JP2009149880A5

JP2009149880A5 -

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Publication number: JP2009149880A5
Authority: JP; Japan
Prior art keywords: particles; silicone; meth; acrylate; groups
Prior art date: 2008-12-03
Legal status : Granted

Application number

JP2008308124A

Other languages

English (en)

Japanese (ja)

Other versions

JP5590539B2 (ja

JP2009149880A (ja

Filing date

2008-12-03

Publication date

2014-02-13

2007-12-06 Priority claimed from DE200710058713 external-priority patent/DE102007058713A1/de

2008-12-03 Application filed filed Critical

2009-07-09 Publication of JP2009149880A publication Critical patent/JP2009149880A/ja

2014-02-13 Publication of JP2009149880A5 publication Critical patent/JP2009149880A5/ja

2014-09-17 Application granted granted Critical

2014-09-17 Publication of JP5590539B2 publication Critical patent/JP5590539B2/ja

Status Expired - Fee Related legal-status Critical Current

2028-12-03 Anticipated expiration legal-status Critical

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239000002245 particle Substances 0.000 claims description 163
229920001296 polysiloxane Polymers 0.000 claims description 129
-1 polyalkoxy Chemical group 0.000 claims description 102
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 89
239000000203 mixture Substances 0.000 claims description 77
239000000839 emulsion Substances 0.000 claims description 68
238000000034 method Methods 0.000 claims description 61
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 59
239000003995 emulsifying agent Substances 0.000 claims description 37
239000006185 dispersion Substances 0.000 claims description 32
230000008569 process Effects 0.000 claims description 26
239000003999 initiator Substances 0.000 claims description 25
239000000463 material Substances 0.000 claims description 25
230000003993 interaction Effects 0.000 claims description 24
150000003254 radicals Chemical class 0.000 claims description 24
150000001875 compounds Chemical class 0.000 claims description 19
239000002537 cosmetic Substances 0.000 claims description 17
229920000642 polymer Polymers 0.000 claims description 17
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 16
239000012074 organic phase Substances 0.000 claims description 16
239000007787 solid Substances 0.000 claims description 15
239000008346 aqueous phase Substances 0.000 claims description 14
239000007957 coemulsifier Substances 0.000 claims description 14
239000011258 core-shell material Substances 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 13
239000000843 powder Substances 0.000 claims description 12
239000000126 substance Substances 0.000 claims description 12
125000004432 carbon atom Chemical group C* 0.000 claims description 11
239000012071 phase Substances 0.000 claims description 11
239000000654 additive Substances 0.000 claims description 10
125000003118 aryl group Chemical group 0.000 claims description 10
239000000049 pigment Substances 0.000 claims description 10
238000004140 cleaning Methods 0.000 claims description 9
239000003795 chemical substances by application Substances 0.000 claims description 8
238000000576 coating method Methods 0.000 claims description 8
125000002877 alkyl aryl group Chemical group 0.000 claims description 7
239000011248 coating agent Substances 0.000 claims description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
125000003545 alkoxy group Chemical group 0.000 claims description 6
125000003710 aryl alkyl group Chemical group 0.000 claims description 6
235000014113 dietary fatty acids Nutrition 0.000 claims description 6
239000000194 fatty acid Substances 0.000 claims description 6
229930195729 fatty acid Natural products 0.000 claims description 6
239000000047 product Substances 0.000 claims description 6
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 5
125000003342 alkenyl group Chemical group 0.000 claims description 5
125000004122 cyclic group Chemical group 0.000 claims description 5
239000010954 inorganic particle Substances 0.000 claims description 5
229920000620 organic polymer Polymers 0.000 claims description 5
239000004094 surface-active agent Substances 0.000 claims description 5
239000000853 adhesive Substances 0.000 claims description 4
230000001070 adhesive effect Effects 0.000 claims description 4
229920006317 cationic polymer Polymers 0.000 claims description 4
239000003599 detergent Substances 0.000 claims description 4
239000003814 drug Substances 0.000 claims description 4
150000004665 fatty acids Chemical class 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000007788 liquid Substances 0.000 claims description 4
229910044991 metal oxide Inorganic materials 0.000 claims description 4
239000003566 sealing material Substances 0.000 claims description 4
229910000077 silane Inorganic materials 0.000 claims description 4
150000004760 silicates Chemical class 0.000 claims description 4
229920002050 silicone resin Polymers 0.000 claims description 4
238000009736 wetting Methods 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
150000004649 carbonic acid derivatives Chemical class 0.000 claims description 3
