JPH0337579B2 - - Google Patents
Info
- Publication number
- JPH0337579B2 JPH0337579B2 JP58188038A JP18803883A JPH0337579B2 JP H0337579 B2 JPH0337579 B2 JP H0337579B2 JP 58188038 A JP58188038 A JP 58188038A JP 18803883 A JP18803883 A JP 18803883A JP H0337579 B2 JPH0337579 B2 JP H0337579B2
- Authority
- JP
- Japan
- Prior art keywords
- mercaptopropionate
- tris
- bis
- formula
- monomethyltin
- 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 - Lifetime
Links
- -1 tin 3-mercaptopropionic acid ester Chemical class 0.000 claims description 89
- 229920005989 resin Polymers 0.000 claims description 13
- 239000011347 resin Substances 0.000 claims description 13
- 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 claims description 10
- 229960001545 hydrotalcite Drugs 0.000 claims description 10
- 229910001701 hydrotalcite Inorganic materials 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 239000011342 resin composition Substances 0.000 claims description 4
- 230000002459 sustained effect Effects 0.000 description 11
- 229920001577 copolymer Polymers 0.000 description 9
- PMNLUUOXGOOLSP-UHFFFAOYSA-M 2-sulfanylpropanoate Chemical compound CC(S)C([O-])=O PMNLUUOXGOOLSP-UHFFFAOYSA-M 0.000 description 7
- 239000007983 Tris buffer Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 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 4
- DKIDEFUBRARXTE-UHFFFAOYSA-M 3-mercaptopropionate Chemical compound [O-]C(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-M 0.000 description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
- JPLYYEIOHUCWPI-UHFFFAOYSA-L [dimethyl-(2-methyl-3-sulfanylpropanoyl)oxystannyl] 2-methyl-3-sulfanylpropanoate Chemical compound C[Sn+2]C.SCC(C)C([O-])=O.SCC(C)C([O-])=O JPLYYEIOHUCWPI-UHFFFAOYSA-L 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 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 3
- 230000000694 effects Effects 0.000 description 3
- 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 3
- 150000002736 metal compounds Chemical class 0.000 description 3
- 230000000087 stabilizing effect Effects 0.000 description 3
- ZHUWXKIPGGZNJW-UHFFFAOYSA-N 6-methylheptyl 3-sulfanylpropanoate Chemical compound CC(C)CCCCCOC(=O)CCS ZHUWXKIPGGZNJW-UHFFFAOYSA-N 0.000 description 2
- 229910018626 Al(OH) Inorganic materials 0.000 description 2
- PPGQKWKKPNJHAN-UHFFFAOYSA-L C(CCCCCCCCCCC)C(C(=O)[O-])CS.C(CCCCCCC)[Sn+2]CCCCCCCC.C(CCCCCCCCCCC)C(C(=O)[O-])CS Chemical compound C(CCCCCCCCCCC)C(C(=O)[O-])CS.C(CCCCCCC)[Sn+2]CCCCCCCC.C(CCCCCCCCCCC)C(C(=O)[O-])CS PPGQKWKKPNJHAN-UHFFFAOYSA-L 0.000 description 2
- RLIKVFCLBKUQRF-UHFFFAOYSA-K CCCCC(CS)C(=O)O[Sn](C)(OC(=O)C(CCCC)CS)OC(=O)C(CCCC)CS Chemical compound CCCCC(CS)C(=O)O[Sn](C)(OC(=O)C(CCCC)CS)OC(=O)C(CCCC)CS RLIKVFCLBKUQRF-UHFFFAOYSA-K 0.000 description 2
- 239000004593 Epoxy Chemical class 0.000 description 2
- 229910019440 Mg(OH) Inorganic materials 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
- 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
- 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 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
- PWEVMPIIOJUPRI-UHFFFAOYSA-N dimethyltin Chemical compound C[Sn]C PWEVMPIIOJUPRI-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 150000002484 inorganic compounds Chemical class 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- LWNSNYBMYBWJDN-UHFFFAOYSA-N octyl 3-sulfanylpropanoate Chemical compound CCCCCCCCOC(=O)CCS LWNSNYBMYBWJDN-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 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 2
- 150000003606 tin compounds Chemical class 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- XRNQGQCZWDPVRK-UHFFFAOYSA-K 2-cyclohexyl-3-sulfanylpropanoate;octyltin(3+) Chemical compound CCCCCCCC[Sn+3].[O-]C(=O)C(CS)C1CCCCC1.[O-]C(=O)C(CS)C1CCCCC1.[O-]C(=O)C(CS)C1CCCCC1 XRNQGQCZWDPVRK-UHFFFAOYSA-K 0.000 description 1
- OSJAAYAWZBUHDN-UHFFFAOYSA-L 2-ethylhexyl 3-[[3-(2-ethylhexoxy)-3-oxopropyl]sulfanyl-dimethylstannyl]sulfanylpropanoate Chemical compound CCCCC(CC)COC(=O)CCS[Sn](C)(C)SCCC(=O)OCC(CC)CCCC OSJAAYAWZBUHDN-UHFFFAOYSA-L 0.000 description 1
- 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 1
- IDZOFXZSEPNDPJ-UHFFFAOYSA-K 2-methyl-3-sulfanylpropanoate methyltin(3+) Chemical compound [Sn+3]C.SCC(C)C([O-])=O.SCC(C)C([O-])=O.SCC(C)C([O-])=O IDZOFXZSEPNDPJ-UHFFFAOYSA-K 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- NIVHKDWMWJUNNR-UHFFFAOYSA-L C(C)OCCCCC(C(=O)[O-])CS.C(C)OCCCCC(C(=O)[O-])CS.C(CCC)[Sn+2]CCCC Chemical compound C(C)OCCCCC(C(=O)[O-])CS.C(C)OCCCCC(C(=O)[O-])CS.C(CCC)[Sn+2]CCCC NIVHKDWMWJUNNR-UHFFFAOYSA-L 0.000 description 1
- HFYMWKJUUAMKIW-UHFFFAOYSA-L CCCCCCCCCCCCC(CS)C(=O)O[Sn](C)(C)OC(=O)C(CCCCCCCCCCCC)CS Chemical compound CCCCCCCCCCCCC(CS)C(=O)O[Sn](C)(C)OC(=O)C(CCCCCCCCCCCC)CS HFYMWKJUUAMKIW-UHFFFAOYSA-L 0.000 description 1
- RVORGJMKRLVXII-UHFFFAOYSA-K CCCCCCCCCCCCC(CS)C(=O)O[Sn](CCCCCCCC)(OC(=O)C(CCCCCCCCCCCC)CS)OC(=O)C(CCCCCCCCCCCC)CS Chemical compound CCCCCCCCCCCCC(CS)C(=O)O[Sn](CCCCCCCC)(OC(=O)C(CCCCCCCCCCCC)CS)OC(=O)C(CCCCCCCCCCCC)CS RVORGJMKRLVXII-UHFFFAOYSA-K 0.000 description 1
- JLNBIOKGRORYGP-UHFFFAOYSA-L CCCCCCCCCCCCCCCCCCCCCCC(CS)C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)C(CCCCCCCCCCCCCCCCCCCCCC)CS Chemical compound CCCCCCCCCCCCCCCCCCCCCCC(CS)C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)C(CCCCCCCCCCCCCCCCCCCCCC)CS JLNBIOKGRORYGP-UHFFFAOYSA-L 0.000 description 1
- CUVYDWOUDAZBMA-BGSQTJHASA-L CCCCCCCC[Sn+2]CCCCCCCC.CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O.CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O Chemical compound CCCCCCCC[Sn+2]CCCCCCCC.CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O.CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O CUVYDWOUDAZBMA-BGSQTJHASA-L 0.000 description 1
- BLOWYPKXIVYNPN-UHFFFAOYSA-K CCCCCCCC[Sn+3].CCCCCCCCCCCCCC(CS)C([O-])=O.CCCCCCCCCCCCCC(CS)C([O-])=O.CCCCCCCCCCCCCC(CS)C([O-])=O Chemical compound CCCCCCCC[Sn+3].CCCCCCCCCCCCCC(CS)C([O-])=O.CCCCCCCCCCCCCC(CS)C([O-])=O.CCCCCCCCCCCCCC(CS)C([O-])=O BLOWYPKXIVYNPN-UHFFFAOYSA-K 0.000 description 1
- 229920006385 Geon Polymers 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- SXABRHRXLJEYQQ-UHFFFAOYSA-L SCC(C)C([O-])=O.SCC(C)C([O-])=O.CCCCCCCC[Sn+2]CCCCCCCC Chemical compound SCC(C)C([O-])=O.SCC(C)C([O-])=O.CCCCCCCC[Sn+2]CCCCCCCC SXABRHRXLJEYQQ-UHFFFAOYSA-L 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- YVXGOQDXPBIWHN-UHFFFAOYSA-L [(2-benzyl-3-sulfanylpropanoyl)oxy-dibutylstannyl] 2-benzyl-3-sulfanylpropanoate Chemical compound C(C1=CC=CC=C1)C(C(=O)[O-])CS.C(C1=CC=CC=C1)C(C(=O)[O-])CS.C(CCC)[Sn+2]CCCC YVXGOQDXPBIWHN-UHFFFAOYSA-L 0.000 description 1
- YOXNIYZHHKSXEJ-UHFFFAOYSA-L [(2-benzyl-3-sulfanylpropanoyl)oxy-dioctylstannyl] 2-benzyl-3-sulfanylpropanoate Chemical compound CCCCCCCC[Sn](CCCCCCCC)(OC(=O)C(CC1=CC=CC=C1)CS)OC(=O)C(CC2=CC=CC=C2)CS YOXNIYZHHKSXEJ-UHFFFAOYSA-L 0.000 description 1
- QXLWQKUDQTWNDA-UHFFFAOYSA-L [(2-cyclohexyl-3-sulfanylpropanoyl)oxy-dioctylstannyl] 2-cyclohexyl-3-sulfanylpropanoate Chemical compound CCCCCCCC[Sn](CCCCCCCC)(OC(=O)C(CS)C1CCCCC1)OC(=O)C(CS)C2CCCCC2 QXLWQKUDQTWNDA-UHFFFAOYSA-L 0.000 description 1
