LU84608A1 - Compositions cosmetiques contenant des essences naturelles et des derives du benzylidene camphre - Google Patents

Compositions cosmetiques contenant des essences naturelles et des derives du benzylidene camphre Download PDF

Info

Publication number: LU84608A1
Authority: LU; Luxembourg
Prior art keywords: denotes; radical; alkyl; hydrogen atom; group
Prior art date: 1983-01-26

Application number

LU84608A

Other languages

English (en)

French (fr)

Original Assignee

Oreal

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.)

1983-01-26

Filing date

1983-01-26

Publication date

1984-10-24

1983-01-26 Application filed by Oreal filed Critical Oreal

1983-01-26 Priority to LU84608A priority Critical patent/LU84608A1/fr

1984-01-23 Priority to US06/573,143 priority patent/US4950478A/en

1984-01-25 Priority to FR8401151A priority patent/FR2539623B1/fr

1984-01-26 Priority to GB08402024A priority patent/GB2133985B/en

1984-01-26 Priority to DE3402645A priority patent/DE3402645C2/de

1984-10-24 Publication of LU84608A1 publication Critical patent/LU84608A1/fr

Links

239000002537 cosmetic Substances 0.000 title claims description 26
OIQXFRANQVWXJF-QBFSEMIESA-N (2z)-2-benzylidene-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one Chemical class CC1(C)C2CCC1(C)C(=O)\C2=C/C1=CC=CC=C1 OIQXFRANQVWXJF-QBFSEMIESA-N 0.000 title claims description 23
239000000203 mixture Substances 0.000 title claims description 22
239000000686 essence Substances 0.000 title description 32
-1 quaternary ammonium radical Chemical class 0.000 claims description 70
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 44
150000003254 radicals Chemical class 0.000 claims description 36
125000000217 alkyl group Chemical group 0.000 claims description 35
229910052739 hydrogen Inorganic materials 0.000 claims description 21
239000001257 hydrogen Substances 0.000 claims description 19
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 18
125000003118 aryl group Chemical group 0.000 claims description 18
125000004432 carbon atom Chemical group C* 0.000 claims description 17
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 16
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 15
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
244000179970 Monarda didyma Species 0.000 claims description 13
235000010672 Monarda didyma Nutrition 0.000 claims description 13
235000014113 dietary fatty acids Nutrition 0.000 claims description 13
239000000194 fatty acid Substances 0.000 claims description 13
229930195729 fatty acid Natural products 0.000 claims description 13
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 13
125000003545 alkoxy group Chemical group 0.000 claims description 11
239000003921 oil Substances 0.000 claims description 11
125000003342 alkenyl group Chemical group 0.000 claims description 10
150000003839 salts Chemical class 0.000 claims description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
150000007530 organic bases Chemical class 0.000 claims description 9
241000723346 Cinnamomum camphora Species 0.000 claims description 8
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 8
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 8
229930008380 camphor Natural products 0.000 claims description 8
229960000846 camphor Drugs 0.000 claims description 8
239000006071 cream Substances 0.000 claims description 8
235000011187 glycerol Nutrition 0.000 claims description 8
239000002253 acid Substances 0.000 claims description 7
125000005843 halogen group Chemical group 0.000 claims description 7
HEOCBCNFKCOKBX-RELGSGGGSA-N (1s,2e,4r)-4,7,7-trimethyl-2-[(4-methylphenyl)methylidene]bicyclo[2.2.1]heptan-3-one Chemical group C1=CC(C)=CC=C1\C=C/1C(=O)[C@]2(C)CC[C@H]\1C2(C)C HEOCBCNFKCOKBX-RELGSGGGSA-N 0.000 claims description 6
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 6
229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 6
125000000753 cycloalkyl group Chemical group 0.000 claims description 6
239000000839 emulsion Substances 0.000 claims description 6
150000004665 fatty acids Chemical class 0.000 claims description 6
125000000623 heterocyclic group Chemical group 0.000 claims description 6
150000002431 hydrogen Chemical class 0.000 claims description 6
235000013336 milk Nutrition 0.000 claims description 6
239000008267 milk Substances 0.000 claims description 6
210000004080 milk Anatomy 0.000 claims description 6
229910052757 nitrogen Inorganic materials 0.000 claims description 6
125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 5
125000004429 atom Chemical group 0.000 claims description 5
229960004697 enzacamene Drugs 0.000 claims description 5
150000007529 inorganic bases Chemical class 0.000 claims description 5
239000006210 lotion Substances 0.000 claims description 5
239000000243 solution Substances 0.000 claims description 5
239000001993 wax Substances 0.000 claims description 5
235000005979 Citrus limon Nutrition 0.000 claims description 4
244000131522 Citrus pyriformis Species 0.000 claims description 4
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
150000001298 alcohols Chemical class 0.000 claims description 4
