US2268736A - Water-dispersible vitamin-containing composition and cosmetic including the same - Google Patents
Water-dispersible vitamin-containing composition and cosmetic including the same Download PDFInfo
- Publication number
- US2268736A US2268736A US252072A US25207239A US2268736A US 2268736 A US2268736 A US 2268736A US 252072 A US252072 A US 252072A US 25207239 A US25207239 A US 25207239A US 2268736 A US2268736 A US 2268736A
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- Prior art keywords
- vitamin
- morpholine
- soap
- concentrate
- substance
- Prior art date
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- 239000000203 mixture Substances 0.000 title description 21
- 239000002537 cosmetic Substances 0.000 title description 10
- 229940088594 vitamin Drugs 0.000 title description 10
- 229930003231 vitamin Natural products 0.000 title description 10
- 235000013343 vitamin Nutrition 0.000 title description 10
- 239000011782 vitamin Substances 0.000 title description 10
- 150000003722 vitamin derivatives Chemical class 0.000 title description 8
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Natural products C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 41
- 239000000126 substance Substances 0.000 description 25
- 239000012141 concentrate Substances 0.000 description 18
- 239000000463 material Substances 0.000 description 18
- 235000019166 vitamin D Nutrition 0.000 description 17
- 239000011710 vitamin D Substances 0.000 description 17
- 239000000344 soap Substances 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- 229930003316 Vitamin D Natural products 0.000 description 15
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 15
- 150000003710 vitamin D derivatives Chemical class 0.000 description 15
- 229940046008 vitamin d Drugs 0.000 description 15
- 235000019155 vitamin A Nutrition 0.000 description 14
- 239000011719 vitamin A Substances 0.000 description 14
- 235000014113 dietary fatty acids Nutrition 0.000 description 13
- 229930195729 fatty acid Natural products 0.000 description 13
- 239000000194 fatty acid Substances 0.000 description 13
- 150000004665 fatty acids Chemical class 0.000 description 13
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 12
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 12
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical group OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 12
- 229940045997 vitamin a Drugs 0.000 description 12
- OBMBYGXRLQQDHH-KVVVOXFISA-N morpholin-4-ium;(z)-octadec-9-enoate Chemical compound C1COCCN1.CCCCCCCC\C=C/CCCCCCCC(O)=O OBMBYGXRLQQDHH-KVVVOXFISA-N 0.000 description 10
- -1 morpholine compound Chemical class 0.000 description 9
- 239000008271 cosmetic emulsion Substances 0.000 description 6
- 239000006071 cream Substances 0.000 description 6
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 6
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 4
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 4
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 4
- 239000005642 Oleic acid Substances 0.000 description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 4
- 239000006210 lotion Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 239000002674 ointment Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 3
- GLMCOBSUGSPCHB-DPMBMXLASA-N (z,12r)-12-hydroxyoctadec-9-enoic acid;morpholine Chemical compound C1COCCN1.CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O GLMCOBSUGSPCHB-DPMBMXLASA-N 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- DTOSIQBPPRVQHS-PDBXOOCHSA-M linolenate Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC([O-])=O DTOSIQBPPRVQHS-PDBXOOCHSA-M 0.000 description 2
- 229940040452 linolenate Drugs 0.000 description 2
- 210000004185 liver Anatomy 0.000 description 2
- 239000008149 soap solution Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 235000015961 tonic Nutrition 0.000 description 2
- 230000001256 tonic effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- FHQRDEDZJIFJAL-UHFFFAOYSA-N 4-phenylmorpholine Chemical compound C1COCCN1C1=CC=CC=C1 FHQRDEDZJIFJAL-UHFFFAOYSA-N 0.000 description 1
- 244000062730 Melissa officinalis Species 0.000 description 1
- 235000010654 Melissa officinalis Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000005313 fatty acid group Chemical group 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical class CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 229960000716 tonics Drugs 0.000 description 1
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
-
- 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
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/361—Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
-
- 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
- A61K8/67—Vitamins
-
- 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
- A61K8/67—Vitamins
- A61K8/671—Vitamin A; Derivatives thereof, e.g. ester of vitamin A acid, ester of retinol, retinol, retinal
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- 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
Definitions
- the invention relates to a new composition of matter.