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 3
150000004679 hydroxides Chemical class 0.000 claims description 3
239000008384 inner phase Substances 0.000 claims description 3
239000000314 lubricant Substances 0.000 claims description 3
150000004767 nitrides Chemical class 0.000 claims description 3
230000000379 polymerizing effect Effects 0.000 claims description 3
229920006395 saturated elastomer Polymers 0.000 claims description 3
125000005248 alkyl aryloxy group Chemical group 0.000 claims description 2
150000001450 anions Chemical class 0.000 claims description 2
239000002518 antifoaming agent Substances 0.000 claims description 2
238000009499 grossing Methods 0.000 claims description 2
125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 2
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
125000005027 hydroxyaryl group Chemical group 0.000 claims description 2
230000000051 modifying effect Effects 0.000 claims description 2
239000008385 outer phase Substances 0.000 claims description 2
230000003578 releasing effect Effects 0.000 claims description 2
239000000758 substrate Substances 0.000 claims description 2
239000002562 thickening agent Substances 0.000 claims description 2
235000018936 Vitellaria paradoxa Nutrition 0.000 claims 2
239000000825 pharmaceutical preparation Substances 0.000 claims 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 42
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 37
239000000243 solution Substances 0.000 description 34
229910052757 nitrogen Inorganic materials 0.000 description 28
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 25
238000006116 polymerization reaction Methods 0.000 description 22
238000003756 stirring Methods 0.000 description 21
239000003921 oil Substances 0.000 description 20
235000019198 oils Nutrition 0.000 description 20
238000002360 preparation method Methods 0.000 description 17
230000004048 modification Effects 0.000 description 15
238000012986 modification Methods 0.000 description 15
238000004090 dissolution Methods 0.000 description 14
125000000524 functional group Chemical group 0.000 description 14
LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 13
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 13
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
235000013870 dimethyl polysiloxane Nutrition 0.000 description 12
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 12
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 11
239000012935 ammoniumperoxodisulfate Substances 0.000 description 11
239000007864 aqueous solution Substances 0.000 description 11
125000002091 cationic group Chemical group 0.000 description 11
150000002148 esters Chemical group 0.000 description 11
238000009472 formulation Methods 0.000 description 11
WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 11
229910000342 sodium bisulfate Inorganic materials 0.000 description 11
BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 10
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 10
125000001931 aliphatic group Chemical group 0.000 description 9
239000004205 dimethyl polysiloxane Substances 0.000 description 9
239000011246 composite particle Substances 0.000 description 8
239000000178 monomer Substances 0.000 description 8
239000002253 acid Substances 0.000 description 7
150000003839 salts Chemical class 0.000 description 7
229920002545 silicone oil Polymers 0.000 description 7
238000001291 vacuum drying Methods 0.000 description 7
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
239000004721 Polyphenylene oxide Substances 0.000 description 6
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
229910004298 SiO 2 Inorganic materials 0.000 description 6
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
229920001577 copolymer Polymers 0.000 description 6
239000004615 ingredient Substances 0.000 description 6
229920000570 polyether Polymers 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
238000010557 suspension polymerization reaction Methods 0.000 description 6
NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 5
XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 5
229960003237 betaine Drugs 0.000 description 5
150000001735 carboxylic acids Chemical class 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
238000004132 cross linking Methods 0.000 description 5
238000009826 distribution Methods 0.000 description 5
239000011159 matrix material Substances 0.000 description 5
239000002609 medium Substances 0.000 description 5
229940041616 menthol Drugs 0.000 description 5
239000003607 modifier Substances 0.000 description 5
150000004756 silanes Chemical class 0.000 description 5
230000006641 stabilisation Effects 0.000 description 5
238000011105 stabilization Methods 0.000 description 5
235000007586 terpenes Nutrition 0.000 description 5
229910002012 Aerosil® Inorganic materials 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
241001070941 Castanea Species 0.000 description 4
235000014036 Castanea Nutrition 0.000 description 4
GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 4
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
