CH635091A5 - Riechstoffmischungen. - Google Patents
Riechstoffmischungen. Download PDFInfo
- Publication number
- CH635091A5 CH635091A5 CH1580077A CH1580077A CH635091A5 CH 635091 A5 CH635091 A5 CH 635091A5 CH 1580077 A CH1580077 A CH 1580077A CH 1580077 A CH1580077 A CH 1580077A CH 635091 A5 CH635091 A5 CH 635091A5
- Authority
- CH
- Switzerland
- Prior art keywords
- valerolactone
- fragrance mixture
- mixture according
- ethyl
- fragrance
- Prior art date
Links
- 239000003205 fragrance Substances 0.000 title claims description 31
- 239000000203 mixture Substances 0.000 title claims description 30
- OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000002304 perfume Substances 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 239000002781 deodorant agent Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 239000002537 cosmetic Substances 0.000 claims description 2
- 239000003599 detergent Substances 0.000 claims description 2
- 239000000344 soap Substances 0.000 claims description 2
- 239000007844 bleaching agent Substances 0.000 claims 1
- 238000009835 boiling Methods 0.000 description 13
- 239000000047 product Substances 0.000 description 13
- 238000002360 preparation method Methods 0.000 description 11
- 239000003921 oil Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- IUDMDIPSJXLOHJ-UHFFFAOYSA-N 4-formyl-4-methylheptanenitrile Chemical compound CCCC(C)(C=O)CCC#N IUDMDIPSJXLOHJ-UHFFFAOYSA-N 0.000 description 3
- -1 e.g. natural oils Chemical class 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- 239000012279 sodium borohydride Substances 0.000 description 3
- 229910000033 sodium borohydride Inorganic materials 0.000 description 3
- UNNGUFMVYQJGTD-UHFFFAOYSA-N 2-Ethylbutanal Chemical compound CCC(CC)C=O UNNGUFMVYQJGTD-UHFFFAOYSA-N 0.000 description 2
- FTZILAQGHINQQR-UHFFFAOYSA-N 2-Methylpentanal Chemical compound CCCC(C)C=O FTZILAQGHINQQR-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 244000272264 Saussurea lappa Species 0.000 description 2
- 235000006784 Saussurea lappa Nutrition 0.000 description 2
- 239000002262 Schiff base Substances 0.000 description 2
- 150000004753 Schiff bases Chemical class 0.000 description 2
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 2
- IPWBXORAIBJDDQ-UHFFFAOYSA-N methyl 2-hexyl-3-oxocyclopentane-1-carboxylate Chemical compound CCCCCCC1C(C(=O)OC)CCC1=O IPWBXORAIBJDDQ-UHFFFAOYSA-N 0.000 description 2
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- GDIYABNICDPBCR-UHFFFAOYSA-N (1-tert-butylcyclohexyl) acetate Chemical compound CC(=O)OC1(C(C)(C)C)CCCCC1 GDIYABNICDPBCR-UHFFFAOYSA-N 0.000 description 1
- 239000001724 (4,8-dimethyl-2-propan-2-ylidene-3,3a,4,5,6,8a-hexahydro-1H-azulen-6-yl) acetate Substances 0.000 description 1
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
- PYLMCYQHBRSDND-VURMDHGXSA-N (Z)-2-ethyl-2-hexenal Chemical compound CCC\C=C(\CC)C=O PYLMCYQHBRSDND-VURMDHGXSA-N 0.000 description 1
- LYGMPIZYNJGJKP-BENRWUELSA-N (e)-2-butyl-2-octenal Chemical compound CCCCC\C=C(C=O)\CCCC LYGMPIZYNJGJKP-BENRWUELSA-N 0.000 description 1
- GADNZGQWPNTMCH-NTMALXAHSA-N (z)-2-propylhept-2-enal Chemical compound CCCC\C=C(C=O)\CCC GADNZGQWPNTMCH-NTMALXAHSA-N 0.000 description 1
