FR2483226A1 - Natural colourants prepd. by extn. of Rubiaceae plants - of specified variety used in cosmetics, esp. hair dyeing - Google Patents
Natural colourants prepd. by extn. of Rubiaceae plants - of specified variety used in cosmetics, esp. hair dyeing Download PDFInfo
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- FR2483226A1 FR2483226A1 FR8011880A FR8011880A FR2483226A1 FR 2483226 A1 FR2483226 A1 FR 2483226A1 FR 8011880 A FR8011880 A FR 8011880A FR 8011880 A FR8011880 A FR 8011880A FR 2483226 A1 FR2483226 A1 FR 2483226A1
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- 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
- A61Q5/10—Preparations for permanently dyeing the hair
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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
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B61/00—Dyes of natural origin prepared from natural sources, e.g. vegetable sources
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Cosmetics (AREA)
Abstract
Description
ta présente invention réalisée au Centre de Recherches Pierre Fabre est relative à un colorant capillaire entièrement naturel constitue, par un extrait de Rubia tinctorum.your present invention made at the Pierre Fabre Research Center relates to an all-natural hair dye consisting of an extract of Rubia tinctorum.
Rubia tinctorum, de la famille des Rubiacées, est une plante herbacée dont la racine ligneuse était autrefois utilisée pour la teinture textile. De nos jours cette teinture naturelle, concurrencée par les produits de synthèse, n'est plus utilisée pour la coloration des fibres textiles.Rubia tinctorum, from the Rubiaceae family, is a herbaceous plant whose woody root was once used for textile dyeing. Nowadays this natural dye, competing with synthetic products, is no longer used for dyeing textile fibers.
La présente invention se rapporte à l'utilisation d'un extrait colorant naturel atoxique, et antibactérien, particulièrement approprié à la réalisation de préparations cosmétiques diverses telles que shampooings, lotions, sprays, bains de boue, crèmes et baumes.The present invention relates to the use of an atoxic natural dye extract, and antibacterial, particularly suitable for the production of various cosmetic preparations such as shampoos, lotions, sprays, mud baths, creams and balms.
D'autres plantes de la même famille des Rubiacées, sont également adaptées à la préparation du colorant capillaire objet de l'invention, particulièrement les Coprosma (Australis-, lucida, parviflora, areolata...) les Morinda (tinctoria, longiflora...) Asperula odorata Galium dasypodum et Rubia iberica.Other plants of the same family of Rubiaceae, are also suitable for the preparation of the hair dye object of the invention, particularly the Coprosma (Australis-, lucida, parviflora, areolata ...) the Morinda (tinctoria, longiflora .. .) Asperula odorata Galium dasypodum and Rubia iberica.
Conformément à la présente invention les teintures capillaires à base de
Rubia tinctorum sont obtenues à partir des organes souterrains de préférence par épuisement avec un solvant suffisamment polaire et volatil tel que les alcools, de préférence méthylique, éthylique ou isopropylique éventuellement acidifiés par l'acide phosphorique ou l'acide sulfurique, les cétones de préférence diméthylcétone ou des solvants chlorés tels que le chlorure de méthylène ou le trichloro 1-1-1 éthane.In accordance with the present invention, hair dyes based on
Rubia tinctorum are obtained from underground organs preferably by exhaustion with a sufficiently polar and volatile solvent such as alcohols, preferably methyl, ethyl or isopropyl optionally acidified with phosphoric acid or sulfuric acid, ketones preferably dimethyl ketone or chlorinated solvents such as methylene chloride or trichloro 1-1-1 ethane.
Après une préconcentration du solvant et addition d'un polyol estérifié ou non, l'évaporation est menée jusqu'à élimination complète du solvant d'extraction.After a preconcentration of the solvent and addition of an esterified polyol or not, the evaporation is carried out until complete elimination of the extraction solvent.