239000002250 absorbent Substances 0.000 description 4
230000002745 absorbent Effects 0.000 description 4
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 4
239000004480 active ingredient Substances 0.000 description 4
230000000996 additive effect Effects 0.000 description 4
230000002776 aggregation Effects 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 4
FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 4
150000001408 amides Chemical class 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
239000003093 cationic surfactant Substances 0.000 description 4
IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
CVSVTCORWBXHQV-UHFFFAOYSA-N creatine Chemical compound NC(=[NH2+])N(C)CC([O-])=O CVSVTCORWBXHQV-UHFFFAOYSA-N 0.000 description 4
229940086555 cyclomethicone Drugs 0.000 description 4
238000009792 diffusion process Methods 0.000 description 4
239000000975 dye Substances 0.000 description 4
239000000945 filler Substances 0.000 description 4
FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 4
238000006459 hydrosilylation reaction Methods 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
238000002156 mixing Methods 0.000 description 4
239000002105 nanoparticle Substances 0.000 description 4
239000003755 preservative agent Substances 0.000 description 4
238000010526 radical polymerization reaction Methods 0.000 description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 3
XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
229910019142 PO4 Inorganic materials 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000006096 absorbing agent Substances 0.000 description 3
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150000001252 acrylic acid derivatives Chemical class 0.000 description 3
239000008186 active pharmaceutical agent Substances 0.000 description 3
238000004220 aggregation Methods 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
125000005037 alkyl phenyl group Polymers 0.000 description 3
125000000129 anionic group Chemical group 0.000 description 3
235000010323 ascorbic acid Nutrition 0.000 description 3
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239000000872 buffer Substances 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000005859 coupling reaction Methods 0.000 description 3
GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 3
125000003700 epoxy group Chemical group 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
239000003205 fragrance Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
150000004706 metal oxides Chemical class 0.000 description 3
TWXDDNPPQUTEOV-FVGYRXGTSA-N methamphetamine hydrochloride Chemical compound Cl.CN[C@@H](C)CC1=CC=CC=C1 TWXDDNPPQUTEOV-FVGYRXGTSA-N 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
125000000962 organic group Chemical group 0.000 description 3
239000010452 phosphate Substances 0.000 description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
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239000002904 solvent Substances 0.000 description 3
239000004408 titanium dioxide Substances 0.000 description 3
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GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 3
WTVHAMTYZJGJLJ-UHFFFAOYSA-N (+)-(4S,8R)-8-epi-beta-bisabolol Natural products CC(C)=CCCC(C)C1(O)CCC(C)=CC1 WTVHAMTYZJGJLJ-UHFFFAOYSA-N 0.000 description 2
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
WWUZIQQURGPMPG-UHFFFAOYSA-N (-)-D-erythro-Sphingosine Natural products CCCCCCCCCCCCCC=CC(O)C(N)CO WWUZIQQURGPMPG-UHFFFAOYSA-N 0.000 description 2
RGZSQWQPBWRIAQ-CABCVRRESA-N (-)-alpha-Bisabolol Chemical compound CC(C)=CCC[C@](C)(O)[C@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-CABCVRRESA-N 0.000 description 2
FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 2
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
AERBNCYCJBRYDG-UHFFFAOYSA-N D-ribo-phytosphingosine Natural products CCCCCCCCCCCCCCC(O)C(O)C(N)CO AERBNCYCJBRYDG-UHFFFAOYSA-N 0.000 description 2
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
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239000006057 Non-nutritive feed additive Substances 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 2
239000012963 UV stabilizer Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
125000004450 alkenylene group Chemical group 0.000 description 2
150000008055 alkyl aryl sulfonates Chemical group 0.000 description 2
150000005215 alkyl ethers Chemical group 0.000 description 2
150000008051 alkyl sulfates Chemical class 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 2
RGZSQWQPBWRIAQ-LSDHHAIUSA-N alpha-Bisabolol Natural products CC(C)=CCC[C@@](C)(O)[C@@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-LSDHHAIUSA-N 0.000 description 2
229940024606 amino acid Drugs 0.000 description 2
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150000001413 amino acids Chemical class 0.000 description 2
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230000000844 anti-bacterial effect Effects 0.000 description 2
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JP2008308124A 2007-12-06 2008-12-03 シリコーン（メタ）アクリレート粒子、その調製方法、およびその使用 Expired - Fee Related JP5590539B2 (ja)