- the invention is directed to vitamin-containing externally applicable substances and especially to water-dispersible compositions containing vitamins A or D and to correlated improvements in the preparation of such compositions, and the externally applicable substances may be cosmetics, salves, ointments, rubs and other liquids, creams, pastes and solids which are applied externally to the human or animal body for a wide variety of purposes, such as healing, soothing, beautifying and the like.
- Another object of the invention is to provide a water-dispersible vitamin-containing composition.
- Another object of the invention is to provide an externally applicable substance containing fat-soluble vitamins therein.
- Another object of the invention is to provide a highly stable vitamin-containing cosmetic.
- a soap is prepared by reacting a fatty acid and a morpholine compound.
- An appropriate quantity of the desired notes a fatty acid residue and R denotes a hydrogen atom or an alkyl, aryl or alkaryl group:
- the morpholine compound which is preferably employed is morpholine or phenylmorpholine.
- the soap is preferably prepared by reacting a quantity of desired fatty acid with a stoichiometric quantity of the morpholine compound to produce an acid-free soap whose pH is 6.9 to 7.0.
- compositions of this invention essentially comprise a material rich in fat-soluble vitamins such as vitamins A and/or D, and this substance may be fish oil, fish liver oil, concentrates thereof, irradiated ergosterol preferably dissolved in an oil such as corn oil or the like, and other well known vitamin rich materials, together with the above neutral soap of the fatty acid and the morpholine compound.
- the soap preferably employed is the oleate of morpholine and is formed vitamin is added to the soap and may be dissolved therein.
- This vitamin-soap solution may be added directly to an externally applicable substance and dispersed therein by agitation. It is also within the purview of the invention to incorporate said vitamin-soap solution in the components of said substance in the course of preparing said substance.
- the invention accordingly comprises the several steps and the relation of one or more of such steps with respect to each of the others, and the composition possessing the features, properties and the relation of constituents, which are exemplified in the following detailed disclosure, and the scope of the invention will be indicated in the claims.
- the soap employed in accordance with this invention may be prepared by reacting a fatty acid and a morpholine compound.
- the reaction may be carried out with or without the aid of external heat.
- the fatty acid used may be either saturated or unsaturated and may contain any number of carbon atoms. Among others, found to be especially suitable, are oleic, stearic, linoleic, linolenic, palmitic, ricinoleic, lauric and myristic acids. If the fatty acid is normally solid, it is first melted before the morpholine compound is added thereto. The reaction which is norby adding morpholine and oleic acid in the following ratio: 14.7 parts of morpholine to 50 parts of oleic acid.
- the mixture is stirred until the mass is free from free fatty acid.
- the quantity of vitaminiferous material added to this soap is a matter of choice.
- the soap-vitaminiferous material admixture is stirred until there is a solution formed'of the vitaminiferous material in said soap.
- the solution may be readily dispersed in water to providev a stable dispersion which may be kept indefinitely, provided the same is kept in a closed container.
- the morpholine oleate soap-Nitaminiferous material solution may be added directly to any desired externally applicable substance.
- This substance may be one of the cosmetics, such as shampoos, face tonic, hair tonics, hand lotions, face creams, vanishing cream and the like which usually contain a mucilaginous and/or an oleaginous material. It may also be any one of a wide variety of other externally applicable substances, such as salves, ointments,
- said solution may be added directly to those substances of the cosmetic species known to the trade as "J ergens Lotion, Italian Balm, Frostilla, Wood burys Cream without changing either the color,
- the addition of the morpholine oleate soap-vitaminiferous material solution does not appreciably alter the physical or chemical characteristics of said substance, and as a matter of fact, does not in anyway deleteriously affect the same.
- said solution may be added to the components thereof in the course of preparing the same.
- Example I 282 grams of oleic acid are mixed with 87 grams of morpholine to produce 369 parts of morpholine oleate. To each 100 grams of said morpholine cleate add between 4 and 5 grams of vitamin D tuna fish liver oil concentrate, whose potency is 1,000,000 units of vitamin D per gram. The mixture is stirred to produce a clear solution of vitamin D-concentrate in morpholine oleate.
- This solution is added to a batch of finished hand lotion comprising an emulsion of an oily or waxy material in water, and sold under the name of Jergens Lotion which measures between 400 to 4,000 grams and the entire mass is stirreduntil the solution is emulsified in said cosmetic, uniformly blended therewith and uniformly distributed as very fine particles or globules throughout said cosmetic which now contains between 10,000 to 1,000 units of vitamin D per gram thereof.
- Example 11 282 grams of oleic acid are mixed with 87 grams of morpholine to produce 369 grams of morpholine oleate. To each 100 grams of said morpholine oleate, add between 8 to 10 grams of a concentrate whose potency is 500,000 units of vitamin A and 100,000 units of vitamin D per gram. The mixture is stirred to produce a clear solution of the concentrate in morpholine oleate. This solution is added to a batch of finished cream comprising a water-in-oil emulsion, the oily phase containing materials of.
- a readily emulsifiable composition comprising a soap of a higher fatty acid and a morpholine compound and a vitamin A and D concentrate.
- a readily emulsifiable composition comprising a morpholine soap of a higher fatty acid and a vitamin A concentrate.
- a readily emulsifiable composition comprising a morpholine soap oi' a higher fatty acid and a vitamin D concentrate.
- a readily emulsiflable composition comprising a morpholine soap of a higher fatty acid and a vitamin A and D concentrate.
- a readily emulsifiable composition comprising morpholine oleate and a vitamin A and D concentrate.
- a readily emulslfiable composition comprising morpholine ricinoleate and a vitamin A and D concentrate.
- a readily emulsifiable composition comprising morpholine linolenate and a vitamin A and D concentrate.
- a cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleaginous materials, a morpholine soap of a higher fatty acid and a vitamin A concentrate.
- a cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleaginous materials, a morpholine soap of a higher fatty acid and a vitamin D concentrate.
- a cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleaginous materials, a morpholine soap of a higher fatty acid and a vitamin A and D concentrate.
- a cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleaginous materials, morpholine oleate, and a vitamin.A and D concentrate.
- a cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleaginou's materials, morpholine ricinoleate. and a vitamin A and D concentrate.
- a cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleagincus materials, morpholine linolenate. and a vitamin A and D concentrate.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Chemical & Material Sciences (AREA)
- Dermatology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Emergency Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Cosmetics (AREA)
Description
Patented Jan. 6, 1942 WATER-DISPERSIBLE VITAMIN-CONTAIN- ING COMPOSITION AND- COSMETIC IN- CLUDING THE SAME Loran 0. Buxton. Harrison. and Louis '1. Rosenberg, Bidgefleld Park, N. 1., minors to National Oil Products Company, Harrison, N. 3., a corporation of New Jersey I No Drawing. Application January 21, 1939, Serial No. 252,072
13 Claims.
This invention relates to a new composition of matter. In one of its specific aspects, the invention is directed to vitamin-containing externally applicable substances and especially to water-dispersible compositions containing vitamins A or D and to correlated improvements in the preparation of such compositions, and the externally applicable substances may be cosmetics, salves, ointments, rubs and other liquids, creams, pastes and solids which are applied externally to the human or animal body for a wide variety of purposes, such as healing, soothing, beautifying and the like.
Another object of the invention is to provide a water-dispersible vitamin-containing composition.
Another object of the invention is to provide an externally applicable substance containing fat-soluble vitamins therein.
Another object of the invention is to provide a highly stable vitamin-containing cosmetic.
Other objects of the invention will in part be obvious and will in part appear hereinafter.
According to the invention, a soap is prepared by reacting a fatty acid and a morpholine compound. An appropriate quantity of the desired notes a fatty acid residue and R denotes a hydrogen atom or an alkyl, aryl or alkaryl group:
And, it has been found that the morpholine compound which is preferably employed is morpholine or phenylmorpholine. The soap is preferably prepared by reacting a quantity of desired fatty acid with a stoichiometric quantity of the morpholine compound to produce an acid-free soap whose pH is 6.9 to 7.0.
