US3662061A - Novel lip coloring cosmetics and methods of making same - Google Patents

Novel lip coloring cosmetics and methods of making same Download PDF

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Publication number
US3662061A
US3662061A US738841A US3662061DA US3662061A US 3662061 A US3662061 A US 3662061A US 738841 A US738841 A US 738841A US 3662061D A US3662061D A US 3662061DA US 3662061 A US3662061 A US 3662061A
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US
United States
Prior art keywords
lip
dye
methods
rouge
making same
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US738841A
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English (en)
Inventor
Felix Lachampt
Charles Zviak
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
LOreal SA
Original Assignee
LOreal SA
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Filing date
Publication date
Application filed by LOreal SA filed Critical LOreal SA
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Publication of US3662061A publication Critical patent/US3662061A/en
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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • A61K8/498Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02Preparations containing skin colorants, e.g. pigments
    • A61Q1/04Preparations containing skin colorants, e.g. pigments for lips
    • A61Q1/06Lipsticks

Definitions

  • This invention relates to a process of making lip rouges for use in lipsticks and to new products which may be used in this process.
  • Bromo acids commonly known as eosine acids and as alkaline eosines, are currently used to color lip rouges of the type used in lipsticks.
  • the acid eosines are insoluble in water and in fatty substances so that, when used in lipsticks, those colorants must be incorporated into dispersions in the waxes and fatty substances constituting the inert portion or base of the lip rouge.
  • This dispersion may be formed by introducing eosine acids into a solvent therefor which is also soluble in the base material of the lip rouge, so that after evaporation of the solvent, the eosine acids precipitate, and, at the end of the process, are dispersed within the material making up the lipstick.
  • This dispersion may also be effected by prolonged grinding of a mixture containing the material making up the lipstick and the colorants.
  • Colored pigments may also be incorporated into the lipstick material by first dissolving them in a solvent such as glycol or tetrahydrofurfuric alcohol.
  • Alkaline eosines are soluble in water, but are not soluble in fatty substances, so that they must also be introduced into the lipstick material in the dispersed state.
  • these lip rouges have the practical disadvantage that the color of the lip-stick differs from the color which is imparted to the skin by the application of the lipstick thereto. This is a practical disadvantage which cannot be ignored because it makes it impossible to choose a color by simply looking at the lipstick, so that it is necessary to apply a streak from the lipstick to the skin in order to determine its actual effect in terms of color.
  • lip rouges utilizing bromo acid colorants also suffer from the disadvantage that they change color with the passage of time, after having been applied to the skin, and this disadvantage is quite serious because the color tends to shift toward blue, a color which is not considered esthetic in this context.
  • the present invention relates to a method of manufacturing new lip rouges from colorants derived from bromo acids and, in particular, for eosines, which avoids all the above disadvantages While providing shades which compare favorably with those presently known.
  • bromo acid dyes which may be used in making the compounds according to the invention are the cosine acids and especially those responding to the following formulae:
  • the amines which may be used to produce the amine salts according to the invention are the non-aromatic primary, secondary and tertiary monoamines in which the radicals substituted on the nitrogen comprise a maximum of 6 carbon atoms, which may be separated by one or more hetero atoms, and especially by oxygen atoms.
  • the radicals substituted on the nitrogen may be separated from each other or connected together to form a heterocycle. They may also carry functional groups such as hydroxyl groups.
  • Another object of the present invention is to provide a method of preparing the above amine salts, which method comprises the step of dispersing the dye in a fatty substance in its molten state, and then adding the corresponding amine and permitting the resulting solution to cool.
  • the fatty substance in which the bromo acid dye is dispersed for subsequent salification may be a fatty substance used in the manufacture of make-up or lip rouge.
  • a fatty substance used in the manufacture of make-up or lip rouge may be a phospholipide, in particular, soybean lecithin, the employment of which is especially advantageous in carrying out the process according to the invention.
  • Yet another object of the present invention is to provide as a new article of manufacture a new colored cosmetic composition, and especially a lip rouge or make-up, which contains at least one fatty constituent in which at least one amine salt of a bromo acid dye is dissolved.
  • the amine salts of bromo acid dyes may be advantageously dissolved in a mixture of waxes such as vegetable waxes, like Carnauba wax, animal waxes like beeswax, or mineral Waxes like ozokerite, and vegetable or mineral oils.
  • waxes such as vegetable waxes, like Carnauba wax, animal waxes like beeswax, or mineral Waxes like ozokerite, and vegetable or mineral oils.
  • wax and oil generally constitute the bases of lip rouges and make-up preparations, which may also contain other fatty constituents such as lanolin and its derivatives, various vegetable or animal lecithins and their derivatives, and derivatives of ricin or fatty alcohols.
  • the lip rouges produced in accordance with the invention may, for example, consist of a mixture of soy bean lecithin, ozokerite, lanolin derivatives, Vaseline oils, and, of course, dyes according to the invention.
  • the cosmetic compositions according to the invention may also contain other ingredients conventionally used in cosmetics such, for example, as perfumes.
  • the lip rouges and make-up preparations may contain other base materials or pigments in addition to the dyes according to the invention.
  • a lip rouge having the following composition is prepared:
  • the soy bean lecithin is placed in a corrosion-resistant container, the dye is added, and the mixture kneaded for several minutes at 50 C.
  • triethanolamine is added, while keeping the temperature at 50 C.
  • the mixture is thoroughly kneaded and the lanolin derivative added, after which the mixture is heated to 75 C.
  • the ozokerite is mixed with Vaseline oil.
  • This second mixture is heated to 85 C., and then incorporated into the first mixture. It is left for several minutes at 75 C., while stirring gently, the result is a limpid solution, free of precipitate, which, after cooling, forms a lip rouge having excellent coloring properties.
  • a method for making a lip rouge composition consisting essentially of a base containing wax, oil and soy bean lecithin and, as a coloring agent therefor, an cosine acid dye selected from the group consisting of JIM 1151' 1'51 llir 0 0 no -011 no -0 n Br ⁇ 0 -Br ⁇ 0 and an amine selected from the group consisting of triethanolamine, 2-arnino-2-methyl-1,3-propanediol, diethanolamine, monoisopropanol amine, trihydroxymethylaminomethane, morpholine and diglycolamine, comprising kneading at 50 C.
  • the soy bean lecithin and the dye until a homogenous mixture is obtained, adding the amine and again kneading while keeping the temperature at C., heating in a separate container the wax and oil at 85 C. and incorporating same into the first mixture which has been heated to C., stirring gently for several minutes at 75 C. and then cooling the mixture to form said lip rouge; the amount of said cosine acid dye ranging between about 5-10 weight percent of said soy bean lecithin and said amine being about 26-46 percent by Weight of said eosine acid dye.

