.
  • non-volatile means an oil of which the vapour pressure at 25°C and atmospheric pressure is non-zero and is less than 0.02 mmHg (2.66 Pa) and better still less than 10 -3 mmHg (0.13 Pa) .
  • the present invention provides a composition of oils for caring for keratin material, in particular the hair, comprising the components of:
  • A) at least one non-volatile silicone oil comprising component A1) a synthetic ester of formula R 1 COOR 2 , selected from the group consisting of monoesters of a saturated branched C6-C10 monocarboxylic acid with a saturated branched C6-C10 alcohol and
  • volatile non-phenyl silicone selected from the group consisting of C6-C10 alkylmethicone, preferably caprylyl methicone, in an amount of 10 wt%or more, preferably 15 wt%or more, relative to the total weight of the composition of oils, and
  • C8-C16 isoparaffin in an amount of 40 wt%or more, preferably 50 wt%or more, relative to the total weight of the composition of oils.
  • composition of oils according to the present invention means generally a combination of a plurality of oils, comprising specific non-volatile oils and volatile oils. Accordingly, the composition may comprise at least one non-volatile oil as component A) .
  • Component A1 non-volatile synthetic oil
  • the component A) may comprise non-volatile synthetic oils useful as component A1) .
  • the non-volatile synthetic oil may be for example a synthetic ester of formula R 1 COOR 2 .
  • R 1 represents a linear or branched fatty acid residue containing from 4 to 40 carbon atoms and R 2 represents a hydrocarbon-based chain containing from 4 to 40 carbon atoms, on condition that R 1 +R 2 ⁇ 14, or ⁇ 16.
  • the oil of formula R 1 COOR 2 for use as the synthetic oil may be chosen from mono-, di-, tri-, tetra-esters and polyesters, and mixtures thereof.
  • oil of formula R 1 COOR 2 mention can be made of purcellin oil (cetostearyl octanoate) , diisopropyl adipate, octyl isononanoate, isononyl isononanoate, 2-ethylhexyl palmitate, octyldodecyl neopentanoate, stearyl heptanoate, stearyl caprylate, 2-octyldodecyl stearate, 2-octyldodecyl erucate, oleyl erucate, isostearyl isostearate, 2-octyldodecyl benzoate, isopropyl myristate, isopropyl palmitate, butyl stearate, hexyl laurate, 2-ethylhexyl palmitate, 2-hexyldecyl laurate,
  • the oil of formula R 1 COOR 2 may be selected from esters of a C6-C24 monocarboxylic acid with a C4-C20 monoalcohol, at least one of the acid and the alcohol being branched or unsaturated; or preferably selected from esters of a C4-C10 (preferably C6-C10) monocarboxylic acid with a C4-C10 (preferably C6-C10) alcohol, at least one of the acid and the alcohol being branched.
  • the oil of formula R 1 COOR 2 may be a monoester of a saturated branched C6-C10 monocarboxylic acid with a saturated branched C6-C10 alcohol.
  • octyl isononanoate, and in particular isononyl isononanoate can thus be especially mentioned.
  • the component A1) may be present in an amount ranging from 0.1 wt%-40 wt%, preferably 0.1wt%-30 wt%, or preferably 0.1 wt%-20 wt%, relative to the total weight of the composition of oils.
  • Component A2 non-volatile amino silicone oil
  • the component A) may also comprise non-volatile amino silicone oils useful as component A2) , besides component A1) .
  • silicone and “silicone oil” can be used exchangeable to one another.
  • the non-volatile amino silicone oil for use as component A2) can be preferably free of phenyl group, i.e., a non-phenyl silicone.
  • non-phenyl denotes a compound not bearing any phenyl substituents.
  • Silicone is usually used as an oil for various cosmetic purpose. Amongst others, an amino silicone is particularly interested.
  • the term “amino silicone” is intended to mean any silicone comprising at least one primary, secondary or tertiary amine or a quaternary ammonium group (i.e., a quaternized group) .
  • a silicone may bear the amine group on the skeleton chain in the molecule, called as an amino-terminal silicone, or bear the amine group on the pendent chain, called as an amino-grafted silicone.
  • Amino silicones are described, for example, in US2011/0155163 and US2011/155164, both of which are herein incorporated by reference.
  • Non-limiting examples include amodimethicone, silicone quaternium-22, trimethylsilyl amodimethicone, bis-isobutyl/PEG/PPG-20/35/amodimethicone copolymer, bis-cetearyl amodimethicone, bis-amino PEG/PPG-41/3 aminoethyl PG-propyl dimethicone, PEG-40/PPG-8 methylaminopropyl hydroxypropyl dimethicone copolymer, bis-isobutyl/PEG/PPG-20/35/amodimethicone copolymer, quaternium-80, methoxy PEG/PPG-7/3 aminopropyl dimethicone, silicone quaternium-22, bis (C13-15 Alkoxy) PG-amodimethicone, bis-hydroxy/methoxy amodimethicone, aminopropyl phenyl trimethicone, aminopropyl dimethicone
  • the amino silicone is preferably an amino-terminal silicone.
  • another group of preferable amino silicone according to the present invention may comprise: amino bispropyl dimethicone; aminopropyl dimethicone; amodimethicone; bis-aminopropyl dimethicone; bis-aminopropyl/ethoxy aminopropyl dimethicone; bis-butyloxyamodimethicone/peg-60 copolymer; bis-isobutyl peg-14/amodimethicone copolymer; bis-isobutyl peg-15/amodimethicone copolymer.
  • a bis-amino-terminal silicone is preferably useful, i.e., an amino silicone having both terminal groups of amino groups.
  • such a bis-amino-terminal silicone is called as a bis-amino silicone, or called as ⁇ , ⁇ -aminosilicone, unless otherwise indicated specifically.
  • the amino group in the ⁇ , ⁇ -aminosilicone useful can be further modified with an alkyl or alkoxyl, preferably a (C1-C6) alkyl or alkoxyl, or preferably a (C1-C4) alkyl or alkoxyl, e.g., propyl.
  • bis-aminopropyl dimethicone bis-aminopropyl/ethoxy aminopropyl dimethicone, bis-isobutyl/PEG/PPG-20/35/amodimethicone copolymer, bis-cetearyl amodimethicone, bis-amino PEG/PPG-41/3 aminoethyl PG-propyl dimethicone, bis (C13-15 Alkoxy) PG-amodimethicone, bis-hydroxy/methoxy amodimethicone may be preferred.
  • non-volatile silicone oil useful for the invention may be an ⁇ , ⁇ -aminoalkyl silicone, preferably ⁇ , ⁇ -amino (C1-C6) alkyl silicone, e.g., bis-aminopropyl dimethicone.
  • the non-volatile silicone may preferably have a viscosity of 500-50000 mPa/s, preferably 10000-15000mPa/s.
  • component A2 is particularly beneficial for the smoothness feeling of keratin materials.
  • ⁇ , ⁇ -amino (C1-C6) alkyl silicone especially one having a viscosity of 500-50000 mPa/s, preferably 10000-15000mPa/s, is of particular benefit.
  • the molecule of component A2) is free of phenyl group.
  • component A) especially an ⁇ , ⁇ -amino (C1-C6) alkyl silicone, e.g., bis-aminopropyl dimethicone, preferably having a viscosity of 500-50000 mPa/s, preferably 10000-15000mPa/s, is used as an essential component for the composition of oils, which can bring better smoothness, as well as good lightness, stability and so on.
  • component A especially an ⁇ , ⁇ -amino (C1-C6) alkyl silicone, e.g., bis-aminopropyl dimethicone, preferably having a viscosity of 500-50000 mPa/s, preferably 10000-15000mPa/s
  • the component A2) may be present in an amount ranging from 0.1 wt%-10 wt%, preferably 0.1wt%-5wt%, or preferably 0.1 wt%-3 wt%, relative to the total weight of the composition of oils.
  • the component A) may also comprise additional non-volatile silicone oils useful as component A3) , besides components A2) and A1) .
  • the additional non-volatile silicone oil is different from the “amino silicone” useful as component A2) according to the present invention.
  • examples of the additional non-volatile silicone oil can be made to polydialkylsiloxane family with terminal trimethylsilyl groups, such as oils with a viscosity in the range 0.2 m 2 /s to 2.5 m 2 /s at 25°C, for example oils from the DC200 series from DOW CORNING, in particular that with a viscosity of 60,000 Cst, from the SILBIONE 70047 series, more particularly 70,047 V 500,000 oil provided by the supplier RHODIA CHIMIE, polydialkylsiloxanes with terminal dimethylsilanol groups such as dimethiconol such as the oils of the 48 series from the company Rhodia or polyalkylarylsiloxanes such as SILBIONE 70641 V 200 oil provided by the supplier RHODIA CHIMIE.
  • polydialkylsiloxane family with terminal trimethylsilyl groups such as oils with a viscosity in the range 0.2 m 2 /s to 2.5 m 2 /s
  • the component A3) may be present in an amount ranging from 0.1 wt%-12 wt%, or preferably 3 wt%-9 wt%, relative to the total weight of the composition of oils.
  • Component B) volatile oil
  • composition of oils according to the present invention may comprise at least two volatile oils as component B) .
  • the component B) is at least one volatile selected from the group consisting of: components B1) oil volatile non-phenyl silicone and B2) C8-C16 isoparaffin.
  • Component B1) volatile non-phenyl silicone oil
  • silicone oils are conventionally known to be non-volatile, whilst some non-phenyl silicone oils are known to be volatile, even with relatively low evaporation rate.
  • examples comprise volatile linear or cyclic silicone oils, especially those with a viscosity ⁇ 8 centistokes (cSt) (8 ⁇ 10 -6 m 2 /s) , and especially containing from 2 to 10 silicon atoms and in particular from 2 to 7 silicon atoms, these silicones optionally comprising alkyl or alkoxy groups containing from 1 to 10 carbon atoms.
  • Such volatile non-phenyl silicone oils may be an alkylsilicone.
  • the “alkyl” moiety in the volatile non-phenyl alkylsilicone has a number of carbon atoms similar to the R 1 and/or R 2 groups in the oil of formula R 1 COOR 2 useful as component A1) , the desired smoothness, lightness and shine of hair can be particularly satisfied, which may thanks to the better compatibility between such an alkylsilicone and the oil of formula R 1 COOR 2 .
  • the typical volatile silicone oil may be C6-C10 alkylmethicone.
  • Caprylyl methicone can be provided as an example of C6-C10 alkylmethicone.
  • Commercial product of caprylyl methicone mention can be made of that sold under the tradename DOW CORNING FZ-3196 by the company DOW CORNING (DOW CHEMICAL) .
  • the component B1) in particular caprylyl methicone, may be preferably used in a relatively higher amount.
  • a relatively higher amount of component B1) in particular caprylyl methicone, can benefit the lightness and smoothness of hair. Accordingly, it is important for the invention to use component B1) , in particular caprylyl methicone, in an appropriate amount.
  • the component B1) in particular caprylyl methicone, may be present in an amount ranging from 10 wt%-35 wt%, preferably 15wt%-25 wt%, relative to the total weight of the composition of oils.
  • the component B) of the co00mposition of oils according to the present invention may optionally comprises additional volatile oils, e.g., an oil selected from the group consisting of C8-C16 isoparaffins, as component B2) , which serves generally as a solvent.
  • additional volatile oils e.g., an oil selected from the group consisting of C8-C16 isoparaffins, as component B2) , which serves generally as a solvent.
  • Hydrocarbon-based oils containing from 8 to 16 carbon atoms, and especially C8-C16 branched alkanes are known to be conventional volatile oils and can be used as component B2) alone or as a mixture thereof.
  • Examples may be made of isododecane (also called 2, 2, 4, 4, 6-pentamethylheptane) , isodecane, isohexadecane, and, for example, the oils sold under the trade names or
  • C8-C16 isoparaffins are usually used as organic solvents, e.g., used as co-solvent in a mixture of organic solvents with other conventional organic solvent (s) .
  • the component B2) e.g., isododecane
  • the composition is free substantially of, or free of, other conventional solvents.
  • other conventional solvents e.g., hydrogenated polyisobutene conventionally used in a hair product, if present, comprise no more than 10 wt%, or no more than 5 wt%, preferably no more than 1%, of the composition of oils.
  • the composition of oils according to the present invention may use a C8-C16 isoparaffin or a mixture thereof, e.g., isododecane, as the sole solvent.
  • the component B2) in particular isododecane, may be present in an amount ranging from 40 wt%-95 wt%, preferably 50wt%-95 wt%, or preferably 55wt%-90 wt%, relative to the total weight of the composition of oils.
  • component B1 a volatile non-phenyl silicone oil and B2) C8-C16 isoparaffin
  • component B2 a volatile non-phenyl silicone oil and B2 C8-C16 isoparaffin
  • the composition of oils according to the present invention comprises both components B1) and B2) .
  • Component C) vegetable oil
  • composition of oils according to the present invention may further comprise at least one vegetable oil, especially of triglyceride type for use component C) .
  • the vegetable oils of triglyceride type are selected from sunflower seed oil, corn oil, soybean oil, marrow oil, grapeseed oil, sesame seed oil, hazelnut oil, apricot oil, macadamia oil, castor oil, olive oil; avocado oil; argan oil; camellia oil, palm oil, maize germ oil, cottonseed oil, peanut oil, pumpkin seed oil, wheatgerm oil, babassu oil, coconut oil, rapeseed oil, almond oil, linseed oil, safflower oil, and also mixtures thereof.
  • the vegetable oils of triglyceride type are selected sunflower seed oil, jojoba seed oil, argania spinosa kernel oil, coconut oil, corn oil, soybean oil, marrow oil, grapeseed oil, sesame seed oil, hazelnut oil, apricot oil, macadamia oil, castor oil, and avocado oil.
  • helianthus annuus (sunflower) seed oil sold under the name REFINED SUNFLOWER OIL by the company AAK KAMANI PRIVATE
  • SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL sold under the name JD FFL JOJOBA GOLDEN OIL by the company JOJOBA DESERT
  • cocos nucifera (coconut) oil sold under the name ACTIVATED VIRGIN COCONUT OIL by the company BIOTROPICS
  • ARGANIA SPINOSA KERNEL OIL sold under the name LIPOFRUCTYL ARGAN BE LS 9779 by the company BASF BEAUTY CARE SOLUTION
  • prunus armeniaca (apricot) kernel oil sold under the name APRICOT KERNEL OIL REFINED DAC by the company GUSTAV HEESS.