Suivant le même processus, les substances actives de Rubia tinctorum peuvent également être solubilisées par des huiles ou des graisses ou des tensio-actifs compatibles avec une utilisation cosmétologique.According to the same process, the active substances of Rubia tinctorum can also be dissolved by oils or fats or surfactants compatible with cosmetic use.
Un dosage intermédiaire des substances actives, avant reprise par le solvant porteur permet la dilution de l'extrait à un titre standard, convenablement choisi en fonction des effets attendus.An intermediate dosage of the active substances, before taking up in the carrier solvent allows the dilution of the extract to a standard titre, suitably chosen according to the expected effects.
Les colorants selon la présente invention sont plus particulièrement destinés à la préparation de compositions cosmétiques de teinture capillaire, en particulier shampooing, lotion, spray, bain de boue. tes supports cosmétiques utilisables sont bien entendu tous les supports connus dans ce domaine.The dyes according to the present invention are more particularly intended for the preparation of cosmetic compositions for hair dyeing, in particular shampoo, lotion, spray, mud bath. your usable cosmetic supports are of course all the supports known in this field.
Selon une variante de ce procédé la couleur initiale beige peut etre nuancée par addition de faibles quantités de sels métalliques en particulier de sel d'aluminium et de sel de fer.According to a variant of this process, the initial beige color can be nuanced by adding small amounts of metal salts, in particular aluminum salt and iron salt.
Les exemples suivants sont donnés à titre indicatif,non limitatif. The following examples are given as a non-limiting indication.
Exemple 1 1 Kg de racines de Rubia tinctorum broyées est extrait successivement par 6 1 et 4 1 de méthanol à 0,5 7. phosphorique à reflux pendant 1 h. Après filtration et essorage du marc, les jus méthyliques sont préconcentrés à 2 1 puis évaporés sur 2 1 environ de propanediol jusqu'à élimination totale du méthanol.Example 1 1 kg of crushed Rubia tinctorum roots is extracted successively with 6 1 and 4 1 of methanol at 0.5 7. phosphoric acid at reflux for 1 h. After filtration and draining of the marc, the methyl juices are preconcentrated to 2 1 and then evaporated on approximately 2 1 of propanediol until complete elimination of the methanol.
L'extrait est alors clarifié, dosé en principe actif et standardisé à 1 % en principe colorant pour utilisation dans les spécialités cosmétiques.The extract is then clarified, dosed in active principle and standardized to 1% in coloring principle for use in cosmetic specialties.
Exemple 2 100 g d'écorces broyées de Coprosma Australis sont extraits par 800 ml d'acétone à reflux. Après filtration et lavage du marc par 200 ml de solvant, les filtrats groupés sont concentrés à 200 ml, dilués par 400 ml d'eau et acidifiés à pH 1 à laide d'acide phosphorique.Example 2 100 g of ground bark of Coprosma Australis are extracted with 800 ml of acetone at reflux. After filtration and washing of the marc with 200 ml of solvent, the grouped filtrates are concentrated to 200 ml, diluted with 400 ml of water and acidified to pH 1 with phosphoric acid.
Le principe colorant est extrait en liquide-liquide à l'aide de 2 x 300 ml de trichloréthylène. Après lavage à l'eau et séchage sur sulfate de sodium, le solvant évaporé à sec fournit une poudre brun rougeatre qui est dissoute à raison de 1 % dans une solution aqueuse à 30 % de lauryl sulfate de sodium.The coloring principle is extracted in liquid-liquid using 2 x 300 ml of trichlorethylene. After washing with water and drying over sodium sulfate, the solvent evaporated to dryness provides a reddish brown powder which is dissolved at a rate of 1% in a 30% aqueous solution of sodium lauryl sulfate.
Exemple 3 100 g de racines et tiges broyées de Morinda umbellata sont extraits par 600 ml de soude 0,5 N à température ambiante. Après filtration et lavage du marc par 200 ml d'eau, les filtrats groupés sont acidifiés à pH voisin de 1 à laide diacide phosphorique dilué.Example 3 100 g of crushed roots and stems of Morinda umbellata are extracted with 600 ml of 0.5 N sodium hydroxide solution at room temperature. After filtration and washing of the marc with 200 ml of water, the grouped filtrates are acidified to a pH close to 1 with dilute phosphoric acid.
