JPS6410011B2 - - Google Patents
Info
- Publication number
- JPS6410011B2 JPS6410011B2 JP11458985A JP11458985A JPS6410011B2 JP S6410011 B2 JPS6410011 B2 JP S6410011B2 JP 11458985 A JP11458985 A JP 11458985A JP 11458985 A JP11458985 A JP 11458985A JP S6410011 B2 JPS6410011 B2 JP S6410011B2
- Authority
- JP
- Japan
- Prior art keywords
- bis
- butyltin
- mercaptopropionate
- tris
- octyltin
- 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
- 239000003381 stabilizer Substances 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical class 0.000 claims description 15
- 229920005989 resin Polymers 0.000 claims description 15
- 239000011347 resin Substances 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 13
- 150000003606 tin compounds Chemical class 0.000 claims description 9
- OOULUYZFLXDWDQ-UHFFFAOYSA-L barium perchlorate Chemical compound [Ba+2].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O OOULUYZFLXDWDQ-UHFFFAOYSA-L 0.000 claims description 8
- -1 hydrotalcite compounds Chemical class 0.000 description 120
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 50
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 49
- 239000007983 Tris buffer Substances 0.000 description 45
- WCRDXYSYPCEIAK-UHFFFAOYSA-N dibutylstannane Chemical compound CCCC[SnH2]CCCC WCRDXYSYPCEIAK-UHFFFAOYSA-N 0.000 description 24
- NPAIMXWXWPJRES-UHFFFAOYSA-N butyltin(3+) Chemical compound CCCC[Sn+3] NPAIMXWXWPJRES-UHFFFAOYSA-N 0.000 description 18
- 125000004432 carbon atom Chemical group C* 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 14
- CSHCPECZJIEGJF-UHFFFAOYSA-N methyltin Chemical compound [Sn]C CSHCPECZJIEGJF-UHFFFAOYSA-N 0.000 description 13
- ZMHZSHHZIKJFIR-UHFFFAOYSA-N octyltin Chemical compound CCCCCCCC[Sn] ZMHZSHHZIKJFIR-UHFFFAOYSA-N 0.000 description 13
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 10
- 230000000087 stabilizing effect Effects 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 9
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 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 7
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 229940049964 oleate Drugs 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- PWEVMPIIOJUPRI-UHFFFAOYSA-N dimethyltin Chemical compound C[Sn]C PWEVMPIIOJUPRI-UHFFFAOYSA-N 0.000 description 6
- 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 5
- PMNLUUOXGOOLSP-UHFFFAOYSA-M 2-sulfanylpropanoate Chemical compound CC(S)C([O-])=O PMNLUUOXGOOLSP-UHFFFAOYSA-M 0.000 description 5
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 5
- UTOVMEACOLCUCK-PLNGDYQASA-N butyl maleate Chemical compound CCCCOC(=O)\C=C/C(O)=O UTOVMEACOLCUCK-PLNGDYQASA-N 0.000 description 5
- ONKUFCYOWCZCSR-UHFFFAOYSA-N didodecyltin Chemical compound CCCCCCCCCCCC[Sn]CCCCCCCCCCCC ONKUFCYOWCZCSR-UHFFFAOYSA-N 0.000 description 5
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 5
- 239000011342 resin composition Substances 0.000 description 5
- BOPWWPKQLXCRCI-UHFFFAOYSA-N 2-sulfanylpentadecanoic acid Chemical compound CCCCCCCCCCCCCC(S)C(O)=O BOPWWPKQLXCRCI-UHFFFAOYSA-N 0.000 description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- HYOKQSFYEDVSMC-OAWHIZORSA-M [(z)-4-butoxy-4-oxobut-2-enoyl]oxy-dibutyltin Chemical compound CCCCOC(=O)\C=C/C(=O)O[Sn](CCCC)CCCC HYOKQSFYEDVSMC-OAWHIZORSA-M 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 4
- TVMDUMQNXXNGMG-UHFFFAOYSA-N dodecyl 2-sulfanylacetate Chemical compound CCCCCCCCCCCCOC(=O)CS TVMDUMQNXXNGMG-UHFFFAOYSA-N 0.000 description 4
- 229960001545 hydrotalcite Drugs 0.000 description 4
- 229910001701 hydrotalcite Inorganic materials 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 4
- IIPCXIGUIPAGQB-OUKQBFOZSA-N (e)-4-dodecoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCCCOC(=O)\C=C\C(O)=O IIPCXIGUIPAGQB-OUKQBFOZSA-N 0.000 description 3
- REFZTFPICLNNPM-UHFFFAOYSA-N 2-sulfanyldodecanoic acid Chemical compound CCCCCCCCCCC(S)C(O)=O REFZTFPICLNNPM-UHFFFAOYSA-N 0.000 description 3
- TZVOTYCXLFYAPY-UHFFFAOYSA-N 2-sulfanylhexadecanoic acid Chemical compound CCCCCCCCCCCCCCC(S)C(O)=O TZVOTYCXLFYAPY-UHFFFAOYSA-N 0.000 description 3
- HGIOOMCLOWLFTJ-UHFFFAOYSA-N 3-phenyl-2-sulfanylpropanoic acid Chemical compound OC(=O)C(S)CC1=CC=CC=C1 HGIOOMCLOWLFTJ-UHFFFAOYSA-N 0.000 description 3
- BURDEKNVCUJHGU-UHFFFAOYSA-N 6-methoxy-2-sulfanylhexanoic acid Chemical compound COCCCCC(S)C(O)=O BURDEKNVCUJHGU-UHFFFAOYSA-N 0.000 description 3
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 3
- INESKUJQAULKSC-UHFFFAOYSA-L [dimethyl(propanoyloxy)stannyl] propanoate Chemical compound CCC(=O)O[Sn](C)(C)OC(=O)CC INESKUJQAULKSC-UHFFFAOYSA-L 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- SKGVGRLWZVRZDC-UHFFFAOYSA-N butyl 2-sulfanylacetate Chemical compound CCCCOC(=O)CS SKGVGRLWZVRZDC-UHFFFAOYSA-N 0.000 description 3
- CNJFYEOPSNYWGP-UHFFFAOYSA-K butyltin(3+) 4-ethyl-2-sulfanyloctanoate Chemical compound CCCC[Sn+3].CCCCC(CC)CC(S)C([O-])=O.CCCCC(CC)CC(S)C([O-])=O.CCCCC(CC)CC(S)C([O-])=O CNJFYEOPSNYWGP-UHFFFAOYSA-K 0.000 description 3
- DHQYDHVETSVMKQ-UHFFFAOYSA-N cyclohexyl 2-sulfanylacetate Chemical compound SCC(=O)OC1CCCCC1 DHQYDHVETSVMKQ-UHFFFAOYSA-N 0.000 description 3
- DVKFXBDZXZUTMB-UHFFFAOYSA-L dibutyltin(2+);4-ethyl-2-(sulfanylmethyl)octanoate Chemical compound CCCC[Sn+2]CCCC.CCCCC(CC)CC(CS)C([O-])=O.CCCCC(CC)CC(CS)C([O-])=O DVKFXBDZXZUTMB-UHFFFAOYSA-L 0.000 description 3
- SDTDHTCWRNVNAJ-UHFFFAOYSA-L dimethyltin(2+);diacetate Chemical compound CC(=O)O[Sn](C)(C)OC(C)=O SDTDHTCWRNVNAJ-UHFFFAOYSA-L 0.000 description 3
- QBHHJQBPSBAZID-UHFFFAOYSA-L dimethyltin(2+);prop-2-enoate Chemical compound C[Sn+2]C.[O-]C(=O)C=C.[O-]C(=O)C=C QBHHJQBPSBAZID-UHFFFAOYSA-L 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- JQTFPHLEQLLQOT-UHFFFAOYSA-N octadecyl 2-sulfanylacetate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CS JQTFPHLEQLLQOT-UHFFFAOYSA-N 0.000 description 3
- BPIOJPMTGBLEIV-PLNGDYQASA-N (z)-4-(2-butoxyethoxy)-4-oxobut-2-enoic acid Chemical compound CCCCOCCOC(=O)\C=C/C(O)=O BPIOJPMTGBLEIV-PLNGDYQASA-N 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
- IGMYAFRPSRRXNA-UHFFFAOYSA-L 2-[dibutyl(carboxymethylsulfanyl)stannyl]sulfanylacetic acid Chemical compound [O-]C(=O)CS.[O-]C(=O)CS.CCCC[Sn+2]CCCC IGMYAFRPSRRXNA-UHFFFAOYSA-L 0.000 description 2
- NTKCAHRZWRIYFH-UHFFFAOYSA-N 2-sulfanyloctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(S)C(O)=O NTKCAHRZWRIYFH-UHFFFAOYSA-N 0.000 description 2
- DKIDEFUBRARXTE-UHFFFAOYSA-M 3-mercaptopropionate Chemical compound [O-]C(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-M 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Chemical class 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
- IKOBEOALWFLQST-UHFFFAOYSA-L [[6-methoxy-2-(sulfanylmethyl)hexanoyl]oxy-dimethylstannyl] 6-methoxy-2-(sulfanylmethyl)hexanoate Chemical compound COCCCCC(C(=O)[O-])CS.COCCCCC(C(=O)[O-])CS.C[Sn+2]C IKOBEOALWFLQST-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
- BBOXUIQANHZBAK-UHFFFAOYSA-K [bis[[4-ethyl-2-(sulfanylmethyl)octanoyl]oxy]-octylstannyl] 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(CCCCCCC)[Sn+3] BBOXUIQANHZBAK-UHFFFAOYSA-K 0.000 description 2
- VSQSNAOYNOHQHO-UHFFFAOYSA-K [bis[[8-methyl-2-(sulfanylmethyl)nonanoyl]oxy]-octylstannyl] 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(CCCCCCC)[Sn+3] VSQSNAOYNOHQHO-UHFFFAOYSA-K 0.000 description 2
- QOAKFYPIOAPITK-UHFFFAOYSA-K [butyl-bis(2-sulfanyldecanoyloxy)stannyl] 2-sulfanyldecanoate Chemical compound C(CCCCCCC)C(C(=O)[O-])S.C(CCCCCCC)C(C(=O)[O-])S.C(CCCCCCC)C(C(=O)[O-])S.C(CCC)[Sn+3] QOAKFYPIOAPITK-UHFFFAOYSA-K 0.000 description 2
- SSUJQNHAECAKOS-UHFFFAOYSA-K [butyl-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(CCC)[Sn+3] SSUJQNHAECAKOS-UHFFFAOYSA-K 0.000 description 2
- URZCGKFICPQWPN-UHFFFAOYSA-K [butyl-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(CCC)[Sn+3] URZCGKFICPQWPN-UHFFFAOYSA-K 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
- YLFRJROMPGNJRP-UHFFFAOYSA-L [dibutyl(3-sulfanylpropanoyloxy)stannyl] 3-sulfanylpropanoate Chemical compound [O-]C(=O)CCS.[O-]C(=O)CCS.CCCC[Sn+2]CCCC YLFRJROMPGNJRP-UHFFFAOYSA-L 0.000 description 2
- CHUXJFIWYUUSDJ-UHFFFAOYSA-L [dibutyl(docosanoyloxy)stannyl] docosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCCCCCCCCCCCC CHUXJFIWYUUSDJ-UHFFFAOYSA-L 0.000 description 2