The compositions of this invention essentially comprise a material rich in fat-soluble vitamins such as vitamins A and/or D, and this substance may be fish oil, fish liver oil, concentrates thereof, irradiated ergosterol preferably dissolved in an oil such as corn oil or the like, and other well known vitamin rich materials, together with the above neutral soap of the fatty acid and the morpholine compound. The soap preferably employed is the oleate of morpholine and is formed vitamin is added to the soap and may be dissolved therein. This vitamin-soap solution may be added directly to an externally applicable substance and dispersed therein by agitation. It is also within the purview of the invention to incorporate said vitamin-soap solution in the components of said substance in the course of preparing said substance.
The invention accordingly comprises the several steps and the relation of one or more of such steps with respect to each of the others, and the composition possessing the features, properties and the relation of constituents, which are exemplified in the following detailed disclosure, and the scope of the invention will be indicated in the claims.
The soap employed in accordance with this invention may be prepared by reacting a fatty acid and a morpholine compound. The reaction may be carried out with or without the aid of external heat. The fatty acid usedmay be either saturated or unsaturated and may contain any number of carbon atoms. Among others, found to be especially suitable, are oleic, stearic, linoleic, linolenic, palmitic, ricinoleic, lauric and myristic acids. If the fatty acid is normally solid, it is first melted before the morpholine compound is added thereto. The reaction which is norby adding morpholine and oleic acid in the following ratio: 14.7 parts of morpholine to 50 parts of oleic acid. The mixture is stirred until the mass is free from free fatty acid. The quantity of vitaminiferous material added to this soap is a matter of choice. After the addition, the soap-vitaminiferous material admixture is stirred until there is a solution formed'of the vitaminiferous material in said soap. The solution may be readily dispersed in water to providev a stable dispersion which may be kept indefinitely, provided the same is kept in a closed container. The morpholine oleate soap-Nitaminiferous material solution may be added directly to any desired externally applicable substance. This substance may be one of the cosmetics, such as shampoos, face tonic, hair tonics, hand lotions, face creams, vanishing cream and the like which usually contain a mucilaginous and/or an oleaginous material. It may also be any one of a wide variety of other externally applicable substances, such as salves, ointments,
rubs and the like. Among others, said solution may be added directly to those substances of the cosmetic species known to the trade as "J ergens Lotion, Italian Balm, Frostilla, Wood burys Cream without changing either the color,
- the texture or odor of the same. After adding many exothermic is as follows wherein R dethe appropriate quantity of said solution to the desired substance which may be of an aqueous or oily'base, the mass is agitated by stirring to distribute said solution uniformly throughout said substance. The morpholine oleate-vitaminiferous solution is thus emulsified in said substance and is uniformly blended with the constituents thereof and is uniformly distributed throughout the substance as very fine'particles or globules which will not settle out, the morpholine oleate acting as the emulsifier for said vitaminiferous material in said substance. The addition of the morpholine oleate soap-vitaminiferous material solution does not appreciably alter the physical or chemical characteristics of said substance, and as a matter of fact, does not in anyway deleteriously affect the same. Instead of adding the morpholine oleate-vitaminiferous solution to the finished substance, said solution may be added to the components thereof in the course of preparing the same.
For a fuller understanding of the nature and objects of the invention, reference should be had to the following examples which are given merely to further illustrate the invention and are not to be construed in a limiting sense, all parts given being by weight:
Example I 282 grams of oleic acid are mixed with 87 grams of morpholine to produce 369 parts of morpholine oleate. To each 100 grams of said morpholine cleate add between 4 and 5 grams of vitamin D tuna fish liver oil concentrate, whose potency is 1,000,000 units of vitamin D per gram. The mixture is stirred to produce a clear solution of vitamin D-concentrate in morpholine oleate. This solution is added to a batch of finished hand lotion comprising an emulsion of an oily or waxy material in water, and sold under the name of Jergens Lotion which measures between 400 to 4,000 grams and the entire mass is stirreduntil the solution is emulsified in said cosmetic, uniformly blended therewith and uniformly distributed as very fine particles or globules throughout said cosmetic which now contains between 10,000 to 1,000 units of vitamin D per gram thereof.
Example 11 282 grams of oleic acid are mixed with 87 grams of morpholine to produce 369 grams of morpholine oleate. To each 100 grams of said morpholine oleate, add between 8 to 10 grams of a concentrate whose potency is 500,000 units of vitamin A and 100,000 units of vitamin D per gram. The mixture is stirred to producea clear solution of the concentrate in morpholine oleate. This solution is added to a batch of finished cream comprising a water-in-oil emulsion, the oily phase containing materials of. an oily or waxy nature, and sold under the name of Woodburys All Purpose Cream, varying from 400 to 4,000 grams and the entire mass is stirred until the solution is emulsified in said cosmetic, uniformly blended with the constituents thereof and uniformly distributed as very fine particles or globules throughout said cosmetic which now contains between 10,000 and 1,000 units of vitamin A and between 2,000 and 200 units of vitamin D.
Since certain changes in carrying out the above process and certain modifications in the composition which embody the invention may be made without departing from its scope, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.
It is also to be understood that the following claims are intended to cover allthe generic and specific features of the invention herein described and all statements of the scope of the invention, which as a matter of language might be said to fall therebetween; and that they are intended to be inclusive in scope and notexclusive, in that if desired other materials may be added to our novel composition of matter herein claimed without departing from the spirit of the invention. Particularly it is to be understood that in said claims, ingredients or components recited in the singular are intended to include compatible mixtures of said ingredients wherever the sense permits.
Having described our invention, what weclaim as new and desire to secure by Letters Patent is:
1. A readily emulsifiable composition comprising a soap of a higher fatty acid and a morpholine compound and a vitamin A and D concentrate.
2. A readily emulsifiable composition comprising a morpholine soap of a higher fatty acid and a vitamin A concentrate.
3. A readily emulsifiable composition comprising a morpholine soap oi' a higher fatty acid and a vitamin D concentrate.
4. A readily emulsiflable composition comprising a morpholine soap of a higher fatty acid and a vitamin A and D concentrate.
5. A readily emulsifiable composition comprising morpholine oleate and a vitamin A and D concentrate.
6. A readily emulslfiable composition comprising morpholine ricinoleate and a vitamin A and D concentrate.
7. A readily emulsifiable composition comprising morpholine linolenate and a vitamin A and D concentrate.
8. A cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleaginous materials, a morpholine soap of a higher fatty acid and a vitamin A concentrate.
9. A cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleaginous materials, a morpholine soap of a higher fatty acid and a vitamin D concentrate.
10. A cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleaginous materials, a morpholine soap of a higher fatty acid and a vitamin A and D concentrate.
11. A cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleaginous materials, morpholine oleate, and a vitamin.A and D concentrate.
12. A cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleaginou's materials, morpholine ricinoleate. and a vitamin A and D concentrate.
13. A cosmetic emulsion comprising a substance selected from the class consisting of mucilaginous and oleagincus materials, morpholine linolenate. and a vitamin A and D concentrate.
LORAN o. BUXTON. LOUIS 'r. ROSENBERG
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US252072A US2268736A (en) | 1939-01-21 | 1939-01-21 | Water-dispersible vitamin-containing composition and cosmetic including the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US252072A US2268736A (en) | 1939-01-21 | 1939-01-21 | Water-dispersible vitamin-containing composition and cosmetic including the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2268736A true US2268736A (en) | 1942-01-06 |
Family
ID=22954473
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US252072A Expired - Lifetime US2268736A (en) | 1939-01-21 | 1939-01-21 | Water-dispersible vitamin-containing composition and cosmetic including the same |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2268736A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2940902A (en) * | 1952-01-03 | 1960-06-14 | Vorsatz Fritz Arthur | Process for the prodction of cosmetic creams and thickening agents therefor |
| US4743442A (en) * | 1983-08-02 | 1988-05-10 | Blendax-Werke R. Schneider Gmbh & Co. | Skin care composition |
| US5514672A (en) * | 1981-02-17 | 1996-05-07 | Bazzano; Gail S. | Use of retinoids and compositions containing same for hair growth |
-
1939
- 1939-01-21 US US252072A patent/US2268736A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2940902A (en) * | 1952-01-03 | 1960-06-14 | Vorsatz Fritz Arthur | Process for the prodction of cosmetic creams and thickening agents therefor |
| US5514672A (en) * | 1981-02-17 | 1996-05-07 | Bazzano; Gail S. | Use of retinoids and compositions containing same for hair growth |
| US4743442A (en) * | 1983-08-02 | 1988-05-10 | Blendax-Werke R. Schneider Gmbh & Co. | Skin care composition |
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