CH531313A - Utilisation de composés carbonylés soufrés comme agents aromatisants - Google Patents
Utilisation de composés carbonylés soufrés comme agents aromatisantsInfo
- Publication number
- CH531313A CH531313A CH1254270A CH1254270A CH531313A CH 531313 A CH531313 A CH 531313A CH 1254270 A CH1254270 A CH 1254270A CH 1254270 A CH1254270 A CH 1254270A CH 531313 A CH531313 A CH 531313A
- Authority
- CH
- Switzerland
- Prior art keywords
- mercapto
- butanone
- pentyl
- ionone
- cyclopentanone
- Prior art date
Links
- -1 Carbonyl mercapto Chemical class 0.000 title description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- NFXLXRBRUPAKLV-UHFFFAOYSA-N C1(=CC=CC=C1)C(CC(C)=O)S Chemical compound C1(=CC=CC=C1)C(CC(C)=O)S NFXLXRBRUPAKLV-UHFFFAOYSA-N 0.000 claims description 5
- QRNZMFDCKKEPSX-UHFFFAOYSA-N 4-mercapto-4-methylpentan-2-one Chemical compound CC(=O)CC(C)(C)S QRNZMFDCKKEPSX-UHFFFAOYSA-N 0.000 claims description 4
- IXHBIDIZIVMXCU-UHFFFAOYSA-N C(C)(=O)SC(CCCC)C1C(CCC1)=O Chemical compound C(C)(=O)SC(CCCC)C1C(CCC1)=O IXHBIDIZIVMXCU-UHFFFAOYSA-N 0.000 claims description 4
- MAPABVGSKHEJQQ-UHFFFAOYSA-N C(C)(=O)SC1(C(C(CC1)=O)CCCCC)C Chemical compound C(C)(=O)SC1(C(C(CC1)=O)CCCCC)C MAPABVGSKHEJQQ-UHFFFAOYSA-N 0.000 claims description 4
- GNHAABKDYGVRCX-UHFFFAOYSA-N S-(3-oxo-1-phenylbutyl) ethanethioate Chemical compound C(C)(=O)SC(CC(C)=O)C1=CC=CC=C1 GNHAABKDYGVRCX-UHFFFAOYSA-N 0.000 claims description 4
- AHGXGVMWRSRBND-UHFFFAOYSA-N SC(CCCC)C1C(CCC1)=O Chemical compound SC(CCCC)C1C(CCC1)=O AHGXGVMWRSRBND-UHFFFAOYSA-N 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 241001465754 Metazoa Species 0.000 claims description 3
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 230000000050 nutritive effect Effects 0.000 claims description 3
- QNNAJQYLCHPCQX-UHFFFAOYSA-N CC(=O)CC(S)C1C(=C)CCCC1(C)C Chemical compound CC(=O)CC(S)C1C(=C)CCCC1(C)C QNNAJQYLCHPCQX-UHFFFAOYSA-N 0.000 claims description 2
- ZFHKWPVUDRXTGJ-UHFFFAOYSA-N CC(=O)CC(S)C1C(C)=CCCC1(C)C Chemical compound CC(=O)CC(S)C1C(C)=CCCC1(C)C ZFHKWPVUDRXTGJ-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 235000013305 food Nutrition 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 241000208125 Nicotiana Species 0.000 claims 1
- 238000005899 aromatization reaction Methods 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract description 10
- 235000019568 aromas Nutrition 0.000 abstract description 5
- 235000013399 edible fruits Nutrition 0.000 abstract description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 3
- 235000013311 vegetables Nutrition 0.000 abstract description 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 abstract 2
- 230000002708 enhancing effect Effects 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 description 8
- 235000020357 syrup Nutrition 0.000 description 8
- 239000006188 syrup Substances 0.000 description 8
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 7
- 239000000796 flavoring agent Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- CFNJLPHOBMVMNS-UHFFFAOYSA-N pentyl butyrate Chemical compound CCCCCOC(=O)CCC CFNJLPHOBMVMNS-UHFFFAOYSA-N 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- WMLUPKZFVOZSAF-UHFFFAOYSA-N 2-pentyl-3-sulfanylcyclopentan-1-one Chemical compound C(CCCC)C1C(CCC1S)=O WMLUPKZFVOZSAF-UHFFFAOYSA-N 0.000 description 3
- ILHZVKAXFCDFMT-UHFFFAOYSA-N 2-pentylcyclopent-2-en-1-one Chemical compound CCCCCC1=CCCC1=O ILHZVKAXFCDFMT-UHFFFAOYSA-N 0.000 description 3
- FAUSKJBKYQFIAE-UHFFFAOYSA-N 3-methyl-2-pentyl-3-sulfanylcyclopentan-1-one Chemical compound CC1(C(C(CC1)=O)CCCCC)S FAUSKJBKYQFIAE-UHFFFAOYSA-N 0.000 description 3
- 240000001890 Ribes hudsonianum Species 0.000 description 3
- 235000016954 Ribes hudsonianum Nutrition 0.000 description 3
- 235000001466 Ribes nigrum Nutrition 0.000 description 3
- WYQYZOQVLQITLB-UHFFFAOYSA-N S-(3-oxo-2-pentylcyclopentyl) ethanethioate Chemical compound C(CCCC)C1C(CCC1SC(C)=O)=O WYQYZOQVLQITLB-UHFFFAOYSA-N 0.000 description 3
- 229930006000 Sucrose Natural products 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical class O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 description 3