150000001412 amines Chemical class 0.000 claims description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
150000001555 benzenes Chemical class 0.000 claims description 4
150000002191 fatty alcohols Chemical class 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
229910052751 metal Inorganic materials 0.000 claims description 4
239000002184 metal Substances 0.000 claims description 4
YZTJYBJCZXZGCT-UHFFFAOYSA-N phenylpiperazine Chemical compound C1CNCCN1C1=CC=CC=C1 YZTJYBJCZXZGCT-UHFFFAOYSA-N 0.000 claims description 4
229920005862 polyol Polymers 0.000 claims description 4
150000003077 polyols Chemical class 0.000 claims description 4
239000003755 preservative agent Substances 0.000 claims description 4
125000001453 quaternary ammonium group Chemical group 0.000 claims description 4
229940124530 sulfonamide Drugs 0.000 claims description 4
239000002562 thickening agent Substances 0.000 claims description 4
PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 claims description 3
239000000443 aerosol Substances 0.000 claims description 3
125000004103 aminoalkyl group Chemical group 0.000 claims description 3
229910052799 carbon Inorganic materials 0.000 claims description 3
125000004181 carboxyalkyl group Chemical group 0.000 claims description 3
239000006260 foam Substances 0.000 claims description 3
229910052736 halogen Inorganic materials 0.000 claims description 3
150000002367 halogens Chemical class 0.000 claims description 3
KMBLCQXNWZYMCE-UHFFFAOYSA-N 3-[(4,7,7-trimethyl-3-oxo-2-bicyclo[2.2.1]heptanylidene)methyl]benzenesulfonic acid Chemical compound CC1(C)C2CCC1(C)C(=O)C2=CC1=CC=CC(S(O)(=O)=O)=C1 KMBLCQXNWZYMCE-UHFFFAOYSA-N 0.000 claims description 2
239000004166 Lanolin Substances 0.000 claims description 2
239000002671 adjuvant Substances 0.000 claims description 2
229910052783 alkali metal Inorganic materials 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
125000003282 alkyl amino group Chemical group 0.000 claims description 2
150000008051 alkyl sulfates Chemical class 0.000 claims description 2
150000008052 alkyl sulfonates Chemical class 0.000 claims description 2
125000002947 alkylene group Chemical group 0.000 claims description 2
125000005530 alkylenedioxy group Chemical group 0.000 claims description 2
DSSYKIVIOFKYAU-UHFFFAOYSA-N camphor Chemical class C1CC2(C)C(=O)CC1C2(C)C DSSYKIVIOFKYAU-UHFFFAOYSA-N 0.000 claims description 2
125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 2
125000004663 dialkyl amino group Chemical group 0.000 claims description 2
239000000975 dye Substances 0.000 claims description 2
239000003974 emollient agent Substances 0.000 claims description 2
239000004872 foam stabilizing agent Substances 0.000 claims description 2
150000002334 glycols Chemical class 0.000 claims description 2
229940039717 lanolin Drugs 0.000 claims description 2
235000019388 lanolin Nutrition 0.000 claims description 2
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
239000000049 pigment Substances 0.000 claims description 2
239000008257 shaving cream Substances 0.000 claims description 2
239000000377 silicon dioxide Substances 0.000 claims description 2
239000000344 soap Substances 0.000 claims description 2
239000007787 solid Substances 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
150000003626 triacylglycerols Chemical class 0.000 claims description 2
ZNEOHLHCKGUAEB-UHFFFAOYSA-N trimethylphenylammonium Chemical compound C[N+](C)(C)C1=CC=CC=C1 ZNEOHLHCKGUAEB-UHFFFAOYSA-N 0.000 claims description 2
239000000080 wetting agent Substances 0.000 claims description 2
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 3
IQXWVZRMYFOEQO-UHFFFAOYSA-N 2-methyl-5-[(4,7,7-trimethyl-3-oxo-2-bicyclo[2.2.1]heptanylidene)methyl]benzenesulfonic acid Chemical compound C1=C(S(O)(=O)=O)C(C)=CC=C1C=C1C(=O)C2(C)CCC1C2(C)C IQXWVZRMYFOEQO-UHFFFAOYSA-N 0.000 claims 1
150000004820 halides Chemical class 0.000 claims 1
ZCCUUQDIBDJBTK-UHFFFAOYSA-N furocoumarin Natural products C1=C2OC(=O)C=CC2=CC2=C1OC=C2 ZCCUUQDIBDJBTK-UHFFFAOYSA-N 0.000 description 15
238000000034 method Methods 0.000 description 12
BGEBZHIAGXMEMV-UHFFFAOYSA-N 5-methoxypsoralen Chemical compound O1C(=O)C=CC2=C1C=C1OC=CC1=C2OC BGEBZHIAGXMEMV-UHFFFAOYSA-N 0.000 description 10
238000006243 chemical reaction Methods 0.000 description 9
150000001875 compounds Chemical class 0.000 description 9
239000002904 solvent Substances 0.000 description 9
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 8
235000019198 oils Nutrition 0.000 description 8
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 7
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 6
229910052500 inorganic mineral Inorganic materials 0.000 description 6
239000011707 mineral Substances 0.000 description 6
235000010755 mineral Nutrition 0.000 description 6
231100000760 phototoxic Toxicity 0.000 description 6
230000008569 process Effects 0.000 description 6
239000002585 base Substances 0.000 description 5
229960002045 bergapten Drugs 0.000 description 5
239000003513 alkali Substances 0.000 description 4
150000003934 aromatic aldehydes Chemical class 0.000 description 4
KGZDKFWCIPZMRK-UHFFFAOYSA-N bergapten Natural products COC1C2=C(Cc3ccoc13)C=CC(=O)O2 KGZDKFWCIPZMRK-UHFFFAOYSA-N 0.000 description 4
SQBBOVROCFXYBN-UHFFFAOYSA-N methoxypsoralen Natural products C1=C2OC(=O)C(OC)=CC2=CC2=C1OC=C2 SQBBOVROCFXYBN-UHFFFAOYSA-N 0.000 description 4
229960000541 cetyl alcohol Drugs 0.000 description 3
150000001851 cinnamic acid derivatives Chemical class 0.000 description 3
239000002304 perfume Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
150000003456 sulfonamides Chemical class 0.000 description 3
VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
206010034972 Photosensitivity reaction Diseases 0.000 description 2
208000012641 Pigmentation disease Diseases 0.000 description 2
206010040914 Skin reaction Diseases 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
159000000011 group IA salts Chemical class 0.000 description 2
150000004678 hydrides Chemical class 0.000 description 2
125000004356 hydroxy functional group Chemical group O* 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
238000006317 isomerization reaction Methods 0.000 description 2
JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 2
239000012071 phase Substances 0.000 description 2
208000007578 phototoxic dermatitis Diseases 0.000 description 2
231100000018 phototoxicity Toxicity 0.000 description 2
230000019612 pigmentation Effects 0.000 description 2
229940072033 potash Drugs 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
235000015320 potassium carbonate Nutrition 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
231100000430 skin reaction Toxicity 0.000 description 2
230000035483 skin reaction Effects 0.000 description 2
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 2
OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
229940099259 vaseline Drugs 0.000 description 2
HSVDGMYRFLHPMS-UHFFFAOYSA-N (2-benzylidene-7,7-dimethyl-3-oxo-4-bicyclo[2.2.1]heptanyl)methanesulfonic acid Chemical compound CC1(C)C2CCC1(CS(O)(=O)=O)C(=O)C2=CC1=CC=CC=C1 HSVDGMYRFLHPMS-UHFFFAOYSA-N 0.000 description 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
OIQXFRANQVWXJF-UHFFFAOYSA-N 2-benzylidene-4,7,7-trimethylbicyclo[2.2.1]heptan-3-one Chemical compound CC1(C)C2CCC1(C)C(=O)C2=CC1=CC=CC=C1 OIQXFRANQVWXJF-UHFFFAOYSA-N 0.000 description 1
VXGRJERITKFWPL-UHFFFAOYSA-N 4',5'-Dihydropsoralen Natural products C1=C2OC(=O)C=CC2=CC2=C1OCC2 VXGRJERITKFWPL-UHFFFAOYSA-N 0.000 description 1
HEOCBCNFKCOKBX-UHFFFAOYSA-N 4,7,7-trimethyl-2-[(4-methylphenyl)methylidene]bicyclo[2.2.1]heptan-3-one Chemical compound C1=CC(C)=CC=C1C=C1C(=O)C2(C)CCC1C2(C)C HEOCBCNFKCOKBX-UHFFFAOYSA-N 0.000 description 1
HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
206010015150 Erythema Diseases 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical class OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
235000019568 aromas Nutrition 0.000 description 1
125000005228 aryl sulfonate group Chemical group 0.000 description 1
ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 1
238000006555 catalytic reaction Methods 0.000 description 1
XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
235000001671 coumarin Nutrition 0.000 description 1
238000001784 detoxification Methods 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
239000004205 dimethyl polysiloxane Substances 0.000 description 1
235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
231100000321 erythema Toxicity 0.000 description 1
230000005284 excitation Effects 0.000 description 1
238000000605 extraction Methods 0.000 description 1
230000008570 general process Effects 0.000 description 1
YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
230000005283 ground state Effects 0.000 description 1
239000003906 humectant Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
230000001788 irregular Effects 0.000 description 1
150000002596 lactones Chemical group 0.000 description 1
230000003902 lesion Effects 0.000 description 1
230000003020 moisturizing effect Effects 0.000 description 1
ITFGZZGYXVHOOU-UHFFFAOYSA-N n,n-dimethylmethanamine;methyl hydrogen sulfate Chemical compound C[NH+](C)C.COS([O-])(=O)=O ITFGZZGYXVHOOU-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
239000004006 olive oil Substances 0.000 description 1
235000008390 olive oil Nutrition 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
230000000258 photobiological effect Effects 0.000 description 1
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
239000002243 precursor Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000003380 propellant Substances 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
238000006277 sulfonation reaction Methods 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- 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
- A61K8/35—Ketones, e.g. benzophenone
- 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
- A61K8/41—Amines
- A61K8/416—Quaternary ammonium compounds
- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
- 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
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
- 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
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/05—Stick

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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)
Birds (AREA)
Epidemiology (AREA)
Emergency Medicine (AREA)
Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Dermatology (AREA)
Cosmetics (AREA)

LU84608A 1983-01-26 1983-01-26 Compositions cosmetiques contenant des essences naturelles et des derives du benzylidene camphre LU84608A1 (fr)

Priority Applications (5)

Application Number	Priority Date	Filing Date	Title
LU84608A LU84608A1 (fr)	1983-01-26	1983-01-26	Compositions cosmetiques contenant des essences naturelles et des derives du benzylidene camphre
US06/573,143 US4950478A (en)	1983-01-26	1984-01-23	Cosmetic compositions containing natural essences and benzylidenecamphor derivatives
FR8401151A FR2539623B1 (fr)	1983-01-26	1984-01-25	Compositions cosmetiques contenant des essences naturelles et des derives du benzylidene camphre
GB08402024A GB2133985B (en)	1983-01-26	1984-01-26	Compositions containing natural essences
DE3402645A DE3402645C2 (de)	1983-01-26	1984-01-26	Kosmetische Mittel, welche natürliche Essenzen und Benzylidenkampferderivate enthalten

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
LU84608		1983-01-26
LU84608A LU84608A1 (fr)	1983-01-26	1983-01-26	Compositions cosmetiques contenant des essences naturelles et des derives du benzylidene camphre

Publications (1)

Publication Number	Publication Date
LU84608A1 true LU84608A1 (fr)	1984-10-24

Family

ID=19730024

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU84608A LU84608A1 (fr)	1983-01-26	1983-01-26	Compositions cosmetiques contenant des essences naturelles et des derives du benzylidene camphre

Country Status (5)

Country	Link
US (1)	US4950478A (de)
DE (1)	DE3402645C2 (de)
FR (1)	FR2539623B1 (de)
GB (1)	GB2133985B (de)
LU (1)	LU84608A1 (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
LU85688A1 (fr) *	1984-12-18	1986-07-17	Oreal	Composition cosmetique accelerant le bronzage a base de furochromones
EP0257928A3 (de) *	1986-08-22	1988-05-18	Kays Kaidbey	Sonnenbräunmittel
LU86762A1 (fr) *	1987-02-06	1988-11-17	Oreal	Composition cosmetique filtrante sous forme d'emulsion huile-dans-l'eau comprenant un filtre uv-a et un filtre uv-b et son utilisation pour la protection de la peau contre les radiations ultraviolettes
FR2636530B1 (fr) *	1988-08-24	1992-05-07	Oreal	Composition cosmetique filtrante photostable sous forme d'emulsion contenant un filtre hydrosoluble a large bande d'absorption et au moins un filtre uv-a liposoluble et son utilisation pour la protection de la peau contre le rayonnement ultraviolet
DE4419470B4 (de) *	1993-06-03	2008-02-07	Erich Petritsch	Verfahren zur Herstellung eines Haut- und/oder Haarpflegemittels aus Tensiden und Wasser
FR2797585B1 (fr) *	1999-08-19	2001-10-26	Jean Jacques Goupil	Composition pour administration topique comprenant du 5-methoxypsoralene
WO2024048925A1 (ko) *	2022-08-31	2024-03-07	신성소재 주식회사	자외선 차단 화장료 조성용 테레프탈리덴 디캠퍼 설폰산의 유기염 및 그의 제조방법

