NL8302893A - Parfumcomposities en geparfumeerde produkten die ten minste een of meer esters van 2-ethyl-2-methyl-butaanzuur als parfumgrondstof bevatten. - Google Patents

Parfumcomposities en geparfumeerde produkten die ten minste een of meer esters van 2-ethyl-2-methyl-butaanzuur als parfumgrondstof bevatten. Download PDF

Info

Publication number: NL8302893A
Authority: NL; Netherlands
Prior art keywords: ethyl; methyl; esters; perfume; butanoic acid
Prior art date: 1983-08-17

Application number

NL8302893A

Other languages

English (en)

Dutch (nl)

Original Assignee

Naarden International Nv

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1983-08-17

Filing date

1983-08-17

Publication date

1985-03-18

1983-08-17 Application filed by Naarden International Nv filed Critical Naarden International Nv

1983-08-17 Priority to NL8302893A priority Critical patent/NL8302893A/nl

1984-08-14 Priority to EP84201183A priority patent/EP0134613A1/en

1984-08-16 Priority to JP17008484A priority patent/JPS6067445A/ja

1985-03-18 Publication of NL8302893A publication Critical patent/NL8302893A/nl

Links

239000000203 mixture Substances 0.000 title claims description 30
239000002304 perfume Substances 0.000 title claims description 25
LHJPKLWGGMAUAN-UHFFFAOYSA-N 2-ethyl-2-methyl-butanoic acid Chemical compound CCC(C)(CC)C(O)=O LHJPKLWGGMAUAN-UHFFFAOYSA-N 0.000 title claims description 14
239000012437 perfumed product Substances 0.000 title claims description 4
150000002148 esters Chemical class 0.000 claims description 14
125000004432 carbon atom Chemical group C* 0.000 claims description 5
125000004494 ethyl ester group Chemical group 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
125000003342 alkenyl group Chemical group 0.000 claims description 3
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
125000003710 aryl alkyl group Chemical group 0.000 claims description 3
125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 2
239000003205 fragrance Substances 0.000 description 22
150000001875 compounds Chemical class 0.000 description 11
-1 essential oils Natural products 0.000 description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
238000002360 preparation method Methods 0.000 description 5
241000402754 Erythranthe moschata Species 0.000 description 4
IGODOXYLBBXFDW-UHFFFAOYSA-N alpha-Terpinyl acetate Chemical compound CC(=O)OC(C)(C)C1CCC(C)=CC1 IGODOXYLBBXFDW-UHFFFAOYSA-N 0.000 description 4
QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 4
RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-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
239000003921 oil Substances 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
235000019645 odor Nutrition 0.000 description 3
239000002994 raw material Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
BJLRAKFWOUAROE-UHFFFAOYSA-N 2500-83-6 Chemical compound C12C=CCC2C2CC(OC(=O)C)C1C2 BJLRAKFWOUAROE-UHFFFAOYSA-N 0.000 description 2
ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 2
NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 2
235000014493 Crataegus Nutrition 0.000 description 2
241001092040 Crataegus Species 0.000 description 2
239000005770 Eugenol Substances 0.000 description 2
GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
235000012308 Tagetes Nutrition 0.000 description 2
241000736851 Tagetes Species 0.000 description 2
KGEKLUUHTZCSIP-HOSYDEDBSA-N [(1s,4s,6r)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Chemical compound C1C[C@]2(C)[C@H](OC(=O)C)C[C@H]1C2(C)C KGEKLUUHTZCSIP-HOSYDEDBSA-N 0.000 description 2
229940007550 benzyl acetate Drugs 0.000 description 2
SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 2
QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 2
XSNQECSCDATQEL-UHFFFAOYSA-N dihydromyrcenol Chemical compound C=CC(C)CCCC(C)(C)O XSNQECSCDATQEL-UHFFFAOYSA-N 0.000 description 2
229930008394 dihydromyrcenol Natural products 0.000 description 2
HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 2
239000001813 ethyl (2R)-2-methylbutanoate Substances 0.000 description 2
229940090910 ethyl 2-methylbutyrate Drugs 0.000 description 2
229960002217 eugenol Drugs 0.000 description 2
