CH530459A - Riech- und/oder Geschmackstoffkompositionen - Google Patents

Riech- und/oder Geschmackstoffkompositionen

Info

Publication number: CH530459A
Authority: CH; Switzerland
Prior art keywords: composition according; dependent; content; methylthio; formula
Prior art date: 1969-09-10

Application number

CH1687871A

Other languages

German (de)

English (en)

Inventor

Dietmar Dr Lamparsky

Peter Dr Schudel

Original Assignee

Givaudan & Cie Sa

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.)

1969-09-10

Filing date

1969-09-10

Publication date

1972-11-15

1969-09-10 Application filed by Givaudan & Cie Sa filed Critical Givaudan & Cie Sa

1969-09-10 Priority to CH1687871A priority Critical patent/CH530459A/de

1972-11-15 Publication of CH530459A publication Critical patent/CH530459A/de

Links

125000004414 alkyl thio group Chemical group 0.000 title claims abstract description 5
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 10
-1 alkylthio terpenoids Chemical class 0.000 claims abstract description 7
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 7
239000000203 mixture Substances 0.000 claims description 31
150000001875 compounds Chemical class 0.000 claims description 19
229910052739 hydrogen Inorganic materials 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 10
239000000796 flavoring agent Substances 0.000 claims description 8
235000019634 flavors Nutrition 0.000 claims description 8
239000003205 fragrance Substances 0.000 claims description 8
PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
229910052799 carbon Inorganic materials 0.000 claims description 4
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
BVACDZLXQCWKAF-UHFFFAOYSA-N 2-methyl-3-methylsulfanyl-5-prop-1-en-2-ylcyclohexan-1-one Chemical compound CSC1CC(C(C)=C)CC(=O)C1C BVACDZLXQCWKAF-UHFFFAOYSA-N 0.000 claims description 3
230000001419 dependent effect Effects 0.000 claims 17
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 4
BQQWJKHFPSNFLB-UHFFFAOYSA-N 3,7-dimethyl-3-methylsulfanyloct-6-enal Chemical compound O=CCC(C)(SC)CCC=C(C)C BQQWJKHFPSNFLB-UHFFFAOYSA-N 0.000 claims 1
YDBPGXCMNSBEHK-UHFFFAOYSA-N 4,7,7-trimethyl-3-methylsulfanylbicyclo[4.1.0]heptan-5-one Chemical compound O=C1C(C)C(SC)CC2C(C)(C)C12 YDBPGXCMNSBEHK-UHFFFAOYSA-N 0.000 claims 1
HJFSNLWDUINFTB-UHFFFAOYSA-N 5-methyl-2-(2-methylsulfanylpropan-2-yl)cyclohexan-1-one Chemical compound CSC(C)(C)C1CCC(C)CC1=O HJFSNLWDUINFTB-UHFFFAOYSA-N 0.000 claims 1
KYJOFNFLQSJNHO-UHFFFAOYSA-N 5-methyl-5-methylsulfanyl-2-propan-2-ylcyclohexan-1-one Chemical compound CSC1(C)CCC(C(C)C)C(=O)C1 KYJOFNFLQSJNHO-UHFFFAOYSA-N 0.000 claims 1
239000002537 cosmetic Substances 0.000 abstract description 2
239000003599 detergent Substances 0.000 abstract description 2
239000002304 perfume Substances 0.000 abstract description 2
IPZJQDSFZGZEOY-UHFFFAOYSA-N dimethylmethylene Chemical group C[C]C IPZJQDSFZGZEOY-UHFFFAOYSA-N 0.000 abstract 3
RMIANEGNSBUGDJ-UHFFFAOYSA-N Isopulegone Chemical compound CC1CCC(C(C)=C)C(=O)C1 RMIANEGNSBUGDJ-UHFFFAOYSA-N 0.000 abstract 2
229930007459 p-menth-8-en-3-one Natural products 0.000 abstract 2
CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 abstract 2
NZGWDASTMWDZIW-MRVPVSSYSA-N (+)-pulegone Chemical compound C[C@@H]1CCC(=C(C)C)C(=O)C1 NZGWDASTMWDZIW-MRVPVSSYSA-N 0.000 abstract 1
NZGWDASTMWDZIW-UHFFFAOYSA-N Pulegone Natural products CC1CCC(=C(C)C)C(=O)C1 NZGWDASTMWDZIW-UHFFFAOYSA-N 0.000 abstract 1
USMNOWBWPHYOEA-UHFFFAOYSA-N alpha-thujone Natural products CC1C(=O)CC2(C(C)C)C1C2 USMNOWBWPHYOEA-UHFFFAOYSA-N 0.000 abstract 1
125000003118 aryl group Chemical group 0.000 abstract 1
229930004008 p-menthane Natural products 0.000 abstract 1
FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 8
235000014347 soups Nutrition 0.000 description 6
235000013305 food Nutrition 0.000 description 5
239000000047 product Substances 0.000 description 5
KSEZPRJUTHMFGZ-UHFFFAOYSA-N 1-(3-ethyl-5,5,8,8-tetramethyl-6,7-dihydronaphthalen-2-yl)ethanone Chemical compound CC1(C)CCC(C)(C)C2=C1C=C(C(C)=O)C(CC)=C2 KSEZPRJUTHMFGZ-UHFFFAOYSA-N 0.000 description 4
ZITBETUVISHUJS-UHFFFAOYSA-N 2-methyl-5-prop-1-en-2-yl-3-sulfanylcyclohexan-1-one Chemical compound CC1C(S)CC(C(C)=C)CC1=O ZITBETUVISHUJS-UHFFFAOYSA-N 0.000 description 4
UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 4
150000003505 terpenes Chemical class 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
235000013575 mashed potatoes Nutrition 0.000 description 3
240000006108 Allium ampeloprasum Species 0.000 description 2
235000005254 Allium ampeloprasum Nutrition 0.000 description 2
244000291564 Allium cepa Species 0.000 description 2
235000002732 Allium cepa var. cepa Nutrition 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
235000021028 berry Nutrition 0.000 description 2
235000013361 beverage Nutrition 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
BWRHOYDPVJPXMF-UHFFFAOYSA-N carane Chemical compound C1C(C)CCC2C(C)(C)C12 BWRHOYDPVJPXMF-UHFFFAOYSA-N 0.000 description 2
235000009508 confectionery Nutrition 0.000 description 2
ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
238000009792 diffusion process Methods 0.000 description 2
239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 2
CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
WTEVQBCEXWBHNA-YFHOEESVSA-N neral Chemical compound CC(C)=CCC\C(C)=C/C=O WTEVQBCEXWBHNA-YFHOEESVSA-N 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
239000003921 oil Substances 0.000 description 2
