JP6203756B2 - 香料系 - Google Patents
香料系 Download PDFInfo
- Publication number
- JP6203756B2 JP6203756B2 JP2014553421A JP2014553421A JP6203756B2 JP 6203756 B2 JP6203756 B2 JP 6203756B2 JP 2014553421 A JP2014553421 A JP 2014553421A JP 2014553421 A JP2014553421 A JP 2014553421A JP 6203756 B2 JP6203756 B2 JP 6203756B2
- Authority
- JP
- Japan
- Prior art keywords
- perfume
- methyl
- delivery system
- cyclohex
- 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.)
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- 239000002304 perfume Substances 0.000 title claims description 140
- 239000000203 mixture Substances 0.000 claims description 130
- 238000004140 cleaning Methods 0.000 claims description 43
- 150000001412 amines Chemical class 0.000 claims description 37
- 239000004744 fabric Substances 0.000 claims description 35
- 239000003599 detergent Substances 0.000 claims description 30
- 239000002994 raw material Substances 0.000 claims description 25
- 238000011282 treatment Methods 0.000 claims description 23
- 229920000642 polymer Polymers 0.000 claims description 21
- 239000011159 matrix material Substances 0.000 claims description 14
- 239000003094 microcapsule Substances 0.000 claims description 14
- FYARZVBULLSAII-UHFFFAOYSA-N 4-(2,4-dimethylcyclohex-3-en-1-ylidene)butan-2-one Chemical compound CC1C=C(C)CCC1=CCC(C)=O FYARZVBULLSAII-UHFFFAOYSA-N 0.000 claims description 8
- 239000004615 ingredient Substances 0.000 claims description 8
- YHFPADQBRHKDEB-UHFFFAOYSA-N 1-(2,4,6-trimethylcyclohex-3-en-1-yl)propan-1-one Chemical compound CCC(=O)C1C(C)CC(C)=CC1C YHFPADQBRHKDEB-UHFFFAOYSA-N 0.000 claims description 6
- UVSMZUFSZJQNGU-UHFFFAOYSA-N 3-ethenyl-2-(3-methylbutyl)cyclopentan-1-one Chemical compound CC(C)CCC1C(C=C)CCC1=O UVSMZUFSZJQNGU-UHFFFAOYSA-N 0.000 claims description 6
- 239000002088 nanocapsule Substances 0.000 claims description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 239000000047 product Substances 0.000 description 78
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 67
- 239000011541 reaction mixture Substances 0.000 description 53
- 239000003205 fragrance Substances 0.000 description 45
- -1 facial tissue Substances 0.000 description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 35
- 238000000034 method Methods 0.000 description 34
- 239000000463 material Substances 0.000 description 33
- 238000002360 preparation method Methods 0.000 description 32
- 239000000243 solution Substances 0.000 description 31
- 239000003795 chemical substances by application Substances 0.000 description 29
- 238000006243 chemical reaction Methods 0.000 description 28
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 24
- 230000015572 biosynthetic process Effects 0.000 description 24
- 239000007788 liquid Substances 0.000 description 24
- 238000003786 synthesis reaction Methods 0.000 description 23
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- 229920002472 Starch Polymers 0.000 description 19
- 239000008107 starch Substances 0.000 description 19
- 235000019698 starch Nutrition 0.000 description 19
- 235000019645 odor Nutrition 0.000 description 17
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 16
- 238000009472 formulation Methods 0.000 description 16
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 13
- 239000007789 gas Substances 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 229940088598 enzyme Drugs 0.000 description 12
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- 230000008569 process Effects 0.000 description 12
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 12
- 102000004190 Enzymes Human genes 0.000 description 11
- 108090000790 Enzymes Proteins 0.000 description 11
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 11
- 239000007844 bleaching agent Substances 0.000 description 11
- 239000007795 chemical reaction product Substances 0.000 description 11
- 229910000029 sodium carbonate Inorganic materials 0.000 description 11
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 10
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- 238000009835 boiling Methods 0.000 description 10
- 239000000975 dye Substances 0.000 description 10
- 238000004817 gas chromatography Methods 0.000 description 10