150000002576 ketones Chemical class 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
229930014626 natural product Natural products 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
MDHYEMXUFSJLGV-UHFFFAOYSA-N phenethyl acetate Chemical compound CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 description 2
238000010992 reflux Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 2
BGEHHAVMRVXCGR-UHFFFAOYSA-N tridecanal Chemical compound CCCCCCCCCCCCC=O BGEHHAVMRVXCGR-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
HLCSDJLATUNSSI-JXMROGBWSA-N (2e)-3,7-dimethylocta-2,6-dienenitrile Chemical compound CC(C)=CCC\C(C)=C\C#N HLCSDJLATUNSSI-JXMROGBWSA-N 0.000 description 1
239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
VCOCESNMLNDPLX-BTXGZQJSSA-N (3s,6s)-2,2,8,8-tetramethyl-octahydro-1h-2,4a-methanonapthalene-10-one Chemical compound O=C1CCC(C)(C)[C@@]2(C3)C1C(C)(C)[C@H]3CC2 VCOCESNMLNDPLX-BTXGZQJSSA-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
CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 1
QUMXDOLUJCHOAY-UHFFFAOYSA-N 1-Phenylethyl acetate Chemical compound CC(=O)OC(C)C1=CC=CC=C1 QUMXDOLUJCHOAY-UHFFFAOYSA-N 0.000 description 1
239000001875 1-phenylethyl acetate Substances 0.000 description 1
ZTNFZIHZMITMGE-UHFFFAOYSA-N 2,6-dimethylcyclohex-2-ene-1-carbaldehyde Chemical compound CC1CCC=C(C)C1C=O ZTNFZIHZMITMGE-UHFFFAOYSA-N 0.000 description 1
BEARMGATPGLSKG-UHFFFAOYSA-N 2,6-dimethyloct-7-en-2-yl acetate Chemical compound C=CC(C)CCCC(C)(C)OC(C)=O BEARMGATPGLSKG-UHFFFAOYSA-N 0.000 description 1
WRFXXJKURVTLSY-UHFFFAOYSA-N 2,6-dimethyloctan-2-ol Chemical compound CCC(C)CCCC(C)(C)O WRFXXJKURVTLSY-UHFFFAOYSA-N 0.000 description 1
ROKSAUSPJGWCSM-UHFFFAOYSA-N 2-(7,7-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)ethanol Chemical compound C1C2C(C)(C)C1CC=C2CCO ROKSAUSPJGWCSM-UHFFFAOYSA-N 0.000 description 1
FLUWAIIVLCVEKF-UHFFFAOYSA-N 2-Methyl-1-phenyl-2-propanyl acetate Chemical compound CC(=O)OC(C)(C)CC1=CC=CC=C1 FLUWAIIVLCVEKF-UHFFFAOYSA-N 0.000 description 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
QUBNQDBPPTZYJL-UHFFFAOYSA-N 2-butyl-4,4,6-trimethyl-1,3-dioxane Chemical compound CCCCC1OC(C)CC(C)(C)O1 QUBNQDBPPTZYJL-UHFFFAOYSA-N 0.000 description 1
PJXHBTZLHITWFX-UHFFFAOYSA-N 2-heptylcyclopentan-1-one Chemical compound CCCCCCCC1CCCC1=O PJXHBTZLHITWFX-UHFFFAOYSA-N 0.000 description 1
TVNMPNXDTXVZKV-UHFFFAOYSA-N 2-methylpropyl 2-ethyl-2-methylbutanoate Chemical compound CCC(C)(CC)C(=O)OCC(C)C TVNMPNXDTXVZKV-UHFFFAOYSA-N 0.000 description 1
GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 description 1
YCIXWYOBMVNGTB-UHFFFAOYSA-N 3-Methyl-2-pentyl-2-cyclopentenone Natural products CCCCCC1=C(C)CCC1=O YCIXWYOBMVNGTB-UHFFFAOYSA-N 0.000 description 1
HTLBMZKXJYNJSK-UHFFFAOYSA-N 3-naphthalen-2-yl-1,2-oxazol-5-amine Chemical compound O1C(N)=CC(C=2C=C3C=CC=CC3=CC=2)=N1 HTLBMZKXJYNJSK-UHFFFAOYSA-N 0.000 description 1
INIOTLARNNSXAE-UHFFFAOYSA-N 4,8-dimethyl-2-propan-2-ylidene-3,3a,4,5,6,8a-hexahydro-1h-azulen-6-ol Chemical compound CC1CC(O)C=C(C)C2CC(=C(C)C)CC12 INIOTLARNNSXAE-UHFFFAOYSA-N 0.000 description 1
MQBIZQLCHSZBOI-UHFFFAOYSA-N 4-(4-Methyl-3-pentenyl)-3-cyclohexene-1-carboxaldehyde Chemical compound CC(C)=CCCC1=CCC(C=O)CC1 MQBIZQLCHSZBOI-UHFFFAOYSA-N 0.000 description 1
ZQJZZXUXSPBKPE-UHFFFAOYSA-N 4-pentan-3-yloxane Chemical compound CCC(CC)C1CCOCC1 ZQJZZXUXSPBKPE-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
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
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
240000007436 Cananga odorata Species 0.000 description 1
NPOJQCVWMSKXDN-UHFFFAOYSA-N Dacthal Chemical compound COC(=O)C1=C(Cl)C(Cl)=C(C(=O)OC)C(Cl)=C1Cl NPOJQCVWMSKXDN-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
235000018958 Gardenia augusta Nutrition 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
235000019502 Orange oil Nutrition 0.000 description 1
241000896103 Pinus sibirica Species 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
YMOONIIMQBGTDU-VOTSOKGWSA-N [(e)-2-bromoethenyl]benzene Chemical compound Br\C=C\C1=CC=CC=C1 YMOONIIMQBGTDU-VOTSOKGWSA-N 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
229940022663 acetate Drugs 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000002386 air freshener Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
150000007824 aliphatic compounds Chemical class 0.000 description 1
UZFLPKAIBPNNCA-BQYQJAHWSA-N alpha-ionone Chemical compound CC(=O)\C=C\C1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-BQYQJAHWSA-N 0.000 description 1
UZFLPKAIBPNNCA-UHFFFAOYSA-N alpha-ionone Natural products CC(=O)C=CC1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-UHFFFAOYSA-N 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
229940062909 amyl salicylate Drugs 0.000 description 1
230000001166 anti-perspirative effect Effects 0.000 description 1
239000003213 antiperspirant Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000003788 bath preparation Substances 0.000 description 1
KVOPHPAPHNEQLH-UHFFFAOYSA-N benzyl 2-ethyl-2-methylbutanoate Chemical compound CCC(C)(CC)C(=O)OCC1=CC=CC=C1 KVOPHPAPHNEQLH-UHFFFAOYSA-N 0.000 description 1
229960002903 benzyl benzoate Drugs 0.000 description 1
JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
229940115397 bornyl acetate Drugs 0.000 description 1
FZJUFJKVIYFBSY-UHFFFAOYSA-N bourgeonal Chemical compound CC(C)(C)C1=CC=C(CCC=O)C=C1 FZJUFJKVIYFBSY-UHFFFAOYSA-N 0.000 description 1
150000001717 carbocyclic compounds Chemical class 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
235000000484 citronellol Nutrition 0.000 description 1
239000004567 concrete Substances 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
239000006071 cream Substances 0.000 description 1
QSXOMHOVPSVYLB-UHFFFAOYSA-N cyclohexyl 2-ethyl-2-methylbutanoate Chemical compound CCC(C)(CC)C(=O)OC1CCCCC1 QSXOMHOVPSVYLB-UHFFFAOYSA-N 0.000 description 1
BYLXLDKSNAVZTP-UHFFFAOYSA-N dec-9-en-1-ol;1-phenoxyethyl 2-methylpropanoate Chemical compound OCCCCCCCCC=C.CC(C)C(=O)OC(C)OC1=CC=CC=C1 BYLXLDKSNAVZTP-UHFFFAOYSA-N 0.000 description 1
SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
239000002781 deodorant agent Substances 0.000 description 1
239000003599 detergent Substances 0.000 description 1
XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
229940095104 dimethyl benzyl carbinyl acetate Drugs 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
238000004043 dyeing Methods 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
NYNCZOLNVTXTTP-UHFFFAOYSA-N ethyl 2-(1,3-dioxoisoindol-2-yl)acetate Chemical compound C1=CC=C2C(=O)N(CC(=O)OCC)C(=O)C2=C1 NYNCZOLNVTXTTP-UHFFFAOYSA-N 0.000 description 1
NPNMNANLCUXXQR-UHFFFAOYSA-N ethyl 2-ethyl-2-methylbutanoate Chemical compound CCOC(=O)C(C)(CC)CC NPNMNANLCUXXQR-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
229940113087 geraniol Drugs 0.000 description 1
HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
150000002391 heterocyclic compounds Chemical class 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000001469 lavandula hydrida abrial herb 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
239000001289 litsea cubeba fruit oil Substances 0.000 description 1
239000006210 lotion Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
HRGPYCVTDOECMG-RHBQXOTJSA-N methyl cedryl ether Chemical compound C1[C@@]23[C@H](C)CC[C@H]2C(C)(C)[C@]1([H])[C@@](OC)(C)CC3 HRGPYCVTDOECMG-RHBQXOTJSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
239000002674 ointment Substances 0.000 description 1
239000010502 orange oil Substances 0.000 description 1
ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000010666 rose oil Substances 0.000 description 1
235000019719 rose oil Nutrition 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000002453 shampoo Substances 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
239000000454 talc Substances 0.000 description 1
229940116411 terpineol Drugs 0.000 description 1
239000000341 volatile oil Substances 0.000 description 1
239000003643 water by type Substances 0.000 description 1
ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 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
- C11B9/0007—Aliphatic compounds
- C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
- C11B9/0019—Aliphatic compounds containing oxygen as the only heteroatom carbocylic acids; Salts or esters thereof

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Fats And Perfumes (AREA)
Cosmetics (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NL8302893A 1983-08-17 1983-08-17 Parfumcomposities en geparfumeerde produkten die ten minste een of meer esters van 2-ethyl-2-methyl-butaanzuur als parfumgrondstof bevatten. NL8302893A (nl)

Priority Applications (3)

Application Number	Priority Date	Filing Date	Title
NL8302893A NL8302893A (nl)	1983-08-17	1983-08-17	Parfumcomposities en geparfumeerde produkten die ten minste een of meer esters van 2-ethyl-2-methyl-butaanzuur als parfumgrondstof bevatten.
EP84201183A EP0134613A1 (en)	1983-08-17	1984-08-14	Perfume compositions and perfumed products which contain at least one or more esters of 2-ethyl-2-methyl-butanoic acid as the perfume base
JP17008484A JPS6067445A (ja)	1983-08-17	1984-08-16	香料組成物及び香料化された製品

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL8302893		1983-08-17
NL8302893A NL8302893A (nl)	1983-08-17	1983-08-17	Parfumcomposities en geparfumeerde produkten die ten minste een of meer esters van 2-ethyl-2-methyl-butaanzuur als parfumgrondstof bevatten.

Publications (1)

Publication Number	Publication Date
NL8302893A true NL8302893A (nl)	1985-03-18

Family

ID=19842279

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8302893A NL8302893A (nl)	1983-08-17	1983-08-17	Parfumcomposities en geparfumeerde produkten die ten minste een of meer esters van 2-ethyl-2-methyl-butaanzuur als parfumgrondstof bevatten.

Country Status (3)

Country	Link
EP (1)	EP0134613A1 (ja)
JP (1)	JPS6067445A (ja)
NL (1)	NL8302893A (ja)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP5080776B2 (ja) *	2006-10-06	2012-11-21	花王株式会社	エステル化合物
EP3597626A1 (en) *	2018-07-19	2020-01-22	Basf Se	Alpha,alpha-disubstituted carboxylic acid esters for use as aroma chemicals

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2626142A1 (de) *	1976-06-11	1977-12-22	Henkel Kgaa	Verwendung von aliphatischen 2-methyl- 2-alkyl-alkansaeureestern als riechstoffe sowie diese enthaltende riechstoffkompositionen