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 3
- 235000019634 flavors Nutrition 0.000 description 3
- 235000013355 food flavoring agent Nutrition 0.000 description 3
- 235000021056 liquid food Nutrition 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 235000020374 simple syrup Nutrition 0.000 description 3
- 239000005720 sucrose Substances 0.000 description 3
- 150000003463 sulfur Chemical class 0.000 description 3
- HNAGHMKIPMKKBB-UHFFFAOYSA-N 1-benzylpyrrolidine-3-carboxamide Chemical compound C1C(C(=O)N)CCN1CC1=CC=CC=C1 HNAGHMKIPMKKBB-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- YCIXWYOBMVNGTB-UHFFFAOYSA-N 3-Methyl-2-pentyl-2-cyclopentenone Natural products CCCCCC1=C(C)CCC1=O YCIXWYOBMVNGTB-UHFFFAOYSA-N 0.000 description 2
- BWHOZHOGCMHOBV-UHFFFAOYSA-N Benzalacetone Natural products CC(=O)C=CC1=CC=CC=C1 BWHOZHOGCMHOBV-UHFFFAOYSA-N 0.000 description 2
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 244000061176 Nicotiana tabacum Species 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 229940072049 amyl acetate Drugs 0.000 description 2
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- OBNCKNCVKJNDBV-UHFFFAOYSA-N butanoic acid ethyl ester Natural products CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 229940043350 citral Drugs 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 2
- 229930002839 ionone Natural products 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- KOUKXHPPRFNWPP-UHFFFAOYSA-N pyrazine-2,5-dicarboxylic acid;hydrate Chemical compound O.OC(=O)C1=CN=C(C(O)=O)C=N1 KOUKXHPPRFNWPP-UHFFFAOYSA-N 0.000 description 2
- 150000003573 thiols Chemical class 0.000 description 2
- BWHOZHOGCMHOBV-BQYQJAHWSA-N trans-benzylideneacetone Chemical compound CC(=O)\C=C\C1=CC=CC=C1 BWHOZHOGCMHOBV-BQYQJAHWSA-N 0.000 description 2
- PSQYTAPXSHCGMF-BQYQJAHWSA-N β-ionone Chemical compound CC(=O)\C=C\C1=C(C)CCCC1(C)C PSQYTAPXSHCGMF-BQYQJAHWSA-N 0.000 description 2
- SFEOKXHPFMOVRM-UHFFFAOYSA-N (+)-(S)-gamma-ionone Natural products CC(=O)C=CC1C(=C)CCCC1(C)C SFEOKXHPFMOVRM-UHFFFAOYSA-N 0.000 description 1
- 239000001074 1-methoxy-4-[(E)-prop-1-enyl]benzene Substances 0.000 description 1
- RCSBILYQLVXLJG-UHFFFAOYSA-N 2-Propenyl hexanoate Chemical compound CCCCCC(=O)OCC=C RCSBILYQLVXLJG-UHFFFAOYSA-N 0.000 description 1
- MIDXCONKKJTLDX-UHFFFAOYSA-N 3,5-dimethylcyclopentane-1,2-dione Chemical compound CC1CC(C)C(=O)C1=O MIDXCONKKJTLDX-UHFFFAOYSA-N 0.000 description 1
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
- CIBUHUTVSRPCRO-UHFFFAOYSA-N 4,4'-Thiobis-2-butanone Chemical compound CC(=O)CCSCCC(C)=O CIBUHUTVSRPCRO-UHFFFAOYSA-N 0.000 description 1
- 241000234282 Allium Species 0.000 description 1
- 240000006108 Allium ampeloprasum Species 0.000 description 1
- 235000005254 Allium ampeloprasum Nutrition 0.000 description 1
- 244000144730 Amygdalus persica Species 0.000 description 1
- 235000004936 Bromus mango Nutrition 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- ICMAFTSLXCXHRK-UHFFFAOYSA-N Ethyl pentanoate Chemical compound CCCCC(=O)OCC ICMAFTSLXCXHRK-UHFFFAOYSA-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
- 240000007228 Mangifera indica Species 0.000 description 1
- 235000014826 Mangifera indica Nutrition 0.000 description 1
- 235000006040 Prunus persica var persica Nutrition 0.000 description 1
- 235000011552 Rhamnus crocea Nutrition 0.000 description 1
- 235000009184 Spondias indica Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 241000759263 Ventia crocea Species 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000013736 caramel Nutrition 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000004508 fractional distillation Methods 0.000 description 1
- 235000021022 fresh fruits Nutrition 0.000 description 1
- 229940113087 geraniol Drugs 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 235000020440 raspberry syrup Nutrition 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
Classifications
-
- 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
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/20—Synthetic spices, flavouring agents or condiments