Le principe colorant est extrait en liquide-liquide à l'aide de 3 x 200 ml de méthyl-éthyl-cétone. Après lavage à l'eau, le solvant est concentré à 200 ml et évaporé sur 200 ml propanediol.The coloring principle is extracted in liquid-liquid using 3 x 200 ml of methyl ethyl ketone. After washing with water, the solvent is concentrated to 200 ml and evaporated on 200 ml propanediol.
Après clarification, l'extrait est dosé en principe actif et standardisé à 0,5 Z0 en principe colorant pour utilisation dans les spécialités cosmétiques.After clarification, the extract is dosed in active principle and standardized to 0.5 Z0 in coloring principle for use in cosmetic specialties.
A titre d'exemples non limitatifs de préparations cosmétologiques selon l'invention on mentionnera ci-après 3 exemples de formulation de shampooing
Exemple A
Alkyl éther sulfate de sodium * 10 7
Carboxy méthyl cellulose sodique e 2 7.By way of nonlimiting examples of cosmetic preparations according to the invention, 3 examples of shampoo formulation will be mentioned below.
Example A
Alkyl ether sodium sulfate * 10 7
Carboxy methyl sodium cellulose e 2 7.
2-bromo-2-nitro-propane-1,3-diol............ 0,25 %
Parfum...................................... 0,25 %
Extrait de Rubia standardisé à 0,5 % .............................. 2 %
Eau distillée............................. Q.S.P.100 ml
Exemple B
Alkyl éther sulfate de sodium et magnésium ............. 10 %
Alkyl sorbate éthoxylé ............................ 5 %
Bentone..................................... 0,5 %
Parahydroxy benzoate........................ 0,15 %
Parfum...................................... 0,25 %
Extrait de Rubia standardisé à 0,5 % .................. 2 %
Eau....................................... 100 %
Exemple C
Alkyl éther sulfate de sodium............... 10 %
Carboxy méthyl cellulose sodique............ 2 % 2-Bromo-2-nitro-propane-1,3-diol............ 0,05 %
Parfum ............................................... 0,25 %
Extrait de Rubia standardisé à 0,5 % .......................... 2 %
Chlorure ferrique......................... 0,1 %
Eau distillée . . .. .. . .. ... .. .. . . Q. S.P. QoSPo 100 ml 2-bromo-2-nitro-propane-1,3-diol ............ 0.25%
Perfume ...................................... 0.25%
Rubia extract standardized to 0.5% .............................. 2%
Distilled water ............................. QSP100 ml
Example B
Alkyl ether sodium and magnesium sulfate ............. 10%
Alkyl ethoxylated sorbate ............................ 5%
Bentone ..................................... 0.5%
Parahydroxy benzoate ........................ 0.15%
Perfume ...................................... 0.25%
Rubia extract standardized to 0.5% .................. 2%
Water ....................................... 100%
Example C
Alkyl ether sodium sulfate ............... 10%
Carboxy methyl cellulose sodium ............ 2% 2-Bromo-2-nitro-propane-1,3-diol ............ 0.05%
Perfume ............................................... 0, 25%
Rubia extract standardized to 0.5% .......................... 2%
Ferric chloride ......................... 0.1%
Distilled water . . .. ... .. ... .. ... . QSP QoSPo 100 ml
Claims (12)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8011880A FR2483226A1 (en) | 1980-05-28 | 1980-05-28 | Natural colourants prepd. by extn. of Rubiaceae plants - of specified variety used in cosmetics, esp. hair dyeing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8011880A FR2483226A1 (en) | 1980-05-28 | 1980-05-28 | Natural colourants prepd. by extn. of Rubiaceae plants - of specified variety used in cosmetics, esp. hair dyeing |
