GB1590909A - Perfume compositions containing substituted 1,3-dioxans - Google Patents
Perfume compositions containing substituted 1,3-dioxans Download PDFInfo
- Publication number
- GB1590909A GB1590909A GB43837/77A GB4383777A GB1590909A GB 1590909 A GB1590909 A GB 1590909A GB 43837/77 A GB43837/77 A GB 43837/77A GB 4383777 A GB4383777 A GB 4383777A GB 1590909 A GB1590909 A GB 1590909A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dioxan
- isopropyl
- perfume composition
- perfume
- dimethyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 239000002304 perfume Substances 0.000 title claims description 35
- 239000000203 mixture Substances 0.000 title claims description 24
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical class C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 title description 2
- KBYHWUXTLMRZHL-UHFFFAOYSA-N 5,5-dimethyl-4-propan-2-yl-1,3-dioxane Chemical compound CC(C)C1OCOCC1(C)C KBYHWUXTLMRZHL-UHFFFAOYSA-N 0.000 claims description 9
- -1 alkyl radical Chemical class 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 239000012459 cleaning agent Substances 0.000 claims description 3
- 239000002537 cosmetic Substances 0.000 claims description 3
- 239000000645 desinfectant Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 239000004753 textile Substances 0.000 claims description 3
- COIFDECZEGUHRB-UHFFFAOYSA-N 2-cyclopropyl-2,5,5-trimethyl-4-propan-2-yl-1,3-dioxane Chemical compound O1CC(C)(C)C(C(C)C)OC1(C)C1CC1 COIFDECZEGUHRB-UHFFFAOYSA-N 0.000 claims description 2
- NSCSXGFRAYAHIL-UHFFFAOYSA-N 2-ethyl-5,5-dimethyl-4-propan-2-yl-1,3-dioxane Chemical compound CCC1OCC(C)(C)C(C(C)C)O1 NSCSXGFRAYAHIL-UHFFFAOYSA-N 0.000 claims description 2
- XIPUIGPNIDKXJU-UHFFFAOYSA-N [CH]1CC1 Chemical compound [CH]1CC1 XIPUIGPNIDKXJU-UHFFFAOYSA-N 0.000 claims description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 5
- CHDWHRVQAASQBA-UHFFFAOYSA-N 2,2-diethyl-5,5-dimethyl-4-propan-2-yl-1,3-dioxane Chemical compound CCC1(CC)OCC(C)(C)C(C(C)C)O1 CHDWHRVQAASQBA-UHFFFAOYSA-N 0.000 claims 1
- HSIQLWDLQSZTCV-UHFFFAOYSA-N 2,5,5-trimethyl-4-propan-2-yl-1,3-dioxane Chemical compound CC(C)C1OC(C)OCC1(C)C HSIQLWDLQSZTCV-UHFFFAOYSA-N 0.000 claims 1
- 239000003205 fragrance Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 3
- 241000723346 Cinnamomum camphora Species 0.000 description 3
- 229930008380 camphor Natural products 0.000 description 3
- 229960000846 camphor Drugs 0.000 description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-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
- 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
- 229910052799 carbon Inorganic materials 0.000 description 2
- HQKQRXZEXPXXIG-VJOHVRBBSA-N chembl2333940 Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@H]1[C@@](OC(C)=O)(C)CC2 HQKQRXZEXPXXIG-VJOHVRBBSA-N 0.000 description 2
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 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-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-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
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
- 239000001147 (3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran Substances 0.000 description 1
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-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
- JINWMPBLUUKRSV-UHFFFAOYSA-N 2,2,4-trimethyl-1,3-dioxane Chemical compound CC1CCOC(C)(C)O1 JINWMPBLUUKRSV-UHFFFAOYSA-N 0.000 description 1
- WVYKHQRCBWWGFK-UHFFFAOYSA-N 2,2,5,5-tetramethyl-4-propan-2-yl-1,3-dioxane Chemical compound CC(C)C1OC(C)(C)OCC1(C)C WVYKHQRCBWWGFK-UHFFFAOYSA-N 0.000 description 1
- IXOFPNRLOQANTH-UHFFFAOYSA-N 2,5,5-trimethyl-2-propan-2-yl-1,3-dioxane Chemical compound CC(C)C1(C)OCC(C)(C)CO1 IXOFPNRLOQANTH-UHFFFAOYSA-N 0.000 description 1
- AONDLMLDCWYNJB-UHFFFAOYSA-N 2-butyl-2-ethyl-5,5-dimethyl-4-propan-2-yl-1,3-dioxane Chemical compound CCCCC1(CC)OCC(C)(C)C(C(C)C)O1 AONDLMLDCWYNJB-UHFFFAOYSA-N 0.000 description 1
- NRBUBAMYEALGCN-UHFFFAOYSA-N 2-cyclopropyl-5,5-dimethyl-4-propan-2-yl-1,3-dioxane Chemical compound O1CC(C)(C)C(C(C)C)OC1C1CC1 NRBUBAMYEALGCN-UHFFFAOYSA-N 0.000 description 1
- XXISCOJPDPPPPJ-UHFFFAOYSA-N 2-phenylethanol;3-phenylpropanoic acid Chemical compound OCCC1=CC=CC=C1.OC(=O)CCC1=CC=CC=C1 XXISCOJPDPPPPJ-UHFFFAOYSA-N 0.000 description 1
- WXCMHFPAUCOJIG-UHFFFAOYSA-N 4'-tert-Butyl-2',6'-dimethyl-3',5'-dinitroacetophenone Chemical compound CC(=O)C1=C(C)C([N+]([O-])=O)=C(C(C)(C)C)C([N+]([O-])=O)=C1C WXCMHFPAUCOJIG-UHFFFAOYSA-N 0.000 description 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- SVYIRYSQKUXBPY-UHFFFAOYSA-N 5,5-dimethyl-2,4-di(propan-2-yl)-1,3-dioxane Chemical compound CC(C)C1OCC(C)(C)C(C(C)C)O1 SVYIRYSQKUXBPY-UHFFFAOYSA-N 0.000 description 1
- AWSZUOKHFRWQFK-UHFFFAOYSA-N 5,5-dimethyl-2-propan-2-yl-1,3-dioxane Chemical class CC(C)C1OCC(C)(C)CO1 AWSZUOKHFRWQFK-UHFFFAOYSA-N 0.000 description 1
- QCJVKUULZGKQDG-UHFFFAOYSA-N 8,8-Dimethoxy-2,6-dimethyl-2-octanol Chemical compound COC(OC)CC(C)CCCC(C)(C)O QCJVKUULZGKQDG-UHFFFAOYSA-N 0.000 description 1
- 240000007436 Cananga odorata Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000218631 Coniferophyta Species 0.000 description 1
- PQMOXTJVIYEOQL-UHFFFAOYSA-N Cumarin Natural products CC(C)=CCC1=C(O)C(C(=O)C(C)CC)=C(O)C2=C1OC(=O)C=C2CCC PQMOXTJVIYEOQL-UHFFFAOYSA-N 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- 241000723339 Diselma archeri Species 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
- XMLSXPIVAXONDL-PLNGDYQASA-N Jasmone Chemical compound CC\C=C/CC1=C(C)CCC1=O XMLSXPIVAXONDL-PLNGDYQASA-N 0.000 description 1
- 244000178870 Lavandula angustifolia Species 0.000 description 1
- 235000010663 Lavandula angustifolia Nutrition 0.000 description 1
- 241000212322 Levisticum officinale Species 0.000 description 1
- FSOGIJPGPZWNGO-UHFFFAOYSA-N Meomammein Natural products CCC(C)C(=O)C1=C(O)C(CC=C(C)C)=C(O)C2=C1OC(=O)C=C2CCC FSOGIJPGPZWNGO-UHFFFAOYSA-N 0.000 description 1
- 244000227633 Ocotea pretiosa Species 0.000 description 1
- 235000004263 Ocotea pretiosa Nutrition 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 240000004760 Pimpinella anisum Species 0.000 description 1
- 235000012550 Pimpinella anisum Nutrition 0.000 description 1
- 235000010450 Pino mugo Nutrition 0.000 description 1
- 240000000513 Santalum album Species 0.000 description 1
- 235000008632 Santalum album Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000006359 acetalization reaction Methods 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- OOCCDEMITAIZTP-UHFFFAOYSA-N allylic benzylic alcohol Natural products OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-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
- YPZUZOLGGMJZJO-LQKXBSAESA-N ambroxan Chemical compound CC([C@@H]1CC2)(C)CCC[C@]1(C)[C@@H]1[C@]2(C)OCC1 YPZUZOLGGMJZJO-LQKXBSAESA-N 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
- 229940116229 borneol Drugs 0.000 description 1
- 239000001772 cananga odorata hook. f. and thomas. oil Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000010627 cedar oil Substances 0.000 description 1
- 239000010632 citronella oil Substances 0.000 description 1
- 239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 239000010639 cypress oil Substances 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
- 239000010642 eucalyptus oil Substances 0.000 description 1
- 229940044949 eucalyptus oil Drugs 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229940113087 geraniol Drugs 0.000 description 1
- 229940074928 isopropyl myristate Drugs 0.000 description 1
- 238000005907 ketalization reaction Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 1
- 239000001102 lavandula vera Substances 0.000 description 1
- 235000018219 lavender Nutrition 0.000 description 1
- 239000001645 levisticum officinale Substances 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 229940102398 methyl anthranilate Drugs 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
- 230000007935 neutral effect Effects 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 239000001738 pogostemon cablin oil Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000010668 rosemary oil Substances 0.000 description 1
- 229940058206 rosemary oil Drugs 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- XMLSXPIVAXONDL-UHFFFAOYSA-N trans-jasmone Natural products CCC=CCC1=C(C)CCC1=O XMLSXPIVAXONDL-UHFFFAOYSA-N 0.000 description 1
- GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000003643 water by type Substances 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
- C11B9/0069—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
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)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2648109A DE2648109C2 (de) | 1976-10-23 | 1976-10-23 | 4-Isopropyl-5,5-dimethyl-1,3-dioxane enthaltende Riechstoffkompositionen sowie 4-Isopropyl-5,5-dimethyl-1,3-dioxane als solche |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1590909A true GB1590909A (en) | 1981-06-10 |
Family
ID=5991261
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB43837/77A Expired GB1590909A (en) | 1976-10-23 | 1977-10-21 | Perfume compositions containing substituted 1,3-dioxans |
| GB8276/80A Expired GB1590910A (en) | 1976-10-23 | 1977-10-21 | Substituted 1,3-dioxans |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8276/80A Expired GB1590910A (en) | 1976-10-23 | 1977-10-21 | Substituted 1,3-dioxans |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US4146506A (enExample) |
| JP (1) | JPS5352636A (enExample) |
| CH (1) | CH631348A5 (enExample) |
| DE (1) | DE2648109C2 (enExample) |
| FR (1) | FR2368271A1 (enExample) |
| GB (2) | GB1590909A (enExample) |
| IT (1) | IT1087009B (enExample) |
| NL (1) | NL7710741A (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4211674A (en) * | 1978-04-10 | 1980-07-08 | Polak's Frutal Works B.V. | Cyclic acetals and ketals and their use in perfume compositions |
| DE2900421A1 (de) * | 1979-01-08 | 1980-07-24 | Henkel Kgaa | Verwendung hydrierter indenopyrane als riechstoffe sowie diese enthaltende riechstoffkompositionen |
| FR2472839A1 (fr) * | 1979-12-28 | 1981-07-03 | Thomson Csf | Procede d'ajustement du coefficient de temperature d'une diode a jonction et diode de reference |
| DE3016007A1 (de) * | 1980-04-25 | 1981-11-12 | Henkel KGaA, 4000 Düsseldorf | Verwendung substituierter 2-(1-methylbutyl)-1,3-dioxane als riechstoffe sowie diese enthaltende riechstoffkompositionen |
| US4390462A (en) * | 1980-12-04 | 1983-06-28 | International Flavors & Fragrances Inc. | Aliphatic branched olefin dioxolanes, dithiolanes, and oxathiolanes and uses thereof in augmenting or enhancing the aroma and/or taste of consumable materials |
| JPS5939890A (ja) * | 1982-08-26 | 1984-03-05 | Neos Co Ltd | フエニル置換２−（１−アルケニル）−４−イソプロピル−５，５−ジメチル−１，３−ジオキサン誘導体 |
| GB8701961D0 (en) * | 1987-01-29 | 1987-03-04 | Unilever Plc | Perfumery materials |
| US4742044A (en) * | 1987-08-19 | 1988-05-03 | International Flavors & Fragrances Inc. | Aralkoxy, alkoxy, alkadienyloxy and alkenyloxy-1,3,2-dioxaborinane derivatives and uses thereof in augmenting or enhancing the aroma of perfume compositions, perfumed articles and perfumed polymers |
| JP3806773B2 (ja) * | 1995-03-25 | 2006-08-09 | クエスト・インターナショナル・ビー・ブイ | 芳香物質 |
| JPH11502528A (ja) * | 1995-03-25 | 1999-03-02 | クエスト・インターナショナル・ビー・ブイ | 新規１，３−ジオキサン及び香料類におけるその使用 |
| CN100372842C (zh) * | 2006-05-19 | 2008-03-05 | 华东师范大学 | 一种制备2,4-二异丙基-5,5-二甲基-1,3-二噁烷的方法 |
| BR112014017513A8 (pt) * | 2012-01-18 | 2017-07-04 | Procter & Gamble | sistemas de perfume |
| MX2015014949A (es) * | 2013-04-24 | 2016-03-07 | Procter & Gamble | Sistemas de perfume. |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2769014A (en) * | 1951-05-17 | 1956-10-30 | Polak & Schwarz S Essencefabri | Process for the preparation of novel perfumes containing an m-dioxane ring |
| US2829169A (en) * | 1956-02-29 | 1958-04-01 | Eastman Kodak Co | Process of manufacturing isobutyraldol and 2, 2, 4-trimethyl-1, 3-pentanediol |
| US3326746A (en) * | 1962-09-04 | 1967-06-20 | Lever Brothers Ltd | 1, 3-dioxane cleaning compositions |
| CH525207A (de) * | 1970-01-09 | 1972-07-15 | Givaudan & Cie Sa | Verfahren zur Herstellung von neuen Riechstoffen |
| DE2108649C3 (de) * | 1971-02-24 | 1978-12-07 | Basf Ag, 6700 Ludwigshafen | 2-Methyl-2-hepten-6-on-l-al und seine Acetale |
| NL166187C (nl) * | 1973-04-18 | 1981-07-15 | Naarden International Nv | Werkwijze ter bereiding van reukstofcomposities door een 2-gesubstitueerd 4,4,6-trimethyl-1,3-dioxan te mengen met ten minste een andere reukstof en geparfu- meerde voorwerpen. |
| DE2526675A1 (de) * | 1975-06-14 | 1976-12-30 | Henkel & Cie Gmbh | Entzuendungshemmer fuer kosmetische praeparationen |
-
1976
- 1976-10-23 DE DE2648109A patent/DE2648109C2/de not_active Expired
-
1977
- 1977-09-30 NL NL7710741A patent/NL7710741A/xx not_active Application Discontinuation
- 1977-10-18 IT IT28708/77A patent/IT1087009B/it active
- 1977-10-21 GB GB43837/77A patent/GB1590909A/en not_active Expired
- 1977-10-21 GB GB8276/80A patent/GB1590910A/en not_active Expired
- 1977-10-21 CH CH1288077A patent/CH631348A5/de not_active IP Right Cessation
- 1977-10-21 FR FR7731795A patent/FR2368271A1/fr active Granted
- 1977-10-21 US US05/844,281 patent/US4146506A/en not_active Expired - Lifetime
- 1977-10-21 JP JP12588877A patent/JPS5352636A/ja active Pending
-
1978
- 1978-10-27 US US05/955,160 patent/US4220593A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| IT1087009B (it) | 1985-05-31 |
| DE2648109C2 (de) | 1985-08-14 |
| DE2648109A1 (de) | 1978-04-27 |
| GB1590910A (en) | 1981-06-10 |
| US4220593A (en) | 1980-09-02 |
| FR2368271A1 (fr) | 1978-05-19 |
| NL7710741A (nl) | 1978-04-25 |
| JPS5352636A (en) | 1978-05-13 |
| US4146506A (en) | 1979-03-27 |
| CH631348A5 (de) | 1982-08-13 |
| FR2368271B1 (enExample) | 1981-07-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |