CH257578A - Cosmetic product. - Google Patents
Cosmetic product.Info
- Publication number
- CH257578A CH257578A CH257578DA CH257578A CH 257578 A CH257578 A CH 257578A CH 257578D A CH257578D A CH 257578DA CH 257578 A CH257578 A CH 257578A
- Authority
- CH
- Switzerland
- Prior art keywords
- cosmetic product
- substances
- acid
- water
- insect
- Prior art date
Links
- 239000002537 cosmetic Substances 0.000 title claims description 4
- 239000000126 substance Substances 0.000 claims description 5
- 239000000077 insect repellent Substances 0.000 claims description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000002674 ointment Substances 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 230000037072 sun protection Effects 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000000475 sunscreen effect Effects 0.000 description 2
- 239000000516 sunscreening agent Substances 0.000 description 2
- CWLGEPSKQDNHIO-JOBJLJCHSA-N (e)-n-[(e)-benzylideneamino]-1-phenylmethanimine Chemical class C=1C=CC=CC=1/C=N/N=C/C1=CC=CC=C1 CWLGEPSKQDNHIO-JOBJLJCHSA-N 0.000 description 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- FZKCAHQKNJXICB-UHFFFAOYSA-N 2,1-benzoxazole Chemical compound C1=CC=CC2=CON=C21 FZKCAHQKNJXICB-UHFFFAOYSA-N 0.000 description 1
- YTWWBKKPWACPPB-UHFFFAOYSA-N 2-cyclohexylcyclohexan-1-ol Chemical compound OC1CCCCC1C1CCCCC1 YTWWBKKPWACPPB-UHFFFAOYSA-N 0.000 description 1
- AAIBYZBZXNWTPP-UHFFFAOYSA-N 2-phenylcyclohexan-1-ol Chemical compound OC1CCCCC1C1=CC=CC=C1 AAIBYZBZXNWTPP-UHFFFAOYSA-N 0.000 description 1
- BWHOZHOGCMHOBV-UHFFFAOYSA-N Benzalacetone Natural products CC(=O)C=CC1=CC=CC=C1 BWHOZHOGCMHOBV-UHFFFAOYSA-N 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical class C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000013861 fat-free Nutrition 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- SOXAGEOHPCXXIO-DVOMOZLQSA-N menthyl anthranilate Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)C1=CC=CC=C1N SOXAGEOHPCXXIO-DVOMOZLQSA-N 0.000 description 1
- SJOXEWUZWQYCGL-DVOMOZLQSA-N menthyl salicylate Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)C1=CC=CC=C1O SJOXEWUZWQYCGL-DVOMOZLQSA-N 0.000 description 1
- 229960004665 menthyl salicylate Drugs 0.000 description 1
- 229960002248 meradimate Drugs 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- RWZYAGGXGHYGMB-UHFFFAOYSA-N o-aminobenzenecarboxylic acid Natural products NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003883 ointment base Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 229940058287 salicylic acid derivative anticestodals Drugs 0.000 description 1
- 150000003872 salicylic acid derivatives Chemical class 0.000 description 1
- SJOXEWUZWQYCGL-UHFFFAOYSA-N salicylic acid menthyl ester Natural products CC(C)C1CCC(C)CC1OC(=O)C1=CC=CC=C1O SJOXEWUZWQYCGL-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- BWHOZHOGCMHOBV-BQYQJAHWSA-N trans-benzylideneacetone Chemical compound CC(=O)\C=C\C1=CC=CC=C1 BWHOZHOGCMHOBV-BQYQJAHWSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- 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
- A61K8/368—Carboxylic acids; Salts or anhydrides thereof with carboxyl groups directly bound to carbon atoms of aromatic rings
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
- A61K8/445—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof aromatic, i.e. the carboxylic acid directly linked to the aromatic ring
-
- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
- A61K8/498—Cosmetics 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/02—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings containing insect repellants
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
Description
Kosmetisches Erzeugnis.
Es ist bekannt. Ultraviolettstrahlen absorbierende Stoffe zu kosmetischen Produk1en zu verarbeiten und. als Lichtschutzmittel l'ür die menschliche Haut zu verwenden. Es sind dies die sogenannten Sonnenschutz @remen und Sonnenschutz¯le.
Anderseits ist es auch bekannt, dass ge- wisse chemische Verbindungen eine insekten- verh'eibende Wirkung besitzen, obschon sie an sich geruchlos sind.
Es wurde nun gefunden, da¯ sich diese beiden Korperklassen mit. Vorteil kombinie i-,, lassen, wodurch man zu Sonnenschutz- mitteln gelangt, die gleichzeitig insekten abwehrende Eigenschaften a@fweisen.
Als Sonnenschutzsubstanzen eignen sich z. B. masculin. Umbelliferonderiva. te, Chinin- salze. Anthranil- und SalicylsÏurederivate.
Benzimidazole, Benzalaceton und Benzalazin- derivate. Ta. nnin. usw.
Für die Zwecke der Erfindung in Frage kommende, insektenabwehrende Substanzen sind DicarbonsÏurediester insbesondere der aromatischen Reihe, z. B. der DicarbonsÏuren des Benzols, Toluols, Naphthols, wobei vieh die Phthalsäurediester, wie Phtha. lsäure- dimethylester, am wirksamsten erwiesen ha ben. Auch Diester aliphatischer CarbonsÏuren, wie der WeinsÏure, ZitronensÏure, AdipinsÏure, BernsteinsÏure usw., sind anivend- bar. Ferner eignen sich die ¯thylhexandiole, wie 2-Äthyl-hexandiol- (1. 3). 2-Phenyl-cyclo- hexanol, 2-Cyclohexyl-cyclohexanol usw.
Die l TltravioTettstrahlen adsorbierenden und insektenabweisenden Substanzen können als Lösungen in organischen. Lösungsmitteln oder wässerigen Emulsionen, Salben, Ílen, Pudern und Stiften verarbeitet werden.
So können sie einer Salbengrundlage aus tierischen, pflanzlichen oder mineralischen Fetten und Ölen oder Wachsen oder aber auch einer fettfreien Creme einverleibt sein.
Dispergierende oder emulgierende Hilfsmittel sowie Parfümierungsmittel und Konservie- rungsmittel lassen sich ebenfalls mitverwen- den. Ferner kann man sie Pudergrundmassen einverleiben und gegebenenfalls auch mit geeigneten Trägersubstanzen zu kompakten, abreibfähigen Blocken verarbeiten.
Beispiel fiVr eine Salbe (Wasser-in-Ol-Emulsion)
Eine wasserbeständige Salbe wird erhalten durch Vermischen der folgenden Bestandteile und Homogenisierung in einer Wolloid- mühle : Adeps Lanae 20 Gew.-Teile Menthylsalicylat 8 ;' Phthalsäuredimethylester 10 Paraffin¯l 11, 5 @ Wasser 50 Parfüm und d Konservierungsmittel 0. 5
Beispiel fur eine milchige Emulsion :
Eine milchige Emulsion wird erhalten durch Emulgieren von Glyceryl-monostearat 5 Gew.-Teile Menthylanthranilat 3 @ @ Adipinsäurediäthylester 10 @ @ Wasser 81, 5 Parf m und
Konservierungsmittel 0, 5
Cosmetic product.
It is known. To process ultraviolet rays absorbing substances into cosmetic products and. to use as a sunscreen for human skin. These are the so-called sun protection @remen and sun protection ¯le.
On the other hand, it is also known that certain chemical compounds have an insect-repelling effect, although they are inherently odorless.
It has now been found that these two body classes are associated with. Combine the advantages, which leads to sunscreens that also have insect-repellent properties.
As sun protection substances are z. B. masculin. Umbelliferonderiva. te, quinine salts. Anthranil and salicylic acid derivatives.
Benzimidazoles, benzalacetone and benzalazine derivatives. Ta. Nnin. etc.
For the purposes of the invention in question, insect repellent substances are DicarbonsÏurediester in particular of the aromatic series, z. B. the dicarboxylic acids of benzene, toluene, naphthol, with cattle phthalic diesters such as phtha. dimethyl ester, have been shown to be most effective. Diesters of aliphatic carboxylic acids, such as tartaric acid, citric acid, adipic acid, succinic acid, etc., can also be used. The ¯thylhexanediols, such as 2-ethylhexanediol- (1. 3), are also suitable. 2-phenyl-cyclohexanol, 2-cyclohexyl-cyclohexanol, etc.
The substances that adsorb and repel insects can be used as solutions in organic. Solvents or aqueous emulsions, ointments, oils, powders and pens can be processed.
For example, they can be incorporated into an ointment base made from animal, vegetable or mineral fats and oils or waxes or else a fat-free cream.
Dispersing or emulsifying auxiliaries as well as perfuming agents and preservatives can also be used. They can also be incorporated into powder bases and, if appropriate, processed with suitable carriers to give compact, rub-off blocks.
Example of an ointment (water-in-oil emulsion)
A water-resistant ointment is obtained by mixing the following components and homogenizing them in a wolloid mill: Adeps Lanae 20 parts by weight of menthyl salicylate 8; Phthalic acid dimethyl ester 10 paraffin ¯l 11, 5 @ water 50 perfume and d preservative 0.5
Example of a milky emulsion:
A milky emulsion is obtained by emulsifying glyceryl monostearate 5 parts by weight of menthyl anthranilate 3 @ @ adipic acid diethyl ester 10 @ @ water 81, 5 perfume m and
Preservatives 0, 5
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH257578T | 1947-06-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH257578A true CH257578A (en) | 1948-10-15 |
Family
ID=4472245
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH257578D CH257578A (en) | 1947-06-12 | 1947-06-12 | Cosmetic product. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH257578A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2370469A1 (en) * | 1976-11-15 | 1978-06-09 | Basf Ag | LIGHT PROTECTION AGENTS CONTAINING 4-DIALKYLAMINODIPHTHALATES |
-
1947
- 1947-06-12 CH CH257578D patent/CH257578A/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2370469A1 (en) * | 1976-11-15 | 1978-06-09 | Basf Ag | LIGHT PROTECTION AGENTS CONTAINING 4-DIALKYLAMINODIPHTHALATES |
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