- XPUKAXCASLDVTM-UHFFFAOYSA-N 1-(4-hydroxy-4-methylpentyl)cyclohex-3-ene-1-carbaldehyde Chemical compound CC(C)(O)CCCC1(C=O)CCC=CC1 XPUKAXCASLDVTM-UHFFFAOYSA-N 0.000 description 1
- OFHHDSQXFXLTKC-UHFFFAOYSA-N 10-undecenal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- GPWNWKWQOLEVEQ-UHFFFAOYSA-N 2,4-diaminopyrimidine-5-carbaldehyde Chemical compound NC1=NC=C(C=O)C(N)=N1 GPWNWKWQOLEVEQ-UHFFFAOYSA-N 0.000 description 1
- FACFHHMQICTXFZ-UHFFFAOYSA-N 2-(2-phenylimidazo[1,2-a]pyridin-3-yl)ethanamine Chemical compound N1=C2C=CC=CN2C(CCN)=C1C1=CC=CC=C1 FACFHHMQICTXFZ-UHFFFAOYSA-N 0.000 description 1
- XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 description 1
- LGYNIFWIKSEESD-UHFFFAOYSA-N 2-ethylhexanal Chemical compound CCCCC(CC)C=O LGYNIFWIKSEESD-UHFFFAOYSA-N 0.000 description 1
- NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 description 1
- VIIIJFZJKFXOGG-UHFFFAOYSA-N 3-methylchromen-2-one Chemical compound C1=CC=C2OC(=O)C(C)=CC2=C1 VIIIJFZJKFXOGG-UHFFFAOYSA-N 0.000 description 1
- KDELTJKUZFZTCA-UHFFFAOYSA-N 4-butyl-4-formyldec-5-enenitrile Chemical compound CCCCC=CC(CCCC)(CCC#N)C=O KDELTJKUZFZTCA-UHFFFAOYSA-N 0.000 description 1
- GAJPIEOPLIEIOD-UHFFFAOYSA-N 4-formyl-4-propylnon-5-enenitrile Chemical compound CCCC=CC(CCC)(C=O)CCC#N GAJPIEOPLIEIOD-UHFFFAOYSA-N 0.000 description 1
- HQHRSHCAHYFFDC-UHFFFAOYSA-N 5-cyclohex-3-en-1-yl-2-methylpentan-2-ol Chemical compound CC(C)(O)CCCC1CCC=CC1 HQHRSHCAHYFFDC-UHFFFAOYSA-N 0.000 description 1
- ZXGMMHMAGOAFGQ-UHFFFAOYSA-N 6-methyl-3-oxa-13-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2(7),8-trien-4-one Chemical compound C1CCN2CCCC3=C2C1=C1OC(=O)CC(C)C1=C3 ZXGMMHMAGOAFGQ-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 244000144730 Amygdalus persica Species 0.000 description 1
- 241000195940 Bryophyta Species 0.000 description 1
- CVTGBRKVDLHZQL-UHFFFAOYSA-N C1OC(C(C(C)O1)=O)C1=CC=CC=C1 Chemical compound C1OC(C(C(C)O1)=O)C1=CC=CC=C1 CVTGBRKVDLHZQL-UHFFFAOYSA-N 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 239000005770 Eugenol Substances 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
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- UUQHKWMIDYRWHH-UHFFFAOYSA-N Methyl beta-orcinolcarboxylate Chemical compound COC(=O)C1=C(C)C=C(O)C(C)=C1O UUQHKWMIDYRWHH-UHFFFAOYSA-N 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- UAVFEMBKDRODDE-UHFFFAOYSA-N Vetiveryl acetate Chemical compound CC1CC(OC(C)=O)C=C(C)C2CC(=C(C)C)CC12 UAVFEMBKDRODDE-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 230000000172 allergic effect Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- 239000003788 bath preparation Substances 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000010627 cedar oil Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 1
- 235000000484 citronellol Nutrition 0.000 description 1
- 239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- YWVKKYMZIHZCLT-UHFFFAOYSA-N dec-7-en-3-yl acetate Chemical compound CCC=CCCCC(CC)OC(C)=O YWVKKYMZIHZCLT-UHFFFAOYSA-N 0.000 description 1
- XSNQECSCDATQEL-UHFFFAOYSA-N dihydromyrcenol Chemical compound C=CC(C)CCCC(C)(C)O XSNQECSCDATQEL-UHFFFAOYSA-N 0.000 description 1
