JP2006528254A5 - - Google Patents
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- JP2006528254A5 JP2006528254A5 JP2006520825A JP2006520825A JP2006528254A5 JP 2006528254 A5 JP2006528254 A5 JP 2006528254A5 JP 2006520825 A JP2006520825 A JP 2006520825A JP 2006520825 A JP2006520825 A JP 2006520825A JP 2006528254 A5 JP2006528254 A5 JP 2006528254A5
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- Japan
- Prior art keywords
- group
- carbon atoms
- alkyl
- hydrogen atom
- formula
- Prior art date
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- 125000004432 carbon atom Chemical group C* 0.000 claims 144
- 125000000217 alkyl group Chemical group 0.000 claims 49
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 29
- -1 oxyl group Chemical group 0.000 claims 26
- 125000002947 alkylene group Chemical group 0.000 claims 25
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 15
- 125000003118 aryl group Chemical group 0.000 claims 13
- 125000001931 aliphatic group Chemical group 0.000 claims 10
- 239000000203 mixture Substances 0.000 claims 10
- 125000003545 alkoxy group Chemical group 0.000 claims 9
- KSSJBGNOJJETTC-UHFFFAOYSA-N COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC Chemical compound COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC KSSJBGNOJJETTC-UHFFFAOYSA-N 0.000 claims 8
- 125000002252 acyl group Chemical group 0.000 claims 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims 8
- 239000003063 flame retardant Substances 0.000 claims 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 8
- 229910052757 nitrogen Inorganic materials 0.000 claims 8
- 125000003342 alkenyl group Chemical group 0.000 claims 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims 7
- 229910052799 carbon Inorganic materials 0.000 claims 7
- 125000003884 phenylalkyl group Chemical group 0.000 claims 6
- 125000002723 alicyclic group Chemical group 0.000 claims 5
- 125000000732 arylene group Chemical group 0.000 claims 5
- 150000001875 compounds Chemical class 0.000 claims 5
- 125000002993 cycloalkylene group Chemical group 0.000 claims 5
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical group C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims 4
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims 4
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims 4
- 239000003381 stabilizer Substances 0.000 claims 4
- 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 claims 3
- 239000002253 acid Substances 0.000 claims 3
- 150000001412 amines Chemical class 0.000 claims 3
- 125000003277 amino group Chemical group 0.000 claims 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- DYIZJUDNMOIZQO-UHFFFAOYSA-N 4,5,6,7-tetrabromo-2-[2-(4,5,6,7-tetrabromo-1,3-dioxoisoindol-2-yl)ethyl]isoindole-1,3-dione Chemical compound O=C1C(C(=C(Br)C(Br)=C2Br)Br)=C2C(=O)N1CCN1C(=O)C2=C(Br)C(Br)=C(Br)C(Br)=C2C1=O DYIZJUDNMOIZQO-UHFFFAOYSA-N 0.000 claims 2
- AYJOUNOHHNLBJP-UHFFFAOYSA-N 6-chloro-2-n,4-n-bis[4-(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butyl]-1,3,5-triazine-2,4-diamine Chemical compound C1C(C)(C)N(OC2CCCCC2)C(C)(C)CC1CCCCNC(N=1)=NC(Cl)=NC=1NCCCCC(CC1(C)C)CC(C)(C)N1OC1CCCCC1 AYJOUNOHHNLBJP-UHFFFAOYSA-N 0.000 claims 2
- 239000004114 Ammonium polyphosphate Substances 0.000 claims 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 2
- 229920000877 Melamine resin Polymers 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- 239000007983 Tris buffer Substances 0.000 claims 2
- 125000004450 alkenylene group Chemical group 0.000 claims 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims 2
- 229920001276 ammonium polyphosphate Polymers 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000006309 butyl amino group Chemical group 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000005724 cycloalkenylene group Chemical group 0.000 claims 2
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- UGQQAJOWXNCOPY-UHFFFAOYSA-N dechlorane plus Chemical compound C12CCC3C(C4(Cl)Cl)(Cl)C(Cl)=C(Cl)C4(Cl)C3CCC2C2(Cl)C(Cl)=C(Cl)C1(Cl)C2(Cl)Cl UGQQAJOWXNCOPY-UHFFFAOYSA-N 0.000 claims 2
- 125000003073 divalent carboacyl group Chemical group 0.000 claims 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 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 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 229920000747 poly(lactic acid) Polymers 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000006839 xylylene group Chemical group 0.000 claims 2
- DJKGDNKYTKCJKD-BPOCMEKLSA-N (1s,4r,5s,6r)-1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-ene-5,6-dicarboxylic acid Chemical compound ClC1=C(Cl)[C@]2(Cl)[C@H](C(=O)O)[C@H](C(O)=O)[C@@]1(Cl)C2(Cl)Cl DJKGDNKYTKCJKD-BPOCMEKLSA-N 0.000 claims 1
- BGGGMYCMZTXZBY-UHFFFAOYSA-N (3-hydroxyphenyl) phosphono hydrogen phosphate Chemical compound OC1=CC=CC(OP(O)(=O)OP(O)(O)=O)=C1 BGGGMYCMZTXZBY-UHFFFAOYSA-N 0.000 claims 1
- ORYGKUIDIMIRNN-UHFFFAOYSA-N 1,2,3,4-tetrabromo-5-(2,3,4,5-tetrabromophenoxy)benzene Chemical compound BrC1=C(Br)C(Br)=CC(OC=2C(=C(Br)C(Br)=C(Br)C=2)Br)=C1Br ORYGKUIDIMIRNN-UHFFFAOYSA-N 0.000 claims 1
- YVVYMSXDQGDASK-UHFFFAOYSA-N 1,2,3-tribromo-4-[2-(2,3,4-tribromophenoxy)ethoxy]benzene Chemical compound BrC1=C(Br)C(Br)=CC=C1OCCOC1=CC=C(Br)C(Br)=C1Br YVVYMSXDQGDASK-UHFFFAOYSA-N 0.000 claims 1
- NZUPFZNVGSWLQC-UHFFFAOYSA-N 1,3,5-tris(2,3-dibromopropyl)-1,3,5-triazinane-2,4,6-trione Chemical compound BrCC(Br)CN1C(=O)N(CC(Br)CBr)C(=O)N(CC(Br)CBr)C1=O NZUPFZNVGSWLQC-UHFFFAOYSA-N 0.000 claims 1
- LXIZRZRTWSDLKK-UHFFFAOYSA-N 1,3-dibromo-5-[2-[3,5-dibromo-4-(2,3-dibromopropoxy)phenyl]propan-2-yl]-2-(2,3-dibromopropoxy)benzene Chemical compound C=1C(Br)=C(OCC(Br)CBr)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(OCC(Br)CBr)C(Br)=C1 LXIZRZRTWSDLKK-UHFFFAOYSA-N 0.000 claims 1
- FYQOHJWNKFULEZ-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC(C)(O)CON1C(C)(C)CC(O)CC1(C)C FYQOHJWNKFULEZ-UHFFFAOYSA-N 0.000 claims 1
- FUVBNYKKKZSBCG-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-one Chemical compound CC(C)(O)CON1C(C)(C)CC(=O)CC1(C)C FUVBNYKKKZSBCG-UHFFFAOYSA-N 0.000 claims 1
- WICJDHJYOIJBDM-UHFFFAOYSA-N 1-[4-[butyl-[4-[butyl-[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl]amino]-6-(2-hydroxyethylamino)-1,3,5-triazin-2-yl]amino]-2,2,6,6-tetramethylpiperidin-1-yl]oxy-2-methylpropan-2-ol Chemical compound N=1C(NCCO)=NC(N(CCCC)C2CC(C)(C)N(OCC(C)(C)O)C(C)(C)C2)=NC=1N(CCCC)C1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 WICJDHJYOIJBDM-UHFFFAOYSA-N 0.000 claims 1
- OKELZJLBUAZSCL-UHFFFAOYSA-N 1-cyclohexyloxy-2,2,6,6-tetramethyl-n-octadecylpiperidin-4-amine Chemical compound CC1(C)CC(NCCCCCCCCCCCCCCCCCC)CC(C)(C)N1OC1CCCCC1 OKELZJLBUAZSCL-UHFFFAOYSA-N 0.000 claims 1
- SCSMZMBYJMIJTK-UHFFFAOYSA-N 2,4,9,10,11-pentaoxa-5,8-diaza-1lambda5,3lambda5-diphosphatricyclo[6.1.1.13,5]undecane 1,3-dioxide Chemical compound O1P(=O)(O2)ON2CCN2OP1(=O)O2 SCSMZMBYJMIJTK-UHFFFAOYSA-N 0.000 claims 1
- DMRGBBXBFDQADY-UHFFFAOYSA-N 2-[2,3-bis(dichloroamino)phenyl]ethanol Chemical compound OCCC=1C(=C(C=CC1)N(Cl)Cl)N(Cl)Cl DMRGBBXBFDQADY-UHFFFAOYSA-N 0.000 claims 1
- CCJKFLLIJCGHMO-UHFFFAOYSA-N 2-[diethoxyphosphorylmethyl(2-hydroxyethyl)amino]ethanol Chemical compound CCOP(=O)(OCC)CN(CCO)CCO CCJKFLLIJCGHMO-UHFFFAOYSA-N 0.000 claims 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims 1
- RLHGFJMGWQXPBW-UHFFFAOYSA-N 2-hydroxy-3-(1h-imidazol-5-ylmethyl)benzamide Chemical compound NC(=O)C1=CC=CC(CC=2NC=NC=2)=C1O RLHGFJMGWQXPBW-UHFFFAOYSA-N 0.000 claims 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 claims 1
- XIRDTMSOGDWMOX-UHFFFAOYSA-N 3,4,5,6-tetrabromophthalic acid Chemical compound OC(=O)C1=C(Br)C(Br)=C(Br)C(Br)=C1C(O)=O XIRDTMSOGDWMOX-UHFFFAOYSA-N 0.000 claims 1
- WZHHYIOUKQNLQM-UHFFFAOYSA-N 3,4,5,6-tetrachlorophthalic acid Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(O)=O WZHHYIOUKQNLQM-UHFFFAOYSA-N 0.000 claims 1
- 125000003031 C5-C7 cycloalkylene group Chemical group 0.000 claims 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- 229910003849 O-Si Inorganic materials 0.000 claims 1
- YHDJLQXSHIIBAQ-UHFFFAOYSA-N OP(O)OP(O)O.C1(=CC=CC=C1)C1=C(C(=C(C(=C1O)C1=CC=CC=C1)O)C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound OP(O)OP(O)O.C1(=CC=CC=C1)C1=C(C(=C(C(=C1O)C1=CC=CC=C1)O)C1=CC=CC=C1)C1=CC=CC=C1 YHDJLQXSHIIBAQ-UHFFFAOYSA-N 0.000 claims 1
- 229910003872 O—Si Inorganic materials 0.000 claims 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 229920000388 Polyphosphate Polymers 0.000 claims 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
- PQYJRMFWJJONBO-UHFFFAOYSA-N Tris(2,3-dibromopropyl) phosphate Chemical compound BrCC(Br)COP(=O)(OCC(Br)CBr)OCC(Br)CBr PQYJRMFWJJONBO-UHFFFAOYSA-N 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical group NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- KGUHWHHMNQPSRV-UHFFFAOYSA-N [1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 KGUHWHHMNQPSRV-UHFFFAOYSA-N 0.000 claims 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims 1
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 1
- 125000005250 alkyl acrylate group Chemical group 0.000 claims 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- 125000003368 amide group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- COAPBYURHXLGMG-UHFFFAOYSA-N azane;1,3,5-triazine-2,4,6-triamine Chemical compound N.NC1=NC(N)=NC(N)=N1 COAPBYURHXLGMG-UHFFFAOYSA-N 0.000 claims 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- OSIVCXJNIBEGCL-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1 OSIVCXJNIBEGCL-UHFFFAOYSA-N 0.000 claims 1
- DVXRGUXKOSSOHV-UHFFFAOYSA-N bis[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] decanedioate Chemical compound C1C(C)(C)N(OCC(C)(O)C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 DVXRGUXKOSSOHV-UHFFFAOYSA-N 0.000 claims 1
- WUXGYZUOHKJTEY-UHFFFAOYSA-N bis[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl] hexanedioate Chemical compound C1C(C)(C)N(OCC(C)(O)C)C(C)(C)CC1OC(=O)CCCCC(=O)OC1CC(C)(C)N(OCC(C)(C)O)C(C)(C)C1 WUXGYZUOHKJTEY-UHFFFAOYSA-N 0.000 claims 1
- IUTYMBRQELGIRS-UHFFFAOYSA-N boric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OB(O)O.NC1=NC(N)=NC(N)=N1 IUTYMBRQELGIRS-UHFFFAOYSA-N 0.000 claims 1
- 150000001715 carbamic acids Chemical class 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 230000008878 coupling Effects 0.000 claims 1
- 238000010168 coupling process Methods 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims 1
- 239000003822 epoxy resin Substances 0.000 claims 1
- 125000004185 ester group Chemical group 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000001033 ether group Chemical group 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 229930195729 fatty acid Natural products 0.000 claims 1
- 125000002425 furfuryl group Chemical group C(C1=CC=CO1)* 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- VUNCWTMEJYMOOR-UHFFFAOYSA-N hexachlorocyclopentadiene Chemical class ClC1=C(Cl)C(Cl)(Cl)C(Cl)=C1Cl VUNCWTMEJYMOOR-UHFFFAOYSA-N 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000005647 linker group Chemical group 0.000 claims 1
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 claims 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
- DTSDBGVDESRKKD-UHFFFAOYSA-N n'-(2-aminoethyl)propane-1,3-diamine Chemical compound NCCCNCCN DTSDBGVDESRKKD-UHFFFAOYSA-N 0.000 claims 1
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical compound CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 claims 1
- 125000000466 oxiranyl group Chemical group 0.000 claims 1
- 239000012188 paraffin wax Substances 0.000 claims 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 1
- XZTOTRSSGPPNTB-UHFFFAOYSA-N phosphono dihydrogen phosphate;1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N)=N1.OP(O)(=O)OP(O)(O)=O XZTOTRSSGPPNTB-UHFFFAOYSA-N 0.000 claims 1
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 229920000647 polyepoxide Polymers 0.000 claims 1
- 239000011495 polyisocyanurate Substances 0.000 claims 1
- 229920000582 polyisocyanurate Polymers 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 239000001205 polyphosphate Substances 0.000 claims 1
- 235000011176 polyphosphates Nutrition 0.000 claims 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims 1
- 239000004810 polytetrafluoroethylene Substances 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 230000002195 synergetic effect Effects 0.000 claims 1
- AVIZTSRRMBGYCJ-UHFFFAOYSA-N tetraazanium phosphonato phosphate 1,3,5-triazine-2,4,6-triamine Chemical compound [NH4+].[NH4+].[NH4+].[NH4+].NC1=NC(N)=NC(N)=N1.[O-]P([O-])(=O)OP([O-])([O-])=O AVIZTSRRMBGYCJ-UHFFFAOYSA-N 0.000 claims 1
- FAUOSXUSCVJWAY-UHFFFAOYSA-N tetrakis(hydroxymethyl)phosphanium Chemical compound OC[P+](CO)(CO)CO FAUOSXUSCVJWAY-UHFFFAOYSA-N 0.000 claims 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims 1
- JZZBTMVTLBHJHL-UHFFFAOYSA-N tris(2,3-dichloropropyl) phosphate Chemical compound ClCC(Cl)COP(=O)(OCC(Cl)CCl)OCC(Cl)CCl JZZBTMVTLBHJHL-UHFFFAOYSA-N 0.000 claims 1
- BHYQWBKCXBXPKM-UHFFFAOYSA-N tris[3-bromo-2,2-bis(bromomethyl)propyl] phosphate Chemical compound BrCC(CBr)(CBr)COP(=O)(OCC(CBr)(CBr)CBr)OCC(CBr)(CBr)CBr BHYQWBKCXBXPKM-UHFFFAOYSA-N 0.000 claims 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims 1
- 239000004711 α-olefin Substances 0.000 claims 1
- 0 CCN(C1CC(C)(C)*(CC(C)=O)C(C)(C)C1)C(C)=O Chemical compound CCN(C1CC(C)(C)*(CC(C)=O)C(C)(C)C1)C(C)=O 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US48834003P | 2003-07-18 | 2003-07-18 | |
| PCT/EP2004/051436 WO2005014706A1 (en) | 2003-07-18 | 2004-07-09 | Flame retardant polylactic acid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006528254A JP2006528254A (ja) | 2006-12-14 |
| JP2006528254A5 true JP2006528254A5 (enExample) | 2007-08-23 |
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| JP2006520825A Pending JP2006528254A (ja) | 2003-07-18 | 2004-07-09 | 難燃性ポリ乳酸 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20050014871A1 (enExample) |
| EP (1) | EP1646681B1 (enExample) |
| JP (1) | JP2006528254A (enExample) |
| CN (1) | CN100500744C (enExample) |
| AT (1) | ATE346883T1 (enExample) |
| CA (1) | CA2532456A1 (enExample) |
| DE (1) | DE602004003500T2 (enExample) |
| ES (1) | ES2276335T3 (enExample) |
| WO (1) | WO2005014706A1 (enExample) |
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| EP2172520A1 (en) * | 2003-10-14 | 2010-04-07 | Mitsubishi Plastics, Inc. | Flame-retardant injection-molded object |
| CN1914279B (zh) * | 2003-12-19 | 2010-05-05 | 日本电气株式会社 | 阻燃热塑性树脂组合物 |
| JP4548591B2 (ja) * | 2004-12-24 | 2010-09-22 | 信越化学工業株式会社 | 難燃樹脂組成物 |
| US7825179B2 (en) * | 2005-10-05 | 2010-11-02 | Unitika Ltd. | Biodegradable resin composition, production method therefor, and product molded or formed therefrom |
| JP2007138062A (ja) * | 2005-11-21 | 2007-06-07 | Kaneka Corp | ポリ乳酸系樹脂組成物 |
| DE602006013992D1 (de) | 2006-10-04 | 2010-06-10 | Borealis Tech Oy | Migrationsarme Polyolefinzusammensetzung |
| WO2009009006A1 (en) * | 2007-07-06 | 2009-01-15 | Supresta Llc | Flame retardant composition and flexible polyurethane foam prepared therewith |
| ES2356137T3 (es) | 2007-07-13 | 2011-04-05 | Borealis Technology Oy | Composición de poliolefina de baja migración que comprende un estabilizante de tipo vitamina e. |
| KR20110002834A (ko) * | 2008-04-23 | 2011-01-10 | 유니띠까 가부시키가이샤 | 난연성 폴리락트산계 수지 조성물 및 그것을 사용한 성형체 |
| BRPI0917105A2 (pt) * | 2008-08-28 | 2015-11-03 | Basf Se | uso de uma amina estericamente impedida, processo para estabilizar um material orgânico inanimado, amina estericamente impedida, e, material orgânico inanimado. |
| CN101747507B (zh) * | 2008-12-16 | 2012-04-25 | 财团法人工业技术研究院 | 含膦聚合物及包含此含膦聚合物的聚乳酸材料 |
| CN102369243B (zh) | 2009-03-19 | 2014-11-05 | 界面解决方案Ip有限责任公司 | 生物基聚合物组合物 |
| FR2954319B1 (fr) * | 2009-12-22 | 2012-01-20 | Febex S A | Procede de preparation de thpx |
| JP5493999B2 (ja) * | 2010-02-25 | 2014-05-14 | 富士ゼロックス株式会社 | ポリ乳酸系樹脂組成物、ポリ乳酸系樹脂組成物の製造方法及びポリ乳酸系樹脂成形体 |
| EP2550321A1 (en) * | 2010-03-25 | 2013-01-30 | Basf Se | Flame retardant compositions of phosphinic acid salts and nitroxyl derivatives |
| US8937124B2 (en) * | 2010-08-16 | 2015-01-20 | Fuji Xerox Co., Ltd. | Resin composition and resin molded article |
| KR101212543B1 (ko) * | 2010-09-28 | 2012-12-14 | 도레이 카부시키가이샤 | 열가소성 수지 조성물 및 그것으로 이루어지는 성형품 |
| JP2013067681A (ja) * | 2011-09-20 | 2013-04-18 | Fuji Xerox Co Ltd | 木粉含有材料及びその製造方法、並びに、成形体 |
| CN102634181B (zh) * | 2012-04-25 | 2013-09-04 | 中国科学院宁波材料技术与工程研究所 | 一种催化阻燃聚乳酸复合材料 |
| EP2743299A1 (de) * | 2012-12-12 | 2014-06-18 | Zylum Beteiligungsgesellschaft mbH & Co. Patente II KG | Synergistische Zusammensetzung und deren Verwendung als Flammschutzmittel |
| CN103897378A (zh) * | 2012-12-31 | 2014-07-02 | 贵州瓮福剑峰化工股份有限公司 | 聚氨酯泡沫用磷镁铝高效抑烟阻燃剂 |
| US20140200295A1 (en) * | 2013-01-16 | 2014-07-17 | Polyone Corporation | Heat resistant, flame retardant polylactic acid compounds |
| KR101350993B1 (ko) | 2013-10-18 | 2014-01-23 | 이재식 | 마이크로 캡슐을 이용한 난연 및 내열 특성을 가지는 3d 프린터용 pla 필라멘트제조방법 및 이에 의해 제조된 pla 필라멘트 |
| CN103694657B (zh) * | 2013-12-24 | 2015-07-22 | 南京理工大学 | 三元复合阻燃体系阻燃聚乳酸材料及其制备方法 |
| DE102014001222A1 (de) * | 2014-01-29 | 2015-07-30 | Clariant lnternational Ltd | Halogenfreie feste Flammschutzmittelmischung und ihre Verwendung |
| KR101764760B1 (ko) * | 2014-03-20 | 2017-08-03 | 사빅 글로벌 테크놀러지스 비.브이. | 폴리카보네이트 조성물, 이의 제조 방법 및 이의 물품 |
| JP2016190950A (ja) * | 2015-03-31 | 2016-11-10 | 富士ゼロックス株式会社 | 樹脂組成物および樹脂成形体 |
| CN105671672B (zh) * | 2016-02-25 | 2017-10-24 | 东华大学 | 只含碳、氢、氧三元素的阻燃聚乳酸纤维及其制备方法 |
| CN109068780B (zh) * | 2016-04-28 | 2021-02-26 | 电化株式会社 | 人工毛发纤维 |
| CN106349670B (zh) * | 2016-09-27 | 2018-07-13 | 北京服装学院 | 一种改性聚乳酸体系及其制备方法 |
| US11697898B2 (en) * | 2017-03-10 | 2023-07-11 | Biome Bioplastics Limited | Fabric |
| WO2025223984A1 (en) | 2024-04-22 | 2025-10-30 | Basf Se | Flame retardant articles comprising polylactic acid |
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| US5096950A (en) * | 1988-10-19 | 1992-03-17 | Ciba-Geigy Corporation | Polyolefin compositions stabilized with NOR-substituted hindered amines |
| KR100209818B1 (ko) * | 1992-09-04 | 1999-07-15 | 사또 아끼오 | 분해성점착필름 및 분해성수지조성물 |
| US5393812A (en) * | 1993-08-31 | 1995-02-28 | Hercules Incorporated | Flame retardant, light stable composition |
| TW401437B (en) * | 1995-02-10 | 2000-08-11 | Ciba Sc Holding Ag | Synergistic stabilizer mixture |
| US6262161B1 (en) * | 1997-06-26 | 2001-07-17 | The Dow Chemical Company | Compositions having improved ignition resistance |
| BR9810957A (pt) * | 1997-06-30 | 2000-09-26 | Ciba Sc Holding Ag | "composições retardadoras de chama" |
| US5844026A (en) * | 1997-06-30 | 1998-12-01 | Ciba Specialty Chemicals Corporation | N,N',N''-tris{2,4-bis Hydrocarbyloxy-2,2,6,6-tetra-methylpiperidin-4-yl)alkylamino!-s-triazin-6-yl}-3,3'-ethylenediiminodipropylamines, their isomers and bridged derivatives and polymer compositions stabilized therewith |
| US6472456B1 (en) * | 1997-06-30 | 2002-10-29 | Ciba Specialty Chemicals Corp. | Flame retardant compositions |
| DE69811573T2 (de) * | 1997-07-31 | 2003-12-11 | Teijin Ltd., Osaka | Mehrschichtmaterial und damit hergestelltes Zelt |
| JP2870529B2 (ja) * | 1997-10-27 | 1999-03-17 | 住友電気工業株式会社 | 難燃ポリエステルエラストマー組成物 |
| ITMI980366A1 (it) * | 1998-02-25 | 1999-08-25 | Ciba Spec Chem Spa | Preparazione di eteri amminici stericamente impediti |
| EP1086263A4 (en) * | 1998-04-20 | 2007-05-02 | Bba Nonwovens Simpsonville Inc | LUBRICANT WITH UV RESISTANCE AND FLAME INHIBITION AND METHOD FOR THE PRODUCTION THEREOF |
| US6271377B1 (en) * | 1999-02-25 | 2001-08-07 | Ciba Specialty Chemicals Corporation | Hydroxy-substituted N-alkoxy hindered amines and compositions stabilized therewith |
| JP4168128B2 (ja) * | 1999-12-03 | 2008-10-22 | 日華化学株式会社 | ポリ乳酸繊維用防炎加工剤およびポリ乳酸繊維構造物の防炎加工方法 |
| DE60133181T2 (de) * | 2000-02-22 | 2009-03-12 | Ciba Holding Inc. | Stabilisatormischungen für polyolefine |
| TWI273115B (en) * | 2000-12-12 | 2007-02-11 | Ciba Sc Holding Ag | Improved weatherability of flame retardant polyolefin |
| US6987139B2 (en) * | 2001-10-19 | 2006-01-17 | Matsushita Electric Industrial Co., Ltd. | Polymer composition |
| JP2003192921A (ja) * | 2001-10-19 | 2003-07-09 | Matsushita Electric Ind Co Ltd | 高分子組成物 |
| JP4243761B2 (ja) * | 2001-12-21 | 2009-03-25 | チバ ホールディング インコーポレーテッド | 新規難燃性化合物 |
| US6869985B2 (en) * | 2002-05-10 | 2005-03-22 | Awi Licensing Company | Environmentally friendly polylactide-based composite formulations |
-
2004
- 2004-07-09 CA CA002532456A patent/CA2532456A1/en not_active Abandoned
- 2004-07-09 AT AT04766175T patent/ATE346883T1/de not_active IP Right Cessation
- 2004-07-09 WO PCT/EP2004/051436 patent/WO2005014706A1/en not_active Ceased
- 2004-07-09 JP JP2006520825A patent/JP2006528254A/ja active Pending
- 2004-07-09 DE DE602004003500T patent/DE602004003500T2/de not_active Expired - Lifetime
- 2004-07-09 ES ES04766175T patent/ES2276335T3/es not_active Expired - Lifetime
- 2004-07-09 EP EP04766175A patent/EP1646681B1/en not_active Expired - Lifetime
- 2004-07-09 CN CNB2004800206070A patent/CN100500744C/zh not_active Expired - Fee Related
- 2004-07-13 US US10/890,453 patent/US20050014871A1/en not_active Abandoned
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