- A23L27/203—Alicyclic compounds
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
- A24B15/32—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by acyclic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Toxicology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Nutrition Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
Claims (1)
- REVENDICATION Utilisation d'au moins un des composés carbonylés soufrés de formule:comportant une double liaison dans l'une des positions indiquées par les pointillés et dans laquelle R représente un atome d'hydrogène ou un groupe acétyle, oudans laquelle R est défini selon I, oudans laquelle Rt représente un atome d'hydrogène ou un groupe méthyle et dans laquelle R est défini selon I, oudans laquelle a) R2 représente un atome d'hydrogène ou un groupe méthyle ou phényle et R3 un atome d'hydrogène ou un groupe méthyle et dans laquelle R4 possède le même sens que R ou b) R2 et R3 représentent chacun un ato me d'hydrogène et R4 un groupecomme agents aromatisants pour l'aromatisation d'aliments solides et liquides pour les hommes et les animaux, de boissons non nutritives ou du tabac.SOUS-REVENDICATION Utilisation suivant la revendication d'au moins un des composés suivants: 1- [2,6,6-triméthyl-2-cyclohexène-1-yl] -1-mercapto-3- butanone ou a-ionone-thiol, 1 [2,6, 6-triméthyl- t -cyclo- hexène-1-yl]-1-mercapto-3-butanone ou ,8-ionone-thiol, 1-[2-méthylène-6,6-diméthyl-cyclohexyl]-1 -mercapto-3 butanone ou Y-ionone-thiol, 5-thio-2,8-nonadione, 4-phényl-4-mercapto-2-butanone, 4-acétylthio-4-phényl-2-butanone, 3 -acétylthio-3-méthyl-2-pentyl-cyclopentanone ou 3-acétylthio-dihydrojasmone, 2-[1-mercaptopentyl]-cyclo- pentanone, 2-[1-acétylthio-pentyl]-cyclopentanone, 2-pen tyl-3-mercaptocyolopentanone 4-méthyl-4-mercapto-2pentanone, et 3 méthyl-3-mercapto-2-pentyl-cyclopenta- none.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH972772A CH531559A (fr) | 1970-08-21 | 1970-08-21 | Utilisation de composés carbonylés soufrés comme agents parfumants |
| CH1254270A CH531313A (fr) | 1970-08-21 | 1970-08-21 | Utilisation de composés carbonylés soufrés comme agents aromatisants |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1254270A CH531313A (fr) | 1970-08-21 | 1970-08-21 | Utilisation de composés carbonylés soufrés comme agents aromatisants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH531313A true CH531313A (fr) | 1972-12-15 |
Family
ID=4384001
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH972772A CH531559A (fr) | 1970-08-21 | 1970-08-21 | Utilisation de composés carbonylés soufrés comme agents parfumants |
| CH1254270A CH531313A (fr) | 1970-08-21 | 1970-08-21 | Utilisation de composés carbonylés soufrés comme agents aromatisants |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH972772A CH531559A (fr) | 1970-08-21 | 1970-08-21 | Utilisation de composés carbonylés soufrés comme agents parfumants |
Country Status (1)
| Country | Link |
|---|---|
| CH (2) | CH531559A (it) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3883572A (en) * | 1971-11-26 | 1975-05-13 | Givaudan Corp | Novel mercaptoderivatives of ionones and irones |
| US3979422A (en) * | 1972-10-17 | 1976-09-07 | Givaudan Corporation | Cycloaliphatic ketones, process for making same and odorant and flavoring compositions containing same |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005521726A (ja) * | 2002-03-27 | 2005-07-21 | チャーターハウス セラピューティックス リミテッド | 医薬化合物における改良 |
-
1970
- 1970-08-21 CH CH972772A patent/CH531559A/fr not_active IP Right Cessation
- 1970-08-21 CH CH1254270A patent/CH531313A/fr not_active IP Right Cessation
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3883572A (en) * | 1971-11-26 | 1975-05-13 | Givaudan Corp | Novel mercaptoderivatives of ionones and irones |
| US3979422A (en) * | 1972-10-17 | 1976-09-07 | Givaudan Corporation | Cycloaliphatic ketones, process for making same and odorant and flavoring compositions containing same |
Also Published As
| Publication number | Publication date |
|---|---|
| CH531559A (fr) | 1972-12-15 |
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