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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)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)
US738841A 1967-06-30 1968-06-21 Novel lip coloring cosmetics and methods of making same Expired - Lifetime US3662061A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
LU54005 1967-06-30

Publications (1)

Publication Number Publication Date
US3662061A true US3662061A (en) 1972-05-09

Family

ID=19725259

Family Applications (1)

Application Number Title Priority Date Filing Date
US738841A Expired - Lifetime US3662061A (en) 1967-06-30 1968-06-21 Novel lip coloring cosmetics and methods of making same

Country Status (7)

Country Link
US (1) US3662061A (enrdf_load_stackoverflow)
BE (1) BE717070A (enrdf_load_stackoverflow)
CH (1) CH487647A (enrdf_load_stackoverflow)
DE (1) DE1768740A1 (enrdf_load_stackoverflow)
FR (1) FR1588210A (enrdf_load_stackoverflow)
GB (1) GB1206542A (enrdf_load_stackoverflow)
LU (1) LU54005A1 (enrdf_load_stackoverflow)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001015514A1 (en) 1999-09-02 2001-03-08 Zero Grass International Limited Seed processing apparatus
US6319508B1 (en) 1991-09-30 2001-11-20 L'oreal Anhydrous cosmetic composition containing a fatty phase and pro-liposomes
CN102302428A (zh) * 2011-05-19 2012-01-04 大连九羊食品有限公司 一种含有羊乳脂的唇膏及其制备方法

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54113445A (en) * 1978-02-23 1979-09-05 Kanebo Ltd Lipstick having sheath-core structure
FR2514639B1 (fr) * 1981-10-15 1986-08-01 Oreal Compositions cosmetiques pour le maquillage contenant en tant que pigments colores un sel d'un colorant acide et d'un polymere porteur de fonctions amines salifiees ou quaternisees

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6319508B1 (en) 1991-09-30 2001-11-20 L'oreal Anhydrous cosmetic composition containing a fatty phase and pro-liposomes
US6572870B2 (en) 1991-09-30 2003-06-03 L'oreal Anhydrous cosmetic makeup composition containing a fatty phase
US20040247629A1 (en) * 1991-09-30 2004-12-09 L'oreal Anhydrous cosmetic makeup composition containing a fatty phase and a cosmetic treatment process using the composition
WO2001015514A1 (en) 1999-09-02 2001-03-08 Zero Grass International Limited Seed processing apparatus
CN102302428A (zh) * 2011-05-19 2012-01-04 大连九羊食品有限公司 一种含有羊乳脂的唇膏及其制备方法

Also Published As

Publication number Publication date
FR1588210A (enrdf_load_stackoverflow) 1970-04-10
LU54005A1 (enrdf_load_stackoverflow) 1969-03-24
CH487647A (fr) 1970-03-31
DE1768740A1 (de) 1971-11-25
GB1206542A (en) 1970-09-23
BE717070A (enrdf_load_stackoverflow) 1968-12-24

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