JP2009534469A5 - - Google Patents

Info

Publication number

JP2009534469A5

JP2009534469A5 JP2009507914A JP2009507914A JP2009534469A5 JP 2009534469 A5 JP2009534469 A5 JP 2009534469A5 JP 2009507914 A JP2009507914 A JP 2009507914A JP 2009507914 A JP2009507914 A JP 2009507914A JP 2009534469 A5 JP2009534469 A5 JP 2009534469A5

Authority

JP

Japan

Prior art keywords

alkyl

substituted

phosphate

weight

range

Prior art date

2007-04-23

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.)

Pending

Links

• Espacenet
• Global Dossier
• Discuss

• 150000002148 esters Chemical class 0.000 claims 19
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 16
• 125000000217 alkyl group Chemical group 0.000 claims 16
• 229910019142 PO4 Inorganic materials 0.000 claims 14
• 235000021317 phosphate Nutrition 0.000 claims 14
• 239000010452 phosphate Substances 0.000 claims 13
• 238000000034 method Methods 0.000 claims 10
• 150000002989 phenols Chemical class 0.000 claims 8
• -1 phosphate ester Chemical class 0.000 claims 8
• AYEKOFBPNLCAJY-UHFFFAOYSA-O thiamine pyrophosphate Chemical compound CC1=C(CCOP(O)(=O)OP(O)(O)=O)SC=[N+]1CC1=CN=C(C)N=C1N AYEKOFBPNLCAJY-UHFFFAOYSA-O 0.000 claims 8
• 239000003054 catalyst Substances 0.000 claims 7
• 239000007795 chemical reaction product Substances 0.000 claims 7
• NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 6
• OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 5
• CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical class OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 claims 5
• 229910052698 phosphorus Inorganic materials 0.000 claims 5
• 239000011574 phosphorus Substances 0.000 claims 5
• 239000000047 product Substances 0.000 claims 5
• 239000000203 mixture Substances 0.000 claims 4
• XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 claims 4
• 125000005233 alkylalcohol group Chemical group 0.000 claims 3
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
• 229920001577 copolymer Polymers 0.000 claims 3
• ASMQGLCHMVWBQR-UHFFFAOYSA-M diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)([O-])OC1=CC=CC=C1 ASMQGLCHMVWBQR-UHFFFAOYSA-M 0.000 claims 3
• NUHSROFQTUXZQQ-UHFFFAOYSA-N isopentenyl diphosphate Chemical compound CC(=C)CCO[P@](O)(=O)OP(O)(O)=O NUHSROFQTUXZQQ-UHFFFAOYSA-N 0.000 claims 3
• HPEUEJRPDGMIMY-IFQPEPLCSA-N molybdopterin Chemical compound O([C@H]1N2)[C@H](COP(O)(O)=O)C(S)=C(S)[C@@H]1NC1=C2N=C(N)NC1=O HPEUEJRPDGMIMY-IFQPEPLCSA-N 0.000 claims 3
• 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 3
• RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical class ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 claims 3
• 229920002554 vinyl polymer Polymers 0.000 claims 3
• 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 2
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 2
• 125000005037 alkyl phenyl group Chemical group 0.000 claims 2
• TXFOLHZMICYNRM-UHFFFAOYSA-N dichlorophosphoryloxybenzene Chemical class ClP(Cl)(=O)OC1=CC=CC=C1 TXFOLHZMICYNRM-UHFFFAOYSA-N 0.000 claims 2
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
• 239000003063 flame retardant Substances 0.000 claims 2
• 229920001519 homopolymer Polymers 0.000 claims 2
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
• 239000012948 isocyanate Substances 0.000 claims 2
• 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 2
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
• 239000000178 monomer Substances 0.000 claims 2
• 229920005862 polyol Chemical group 0.000 claims 2
• 150000003077 polyols Chemical group 0.000 claims 2
• 239000011347 resin Substances 0.000 claims 2
• 229920005989 resin Polymers 0.000 claims 2
• ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical group CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 claims 1
• 239000004604 Blowing Agent Substances 0.000 claims 1
• 239000004215 Carbon black (E152) Substances 0.000 claims 1
• 125000002015 acyclic group Chemical group 0.000 claims 1
• 150000001298 alcohols Chemical class 0.000 claims 1
• WWDMDHUOYPEXQH-UHFFFAOYSA-N chloro(phenoxy)phosphinic acid Chemical compound OP(Cl)(=O)OC1=CC=CC=C1 WWDMDHUOYPEXQH-UHFFFAOYSA-N 0.000 claims 1
• 238000004821 distillation Methods 0.000 claims 1
• 125000000524 functional group Chemical group 0.000 claims 1
• 229930195733 hydrocarbon Natural products 0.000 claims 1
• 150000002430 hydrocarbons Chemical class 0.000 claims 1
• IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 1
• 150000002513 isocyanates Chemical class 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
• 238000005191 phase separation Methods 0.000 claims 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
• 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
• QVLTXCYWHPZMCA-UHFFFAOYSA-N po4-po4 Chemical compound OP(O)(O)=O.OP(O)(O)=O QVLTXCYWHPZMCA-UHFFFAOYSA-N 0.000 claims 1
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
• 125000003107 substituted aryl group Chemical group 0.000 claims 1