CA2053855C - Mineral oil free and lanolin free cosmetic composition - Google Patents

Mineral oil free and lanolin free cosmetic composition

Info

Publication number
CA2053855C
CA2053855C CA002053855A CA2053855A CA2053855C CA 2053855 C CA2053855 C CA 2053855C CA 002053855 A CA002053855 A CA 002053855A CA 2053855 A CA2053855 A CA 2053855A CA 2053855 C CA2053855 C CA 2053855C
Authority
CA
Canada
Prior art keywords
weight
composition
amounts
mixture
esters
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 - Fee Related
Application number
CA002053855A
Other languages
French (fr)
Other versions
CA2053855A1 (en
Inventor
Robert J. Edmundson
Brian K. Mattox
Terry Jacks
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.)
Intellectual Property Holding Co
Original Assignee
Maybe Holding Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Maybe Holding Co filed Critical Maybe Holding Co
Priority to PCT/US1990/002211 priority Critical patent/WO1991016879A1/en
Priority to CA002053855A priority patent/CA2053855C/en
Priority claimed from PCT/US1990/002211 external-priority patent/WO1991016879A1/en
Publication of CA2053855A1 publication Critical patent/CA2053855A1/en
Application granted granted Critical
Publication of CA2053855C publication Critical patent/CA2053855C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0216Solid or semisolid forms
    • A61K8/0229Sticks
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/732Starch; Amylose; Amylopectin; Derivatives thereof
    • 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
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • 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
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • 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
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/925Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of animal origin
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Birds (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical & Material Sciences (AREA)
  • Emergency Medicine (AREA)
  • Zoology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

ABSTRACT

A cosmetic composition free of mineral oil and free of lanolin is disclosed. The composition comprises effective amounts of the following cosmetically acceptable ingredients (components): (A) at least one wax; (B) at least one triglyceride; (C) a mixture of esters comprising (I) a mixture of esters with said mixture (i) having a maximum acid value of 0.5 and a saponification value of 268-288; and (ii) a mixture of esters with said mixture (II) having a maximum acid value of 0.5 and a saponification value of 206-226; (D) distarch phosphate; (E) at least one bulking agent; (F) at least one colorant; and (G) optionally, at least one preservative.
The composition is preferably formed into a cosmetic stick shape.

Description

PAT ENT
CASE NO. MY0054 MINERAL OIL FREE AND LANOLIN FREE COSMETI~

BACKGRQUN~

This invention relates to cosmetic cover compositions 15 which are mineral oil free and lanolin free --i.e., contain no mineral oil and no lanolin (wool fat).
U.S. 4,659,573 issued to Frischling et al. on April 21, 1987 discloses an ester blend comprising tridecyl trimellitate blended with at least one additional ester selected from the group consisting of 20 dipentasrythritol hexacaprylata/hexacaprate, tridecyl stearate and neopentyl glycol dicaprylate/dicaprate. It is disclosed that the blend contains about 5 to about 85 wt% tridecyl trimellitate based on the weight of the blend. It is aiso disclosed that these ester blends are a substitute for mineral oil in toiletry and cosmetics. According to U.S.
25 4,65g,573 the disclosed ester blends are suitable for use in night creams, moisturizers, lotions, make-ups, face creams, day creams, body lotions, lipsticks and lip glosses.
The technical information brochure for SOFTISAN~649 (Huls Troisdorf AG) discloses that this product is the glycerin ester of 30 natural vegetable fatty acids, of an jsoctearic acid, and of the adipic acid, and that this product has the CTFA adopted name: caprylic/capric/
isostearic/adipic triglyceride. It is disclosed that when SOFTISAN 649 is stirred in warm water it will form an emulsion having the properties of woolwax. It is also disclosed that emulsions containing SOFTISAN 649 35 have a better heat stabiiity than emulsions with natural woolwax, they 20538~

have a softer consistency, a good adhesion and leave a pleasant feeling on the skin. According to this brochure, SOFTiSAN 649 is particularly suitable for skin care products, baby creams, sticks and other decorative cosmetics. The brochure gives formulations of several products 5 containing SOFTISAN 649, amongst which there is included a sports cream stick on page 5.
Cosmetic cover compositions containing mineral oil and lanolin are known, and such compositions may not be ideally suitable for consumers who have oily skin andtor are sensitive to lanolin. These 10 consumers would benefit from a composition that was free of mineral oil and free of lanolin, and they would further benefit if such a composition could also absorb some excess oil from the user's skin. Thus, a cosmetic cover composition free of mineral oil and free of lanolin, which could also absorb some excess oil from the user's skin, would be a 15 welcome contribution to the art. Such a contribution is provided by this invention.

