JPS6241980B2 - - Google Patents
Info
- Publication number
- JPS6241980B2 JPS6241980B2 JP52138694A JP13869477A JPS6241980B2 JP S6241980 B2 JPS6241980 B2 JP S6241980B2 JP 52138694 A JP52138694 A JP 52138694A JP 13869477 A JP13869477 A JP 13869477A JP S6241980 B2 JPS6241980 B2 JP S6241980B2
- Authority
- JP
- Japan
- Prior art keywords
- maleate
- bis
- dibutyltin
- dioctyltin
- mercaptopropionate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 141
- -1 maleate compound Chemical class 0.000 claims description 52
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- 229910052717 sulfur Inorganic materials 0.000 claims description 13
- 239000011593 sulfur Substances 0.000 claims description 13
- 239000011342 resin composition Substances 0.000 claims description 10
- 230000000087 stabilizing effect Effects 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 7
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 5
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 5
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 5
- 239000000347 magnesium hydroxide Substances 0.000 claims description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 1
- 229920003002 synthetic resin Polymers 0.000 claims 1
- 239000000057 synthetic resin Substances 0.000 claims 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 96
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 25
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 25
- PWEVMPIIOJUPRI-UHFFFAOYSA-N dimethyltin Chemical compound C[Sn]C PWEVMPIIOJUPRI-UHFFFAOYSA-N 0.000 description 18
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 16
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 16
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 15
- 238000011156 evaluation Methods 0.000 description 13
- 239000004800 polyvinyl chloride Substances 0.000 description 11
- 229920000915 polyvinyl chloride Polymers 0.000 description 11
- FDNBQVCBHKEDOJ-FPLPWBNLSA-N (z)-4-(6-methylheptoxy)-4-oxobut-2-enoic acid Chemical compound CC(C)CCCCCOC(=O)\C=C/C(O)=O FDNBQVCBHKEDOJ-FPLPWBNLSA-N 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- 239000003063 flame retardant Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 230000002195 synergetic effect Effects 0.000 description 9
- 239000007983 Tris buffer Substances 0.000 description 8
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- OZDOQMMXEACZAA-NRFIWDAESA-L (z)-4-butoxy-4-oxobut-2-enoate;dibutyltin(2+) Chemical compound CCCCOC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OCCCC OZDOQMMXEACZAA-NRFIWDAESA-L 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- NJMGRJLQRLFQQX-HYXAFXHYSA-N 2-isopropylmaleic acid Chemical compound CC(C)C(\C(O)=O)=C\C(O)=O NJMGRJLQRLFQQX-HYXAFXHYSA-N 0.000 description 5
- NBZNVCBJBGDRJI-KKUWAICFSA-L dibutyltin(2+);(z)-4-(2-ethylhexoxy)-4-oxobut-2-enoate Chemical compound CCCCC(CC)COC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OCC(CC)CCCC NBZNVCBJBGDRJI-KKUWAICFSA-L 0.000 description 5
- 229940097413 isopropyl maleate Drugs 0.000 description 5
- GKOTWPKLOWTGAG-NRFIWDAESA-L (z)-4-butoxy-4-oxobut-2-enoate;dioctyltin(2+) Chemical compound CCCCOC(=O)\C=C/C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)\C=C/C(=O)OCCCC GKOTWPKLOWTGAG-NRFIWDAESA-L 0.000 description 4
- KRKQRRUGEKWXIV-KUAKSMGGSA-L 1-O-cyclohexyl 4-O-[[(Z)-4-cyclohexyloxy-4-oxobut-2-enoyl]oxy-dioctylstannyl] (Z)-but-2-enedioate Chemical compound [Sn++].[CH2]CCCCCCC.[CH2]CCCCCCC.[O-]C(=O)\C=C/C(=O)OC1CCCCC1.[O-]C(=O)\C=C/C(=O)OC1CCCCC1 KRKQRRUGEKWXIV-KUAKSMGGSA-L 0.000 description 4
- RZBBHEJLECUBJT-UHFFFAOYSA-N 6-methylheptyl 2-sulfanylacetate Chemical compound CC(C)CCCCCOC(=O)CS RZBBHEJLECUBJT-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- UTOVMEACOLCUCK-PLNGDYQASA-N butyl maleate Chemical compound CCCCOC(=O)\C=C/C(O)=O UTOVMEACOLCUCK-PLNGDYQASA-N 0.000 description 4
- NPAIMXWXWPJRES-UHFFFAOYSA-N butyltin(3+) Chemical compound CCCC[Sn+3] NPAIMXWXWPJRES-UHFFFAOYSA-N 0.000 description 4
- TUALPPJDVFLVNQ-KUAKSMGGSA-L dibutyltin(2+);(z)-4-oxo-4-phenylmethoxybut-2-enoate Chemical compound C=1C=CC=CC=1COC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OCC1=CC=CC=C1 TUALPPJDVFLVNQ-KUAKSMGGSA-L 0.000 description 4
- VXGIVDFKZKMKQO-UHFFFAOYSA-L dioctyltin isooctylthioglycolate Chemical compound CCCCC(CC)COC(=O)CS[Sn](CCCCCCCC)(CCCCCCCC)SCC(=O)OCC(CC)CCCC VXGIVDFKZKMKQO-UHFFFAOYSA-L 0.000 description 4
- 125000001117 oleyl 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])=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])[H] 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- QKUGKZFASYQCGO-SREVYHEPSA-N (z)-4-oxo-4-phenylmethoxybut-2-enoic acid Chemical compound OC(=O)\C=C/C(=O)OCC1=CC=CC=C1 QKUGKZFASYQCGO-SREVYHEPSA-N 0.000 description 3
- PSSJZBIVTOSSIU-UHFFFAOYSA-L 2,2,4-trimethylpentyl 3-[dibutyl-[3-oxo-3-(2,2,4-trimethylpentoxy)propyl]sulfanylstannyl]sulfanylpropanoate Chemical compound CC(C)CC(C)(C)COC(=O)CCS[Sn](CCCC)(CCCC)SCCC(=O)OCC(C)(C)CC(C)C PSSJZBIVTOSSIU-UHFFFAOYSA-L 0.000 description 3
- RFPITRAFRHNSRB-UHFFFAOYSA-L 2-ethylhexyl 3-[dibutyl-[3-(2-ethylhexoxy)-3-oxopropyl]sulfanylstannyl]sulfanylpropanoate Chemical compound CCCCC(CC)COC(=O)CCS[Sn](CCCC)(CCCC)SCCC(=O)OCC(CC)CCCC RFPITRAFRHNSRB-UHFFFAOYSA-L 0.000 description 3
- DKIDEFUBRARXTE-UHFFFAOYSA-M 3-mercaptopropionate Chemical compound [O-]C(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-M 0.000 description 3
- ZHUWXKIPGGZNJW-UHFFFAOYSA-N 6-methylheptyl 3-sulfanylpropanoate Chemical compound CC(C)CCCCCOC(=O)CCS ZHUWXKIPGGZNJW-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 3
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- JNKCYBSAZHJNIZ-LHJYRGMRSA-L dibutyltin(2+);(z)-4-oxo-4-tridecoxybut-2-enoate Chemical compound CCCCCCCCCCCCCOC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OCCCCCCCCCCCCC JNKCYBSAZHJNIZ-LHJYRGMRSA-L 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 150000002688 maleic acid derivatives Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- ZMHZSHHZIKJFIR-UHFFFAOYSA-N octyltin Chemical compound CCCCCCCC[Sn] ZMHZSHHZIKJFIR-UHFFFAOYSA-N 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- BTSHKFIHOPUJCA-NRFIWDAESA-L (Z)-4-butoxy-4-oxobut-2-enoate dimethyltin(2+) Chemical compound C[Sn+2]C.CCCCOC(=O)\C=C/C([O-])=O.CCCCOC(=O)\C=C/C([O-])=O BTSHKFIHOPUJCA-NRFIWDAESA-L 0.000 description 2
- IQBLWPLYPNOTJC-FPLPWBNLSA-N (z)-4-(2-ethylhexoxy)-4-oxobut-2-enoic acid Chemical compound CCCCC(CC)COC(=O)\C=C/C(O)=O IQBLWPLYPNOTJC-FPLPWBNLSA-N 0.000 description 2
- VTWCVXKFWPSSNK-PLNGDYQASA-N (z)-4-(4-methoxybutoxy)-4-oxobut-2-enoic acid Chemical compound COCCCCOC(=O)\C=C/C(O)=O VTWCVXKFWPSSNK-PLNGDYQASA-N 0.000 description 2
- WBYOSZYSBZQGDJ-KUAKSMGGSA-L (z)-4-cyclohexyloxy-4-oxobut-2-enoate;dibutyltin(2+) Chemical compound C1CCCCC1OC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OC1CCCCC1 WBYOSZYSBZQGDJ-KUAKSMGGSA-L 0.000 description 2
- ZMQWRASVUXJXGM-SREVYHEPSA-N (z)-4-cyclohexyloxy-4-oxobut-2-enoic acid Chemical compound OC(=O)\C=C/C(=O)OC1CCCCC1 ZMQWRASVUXJXGM-SREVYHEPSA-N 0.000 description 2
- VPTNWGPGDXUKCY-KHPPLWFESA-N (z)-4-decoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCOC(=O)\C=C/C(O)=O VPTNWGPGDXUKCY-KHPPLWFESA-N 0.000 description 2
- IIPCXIGUIPAGQB-SEYXRHQNSA-N (z)-4-dodecoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCCCOC(=O)\C=C/C(O)=O IIPCXIGUIPAGQB-SEYXRHQNSA-N 0.000 description 2
- RNERBJNDXXEXTK-SREVYHEPSA-N (z)-4-hexoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCOC(=O)\C=C/C(O)=O RNERBJNDXXEXTK-SREVYHEPSA-N 0.000 description 2
- VTWGIDKXXZRLGH-HJWRWDBZSA-N (z)-4-octoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCOC(=O)\C=C/C(O)=O VTWGIDKXXZRLGH-HJWRWDBZSA-N 0.000 description 2
- FGACNJFGXDUISO-YPKPFQOOSA-N (z)-4-oxo-4-tridecoxybut-2-enoic acid Chemical compound CCCCCCCCCCCCCOC(=O)\C=C/C(O)=O FGACNJFGXDUISO-YPKPFQOOSA-N 0.000 description 2
- NUSQJGCEUADMON-QQUZTSPOSA-J 1-o-benzyl 4-o-[[(z)-4-[dioctyl-[(z)-4-oxo-4-phenylmethoxybut-2-enoyl]oxystannyl]oxy-4-oxobut-2-enoyl]oxy-dioctylstannyl] (z)-but-2-enedioate Chemical compound C=1C=CC=CC=1COC(=O)\C=C/C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)\C=C/C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)\C=C/C(=O)OCC1=CC=CC=C1 NUSQJGCEUADMON-QQUZTSPOSA-J 0.000 description 2
- IRIAEMUUDSWZOX-UHFFFAOYSA-L 2,2-dibutyl-1,3,2-oxathiastanninan-6-one Chemical compound CCCC[Sn]1(CCCC)OC(=O)CCS1 IRIAEMUUDSWZOX-UHFFFAOYSA-L 0.000 description 2
- KVWGXVZLMQTKPV-UHFFFAOYSA-N 2-(4-methoxybutylsulfanyl)acetic acid Chemical compound COCCCCSCC(O)=O KVWGXVZLMQTKPV-UHFFFAOYSA-N 0.000 description 2
- PRIUALOJYOZZOJ-UHFFFAOYSA-L 2-ethylhexyl 2-[dibutyl-[2-(2-ethylhexoxy)-2-oxoethyl]sulfanylstannyl]sulfanylacetate Chemical compound CCCCC(CC)COC(=O)CS[Sn](CCCC)(CCCC)SCC(=O)OCC(CC)CCCC PRIUALOJYOZZOJ-UHFFFAOYSA-L 0.000 description 2
- PMNLUUOXGOOLSP-UHFFFAOYSA-M 2-sulfanylpropanoate Chemical compound CC(S)C([O-])=O PMNLUUOXGOOLSP-UHFFFAOYSA-M 0.000 description 2
- LUHRVCWDUSUHMP-FTHVFMQUSA-L 4-o-[[(e)-4-(2-ethylhexoxy)-4-oxobut-2-enoyl]oxy-dioctylstannyl] 1-o-(2-ethylhexyl) (e)-but-2-enedioate Chemical compound CCCCC(CC)COC(=O)/C=C/C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)\C=C\C(=O)OCC(CC)CCCC LUHRVCWDUSUHMP-FTHVFMQUSA-L 0.000 description 2
- XITDVRBPGQGVFK-FTHVFMQUSA-L 4-o-[[(e)-4-(6-methylheptoxy)-4-oxobut-2-enoyl]oxy-dioctylstannyl] 1-o-(6-methylheptyl) (e)-but-2-enedioate Chemical compound CC(C)CCCCCOC(=O)/C=C/C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)\C=C\C(=O)OCCCCCC(C)C XITDVRBPGQGVFK-FTHVFMQUSA-L 0.000 description 2
- CHOXPWSDXIXQDY-YPKQJYFLSA-L 4-o-[[(z)-4-octadecoxy-4-oxobut-2-enoyl]oxy-dioctylstannyl] 1-o-octadecyl (z)-but-2-enedioate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)\C=C/C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)\C=C/C(=O)OCCCCCCCCCCCCCCCCCC CHOXPWSDXIXQDY-YPKQJYFLSA-L 0.000 description 2
- USFZYMDDRJWGBP-UHFFFAOYSA-N C(C)C(COC(CCS)=O)CCCC.C(CCC)[Sn]CCCC Chemical compound C(C)C(COC(CCS)=O)CCCC.C(CCC)[Sn]CCCC USFZYMDDRJWGBP-UHFFFAOYSA-N 0.000 description 2
- HBGIPOWCFUJKKH-KUAKSMGGSA-L C(\C=C/C(=O)[O-])(=O)OCC1=CC=CC=C1.C[Sn+2]C.C(C1=CC=CC=C1)OC(\C=C/C(=O)[O-])=O Chemical compound C(\C=C/C(=O)[O-])(=O)OCC1=CC=CC=C1.C[Sn+2]C.C(C1=CC=CC=C1)OC(\C=C/C(=O)[O-])=O HBGIPOWCFUJKKH-KUAKSMGGSA-L 0.000 description 2
- MHQJUHSHQGQVTM-HNENSFHCSA-N Octadecyl fumarate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)\C=C/C(O)=O MHQJUHSHQGQVTM-HNENSFHCSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- LYHWLRKJDJPEBQ-UHFFFAOYSA-N SCCC(=O)OCC(CCCC)CC.C(CCCCCCC)[Sn]CCCCCCCC Chemical compound SCCC(=O)OCC(CCCC)CC.C(CCCCCCC)[Sn]CCCCCCCC LYHWLRKJDJPEBQ-UHFFFAOYSA-N 0.000 description 2
- IVBIJGUAZAPDDJ-LHJYRGMRSA-L [Sn++].[CH2]CCCCCCC.[CH2]CCCCCCC.CCCCCCCCCCCCCOC(=O)\C=C/C([O-])=O.CCCCCCCCCCCCCOC(=O)\C=C/C([O-])=O Chemical compound [Sn++].[CH2]CCCCCCC.[CH2]CCCCCCC.CCCCCCCCCCCCCOC(=O)\C=C/C([O-])=O.CCCCCCCCCCCCCOC(=O)\C=C/C([O-])=O IVBIJGUAZAPDDJ-LHJYRGMRSA-L 0.000 description 2
- JDGMQGANESQLIL-UHFFFAOYSA-L [[4-ethyl-2-(sulfanylmethyl)octanoyl]oxy-dioctylstannyl] 4-ethyl-2-(sulfanylmethyl)octanoate Chemical compound CCCCC(CC)CC(CS)C([O-])=O.CCCCC(CC)CC(CS)C([O-])=O.CCCCCCCC[Sn+2]CCCCCCCC JDGMQGANESQLIL-UHFFFAOYSA-L 0.000 description 2
- CYGGDRWPUCJENS-UHFFFAOYSA-L [[8-methyl-2-(sulfanylmethyl)nonanoyl]oxy-dioctylstannyl] 8-methyl-2-(sulfanylmethyl)nonanoate Chemical compound CC(C)CCCCCC(CS)C([O-])=O.CC(C)CCCCCC(CS)C([O-])=O.CCCCCCCC[Sn+2]CCCCCCCC CYGGDRWPUCJENS-UHFFFAOYSA-L 0.000 description 2
- CCRHTZBIGPEKGC-UHFFFAOYSA-K [butyl-bis[[4-ethyl-2-(sulfanylmethyl)octanoyl]oxy]stannyl] 4-ethyl-2-(sulfanylmethyl)octanoate Chemical compound CCCC[Sn+3].CCCCC(CC)CC(CS)C([O-])=O.CCCCC(CC)CC(CS)C([O-])=O.CCCCC(CC)CC(CS)C([O-])=O CCRHTZBIGPEKGC-UHFFFAOYSA-K 0.000 description 2
- YSCDKUPSJMMGGT-UHFFFAOYSA-L [dibutyl-[2-(6-methylheptylsulfanyl)acetyl]oxystannyl] 2-(6-methylheptylsulfanyl)acetate Chemical compound CC(C)CCCCCSCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CSCCCCCC(C)C YSCDKUPSJMMGGT-UHFFFAOYSA-L 0.000 description 2
- SBQQTSREBYOKMO-UHFFFAOYSA-L [dibutyl-[6-methoxy-2-(sulfanylmethyl)hexanoyl]oxystannyl] 6-methoxy-2-(sulfanylmethyl)hexanoate Chemical compound COCCCCC(C(=O)[O-])CS.COCCCCC(C(=O)[O-])CS.C(CCC)[Sn+2]CCCC SBQQTSREBYOKMO-UHFFFAOYSA-L 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- SKGVGRLWZVRZDC-UHFFFAOYSA-N butyl 2-sulfanylacetate Chemical compound CCCCOC(=O)CS SKGVGRLWZVRZDC-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- JJPZOIJCDNHCJP-UHFFFAOYSA-N dibutyl(sulfanylidene)tin Chemical compound CCCC[Sn](=S)CCCC JJPZOIJCDNHCJP-UHFFFAOYSA-N 0.000 description 2
- VLQWDCKTDZZUSU-KKUWAICFSA-L dibutyltin(2+);(z)-4-(6-methylheptoxy)-4-oxobut-2-enoate Chemical compound CC(C)CCCCCOC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OCCCCCC(C)C VLQWDCKTDZZUSU-KKUWAICFSA-L 0.000 description 2
- IPEIQLRNAOQYPJ-NUJFUEHTSA-L dibutyltin(2+);(z)-4-dodecoxy-4-oxobut-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OCCCCCCCCCCCC IPEIQLRNAOQYPJ-NUJFUEHTSA-L 0.000 description 2
- OSGZEAQLLRZGHT-VGKOASNMSA-L dibutyltin(2+);(z)-4-ethoxy-4-oxobut-2-enoate Chemical compound CCOC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OCC OSGZEAQLLRZGHT-VGKOASNMSA-L 0.000 description 2
- WNDWDJLPMLWBHW-UDVCPWNYSA-L dibutyltin(2+);(z)-4-methoxy-4-oxobut-2-enoate Chemical compound COC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OC WNDWDJLPMLWBHW-UDVCPWNYSA-L 0.000 description 2
- WHWTUCZRUDXTMZ-YPKQJYFLSA-L dibutyltin(2+);(z)-4-octadecoxy-4-oxobut-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OCCCCCCCCCCCCCCCCCC WHWTUCZRUDXTMZ-YPKQJYFLSA-L 0.000 description 2
- RFAIKXASDCRKEP-UHFFFAOYSA-N dioctyl(sulfanylidene)tin Chemical compound CCCCCCCC[Sn](=S)CCCCCCCC RFAIKXASDCRKEP-UHFFFAOYSA-N 0.000 description 2
- NHDGUEXYQMLBDM-KUAKSMGGSA-L dioctyltin(2+) (Z)-4-oxo-4-phenylmethoxybut-2-enoate Chemical compound [O-]C(=O)\C=C/C(=O)OCC1=CC=CC=C1.[O-]C(=O)\C=C/C(=O)OCC1=CC=CC=C1.CCCCCCCC[Sn+2]CCCCCCCC NHDGUEXYQMLBDM-KUAKSMGGSA-L 0.000 description 2
- LUHRVCWDUSUHMP-KKUWAICFSA-L dioctyltin(2+);(z)-4-(2-ethylhexoxy)-4-oxobut-2-enoate Chemical compound CCCCC(CC)COC(=O)\C=C/C([O-])=O.CCCCC(CC)COC(=O)\C=C/C([O-])=O.CCCCCCCC[Sn+2]CCCCCCCC LUHRVCWDUSUHMP-KKUWAICFSA-L 0.000 description 2
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- ZUSPUVLQZAKOMX-UHFFFAOYSA-K [butyl-bis[(2-octylsulfanylacetyl)oxy]stannyl] 2-octylsulfanylacetate Chemical compound C(CCCCCCC)SCC(=O)[O-].C(CCCCCCC)SCC(=O)[O-].C(CCCCCCC)SCC(=O)[O-].C(CCC)[Sn+3] ZUSPUVLQZAKOMX-UHFFFAOYSA-K 0.000 description 1
- MHZRVFLVJFHAQG-BQGNPDQISA-K [butyl-bis[[(Z)-2-(sulfanylmethyl)icos-11-enoyl]oxy]stannyl] (Z)-2-(sulfanylmethyl)icos-11-enoate Chemical compound CCCC[Sn+3].CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O.CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O.CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O MHZRVFLVJFHAQG-BQGNPDQISA-K 0.000 description 1
- LLIBVDRNHISOQI-UHFFFAOYSA-K [butyl-bis[[6-methoxy-2-(sulfanylmethyl)hexanoyl]oxy]stannyl] 6-methoxy-2-(sulfanylmethyl)hexanoate Chemical compound COCCCCC(C(=O)[O-])CS.COCCCCC(C(=O)[O-])CS.COCCCCC(C(=O)[O-])CS.C(CCC)[Sn+3] LLIBVDRNHISOQI-UHFFFAOYSA-K 0.000 description 1
- NZGKWBKMYYPEOQ-UHFFFAOYSA-K [butyl-bis[[8-methyl-2-(sulfanylmethyl)nonanoyl]oxy]stannyl] 8-methyl-2-(sulfanylmethyl)nonanoate Chemical compound C(CCCCC(C)C)C(C(=O)[O-])CS.C(CCCCC(C)C)C(C(=O)[O-])CS.C(CCCCC(C)C)C(C(=O)[O-])CS.C(CCC)[Sn+3] NZGKWBKMYYPEOQ-UHFFFAOYSA-K 0.000 description 1
- JXMMBAPTZHDHGJ-UHFFFAOYSA-L [dibutyl-(2-cyclohexyl-3-sulfanylpropanoyl)oxystannyl] 2-cyclohexyl-3-sulfanylpropanoate Chemical compound C1(CCCCC1)C(C(=O)[O-])CS.C1(CCCCC1)C(C(=O)[O-])CS.C(CCC)[Sn+2]CCCC JXMMBAPTZHDHGJ-UHFFFAOYSA-L 0.000 description 1
- DULZKMOPDRLVDS-UHFFFAOYSA-L [dibutyl-(2-octadecylsulfanylacetyl)oxystannyl] 2-octadecylsulfanylacetate Chemical compound C(CCCCCCCCCCCCCCCCC)SCC(=O)[O-].C(CCCCCCCCCCCCCCCCC)SCC(=O)[O-].C(CCC)[Sn+2]CCCC DULZKMOPDRLVDS-UHFFFAOYSA-L 0.000 description 1
- FMOWRAQPFRRNJR-BGSQTJHASA-L [dibutyl-[2-[(Z)-octadec-9-enyl]sulfanylacetyl]oxystannyl] 2-[(Z)-octadec-9-enyl]sulfanylacetate Chemical compound CCCC[Sn+2]CCCC.CCCCCCCC\C=C/CCCCCCCCSCC([O-])=O.CCCCCCCC\C=C/CCCCCCCCSCC([O-])=O FMOWRAQPFRRNJR-BGSQTJHASA-L 0.000 description 1
- KYDGMZSIZYYJJJ-UHFFFAOYSA-L [dimethyl-(2-sulfanylacetyl)oxystannyl] 2-sulfanylacetate Chemical compound C[Sn+2]C.[O-]C(=O)CS.[O-]C(=O)CS KYDGMZSIZYYJJJ-UHFFFAOYSA-L 0.000 description 1
- PAVXXDHLWRXCCX-BGSQTJHASA-L [dimethyl-[(Z)-2-(sulfanylmethyl)icos-11-enoyl]oxystannyl] (Z)-2-(sulfanylmethyl)icos-11-enoate Chemical compound C[Sn+2]C.CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O.CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O PAVXXDHLWRXCCX-BGSQTJHASA-L 0.000 description 1
- IGOGXRAECHXKAS-UHFFFAOYSA-L [dimethyl-[2-(sulfanylmethyl)icosanoyloxy]stannyl] 2-(sulfanylmethyl)icosanoate Chemical compound C(CCCCCCCCCCCCCCCCC)C(C(=O)[O-])CS.C(CCCCCCCCCCCCCCCCC)C(C(=O)[O-])CS.C[Sn+2]C IGOGXRAECHXKAS-UHFFFAOYSA-L 0.000 description 1
- PJASOGQUPMLMRV-UHFFFAOYSA-L [dioctyl-(2-octylsulfanylacetyl)oxystannyl] 2-octylsulfanylacetate Chemical compound C(CCCCCCC)SCC(=O)[O-].C(CCCCCCC)SCC(=O)[O-].C(CCCCCCC)[Sn+2]CCCCCCCC PJASOGQUPMLMRV-UHFFFAOYSA-L 0.000 description 1
- ADVRPFABJGOKFI-UHFFFAOYSA-L [dioctyl-[2-(sulfanylmethyl)decanoyloxy]stannyl] 2-(sulfanylmethyl)decanoate Chemical compound C(CCCCCCC)C(C(=O)[O-])CS.C(CCCCCCC)C(C(=O)[O-])CS.C(CCCCCCC)[Sn+2]CCCCCCCC ADVRPFABJGOKFI-UHFFFAOYSA-L 0.000 description 1
- VRYMWPCWSRTXDU-UHFFFAOYSA-L [dioctyl-[2-(sulfanylmethyl)hexanoyloxy]stannyl] 2-(sulfanylmethyl)hexanoate Chemical compound CCCCC(CS)C([O-])=O.CCCCC(CS)C([O-])=O.CCCCCCCC[Sn+2]CCCCCCCC VRYMWPCWSRTXDU-UHFFFAOYSA-L 0.000 description 1
- LZRWWJSRKHVQBQ-UHFFFAOYSA-K [dodecyl-bis[[4-ethyl-2-(sulfanylmethyl)octanoyl]oxy]stannyl] 4-ethyl-2-(sulfanylmethyl)octanoate Chemical compound C(C)C(CC(C(=O)[O-])CS)CCCC.C(C)C(CC(C(=O)[O-])CS)CCCC.C(C)C(CC(C(=O)[O-])CS)CCCC.C(CCCCCCCCCCC)[Sn+3] LZRWWJSRKHVQBQ-UHFFFAOYSA-K 0.000 description 1
- NTXUTVSZMMZOGJ-UHFFFAOYSA-K [methyl-bis[2-(sulfanylmethyl)icosanoyloxy]stannyl] 2-(sulfanylmethyl)icosanoate Chemical compound C(CCCCCCCCCCCCCCCCC)C(C(=O)[O-])CS.C(CCCCCCCCCCCCCCCCC)C(C(=O)[O-])CS.C(CCCCCCCCCCCCCCCCC)C(C(=O)[O-])CS.C[Sn+3] NTXUTVSZMMZOGJ-UHFFFAOYSA-K 0.000 description 1
- LXJOTZSFXCLGCX-BQGNPDQISA-K [methyl-bis[[(Z)-2-(sulfanylmethyl)icos-11-enoyl]oxy]stannyl] (Z)-2-(sulfanylmethyl)icos-11-enoate Chemical compound C(CCCCCCC\C=C/CCCCCCCC)C(C(=O)[O-])CS.C(CCCCCCC\C=C/CCCCCCCC)C(C(=O)[O-])CS.C(CCCCCCC\C=C/CCCCCCCC)C(C(=O)[O-])CS.C[Sn+3] LXJOTZSFXCLGCX-BQGNPDQISA-K 0.000 description 1
- AFPRNKPRPTVLOM-BQGNPDQISA-K [methyl-bis[[2-[(Z)-octadec-9-enyl]sulfanylacetyl]oxy]stannyl] 2-[(Z)-octadec-9-enyl]sulfanylacetate Chemical compound CCCCCCCC/C=C\CCCCCCCCSCC(=O)O[Sn](OC(=O)CSCCCCCCCC/C=C\CCCCCCCC)(OC(=O)CSCCCCCCCC/C=C\CCCCCCCC)C AFPRNKPRPTVLOM-BQGNPDQISA-K 0.000 description 1
- RPPYRNLPHFTSIN-UHFFFAOYSA-K [octyl-bis[2-(sulfanylmethyl)decanoyloxy]stannyl] 2-(sulfanylmethyl)decanoate Chemical compound C(CCCCCCC)C(C(=O)[O-])CS.C(CCCCCCC)C(C(=O)[O-])CS.C(CCCCCCC)C(C(=O)[O-])CS.C(CCCCCCC)[Sn+3] RPPYRNLPHFTSIN-UHFFFAOYSA-K 0.000 description 1
- AEYDCBMIVYEXJD-UHFFFAOYSA-K [octyl-bis[2-(sulfanylmethyl)hexanoyloxy]stannyl] 2-(sulfanylmethyl)hexanoate Chemical compound C(CCC)C(C(=O)[O-])CS.C(CCC)C(C(=O)[O-])CS.C(CCC)C(C(=O)[O-])CS.C(CCCCCCC)[Sn+3] AEYDCBMIVYEXJD-UHFFFAOYSA-K 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- PTLASYHTXGUCJU-UHFFFAOYSA-N benzyl 2,3,3a,4,5,6,7,7a-octahydro-1h-indole-2-carboxylate;4-methylbenzenesulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1.C1C2CCCCC2NC1C(=O)OCC1=CC=CC=C1 PTLASYHTXGUCJU-UHFFFAOYSA-N 0.000 description 1
- XTCXSNIRIUQZLY-UHFFFAOYSA-N benzyl 2-sulfanylacetate Chemical compound SCC(=O)OCC1=CC=CC=C1 XTCXSNIRIUQZLY-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- PZGVVCOOWYSSGB-UHFFFAOYSA-L but-2-enedioate;dioctyltin(2+) Chemical compound CCCCCCCC[Sn]1(CCCCCCCC)OC(=O)C=CC(=O)O1 PZGVVCOOWYSSGB-UHFFFAOYSA-L 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
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- CTZWBKHVGXKFLI-KUAKSMGGSA-L dibutyltin(2+);(z)-4-hexoxy-4-oxobut-2-enoate Chemical compound CCCC[Sn+2]CCCC.CCCCCCOC(=O)\C=C/C([O-])=O.CCCCCCOC(=O)\C=C/C([O-])=O CTZWBKHVGXKFLI-KUAKSMGGSA-L 0.000 description 1
- OSILQYMASGMTIY-WFTKVDHJSA-L dibutyltin(2+);(z)-4-octoxy-4-oxobut-2-enoate Chemical compound CCCCCCCCOC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OCCCCCCCC OSILQYMASGMTIY-WFTKVDHJSA-L 0.000 description 1
- QWKDQXNGJACGFP-VGKOASNMSA-L dibutyltin(2+);(z)-4-oxo-4-propan-2-yloxybut-2-enoate Chemical compound CC(C)OC(=O)\C=C/C(=O)O[Sn](CCCC)(CCCC)OC(=O)\C=C/C(=O)OC(C)C QWKDQXNGJACGFP-VGKOASNMSA-L 0.000 description 1
- DXIALWHCMIXMAB-UHFFFAOYSA-L dibutyltin(2+);2-(2-ethylhexylsulfanyl)acetate Chemical compound CCCC[Sn+2]CCCC.CCCCC(CC)CSCC([O-])=O.CCCCC(CC)CSCC([O-])=O DXIALWHCMIXMAB-UHFFFAOYSA-L 0.000 description 1
- LTWNGXCAVJUGCF-UHFFFAOYSA-L dibutyltin(2+);2-(sulfanylmethyl)decanoate Chemical compound CCCC[Sn+2]CCCC.CCCCCCCCC(CS)C([O-])=O.CCCCCCCCC(CS)C([O-])=O LTWNGXCAVJUGCF-UHFFFAOYSA-L 0.000 description 1
- ZYIYJSWBGLPVEO-UHFFFAOYSA-L dibutyltin(2+);2-(sulfanylmethyl)hexanoate Chemical compound CCCC[Sn+2]CCCC.CCCCC(CS)C([O-])=O.CCCCC(CS)C([O-])=O ZYIYJSWBGLPVEO-UHFFFAOYSA-L 0.000 description 1
- QGQIZFGMTNYKSZ-UHFFFAOYSA-L dibutyltin(2+);2-(sulfanylmethyl)icosanoate Chemical compound CCCC[Sn+2]CCCC.CCCCCCCCCCCCCCCCCCC(CS)C([O-])=O.CCCCCCCCCCCCCCCCCCC(CS)C([O-])=O QGQIZFGMTNYKSZ-UHFFFAOYSA-L 0.000 description 1
- JQWRJZYBUAZHTK-UHFFFAOYSA-L dibutyltin(2+);2-octylsulfanylacetate Chemical compound CCCC[Sn+2]CCCC.CCCCCCCCSCC([O-])=O.CCCCCCCCSCC([O-])=O JQWRJZYBUAZHTK-UHFFFAOYSA-L 0.000 description 1
- BILPJDUODHSEHZ-UHFFFAOYSA-N dimethyltin 2-ethylhexyl 2-sulfanylacetate Chemical compound C[Sn]C.CCCCC(CC)COC(=O)CS.CCCCC(CC)COC(=O)CS BILPJDUODHSEHZ-UHFFFAOYSA-N 0.000 description 1
- YIYSMOLARSLVBW-VGKOASNMSA-L dimethyltin(2+) (Z)-4-ethoxy-4-oxobut-2-enoate Chemical compound C[Sn+2]C.CCOC(=O)\C=C/C([O-])=O.CCOC(=O)\C=C/C([O-])=O YIYSMOLARSLVBW-VGKOASNMSA-L 0.000 description 1