- YVHDRFKHKGNLNW-UHFFFAOYSA-L [dibutyl(octadecanoyloxy)stannyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCCCCCCCC YVHDRFKHKGNLNW-UHFFFAOYSA-L 0.000 description 2
- FMFSDPBBKMTUIZ-UHFFFAOYSA-L [didodecyl(octadecanoyloxy)stannyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[Sn](CCCCCCCCCCCC)(CCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC FMFSDPBBKMTUIZ-UHFFFAOYSA-L 0.000 description 2
- 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 2
- CXIVPNDPMRNJNC-UHFFFAOYSA-K [octyl-bis(2-sulfanyldecanoyloxy)stannyl] 2-sulfanyldecanoate Chemical compound C(CCCCCCC)C(C(=O)[O-])S.C(CCCCCCC)C(C(=O)[O-])S.C(CCCCCCC)C(C(=O)[O-])S.C(CCCCCCC)[Sn+3] CXIVPNDPMRNJNC-UHFFFAOYSA-K 0.000 description 2
- 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 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 229940116224 behenate Drugs 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-M behenate Chemical compound CCCCCCCCCCCCCCCCCCCCCC([O-])=O UKMSUNONTOPOIO-UHFFFAOYSA-M 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000002704 decyl group Chemical group [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])* 0.000 description 2
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 2
- JJPZOIJCDNHCJP-UHFFFAOYSA-N dibutyl(sulfanylidene)tin Chemical compound CCCC[Sn](=S)CCCC JJPZOIJCDNHCJP-UHFFFAOYSA-N 0.000 description 2
- OASDIMRZYZWNDB-UHFFFAOYSA-L dibutyltin(2+);4-ethyl-2-sulfanyloctanoate Chemical compound CCCC[Sn+2]CCCC.CCCCC(CC)CC(S)C([O-])=O.CCCCC(CC)CC(S)C([O-])=O OASDIMRZYZWNDB-UHFFFAOYSA-L 0.000 description 2
- IEGSIVINRWBXJG-UHFFFAOYSA-L dibutyltin(2+);8-methyl-2-sulfanylnonanoate Chemical compound CCCC[Sn+2]CCCC.CC(C)CCCCCC(S)C([O-])=O.CC(C)CCCCCC(S)C([O-])=O IEGSIVINRWBXJG-UHFFFAOYSA-L 0.000 description 2
- RFAIKXASDCRKEP-UHFFFAOYSA-N dioctyl(sulfanylidene)tin Chemical compound CCCCCCCC[Sn](=S)CCCCCCCC RFAIKXASDCRKEP-UHFFFAOYSA-N 0.000 description 2
- 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 2
- BFWDOVALNSMHNM-UHFFFAOYSA-L dioctyltin(2+);2-sulfanyldecanoate Chemical compound CCCCCCCCC(S)C([O-])=O.CCCCCCCCC(S)C([O-])=O.CCCCCCCC[Sn+2]CCCCCCCC BFWDOVALNSMHNM-UHFFFAOYSA-L 0.000 description 2
- NMICJTGDWUZAEC-UHFFFAOYSA-L dioctyltin(2+);8-methyl-2-sulfanylnonanoate Chemical compound CC(C)CCCCCC(S)C([O-])=O.CC(C)CCCCCC(S)C([O-])=O.CCCCCCCC[Sn+2]CCCCCCCC NMICJTGDWUZAEC-UHFFFAOYSA-L 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 2
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 2
- HTTYRACTMYJREK-UHFFFAOYSA-N hexyl 2-sulfanylacetate Chemical compound CCCCCCOC(=O)CS HTTYRACTMYJREK-UHFFFAOYSA-N 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 229940070765 laurate Drugs 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- MKIJJIMOAABWGF-UHFFFAOYSA-N methyl 2-sulfanylacetate Chemical compound COC(=O)CS MKIJJIMOAABWGF-UHFFFAOYSA-N 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- CIMQDDUJBLLXSF-PUTDEVHMSA-L (e)-but-2-enoate;dibutyltin(2+) Chemical compound C\C=C\C([O-])=O.C\C=C\C([O-])=O.CCCC[Sn+2]CCCC CIMQDDUJBLLXSF-PUTDEVHMSA-L 0.000 description 1
- 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 1
- 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 1
- BMASLOOHTMQIGP-ZOKJKDLISA-H (z)-but-2-enedioate;butyltin(3+) Chemical compound CCCC[Sn+3].CCCC[Sn+3].[O-]C(=O)\C=C/C([O-])=O.[O-]C(=O)\C=C/C([O-])=O.[O-]C(=O)\C=C/C([O-])=O BMASLOOHTMQIGP-ZOKJKDLISA-H 0.000 description 1
- PKZGKWFUCLURJO-GRHBHMESSA-L (z)-but-2-enedioate;dimethyltin(2+) Chemical compound C[Sn+2]C.[O-]C(=O)\C=C/C([O-])=O PKZGKWFUCLURJO-GRHBHMESSA-L 0.000 description 1
- XIDZPWZINDODBR-UHFFFAOYSA-L 2,2-dimethyl-1,3,2-oxathiastannolan-5-one Chemical compound C[Sn]1(C)OC(=O)CS1 XIDZPWZINDODBR-UHFFFAOYSA-L 0.000 description 1
- KEUUHXDTZRYITO-UHFFFAOYSA-L 2,2-dioctyl-1,3,2-oxathiastannolan-5-one Chemical compound CCCCCCCC[Sn]1(CCCCCCCC)OC(=O)CS1 KEUUHXDTZRYITO-UHFFFAOYSA-L 0.000 description 1
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- XLAUUFJKYLULDE-UHFFFAOYSA-L [docosanoyloxy(dioctyl)stannyl] docosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCCCCCC XLAUUFJKYLULDE-UHFFFAOYSA-L 0.000 description 1
- MBPHIRCSMZIBOE-UHFFFAOYSA-L [dodecanoyloxy(didodecyl)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCCCCCCCCCC)(CCCCCCCCCCCC)OC(=O)CCCCCCCCCCC MBPHIRCSMZIBOE-UHFFFAOYSA-L 0.000 description 1
- XQBCVRSTVUHIGH-UHFFFAOYSA-L [dodecanoyloxy(dioctyl)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCCCCCCCC XQBCVRSTVUHIGH-UHFFFAOYSA-L 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
- 239000006096 absorbing agent Substances 0.000 description 1
- 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 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 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
- MGFFVSDRCRVHLC-UHFFFAOYSA-N butyl 3-sulfanylpropanoate Chemical compound CCCCOC(=O)CCS MGFFVSDRCRVHLC-UHFFFAOYSA-N 0.000 description 1
- FAOSYNUKPVJLNZ-UHFFFAOYSA-N butylstannane Chemical compound CCCC[SnH3] FAOSYNUKPVJLNZ-UHFFFAOYSA-N 0.000 description 1
- MDOSPVAVEBHPJP-UHFFFAOYSA-K butyltin(3+) 2-(sulfanylmethyl)octanoate Chemical compound CCCC[Sn+3].CCCCCCC(CS)C([O-])=O.CCCCCCC(CS)C([O-])=O.CCCCCCC(CS)C([O-])=O MDOSPVAVEBHPJP-UHFFFAOYSA-K 0.000 description 1
- APISZPGKQMPHRF-UHFFFAOYSA-K butyltin(3+) 2-methyl-3-sulfanylpropanoate Chemical compound CCCC[Sn+3].SCC(C)C([O-])=O.SCC(C)C([O-])=O.SCC(C)C([O-])=O APISZPGKQMPHRF-UHFFFAOYSA-K 0.000 description 1
- WEOSHZXMNBUUGL-UHFFFAOYSA-K butyltin(3+) 2-sulfanyloctanoate Chemical compound C(CCCCC)C(C(=O)[O-])S.C(CCCCC)C(C(=O)[O-])S.C(CCCCC)C(C(=O)[O-])S.C(CCC)[Sn+3] WEOSHZXMNBUUGL-UHFFFAOYSA-K 0.000 description 1