- 238000002156 mixing Methods 0.000 description 10
- 239000012043 crude product Substances 0.000 description 9
- 238000005516 engineering process Methods 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- 229920000058 polyacrylate Polymers 0.000 description 9
- 229920006395 saturated elastomer Polymers 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- 238000004821 distillation Methods 0.000 description 8
- 239000000835 fiber Substances 0.000 description 8
- 239000003112 inhibitor Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 238000012546 transfer Methods 0.000 description 8
- 229920002873 Polyethylenimine Polymers 0.000 description 7
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 239000002671 adjuvant Substances 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 7
- 230000003197 catalytic effect Effects 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- 235000011888 snacks Nutrition 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- 239000012267 brine Substances 0.000 description 6
- 239000002775 capsule Substances 0.000 description 6
- 239000002738 chelating agent Substances 0.000 description 6
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 6
- 238000004851 dishwashing Methods 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- 239000000499 gel Substances 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 229920001296 polysiloxane Polymers 0.000 description 6
- 239000002453 shampoo Substances 0.000 description 6
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 229920000877 Melamine resin Polymers 0.000 description 5
- 230000003750 conditioning effect Effects 0.000 description 5
- 239000011258 core-shell material Substances 0.000 description 5
- 239000002270 dispersing agent Substances 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 239000012044 organic layer Substances 0.000 description 5
- 238000002470 solid-phase micro-extraction Methods 0.000 description 5
- 239000012086 standard solution Substances 0.000 description 5
- 229910052723 transition metal Inorganic materials 0.000 description 5
- YGHRJJRRZDOVPD-UHFFFAOYSA-N 3-methylbutanal Chemical compound CC(C)CC=O YGHRJJRRZDOVPD-UHFFFAOYSA-N 0.000 description 4
- 229920000858 Cyclodextrin Polymers 0.000 description 4
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 239000013543 active substance Substances 0.000 description 4
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 4
- 235000010675 chips/crisps Nutrition 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000011162 core material Substances 0.000 description 4
- 238000001514 detection method Methods 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 125000005842 heteroatom Chemical group 0.000 description 4
- 239000012943 hotmelt Substances 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 239000012074 organic phase Substances 0.000 description 4
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 239000011257 shell material Substances 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 150000003624 transition metals Chemical class 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- FLANQKVDSAQAGZ-UHFFFAOYSA-N (2,4-dimethyl-1-propan-2-ylcyclohex-3-en-1-yl)methanol Chemical compound CC(C)C1(CO)CCC(C)=CC1C FLANQKVDSAQAGZ-UHFFFAOYSA-N 0.000 description 3
- XVLCMWGWCZXJBY-UHFFFAOYSA-N 1,1,3,3,5-pentamethyl-3a,4,7,7a-tetrahydro-2-benzofuran Chemical compound C1C(C)=CCC2C(C)(C)OC(C)(C)C12 XVLCMWGWCZXJBY-UHFFFAOYSA-N 0.000 description 3
- TVBFZGNTIPSPBP-UHFFFAOYSA-N 1,3,4-trimethylbicyclo[2.2.1]heptane-3-carboxylic acid Chemical compound C1CC2(C)C(C)(C(O)=O)CC1(C)C2 TVBFZGNTIPSPBP-UHFFFAOYSA-N 0.000 description 3
- NCVBOMKCZGXGCG-UHFFFAOYSA-N 2,4-dimethyl-1-propan-2-ylcyclohex-3-ene-1-carbaldehyde Chemical compound CC(C)C1(C=O)CCC(C)=CC1C NCVBOMKCZGXGCG-UHFFFAOYSA-N 0.000 description 3
- BVUSMSOTLWGFKV-UHFFFAOYSA-N 2-(3-methylbutyl)cyclopent-2-en-1-one Chemical compound CC(C)CCC1=CCCC1=O BVUSMSOTLWGFKV-UHFFFAOYSA-N 0.000 description 3
- KZQDEHUTBFUOPD-UHFFFAOYSA-N 2-[6-(2-hydroxypropan-2-yl)-4-methylcyclohex-3-en-1-yl]propan-2-ol Chemical compound CC1=CCC(C(C)(C)O)C(C(C)(C)O)C1 KZQDEHUTBFUOPD-UHFFFAOYSA-N 0.000 description 3
- QUDBAGFQCACQMZ-UHFFFAOYSA-N 3,4-dimethyl-2-methylidenepentanal Chemical compound CC(C)C(C)C(=C)C=O QUDBAGFQCACQMZ-UHFFFAOYSA-N 0.000 description 3
- QOUVUDUTJPGJNG-UHFFFAOYSA-N 3-methyl-2-methylidenebutanal Chemical compound CC(C)C(=C)C=O QOUVUDUTJPGJNG-UHFFFAOYSA-N 0.000 description 3
- NYPOJSCNHYUZRG-UHFFFAOYSA-N 4,8-dimethylnona-3,7-dien-2-ol Chemical compound CC(O)C=C(C)CCC=C(C)C NYPOJSCNHYUZRG-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- GCPWJFKTWGFEHH-UHFFFAOYSA-N acetoacetamide Chemical compound CC(=O)CC(N)=O GCPWJFKTWGFEHH-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 230000001166 anti-perspirative effect Effects 0.000 description 3
- 239000003213 antiperspirant Substances 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 229920006317 cationic polymer Polymers 0.000 description 3
- 239000012459 cleaning agent Substances 0.000 description 3
- 238000005354 coacervation Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 229910021641 deionized water Inorganic materials 0.000 description 3
- 239000000645 desinfectant Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- GODQWBQDOFWJQS-UHFFFAOYSA-N dimethyl 4-methylcyclohex-4-ene-1,2-dicarboxylate Chemical compound COC(=O)C1CC=C(C)CC1C(=O)OC GODQWBQDOFWJQS-UHFFFAOYSA-N 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 238000005194 fractionation Methods 0.000 description 3
- 230000036541 health Effects 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- 229940098779 methanesulfonic acid Drugs 0.000 description 3
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 3
- 208000022018 mucopolysaccharidosis type 2 Diseases 0.000 description 3
- 239000006072 paste Substances 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 229920005646 polycarboxylate Polymers 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
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- 239000000843 powder Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- OHEFFKYYKJVVOX-UHFFFAOYSA-N sulcatol Chemical compound CC(O)CCC=C(C)C OHEFFKYYKJVVOX-UHFFFAOYSA-N 0.000 description 3
- 239000003826 tablet Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 239000010457 zeolite Substances 0.000 description 3
- LBIOIVZFQAHKGP-UHFFFAOYSA-N (1,2-dimethyl-3-propan-2-ylcyclopentyl) acetate Chemical compound CC(C)C1CCC(C)(OC(C)=O)C1C LBIOIVZFQAHKGP-UHFFFAOYSA-N 0.000 description 2
- CIOXZGOUEYHNBF-UHFFFAOYSA-N (carboxymethoxy)succinic acid Chemical compound OC(=O)COC(C(O)=O)CC(O)=O CIOXZGOUEYHNBF-UHFFFAOYSA-N 0.000 description 2
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
- ILVZTOZDOGPBOI-UHFFFAOYSA-N 1,5-dimethyl-4-propan-2-yl-2-oxabicyclo[2.2.2]octane Chemical compound C1CC2(C)CC(C)C1(C(C)C)CO2 ILVZTOZDOGPBOI-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- BKQSMDOYQBNEDA-UHFFFAOYSA-N 1-methyl-4-(3-methylbutan-2-yl)-2-oxabicyclo[2.2.2]octane Chemical compound C1CC2(C)CCC1(C(C)C(C)C)CO2 BKQSMDOYQBNEDA-UHFFFAOYSA-N 0.000 description 2
- MTGRYMBXBGBEAB-UHFFFAOYSA-N 2,2,3a,7-tetramethyl-3,4,5,6,7,7a-hexahydro-1-benzofuran Chemical compound CC1CCCC2(C)CC(C)(C)OC12 MTGRYMBXBGBEAB-UHFFFAOYSA-N 0.000 description 2
- YVIHJMSLCZGXLX-UHFFFAOYSA-N 2,5,5-trimethyl-2-propyl-1,3-dioxane Chemical compound CCCC1(C)OCC(C)(C)CO1 YVIHJMSLCZGXLX-UHFFFAOYSA-N 0.000 description 2
- PIXWACURCSBXIQ-UHFFFAOYSA-N 2,6-dimethyl-2-(2-methylprop-2-enyl)cyclohexan-1-one Chemical compound CC1CCCC(C)(CC(C)=C)C1=O PIXWACURCSBXIQ-UHFFFAOYSA-N 0.000 description 2
- UNYCRXRQVNALHT-UHFFFAOYSA-N 2,6-dimethyl-3a-propan-2-yl-3,4,5,6,7,7a-hexahydro-2h-1-benzofuran Chemical compound C1C(C)CCC2(C(C)C)C1OC(C)C2 UNYCRXRQVNALHT-UHFFFAOYSA-N 0.000 description 2
- SWDGUJRVKJUCNL-UHFFFAOYSA-N 2-(3-methylbutylidene)cyclopentan-1-one Chemical compound CC(C)CC=C1CCCC1=O SWDGUJRVKJUCNL-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- CETWDUZRCINIHU-UHFFFAOYSA-N 2-heptanol Chemical compound CCCCCC(C)O CETWDUZRCINIHU-UHFFFAOYSA-N 0.000 description 2
- URCUNETUGGJHFS-UHFFFAOYSA-N 2-hex-3-enyl-5-methyloxolane Chemical compound CCC=CCCC1CCC(C)O1 URCUNETUGGJHFS-UHFFFAOYSA-N 0.000 description 2
- 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- WIZKUEPBSJBGTO-UHFFFAOYSA-N 4-(cyclopropylmethoxymethyl)-5-methylcyclohexene Chemical compound CC1CC=CCC1COCC1CC1 WIZKUEPBSJBGTO-UHFFFAOYSA-N 0.000 description 2
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 2
- GUOCOOQWZHQBJI-UHFFFAOYSA-N 4-oct-7-enoxy-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)OCCCCCCC=C GUOCOOQWZHQBJI-UHFFFAOYSA-N 0.000 description 2
- PLPHPIBVJUQZNN-UHFFFAOYSA-N 6-methyl-3-propan-2-yl-2-prop-1-enyloxane Chemical compound C(C)(C)C1C(OC(CC1)C)C=CC PLPHPIBVJUQZNN-UHFFFAOYSA-N 0.000 description 2
- GCBRDRITNLZNLC-UHFFFAOYSA-N 8-ethoxy-2,6-dimethylnona-2,6-diene Chemical compound CCOC(C)C=C(C)CCC=C(C)C GCBRDRITNLZNLC-UHFFFAOYSA-N 0.000 description 2
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 239000004382 Amylase Substances 0.000 description 2
- 108010065511 Amylases Proteins 0.000 description 2
- 102000013142 Amylases Human genes 0.000 description 2
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Classifications
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- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
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Description
本明細書で使用するとき、「消費者製品」は、販売される形態での使用又は消費を一般に意図する、ベビーケア、ビューティケア、布地及びホームケア、ファミリーケア、女性用ケア、ヘルスケア、スナック、及び/又は飲料製品若しくは装置を意味する。かかる製品としては、おむつ、よだれかけ、拭き取り用品;脱色、着色、染色、コンディショニング、シャンプー、スタイリングを含む毛髪(ヒト、イヌ、及び/又はネコ)の処理に関連する製品及び/又は方法;防臭剤及び制汗剤;パーソナルクレンジング;化粧品;上質な芳香剤を含む消費者使用のためのクリーム、ローション、及び他の局所塗布製品の塗布を含むスキンケア;並びにシェービング製品、エアフレッシュナー及び芳香送達系を含む空気ケア、車ケア、食器洗浄、布地コンディショニング(柔軟化及び/又はフレッシュニングを含む)、洗濯洗浄、洗濯及びすすぎ添加剤並びに/又はケア、床及び便器洗浄剤を含む硬質表面洗浄及び/又は処理、並びに消費者用又は業務用の他の洗浄などの、布地及びホームケア領域内の布地、硬質表面、及び任意の他の表面処理に関する製品及び/又は方法;トイレットペーパー、フェイシャルティッシュ、紙ハンカチ、及び/又は紙タオルに関連する製品及び/又は方法;タンポン、女性用ナプキン;練り歯磨き、歯用ジェル、歯用リンス、義歯接着剤、歯ホワイトニングを含む口腔ケアに関連する製品及び/又は方法;咳及び風邪治療薬、鎮痛剤、処方薬、ペットヘルス及び栄養を含む店頭販売ヘルスケア;主に慣習的な食事の間又は食事随伴物としての消費が意図される加工食品(非限定的な例としては、ポテトチップス、トルティーヤチップス、ポップコーン、プレッツェル、コーンチップス、シリアルバー、野菜チップス又はクリスプ、スナックミックス、パーティミックス、マルチグレインチップス、スナッククラッカー、チーズスナック、ポークラインズ、コーンスナック、ペレットスナック、押出成形スナック及びベーグルチップが挙げられる)、並びにコーヒーが挙げられるが、これらに限定されない。
本明細書で詳述する香料送達系及び/又は消費者製品での使用に適したPRMには、下の表1に列挙したPRM及びその立体異性体が含まれる。
本明細書に開示される香料原材料及び香料組成物は更に、香料送達系に組み込まれてもよい。好適な香料送達系、香料送達系を製造する方法、及び香料送達系の使用は、米国特許出願第2007/0275866(A1)号に開示されている。かかる香料送達系には以下のものが挙げられる。
a)約20nm〜約500nm、約40nm〜約250nm、又は約60nm〜約150nmのシェル厚、
b)約5:95〜約50:50、約10:90〜約30:70、又は約10:90〜約15:85のシェル対コア比、
c)約0.1MPa〜約16MPa、約0.5MPa〜約8MPa、又は更には約1MPa〜約3MPaの破壊応力、及び
d)約1μ〜約100μ、約5μ〜約80μ、又は更には約15μ〜約50μの平均粒径。
香料を配合するために、表1に開示されたPRMが使用され得る。かかる香料は、表1のPRMの組み合わせ、又は表1のPRMのうちの1つ以上、及び1つ以上の追加的なPRMを含み得るPRMの組み合わせである。香料において使用する場合、表1のPRMは、香料の全重量に対して、約0.01重量%〜約50重量%、約0.1重量%〜約15重量%、約0.1重量%〜約10重量%、又は更には約0.5重量%〜約10重量%濃度で使用され得る。このような香料は、未希釈で部位に塗布する、あるいは、消費者製品、洗浄及び/又は処理組成物、布地及び硬質表面用の洗浄及び/又は処理組成物、洗剤、及び/又は超コンパクト洗剤中で使用することを含む、種々の用途で使用され得る。
本発明の目的のために、以下に例示される補助剤の非限定的なリストは、本明細書に詳述される組成物(例えば、消費者製品、洗浄及び/若しくは処理組成物、布地及び硬質表面用の洗浄及び/若しくは処理組成物、洗剤、並びに/又は超コンパクト化洗剤)中で用いるのに好適である。このような補助物質は、例えば洗浄される基材を処理する目的で、又は香料、着色剤、染料などを用いる場合のように組成物の審美性を変化させる目的で、組成物の性能を支援又は強化するために組成物の特定の実施形態に組み込み得ることが好ましい。かかる補助剤は、本明細書に詳述される本出願人らの香料及び/又は香料系を介して供給される構成成分に追加されることが理解されよう。このような追加的構成成分の正確な性質、及びそれを組み込む濃度は、組成物の物理的形態及び使用されるべき作業の性質に依存する。
本明細書に開示されるいくつかの消費者製品を用いて、部位、とりわけ表面又は布地を洗浄又は処理することができる。通常、この部位の少なくとも一部は、未希釈形態で又は液体、例えば洗浄液に希釈されて本出願人らの組成物の実施形態と接触し、そしてその後、場合により、その部位が洗浄及び/又はすすがれてもよい。一態様では、ある部位が任意により洗浄及び/又はすすがれ、本発明による粒子に又は前記粒子を含む組成物に接触され、次に任意により洗浄及び/又はすすがれる。本発明の目的に関して、洗浄としては、限定するものではないが、こすり洗い及び機械的撹拌が挙げられる。布地は、標準的な消費者の使用条件で洗濯又は処理することが可能な大部分の任意の布地を含んでよい。開示される組成物を含み得る液体は、約3〜約11.5のpHを有してよい。こうした組成物は、典型的には溶液中で約500ppm〜約15,000ppmの濃度で使用される。洗浄溶媒が水であるとき、水温は、典型的には、約5℃〜約90℃であり、部位が布地を含むとき、水と布地との割合は、典型的には、約1:1〜約30:1である。
本出願の「試験方法」の項で開示される試験方法は、本出願人らの発明が本明細書に記載され及び特許請求されているように、本出願人らの発明のパラメータの各値を求めるために使用されるべきであると理解される。
「logPの計算値」(ClogP)は、Hansch及びLeoのフラグメント手法(cf.,A.Leo,in Comprehensive Medicinal Chemistry,Vol.4,C.Hansch,P.G.Sammens,J.B.Taylor,and C.A.Ramsden,Eds.P.295,Pergamon Press,1990,参照によりここに組み込まれる)により決定される。ClogP値は、Daylight Chemical Information Systems Inc.(Irvine,California U.S.A.)から入手可能な「CLOGP」プログラムを用いることにより計算することができる。
沸点は、ASTM法D2887−04a「ガスクロマトグラフィーによる、石油留分の沸点範囲分布のための標準試験方法(Standard Test Method for Boiling Range Distribution of Petroleum Fractions by Gas Chromatograph)」(ASTMインターナショナル)により測定される。
(a)芳香剤非含有消費者製品配合物(シャンプー又はリーブオンコンディショナー)を入手する。
(b)水性スラリー中での香料含有率が25重量%となるように含水率が調整されている芳香剤マイクロカプセルを入手する。
(c)2.0グラムの芳香剤マイクロカプセル水性スラリーを95グラムの芳香剤非含有消費者製品配合物に加えることで試料Aを調製する。次に、3.0グラムの脱イオン水を配合物に加えて100グラムに合わせる。40℃で1週間この配合物をエイジングさせる。
(d)0.50グラムの未希釈の芳香剤を95グラムの芳香剤非含有消費者製品配合物に加えることで、試料Bを調製する。次に、4.5グラムの脱イオン水を配合物に加えて100グラムに合わせる。40℃で1週間この配合物をエイジングさせる。
1.20mLのヘッドスペースバイアル
2.タイマー。
3.ガスクロマトグラフ(GC):CIS−4インジェクター、MPS−2オートサンプラー及びTDUを備えるAgilent model 6890(Gerstel,Mulheim,Germany)SPME分析において、スプリット/スプリットレスインジェクター(CIS−4インジェクターとは異なる)を使用した。
4.GCカラム:J&W DB−5 MS、30M×0.25mm ID、膜厚1.0μm(J&W Scientific of Folsom,California,USAから入手した)。
5.キャリアガス、ヘリウム、流速1.5mL/分。
6.インジェクターライナーは、Supelcoの特定のSPMEライナー(0.75mm ID)である。
7.検出器は、約230℃の供給源温度及び約150℃のMS Quad温度を有する、Agilent Technologies,Inc.,Wilmington,DE,USAから入手したモデル5973質量選択検出器である。
1.試料を適切な試料トレイに移し、SPME−GC−MS分析を続ける。
2.一連の試料装填及び分析を開始する。このステップにおいては、試料をオートサンプラートレイ上で少なくとも2時間均衡化させ、次に、トレイから直接サンプリングする。SPME繊維集合体は、DVB/CAR/PDMS(50/30μm、24ga、長さ1cm)である。サンプリング時間は、5分間である。
3.インジェクター温度は、260℃である。
4.次に、GC−MS分析の実行を開始する。脱着時間は、5分間である。
5.以下の温度プログラムを使用する。
i)約50℃の初期温度を3分間保持する。
ii)約250℃の温度に達するまで約6℃/分の速度で、その後、275℃に達するまで25℃/分の速度で初期温度を上昇させ、約275℃で4.67分間維持する。
6.Hewlett Packardから購入し、使用許諾を受けた、John Wiley & Sons及び米国国立標準技術研究所(NIST)のMSスペクトルライブラリを使用して、香料化合物を特定する。
7.Agilent Technologies,Inc.(Wilmington,DE,USA)から入手したChemstationソフトウェアを使用して、特定イオンのクロマトグラフィーピークを積分する。
8.試料A中の香料原材料のピーク面積を試料B中のピーク面積で割ることで、各PRMの比率を計算する。
9.次に、香料における香料原材料の重量組成によって、各比率を重み付けする。
10.ステップ9で得られた個別の香料原材料比率の合計によって、ヘッドスペース率を計算する。
液体洗剤中の香料マイクロカプセルからの香料の漏れ%を測定する際、等しいレベルの遊離香料(香料マイクロカプセルを有さない)を有する液体洗剤の未加工試料も参照のために並行して分析する必要がある。
−トナリドの原液:70mgのトナリドを秤量し、20mLの試薬用ヘキサンを加える。
−内標準溶液:20mLの試薬用ヘキサンで200μLの原液を希釈する。
−均質化するように混合する。
−液体洗剤製品を2g秤量し、抽出容器に入れる。
−2mLの内標準溶液を加えて、容器を閉じる。
−抽出容器を20回手で上下逆に穏やかにひっくり返し、香料を抽出する。
−硫酸ナトリウムを1匙加える。
−層の分離後、すぐにヘキサン層をガスクロマトグラフオートサンプラーバイアルに入れて、バイアルの蓋をする。
−ガスクロマトグラフ注入ポートにスプリットレス(1.5μL)を注入する。
−ガスクロマトグラフィー質量分析を行う。
−液体洗剤製品を2g秤量し、抽出容器に入れる。
−2mLの内標準溶液を加えて、容器を閉じる。
−抽出容器を20回(手で)上下逆に穏やかにひっくり返し、香料を抽出する。
−硫酸ナトリウムを1匙加える。
−層の分離後、すぐにヘキサン層をガスクロマトグラフオートサンプラーバイアルに入れて、バイアルの蓋をする。
−ガスクロマトグラフ注入ポートにスプリットレス(1.5μL)を注入する。
−ガスクロマトグラフィー質量分析を行う。
−個別の香料原料ごとのカプセルからの香料の漏れ:
香料の漏れ(%)={(カプセルの香料原材料の面積×参照の内標準溶液の面積×参照の重量)/(カプセルの内標準溶液の面積×参照の香料原材料の面積×カプセルの重量)}×100
ガスクロマトグラフを使用して判定した。ガスクロマトグラフを較正して、シリンジにより注入される正確な物質体積、正確なスプリット比、並びに既知の濃度及び鎖長分布の炭化水素標準物質を用いた炭化水素反応を決定する。空気の流量を正確に測定し、ヒトの吸入の持続時間が12秒間であると仮定して、試料体積を計算する。任意の時点の検出器における正確な濃度が既知であるため、吸入された体積当たりの質量、ひいては材料濃度は既知である。
GC:FID検出器、7673オートサンプラーを備える5890シリーズII
カラム:J&W Scientific DB−1
長さ:30メートル、内径0.25メートル、膜厚1マイクロメートル
方法:
−スプリット注入:17/1スプリット比
−オートサンプラー:1.13マイクロリットル/注入
−カラム流量:1.10マイクロリットル/分
−空気流:345ミリリットル/分
−入口温度:245℃
−検出器温度:285℃
−初期温度=50℃、5℃/分の昇温速度、最終温度=280℃、最終時間6分間
−推定導入:1回嗅ぐごとに12秒、GCガスを試料希釈物に加える。
1−(2,4,6−トリメチル−シクロへキセ−3−エニル)−プロパン−1−オンの合成
8−ヒドロキシ−2,6−ジメチル−ノナ−2,6−ジエンの調製:テトラヒドロフラン(THF)(1.6L、1M)中のメチルリチウムを、温度計、機械的撹拌機、凝縮器、及び添加漏斗を備えた火炎乾燥した3L反応フラスコに入れた。シトラールを2〜2.5時間かけて滴加した。転化率が90%を超えるまで反応混合物を熟成させた。反応混合物を30℃を下回るまで冷却し、HCl(pH<5、10%)を徐々に加えて急冷した。水相をトルエン(100mL)で3回抽出し、抽出物を粗反応混合物に加えた。次に、粗反応混合物を飽和重炭酸ナトリウム(500mL)で洗浄し、続いて飽和塩溶液で洗浄し、無水硫酸ナトリウム上で乾燥した。粗反応混合物を濃縮した。溶媒をロータリーエバポレータを介して回収して8−ヒドロキシ−2,6−ジメチル−ノナ−2,6−ジエンを得た。
3a−イソプロピル−2,6−ジメチル−オクタヒドロ−ベンゾフランの調製:メントン(500g)、オルソギ酸メチルエステル(377g)及びメタノール(400mL)を3L反応フラスコに入れた。塩酸(hydrochlorioc acid)(3g)を一度に(In one portion)加え、この混合物は22℃〜40℃の熱を発生させた。反応混合物を6時間熟成させ、ナトリウムメトキシド溶液(35g)で急冷した。反応混合物を90℃まで加熱しながら低沸点物質を除去した。アリルアルコール(404g)及び酢酸(195g)を加え、反応混合物を160℃まで加熱した。反応混合物を160℃で3時間保持し、25℃まで冷却し、ブライン(500mL)で洗浄した。粗生成物を蒸留して、アリルメントン(allyl menthone)の異性体の混合物を得た。
シクロプロパンカルボン酸1−メチル−ヘキシルエステルの調製:2−ヘプタノール(200g、1.72モル)及びシクロプロパンカルボン酸(163g、1.90モル)をトルエン(500mL)に加えた後、p−トルエンスルホン酸(3.2g、0.0172モル)を加えた。反応混合物を6時間にわたり加熱還流させ、室温まで冷却し、重炭酸ナトリウム溶液(1L)で急冷した。次に、反応混合物をブライン(0.5L)で洗浄し、硫酸ナトリウム(50g)上で乾燥させた。溶媒を除去し、反応混合物を蒸留し、生成物シクロプロパンカルボン酸1−メチル−ヘキシルエステル(253g)を得た。
酢酸3−イソプロピル−1,2−ジメチル−シクロペンチルエステルの調製:トランス−ジヒドロピノール(dihydroplinol)(165g)及びジメチルアミノピリジン(2g)を1L丸底フラスコに入れ、80℃まで加熱した。無水酢酸(143g)を得られた混合物に加え、出発物質の大部分が消費されるまで同じ温度で攪拌した。次に反応混合物を室温まで冷却し、水及び炭酸ナトリウムで洗浄し、トルエンで抽出した。有機溶媒を減圧下で除去し、分留により生成物酢酸3−イソプロピル−1,2−ジメチル−シクロペンチルエステル(45g、収率21%)を得た。
4−(2,4−ジメチル−シクロへキセ−3−エニリデン)−ブタン−2−オンの調製:ケトエステル(780g)を2L丸底フラスコに加え、200℃まで加熱した。水(2当量)を滴加し、Bidwell−Sterlingトラップでより軽質な溶媒を除去した。次に、反応混合物を室温まで冷却した。粗生成物を無水硫酸ナトリウムの上で乾燥させた。分留により、生成物4−(2,4−ジメチル−シクロヘキセ−3−エニリデン)−ブタン−2−オン(231g)を得た。
2−[6−(1−ヒドロキシ−1−メチル−エチル)−4−メチル−シクロヘキセ−3−エニル]−プロパン−2−オル(720g、3.3モル、上で詳述した通りに得た)を、Bidwell−Sterlingトラップを取り付けた丸底フラスコに充填し、トルエン(1L)中に溶解した。酸触媒p−トルエンスルホン酸(pTSA、40g、0.18モル)を加え、この混合物を加熱還流させた。還流を1.5時間にわたり維持した。この間に水をBidwell−Sterlingトラップに収集した。GC分析により反応の完了が示された。得られた混合物の体積を減少させ、分留により精製して、1,1,3,3,5−ペンタメチル−1,3,3a,4,7,7a−ヘキサヒドロ−イソベンゾフラン(60g、収率9%)を得た。
3−sec−ブチル−1,5−ジメチル−2−オキサ−ビシクロ[2.2.2]オクタンは、米国特許第4197328号(Schmittら)に開示されているプロセスによって調製することができる。
1−(6−イソプロピル−2−メチル−シクロヘキセ−3−エニル)−エタノンは、欧州特許出願第0231556(A1)号(Van der Weerdtら)に開示されているプロセスによって調製することができる。
1−(6−イソプロピル−4−メチル−シクロヘキセ−3−エニル)−エタノンは、米国特許第4524020号(Sprekerら)に開示されているプロセスによって調製することができる。
4−(3−メトキシ−1−メチル−プロピル)−1−メチル−シクロヘキセンは、欧州特許出願第53716(A1)号(Schaperら)に開示されているプロセスによって調製することができる。
3−(1,1−ジメトキシ−エチル)−1,1−ジメチル−シクロヘキサンは、米国特許第4933320号(Sprekerら)に開示されているプロセスによって調製することができる。
2,4−ジメチル−2−(4−メチル−ペント−3−ニル)−[1,3]ジオキソランは、Huaxue Yanjiu Yu Yingyong,2003,pp〜229−230(Peng,A.,Xia,M.,Jin,X)に開示されているプロセスによって調製することができる。
以下の成分:
1.1つ以上の表1のPRMを含む香料材料を50%、
2.BASFからのLupasol WF(CAS番号09002−98−6)を50%を秤量し、ガラスバイアル瓶に加え、60℃の温水浴中に使用前に1時間載置する。
25グラムのブチルアクリレート−アクリル酸コポリマー乳化剤(Colloid C351、25%固形分、pKa 4.5〜4.7、Kemira Chemicals,Inc.Kennesaw,Georgia U.S.A.)を脱イオン水200グラムに溶解及び混合する。溶液のpHを、水酸化ナトリウム溶液でpH 4.0に調整する。部分メチル化メチロールメラミン樹脂(Cymel 385、80%固形分(Cytec Industries West Paterson,New Jersey,U.S.A.))8グラムを乳化剤溶液に添加する。1つ以上の表1のPRMを含む香油200グラムを、先の混合物に機械撹拌しながら添加したところ、温度は50℃に上昇した。安定なエマルションが得られるまで高速で混合した後に、第2の溶液及び4グラムの硫酸ナトリウム塩をこのエマルションに添加する。この第2の溶液は、ブチルアクリレート−アクリル酸コポリマー乳化剤(Colloid C351、25%固形分、pKa 4.5〜4.7、Kemira)10グラム、蒸留水120グラム、pHを4.8に調整するための水酸化ナトリウム溶液、部分メチル化メチロールメラミン樹脂(Cymel 385、80%固形分、Cytec)25グラムを含有する。この混合物を70℃まで加熱し、連続的に攪拌しながら1晩にわたって維持して、カプセル封入プロセスを完了させる。アセトアセトアミド(Sigma−Aldrich,Saint Louis,Missouri,U.S.A.)23グラムをこの懸濁液に添加する。モデル780 Accusizerにより分析したときに30μmの平均カプセルサイズを得る。
1つ以上の表1のPRMを含む香料組成物を50%、カルボキシル末端Hycar(登録商標)1300X18(CAS番号0068891−50−9)(Noveon製)(混合前に1時間にわたって60℃の温水浴中に置く)を40%、Lupasol(登録商標)WF(CAS番号09002−98−6)(BASF製)(混合前に1時間にわたって60℃の温水浴中に置く)を10%、を含む混合物。ウルトラ−ツラックスT25基本装備(IKA製)を用いて5分間混合することにより、混合を達成する。混合後、混合物を±12時間60℃の温水浴中に置く。均質な、粘稠かつ粘着性のある物質が得られる。
本明細書に開示されたPRM、香料及びアミンを含有する製品配合の非限定的な例を、以下の表に要約する。
b メチル−ビス(タローアミドエチル)−2−ヒドロキシエチルアンモニウムメチルサルフェート。
c 脂肪酸とメチルジエタノールアミンとのモル比1.5:1での反応生成物を塩化メチルで四級化して得られる、N,N−ビス(ステアロイル−オキシ−エチル)N,N−ジメチルアンモニウムクロライドとN−(ステアロイル−オキシ−エチル)N−ヒドロキシエチルN,Nジメチルアンモニウムクロライドとの1:1モル混合物。
d National Starchから商品名CATO(登録商標)で入手可能なカチオン性高アミローストウモロコシデンプン。
e 1つ以上の表1のPRMを含む香料
f 米国特許第5,574,179号、第15段、1〜5行目に記載の式を有する、エチレンオキシドとテレフタレートとのコポリマーであって、式中、各Xはメチルであり、各nは40であり、uは4であり、各R1は本質的に1,4−フェニレン部分であり、各R2は、本質的にエチレン、1,2−プロピレン部分、又はこれらの混合物である。
g WackerからのSE39
h ジエチレントリアミン五酢酸。
i Rohm and Haas Co.から入手可能なKATHON(登録商標)CG。「PPM」は、「百万分の一」。
j グルタルアルデヒド
k DC2310の商標名でDow Corning Corp.から入手可能なシリコーン消泡剤。
l Rohm and Haas Co.から商品名Aculan 44で入手可能な、疎水変性エトキシル化ウレタン。
* 本明細書に開示されているようなアミン部分を含む1種以上の材料。
† 残部
Claims (7)
- 消費者製品の全重量に対して0.005重量%〜2.5重量%の、4−(2,4−ジメチル−シクロへキセ−3−エニリデン)−ブタン−2−オン、2−(3−メチル−ブチル)−3−ビニル−シクロペンタノン、1−(2,4,6−トリメチル−シクロへキセ−3−エニル)−プロパン−1−オン及びそれらの立体異性体から選択される1種以上の香料原材料と、補助成分とを含み、前記消費者製品が洗浄及び/又は処理組成物である、消費者製品。
- 前記消費者製品が布地及び/又は硬質表面用の洗浄及び/又は処理組成物である、請求項1に記載の消費者製品。
- 前記消費者製品が洗剤である、請求項1に記載の消費者製品。
- 香料送達系であって、
香料送達系の全重量に対して0.025%〜5%の、4−(2,4−ジメチル−シクロへキセ−3−エニリデン)−ブタン−2−オン、2−(3−メチル−ブチル)−3−ビニル−シクロペンタノン、1−(2,4,6−トリメチル−シクロへキセ−3−エニル)−プロパン−1−オン及びそれらの立体異性体から選択される1種以上の香料原材料を含み、前記香料送達系が、ポリマー支援型送達系、アミン支援型送達系から選択される、香料送達系。 - 前記香料送達系が、ナノカプセル又はマイクロカプセルの全重量に対して45重量%〜90重量%の、4−(2,4−ジメチル−シクロへキセ−3−エニリデン)−ブタン−2−オン、2−(3−メチル−ブチル)−3−ビニル−シクロペンタノン、1−(2,4,6−トリメチル−シクロへキセ−3−エニル)−プロパン−1−オン及びそれらの立体異性体から選択される1種以上の香料原材料を含むナノカプセル又はマイクロカプセルである、請求項4に記載の香料送達系。
- 前記香料送達系が、ポリマー支援型送達マトリックス系の全重量に対して45重量%〜90重量%の、4−(2,4−ジメチル−シクロへキセ−3−エニリデン)−ブタン−2−オン、2−(3−メチル−ブチル)−3−ビニル−シクロペンタノン、1−(2,4,6−トリメチル−シクロへキセ−3−エニル)−プロパン−1−オン及びそれらの立体異性体から選択される1種以上の香料原材料を含むポリマー支援型送達マトリックス系である、請求項4に記載の香料送達系。
- 前記香料送達系がアミン支援型送達系であり、前記アミン支援型送達系が、アミン支援型送達系の全重量に対して5重量%〜50重量%の、4−(2,4−ジメチル−シクロへキセ−3−エニリデン)−ブタン−2−オン、2−(3−メチル−ブチル)−3−ビニル−シクロペンタノン、1−(2,4,6−トリメチル−シクロへキセ−3−エニル)−プロパン−1−オン及びそれらの立体異性体から選択される1種以上の香料原材料を含む、請求項4に記載の香料送達系。
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3109309B1 (en) | 2012-01-18 | 2022-06-08 | The Procter & Gamble Company | Perfume systems |
EP2993221B1 (de) * | 2014-09-08 | 2019-01-09 | Symrise AG | Verkapselte Duftstoffmischungen |
EP3303534A4 (en) * | 2015-06-04 | 2019-04-10 | P2 Science, Inc. | OLFAKTORISCHE COMPOSITIONS WITH CYCLOHEXYL-ALKYL-CARBINOLENE |
WO2016209863A1 (en) * | 2015-06-22 | 2016-12-29 | The Procter & Gamble Company | Perfume compositions |
BR112018016806B1 (pt) | 2016-02-18 | 2021-11-16 | International Flavors & Fragrances Inc. | Composiqao de microcapsula, e, produtos de consumidor |
EP4209264A1 (en) | 2016-09-16 | 2023-07-12 | International Flavors & Fragrances Inc. | Microcapsule compositions stabilized with viscosity control agents |
CN106620782A (zh) * | 2016-09-22 | 2017-05-10 | 长兴净安环保科技有限公司 | 一种除异味液体芳香剂及其制备方法 |
CN106474514A (zh) * | 2016-09-22 | 2017-03-08 | 长兴净安环保科技有限公司 | 一种液体芳香剂及其制备方法 |
CN106474517A (zh) * | 2016-09-22 | 2017-03-08 | 长兴净安环保科技有限公司 | 一种珠状芳香剂及其制备方法 |
CN106620793A (zh) * | 2016-09-22 | 2017-05-10 | 长兴净安环保科技有限公司 | 一种固体凝胶芳香剂及其制备方法 |
US11111458B2 (en) * | 2018-10-10 | 2021-09-07 | International Flavors & Fragrances Inc. | Cyclopropylmethoxy derivatives |
ES2973083T3 (es) | 2018-10-24 | 2024-06-18 | Procter & Gamble | Productos de consumo y sistemas de suministro que utilizan compuestos organolépticos |
US12016963B2 (en) | 2019-05-10 | 2024-06-25 | The Procter & Gamble Company | Freshening compositions with alkoxylated phenols |
CN110052133B (zh) * | 2019-05-24 | 2021-12-28 | 广州市可达环保科技有限公司 | 一种甲醛净化剂及其制备方法和应用 |
CN112402671A (zh) * | 2020-11-23 | 2021-02-26 | 象鼻山香(杭州)生物科技有限公司 | 野菊叶中清新空气有效部位的提取方法及应用 |
EP4124383A1 (en) | 2021-07-27 | 2023-02-01 | International Flavors & Fragrances Inc. | Biodegradable microcapsules |
EP4154974A1 (en) | 2021-09-23 | 2023-03-29 | International Flavors & Fragrances Inc. | Biodegradable microcapsules |
Family Cites Families (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH583035A5 (ja) * | 1973-03-01 | 1976-12-31 | Givaudan & Cie Sa | |
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. |
JPS5842175B2 (ja) * | 1975-09-22 | 1983-09-17 | ソダコウリヨウ カブシキガイシヤ | 2− アルキル−シクロペンテノンノ セイゾウホウ |
DE2648109C2 (de) * | 1976-10-23 | 1985-08-14 | Henkel KGaA, 4000 Düsseldorf | 4-Isopropyl-5,5-dimethyl-1,3-dioxane enthaltende Riechstoffkompositionen sowie 4-Isopropyl-5,5-dimethyl-1,3-dioxane als solche |
US4162687A (en) | 1978-06-06 | 1979-07-31 | Lorch Leonard G | Dental flossing device |
US4208308A (en) * | 1978-10-20 | 1980-06-17 | International Flavors & Fragrances Inc. | 2-Oxabicyclooctane derivatives in perfume compositions |
US4197328A (en) | 1978-10-20 | 1980-04-08 | International Flavors & Fragrances Inc. | 2-Oxabicyclooctane derivatives in augmenting or enhancing the aroma or taste of foodstuffs |
NL8003068A (nl) * | 1980-05-28 | 1982-01-04 | Naarden & Shell Aroma Chem | Parfumcomposities en geparfumeerde materialen en voorwerpen die esters van bicyclische monoterpeenzuren als grondstof bevatten. |
DE3045960A1 (de) | 1980-12-05 | 1982-07-22 | Henkel KGaA, 4000 Düsseldorf | Terpenether, deren herstellung und verwendung sowie diese enthaltende riechstoffkompositionen |
GR76237B (ja) | 1981-08-08 | 1984-08-04 | Procter & Gamble | |
US4515711A (en) * | 1982-09-27 | 1985-05-07 | Givaudan Corporation | Alkenoxy octadienes as odorants |
DE3475472D1 (en) * | 1983-10-21 | 1989-01-12 | Firmenich & Cie | Use of alpha-terpenyl methyl ether as a compounding ingredient in perfumed sanitizing compositions |
US4524020A (en) * | 1984-08-24 | 1985-06-18 | International Flavors & Fragrances Inc. | Isopropyl substituted cyclohexenyl methyl ketones and perfumery uses thereof |
US4627935A (en) * | 1985-02-06 | 1986-12-09 | International Flavors & Fragrances Inc. | 2-isopropenyl-5-methylcyclopentanealkanols, esters thereof and organoleptic uses of same |
JPS62123183A (ja) * | 1985-11-22 | 1987-06-04 | Taiyo Koryo Kk | 新規テルペンテトラヒドロフラン誘導体および該誘導体を含む香料組成物 |
EP0231556A1 (en) | 1986-01-23 | 1987-08-12 | Naarden International N.V. | Isopropyl-methyl-butenoyl-cyclohexenes and -cyclohexenes and -cyclohexadienes, and also perfume compositions and perfumed articles and materials which contain said compounds as a perfume ingredient |
US4933320A (en) | 1986-05-16 | 1990-06-12 | International Flavors & Fragrances Inc. | Isomer-directed process for producing asymmetric ketones using catalytic Claisen rearrangement of allylic ethers, intermediates, and uses of products and intermediates of process in perfumery |
US4776358A (en) | 1986-09-23 | 1988-10-11 | Leonard Lorch | Floss employing microporous tapes sandwiching paste dentifrice |
FR2634203A1 (fr) * | 1988-07-13 | 1990-01-19 | Inst Rech Controles Techn | Dihydro-2,3-benzofurannes a odeur musquee et parfums et produits parfumes les contenant |
CA2004270A1 (en) | 1988-12-29 | 1990-06-29 | William R. Michael | Perfume microcapsules for use in granular detergent compositions |
US5118865A (en) * | 1990-03-26 | 1992-06-02 | Firmenich Sa | Cyclic ketones and their use as perfuming ingredients |
CN1066188C (zh) | 1993-03-01 | 2001-05-23 | 普罗格特-甘布尔公司 | 浓的可生物降解季铵织物柔软剂组合物和含有中等碘值不饱和脂肪酸链的化合物 |
US5283237A (en) * | 1993-07-01 | 1994-02-01 | International Flavors & Fragrances Inc. | Use in perfumery of 2(1-vinyl-5-hexenyl) cyclopentanone, a process for preparing same, and process intermediates |
US5534179A (en) | 1995-02-03 | 1996-07-09 | Procter & Gamble | Detergent compositions comprising multiperacid-forming bleach activators |
US5597936A (en) | 1995-06-16 | 1997-01-28 | The Procter & Gamble Company | Method for manufacturing cobalt catalysts |
US5576282A (en) | 1995-09-11 | 1996-11-19 | The Procter & Gamble Company | Color-safe bleach boosters, compositions and laundry methods employing same |
MA24136A1 (fr) | 1996-04-16 | 1997-12-31 | Procter & Gamble | Fabrication d'agents de surface . |
DE19635655A1 (de) * | 1996-09-03 | 1998-03-05 | Haarmann & Reimer Gmbh | Verwendung substituierter 2-Acetylbenzofurane als Riechstoffe |
BR9812093B1 (pt) | 1997-03-07 | 2009-12-01 | composição detergente alvejante. | |
US6225464B1 (en) | 1997-03-07 | 2001-05-01 | The Procter & Gamble Company | Methods of making cross-bridged macropolycycles |
US5767305A (en) * | 1997-04-03 | 1998-06-16 | International Flavors & Fragrances Inc. | Cyclopropyl carboxylic acid esters and uses thereof in imparting, augmenting and enhancing aromas |
AU2026100A (en) | 1998-11-30 | 2000-06-19 | Procter & Gamble Company, The | Process for preparing cross-bridged tetraaza macrocycles |
EP1318190A1 (en) * | 2001-12-07 | 2003-06-11 | Givaudan SA | Organic compounds |
JP4551225B2 (ja) * | 2003-03-26 | 2010-09-22 | カウンシル オブ サイエンティフィク アンド インダストリアル リサーチ | 香料およびフレーバ剤としての新規セスキテルペン酸化物 |
US7281541B2 (en) | 2004-06-16 | 2007-10-16 | Lorch Leonard G | Dental floss |
US20070275866A1 (en) * | 2006-05-23 | 2007-11-29 | Robert Richard Dykstra | Perfume delivery systems for consumer goods |
DE102006043587A1 (de) * | 2006-09-16 | 2008-03-27 | Symrise Gmbh & Co. Kg | 2-Methyl-2-alkenyl-substituierte 1,3-Dioxane als Riechstoffe |
JP2010528161A (ja) * | 2007-06-05 | 2010-08-19 | ザ プロクター アンド ギャンブル カンパニー | 香料システム |
US8114823B2 (en) * | 2008-10-14 | 2012-02-14 | International Flavors & Fragrances Inc. | Isomers of bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester and their use in perfume compositions |
US7700529B1 (en) * | 2008-10-14 | 2010-04-20 | International Flavors & Fragrances Inc. | Isomers of bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester and their use in perfume compositions |
US8754028B2 (en) | 2008-12-16 | 2014-06-17 | The Procter & Gamble Company | Perfume systems |
CN107028801A (zh) * | 2009-12-18 | 2017-08-11 | 宝洁公司 | 香料和香料包封物 |
EP3109309B1 (en) | 2012-01-18 | 2022-06-08 | The Procter & Gamble Company | Perfume systems |
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- 2013-01-18 CN CN201380005845.3A patent/CN104066828B/zh not_active Expired - Fee Related
- 2013-01-18 ES ES13702163.0T patent/ES2673844T3/es active Active
- 2013-01-18 JP JP2014553421A patent/JP6203756B2/ja active Active
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EP2804939B1 (en) | 2018-04-04 |
EP2804939A2 (en) | 2014-11-26 |
EP3101112A3 (en) | 2017-05-03 |
CN104066828B (zh) | 2017-06-06 |
WO2013109798A2 (en) | 2013-07-25 |
EP3109309A3 (en) | 2017-04-05 |
BR112014017513A2 (pt) | 2017-06-13 |
EP3109308A2 (en) | 2016-12-28 |
US20160340607A1 (en) | 2016-11-24 |
MX2014008774A (es) | 2014-08-27 |
EP3109307A2 (en) | 2016-12-28 |
CN104066828A (zh) | 2014-09-24 |
EP3109309A2 (en) | 2016-12-28 |
WO2013109798A3 (en) | 2013-11-07 |
EP3109308B1 (en) | 2022-06-01 |
US9441185B2 (en) | 2016-09-13 |
EP3101112B1 (en) | 2019-04-03 |
JP2015504115A (ja) | 2015-02-05 |
US20140329733A1 (en) | 2014-11-06 |
EP3109308A3 (en) | 2017-03-29 |
BR112014017513A8 (pt) | 2017-07-04 |
US10144903B2 (en) | 2018-12-04 |
EP3109307B1 (en) | 2021-03-31 |
EP3109309B1 (en) | 2022-06-08 |
EP3109307A3 (en) | 2017-05-03 |
ES2673844T3 (es) | 2018-06-26 |
EP3101112A2 (en) | 2016-12-07 |
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