- 229930008394 dihydromyrcenol Natural products 0.000 description 1
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229940073505 ethyl vanillin Drugs 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229940113087 geraniol Drugs 0.000 description 1
- 239000001927 guaiacum sanctum l. gum oil Substances 0.000 description 1
- 239000003676 hair preparation Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 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
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 229940102398 methyl anthranilate Drugs 0.000 description 1
- YAHNYLGSSPTTAG-UHFFFAOYSA-N methyl n-(3,4-dichlorophenyl)carbamodithioate Chemical compound CSC(=S)NC1=CC=C(Cl)C(Cl)=C1 YAHNYLGSSPTTAG-UHFFFAOYSA-N 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- 229940067137 musk ketone Drugs 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- BOPPSUHPZARXTH-UHFFFAOYSA-N ocean propanal Chemical compound O=CC(C)CC1=CC=C2OCOC2=C1 BOPPSUHPZARXTH-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000013580 sausages Nutrition 0.000 description 1
- 239000001290 saussurea lappa clarke root oil Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D315/00—Heterocyclic compounds containing rings having one oxygen atom as the only ring hetero atom according to more than one of groups C07D303/00 - C07D313/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/008—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing six atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Cosmetics (AREA)
- Fats And Perfumes (AREA)
- Pyrane Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB53707/76A GB1594579A (en) | 1976-12-23 | 1976-12-23 | Perfume compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH635091A5 true CH635091A5 (de) | 1983-03-15 |
Family
ID=10468722
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1580077A CH635091A5 (de) | 1976-12-23 | 1977-12-21 | Riechstoffmischungen. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4288350A (en, 2012) |
| JP (1) | JPS5384975A (en, 2012) |
| AU (1) | AU512313B2 (en, 2012) |
| BE (1) | BE862229A (en, 2012) |
| CA (1) | CA1117425A (en, 2012) |
| CH (1) | CH635091A5 (en, 2012) |
| DE (1) | DE2756772A1 (en, 2012) |
| FR (2) | FR2385394A1 (en, 2012) |
| GB (1) | GB1594579A (en, 2012) |
| IL (1) | IL53666A (en, 2012) |
| IT (1) | IT1089211B (en, 2012) |
| NL (1) | NL186490C (en, 2012) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2818244C2 (de) * | 1978-04-26 | 1986-10-30 | Henkel KGaA, 4000 Düsseldorf | Verwendung der 4,6,6- bzw. 4,4,6-Trimethyltetrahydropyran-2-one als Riechstoffe sowie diese enthaltende Riechstoffkompositionen |
| CH634479A5 (fr) * | 1978-09-29 | 1983-02-15 | Firmenich & Cie | Utilisation de la 6-n-butyl-5,6-dihydro-2h-pyran-2-one en tant qu'agent parfumant. |
| EP0054316A1 (fr) * | 1980-12-09 | 1982-06-23 | Firmenich Sa | Nouveaux composés lactoniques, procédé pour leur préparation et leur utilisation à titre d'ingrédients parfumants ou aromatisants |
| JP5137249B2 (ja) * | 2002-09-27 | 2013-02-06 | 花王株式会社 | 香料組成物 |
| JP4323271B2 (ja) * | 2002-09-27 | 2009-09-02 | 花王株式会社 | バレロラクトン化合物及び香料組成物 |
