CH620120A5 - - Google Patents

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Info

Publication number: CH620120A5
Authority: CH; Switzerland
Prior art keywords: derivative; perfume; sample; perfumes; essence
Prior art date: 1977-05-24

Application number

CH637777A

Other languages

English (en)

French (fr)

Inventor

Guenter Holzner

Original Assignee

Firmenich & Cie

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.)

1977-05-24

Filing date

1977-05-24

Publication date

1980-11-14

1977-05-24 Application filed by Firmenich & Cie filed Critical Firmenich & Cie

1977-05-24 Priority to CH637777A priority Critical patent/CH620120A5/fr

1978-05-09 Priority to BE187506A priority patent/BE866842A/xx

1978-05-16 Priority to GB19765/78A priority patent/GB1572687A/en

1978-05-16 Priority to US05/906,659 priority patent/US4217250A/en

1978-05-22 Priority to FR7815116A priority patent/FR2391720A1/fr

1978-05-23 Priority to JP6158978A priority patent/JPS53145933A/ja

1978-05-23 Priority to DE19782822525 priority patent/DE2822525A1/de

1978-05-24 Priority to IT7823757A priority patent/IT1096319B/it

1980-11-14 Publication of CH620120A5 publication Critical patent/CH620120A5/fr

Links

239000002304 perfume Substances 0.000 claims description 44
239000004615 ingredient Substances 0.000 claims description 23
229910001385 heavy metal Inorganic materials 0.000 claims description 10
238000000034 method Methods 0.000 claims description 10
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 8
239000008139 complexing agent Substances 0.000 claims description 7
230000000087 stabilizing effect Effects 0.000 claims description 7
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 4
239000003963 antioxidant agent Substances 0.000 claims description 4
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
239000005977 Ethylene Substances 0.000 claims description 3
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 3
229920001577 copolymer Polymers 0.000 claims description 3
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
230000003078 antioxidant effect Effects 0.000 claims description 2
XQRLCLUYWUNEEH-UHFFFAOYSA-N diphosphonic acid Chemical compound OP(=O)OP(O)=O XQRLCLUYWUNEEH-UHFFFAOYSA-N 0.000 claims description 2
150000002191 fatty alcohols Chemical class 0.000 claims description 2
229910052751 metal Inorganic materials 0.000 claims description 2
239000002184 metal Substances 0.000 claims description 2
150000003016 phosphoric acids Chemical class 0.000 claims description 2
230000006641 stabilisation Effects 0.000 claims description 2
238000011105 stabilization Methods 0.000 claims description 2
150000007530 organic bases Chemical class 0.000 claims 1
150000002895 organic esters Chemical class 0.000 claims 1
238000003860 storage Methods 0.000 description 13
239000000654 additive Substances 0.000 description 9
239000000344 soap Substances 0.000 description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
229920002359 Tetronic® Polymers 0.000 description 8
230000000996 additive effect Effects 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
239000003205 fragrance Substances 0.000 description 6
239000002253 acid Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
239000000341 volatile oil Substances 0.000 description 5
KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 4
238000004925 denaturation Methods 0.000 description 4
230000036425 denaturation Effects 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
235000019441 ethanol Nutrition 0.000 description 4
229910052742 iron Inorganic materials 0.000 description 4
239000000203 mixture Substances 0.000 description 4
230000000717 retained effect Effects 0.000 description 4
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
240000002505 Pogostemon cablin Species 0.000 description 3
235000011751 Pogostemon cablin Nutrition 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
229910000147 aluminium phosphate Inorganic materials 0.000 description 3
235000006708 antioxidants Nutrition 0.000 description 3
238000011109 contamination Methods 0.000 description 3
239000003599 detergent Substances 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
-1 fatty alcohol Ester Chemical class 0.000 description 3
230000003647 oxidation Effects 0.000 description 3
238000007254 oxidation reaction Methods 0.000 description 3
239000002994 raw material Substances 0.000 description 3
229960004418 trolamine Drugs 0.000 description 3
WEFHSZAZNMEWKJ-KEDVMYETSA-N (6Z,8E)-undeca-6,8,10-trien-2-one (6E,8E)-undeca-6,8,10-trien-2-one (6Z,8E)-undeca-6,8,10-trien-3-one (6E,8E)-undeca-6,8,10-trien-3-one (6Z,8E)-undeca-6,8,10-trien-4-one (6E,8E)-undeca-6,8,10-trien-4-one Chemical compound CCCC(=O)C\C=C\C=C\C=C.CCCC(=O)C\C=C/C=C/C=C.CCC(=O)CC\C=C\C=C\C=C.CCC(=O)CC\C=C/C=C/C=C.CC(=O)CCC\C=C\C=C\C=C.CC(=O)CCC\C=C/C=C/C=C WEFHSZAZNMEWKJ-KEDVMYETSA-N 0.000 description 2
KEBDNKNVCHQIJU-UHFFFAOYSA-N 2-Methylpropyl 3-methylbutanoate Chemical compound CC(C)COC(=O)CC(C)C KEBDNKNVCHQIJU-UHFFFAOYSA-N 0.000 description 2
NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 description 2
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
244000183685 Citrus aurantium Species 0.000 description 2
235000007716 Citrus aurantium Nutrition 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
241000116713 Ferula gummosa Species 0.000 description 2
GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
235000010672 Monarda didyma Nutrition 0.000 description 2
244000179970 Monarda didyma Species 0.000 description 2
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric Acid Chemical compound [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 2
230000003254 anti-foaming effect Effects 0.000 description 2
239000002518 antifoaming agent Substances 0.000 description 2
239000002216 antistatic agent Substances 0.000 description 2
239000003899 bactericide agent Substances 0.000 description 2
235000001053 badasse Nutrition 0.000 description 2
QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000004040 coloring Methods 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 2
239000002781 deodorant agent Substances 0.000 description 2
230000006866 deterioration Effects 0.000 description 2
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 2
239000004864 galbanum Substances 0.000 description 2
WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 2
PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 2
235000009606 lavandin Nutrition 0.000 description 2
244000056931 lavandin Species 0.000 description 2
UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 2
KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
150000003014 phosphoric acid esters Chemical class 0.000 description 2
239000003380 propellant Substances 0.000 description 2
ZNCPFRVNHGOPAG-UHFFFAOYSA-L sodium oxalate Chemical compound [Na+].[Na+].[O-]C(=O)C([O-])=O ZNCPFRVNHGOPAG-UHFFFAOYSA-L 0.000 description 2
229940039790 sodium oxalate Drugs 0.000 description 2
229940116411 terpineol Drugs 0.000 description 2
HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 2
WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 1
PCFHYANYPQEMPU-UHFFFAOYSA-N 4-(2,2,3-trimethyl-5-bicyclo[2.2.1]heptanyl)cyclohexan-1-ol Chemical compound CC1(C)C(C)C2CC1CC2C1CCC(O)CC1 PCFHYANYPQEMPU-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
PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical class NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 description 1
WWJLCYHYLZZXBE-UHFFFAOYSA-N 5-chloro-1,3-dihydroindol-2-one Chemical compound ClC1=CC=C2NC(=O)CC2=C1 WWJLCYHYLZZXBE-UHFFFAOYSA-N 0.000 description 1
244000137282 Agathosma betulina Species 0.000 description 1
235000013388 Agathosma crenulata Nutrition 0.000 description 1
235000009269 Barosma crenulata Nutrition 0.000 description 1
206010007134 Candida infections Diseases 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
241000746418 Dalbergia nigra Species 0.000 description 1
241000402754 Erythranthe moschata Species 0.000 description 1
YIKYNHJUKRTCJL-UHFFFAOYSA-N Ethyl maltol Chemical compound CCC=1OC=CC(=O)C=1O YIKYNHJUKRTCJL-UHFFFAOYSA-N 0.000 description 1
WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 1
239000005792 Geraniol Substances 0.000 description 1
GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
241000208152 Geranium Species 0.000 description 1
KGEKLUUHTZCSIP-UHFFFAOYSA-N Isobornyl acetate Natural products C1CC2(C)C(OC(=O)C)CC1C2(C)C KGEKLUUHTZCSIP-UHFFFAOYSA-N 0.000 description 1
208000007027 Oral Candidiasis Diseases 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
241000896103 Pinus sibirica Species 0.000 description 1
244000178231 Rosmarinus officinalis Species 0.000 description 1
240000000513 Santalum album Species 0.000 description 1
235000008632 Santalum album Nutrition 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
241000287411 Turdidae Species 0.000 description 1
244000284012 Vetiveria zizanioides Species 0.000 description 1
235000007769 Vetiveria zizanioides Nutrition 0.000 description 1
239000001940 [(1R,4S,6R)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Substances 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 description 1
GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
230000001166 anti-perspirative effect Effects 0.000 description 1
239000003213 antiperspirant Substances 0.000 description 1
235000010323 ascorbic acid Nutrition 0.000 description 1
229960005070 ascorbic acid Drugs 0.000 description 1
239000011668 ascorbic acid Substances 0.000 description 1
229940007550 benzyl acetate Drugs 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
229940062650 buchu Drugs 0.000 description 1
201000003984 candidiasis Diseases 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
229960005233 cineole Drugs 0.000 description 1
235000015165 citric acid Nutrition 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid group Chemical class C(CC(O)(C(=O)O)CC(=O)O)(=O)O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
230000000536 complexating effect Effects 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
229960000956 coumarin Drugs 0.000 description 1
235000001671 coumarin Nutrition 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical class CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
OVESPWUILKSVDV-UHFFFAOYSA-N ethyl acetate;hexyl acetate Chemical compound CCOC(C)=O.CCCCCCOC(C)=O OVESPWUILKSVDV-UHFFFAOYSA-N 0.000 description 1
229940093503 ethyl maltol Drugs 0.000 description 1
229940073505 ethyl vanillin Drugs 0.000 description 1
229940113087 geraniol Drugs 0.000 description 1
239000011521 glass Substances 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
125000001245 hexylamino group Chemical group [H]N([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
239000004571 lime Substances 0.000 description 1
UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
AFRVIZIPSOUEBO-UHFFFAOYSA-N methyl 2,4-dihydroxy-3,5-dimethylbenzoate Chemical compound COC(=O)C1=CC(C)=C(O)C(C)=C1O AFRVIZIPSOUEBO-UHFFFAOYSA-N 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
FVEINXLJOJPHLH-UHFFFAOYSA-N p-tert-Butylbenzyl alcohol Chemical compound CC(C)(C)C1=CC=C(CO)C=C1 FVEINXLJOJPHLH-UHFFFAOYSA-N 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
239000012437 perfumed product Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000002453 shampoo Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
238000011282 treatment Methods 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume 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
- A61K8/40—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
- 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
- A61K8/55—Phosphorus compounds
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/51—Chelating agents

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Detergent Compositions (AREA)
Fats And Perfumes (AREA)
Beans For Foods Or Fodder (AREA)
Cosmetics (AREA)

CH637777A 1977-05-24 1977-05-24 CH620120A5 (da)

Priority Applications (8)

Application Number	Priority Date	Filing Date	Title
CH637777A CH620120A5 (da)	1977-05-24	1977-05-24
BE187506A BE866842A (fr)	1977-05-24	1978-05-09	Procede pour la stabilisation de parfums
GB19765/78A GB1572687A (en)	1977-05-24	1978-05-16	Process for the stabilization of perfumes
US05/906,659 US4217250A (en)	1977-05-24	1978-05-16	Process for the stabilization of perfumes
FR7815116A FR2391720A1 (fr)	1977-05-24	1978-05-22	Procede pour la stabilisation de parfums
JP6158978A JPS53145933A (en)	1977-05-24	1978-05-23	Perfume stabilizing method
DE19782822525 DE2822525A1 (de)	1977-05-24	1978-05-23	Stabilisierung von parfuem bzw. parfuembestandteilen
IT7823757A IT1096319B (it)	1977-05-24	1978-05-24	Procedimento per la stabilizzazione di profumi

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH637777A CH620120A5 (da)	1977-05-24	1977-05-24

Publications (1)

Publication Number	Publication Date
CH620120A5 true CH620120A5 (da)	1980-11-14

Family

ID=4308616

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH637777A CH620120A5 (da)	1977-05-24	1977-05-24

Country Status (8)

Country	Link
US (1)	US4217250A (da)
JP (1)	JPS53145933A (da)
BE (1)	BE866842A (da)
CH (1)	CH620120A5 (da)
DE (1)	DE2822525A1 (da)
FR (1)	FR2391720A1 (da)
GB (1)	GB1572687A (da)
IT (1)	IT1096319B (da)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4440663A (en) *	1981-09-14	1984-04-03	The Procter & Gamble Company	Alkaline aqueous liquid detergent compositions containing normally unstable ester perfumes
US5198218A (en) *	1991-02-08	1993-03-30	Chesebrough-Pond's Usa Co., Division Of Conopco, Inc.	Clear cosmetic sticks with compatible fragrance components
US5128123A (en) *	1991-02-08	1992-07-07	Chesebrough-Pond's Usa Co., Division Of Conopco, Inc.	Clear cosmetic sticks
US5114717A (en) *	1991-02-08	1992-05-19	Chesebrough-Pond's Usa Co., Division Of Conopco, Inc.	Clear cosmetic sticks with compatible fragrance components
DE69305615T2 (de) *	1992-06-16	1997-02-20	Franz Buchli	Parfümiertes mittel
SE512222C2 (sv) *	1998-06-29	2000-02-14	Johan Sterte	Förfarande för framställning av makrostrukturer av mikroporösa material
US6908604B2 (en)	1999-05-17	2005-06-21	Exxonmobil Chemical Patents Inc.	Macrostructures of porous inorganic material and process for their preparation
EP1872831A1 (de) *	2006-06-21	2008-01-02	Symrise GmbH & Co. KG	Riechstoffhaltige Zusammensetzungen umfassend deliqueszente Stoffe
US20070298995A1 (en) *	2006-06-21	2007-12-27	Symrise Gmbh & Co. Kg	Fragrance-containing compositions comprising deliquescent substances
EP1875942A1 (de) *	2006-06-21	2008-01-09	Symrise GmbH & Co. KG	Riechstoffhaltige Zusammensetzungen umfassend deliqueszente Stoffe
FR2908982A1 (fr) *	2006-11-23	2008-05-30	Oreal	Composition cosmetique comprenant au moins un solvant volatil hydrocarbone aprotique
FR2908989B1 (fr) *	2006-11-23	2012-08-17	Oreal	Composition cosmetique comprenant au moins un ester volatil
US20080161394A1 (en) *	2006-11-23	2008-07-03	Jean-Yves Fouron	Cosmetic composition comprising at least one volatile carbonic acid ester
FR3147718A1 (fr) *	2023-04-13	2024-10-18	Jafer Enterprises R&D Sl.	Composition, notamment parfumante, comprenant du succinate de diéthyle et une amine tertiaire

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NL126096C (da) *	1959-02-06
DE1114613B (de) *	1959-04-11	1961-10-05	Lingner Werke G M B H	Verfahren zum Herstellen von in Behaeltern, insbesondere Spruehbehaeltern, aus Kunststoffen verpackten fluessigen kosmetischen Praeparaten, die aetherische OEle enthalten, welche den Kunststoff des Behaelters angreifen
BE594070A (da) *	1959-08-12
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JPS52122639A (en) *	1976-04-06	1977-10-15	Shiseido Co Ltd	Toiletry

1977
- 1977-05-24 CH CH637777A patent/CH620120A5/fr not_active IP Right Cessation
1978
- 1978-05-09 BE BE187506A patent/BE866842A/xx not_active IP Right Cessation
- 1978-05-16 GB GB19765/78A patent/GB1572687A/en not_active Expired
- 1978-05-16 US US05/906,659 patent/US4217250A/en not_active Expired - Lifetime
- 1978-05-22 FR FR7815116A patent/FR2391720A1/fr active Granted
- 1978-05-23 DE DE19782822525 patent/DE2822525A1/de not_active Withdrawn
- 1978-05-23 JP JP6158978A patent/JPS53145933A/ja active Pending
- 1978-05-24 IT IT7823757A patent/IT1096319B/it active

Also Published As

Publication number	Publication date
IT7823757A0 (it)	1978-05-24
FR2391720B1 (da)	1981-02-27
BE866842A (fr)	1978-11-09
GB1572687A (en)	1980-07-30
US4217250A (en)	1980-08-12
JPS53145933A (en)	1978-12-19
IT1096319B (it)	1985-08-26
FR2391720A1 (fr)	1978-12-22
DE2822525A1 (de)	1978-12-07

Publication	Publication Date	Title
CH620120A5 (da)	1980-11-14
FR2563430A1 (fr)	1985-10-31	Lotion d'ondulation pour permanente a froid
FR2676924A1 (fr)	1992-12-04	Microemulsion contenant un concentre parfumant et produit correspondant.
FR2729307A1 (fr)	1996-07-19	Utilisation d'esters d'acides gras ethoxyles comme composants auto-emulsionnables notamment utiles pour la preparation de produits de traitement phytosanitaires ou de medicaments a usage veterinaire ou humain
EP3630057B1 (fr)	2021-08-18	Parfums sous forme de microémulsions aqueuses
EP1115818A1 (fr)	2001-07-18	Concentre hydrosoluble obtenu a partir d'une phase emulgatrice ou hydrosolubilisante et d'un complexe de matieres lipophiles liquides d'origine vegetale
FR2897533A1 (fr)	2007-08-24	Agent oxydant pour le traitement des cheveux
EP1043015B1 (fr)	2005-02-23	Composition parfumante liquide homogène à base de silicones volatiles
EP3697379A1 (en)	2020-08-26	Prevention of the oxidation of perfumery raw materials
EP3463585B1 (fr)	2020-07-08	Parfums sous forme de microémulsions aqueuses
EP0051546B1 (fr)	1984-10-03	Procédé d'obtention de compositions parfumantes et de produits parfumés et compositions et produits ainsi obtenus
EP0809485B1 (fr)	2001-11-07	Utilisation du 4-tert-butyl-1-cyclohexanol en tant qu'antioxydant
EP4262766A1 (fr)	2023-10-25	Composition désinfectante comprenant un mélange de phénol, d'aldéhyde et d'alcool, et son utilisation pour désinfecter une surface ou en cosmétique pour désinfecter la peau, notamment les mains
FR2552328A1 (fr)	1985-03-29	Procede de fabrication d'une composition parfumee et composition obtenue par ce procede
CH636009A5 (fr)	1983-05-13	Utilisation d'un derive hydroxy-acetylenique en tant qu'ingredient parfumant.
EP0056500A2 (fr)	1982-07-28	Esters de l'acide 2,2-diméthyl-propionique, leur utilisation à titre d'ingrédients parfumants et composition contenant l'un d'entre eux
WO2020128321A1 (fr)	2020-06-25	Composition d'acide thioglycolique à faible odeur
FR2786408A1 (fr)	2000-06-02	Emulsions transparentes fluides et leur procede de preparation
EP0045534B1 (fr)	1983-12-21	Utilisation de phényl-n-hexyl cétone à titre d'ingrédient parfumant et compositions parfumantes contenant ladite cétone
FR2513491A1 (fr)	1983-04-01	Composition antioxydante pour aliments pour animaux et aliments pour animaux, graisses ou huiles la contenant
EP0050577B1 (fr)	1984-10-17	Procédé d'obtention de compositions parfumantes et de produits parfumés et compositions et produits ainsi obtenus
US4031034A (en)	1977-06-21	Altering perfume green notes using trithioacetone
CH622946A5 (en)	1981-05-15	Use of novel sesquiterpenoids as fragrance materials
JP2024517791A (ja)	2024-04-23	香料および食用油の自動酸化を防止または低減するための組成物および方法
US20250032375A1 (en)	2025-01-30	Solvent mixtures comprising 1,3-butylene glycol and triethyl-citrate

Legal Events

Date	Code	Title	Description
1986-01-31	PL	Patent ceased
2024-10-31	PL	Patent ceased