SUMMARY OF THE INVENTION

This invention provides a cosmetic composition, useful as a cover composition, which is tree of mineral oil and free of lanolin.
These compositions contain certain esters which can completely replace mineral oil in cosmetic cover compositions. Suitable esters useful as a mineral oil substitute are those which have mineral oil-like properties --i.e., suitabl0 esters impart to the composition or provide the composition with characteristics which are the same as or similar to those characteristics which would have been impar~ed to or provided by mineral oil if the mineral oil had been present in the composition.
The compositions of this invention ars also free of lanolin.
Thesq compositions contain triglyceride (glyceryl esters of fatty acids) which can completely replace lanolin in cosmetic compositions.
Suitable triglycerides useful as a lanolin subsitute are those triglycerides which have lanolin-like properties -- i.e., suitable triglycerides impart to the composition or provide the composition with characteris~ics which are the same as or similar to those characteristics which would have been imparted to or provided by lanolin if the lanolin had been present in the composition The compositions of this invention also contain distarch phosphate which, without wishing to be bound by theory, is believed to function as an absorber of oil from the skin of the user.
The compositions of this invention also contain at least one wax, triglyceride, bulking agent, colorant, and optionally, preservative.
The term "at least one" as used herein means one, more than one, or a 1 0 mixture.
The term "suitable for use in cosmetic compositions", as used herein, means cosmetically acceptable and refers to those materials known in the art as being useable in cosmetic compositions, such as those materials disclosed in Nikitakis, J.M., editor, ~
Cosmetic Ingredient Handbook, First Edition, copyright 1988, published by The Cosmetic, Toiletry and Fragance Association, Inc., 1110 Vermont Avenue, N.W., Washington, D.C., 20005, the disclosure of which is incorporated herein by reference thereto, and which is hereinafter referred to as the ~CTFA Handbook."
DETAILED DESCRIPTION OF THE INVENTION

This invention provides a cosmetic composition free of mineral oil and free of lanolin comprising:
(A) an effective amount of at least one wax suitable for use in cosmetic compositions;
(B) an effective amount of at least one triglyceride suitable for use in cosmetic compositions;
(C) an effective amount of a mixture of esters suitable for use in cosmetic compositions, said mixture comprising:

(i) an effective amount of a mixture of esters with said mixtura (i~ having a ==

4 20~38~5 maximum acid value of 0.5 and a saponificaiton value of 268-288; and (ii) an effective amount of a mixture of esters with said mixture (ii) having a maximum acid value of 0.5 and a saponification value of 206-266;

(D) an effective amount of distarch phosphate;
(E) an effective amount of at least one bulking agent suitable for use in cosmetic compositions;
(F) an effective amount of at least one colorant suitable for use in cosmetic compositions; and (G) optionally, an effective amount of at least one praservative suitable for use in cosmetic compositions.
This invention also provides articles of manufacture comprising the compositions of this invention manufactured in a solid rigid form suitable for use as a cosmetic. Preferably the compositions are manufactured in the form or shape of a cover stick.
Although the compositions can be formed by known procedures into any suitable solid shape for the ultimate end product, preferably the composition is formed into a cosmetic stick shape -- e.g., a cylindrical shape having a slanted tip such as a "lipstick shape." The shaped composition can then be placed in any suitable dispensing package such as a lipstick type container wherein the composition is advanced by, for example, turning the barrel of the dispensing package or container. Thus, for example, the composition can be cylindrical in shape wherein the cylinder is about 6.3 to about 7.6 cm in length and preferably about 6.8 to about 7.1, the diameter is about 0.72 to about 0.77 cm with about 0.73 to about 0.75 being preferred, and the tip of the cyclinder is formed so as to have an angle of about 43 to about 47 degrees and preferably about 44 to about 46 degrees.
The compositions of this invention contain an effective amount of at least one a cosmetically acceptable wax. Waxes which 20~3855 may prove useful include those listed in the CTFA Handbook cited above and already incorporated herein by reference thereto. Thus, representative examples include ozokertie, ceresin, paraffin, candelilla, carnauba, and the like. Preferably the wax is selected from the group 5 consisting of: ozokerite and ceresin. Most preferably ozokerite is used.
Usually, the wax is present in amounts of about 10.0% to about 15% by weight of the total composition with about 13% to about 14% by weight being preferred.
The compositions of this invention also contain an effective 10 amount of at least one cosmetically acceptable triglyceride. Triglyceride, as used herein, refers to the glyceryl esters of fatty acids and includes those esters which have been hydrogenated to reduce or eliminate unsaturation. Those skilled in the art will appreciate that th triglycerides are the chief constituent of fats and oils, and that the 15 triglycerides have the general formula:

CH2(00CR1 )CH(OOCR2)CH2(00CR3) wherein R1, R2 and R3 are usually of different chain lengths, e.g., C1-20 C31 and more usually C2-C24. Fatty acids are well known in the a~, see for example, ~i~ch~ cals rganic Compounds for Research ~
ni~nostic Reagents, Sigma Chamical Company, pp 924-925, 1989, the disclosure of which is incorporated herein by reference thereto.
Thus, the triglycerides which are useable include those 25 materials (substances) which are known to those skilled in the art as fals and oils. Suitable triglycerides which may prove useful include, those materials listed as fats and oils in the CTFA Handbook cited above and already incorporated herein by reference thereto. Preferably, triglycerides are used rather than a fat or oil containing triglycerides.
30 Representative triglycerides include the glyceryl esters of caprylic aci~
capric acid, isostearic acid (identified in the CTFA Handbook as a mixture of branched chain 18 carbon aliphatic acids), adipic acid, laur;
acid and stearic acid.

==

-6- 20~385~

The preferred fatty acids are selected from the group consisting of caprylic acid, capric acid, isostearic acid and adipic acid.
Preferably a mixture of the glyceryl esters of the above mentioned preferred fatty acids are used. The preferred ester mixture normally 5 contains, by weight of the ester mixture, about 10 to about 14 % glyceryl ester of caprylic acid, about 7.0 to about 11.0% glyceryl ester of capric acid, about 39.0 to about 41.0 % glyceryl ester of isostearic acid, and about 17.0 to about 21.0% glyceryl ester of adipic.
The preferred triglyceride is caprylic/capric/isostearic/
10 adipic triglyceride which is identified by the CTFA Handbook as the mixed ester of caprylic, capric, isostearic acids with a dimer of glycerin.
Caprylic/capric/isostearic/ adipic triglyceride is commercially available under the product designation SOFTISAN 649 from Huls American, Inc., Rockleigh, N.J. SOFTISAN 649 is reported to contain: 12% caprylic 15 acid, 9/O capric acid, 19% adipic acid, 41% isostearic acid, and 10% 12-hydroxystearic acid with the remainder being a mixture of C6, C12, C14 and C16 fatty acids.
Other triglycerides which may prove suitable include:
caprylic/capric/lauric trigiyceride; caprylic/capric/linolaic triglyceride;
20 caprylic/capriclstearic triglyceride; and caprylic/carpic triglyceride.
These triglycerides are known In the art --see the CTFA Handbook for example.
Normally, the triglyceride is used in amounts of about 3 to about 10% by weight of the total composition with about 4 to about 5%
25 by weight being preferred and about 5 to about 6% by weight being most preferred.
The compositions of this invention, as stated previously, contain no mineral oil. In place of the mineral oil there is used an effective amount of a mineral oil substituts. The minerai oil substitue 30 provides the same or similar characteristics to the composition that mineral oil would have provided had the mineral oil been present. It is contemplated that one or more esters having mineral oil characteristics or imparting mineral oil lika characteristics to the composition, may be used.

=~

7 20~38~5 An effective amount of a mixture of esters may be used as a mineral oil substitute in the compositions of this invention. Thus, an effective amount of a mixture of esters comprising:

(i) an effective amount of a mixture of esters with said mixture (i) having a maximum acid value of 0.~ and a saponification value of 268-288; and (ii) an effective amount of a mixture of esters with said mixture (ii) having a maximum acid value of 0.5 and a saponification value of 206-266 may be used in the compositions of this invention.
The ratio of ester mixture (i) above to (ii) above is normally about 1.5 to about 1 with about 1 to about 1 being preferred. Thus, (i) and (ii) are each usually present in the amounts of about 15 to about 25% (about 30 to about 50% total of (i) plus (ii)) by weight of the total composition with about 17 to about 23% (about 34 to about 46% ~otal of (i) plus (ii)) being preferred and about 18 to about 22% (about 36 to about 44% total of (i) plus (ii)) being most preferred and about 19 to about 21% (about 38 to about 42% total of (i) plus (ii)) being even more preferred.
Tridecyl trimellitate (TDTM) can be blended with at least one other ester, preferably at least two other esters, to formulate a blend which duplicates the viscosity and feel of mineral oil for use in cosmetics. The esters generally blended with TDTM will be lower in viscosity than TDTM. The preferred esters for blending with TDTM are tridecyl stearate (TDS), neopentylglycol dicaprylate/dicaprate (NPGC) and dipentaerythritol hexacaprylatelhexacaprate (DPHC). Particularly advantageous results are achieved when TDTM is blended with TDS, NPGC and DPHC. The selection and quantity of the esters which are 2053~