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1024465A (fr) *	1950-09-11	1953-04-01		Huile brunissante écran solaire
DE1492322A1 (de) *	1964-06-08	1970-01-15	Domekos Dr H Doering Gmbh	Verwendung UV-absorbierender Substanzen als Zusaetze fuer Kosmetika
LU55702A1 (de) *	1968-03-18	1969-10-02
DE2051824C3 (de) *	1970-10-22	1975-11-27	Merck Patent Gmbh, 6100 Darmstadt	Kosmetisches Lichtschutzmittel
GB1367539A (en) *	1971-11-26	1974-09-18	Int Flavors & Fragrances Inc	Coumarin sun-screening compounds and compositions containing them
LU66156A1 (de) *	1972-09-25	1974-04-02
US4061730A (en) *	1972-09-25	1977-12-06	Societe Anonyme Dite: L'oreal	Anti-solar agent and compositions containing the same
LU67061A1 (de) *	1973-02-19	1974-09-25
DE2336219A1 (de) *	1973-07-17	1975-02-20	Merck Patent Gmbh	Campherderivate
FR2282426A2 (fr) *	1974-08-19	1976-03-19	Oreal	Nouveaux agents sulfones, pour la protection contre les rayons actiniques et compositions cosmetiques les contenant
FR2360301A1 (fr) *	1976-08-04	1978-03-03	Goupil Jean Jacques	Nouveaux produits solaires
LU76955A1 (de) *	1977-03-15	1978-10-18
FR2402647A1 (fr) *	1977-09-09	1979-04-06	Oreal	Nouveaux benzylidene camphres, leur procede de preparation et compositions cosmetiques les contenant
FR2383904A1 (fr) *	1977-03-15	1978-10-13	Oreal	Nouveaux benzylidene camphres, leur procede de preparation et compositions cosmetiques les contenant
IT1111618B (it) *	1977-03-15	1986-01-13	Oreal	Derivati della canfora e loro impiego nel campo cosmetico
FR2409751A1 (fr) *	1977-11-29	1979-06-22	Thorel Jean Noel	Composition dotee de proprietes protectrices et pigmentogenes de la peau
FR2421878A2 (fr) *	1978-04-05	1979-11-02	Oreal	Nouveaux benzylidene camphres, leur procede de preparation et compositions cosmetiques les contenant
FR2430938A1 (fr) *	1978-07-11	1980-02-08	Oreal	Nouvelles oxybenzylidenes bornanones, leur procede de preparation, et compositions cosmetiques les contenant
FR2528420A1 (fr) *	1982-06-15	1983-12-16	Oreal	Nouveaux 3-benzylidene camphres, leur procede de preparation et leur utilisation pour la protection contre les rayons uv
US4654434A (en) *	1982-06-15	1987-03-31	L'oreal	3-benzylidene-camphors, process for their preparation and their use in protection against UV rays
US4663088A (en) *	1982-06-15	1987-05-05	L'oreal	3-benzylidene-camphors, process for their preparation and their use in protection against UV rays
LU84264A1 (fr) *	1982-07-08	1984-03-22	Oreal	Nouveaux sulfonamides derives du 3-benzylidene camphre et leur application en tant que filtres u.v.,notamment dans des compositions cosmetiques
LU84607A1 (fr) *	1983-01-26	1984-10-24	Oreal	Compositions alcooliques ou hydroalcooliques contenant des essences naturelles et du benzylidene camphre ou ses derives

1983
- 1983-01-26 LU LU84608A patent/LU84608A1/fr unknown
1984
- 1984-01-23 US US06/573,143 patent/US4950478A/en not_active Expired - Fee Related
- 1984-01-25 FR FR8401151A patent/FR2539623B1/fr not_active Expired
- 1984-01-26 DE DE3402645A patent/DE3402645C2/de not_active Expired - Fee Related
- 1984-01-26 GB GB08402024A patent/GB2133985B/en not_active Expired