- CUHFNERITPIOBB-UHFFFAOYSA-L dimethyltin(2+);2-(2-ethylhexylsulfanyl)acetate Chemical compound C[Sn+2]C.CCCCC(CC)CSCC([O-])=O.CCCCC(CC)CSCC([O-])=O CUHFNERITPIOBB-UHFFFAOYSA-L 0.000 description 1
- IRFPIPNMASANJY-UHFFFAOYSA-L dimethyltin(2+);2-(6-methylheptoxy)-2-oxoethanethiolate Chemical compound CC(C)CCCCCOC(=O)CS[Sn](C)(C)SCC(=O)OCCCCCC(C)C IRFPIPNMASANJY-UHFFFAOYSA-L 0.000 description 1
- JCGSLDBLJGDNHD-UHFFFAOYSA-L dimethyltin(2+);3-sulfanylpropanoate Chemical compound C[Sn+2]C.[O-]C(=O)CCS.[O-]C(=O)CCS JCGSLDBLJGDNHD-UHFFFAOYSA-L 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- OWDPVSGEPJRRNV-NUJFUEHTSA-L dioctyltin(2+);(z)-4-dodecoxy-4-oxobut-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)\C=C/C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)\C=C/C(=O)OCCCCCCCCCCCC OWDPVSGEPJRRNV-NUJFUEHTSA-L 0.000 description 1
- DVIRNKJIPPLYCT-UHFFFAOYSA-L dioctyltin(2+);2-(2-ethylhexylsulfanyl)acetate Chemical compound CCCCC(CC)CSCC([O-])=O.CCCCC(CC)CSCC([O-])=O.CCCCCCCC[Sn+2]CCCCCCCC DVIRNKJIPPLYCT-UHFFFAOYSA-L 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical class [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- CSHCPECZJIEGJF-UHFFFAOYSA-N methyltin Chemical compound [Sn]C CSHCPECZJIEGJF-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- MADOXCFISYCULS-UHFFFAOYSA-N octyl 2-sulfanylacetate Chemical compound CCCCCCCCOC(=O)CS MADOXCFISYCULS-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920005671 poly(vinyl chloride-propylene) Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13869477A JPS5471156A (en) | 1977-11-18 | 1977-11-18 | Stabilization of synthetic resin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13869477A JPS5471156A (en) | 1977-11-18 | 1977-11-18 | Stabilization of synthetic resin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5471156A JPS5471156A (en) | 1979-06-07 |
| JPS6241980B2 true JPS6241980B2 (xx) | 1987-09-05 |
Family
ID=15227924
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13869477A Granted JPS5471156A (en) | 1977-11-18 | 1977-11-18 | Stabilization of synthetic resin |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5471156A (xx) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH075805B2 (ja) * | 1984-02-23 | 1995-01-25 | 日東化成株式会社 | 安定化されたハロゲン含有樹脂組成物 |
| EP0748844A1 (de) * | 1995-05-17 | 1996-12-18 | Ciba-Geigy Ag | Stabilisierte PVC-Zusammensetzungen |
| KR100379882B1 (ko) * | 2000-12-28 | 2003-04-11 | 제일모직주식회사 | 난연성 아크릴로니트릴-부타디엔-스티렌 수지 조성물 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS494827A (xx) * | 1972-05-04 | 1974-01-17 | ||
| JPS4997853A (xx) * | 1973-01-08 | 1974-09-17 | ||
| JPS5146341A (ja) * | 1974-10-18 | 1976-04-20 | Mitsubishi Petrochemical Co | Jishoseijushisoseibutsu |
-
1977
- 1977-11-18 JP JP13869477A patent/JPS5471156A/ja active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS494827A (xx) * | 1972-05-04 | 1974-01-17 | ||
| JPS4997853A (xx) * | 1973-01-08 | 1974-09-17 | ||
| JPS5146341A (ja) * | 1974-10-18 | 1976-04-20 | Mitsubishi Petrochemical Co | Jishoseijushisoseibutsu |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5471156A (en) | 1979-06-07 |
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