blended with TDTM will vary depending on the desired viscosity of the final blend and the feel which the final blend is intended to have.
Illustrative, non-limiting examples of other esters which may be blended with TDTM are isodecyl trimellitate, isopropyl myristate, 5 isopropyl palmitate, tridecyl myristate, tridecyl palmitate, isodecyl trimellitate, propylene glycol dicaprate/dicaprylate, neopentyl glycol dicaprat~ and trisodecyl trimellitate.
Depending on the desired viscosity and other properties desired, the amount of TDTM in a particular bland can vary from about 5 10 to about 85 wt%, based on the ester blend, preferably about 5 to about 60 wt%, more preferably about 8 to about 45 wt %, most preferably about 10 to about 38 wt%, e.g., about 12 to about 37 wt%. Whsre the ester blend is a low viscosity blend, e.g., 70 S.S.U. at 100 F., the TDTM
is preferably utilized at about 10 to about 14 wt%. For an intermediate 15 viscosity blend, e.g., 130 S.S.U. at 100 F., the TDTM is prefarably u~ilized at about 33 to about 38 wt% based on the ester blend, and for a high viscosity blend, e.~., 350 S.S.U. at 100 F., the TDTM is preferably utilized at about 38 to about 42 wt%, based on the ester blend. The balance of the ester blend can be at least one additional ester, 20 preferably at least two additional esters, each of the two esters being utilized at about 2 to about 60 wt% based on the ester blend depending on the particular properties desired. In a preferred blend where TDS is one of the two or more additional esters blended with the TDTM, it can be utilized at about 5 to about 55 wt%. Where the ester blend is a low 26 viscosity blend, e.g., less than 150 S.S.U., the TDS is preferably utilized at about 40 to about 60 wt%, more preferably about 42 to about 46 wt%, based on the ester blend. Where the ester blend is a higher viscosity blend, the TDS is preferably utilizied at about 5 to about 20 wt%, more preferably at about 5 to about 12 wt%, most preferably at about 6 to 30 about 9 wt % based on the ester blend.
Where NPGC is one of the additional esters, it is preferably utilized at about 2 to about 65 wt% based on the ester blend. For lower viscosity blends, the NPGC is preferably utilized at about 40 to about 50 wt% based on ~he ester blend, more preferably about 42 to about 45 20~3855 g wt%. For higher viscosity blends, the NPGC is preferably utilized at about 2 to about 10 wt%, more preferably about 3 to about 5 wt%.
Where DPHC is one of the additional ester blends it can be utilized at about 10 to about 55 wt%. For lower viscosity blends the 5 DPHC is preferably utilized at about 12 to about 25 wt% based on the ester blend, more preferably at abou~ 16 to about 20 wt%, most prefarably at about 17 to about 19 wt% based on the ester blend. For higher viscosity blends, the DPHC is preferably utilized at about 40 to about 55 wt% based on the ester blend, more preferably about 42 to 10 about 52 wt%, most preferably about 46 to about 50 wt%.
These blends are known in the art, for example, see U.S.
4,659,573 issued to Frischling et al. on April 21, 1987, the disclosure of which is incorporated herein by reference thereto.

Generally, the ester mixture used in the compositions of this invention contains:

(A) Tridecyl stearate in amounts of about 9 to abou~
12% by wt of the total composition with about 9.0 to about 11.0% being 20 preferred and about 10 to about 11% being most preferred;
(B) neopentylglycol dicaprylate/dicaprate in amounts of about 8 to about 11% by wt of the total composition with about 9 to about 11% being preferred and about 9 to about 10% being most preferred;
(C) tridecyi trimellitate in amounts of about 9 to about 25 12% by weight of the total composition with about 9 to about 11% being preferred and about 10 to about 11% being most preferred;
(D) dipentaerythrityl (dipentaerythritol) hexacaprylate/hexacaprate in amounts of about 8 to about 11.5% by weight of the composition with about 9 to about 11% being preferred 30 and about 9 to about 10% being most preferred.

A mixture of esters having the maximum acid value (0.5) and saponification value (268-288) of (i) above is available commercially under the product designation LIPOVOL MOS-350 from - 10- 20~38~

LIPO CHEMICALS INC, Pattsrson, NJ. LIPOVOL MOS-350 is reported to contain: (1 ) 47.55% by weight of dipsntaerylthrityl hexacaparylate/
hexacaprate; (2) 40.25% by weight of tridecyl trimellitate; (3) 8.80% by weight ot tridecyl stearate; and (4) 3.40% by wt of neopentylglycol dicaprylateldicaprate.
A mixture of esters having the maximum acid value (0.5) and saponification value (206-2~6) of (ii) above is available commercially under the product designation LIPOVOL MOS-70 from LIPO CHEMICALS INC., Patterson, N.J. LIPOVOL MOS-70 is reported to contain (i) 44.00% by wt tridecyl stearate; (2) 44.00% by wt neopentylglycol decaprylate/decaprate; and (3) 12.00% by wt tridecyl trimellitate.
Effective amounts of distarch phosphate are used in the compositions of this invention. Distarch phosphate, according to the CTFA Handbook, is the product produced by the cross-linking of starch with sodium metaphosphate. Distarch phosphate is commercially available from, for example, National Starch Co. In general, suitable amounts of distarch phosphate are within the range of about 2.5 to about ' 7.5% by weight of the total composition with about 3 to about 7% by , 20 weight being preferred and about 4 to about 6% by wt being mostpreferred and about 4.5 to about 5.5% being even more preferred.
Bulking agents suitable for use in cosmetics are also present in effective amounts in the compositions of this invention.
Suitable bulking agents which may prove useful include those bulking agents disclosed in the CTFA Handbook which has already been cited above and has already been incorporated herein by reference thereto.
Thus, representative bulklng agents include talc, kaolin, mica, zinc stearate, zinc oxide, and the like. Preferably, the bulking agent is selected from the group consisting of talc, kaolin, mica, and zinc oxide.
Most preferably kaolin is used.
In general the total amount of bulking agent used is about 3 to about 6% by weight of ths total composition with about 3 to about 4.5 % by wt being preferred and about 3.0 to about 4.0% being most preferred.
., .

20~3855 Cosmetically acceptable colorants are also present in effective arnounts in the compositions of this invention. Colorants which may prove useful include those colorants disclosed in the CTFA
Handbook which, as stated previously, has already been cited herein 5 and has already been incorporated herein by reference thereto.
Representative colorants (coloring agents) may include: titantium dioxide; lomicron pink (a commercially available blend of iron oxides and talc); iron oxides such as yellow oxide, and black oxide; and the like. Preferably the colorants are selected from the group consisting of:
10 titanium dioxlde; lomlcron pink; and the iron oxides known as yellow oxide and black oxids.
Generally, the colorant is present in amounts of about 28 ~o about 35% by weight of the total composition with about 29 to about 32% by wt being preferred and about 30 to about 32% by wt being most 15 preferred. Preferably the composition contains about 27 to about 33%
by weight of the composition of titantium dioxide with about 29 to about 30% by wt being preferred. It is preferred that, in addition to the titanium dioxide, the composition also contain: (a) lomicron pink in amounts of about 0.5 to about 1.00% by weight of the total composition with about 20 0.80 to about 1.00% by wt being preferred and about 0.80 to about 0.~0% by wt being most preferred; (b) yellow oxide (an iron oxide) in amounts of about 0.50 to about 1.00% by weight of the total composition with about 0.80 to about 1.00% by wt being preferred and about 0.80 to about 0.90% by weight being most preferred; and (c) black oxide (an 25 iron oxide) in amounts of about 0.01 to about ~.05% by weight of the total composition and about 0.02 to about 0.04% by wt being preferred.
The compositions of this invention optionally contain an effective amount of at least one preservative. Preferably the preservative is present. Preservatives which may prove useful include 30 those preservatives disclosed in the CTFA Handbook which has already been cited above and which has already been incorporated herein by reference thereto. Examples of preservatives include: butylated hydroxyanisole, butyl paraben, propyl paraben, methyl paraben, and the like. Preferably the preservative is selected from the group consisting of - 12- 20538~

butylated hydroxyanisole (e.g, such as that available under the product designation TENOX), butyl paraben, and propyl paraben. A suitable combination of preservatives for use is butylated hydroxyanisole, butyl paraben, and propyl paraben.
Generally, the preservative Is present in an amount ot about 0.20 to about 0.5% by weight of the total composition with about 0.20 to about 0.3% by wt being preferred and about 0.2 to about 0.25%
by wt being most preferred. Preferably the composition contains: (1 ) butylated hydroxyanisole in an amount of about 0.02 to about 0.04 % by weight of the total composition with about 0.025 to about 0.035% by wt being preferred and about 0.03% by wt being most preferred; (2) butyl paraben in an amount of about 0.05 to about 0.2% by weight of the total . composition with about 0.05 to about 0.15% by wt being preferred and about 0.1% by wt being most preferred; (3) propyl paraben in an amount of about 0.05 to about 0.2% by wt of the total composition with about 0.05 to about 0.15% by wt being preferred and about 0.1% by wt being most preferred.
The ingredients forming the compositions of this invention may be blended together In any suitable mixing device capable of adequately mixing the ingredients together at a suitable temperature to produce a uniform blend. Generally, the temperature needed to adequately blend the ingredients together is dependent upon the temperature needed to melt the particular wax being used. The , temperaturG selected is high enough to melt the wax and allow uniform 25 blending of ingredients but not so high as to cause undue degradation of the various ingredients used. Normally, a temperature within the range of about 70 to about 85C will suffice with about 80 to about 83C
being preferred. The ingredients are blended together using sufficient shear to yield a uniform blend of ingredients in a reasonable amount of time. Normally mixing devices which can provide a shear rate of about 800 to about 1200 RPM, with about 850 to about 950 RPM being preferred, will be suitable. A reasonable amount of time will usually be about 30 to about 50 minutes with about 35 to about 45 minutes being preferred.

=:~

- 13- ~o~38~

Although the order of blending ingredients is not critical, it is preferred to: (1 ) melt the wax; (2) then add the triglyceride and mineral-oil substitue (the mixture of esters having or imparting mineral-oil characteristics); (3) blend (1) and (2) together along with the 5 preservatlves; ~4) blend the distarch phosphate with the resulting mixture of (3); (5) add the colorants and bulking agents, preferably as a premix, to the resulting mixture from (4) (note, the premix may have a preservative added to it to maintain its integrity until use); and (6) blend the resulting mixture from (5) together until uniform. During the blending 10 steps a temperature is maintained that is high enough to prevent the wax from solidifying but not so high as to cause undue degradation of the ingredients. The resulting final mixture can be strained through a suitable material --e.g., cheese cloth-- and stored in suitable containers.
The composition can be formed into suitable shapes, e.g., 15 a stick shape similar to that of lipstick, by methods known in the art. For example, pouring the molten mass into metal molds.
The following examples are illustrative only and should not be construed as limiting the invention in any way. Those skilled in the art will appreciate that variations are possible which are within the spirit 20 and scope of the appended claims.
EXAMPLE I
A composition of this invention was prepared from the ingredients given in Table I.

==~

2û~38~

~L~

Ingredient % by wt White ozokerite 170 MF 13.030 SOFTISAN 649 5.800 LIPOVOL MOS 70 20.110 LIPOVOL MOS 350 20.727 Butylated hydroxyanisole 0.030 Butyl paraben 0.100 Distarch phosphate 5.000 Titanium dioxide 28.209 Kaolin 2.942 Lomicron Pink 2.009 Yellow Oxide 1.878 Black Oxide 0.065 Propyl paraben _ 0.100 The ingredients in Table I were combined together using 5 the following proeedure. A sample portion (i.e., about 5.0%) of LIPOVOL
MOS 70 was added to a steam jacketed kettle (A) equipped with an.
appropriate mixer and maintained at about 85C. The white ozokerite (obtained from Strahl 8 Pitsch) was melted in this kettle.
Ne)h the SOFTISAN 649, the remainder of the LIPOVOL
1 0 MOS 70, and the LIPOVOL MOS 350 was added to another steam jacketed kettle (B) equipped with a high shear mixer. These ingredients were heated to about 80C to about 85C and mixed until uniform.
Next the melted ozokerite from kettls (A) was added to kettle (B). Also added to kettle (B) was the butylated hydroxyanisole 1 5 (obtained under the tradename TENOX) and the butyl paraben. The ingredients in kettle (B) were mixed well. While maintaining the temperature of kettle (B) at about 80 to about 85C, the distarch phosphate (obtained ~rom National Starch Co.) was added. The resulting blend is mixed about 15-~0 minutes or until uniform.

-20~38~

The titanium dioxide, kaolin, lomicron pink, yellow oxide, black oxide and propyl paraben were premixed together using a CBM
mixer to form a color mix.
With the resulting mixture in kettle (B) at about 80C to 5 about 85C, the mixer and high shear was started. The high shear was brought to about 900 RPM. The color mix was added slowly to kettle (B) and the RPM were increased as necessary to effect good movement of the batch. The resulting mixture was mixed for about 30-40 minutes.
Then the mixer was stopped to check a sample for 10 undispersed pigment or color spots (an amount of pigment spots will be evident but should not be excessive). If the dispersion is not acceptable the mixture is maintained at about 80-85C and mixing is continued with high RPM for about an additional 25 to 30 minutes. Repeat mixing if necessary.
The temperature should not exceed 95C.
When the mixture was uniform it was strained through cheese cloth into appropriate containers.

~AMPLE 2 Following the procedure of Example 1, the ingredients in Table 1I were blended together to produce a composition of this invention.

-16- 20538~5 TABLE lI

In~redient % by wt Whits Ozokerite 170 MF 13.030 SOFTISAN 649 5.800 LIPOVOL MOS 70 20.1 10 LIPOVOL MOS 350 20.727 Butylated hydroxyanisole (Tenox) 0.030 Butyl paraben 0.100 Distarch phosphate 5.00 rltanium dioxide 29.236 Kaolin 4.1 92 Lomicron Pink 0.805 Yellow oxide 0.835 Black oxide 0-035 Pro I araven 0 100 PY P
Those skilled in the art will appreciate that the total amount of all ingredients (components) used in the compositions of this invention equals 100% by weight of the total composition. Also, unless stated otherwise, all percents herein are percent by weight of the total composition.
The invention being thus described, it will be obvious that the same may be varied in many ways. Such variations are not to be regarded as a departure from the spirit and scope of the invention, and all such modifications are intended to be included within the scope of the claims.

Claims (14)

WHAT IS CLAIMED IS:
1. A cosmetic composition free of mineral oil and free of lanolin comprising:

(A) an effective amount of at least one wax suitable for use in cosmetic compositions;
(B) an effective amount of at least one triglyceride suitable for use in cosmetic compositions;
(C) an effective amount of a mixture of esters suitable for use in cosmetic compositions, said mixture comprising:

(i) an effective amount of a mixture of esters with said mixture (i) having a maximum acid value of 0.5 and a saponification value of 268-288; and (ii) an effective amount of a mixture of esters with said mixture (ii) having a maximum acid value of 0.5 and a saponification value of 206-226;

(D) an effective amount of distarch phosphate;
(E) an effective amount of at least one bulking agent suitable for use in cosmetic compositions;
(F) an effective amount of at least one colorant suitable for use in cosmetic compositions; and (G) optionally, an effective amount of at least one preservative suitable for use in cosmetic compositions.
2. The compositions of Claim 1 wherein:

(A) said wax is present in amounts of about 13 to about 14% by weight;
(B) said triglycerides are present in amounts of about 4 to about 5% by weight;
(C) said mixture of esters (C) is present in amounts of about 36 to about 44% by weight;
(D) said distarch phosphate is present in amounts of about 4 to about 6% by weight;
(E) said bulking agent is present in amounts of about 3.0 to about 4.5 % by weight;
(F) said colorant is present in amount of about 29 to about 32% by weight; and (G) optionally, said preservative is present in amounts of about 0.2 to about 0.3% by weight;

wherein the % by weight is by weight of the total composition and the total amount of components (A)-(G) equals 100%
by weight of the composition.
3. The composition of Claim 1 wherein said mixture of esters of (C) comprises said ester mixture (i) in amounts of about 19 to about 21% by weight of said composition, and said ester mixture (ii) in amounts of about 19 to about 21% by weight of said composition.
4. The composition of Claim 1 wherein said mixture of esters of (C) comprises:

(A) tridecyl stearate in amounts of about 9 to about 11 by weight of said composition;
(B) neopentylglycol dicaprylate/dicaprate in amounts about 9 to about 11% by weight of said composition;

(C) tridecyl trimellitate in amounts of about 9 to about 11% by weight of said composition; and (D) dipentaerythrityl hexacaprylate/hexacaprate in amounts of about 9 to about 11% by weight of said composition.
5. The composition of Claim 1 wherein said wax is selected from the group consisting of ozokerite, ceresin, and carnauba.
6. The composition of Claim 1 wherein said triglyceride is a glyceryl ester of carboxylic acids selected from the group consisting of caprylic acid, capric acid, isostearic acid, adipic acid, lauric acid, and stearic acid.
7. The composition of Claim 1 wherein said bulking agent is selected from the group consisting of talc, kaolin, mica, zinc stearate, and zinc oxide.
8. The composition of Claim 1 wherein said colorant is selected from the group consisting of titanium dioxide, yellow oxide, black oxide, and lomicron pink.
9. The composition of Claim 1 wherein said preservatives are selected from the group consisting of butylated hydroxyanisole, butyl paraben, propyl paraben, and methyl paraben.
10. The composition of Claim 4 wherein:

(A) the wax is ozokerite;
(B) the triglyceride is a mixture of the glyceryl esters of caprylic acid, capric acid, isostearic acid, and adipic acid;
(C) the bulking agent is kaolin; and (D) the colorants are titanium dioxide, yellow oxide, black oxide and lomicron pink.
11. The composition of Claim 1 wherein:

(A) said wax is ozokerite present in amounts of 13 to about 14% by weight of said composition;
(B) said triglyceride is present in amounts of about 4 to about 5% by weight of said composition, and said triglyceride is a mixture of the glyceryl esters of caprylic acid, capric acid, isostearic acid, and adipic acid;
(C) said mixture of esters of (C) comprises:

(i) about 9 to about 11% by weight of the total composition of tridecyl stearate;
(ii) about 9 to about 11% by weight of the total composition of neopentylglycol dicaprylate/
dicaprate;
(iii) about 9 to about 11% by weight of the total composition of tridecyl trimellitate; and (iv) about 9 to about 11% by weight of the total composition of dipentaerythrityl hexacaprylate/
hexacaprate;

(D) said distarch phosphate is present in amounts of about 4 to about 6% by weight of said compsition;
(E) said bulking agent is kaolin present in amounts of about 3 to about 4.5% by weight of said composition;
(F) said colorants are:

(i) about 29 to about 30% by weight of said composition of titanium dioxide;

(ii) about 0.8 to about 1.0% by weight of said composition of lomicron pink;
(iii) about 0.8 to about 1.0% by weight of said composition of yellow oxide; and (iv) about 0.02 to about 0.04% by weight of said composition of black oxide; and (G) said preservative are:

(i) about 0.025 to about 0.035% by weight of said composition of butylated hydroxyanisole;
(ii) about 0.05 to about 0.15% by weight of said composition of butylparaben; and (iii) about 0.05 to about 0.15% by weight of said composition of propyl paraben.
12. The composition of 11 wherein:
(A) said triglyceride is present in amounts of about 5 to about 6% by weight;

(B) said mixture of esters (C) comprises:

(i) about 10 to about 11% by weight of tridecyl stearate;

(ii) about 9 to about 11% by weight of neopentylglycol dicaprylate/dicaprate;

(iii) about 10 to 11% by weight of tridecyl trimellitate;
and (iv) about 9 to 10% by weight of dipentaerythrityl hexacaprylate/hexacaprate;

(C) said distarch phosphate is present in amounts of about 4.5 to about 5.5% by weight; and (D) said bulking agent is present in amounts of about 3 to about 4% by weight.
13. The composition of Claim 1 manufactured in a solid, rigid form suitable for use as a cosmetic.
14. The composition of Claim 1 manufactured in the form of a cover stick.
CA002053855A 1990-04-27 1990-04-27 Mineral oil free and lanolin free cosmetic composition Expired - Fee Related CA2053855C (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
PCT/US1990/002211 WO1991016879A1 (en) 1990-04-27 1990-04-27 Mineral oil free and lanolin free cosmetic composition
CA002053855A CA2053855C (en) 1990-04-27 1990-04-27 Mineral oil free and lanolin free cosmetic composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
PCT/US1990/002211 WO1991016879A1 (en) 1990-04-27 1990-04-27 Mineral oil free and lanolin free cosmetic composition
CA002053855A CA2053855C (en) 1990-04-27 1990-04-27 Mineral oil free and lanolin free cosmetic composition

Publications (2)

Publication Number Publication Date
CA2053855A1 CA2053855A1 (en) 1991-10-28
CA2053855C true CA2053855C (en) 1994-02-22

Family

ID=4148610

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002053855A Expired - Fee Related CA2053855C (en) 1990-04-27 1990-04-27 Mineral oil free and lanolin free cosmetic composition

Country Status (1)

Country Link
CA (1) CA2053855C (en)

Also Published As

Publication number Publication date
CA2053855A1 (en) 1991-10-28

Similar Documents

Publication Publication Date Title
CA1333572C (en) High gloss, high-shine lipstick
US4996044A (en) Lipstick formulation and method
US5538718A (en) Cosmetic sticks
CA2072028C (en) Coloured cosmetic sticks
AU666343B2 (en) Coloured cosmetic stick of improved hardness
EP0975320B1 (en) Solid cosmetic compositions on the basis of solidified oils and lanosterin
ES2221328T3 (en) TOPICAL COMPOSITION CONTAINING AN ESTER OF ACID OR ALCOHOL FAT RAMIFIED IN C24 TO C28.
US8333955B2 (en) High shine, stick-shaped cosmetic products
US5667770A (en) Long wearing lipstick
US5466457A (en) Cosmetic sticks
JP2007532695A (en) Skin care composition
HU215205B (en) Cosmetical or dermatological composition in soft form and process for producing the same
CA2199702A1 (en) Color cosmetic composition containing alcohol modified wax
US6667047B2 (en) Ultra-stable composition comprising moringa oil and its derivatives and uses thereof
EP0508591A2 (en) Lipstick composition
US4360387A (en) Isomorphous jojoba oil compositions containing trans-isomerized jojoba oil
US20130272982A1 (en) Shiny, transfer resistant lipstick and method of making
EP3248588A1 (en) Makeup cosmetic
US5279830A (en) Mineral oil free and lanolin free cosmetic composition
EP0195575B1 (en) Improved lipstick formulation and method
MXPA01001681A (en) Aqueous solid gel comprising a hydrophilic gelling agent and a particular polyethylene glycol, composition comprising same and uses.
US6274153B1 (en) Structured cosmetic material comprising κ-carragheen which forms a three-dimensional network
WO1991016879A1 (en) Mineral oil free and lanolin free cosmetic composition
JP2831552B2 (en) Oily solid cosmetics containing acid dyes
CA2053855C (en) Mineral oil free and lanolin free cosmetic composition

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed