CN1423661A - 包括有气味组分的聚合纳米粒子 - Google Patents
包括有气味组分的聚合纳米粒子 Download PDFInfo
- Publication number
- CN1423661A CN1423661A CN01808102A CN01808102A CN1423661A CN 1423661 A CN1423661 A CN 1423661A CN 01808102 A CN01808102 A CN 01808102A CN 01808102 A CN01808102 A CN 01808102A CN 1423661 A CN1423661 A CN 1423661A
- Authority
- CN
- China
- Prior art keywords
- component
- nanoparticle
- scent
- temperature
- reaction mixture
- 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.)
- Granted
Links
- 239000002105 nanoparticle Substances 0.000 title claims abstract description 41
- 239000000178 monomer Substances 0.000 claims abstract description 42
- 239000007788 liquid Substances 0.000 claims abstract description 30
- 239000003999 initiator Substances 0.000 claims abstract description 25
- 239000011541 reaction mixture Substances 0.000 claims abstract description 22
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 14
- 239000007864 aqueous solution Substances 0.000 claims abstract description 13
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims description 55
- 239000004816 latex Substances 0.000 claims description 20
- 229920000126 latex Polymers 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 19
- 229920000642 polymer Polymers 0.000 claims description 17
- 239000000126 substance Substances 0.000 claims description 17
- 239000004744 fabric Substances 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 14
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 11
- 238000005406 washing Methods 0.000 claims description 11
- 230000008859 change Effects 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 8
- 239000013543 active substance Substances 0.000 claims description 7
- 241000282326 Felis catus Species 0.000 claims description 6
- 239000002979 fabric softener Substances 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 4
- 230000007704 transition Effects 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000004793 Polystyrene Substances 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 229920000058 polyacrylate Polymers 0.000 claims description 2
- 229920002223 polystyrene Polymers 0.000 claims description 2
- 239000008346 aqueous phase Substances 0.000 claims 1
- ONJMNXFNTYIEEA-UHFFFAOYSA-N benzene ethene Chemical compound C1=CC=CC=C1.C=C.C=C.C=C ONJMNXFNTYIEEA-UHFFFAOYSA-N 0.000 claims 1
- 239000011247 coating layer Substances 0.000 claims 1
- 239000011521 glass Substances 0.000 abstract 1
- 235000013599 spices Nutrition 0.000 description 58
- 239000000047 product Substances 0.000 description 21
- 239000002245 particle Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 150000002500 ions Chemical class 0.000 description 16
- 239000000758 substrate Substances 0.000 description 16
- 239000006185 dispersion Substances 0.000 description 15
- -1 polyoxytrimethylene Polymers 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 239000002304 perfume Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 11
- 230000002045 lasting effect Effects 0.000 description 11
- 239000007787 solid Substances 0.000 description 10
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 9
- 230000000474 nursing effect Effects 0.000 description 9
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 9
- 239000000796 flavoring agent Substances 0.000 description 7
- 235000019634 flavors Nutrition 0.000 description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 6
- 230000008021 deposition Effects 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 238000013268 sustained release Methods 0.000 description 6
- 239000012730 sustained-release form Substances 0.000 description 6
- LDHQCZJRKDOVOX-UHFFFAOYSA-N 2-butenoic acid Chemical compound CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 5
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000009792 diffusion process Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 238000007046 ethoxylation reaction Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N ethyl acetate Substances CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 239000000284 extract Substances 0.000 description 4
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000006386 neutralization reaction Methods 0.000 description 4
- 239000012074 organic phase Substances 0.000 description 4
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 4
- 230000002572 peristaltic effect Effects 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Natural products CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 235000003891 ferrous sulphate Nutrition 0.000 description 3
- 239000011790 ferrous sulphate Substances 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 3
- 239000000416 hydrocolloid Substances 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 3
- 238000005304 joining Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 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 3
- 239000012071 phase Substances 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- 238000010926 purge Methods 0.000 description 3
- 239000013074 reference sample Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- 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 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- YGFGZTXGYTUXBA-UHFFFAOYSA-N (±)-2,6-dimethyl-5-heptenal Chemical compound O=CC(C)CCC=C(C)C YGFGZTXGYTUXBA-UHFFFAOYSA-N 0.000 description 2
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 2
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- GNKZMNRKLCTJAY-UHFFFAOYSA-N 4'-Methylacetophenone Chemical compound CC(=O)C1=CC=C(C)C=C1 GNKZMNRKLCTJAY-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- 239000004160 Ammonium persulphate Substances 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 2
- 229920000858 Cyclodextrin Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CRZQGDNQQAALAY-UHFFFAOYSA-N Methyl benzeneacetate Chemical compound COC(=O)CC1=CC=CC=C1 CRZQGDNQQAALAY-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000004141 Sodium laurylsulphate Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N acrylic acid methyl ester Natural products COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 235000019395 ammonium persulphate Nutrition 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- HCRBXQFHJMCTLF-ZCFIWIBFSA-N ethyl (2r)-2-methylbutanoate Chemical compound CCOC(=O)[C@H](C)CC HCRBXQFHJMCTLF-ZCFIWIBFSA-N 0.000 description 2
- SHZIWNPUGXLXDT-UHFFFAOYSA-N ethyl hexanoate Chemical compound CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 2
- WDAXFOBOLVPGLV-UHFFFAOYSA-N ethyl isobutyrate Chemical compound CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 229960004275 glycolic acid Drugs 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- OTTZHAVKAVGASB-UHFFFAOYSA-N hept-2-ene Chemical compound CCCCC=CC OTTZHAVKAVGASB-UHFFFAOYSA-N 0.000 description 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical compound COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 description 2
- 238000012703 microemulsion polymerization Methods 0.000 description 2
- 239000013618 particulate matter Substances 0.000 description 2
- PGMYKACGEOXYJE-UHFFFAOYSA-N pentyl acetate Chemical compound CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 2
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 229920000136 polysorbate Polymers 0.000 description 2
- 230000002000 scavenging effect Effects 0.000 description 2
- 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 2
- 230000035807 sensation Effects 0.000 description 2
- 235000019615 sensations Nutrition 0.000 description 2
- 239000003352 sequestering agent Substances 0.000 description 2
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 2
- 238000002470 solid-phase micro-extraction Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- NPNUFJAVOOONJE-ZIAGYGMSSA-N β-(E)-Caryophyllene Chemical compound C1CC(C)=CCCC(=C)[C@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-ZIAGYGMSSA-N 0.000 description 2
- ZHHYXNZJDGDGPJ-BSWSSELBSA-N (2e,4e)-nona-2,4-dienal Chemical compound CCCC\C=C\C=C\C=O ZHHYXNZJDGDGPJ-BSWSSELBSA-N 0.000 description 1
- GDDAJHJRAKOILH-QFXXITGJSA-N (2e,5e)-octa-2,5-diene Chemical compound CC\C=C\C\C=C\C GDDAJHJRAKOILH-QFXXITGJSA-N 0.000 description 1
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
- JQQDKNVOSLONRS-JEGFTUTRSA-N (3e,5e)-undeca-1,3,5-triene Chemical compound CCCCC\C=C\C=C\C=C JQQDKNVOSLONRS-JEGFTUTRSA-N 0.000 description 1
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 1
- YDXQPTHHAPCTPP-AATRIKPKSA-N (E)-3-Octen-1-ol Chemical compound CCCC\C=C\CCO YDXQPTHHAPCTPP-AATRIKPKSA-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
- UFLHIIWVXFIJGU-ARJAWSKDSA-N (Z)-hex-3-en-1-ol Chemical compound CC\C=C/CCO UFLHIIWVXFIJGU-ARJAWSKDSA-N 0.000 description 1
- XJHRZBIBSSVCEL-ARJAWSKDSA-N (Z)-non-6-en-1-ol Chemical compound CC\C=C/CCCCCO XJHRZBIBSSVCEL-ARJAWSKDSA-N 0.000 description 1
- WVAFEFUPWRPQSY-UHFFFAOYSA-N 1,2,3-tris(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1C=C WVAFEFUPWRPQSY-UHFFFAOYSA-N 0.000 description 1
- BZJTUOGZUKFLQT-UHFFFAOYSA-N 1,3,5,7-tetramethylcyclooctane Chemical group CC1CC(C)CC(C)CC(C)C1 BZJTUOGZUKFLQT-UHFFFAOYSA-N 0.000 description 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-butanediol Substances OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
- SPPWGCYEYAMHDT-UHFFFAOYSA-N 1,4-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=C(C(C)C)C=C1 SPPWGCYEYAMHDT-UHFFFAOYSA-N 0.000 description 1
- WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 1
- VPKMGDRERYMTJX-CMDGGOBGSA-N 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one Chemical compound CCC(=O)\C=C\C1C(C)=CCCC1(C)C VPKMGDRERYMTJX-CMDGGOBGSA-N 0.000 description 1
- KBHWKXNXTURZCD-UHFFFAOYSA-N 1-Methoxy-4-propylbenzene Chemical compound CCCC1=CC=C(OC)C=C1 KBHWKXNXTURZCD-UHFFFAOYSA-N 0.000 description 1
- HNAGHMKIPMKKBB-UHFFFAOYSA-N 1-benzylpyrrolidine-3-carboxamide Chemical compound C1C(C(=O)N)CCN1CC1=CC=CC=C1 HNAGHMKIPMKKBB-UHFFFAOYSA-N 0.000 description 1
- NIBFJPXGNVPNHK-UHFFFAOYSA-N 2,2-difluoro-1,3-benzodioxole-4-carbaldehyde Chemical group C1=CC(C=O)=C2OC(F)(F)OC2=C1 NIBFJPXGNVPNHK-UHFFFAOYSA-N 0.000 description 1
- WNJSKZBEWNVKGU-UHFFFAOYSA-N 2,2-dimethoxyethylbenzene Chemical compound COC(OC)CC1=CC=CC=C1 WNJSKZBEWNVKGU-UHFFFAOYSA-N 0.000 description 1
- ZEMPKEQAKRGZGQ-AAKVHIHISA-N 2,3-bis[[(z)-12-hydroxyoctadec-9-enoyl]oxy]propyl (z)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCC(O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CC(O)CCCCCC)COC(=O)CCCCCCC\C=C/CC(O)CCCCCC ZEMPKEQAKRGZGQ-AAKVHIHISA-N 0.000 description 1
- XGTXFAUKOSHYSX-UHFFFAOYSA-N 2,4-dimethyl-6-phenyl-3,4-dihydro-2h-pyran Chemical compound O1C(C)CC(C)C=C1C1=CC=CC=C1 XGTXFAUKOSHYSX-UHFFFAOYSA-N 0.000 description 1
- 229940029225 2,6-dimethyl-5-heptenal Drugs 0.000 description 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
- LTHJXDSHSVNJKG-UHFFFAOYSA-N 2-[2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(C)=C LTHJXDSHSVNJKG-UHFFFAOYSA-N 0.000 description 1
- LBICMZLDYMBIGA-UHFFFAOYSA-N 2-methyldecanal Chemical compound CCCCCCCCC(C)C=O LBICMZLDYMBIGA-UHFFFAOYSA-N 0.000 description 1
- NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 description 1
- ILPBINAXDRFYPL-UHFFFAOYSA-N 2-octene Chemical compound CCCCCC=CC ILPBINAXDRFYPL-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- IQVAERDLDAZARL-UHFFFAOYSA-N 2-phenylpropanal Chemical compound O=CC(C)C1=CC=CC=C1 IQVAERDLDAZARL-UHFFFAOYSA-N 0.000 description 1
- PANBRUWVURLWGY-UHFFFAOYSA-N 2-undecenal Chemical compound CCCCCCCCC=CC=O PANBRUWVURLWGY-UHFFFAOYSA-N 0.000 description 1
- WTPYRCJDOZVZON-UHFFFAOYSA-N 3,5,5-Trimethylhexanal Chemical compound O=CCC(C)CC(C)(C)C WTPYRCJDOZVZON-UHFFFAOYSA-N 0.000 description 1
- ZHDQGHCZWWDMRS-UHFFFAOYSA-N 3,5-dimethylcyclohex-3-ene-1-carbaldehyde Chemical compound CC1CC(C=O)CC(C)=C1 ZHDQGHCZWWDMRS-UHFFFAOYSA-N 0.000 description 1
- UCSIFMPORANABL-UHFFFAOYSA-N 3,7-dimethyloctanal Chemical compound CC(C)CCCC(C)CC=O UCSIFMPORANABL-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- OHRBQTOZYGEWCJ-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)butanal Chemical compound CC(C)C1=CC=CC(C(C)CC=O)=C1 OHRBQTOZYGEWCJ-UHFFFAOYSA-N 0.000 description 1
- DKHJONPHCWFBAX-UHFFFAOYSA-N 3-butyl-3h-1-benzofuran-2-one Chemical compound C1=CC=C2C(CCCC)C(=O)OC2=C1 DKHJONPHCWFBAX-UHFFFAOYSA-N 0.000 description 1
- PNWDAMQMBGMVCR-UHFFFAOYSA-N 3-cyclohexyloxyprop-2-enyl acetate Chemical compound CC(=O)OCC=COC1CCCCC1 PNWDAMQMBGMVCR-UHFFFAOYSA-N 0.000 description 1
- YNTDEAJPDJLXKN-UHFFFAOYSA-N 3-methyloxonan-2-one Chemical compound CC1CCCCCCOC1=O YNTDEAJPDJLXKN-UHFFFAOYSA-N 0.000 description 1
- YGCZTXZTJXYWCO-UHFFFAOYSA-N 3-phenylpropanal Chemical compound O=CCCC1=CC=CC=C1 YGCZTXZTJXYWCO-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- XRUKRHLZDVJJSX-UHFFFAOYSA-N 4-cyanopentanoic acid Chemical compound N#CC(C)CCC(O)=O XRUKRHLZDVJJSX-UHFFFAOYSA-N 0.000 description 1
- OALYTRUKMRCXNH-UHFFFAOYSA-N 5-pentyloxolan-2-one Chemical compound CCCCCC1CCC(=O)O1 OALYTRUKMRCXNH-UHFFFAOYSA-N 0.000 description 1
- NKCQEIXYLHACJC-UHFFFAOYSA-N 6-propan-2-ylquinoline Chemical compound N1=CC=CC2=CC(C(C)C)=CC=C21 NKCQEIXYLHACJC-UHFFFAOYSA-N 0.000 description 1
- JRLTTZUODKEYDH-UHFFFAOYSA-N 8-methylquinoline Chemical group C1=CN=C2C(C)=CC=CC2=C1 JRLTTZUODKEYDH-UHFFFAOYSA-N 0.000 description 1
- NVEQFIOZRFFVFW-UHFFFAOYSA-N 9-epi-beta-caryophyllene oxide Natural products C=C1CCC2OC2(C)CCC2C(C)(C)CC21 NVEQFIOZRFFVFW-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- ZZXUWRKAAKRMEK-UHFFFAOYSA-N C12CC3CC(CC(C1)C3)C2.CC=CC(=O)O Chemical class C12CC3CC(CC(C1)C3)C2.CC=CC(=O)O ZZXUWRKAAKRMEK-UHFFFAOYSA-N 0.000 description 1
- ZVQUYMKKXHCGGQ-UHFFFAOYSA-N CC(=O)OCC1=CC=CC=C1.OC(=O)CCC1=CC=CC=C1 Chemical compound CC(=O)OCC1=CC=CC=C1.OC(=O)CCC1=CC=CC=C1 ZVQUYMKKXHCGGQ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 244000089742 Citrus aurantifolia Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- YYLLIJHXUHJATK-UHFFFAOYSA-N Cyclohexyl acetate Chemical compound CC(=O)OC1CCCCC1 YYLLIJHXUHJATK-UHFFFAOYSA-N 0.000 description 1
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 1
- HZPKNSYIDSNZKW-UHFFFAOYSA-N Ethyl 2-methylpentanoate Chemical compound CCCC(C)C(=O)OCC HZPKNSYIDSNZKW-UHFFFAOYSA-N 0.000 description 1
- DULCUDSUACXJJC-UHFFFAOYSA-N Ethyl phenylacetate Chemical compound CCOC(=O)CC1=CC=CC=C1 DULCUDSUACXJJC-UHFFFAOYSA-N 0.000 description 1
- WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 1
- 101000648997 Homo sapiens Tripartite motif-containing protein 44 Proteins 0.000 description 1
- 238000012695 Interfacial polymerization Methods 0.000 description 1
- FRLZQXRXIKQFNS-UHFFFAOYSA-N Methyl 2-octynoate Chemical compound CCCCCC#CC(=O)OC FRLZQXRXIKQFNS-UHFFFAOYSA-N 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 239000004159 Potassium persulphate Substances 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- CDJJKTLOZJAGIZ-UHFFFAOYSA-N Tolylacetate Chemical compound CC(=O)OC1=CC=C(C)C=C1 CDJJKTLOZJAGIZ-UHFFFAOYSA-N 0.000 description 1
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 1
- 102100028017 Tripartite motif-containing protein 44 Human genes 0.000 description 1
- XJHRZBIBSSVCEL-UHFFFAOYSA-N Z-Non-6-en-1-ol Natural products CCC=CCCCCCO XJHRZBIBSSVCEL-UHFFFAOYSA-N 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000002386 air freshener Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- FAMPSKZZVDUYOS-UHFFFAOYSA-N alpha-Caryophyllene Natural products CC1=CCC(C)(C)C=CCC(C)=CCC1 FAMPSKZZVDUYOS-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000012874 anionic emulsifier Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- NPNUFJAVOOONJE-UHFFFAOYSA-N beta-cariophyllene Natural products C1CC(C)=CCCC(=C)C2CC(C)(C)C21 NPNUFJAVOOONJE-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- WNHXJHGRIHUOTG-UHFFFAOYSA-N but-2-enyl acetate Chemical compound CC=CCOC(C)=O WNHXJHGRIHUOTG-UHFFFAOYSA-N 0.000 description 1
- OBNCKNCVKJNDBV-UHFFFAOYSA-N butanoic acid ethyl ester Natural products CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 description 1
- 229940043232 butyl acetate Drugs 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229940117948 caryophyllene Drugs 0.000 description 1
- NPNUFJAVOOONJE-UONOGXRCSA-N caryophyllene Natural products C1CC(C)=CCCC(=C)[C@@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-UONOGXRCSA-N 0.000 description 1
- 150000001768 cations Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229960000800 cetrimonium bromide Drugs 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 229960005233 cineole Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 1
- 229940073507 cocamidopropyl betaine Drugs 0.000 description 1
- 235000020057 cognac Nutrition 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 1
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 239000004815 dispersion polymer Substances 0.000 description 1
- 238000012674 dispersion polymerization Methods 0.000 description 1
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 1
- 230000005520 electrodynamics Effects 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
- 239000001813 ethyl (2R)-2-methylbutanoate Substances 0.000 description 1
- 229940090910 ethyl 2-methylbutyrate Drugs 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Substances OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 150000002334 glycols Chemical group 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
- YMBZEYUTGXVZPA-UHFFFAOYSA-N heptanoic acid;pentyl acetate Chemical compound CCCCCCC(O)=O.CCCCCOC(C)=O YMBZEYUTGXVZPA-UHFFFAOYSA-N 0.000 description 1
- UFLHIIWVXFIJGU-UHFFFAOYSA-N hex-3-en-1-ol Natural products CCC=CCCO UFLHIIWVXFIJGU-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000002475 indoles Chemical class 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 150000002561 ketenes Chemical class 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- CXHHBNMLPJOKQD-UHFFFAOYSA-N methyl hydrogen carbonate Chemical compound COC(O)=O CXHHBNMLPJOKQD-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- LUKNLVTZDZMBOU-UHFFFAOYSA-N n-ethoxymethanamine Chemical compound CCONC LUKNLVTZDZMBOU-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- DBSDMAPJGHBWAL-UHFFFAOYSA-N penta-1,4-dien-3-ylbenzene Chemical compound C=CC(C=C)C1=CC=CC=C1 DBSDMAPJGHBWAL-UHFFFAOYSA-N 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- KRIOVPPHQSLHCZ-UHFFFAOYSA-N phenyl propionaldehyde Natural products CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 description 1
- 229940100595 phenylacetaldehyde Drugs 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229940068977 polysorbate 20 Drugs 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229940068968 polysorbate 80 Drugs 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 235000019394 potassium persulphate Nutrition 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000008786 sensory perception of smell Effects 0.000 description 1
- 229940074386 skatole Drugs 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229950011392 sorbitan stearate Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- UHUFTBALEZWWIH-UHFFFAOYSA-N tetradecanal Chemical compound CCCCCCCCCCCCCC=O UHUFTBALEZWWIH-UHFFFAOYSA-N 0.000 description 1
- RBNWAMSGVWEHFP-UHFFFAOYSA-N trans-p-Menthane-1,8-diol Chemical compound CC(C)(O)C1CCC(C)(O)CC1 RBNWAMSGVWEHFP-UHFFFAOYSA-N 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- KMPQYAYAQWNLME-UHFFFAOYSA-N undecanal Chemical compound CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- YEIGUXGHHKAURB-UHFFFAOYSA-N viridine Natural products O=C1C2=C3CCC(=O)C3=CC=C2C2(C)C(O)C(OC)C(=O)C3=COC1=C23 YEIGUXGHHKAURB-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0039—Coated compositions or coated components in the compositions, (micro)capsules
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
- C11D3/502—Protected perfumes
- C11D3/505—Protected perfumes encapsulated or adsorbed on a carrier, e.g. zeolite or clay
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/413—Nanosized, i.e. having sizes below 100 nm
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2984—Microcapsule with fluid core [includes liposome]
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Nanotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Birds (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Medical Informatics (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Pharmacology & Pharmacy (AREA)
- Crystallography & Structural Chemistry (AREA)
- Biophysics (AREA)
- Polymers & Plastics (AREA)
- Dispersion Chemistry (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Fats And Perfumes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
Abstract
Description
商品名 | 通用名称 | 注释 |
RewoquatRTM50 | 甲基硫酸蓖麻油酰胺基丙基三甲基铵 | 阳离子 |
RewoquatCPEM | 甲基硫酸椰油戊基乙氧基甲基铵 | 阳离子 |
EthoquatC12 | 氯化椰油基二(2-羟乙基)甲基铵 | 阳离子 |
CTAB | 溴化十六烷基三甲基铵 | 阳离子 |
LexemulAR | 甘油硬脂酸酯(和)硬脂酰胺基乙基二乙胺 | 阳离子 |
DisponilA1080 | 乙氧基化线性脂肪醇的混合物 | 非离子 |
DisponalA3065 | 乙氧基化线性脂肪醇的混合物 | 非离子 |
MergitalLM4L | 用4mol环氧乙烷进行乙氧基化的C12-C13脂肪醇的混合物 | 非离子 |
Lauropal12 | 用6-15mol环氧乙烷进行乙氧基化的C12-C14脂肪醇的混合物 | 非离子 |
Montane60 | 脱水山梨糖醇硬脂酸酯 | 非离子 |
Tween20 | 聚山梨酸酯20 | 非离子 |
Tween80 | 聚山梨酸酯80 | 非离子 |
TritonX 165 | 硬脂酸酯 | 非离子 |
Tego Betain F 50 | 椰油酰胺基丙基甜菜碱 | 两性离子 |
Betain Tego CK | 脂肪酸烷基酰胺基烷基甜菜碱 | 两性离子 |
Dowfax2Al | 具有四丙烯疏水物源的二磺酸化表面活性剂 | 阴离子 |
SDS | 十二烷基硫酸钠 | 阴离子 |
Abex3594 | 阴离子 | |
AbexEP-227 | nonoxynol-77硫酸铵 | 阴离子 |
LexemulAS | 甘油硬脂酸酯(和)十二烷基硫酸钠 | 阴离子 |
化学文摘名称 | OV |
2-甲基戊酸乙酯 | 62586530 |
异丁酸乙酯FCC | 39200330 |
1-(2,6,6-三甲基-1,3-环己二烯-1-基)-丁-2-烯-1-酮 | 21672290 |
壬二烯醛1%柠檬酸三乙酯 | 17446920 |
苯基乙醛85 | 14342060 |
3-甲基吲哚 | 10531770 |
己酸乙酯 | 10296830 |
1,8-环氧-对-甲烷 | 9931397 |
醛C12 MNA | 9648383 |
乙酸乙酯 | 7672145 |
2-甲基丁酸乙酯 | 6716841 |
醛C8 | 5678510 |
反式癸烯-4-醛 | 4668142 |
十一碳三烯(UNDECATRIENE) | 4482573 |
甲基辛基乙醛 | 4469274 |
醛C7 | 3699238 |
2,6-二甲基-5-庚烯醛 | 3674714 |
二氢2-甲氧基-4-(2-丙烯基)苯酚 | 3472000 |
丁基2-苯并呋喃酮 | 3266946 |
酸柠檬氧化物(lime oxide) | 2161723 |
丁酸乙酯 | 1764598 |
顺式-6-壬烯醇 | 1712805 |
对-甲苯基醛提取物(EXTRA) | 1475808 |
二氢茴香脑FCC | 1313749 |
乙酸环己酯 | 1292485 |
乙酸对甲苯酯 | 1273204 |
2,4-二甲基-6-苯基-二氢吡喃 | 1193400 |
3-(3-异丙基苯基)丁醛 | 1187323 |
1-(2,6,6,-三甲基环己-1-烯-1-基)丁-2-烯-1-酮 | 1122995 |
2-辛炔酸甲酯 | 1094551 |
异醋酸丁酯FCC | 979809.6 |
7-甲基-3,4-二氢-2H-1,5-苯并二氧杂环庚三烯-3-酮 | 973365.4 |
1-(2,6,6-三甲基-1,3-环己烯-1-基)2-丁烯-1-酮 | 961551.6 |
2-甲氧基-4-甲基苯酚 | 943751.4 |
4-甲氧基苯甲醛 | 941980.3 |
辛烯醇 | 925978.5 |
6,6-二甲基双环[3.1.1]庚-2-烯-2-丙醛 | 904490.6 |
乙酸3-甲基-2-丙烯基酯 | 877798.3 |
醛异C11 | 854722 |
3,7-二甲基-2,6-辛二烯腈 | 832569 |
氨茴酸甲酯 | 827264.3 |
甲基辛内酯 | 826643 |
苯乙酸甲酯 | 792198.8 |
甲基紫罗兰酮/IRISANTHEME | 778605.1 |
2,4-二甲基苯乙酮 | 754754.7 |
8-乙基-1-氧杂螺[4.5]癸-2-酮 | 734286 |
4-甲氧苯甲醛 | 683617.5 |
2-甲基-5-(1-甲基乙烯基)环己-2-烯-1-酮 | 673272.8 |
苯基丙醛 | 589314.7 |
戊基羟乙酸烯丙基酯 | 587664.6 |
2,4-二甲基3-环己烯-1-甲醛 | 587309.8 |
1-甲醛-2,4-二甲基-环己-3-烯 | 585468 |
顺式-3-乙酸己烯酯 | 575465.8 |
7-甲基-3-亚甲基-1,6-辛二烯 | 546499.8 |
对甲酚 | 524810.3 |
异壬醛 | 510654.2 |
醛C18 | 507873.9 |
戊基羟乙酸烯丙基酯 | 503042.8 |
2-己基-环戊-2-烯-1-酮 | 485812.6 |
异丙基喹啉/碱3 | 479565.3 |
2-苯基丙醛 | 477838.4 |
乙酸戊酯 | 441261.3 |
乙酸丁酯 | 435143.8 |
甲基LAITONE | 420065.1 |
醛C14 | 419891.6 |
顺式-3-己烯醇 | 391510 |
醛C10 | 387743.2 |
丁酸2-甲基-己基酯 | 382190.6 |
苯乙酸乙酯 | 375894.8 |
乙酸(环己氧基)-2-丙烯基酯 | 372893.1 |
癸-4-烯-1-醛 | 367957 |
甲基己基甲酮 | 361139.4 |
甲酰基-7-异丙基-5-甲基-2-双环[2.2.2.]辛-2-烯 | 355730.8 |
2,6-二甲基庚烷-2-醇 | 352155.6 |
醛C11十一碳烯醛 | 351095 |
反式2-己烯醛 | 350064.3 |
2-甲氧基-4-(2-丙烯基)苯酚 | 346904.9 |
3,7-二甲基辛醛 | 311427.9 |
庚酸乙酯 | 310684.7 |
3,7-二甲基-2,6-辛二烯腈 | 298260.5 |
4-甲醛-1,3,5-三甲基-环己-1-烯 | 295165.8 |
四氢-4-甲基-2-(2-甲基-1-丙烯基)-2H-吡喃 | 291002 |
甲基苯基乙基氧化物 | 287117.9 |
顺式-3-甲酸己烯酯 | 282721.5 |
4-82,6,6-三甲基环己-1-烯-1-基)-丁-3-烯-2-酮 | 280385 |
己-5-烯-2-酮 | 278762.7 |
石竹烯FCC,天然NKFP | 278378 |
对甲基苯乙酮 | 271792.6 |
JASVERATE | 265515.9 |
2,4,4,7-四甲基-壬-6,8-二烯-3-酮 | 252222 |
二氢3,7-二甲基-1,6-辛二烯-3-醇 | 250072.3 |
2,6-二甲基辛-7-烯-2-醇 | 248873.6 |
1-(2,6,6-三甲基-2-环己烯-1-基)-2-丁烯-1-酮 | 245891.4 |
1-(2,6,6-三甲基-3-环己烯-1-基)-丁-2-烯-1-酮 | 243343.3 |
甲基·戊基酮 | 239523.8 |
1-甲基-4-(1-甲基乙叉基)环己烯 | 234817.8 |
CITRODYLE | 230257.8 |
α-异甲基紫罗兰酮 | 218736.2 |
3,7-二甲基-1,6-辛二烯-3-醇 | 218426.5 |
辛炔碳酸甲基酯 | 216945.5 |
苯乙酮萃取物 | 212908.8 |
3-甲基-5-(2,2,3-三甲基-3-环戊烯-1-基)-4-戊烯-2-醇 | 212557.4 |
γ-辛内酯 | 210058.7 |
纯吲哚 | 207042.8 |
甲基丙烯酸量[%] | 气味性能24h 48h >72h | 聚合物分散体的稳定性* | ||
0 | ++ | + | + | - |
2.6 | +++ | ++ | + | + |
5.2 | +++ | ++ | ++ | + |
7.8 | ++ | ++ | ++ | + |
香料量[%] | 气味性能香料A 香料B | |
5.9 | ++ | ++ |
11.7 | ++ | ++ |
香料量[%] | 气味性能 | 胶乳稳定性 |
2.9 | + | + |
5.9 | ++ | + |
11.7 | ++ | + |
17.7 | + | + |
35 | + | 稳定性限制 |
软化剂的量 | 分散体的量 | 1天 | 4天 | 10天 | 1个月 |
7g | 1.200g | 凝胶 | 凝胶 | 凝胶 | 凝胶 |
7g | 1.008g | 液体 | 凝胶 | 凝胶 | 凝胶 |
7g | 0.806g | 液体 | 液体 | 液体 | 液体 |
7g | 0.495g | 液体 | 液体 | 液体 | 液体 |
7g | 0.310g | 液体 | 液体 | 液体 | 液体 |
香料组分 | tR | 24小时后面积计数 | 24小时后面积计数 |
参考 | 样品 | ||
乙酸戊酯(Amylacetat) | 8.82 | 0 | 730 |
桉叶油素 | 9.60 | 27 | 6664 |
二甲基辛烯酮 | 12.52 | 20 | 4086 |
四氮环十五烷C | 13.54 | 0 | 3266 |
里哪醇 | 16.99 | 0 | 14 |
醛C12 | 19.33 | 67 | 984 |
苯乙醛二甲缩醛 | 21.15 | 0 | 0 |
萜品醇 | 21.60 | 0 | 253 |
乙酸苄基酯(benzylacetat) | 22.64 | 0 | 21 |
α-紫罗兰酮 | 26.52 | 0 | 238 |
化合物X | 27.54 | 0 | 237 |
苯基乙醇 | 28.77 | 9 | 13 |
二苯基氧化物 | 31.66 | 30 | 747 |
化合物Y | 32.28 | 11 | 130 |
α-甲基对叔丁基苯丙醛 | 33.00 | 116 | 131 |
Claims (20)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00108313A EP1146057A1 (en) | 2000-04-15 | 2000-04-15 | Polymeric nanoparticles including olfactive molecules |
EP00108313.8 | 2000-04-15 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1423661A true CN1423661A (zh) | 2003-06-11 |
CN1247617C CN1247617C (zh) | 2006-03-29 |
Family
ID=8168487
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB018081029A Expired - Fee Related CN1247617C (zh) | 2000-04-15 | 2001-04-06 | 包括有气味组分的聚合纳米粒子 |
Country Status (7)
Country | Link |
---|---|
US (2) | US7205340B2 (zh) |
EP (2) | EP1146057A1 (zh) |
JP (1) | JP2003531225A (zh) |
CN (1) | CN1247617C (zh) |
AU (1) | AU6384301A (zh) |
BR (1) | BR0110015A (zh) |
WO (1) | WO2001079303A1 (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104812447A (zh) * | 2012-11-23 | 2015-07-29 | 荷兰联合利华有限公司 | 有益剂递送颗粒、包含所述颗粒的组合物和处理基体的方法 |
CN107708652A (zh) * | 2015-06-12 | 2018-02-16 | 宝洁公司 | 芳香剂组合物及其用途 |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1146057A1 (en) * | 2000-04-15 | 2001-10-17 | Givaudan SA | Polymeric nanoparticles including olfactive molecules |
FR2813313B1 (fr) * | 2000-08-25 | 2007-06-15 | Rhodia Chimie Sa | Composition a base de nanoparticules ou de nanolatex de polymeres pour le soin du linge |
DE10063428A1 (de) * | 2000-12-20 | 2002-07-11 | Henkel Kgaa | Dispersionen nanopartikulärer riechstoffhaltiger Kompositmaterialien |
ATE440938T1 (de) | 2001-07-11 | 2009-09-15 | Procter & Gamble | Verfahren zur oberflächenreinigung mittels eines dispergierten polymers |
US6740631B2 (en) * | 2002-04-26 | 2004-05-25 | Adi Shefer | Multi component controlled delivery system for fabric care products |
US6825161B2 (en) * | 2002-04-26 | 2004-11-30 | Salvona Llc | Multi component controlled delivery system for soap bars |
DE60324225D1 (de) * | 2002-06-14 | 2008-12-04 | Rohm & Haas | Farbmittel, Dispergiermittel und Dispersionen enthaltend polymere Nanopartikel |
US7316994B2 (en) | 2002-11-01 | 2008-01-08 | The Procter & Gamble Company | Perfume polymeric particles |
US8187580B2 (en) | 2002-11-01 | 2012-05-29 | The Procter & Gamble Company | Polymeric assisted delivery using separate addition |
US8409618B2 (en) | 2002-12-20 | 2013-04-02 | Kimberly-Clark Worldwide, Inc. | Odor-reducing quinone compounds |
US7666410B2 (en) * | 2002-12-20 | 2010-02-23 | Kimberly-Clark Worldwide, Inc. | Delivery system for functional compounds |
EP1443058A1 (en) | 2003-01-29 | 2004-08-04 | Firmenich Sa | Polymeric particles and fragrance delivery systems |
EP2428278A3 (en) | 2003-05-27 | 2012-04-25 | Panasonic Electric Works Co., Ltd | Charged fine particulate water, and method of creating environment where mist of the charged fine particulate water is dispersed |
US7794737B2 (en) | 2003-10-16 | 2010-09-14 | Kimberly-Clark Worldwide, Inc. | Odor absorbing extrudates |
US7837663B2 (en) | 2003-10-16 | 2010-11-23 | Kimberly-Clark Worldwide, Inc. | Odor controlling article including a visual indicating device for monitoring odor absorption |
US7488520B2 (en) | 2003-10-16 | 2009-02-10 | Kimberly-Clark Worldwide, Inc. | High surface area material blends for odor reduction, articles utilizing such blends and methods of using same |
US7754197B2 (en) | 2003-10-16 | 2010-07-13 | Kimberly-Clark Worldwide, Inc. | Method for reducing odor using coordinated polydentate compounds |
US7879350B2 (en) | 2003-10-16 | 2011-02-01 | Kimberly-Clark Worldwide, Inc. | Method for reducing odor using colloidal nanoparticles |
US7413550B2 (en) | 2003-10-16 | 2008-08-19 | Kimberly-Clark Worldwide, Inc. | Visual indicating device for bad breath |
US7678367B2 (en) | 2003-10-16 | 2010-03-16 | Kimberly-Clark Worldwide, Inc. | Method for reducing odor using metal-modified particles |
EP1711231A1 (en) | 2003-10-31 | 2006-10-18 | Firmenich Sa | Fragrance delivery system for surface cleaners and conditioners |
GB0328849D0 (en) * | 2003-12-12 | 2004-01-14 | Unilever Plc | Fabric conditioning composition |
GB0328846D0 (en) * | 2003-12-12 | 2004-01-14 | Unilever Plc | Fabric conditioning composition |
GB0328844D0 (en) * | 2003-12-12 | 2004-01-14 | Unilever Plc | Fabric conditioning composition |
GB0328847D0 (en) * | 2003-12-12 | 2004-01-14 | Unilever Plc | Fabric conditioning composition |
GB0328838D0 (en) * | 2003-12-12 | 2004-01-14 | Unilever Plc | Fabric conditioning composition |
GB0328848D0 (en) * | 2003-12-12 | 2004-01-14 | Unilever Plc | Fabric conditioning composition |
GB0328842D0 (en) * | 2003-12-12 | 2004-01-14 | Unilever Plc | Fabric conditioning composition |
US7576170B2 (en) | 2003-12-19 | 2009-08-18 | Momentive Performance Materials | Cyclic siloxane compositions for the release of active ingredients |
US7579495B2 (en) | 2003-12-19 | 2009-08-25 | Momentive Performance Materials Inc. | Active-releasing cyclic siloxanes |
US7238732B2 (en) | 2004-02-18 | 2007-07-03 | Eastman Chemical Company | Radiation-curable adhesive compositions |
US7262242B2 (en) * | 2004-02-18 | 2007-08-28 | Eastman Chemical Company | Aromatic/acrylate tackifier resin and acrylic polymer blends |
US7332540B2 (en) * | 2004-02-18 | 2008-02-19 | Eastman Chemical Company | Aromatic-acrylate tackifier resins |
US7077463B2 (en) * | 2004-04-06 | 2006-07-18 | Lear Corporation | Rear fold down cargo seat with tilt down cushion |
US20060047025A1 (en) * | 2004-06-29 | 2006-03-02 | Matthew Piazza | Viscous materials and method for producing |
US7723285B2 (en) | 2004-07-20 | 2010-05-25 | Michigan Molecular Institute | Beneficial agent delivery systems |
US7517840B2 (en) | 2005-04-07 | 2009-04-14 | Givaudan Fragrances Corporation | Optimized perfumery for rinse-off products |
US7446079B2 (en) * | 2005-04-07 | 2008-11-04 | Givaudan Fragrances Corporation | Perfumes for rinse-off systems |
US20060269441A1 (en) * | 2005-05-25 | 2006-11-30 | Ochomogo Maria G | Nanosilica-based food contact sanitizer |
EP1996627B1 (de) * | 2006-03-13 | 2011-08-31 | Basf Se | Verfahren zur herstellung von polymeren nanopartikeln |
US7977103B2 (en) | 2006-04-20 | 2011-07-12 | Kimberly-Clark Worldwide, Inc. | Method for detecting the onset of ovulation |
US9345649B2 (en) | 2006-12-21 | 2016-05-24 | Avon Products, Inc. | Cosmetic composition containing novel fractal particle-based gels |
US20100144919A1 (en) * | 2007-11-28 | 2010-06-10 | Janos Borbely | Reactive polymeric nanoparticles (RPNPS) for restoration materials in dentistry |
TWI411448B (zh) | 2007-12-27 | 2013-10-11 | Avon Prod Inc | 適合用於化妝品之光學模糊色素組合物 |
TWI468185B (zh) * | 2007-12-27 | 2015-01-11 | Avon Prod Inc | 適合用於化妝品組合物之凝膠技術 |
EP2254545A2 (en) * | 2008-02-21 | 2010-12-01 | Basf Se | Preparation of cationic nanoparticles and personal care compositions comprising said nanoparticles |
FR2999918B1 (fr) | 2012-12-26 | 2015-06-19 | Oreal | Polymere de type sol-gel a empreinte moleculaire pour pieger selectivement les molecules odorantes |
FR2999917B1 (fr) * | 2012-12-26 | 2017-06-23 | Oreal | Polymere a empreinte moleculaire pour pieger selectivement les molecules odorantes |
FR3000074B1 (fr) | 2012-12-26 | 2015-01-16 | Oreal | Polymeres a empreinte moleculaire et leur utilisation comme agent antipelliculaire |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE967860C (de) * | 1954-07-02 | 1957-12-19 | Boehringer Sohn Ingelheim | Verfahren zur Herstellung von Loesungen von Riechstoffen in festen Koerpern |
JPS63122796A (ja) | 1986-11-11 | 1988-05-26 | 花王株式会社 | 液体洗浄剤組成物 |
JPS644237A (en) * | 1987-03-12 | 1989-01-09 | Dainippon Ink & Chemicals | Manufacture of slowly-releasing non-film-forming polymer dispersed liquid |
EP0330692A1 (en) * | 1987-08-24 | 1989-09-06 | Ciba Specialty Chemicals Water Treatments Limited | Polymeric compositions |
US4919841A (en) | 1988-06-06 | 1990-04-24 | Lever Brothers Company | Wax encapsulated actives and emulsion process for their production |
US5155193A (en) * | 1990-07-02 | 1992-10-13 | Xerox Corporation | Suspension polymerization processes |
US5506201A (en) * | 1994-04-29 | 1996-04-09 | International Flavors & Fragrances Inc. | Formulation of a fat surfactant vehicle containing a fragrance |
US6126953A (en) * | 1996-08-19 | 2000-10-03 | The Procter & Gamble Company | Fragrance delivery systems for personal care articles |
US6150310A (en) * | 1996-08-19 | 2000-11-21 | The Procter & Gamble Company | Laundry detergent compositions comprising β-ketoester pro-fragrances |
CN1233282A (zh) * | 1996-08-19 | 1999-10-27 | 普罗格特-甘布尔公司 | 包含β-酮酯香料前体的洗衣洗涤剂组合物 |
DE19645024A1 (de) * | 1996-10-31 | 1998-05-07 | Basf Ag | Bleichhilfsmittel enthaltende Mikrokapseln |
NZ336352A (en) * | 1996-12-19 | 2000-11-24 | S | Preparation of polycarboxypolyamide resins for use as coating compositions |
WO1998028398A1 (en) | 1996-12-23 | 1998-07-02 | Quest International B.V. | Particles containing absorbed liquids and methods of making them |
EP0925776A3 (en) | 1997-12-16 | 2001-08-29 | Givaudan SA | Polymer with binding capacity for organoleptic substances |
US6051540A (en) * | 1998-11-05 | 2000-04-18 | International Flavors & Fragrances Inc. | Method employing drum chilling and apparatus therefor for producing fragrance-containing long lasting solid particle |
EP1146057A1 (en) * | 2000-04-15 | 2001-10-17 | Givaudan SA | Polymeric nanoparticles including olfactive molecules |
-
2000
- 2000-04-15 EP EP00108313A patent/EP1146057A1/en not_active Withdrawn
-
2001
- 2001-04-06 AU AU63843/01A patent/AU6384301A/en not_active Abandoned
- 2001-04-06 CN CNB018081029A patent/CN1247617C/zh not_active Expired - Fee Related
- 2001-04-06 WO PCT/EP2001/003986 patent/WO2001079303A1/en active Application Filing
- 2001-04-06 EP EP01938094A patent/EP1274739A1/en not_active Withdrawn
- 2001-04-06 US US10/240,978 patent/US7205340B2/en not_active Expired - Fee Related
- 2001-04-06 JP JP2001576897A patent/JP2003531225A/ja not_active Ceased
- 2001-04-06 BR BR0110015-7A patent/BR0110015A/pt active Search and Examination
-
2007
- 2007-03-12 US US11/684,735 patent/US7776939B2/en not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104812447A (zh) * | 2012-11-23 | 2015-07-29 | 荷兰联合利华有限公司 | 有益剂递送颗粒、包含所述颗粒的组合物和处理基体的方法 |
CN104812447B (zh) * | 2012-11-23 | 2017-08-25 | 荷兰联合利华有限公司 | 有益剂递送颗粒、包含所述颗粒的组合物和处理基体的方法 |
CN107708652A (zh) * | 2015-06-12 | 2018-02-16 | 宝洁公司 | 芳香剂组合物及其用途 |
CN107708652B (zh) * | 2015-06-12 | 2021-09-21 | 宝洁公司 | 芳香剂组合物及其用途 |
Also Published As
Publication number | Publication date |
---|---|
US7205340B2 (en) | 2007-04-17 |
EP1146057A1 (en) | 2001-10-17 |
US20070207052A1 (en) | 2007-09-06 |
EP1274739A1 (en) | 2003-01-15 |
WO2001079303A1 (en) | 2001-10-25 |
AU6384301A (en) | 2001-10-30 |
US20030181540A1 (en) | 2003-09-25 |
US7776939B2 (en) | 2010-08-17 |
CN1247617C (zh) | 2006-03-29 |
JP2003531225A (ja) | 2003-10-21 |
BR0110015A (pt) | 2003-12-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1247617C (zh) | 包括有气味组分的聚合纳米粒子 | |
JP6793713B2 (ja) | マイクロカプセル | |
CN112638352B (zh) | 包含含有有益剂的递送颗粒的组合物 | |
JP6827961B2 (ja) | カプセル封入された香料組成物における、またはこれに関する改善 | |
JP4495720B2 (ja) | ポリマー粒子および芳香デリバリーシステムの製造方法および前記方法により得られたポリマー粒子および芳香デリバリーシステム | |
RU2639909C2 (ru) | Система носителя для отдушки | |
US10059907B2 (en) | Microcapsules | |
CN105431227B (zh) | 微囊 | |
CN110036038B (zh) | 微胶囊的制造方法 | |
JP2006514704A (ja) | ポリマー補助された有益剤デリバリーシステム | |
DE60315241T2 (de) | Zusammensetzungen mehrstufiger Polymere mit ausgelöster Freisetzung | |
JP2023543577A (ja) | 封入体の集団を含む消費者製品組成物 | |
JP2022507552A (ja) | 封入体を含む組成物 | |
TWI417438B (zh) | Fiber treatment agent | |
WO2022109127A1 (en) | Biodegradable delivery particles | |
KR102159515B1 (ko) | 중합성 조성물, 고분자 캡슐 및 이를 포함하는 섬유 유연제 조성물 | |
JP2023549862A (ja) | 高いコア:壁比を有する送達粒子を含む消費者製品 | |
JP2023543579A (ja) | 高コア対壁比を有する送達粒子を含む消費者製品 | |
CN107118296A (zh) | 一种具有可控薄荷醇包覆量的高分子树脂复合微球及其制备方法 | |
JPH1072776A (ja) | エマルジョン型洗濯糊およびその製造方法 | |
CN117177808A (zh) | 具有高芯:壁比的递送颗粒 | |
WO2005059074A1 (en) | Fabric conditioning composition | |
US20140065197A1 (en) | Carrier system for frangrances |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
EE01 | Entry into force of recordation of patent licensing contract |
Assignee: Shanghai qihuadun Co. Ltd. Assignor: Givaudan S. A. Contract fulfillment period: 2007.1.1 to 2012.12.31 contract change Contract record no.: 2009990001148 Denomination of invention: Polymeric nano particles including olfactive components Granted publication date: 20060329 License type: Exclusive license Record date: 20091014 |
|
LIC | Patent licence contract for exploitation submitted for record |
Free format text: EXCLUSIVE LICENSE; TIME LIMIT OF IMPLEMENTING CONTACT: 2007.1.1 TO 2012.12.31; CHANGE OF CONTRACT Name of requester: SHANGHAI GIVAUDAN CO., LTD. Effective date: 20091014 |
|
C56 | Change in the name or address of the patentee |
Owner name: GIVAUDAN CO., LTD. Free format text: FORMER NAME: GIVAUDAN SA |
|
CP01 | Change in the name or title of a patent holder |
Address after: Swiss Wei Ernie Patentee after: Givaudan SA Address before: Swiss Wei Ernie Patentee before: Givaudan S. A. |
|
EC01 | Cancellation of recordation of patent licensing contract |
Assignee: Shanghai qihuadun Co. Ltd. Assignor: Givaudan S. A. Contract record no.: 2009990001148 Date of cancellation: 20100805 |
|
EE01 | Entry into force of recordation of patent licensing contract |
Assignee: Chiverton daily Flavors & fragrances (Shanghai) Co., Ltd. Assignor: Givaudan SA Contract record no.: 2010990000597 Denomination of invention: Polymeric nano particles including olfactive components Granted publication date: 20060329 License type: Exclusive License Open date: 20030611 Record date: 20100805 |
|
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20060329 Termination date: 20150406 |
|
EXPY | Termination of patent right or utility model |