- AVWIXKISMQYFFD-UHFFFAOYSA-K butyltin(3+) 8-methyl-2-sulfanylnonanoate Chemical compound CCCC[Sn+3].CC(C)CCCCCC(S)C([O-])=O.CC(C)CCCCCC(S)C([O-])=O.CC(C)CCCCCC(S)C([O-])=O AVWIXKISMQYFFD-UHFFFAOYSA-K 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- KRGNPJFAKZHQPS-UHFFFAOYSA-N chloroethene;ethene Chemical group C=C.ClC=C KRGNPJFAKZHQPS-UHFFFAOYSA-N 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- XIZMMPKZMJWKFV-UHFFFAOYSA-N decyl 3-sulfanylpropanoate Chemical compound CCCCCCCCCCOC(=O)CCS XIZMMPKZMJWKFV-UHFFFAOYSA-N 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 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 1
- 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 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
- ZXPGMQQBXUCROI-UHFFFAOYSA-L dibutyltin(2+);2-(sulfanylmethyl)hexadecanoate Chemical compound CCCC[Sn+2]CCCC.CCCCCCCCCCCCCCC(CS)C([O-])=O.CCCCCCCCCCCCCCC(CS)C([O-])=O ZXPGMQQBXUCROI-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
- WUZHLENJCMZKAP-UHFFFAOYSA-L dibutyltin(2+);2-methyl-3-sulfanylpropanoate Chemical compound SCC(C)C([O-])=O.SCC(C)C([O-])=O.CCCC[Sn+2]CCCC WUZHLENJCMZKAP-UHFFFAOYSA-L 0.000 description 1
- LGUARMJKHONSQN-UHFFFAOYSA-L dibutyltin(2+);2-sulfanyldecanoate Chemical compound CCCC[Sn+2]CCCC.CCCCCCCCC(S)C([O-])=O.CCCCCCCCC(S)C([O-])=O LGUARMJKHONSQN-UHFFFAOYSA-L 0.000 description 1
- DDWSKYCNLHDAFV-UHFFFAOYSA-L dibutyltin(2+);2-sulfanylhexanoate Chemical compound CCCC[Sn+2]CCCC.CCCCC(S)C([O-])=O.CCCCC(S)C([O-])=O DDWSKYCNLHDAFV-UHFFFAOYSA-L 0.000 description 1
- OLCGOMDQTJMIPX-UHFFFAOYSA-L dibutyltin(2+);2-sulfanyloctanoate Chemical compound CCCC[Sn+2]CCCC.CCCCCCC(S)C([O-])=O.CCCCCCC(S)C([O-])=O OLCGOMDQTJMIPX-UHFFFAOYSA-L 0.000 description 1
- VVKVIDFEFWYOLN-UHFFFAOYSA-L dibutyltin(2+);2-sulfanylpropanoate Chemical compound CC(S)C([O-])=O.CC(S)C([O-])=O.CCCC[Sn+2]CCCC VVKVIDFEFWYOLN-UHFFFAOYSA-L 0.000 description 1
- WPOOSSRZRBISJU-UHFFFAOYSA-L dibutyltin(2+);8-methyl-2-(sulfanylmethyl)nonanoate Chemical compound CCCC[Sn+2]CCCC.CC(C)CCCCCC(CS)C([O-])=O.CC(C)CCCCCC(CS)C([O-])=O WPOOSSRZRBISJU-UHFFFAOYSA-L 0.000 description 1
- OTTUHBAOXMCCDS-UHFFFAOYSA-N didodecyl(sulfanylidene)tin Chemical compound CCCCCCCCCCCC[Sn](=S)CCCCCCCCCCCC OTTUHBAOXMCCDS-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZGDZBVDQDGMHIJ-BGSQTJHASA-L dimethyltin(2+) (Z)-2-sulfanylicos-11-enoate Chemical compound C[Sn+2]C.CCCCCCCC\C=C/CCCCCCCCC(S)C([O-])=O.CCCCCCCC\C=C/CCCCCCCCC(S)C([O-])=O ZGDZBVDQDGMHIJ-BGSQTJHASA-L 0.000 description 1
- MAIVVHWVCDQBOP-UDVCPWNYSA-L dimethyltin(2+) (Z)-4-methoxy-4-oxobut-2-enoate Chemical compound C[Sn+2]C.COC(=O)\C=C/C([O-])=O.COC(=O)\C=C/C([O-])=O MAIVVHWVCDQBOP-UDVCPWNYSA-L 0.000 description 1
- ISHVYKAWSPILKE-UHFFFAOYSA-L dimethyltin(2+) 2-sulfanyldodecanoate Chemical compound C[Sn+2]C.CCCCCCCCCCC(S)C([O-])=O.CCCCCCCCCCC(S)C([O-])=O ISHVYKAWSPILKE-UHFFFAOYSA-L 0.000 description 1
- WDVGZZNLIOAJNO-UHFFFAOYSA-L dimethyltin(2+) 2-sulfanylhexanoate Chemical compound C[Sn+2]C.CCCCC(S)C([O-])=O.CCCCC(S)C([O-])=O WDVGZZNLIOAJNO-UHFFFAOYSA-L 0.000 description 1
- VSGRKLWYHXHXHB-UHFFFAOYSA-L dimethyltin(2+) 2-sulfanylicosanoate Chemical compound C[Sn+2]C.CCCCCCCCCCCCCCCCCCC(S)C([O-])=O.CCCCCCCCCCCCCCCCCCC(S)C([O-])=O VSGRKLWYHXHXHB-UHFFFAOYSA-L 0.000 description 1
- JUNMITBCGRUHOV-UHFFFAOYSA-L dimethyltin(2+) 2-sulfanyltetradecanoate Chemical compound C[Sn+2]C.CCCCCCCCCCCCC(S)C([O-])=O.CCCCCCCCCCCCC(S)C([O-])=O JUNMITBCGRUHOV-UHFFFAOYSA-L 0.000 description 1
- YAHBZWSDRFSFOO-UHFFFAOYSA-L dimethyltin(2+);2-(2-ethylhexoxy)-2-oxoethanethiolate Chemical compound CCCCC(CC)COC(=O)CS[Sn](C)(C)SCC(=O)OCC(CC)CCCC YAHBZWSDRFSFOO-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
- WLTCMZJXLZLPDW-UHFFFAOYSA-L dimethyltin(2+);2-(sulfanylmethyl)pentadecanoate Chemical compound C[Sn+2]C.CCCCCCCCCCCCCC(CS)C([O-])=O.CCCCCCCCCCCCCC(CS)C([O-])=O WLTCMZJXLZLPDW-UHFFFAOYSA-L 0.000 description 1
- HKPPFWSHODSGMF-UHFFFAOYSA-L dimethyltin(2+);2-sulfanyldecanoate Chemical compound C[Sn+2]C.CCCCCCCCC(S)C([O-])=O.CCCCCCCCC(S)C([O-])=O HKPPFWSHODSGMF-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
- IRWQVZSQGDKREP-UHFFFAOYSA-L dimethyltin(2+);octadecanoate Chemical compound C[Sn+2]C.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O IRWQVZSQGDKREP-UHFFFAOYSA-L 0.000 description 1
- 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 1
- 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 1
- KBPYBYIUWWZSGD-UHFFFAOYSA-L dioctyltin(2+);2-sulfanyloctadecanoate Chemical compound CCCCCCCC[Sn+2]CCCCCCCC.CCCCCCCCCCCCCCCCC(S)C([O-])=O.CCCCCCCCCCCCCCCCC(S)C([O-])=O KBPYBYIUWWZSGD-UHFFFAOYSA-L 0.000 description 1
- JXQGQOSVTCVADL-UHFFFAOYSA-L dioctyltin(2+);2-sulfanyltetradecanoate Chemical compound CCCCCCCCCCCCC(S)C([O-])=O.CCCCCCCCCCCCC(S)C([O-])=O.CCCCCCCC[Sn+2]CCCCCCCC JXQGQOSVTCVADL-UHFFFAOYSA-L 0.000 description 1
- PWRPYOJPQUDGJK-UHFFFAOYSA-L dioctyltin(2+);prop-2-enoate Chemical compound [O-]C(=O)C=C.[O-]C(=O)C=C.CCCCCCCC[Sn+2]CCCCCCCC PWRPYOJPQUDGJK-UHFFFAOYSA-L 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 125000005469 ethylenyl group Chemical group 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000755 henicosyl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 125000002960 margaryl 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])[H] 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- UJUNCQGPYVUDNO-BQGNPDQISA-K methyltin(3+) (Z)-2-sulfanylicos-11-enoate Chemical compound [Sn+3]C.CCCCCCCC\C=C/CCCCCCCCC(S)C([O-])=O.CCCCCCCC\C=C/CCCCCCCCC(S)C([O-])=O.CCCCCCCC\C=C/CCCCCCCCC(S)C([O-])=O UJUNCQGPYVUDNO-BQGNPDQISA-K 0.000 description 1
- RKZNLZBDLFFKJP-UHFFFAOYSA-K methyltin(3+) 2-sulfanyldecanoate Chemical compound [Sn+3]C.CCCCCCCCC(S)C([O-])=O.CCCCCCCCC(S)C([O-])=O.CCCCCCCCC(S)C([O-])=O RKZNLZBDLFFKJP-UHFFFAOYSA-K 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- OMBIMRMWSOADNO-UHFFFAOYSA-K octyltin(3+) 2-sulfanyldodecanoate Chemical compound C(CCCCCCCCC)C(C(=O)[O-])S.C(CCCCCCCCC)C(C(=O)[O-])S.C(CCCCCCCCC)C(C(=O)[O-])S.C(CCCCCCC)[Sn+3] OMBIMRMWSOADNO-UHFFFAOYSA-K 0.000 description 1
- 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 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000000913 palmityl 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])[H] 0.000 description 1
- 150000008301 phosphite esters Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920005671 poly(vinyl chloride-propylene) Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005470 propylenyl group Chemical group 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000008117 stearic acid 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
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- ZFPOOXOHYITZFO-UHFFFAOYSA-N tetradecyl 3-sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCS ZFPOOXOHYITZFO-UHFFFAOYSA-N 0.000 description 1
- BANFORNDDZWGFX-UHFFFAOYSA-N tridecyl 2-sulfanylacetate Chemical compound CCCCCCCCCCCCCOC(=O)CS BANFORNDDZWGFX-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl 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])[H] 0.000 description 1
- 125000002948 undecyl 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])[H] 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 |
|---|---|---|---|
| JP11458985A JPS61272258A (ja) | 1985-05-28 | 1985-05-28 | ハロゲン含有樹脂組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11458985A JPS61272258A (ja) | 1985-05-28 | 1985-05-28 | ハロゲン含有樹脂組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61272258A JPS61272258A (ja) | 1986-12-02 |
| JPS6410011B2 true JPS6410011B2 (enrdf_load_stackoverflow) | 1989-02-21 |
Family
ID=14641636
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11458985A Granted JPS61272258A (ja) | 1985-05-28 | 1985-05-28 | ハロゲン含有樹脂組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61272258A (enrdf_load_stackoverflow) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2801036B2 (ja) * | 1989-09-14 | 1998-09-21 | 旭電化工業株式会社 | 含塩素樹脂用粉末安定剤 |
| AU2003255040A1 (en) * | 2002-09-13 | 2004-04-30 | Kaneka Corporation | Polymer composition containing double salt whose metal components are magnesium and aluminum |
-
1985
- 1985-05-28 JP JP11458985A patent/JPS61272258A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61272258A (ja) | 1986-12-02 |
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