235000019198 oils Nutrition 0.000 description 2
XOKSLPVRUOBDEW-UHFFFAOYSA-N pinane Chemical compound CC1CCC2C(C)(C)C1C2 XOKSLPVRUOBDEW-UHFFFAOYSA-N 0.000 description 2
GCTNBVHDRFKLLK-UHFFFAOYSA-N thujane Chemical compound CC1CCC2(C(C)C)C1C2 GCTNBVHDRFKLLK-UHFFFAOYSA-N 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
FQTLCLSUCSAZDY-UHFFFAOYSA-N (+) E(S) nerolidol Natural products CC(C)=CCCC(C)=CCCC(C)(O)C=C FQTLCLSUCSAZDY-UHFFFAOYSA-N 0.000 description 1
239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 1
QQLIGMASAVJVON-UHFFFAOYSA-N 1-naphthalen-1-ylethanone Chemical compound C1=CC=C2C(C(=O)C)=CC=CC2=C1 QQLIGMASAVJVON-UHFFFAOYSA-N 0.000 description 1
OFHHDSQXFXLTKC-UHFFFAOYSA-N 10-undecenal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 description 1
MBZRJSQZCBXRGK-UHFFFAOYSA-N 4-tert-Butylcyclohexyl acetate Chemical compound CC(=O)OC1CCC(C(C)(C)C)CC1 MBZRJSQZCBXRGK-UHFFFAOYSA-N 0.000 description 1
240000003291 Armoracia rusticana Species 0.000 description 1
235000011330 Armoracia rusticana Nutrition 0.000 description 1
244000223760 Cinnamomum zeylanicum Species 0.000 description 1
WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
229920002261 Corn starch Polymers 0.000 description 1
108010082495 Dietary Plant Proteins Proteins 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
244000178870 Lavandula angustifolia Species 0.000 description 1
235000010663 Lavandula angustifolia Nutrition 0.000 description 1
235000019501 Lemon oil Nutrition 0.000 description 1
FQTLCLSUCSAZDY-ATGUSINASA-N Nerolidol Chemical compound CC(C)=CCC\C(C)=C\CC[C@](C)(O)C=C FQTLCLSUCSAZDY-ATGUSINASA-N 0.000 description 1
235000019502 Orange oil Nutrition 0.000 description 1
108091006629 SLC13A2 Proteins 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
125000002015 acyclic group Chemical group 0.000 description 1
229930003651 acyclic monoterpene Natural products 0.000 description 1
150000002841 acyclic monoterpene derivatives Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
125000002619 bicyclic group Chemical group 0.000 description 1
229930003642 bicyclic monoterpene Chemical class 0.000 description 1
150000001604 bicyclic monoterpene derivatives Chemical class 0.000 description 1
229930006741 carane Natural products 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
235000017803 cinnamon Nutrition 0.000 description 1
229940043350 citral Drugs 0.000 description 1
239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 description 1
239000001524 citrus aurantium oil Substances 0.000 description 1
239000008120 corn starch Substances 0.000 description 1
229960000956 coumarin Drugs 0.000 description 1
235000001671 coumarin Nutrition 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
PXEDJBXQKAGXNJ-QTNFYWBSSA-L disodium L-glutamate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](N)CCC([O-])=O PXEDJBXQKAGXNJ-QTNFYWBSSA-L 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000001102 lavandula vera Substances 0.000 description 1
235000018219 lavender Nutrition 0.000 description 1
239000010501 lemon oil Substances 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
229930007744 linalool Natural products 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000001525 mentha piperita l. herb oil Substances 0.000 description 1
235000020124 milk-based beverage Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
125000002950 monocyclic group Chemical group 0.000 description 1
229930003647 monocyclic monoterpene Chemical class 0.000 description 1
150000002767 monocyclic monoterpene derivatives Chemical class 0.000 description 1
235000013923 monosodium glutamate Nutrition 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 description 1
239000010502 orange oil Substances 0.000 description 1
235000019477 peppermint oil Nutrition 0.000 description 1
239000012437 perfumed product Substances 0.000 description 1
229930006728 pinane Natural products 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
235000011888 snacks Nutrition 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
229940073490 sodium glutamate Drugs 0.000 description 1
239000007787 solid Substances 0.000 description 1
235000013599 spices Nutrition 0.000 description 1
239000000271 synthetic detergent Substances 0.000 description 1
229940116411 terpineol Drugs 0.000 description 1
235000013618 yogurt 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
- C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
- 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
- A23L27/202—Aliphatic compounds
- A23L27/2022—Aliphatic compounds containing sulfur
- 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/22—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and doubly-bound oxygen atoms bound to the same carbon skeleton
- 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
- C11B9/0007—Aliphatic compounds
- C11B9/0011—Aliphatic compounds containing S
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/14—All rings being cycloaliphatic
- C07C2602/20—All rings being cycloaliphatic the ring system containing seven carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
- C07C2602/42—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Food Science & Technology (AREA)
Polymers & Plastics (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Nutrition Science (AREA)
Fats And Perfumes (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Cosmetics (AREA)
Seasonings (AREA)
Seeds, Soups, And Other Foods (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

CH1687871A 1969-09-10 1969-09-10 Riech- und/oder Geschmackstoffkompositionen CH530459A (de)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CH1687871A CH530459A (de)	1969-09-10	1969-09-10	Riech- und/oder Geschmackstoffkompositionen

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH1687871A CH530459A (de)	1969-09-10	1969-09-10	Riech- und/oder Geschmackstoffkompositionen
CH1374869A CH525198A (de)	1969-09-10	1969-09-10	Verfahren zur Herstellung von neuen mercapto- oder alkylthio-substituierten Terpenoiden

Publications (1)

Publication Number	Publication Date
CH530459A true CH530459A (de)	1972-11-15

Family

ID=4394953

Family Applications (3)

Application Number	Title	Priority Date	Filing Date
CH1687871A CH530459A (de)	1969-09-10	1969-09-10	Riech- und/oder Geschmackstoffkompositionen
CH1331170A CH524581A (de)	1969-09-10	1969-09-10	Verfahren zur Herstellung eines mercapto-substituierten Terpenoids
CH1374869A CH525198A (de)	1969-09-10	1969-09-10	Verfahren zur Herstellung von neuen mercapto- oder alkylthio-substituierten Terpenoiden

Family Applications After (2)

Application Number	Title	Priority Date	Filing Date
CH1331170A CH524581A (de)	1969-09-10	1969-09-10	Verfahren zur Herstellung eines mercapto-substituierten Terpenoids
CH1374869A CH525198A (de)	1969-09-10	1969-09-10	Verfahren zur Herstellung von neuen mercapto- oder alkylthio-substituierten Terpenoiden

Country Status (18)

Country	Link
US (2)	US3819712A (2)
JP (3)	JPS5231862B1 (2)
AT (2)	AT308283B (2)
AU (1)	AU1944870A (2)
BE (2)	BE755503A (2)
CA (2)	CA991084A (2)
CH (3)	CH530459A (2)
DE (2)	DE2043341C3 (2)
ES (2)	ES383475A1 (2)
FR (2)	FR2061637B1 (2)
GB (2)	GB1323167A (2)
GT (1)	GT197122379A (2)
IL (1)	IL35166A (2)
IT (2)	IT1050116B (2)
NL (2)	NL7012644A (2)
SE (1)	SE391728B (2)
SU (1)	SU379087A3 (2)
ZA (2)	ZA705808B (2)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3914316A (en) *	1972-12-29	1975-10-21	Dow Chemical Co	Preparation of 2-(sulfur-substituted)-3-hydroxy-5,5-dimethyl-2-cyclohexen-1-ones
US4024289A (en) *	1976-09-15	1977-05-17	International Flavors & Fragrances Inc.	Flavoring with α-oxy(oxo)mercaptans
US4044164A (en) *	1976-10-07	1977-08-23	International Flavors & Fragrances Inc.	Uses of α-oxy(oxo) sulfides and ethers in foodstuffs and flavors for foodstuffs
US4045491A (en) *	1976-10-07	1977-08-30	International Flavors & Fragrances Inc.	α-Oxy(oxo) sulfides and ethers
US4053654A (en) *	1976-10-07	1977-10-11	International Flavors & Fragrances Inc.	Uses of α-oxy(oxo) sulfides and ethers in foodstuffs and flavors for foodstuffs
US4055691A (en) *	1976-10-07	1977-10-25	International Flavors & Fragrances Inc.	Uses of α-oxy(oxo) sulfides and ethers in foodstuffs and flavors for foodstuffs
US4053655A (en) *	1976-10-07	1977-10-11	International Flavors & Fragrances Inc.	Uses of α-oxy(oxo) sulfides and ethers in foodstuffs and flavors for foodstuffs
US4502985A (en) *	1982-07-21	1985-03-05	Dragoco Gerberding & Co. Gmbh	Use of 1,5-dimethyl-8-hydroximino-bicyclo[3.2.1]octane as perfuming ingredient
JPS5949339U (ja) *	1982-09-27	1984-04-02	三菱電機株式会社	フロ−スイツチ
NL8700240A (nl) *	1987-01-30	1988-08-16	Tno	Werkwijze voor het bereiden van thiolverbindingen.
US5578470A (en) *	1987-01-30	1996-11-26	Nederlandse Organisatie Voor Toegepast	Method for preparing thiol compounds with bacterial β-lyase
ES2312635T3 (es) *	2001-12-13	2009-03-01	Firmenich Sa	Compuestos para una liberacion controlada de moleculas activas.
DE102009026698A1 (de) *	2009-06-03	2010-12-09	Symrise Gmbh & Co. Kg	Verwendung bestimmter Isopropylmethylcyclohexenthiole als Riech- und/oder Aromastoffe
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DE102013226216A1 (de) *	2013-12-17	2015-06-18	Henkel Ag & Co. Kgaa	Michael-Systeme für die Duftstoff-Stabilisierung
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1969
- 1969-09-10 CH CH1687871A patent/CH530459A/de not_active IP Right Cessation
- 1969-09-10 CH CH1331170A patent/CH524581A/de not_active IP Right Cessation
- 1969-09-10 CH CH1374869A patent/CH525198A/de not_active IP Right Cessation
1970
- 1970-08-24 ZA ZA705808A patent/ZA705808B/xx unknown
- 1970-08-24 ZA ZA705807A patent/ZA705807B/xx unknown
- 1970-08-25 IL IL35166A patent/IL35166A/xx unknown
- 1970-08-26 NL NL7012644A patent/NL7012644A/xx unknown
- 1970-08-26 NL NL7012643A patent/NL7012643A/xx unknown
- 1970-08-31 BE BE755503A patent/BE755503A/xx not_active IP Right Cessation
- 1970-08-31 BE BE755504D patent/BE755504A/xx unknown
- 1970-09-01 DE DE2043341A patent/DE2043341C3/de not_active Expired
- 1970-09-01 DE DE2043366A patent/DE2043366C2/de not_active Expired
- 1970-09-02 AU AU19448/70A patent/AU1944870A/en not_active Expired
- 1970-09-03 US US00069457A patent/US3819712A/en not_active Expired - Lifetime
- 1970-09-08 GB GB4288670A patent/GB1323167A/en not_active Expired
- 1970-09-08 GB GB4288770A patent/GB1323467A/en not_active Expired
- 1970-09-09 FR FR707032707A patent/FR2061637B1/fr not_active Expired
- 1970-09-09 ES ES383475A patent/ES383475A1/es not_active Expired
- 1970-09-09 FR FR7032708A patent/FR2061158A5/fr not_active Expired
- 1970-09-09 SU SU1482987A patent/SU379087A3/ru active
- 1970-09-09 AT AT816470A patent/AT308283B/de active
- 1970-09-09 SE SE7317031A patent/SE391728B/xx unknown
- 1970-09-09 ES ES383474A patent/ES383474A1/es not_active Expired
- 1970-09-09 CA CA092,642A patent/CA991084A/en not_active Expired
- 1970-09-09 AT AT155172A patent/AT311324B/de not_active IP Right Cessation
- 1970-09-10 CA CA092,755A patent/CA1040654A/en not_active Expired
- 1970-09-10 JP JP45079630A patent/JPS5231862B1/ja active Pending
- 1970-09-10 IT IT29592/70A patent/IT1050116B/it active
- 1970-09-10 IT IT29591/70A patent/IT1034017B/it active
- 1970-09-10 JP JP45079631A patent/JPS5031144B1/ja active Pending
1971
- 1971-11-05 GT GT197122379A patent/GT197122379A/es unknown
1973
- 1973-08-21 JP JP48093789A patent/JPS519015B1/ja active Pending
1975
- 1975-04-17 US US05/569,120 patent/US3974222A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
GT197122379A (es)	1973-04-28
BE755504A (fr)	1971-03-01
ZA705807B (en)	1971-04-28
DE2043341C3 (de)	1981-10-15
GB1323467A (en)	1973-07-18
ES383474A1 (es)	1973-02-16
JPS5031144B1 (2)	1975-10-07
US3974222A (en)	1976-08-10
IL35166A0 (en)	1970-10-30
FR2061158A5 (2)	1971-06-18
FR2061637B1 (2)	1973-01-12
SE391728B (sv)	1977-02-28
AT311324B (de)	1973-11-12
DE2043341A1 (de)	1971-03-11
DE2043341B2 (de)	1980-11-20
IT1050116B (it)	1981-03-10
ES383475A1 (es)	1973-02-16
SU379087A3 (2)	1973-04-18
CA1040654A (en)	1978-10-17
NL7012643A (2)	1971-03-12
AT308283B (de)	1973-06-25
CH525198A (de)	1972-07-15
DE2043366A1 (de)	1971-03-11
ZA705808B (en)	1971-04-28
CH524581A (de)	1972-06-30
CA991084A (en)	1976-06-15
IT1034017B (it)	1979-09-10
FR2061637A1 (2)	1971-06-25
AU1944870A (en)	1972-03-09
US3819712A (en)	1974-06-25
DE2043366C2 (de)	1983-12-29
NL7012644A (2)	1971-03-12
GB1323167A (en)	1973-07-11
JPS5231862B1 (2)	1977-08-17
IL35166A (en)	1973-06-29
JPS519015B1 (2)	1976-03-23
BE755503A (fr)	1971-03-01