  • the vegetable oil of triglyceride type may be present in an amount ranging from 0.5 wt%to 15 wt%, preferably from 0.1 wt%to 10 wt%, or preferably from 0.1 wt%to 5 wt%, relative to the total weight of the composition of oils.
  • all or substantially all of the useful components is each free of phenyl.
  • a hair product especially a hair oil
  • the presence of phenyl in some components, e.g., in a silicone may usually benefit the effect of shininess.
  • a phenyl-containing compound may often be non-environmental-friendly.
  • the inventors of the present invention have discovered surprisingly that using the composition of oils according to the present invention comprising the specific combination of the components A) and B) , the desired shininess can be still achieved.
  • the composition of oils consists essentially of, or consists of components A1) , A2) , A3) , B1) and B2) described here. According to an embodiment of the present invention, it is preferable that the composition of oils consists essentially of, or consists of components A1) , A2) , B1) and B2) described here.
  • composition of oils of the present invention may comprise conventional cosmetic adjuvants or additives, for instance fragrances, fillers, antioxidant (for example, tocopherols, such as d-alpha-tocopherol, d-beta-tocopherol, d-gamma-tocopherol, d-delta-tocopherol) , and mixtures thereof.
  • fragrances for instance, fragrances, fillers, antioxidant (for example, tocopherols, such as d-alpha-tocopherol, d-beta-tocopherol, d-gamma-tocopherol, d-delta-tocopherol) , and mixtures thereof.
  • antioxidant for example, tocopherols, such as d-alpha-tocopherol, d-beta-tocopherol, d-gamma-tocopherol, d-delta-tocopherol
  • the composition according to the present invention can be essentially in an anhydrous form.
  • water or moisture is preferably avoided to be included in the composition; however, it is easily understood by those skilled that water may not be 100%removed.
  • water may be provided by ingredients of the composition that contain it in residual amount, may be incorporated during the production, or may be absorbed from ambient during production and/or storage.
  • anhydrous means absence of water, or the presence of water in such an amount those skilled can determine it as free or substantially free of water.
  • an “anhydrous” composition according to the present invention may comprise less than 2%, preferably less than 0.5%by weight of water, relative to the total weight of the composition.
  • an “anhydrous” composition according to the present invention does not comprise a detectable amount of water, wherein the “detectable amount” means an amount can be detected by a device conventionally used in the art to measure the water content.
  • the components A) to C) are subjected to a water removal step before being incorporated into the composition of the present invention.
  • the technical means for the water removal is not particularly limited, as long as the composition obtained is "anhydrous" .
  • composition of oils of the present invention can be in the form of oil gel or oil balm.
  • compositions according to the invention can be manufactured by known processes, generally used in the cosmetic or dermatological field.
  • the present invention relates to a non-therapeutic method for caring for keratin material, in particular the hair, comprising applying the composition of oils according to the present invention to the skin, in particular the hair.
  • compositions/formulas described below are expressed in %by weight, relative to the total weight of each composition/formula.
  • composition according to invention formula (Inv. ) 1 and comparative formula (Comp. ) 1-3 were prepared according to the contents given in Table 1.
  • compositions of oils listed above were prepared as follows, taking the composition of oils of invention formula 1 as an example: mixing the components to obtain a mixture and homogenizing the mixture by stirring.
  • compositions according to invention formula (Inv. ) 1 and comparative formula (Comp. ) 1-3 were evaluated for the hair conditioning performances.
  • compositions A-E with different amounts of component B1) were prepared according to the contents given in Table 3-1.
  • the scores were provided twice, 0 hour (instant) and 4 hours after applying the compositions.
  • compositions F-G with different amounts of component B2) were prepared according to the contents given in Table 4-1.
  • composition D served as the benchmark.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
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  • Epidemiology (AREA)
  • Dermatology (AREA)
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  • Cosmetics (AREA)