- NCHPANLKGNXFRX-UHFFFAOYSA-K [Sn+3]C.CCCCCCCCC(CS)C([O-])=O.CCCCCCCCC(CS)C([O-])=O.CCCCCCCCC(CS)C([O-])=O Chemical compound [Sn+3]C.CCCCCCCCC(CS)C([O-])=O.CCCCCCCCC(CS)C([O-])=O.CCCCCCCCC(CS)C([O-])=O NCHPANLKGNXFRX-UHFFFAOYSA-K 0.000 description 1
- 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 1
- KTAWZHKXLUYKNC-UHFFFAOYSA-L [[6-methoxy-2-(sulfanylmethyl)hexanoyl]oxy-dioctylstannyl] 6-methoxy-2-(sulfanylmethyl)hexanoate Chemical compound CCCCCCCC[Sn](CCCCCCCC)(OC(=O)C(CCCCOC)CS)OC(=O)C(CCCCOC)CS KTAWZHKXLUYKNC-UHFFFAOYSA-L 0.000 description 1
- 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 1
- LAZDLLVVLXLISH-UHFFFAOYSA-K [bis[(2-benzyl-3-sulfanylpropanoyl)oxy]-butylstannyl] 2-benzyl-3-sulfanylpropanoate Chemical compound C(C1=CC=CC=C1)C(C(=O)[O-])CS.C(C1=CC=CC=C1)C(C(=O)[O-])CS.C(C1=CC=CC=C1)C(C(=O)[O-])CS.C(CCC)[Sn+3] LAZDLLVVLXLISH-UHFFFAOYSA-K 0.000 description 1
- HZPXXOQDOAOSBQ-UHFFFAOYSA-K [bis[[4-ethyl-2-(sulfanylmethyl)octanoyl]oxy]-methylstannyl] 4-ethyl-2-(sulfanylmethyl)octanoate Chemical compound [Sn+3]C.CCCCC(CC)CC(CS)C([O-])=O.CCCCC(CC)CC(CS)C([O-])=O.CCCCC(CC)CC(CS)C([O-])=O HZPXXOQDOAOSBQ-UHFFFAOYSA-K 0.000 description 1
- 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 1
- SVGSOCPXMWAZOK-UHFFFAOYSA-K [bis[[6-methoxy-2-(sulfanylmethyl)hexanoyl]oxy]-methylstannyl] 6-methoxy-2-(sulfanylmethyl)hexanoate Chemical compound COCCCCC(C(=O)[O-])CS.COCCCCC(C(=O)[O-])CS.COCCCCC(C(=O)[O-])CS.C[Sn+3] SVGSOCPXMWAZOK-UHFFFAOYSA-K 0.000 description 1
- 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 1
- 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 1
- QNZSBKCIVRSFHR-UHFFFAOYSA-K [butyl-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(CCC)[Sn+3] QNZSBKCIVRSFHR-UHFFFAOYSA-K 0.000 description 1
- 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 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
- YPPXRFJIUCROQP-BGSQTJHASA-L [dibutyl-[(Z)-2-(sulfanylmethyl)icos-11-enoyl]oxystannyl] (Z)-2-(sulfanylmethyl)icos-11-enoate Chemical compound CCCC[Sn+2]CCCC.CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O.CCCCCCCC\C=C/CCCCCCCCC(CS)C([O-])=O YPPXRFJIUCROQP-BGSQTJHASA-L 0.000 description 1
- 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 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
- OXDSRJYUPSCKIX-UHFFFAOYSA-L [dimethyl-[2-(sulfanylmethyl)decanoyloxy]stannyl] 2-(sulfanylmethyl)decanoate Chemical compound C[Sn+2]C.CCCCCCCCC(CS)C([O-])=O.CCCCCCCCC(CS)C([O-])=O OXDSRJYUPSCKIX-UHFFFAOYSA-L 0.000 description 1
- FDRAISLZUAHUSR-UHFFFAOYSA-L [dimethyl-[2-(sulfanylmethyl)hexanoyloxy]stannyl] 2-(sulfanylmethyl)hexanoate Chemical compound CCCCC(CS)C(=O)O[Sn](C)(C)OC(=O)C(CCCC)CS FDRAISLZUAHUSR-UHFFFAOYSA-L 0.000 description 1
- LIKRGYHPRSUSSB-UHFFFAOYSA-L [dimethyl-[2-(sulfanylmethyl)tetracosanoyloxy]stannyl] 2-(sulfanylmethyl)tetracosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCCC(CS)C(=O)O[Sn](C)(C)OC(=O)C(CCCCCCCCCCCCCCCCCCCCCC)CS LIKRGYHPRSUSSB-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
- BVOUVSBEICUNQU-UHFFFAOYSA-L [dioctyl-[2-(sulfanylmethyl)icosanoyloxy]stannyl] 2-(sulfanylmethyl)icosanoate Chemical compound CCCCCCCCCCCCCCCCCCC(CS)C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)C(CCCCCCCCCCCCCCCCCC)CS BVOUVSBEICUNQU-UHFFFAOYSA-L 0.000 description 1
- CLUZTHQDKTXPLL-UHFFFAOYSA-L [dioctyl-[2-(sulfanylmethyl)pentadecanoyloxy]stannyl] 2-(sulfanylmethyl)pentadecanoate Chemical compound CCCCCCCCCCCCCC(CS)C(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)C(CCCCCCCCCCCCC)CS CLUZTHQDKTXPLL-UHFFFAOYSA-L 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
- 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
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000001204 arachidyl 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])[H] 0.000 description 1
- 125000002511 behenyl 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])C([H])([H])[H] 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
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 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
- 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
- 238000004040 coloring Methods 0.000 description 1
- 230000002301 combined effect Effects 0.000 description 1
- 230000000052 comparative effect Effects 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
- 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
- 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 1
- 235000014113 dietary fatty acids Nutrition 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
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 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
- 238000000465 moulding Methods 0.000 description 1
- 125000001421 myristyl 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])[H] 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZMHZSHHZIKJFIR-UHFFFAOYSA-N octyltin Chemical compound CCCCCCCC[Sn] ZMHZSHHZIKJFIR-UHFFFAOYSA-N 0.000 description 1
- 125000005461 organic phosphorous group Chemical group 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
- 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
- 239000008117 stearic acid Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- ZOIIFFYQXPDJOK-UHFFFAOYSA-L tetradecyl 3-[dibutyl-(3-oxo-3-tetradecoxypropyl)sulfanylstannyl]sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCS[Sn](CCCC)(CCCC)SCCC(=O)OCCCCCCCCCCCCCC ZOIIFFYQXPDJOK-UHFFFAOYSA-L 0.000 description 1
- NOQSBIQABOFHKR-UHFFFAOYSA-L tridecyl 3-[dibutyl-(3-oxo-3-tridecoxypropyl)sulfanylstannyl]sulfanylpropanoate Chemical compound CCCCCCCCCCCCCOC(=O)CCS[Sn](CCCC)(CCCC)SCCC(=O)OCCCCCCCCCCCCC NOQSBIQABOFHKR-UHFFFAOYSA-L 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
- 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 |
|---|---|---|---|
| JP18803883A JPS6079049A (ja) | 1983-10-07 | 1983-10-07 | ハロゲン含有樹脂組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18803883A JPS6079049A (ja) | 1983-10-07 | 1983-10-07 | ハロゲン含有樹脂組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6079049A JPS6079049A (ja) | 1985-05-04 |
| JPH0337579B2 true JPH0337579B2 (ru) | 1991-06-06 |
Family
ID=16216580
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18803883A Granted JPS6079049A (ja) | 1983-10-07 | 1983-10-07 | ハロゲン含有樹脂組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6079049A (ru) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60199043A (ja) * | 1984-03-22 | 1985-10-08 | Nitto Kasei Kk | 安定化されたハロゲン含有樹脂組成物 |
| EP0709427B1 (en) * | 1994-10-27 | 2000-05-03 | Kyowa Chemical Industry Co., Ltd. | Resin composition and molded article |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57209943A (en) * | 1981-06-18 | 1982-12-23 | Adeka Argus Chem Co Ltd | Stabilized halogen-containing resin composition |
-
1983
- 1983-10-07 JP JP18803883A patent/JPS6079049A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57209943A (en) * | 1981-06-18 | 1982-12-23 | Adeka Argus Chem Co Ltd | Stabilized halogen-containing resin composition |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6079049A (ja) | 1985-05-04 |
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