Also Published As

Publication number	Publication date
DE3402645A1 (de)	1984-07-26
FR2539623A1 (fr)	1984-07-27
US4950478A (en)	1990-08-21
GB2133985A (en)	1984-08-08
FR2539623B1 (fr)	1987-06-05
GB8402024D0 (en)	1984-02-29
DE3402645C2 (de)	1995-02-02
GB2133985B (en)	1986-04-16

Publication	Publication Date	Title
CA1211451A (fr)	1986-09-16	Sulfonamides derives du 3-benzylidene camphre et leur application en tant que filtres u.v., notamment dans des compositions cosmetiques
CA1204779A (fr)	1986-05-20	3-benzylidene camphres, leur procede de preparation et leur utilisation pour la protection contre les rayons uv
CA1299581C (fr)	1992-04-28	Composition cosmetique contenant des derives hydroxyles de chalcone et son utilisation pour la protection de la peau et des cheveux contre les radiations lumineuses, nouveaux derives hydroxyles de chalcone utilises et leur procede de preparation
CA1112179A (fr)	1981-11-10	Compositions tinctoriales a base de colorants d'oxydation domprenant un acide (2,5-dihydroxyphenyl) alcanoique ou l'un de ses sels a titre d'anti- oxydant
CA1110654A (fr)	1981-10-13	Benzylidene camphres, leur procede de preparation et compositions cosmetiques les contenant
CH653254A5 (fr)	1985-12-31	Compositions cosmetiques contenant des derives hydroxyles du dibenzoylmethane, derives hydroxyles du dibenzoylmethane utilises et leur procede de preparation.
EP0368717B1 (de)	1993-01-20	Derivate der 5-Benzyliden-3-oxacyclopentanone, ihr Herstellungsverfahren und ihre Verwendung in kosmetischen Zusammensetzungen zum Schutz der Haut und der Haare gegen Sonnenstrahlung
CH650490A5 (fr)	1985-07-31	Oligomeres tensio-actifs, leurs procedes de preparation et les compositions les contenant.
CA1167070A (fr)	1984-05-08	Nouveaux agents de surface non-ioniques polyoxyethylenes a deux chaines lipophiles, leur procede de preparation et compositions les contenant
LU87271A1 (fr)	1990-02-07	Nouveaux derives insatures liposolubles des benzalmalonates et leur utilisation en tant qu'absorbeurs du rayonnement ultra-violet en cosmetique
CA2141062A1 (fr)	1994-12-08	Utilisation pour la teinture des fibres keratiniques de para-aminophenols 3-substitues et nouveaux para-aminophenols 3-substitues
JPH01153617A (ja)	1989-06-15	皮脂分泌抑制局所適用用製剤
FR2593509A1 (fr)	1987-07-31	Nouveaux ethers de polyglycerols et leur utilisation en cosmetique et en pharmacie
CH671577A5 (de)	1989-09-15
LU84608A1 (fr)	1984-10-24	Compositions cosmetiques contenant des essences naturelles et des derives du benzylidene camphre
FR2717808A1 (fr)	1995-09-29	Composition cosmétique stable à la lumière.
CA1180283A (fr)	1985-01-02	Utilisation de benzoquinones pour la coloration directe des fibres keratiniques
CH663017A5 (fr)	1987-11-13	Derives du 3-benzylidene camphre, leur procede de preparation et leur utilisation en tant qu'agents de protection contre les rayons uv et en tant que medicaments.
CA1210332A (fr)	1986-08-26	Compositions alcooliques ou hydroalcooliques contenant des essences naturelles et des derives du benzylidene camphre
EP0370868B1 (de)	1993-03-03	Verwendung modifizierter Diorganopolysiloxane als Antioxydantien in der Kosmetik und Dermatologie
FR2693206A1 (fr)	1994-01-07	Utilisation dans des solutions d'agents tensioactifs de carbamates d'aminopolyols en tant qu'épaississants et compositions les contenant.
CH677111A5 (de)	1991-04-15
JPH01160945A (ja)	1989-06-23	新規アルキルアリールエーテル誘導体およびそれを含む皮脂分泌抑制局所適用用製剤
JPS6061515A (ja)	1985-04-09	アルコキシアリ−ル−アルカノ−ルを含有する脂漏抑制化粧料
CA1307467C (fr)	1992-09-15	Composition destinee au traitement de l'acne et de la seborrhee contenant en tant qu'agent actif un hydroperoxyde