Abstract

Une composition d'huiles pour le soin des matières kératiniques, en particulier des cheveux, comprend les composants suivants : A) au moins une huile non volatile comprenant le composant A1) un ester synthétique de formule R 1COOR 2 ; et B) au moins deux huiles volatiles choisies dans le groupe constitué par : les composants B1) de la silicone volatile et B2) de l'isoparaffine en C8-C16.
PCT/CN2021/143017 2021-12-30 2021-12-30 Composition d'huiles pour le soin des matières kératiniques Ceased WO2023123196A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
PCT/CN2021/143017 WO2023123196A1 (fr) 2021-12-30 2021-12-30 Composition d'huiles pour le soin des matières kératiniques
CN202180105325.4A CN118488827A (zh) 2021-12-30 2021-12-30 用于护理角蛋白材料的油的组合物
FR2201191A FR3131533B1 (fr) 2021-12-30 2022-02-11 Composition d'huiles pour le soin de matière kératineuse

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2021/143017 WO2023123196A1 (fr) 2021-12-30 2021-12-30 Composition d'huiles pour le soin des matières kératiniques

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WO2023123196A1 true WO2023123196A1 (fr) 2023-07-06

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070071703A1 (en) * 2005-09-28 2007-03-29 Lin Samuel Qcheng S High efficiency master gels for thickening oil based compositions
WO2012024364A2 (fr) * 2010-08-18 2012-02-23 Kao Corporation Compositions de revitalisant pour cheveux et peau
US20130039873A1 (en) * 2011-08-12 2013-02-14 Kao Corporation Hair and skin conditioning compositions
WO2013160364A1 (fr) * 2012-04-26 2013-10-31 L'oreal Composition comprenant un silane et un tensioactif gemini
JP2020193192A (ja) * 2019-05-24 2020-12-03 株式会社マンダム 油性毛髪化粧料

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2954135B1 (fr) 2009-12-23 2012-02-24 Oreal Composition cosmetique comprenant au moins un compose organique du silicium, au moins un tensioactif anionique et au moins une silicone aminee ainsi qu'un procede mettant en oeuvre ladite composition
FR2954128B1 (fr) 2009-12-23 2012-02-17 Oreal Composition cosmetique comprenant au moins un compose organique du silicium, au moins un tensioactif anionique et au moins un agent epaississant non ionique ainsi qu'un procede mettant en oeuvre la composition
EP2550956A1 (fr) * 2011-07-26 2013-01-30 KPSS-Kao Professional Salon Services GmbH Composition non aqueuse pour cheveux
FR3007972B1 (fr) * 2013-07-04 2015-08-07 Oreal Composition cosmetique comprenant des esters gras liquides, des huiles volatiles et des epaississants, et procede de traitement cosmetique

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070071703A1 (en) * 2005-09-28 2007-03-29 Lin Samuel Qcheng S High efficiency master gels for thickening oil based compositions
WO2012024364A2 (fr) * 2010-08-18 2012-02-23 Kao Corporation Compositions de revitalisant pour cheveux et peau
US20130039873A1 (en) * 2011-08-12 2013-02-14 Kao Corporation Hair and skin conditioning compositions
WO2013160364A1 (fr) * 2012-04-26 2013-10-31 L'oreal Composition comprenant un silane et un tensioactif gemini
JP2020193192A (ja) * 2019-05-24 2020-12-03 株式会社マンダム 油性毛髪化粧料

Also Published As

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FR3131533B1 (fr) 2025-03-07
FR3131533A1 (fr) 2023-07-07
CN118488827A (zh) 2024-08-13

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