Legal Events

Date	Code	Title	Description
1989-11-30	PL	Patent ceased

Publication	Publication Date	Title
CH530459A (de)	1972-11-15	Riech- und/oder Geschmackstoffkompositionen
DE2427609C3 (de)	1984-02-02	4-Isopropenylcyclohexyl-methylester bzw. -methyläther und 4-Isopropylcyclohexyl-methylester bzw.-methyläther sowie die Verwendung dieser Verbindungen als Riechstoff bzw. Riechstoffkomponente und als Geschmacksstoffe oder Geschmacksstoffzusätze
DE3307869A1 (de)	1984-09-06	Methylsubstituierte 1-((3-methylthio)-1-oxo-butyl)-cyclohex-2-ene, verfahren zu deren herstellung und deren verwendung als riech- und aromastoffe
DE1807568C3 (de)	1982-05-13	Cycloaliphatische ungesättigte Ketone, Verfahren zu deren Herstellung und deren Verwendung als Riech- und Geschmacksstoffe
DE2405568B2 (de)	1977-06-16	Cycloaliphatische verbindungen und deren verwendung als riech- und geschmacksstoffe
DE2752787A1 (de)	1978-05-24	Substituierte cyclohexanone als riech- und geschmacksstoffe
DE2540624A1 (de)	1976-04-08	Wuerz- und aromastoff
DE2350178A1 (de)	1974-04-25	Neue cycloaliphatische ketone
DE2159924C3 (de)	1978-10-12	Jonon- und Ironderivate, Verfahren zu ihrer Herstellung und Riech- und/oder Geschmackstoffkompositionen
EP0041122B1 (de)	1985-07-17	Di- und Tetrahydrobenzofuranonderivate enthaltende Riechstoffkompositionen
DE2443191C3 (de)	1980-01-10	Verwendung von Bicycle- [2,2,2] -oetanderivaten als Parfümierungs- und Aromatisierungsmittel
DE2951508C2 (de)	1982-12-30	Methoxy- und Aethoxy-1,4,8-trimethyl-cyclododeca-4,8-diene, Verfahren zu ihrer Herstellung und sie enthaltende Parfüm- und Aromakompositionen
DE60107317T2 (de)	2005-11-10	Organoleptische Zusammensetzung
DE2721002C3 (de)	1980-04-30	Cyclopentanonderivate und diese enthaltende Riechstoff- und Geschmacksstoffkompositionen
DE2840823A1 (de)	1979-05-17	Trans, trans- delta -damascon und dessen verwendung als wuerzstoff
EP0684299B1 (de)	2000-11-22	Dihydrofarnesal
DE2559751C2 (de)	1980-11-20	Verwendung einer Spiranverbindung als Riech- bzw. Aromastoff
DE69024650T3 (de)	2004-03-04	Aroma-Zusammensetzung enthaltende Gamma-Jasmolactone, die Verwendung solch einer Aromazusammensetzung oder Gamma-lactone für die Aromatisierung von Nahrungsmitteln, und die aromatisierte Nahrungsmitteln
US3896175A (en)	1975-07-22	3,7-dimethyl-octa-2,6-dienyl-mercaptan
DE2700688B2 (de)	1979-12-06	Carbonylverbindungen, Verfahren zu deren Herstellung sowie deren Verwendung als Würzstoff für Nahrungsmittel, Getränke, Tabak und/oder Parfümerieartikel
DE2455975A1 (de)	1975-07-10	Verwendung von neuen acetalen als riech- und geschmacksstoffe
DE2242464A1 (de)	1973-03-15	Neuer riech- und/oder aromastoff
DE2351057C2 (de)	1982-06-09	2,5,5-Trimethyl-hepta-2,6-dienal und seine niederen Alkylacetate, deren Herstellung und deren Verwendung
EP0215799B1 (de)	1988-08-24	Tricyclo [5.2.1.0/2,6] decan/decen-derivate mit funktionalisierter alkyliden-seitenkette und deren verwendung als riechstoffe
DE2347454C2 (de)	1982-07-15	Verfahren zur Herstellung von Geschmacksstoffkompositionen