1983
- 1983-08-17 NL NL8302893A patent/NL8302893A/nl not_active Application Discontinuation
1984
- 1984-08-14 EP EP84201183A patent/EP0134613A1/en not_active Withdrawn
- 1984-08-16 JP JP17008484A patent/JPS6067445A/ja active Pending

Also Published As

Publication number	Publication date
JPS6067445A (ja)	1985-04-17
EP0134613A1 (en)	1985-03-20

Legal Events

Date	Code	Title	Description
1985-03-18	A1B	A search report has been drawn up
1986-04-01	BV	The patent application has lapsed

Publication	Publication Date	Title
SU814283A3 (ru)	1981-03-15	Ароматизирующа композици
CA2309449C (en)	2005-08-16	Esters with musky odor and their use in perfumery
NL8003068A (nl)	1982-01-04	Parfumcomposities en geparfumeerde materialen en voorwerpen die esters van bicyclische monoterpeenzuren als grondstof bevatten.
JP2933719B2 (ja)	1999-08-16	香料製造におけるジメチル‐シクロヘキサンカルボン酸エステル
JP5689135B2 (ja)	2015-03-25	付香成分としてのエステル
JP5543218B2 (ja)	2014-07-09	フレグランス組成物および化合物
EP0841333A1 (en)	1998-05-13	14-Methyl-hexadecenolide and 14-methyl-hexadecanolide
US6384269B1 (en)	2002-05-07	Esters with musky odor and their use in perfumery
US4843061A (en)	1989-06-27	Cyclohexane-, cyclohexene- and cyclohexadiene-, bicyclo (2.2.1)-heptenecarboxylic acid esters, and also perfume compositions and perfumed products which contain one or more of said compounds as perfume component
NL8302893A (nl)	1985-03-18	Parfumcomposities en geparfumeerde produkten die ten minste een of meer esters van 2-ethyl-2-methyl-butaanzuur als parfumgrondstof bevatten.
JP3715387B2 (ja)	2005-11-09	香料中のシクロペンチリデン−シクロペンタノール
US5849685A (en)	1998-12-15	Fragrance material
EP0770671B1 (en)	1999-09-22	Cyclopentylidene-cyclopentanol in perfumery
NL8104271A (nl)	1983-04-18	Parfumcomposities en geparfumeerde produkten die spiroundecanonen en -undecenonen als parfumgrondstof bevatten.
JP5689134B2 (ja)	2015-03-25	アニスノートを有する着臭剤
JP4125966B2 (ja)	2008-07-30	香料成分としての不飽和エステルの使用、香料組成物、香料添加製品、および不飽和エステル化合物
ES2355118T3 (es)	2011-03-23	Compuestos orgánicos.
US20140148376A1 (en)	2014-05-29	Penta/hexamethyl-3,4,5,8-tetrahydro-1(2h)-naphthalenone derivatives with aromatic notes
US4749682A (en)	1988-06-07	Perfume compositions and perfumed products which contain an alkyl 2-mercaptobenzoate as fragrance material
CA2941402A1 (en)	2016-02-25	Perfume compositons containing isomeric alkadienenitriles
NL8701489A (nl)	1989-01-16	Trimethylcyclohexenyl- en tetramethylcyclohexenyl-methyl-alkenylcarbinolen, alsmede parfumcomposities en geparfumeerde produkten die een of meer van deze verbindingen als parfumgrondstof bevatten.
NL8104274A (nl)	1983-04-18	Parfumcomposities en geparfumeerde produkten die alifatische ketonen als parfumgrondstof bevatten alsmede alifatisch keton geschikt voor gebruik als parfumgrondstof.
NL8800215A (nl)	1989-08-16	Parfumcomposities alsmede geparfumeerde produkten, die een of meer bicyclo 3,3,0 octyl-alkyl-ketonen als parfumgrondstof bevatten.
NL8400657A (nl)	1985-09-16	Parfumcomposities en geparfumeerde voorwerpen en materialen, die tetrahydro-naftol als parfumgrondstof bevatten.
JP2004528289A (ja)	2004-09-16	芳香性化合物