| FR2873922B1 (fr) * | 2004-08-06 | 2008-10-17 | Mane Fils Sa V | Tetrahydropyran(on)es substitues en beta, leur procede de synthese et leur utilisation en parfumerie |
| EP1847588B1 (de) * | 2006-04-19 | 2009-02-18 | Symrise GmbH & Co. KG | Neue Verwendungen von 4-Methyl-5-hydroxy-hexansäurelacton |
| JP7332563B2 (ja) * | 2020-10-20 | 2023-08-23 | 長谷川香料株式会社 | ラクトン化合物 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE854503C (de) | 1942-10-18 | 1952-11-04 | Basf Ag | Verfahren zur Herstellung von hoehermolekularen Umwandlungs-produkten von Allylverbindungen |
| US2526702A (en) * | 1948-09-20 | 1950-10-24 | Shell Dev | Preparation of lactones |
| US2576901A (en) * | 1950-10-16 | 1951-11-27 | Shell Dev | Preparation of delta-valero-lactones |
| US2680118A (en) * | 1950-12-13 | 1954-06-01 | Monsanto Chemicals | Lactone preparation |
| DE962429C (de) | 1955-04-28 | 1957-04-25 | Basf Ag | Verfahren zur Herstellung von ª€ú¼ ªŠ-ungesaettigten Carbonsaeuren bzw. ihren Abkoemmlingen |
| US3479327A (en) * | 1965-11-19 | 1969-11-18 | Gaf Corp | Polymers of vinyl esters and n-vinyl-3-alkyl-lactams |
| US3531501A (en) * | 1967-10-16 | 1970-09-29 | Int Flavors & Fragrances Inc | Process for the production of unsaturated delta-decalactone |
| US3607885A (en) * | 1968-08-15 | 1971-09-21 | Universal Oil Prod Co | Preparation of lactones such as substituted delta valerolactones |
-
1976
- 1976-12-23 GB GB53707/76A patent/GB1594579A/en not_active Expired
-
1977
- 1977-12-12 CA CA000292868A patent/CA1117425A/en not_active Expired
- 1977-12-20 DE DE19772756772 patent/DE2756772A1/de active Granted
- 1977-12-21 IL IL53666A patent/IL53666A/xx unknown
- 1977-12-21 CH CH1580077A patent/CH635091A5/de not_active IP Right Cessation
- 1977-12-22 IT IT31136/77A patent/IT1089211B/it active
- 1977-12-22 AU AU31880/77A patent/AU512313B2/en not_active Expired
- 1977-12-23 NL NLAANVRAGE7714323,A patent/NL186490C/xx not_active IP Right Cessation
- 1977-12-23 FR FR7738941A patent/FR2385394A1/fr active Granted
- 1977-12-23 JP JP15546477A patent/JPS5384975A/ja active Granted
- 1977-12-23 BE BE2056539A patent/BE862229A/xx not_active IP Right Cessation
-
1978
- 1978-08-07 FR FR7823224A patent/FR2385711A1/fr active Granted
-
1980
- 1980-03-26 US US06/134,010 patent/US4288350A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| GB1594579A (en) | 1981-07-30 |
| IL53666A (en) | 1981-10-30 |
| DE2756772C2 (en, 2012) | 1988-01-21 |
| IL53666A0 (en) | 1978-03-10 |
| FR2385711A1 (fr) | 1978-10-27 |
| NL186490C (nl) | 1990-12-17 |
| NL7714323A (nl) | 1978-06-27 |
| FR2385394A1 (fr) | 1978-10-27 |
| BE862229A (nl) | 1978-06-23 |
| FR2385711B1 (en, 2012) | 1982-11-05 |
| CA1117425A (en) | 1982-02-02 |
| AU3188077A (en) | 1979-06-28 |
| IT1089211B (it) | 1985-06-18 |
| FR2385394B1 (en, 2012) | 1982-11-05 |
| JPS5384975A (en) | 1978-07-26 |
| JPS6310705B2 (en, 2012) | 1988-03-08 |
| DE2756772A1 (de) | 1978-06-29 |
| AU512313B2 (en) | 1980-10-02 |
| US4288350A (en) | 1981-09-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PFA | Name/firm changed |
Owner name: P.F.W. (NEDERLAND) B.V. |
|
| PUE | Assignment |
Owner name: PFW AROMA CHEMICALS B.V. |
|
| PL | Patent ceased |