Publications (2)
Publication Number | Publication Date |
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FR2483226A1 true FR2483226A1 (en) | 1981-12-04 |
FR2483226B1 FR2483226B1 (en) | 1983-06-10 |
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Application Number | Title | Priority Date | Filing Date |
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FR8011880A Granted FR2483226A1 (en) | 1980-05-28 | 1980-05-28 | Natural colourants prepd. by extn. of Rubiaceae plants - of specified variety used in cosmetics, esp. hair dyeing |
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FR (1) | FR2483226A1 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2549721A1 (en) * | 1983-07-28 | 1985-02-01 | Secta Labo Cosmetologie Y Roch | Method and compositions for colouring superficial body growths |
EP0133129A2 (en) * | 1983-07-28 | 1985-02-13 | Secta-Laboratoires De Cosmetologie Yves Rocher | Process and compositions for dyeing the annexes of the epidermis |
FR2567400A2 (en) * | 1984-07-12 | 1986-01-17 | Secta Lab Cosmetologie Y Roche | Process and compositions for dyeing exoskeletons. |
EP0440494A2 (en) * | 1990-02-02 | 1991-08-07 | Tokiwa Kanpo Pharmaceutical Co., Ltd. | Hair dyeing |
EP1191070A1 (en) * | 2000-09-26 | 2002-03-27 | Coöperatie Rubia | Method for the production of a dye preparation based on madder root |
WO2004105718A1 (en) * | 2003-06-03 | 2004-12-09 | Unilever Plc | Skin lightening composition comprising an extract of plants from the families of symplocos or rubia |
WO2011045150A2 (en) * | 2009-10-12 | 2011-04-21 | Unilever Nv | A personal care composition |
-
1980
- 1980-05-28 FR FR8011880A patent/FR2483226A1/en active Granted
Non-Patent Citations (1)
Title |
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EXBK/52 * |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2549721A1 (en) * | 1983-07-28 | 1985-02-01 | Secta Labo Cosmetologie Y Roch | Method and compositions for colouring superficial body growths |
EP0133129A2 (en) * | 1983-07-28 | 1985-02-13 | Secta-Laboratoires De Cosmetologie Yves Rocher | Process and compositions for dyeing the annexes of the epidermis |
EP0133129A3 (en) * | 1983-07-28 | 1985-07-10 | Secta-Laboratoires De Cosmetologie Yves Rocher | Process and compositions for dyeing the annexes of the epidermis |
AU570706B2 (en) * | 1983-07-28 | 1988-03-24 | Secta-Laboratoires De Cosmetologie Yves Rocher | Process and composition for colouration of phanera |
FR2567400A2 (en) * | 1984-07-12 | 1986-01-17 | Secta Lab Cosmetologie Y Roche | Process and compositions for dyeing exoskeletons. |
EP0440494A2 (en) * | 1990-02-02 | 1991-08-07 | Tokiwa Kanpo Pharmaceutical Co., Ltd. | Hair dyeing |
EP0440494A3 (en) * | 1990-02-02 | 1992-06-10 | Tokiwa Kanpo Pharmaceutical Co., Ltd. | Hair dyeing |
EP1191070A1 (en) * | 2000-09-26 | 2002-03-27 | Coöperatie Rubia | Method for the production of a dye preparation based on madder root |
US6596036B2 (en) | 2000-09-26 | 2003-07-22 | Coöperatie Rubia U.A. | Method for the production of a dye preparation based on madder root |
WO2004105718A1 (en) * | 2003-06-03 | 2004-12-09 | Unilever Plc | Skin lightening composition comprising an extract of plants from the families of symplocos or rubia |
WO2011045150A2 (en) * | 2009-10-12 | 2011-04-21 | Unilever Nv | A personal care composition |
WO2011045150A3 (en) * | 2009-10-12 | 2011-11-03 | Unilever Nv | A personal care composition |
Also Published As
Publication number | Publication date |
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FR2483226B1 (en) | 1983-06-10 |
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