NO763800L - - Google Patents

Info

Publication number: NO763800L
Authority: NO; Norway
Prior art keywords: coester; synthetic resin; acid; phenol; stabilizer
Prior art date: 1975-11-10

Application number

NO763800A

Other languages

English (en)

Norwegian (no)

Inventor

W E Leistner

M Minagawa

Y Nakahara

T Haruna

Original Assignee

Argus Chem

Priority date (The priority date 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 date listed.)

1975-11-10

Filing date

1976-11-09

Publication date

1977-05-11

1976-11-09 Application filed by Argus Chem filed Critical Argus Chem

1977-05-11 Publication of NO763800L publication Critical patent/NO763800L/no

Links

ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 80
239000003381 stabilizer Substances 0.000 claims description 59
-1 alkylidene bisphenol Chemical compound 0.000 claims description 50
239000000203 mixture Substances 0.000 claims description 50
229920003002 synthetic resin Polymers 0.000 claims description 27
125000001931 aliphatic group Chemical group 0.000 claims description 26
239000000057 synthetic resin Substances 0.000 claims description 26
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 25
229920000642 polymer Polymers 0.000 claims description 20
125000004432 carbon atom Chemical group C* 0.000 claims description 15
229920005989 resin Polymers 0.000 claims description 10
239000011347 resin Substances 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 9
230000015556 catabolic process Effects 0.000 claims description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 7
239000003490 Thiodipropionic acid Substances 0.000 claims description 6
239000006096 absorbing agent Substances 0.000 claims description 6
238000006731 degradation reaction Methods 0.000 claims description 6
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 6
235000019303 thiodipropionic acid Nutrition 0.000 claims description 6
ODJQKYXPKWQWNK-UHFFFAOYSA-N 3,3'-Thiobispropanoic acid Chemical compound OC(=O)CCSCCC(O)=O ODJQKYXPKWQWNK-UHFFFAOYSA-N 0.000 claims description 5
239000004215 Carbon black (E152) Substances 0.000 claims description 5
GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 claims description 5
229930195733 hydrocarbon Natural products 0.000 claims description 5
229920000098 polyolefin Polymers 0.000 claims description 5
239000004800 polyvinyl chloride Substances 0.000 claims description 5
229920000915 polyvinyl chloride Polymers 0.000 claims description 5
235000012424 soybean oil Nutrition 0.000 claims description 5
239000003549 soybean oil Substances 0.000 claims description 5
229930185605 Bisphenol Natural products 0.000 claims description 4
239000003508 Dilauryl thiodipropionate Substances 0.000 claims description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 4
235000019304 dilauryl thiodipropionate Nutrition 0.000 claims description 4
238000010438 heat treatment Methods 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 4
150000005846 sugar alcohols Polymers 0.000 claims description 4
ODJQKYXPKWQWNK-UHFFFAOYSA-L 3-(2-carboxylatoethylsulfanyl)propanoate Chemical class [O-]C(=O)CCSCCC([O-])=O ODJQKYXPKWQWNK-UHFFFAOYSA-L 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 3
150000001735 carboxylic acids Chemical class 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
229920001083 polybutene Polymers 0.000 claims description 3
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
239000005864 Sulphur Substances 0.000 claims description 2
239000001361 adipic acid Substances 0.000 claims description 2
235000011037 adipic acid Nutrition 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
229910052788 barium Inorganic materials 0.000 claims description 2
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 2
239000008116 calcium stearate Substances 0.000 claims description 2
235000013539 calcium stearate Nutrition 0.000 claims description 2
229910052749 magnesium Inorganic materials 0.000 claims description 2
239000011777 magnesium Substances 0.000 claims description 2
150000002763 monocarboxylic acids Chemical class 0.000 claims description 2
229910052712 strontium Inorganic materials 0.000 claims description 2
CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 2
150000007933 aliphatic carboxylic acids Chemical class 0.000 claims 2
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 1
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims 1
229910052759 nickel Inorganic materials 0.000 claims 1
239000001384 succinic acid Substances 0.000 claims 1
229910052718 tin Inorganic materials 0.000 claims 1
150000003751 zinc Chemical class 0.000 claims 1
238000006243 chemical reaction Methods 0.000 description 24
150000001732 carboxylic acid derivatives Chemical class 0.000 description 15
150000002989 phenols Chemical class 0.000 description 14
ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 13
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 10
230000002829 reductive effect Effects 0.000 description 10
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
239000003570 air Substances 0.000 description 9
150000001875 compounds Chemical class 0.000 description 9
229910001385 heavy metal Inorganic materials 0.000 description 9
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 8
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
239000002253 acid Substances 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 8
238000000034 method Methods 0.000 description 8
239000004743 Polypropylene Substances 0.000 description 7
229920001155 polypropylene Polymers 0.000 description 7
238000012360 testing method Methods 0.000 description 7
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 6
239000000654 additive Substances 0.000 description 6
235000010290 biphenyl Nutrition 0.000 description 6
239000004305 biphenyl Substances 0.000 description 6
239000013068 control sample Substances 0.000 description 6
229920001577 copolymer Polymers 0.000 description 6
150000002148 esters Chemical class 0.000 description 6
238000002844 melting Methods 0.000 description 6
230000008018 melting Effects 0.000 description 6
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 6
229910000027 potassium carbonate Inorganic materials 0.000 description 6
239000000047 product Substances 0.000 description 6
239000007787 solid Substances 0.000 description 6
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 5
239000006227 byproduct Substances 0.000 description 5
239000003054 catalyst Substances 0.000 description 5
238000009472 formulation Methods 0.000 description 5
239000006078 metal deactivator Substances 0.000 description 5
239000000376 reactant Substances 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
239000000243 solution Substances 0.000 description 5
230000000087 stabilizing effect Effects 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
239000002656 Distearyl thiodipropionate Substances 0.000 description 4
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 4
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 4
239000004676 acrylonitrile butadiene styrene Substances 0.000 description 4
230000000996 additive effect Effects 0.000 description 4
239000001273 butane Substances 0.000 description 4
150000004649 carbonic acid derivatives Chemical class 0.000 description 4
238000000748 compression moulding Methods 0.000 description 4
PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 4
235000019305 distearyl thiodipropionate Nutrition 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
239000004417 polycarbonate Substances 0.000 description 4
229920000515 polycarbonate Polymers 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000003513 alkali Substances 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
239000003963 antioxidant agent Substances 0.000 description 3
230000003078 antioxidant effect Effects 0.000 description 3
239000012298 atmosphere Substances 0.000 description 3
AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 3
238000001816 cooling Methods 0.000 description 3
238000002845 discoloration Methods 0.000 description 3
239000011888 foil Substances 0.000 description 3
239000011521 glass Substances 0.000 description 3
125000005027 hydroxyaryl group Chemical group 0.000 description 3
239000004615 ingredient Substances 0.000 description 3
239000000463 material Substances 0.000 description 3
239000012299 nitrogen atmosphere Substances 0.000 description 3
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
238000010992 reflux Methods 0.000 description 3
239000011342 resin composition Substances 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 2
WXUAQHNMJWJLTG-UHFFFAOYSA-N 2-methylbutanedioic acid Chemical compound OC(=O)C(C)CC(O)=O WXUAQHNMJWJLTG-UHFFFAOYSA-N 0.000 description 2
PFANXOISJYKQRP-UHFFFAOYSA-N 2-tert-butyl-4-[1-(5-tert-butyl-4-hydroxy-2-methylphenyl)butyl]-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(CCC)C1=CC(C(C)(C)C)=C(O)C=C1C PFANXOISJYKQRP-UHFFFAOYSA-N 0.000 description 2
XJMMNTGIMDZPMU-UHFFFAOYSA-N 3-methylglutaric acid Chemical compound OC(=O)CC(C)CC(O)=O XJMMNTGIMDZPMU-UHFFFAOYSA-N 0.000 description 2
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
229920000877 Melamine resin Polymers 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
239000000370 acceptor Substances 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
125000003710 aryl alkyl group Chemical group 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
229920003020 cross-linked polyethylene Polymers 0.000 description 2
239000004703 cross-linked polyethylene Substances 0.000 description 2
230000003247 decreasing effect Effects 0.000 description 2
238000004821 distillation Methods 0.000 description 2
230000008030 elimination Effects 0.000 description 2
238000003379 elimination reaction Methods 0.000 description 2
239000005038 ethylene vinyl acetate Substances 0.000 description 2
238000000227 grinding Methods 0.000 description 2
150000002430 hydrocarbons Chemical group 0.000 description 2
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
229910000041 hydrogen chloride Inorganic materials 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
238000004898 kneading Methods 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
TXXHDPDFNKHHGW-UHFFFAOYSA-N muconic acid Chemical compound OC(=O)C=CC=CC(O)=O TXXHDPDFNKHHGW-UHFFFAOYSA-N 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
235000019198 oils Nutrition 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
238000005192 partition Methods 0.000 description 2
WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
229920000573 polyethylene Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
230000000717 retained effect Effects 0.000 description 2
239000000523 sample Substances 0.000 description 2
239000011343 solid material Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
238000011105 stabilization Methods 0.000 description 2
239000007858 starting material Substances 0.000 description 2
238000003860 storage Methods 0.000 description 2
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
150000003512 tertiary amines Chemical class 0.000 description 2
HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical class OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 1
ZNEMGFATAVGQSF-UHFFFAOYSA-N 1-(2-amino-6,7-dihydro-4H-[1,3]thiazolo[4,5-c]pyridin-5-yl)-2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]ethanone Chemical compound NC=1SC2=C(CN(CC2)C(CC=2OC(=NN=2)C=2C=NC(=NC=2)NC2CC3=CC=CC=C3C2)=O)N=1 ZNEMGFATAVGQSF-UHFFFAOYSA-N 0.000 description 1
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
AUFZRCJENRSRLY-UHFFFAOYSA-N 2,3,5-trimethylhydroquinone Chemical compound CC1=CC(O)=C(C)C(C)=C1O AUFZRCJENRSRLY-UHFFFAOYSA-N 0.000 description 1
ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 1
ANJHKVLUGKEZJB-UHFFFAOYSA-N 2,4-ditert-butyl-6-(3,5-ditert-butyl-2-hydroxyphenyl)sulfanylphenol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(SC=2C(=C(C=C(C=2)C(C)(C)C)C(C)(C)C)O)=C1O ANJHKVLUGKEZJB-UHFFFAOYSA-N 0.000 description 1
NMJMUSGKTCPFOK-UHFFFAOYSA-N 2,4-ditert-butylbenzene-1,3-diol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1O NMJMUSGKTCPFOK-UHFFFAOYSA-N 0.000 description 1
JZODKRWQWUWGCD-UHFFFAOYSA-N 2,5-di-tert-butylbenzene-1,4-diol Chemical compound CC(C)(C)C1=CC(O)=C(C(C)(C)C)C=C1O JZODKRWQWUWGCD-UHFFFAOYSA-N 0.000 description 1
ATYJAGSSMXWONK-UHFFFAOYSA-N 2,5-diethylhexanedioic acid Chemical compound CCC(C(O)=O)CCC(CC)C(O)=O ATYJAGSSMXWONK-UHFFFAOYSA-N 0.000 description 1
UDFARPRXWMDFQU-UHFFFAOYSA-N 2,6-ditert-butyl-4-[(3,5-ditert-butyl-4-hydroxyphenyl)methylsulfanylmethyl]phenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CSCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 UDFARPRXWMDFQU-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
DMAXMXPDVWTIRV-UHFFFAOYSA-N 2-(2-phenylethyl)phenol Chemical compound OC1=CC=CC=C1CCC1=CC=CC=C1 DMAXMXPDVWTIRV-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
YQQAAUCBTNZUQQ-UHFFFAOYSA-N 2-[1-(2-hydroxy-3,5-dimethylphenyl)butyl]-4,6-dimethylphenol Chemical compound C=1C(C)=CC(C)=C(O)C=1C(CCC)C1=CC(C)=CC(C)=C1O YQQAAUCBTNZUQQ-UHFFFAOYSA-N 0.000 description 1
PTJWCLYPVFJWMP-UHFFFAOYSA-N 2-[[3-hydroxy-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)COCC(CO)(CO)CO PTJWCLYPVFJWMP-UHFFFAOYSA-N 0.000 description 1
LOVMVPJGMHASBH-UHFFFAOYSA-N 2-cyclohexyl-3-[1-(2-cyclohexyl-3-hydroxyphenyl)cyclohexyl]phenol Chemical compound OC1=CC=CC(C2(CCCCC2)C=2C(=C(O)C=CC=2)C2CCCCC2)=C1C1CCCCC1 LOVMVPJGMHASBH-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/64—Polyesters containing both carboxylic ester groups and carbonate groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Polyesters Or Polycarbonates (AREA)

NO763800A 1975-11-10 1976-11-09 NO763800L (xx)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP50134971A JPS5928226B2 (ja)	1975-11-10	1975-11-10	アンテイカサレタゴウセイジユシソセイブツ

Publications (1)

Publication Number	Publication Date
NO763800L true NO763800L (xx)	1977-05-11

Family

ID=15140870

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO763800A NO763800L (xx)	1975-11-10	1976-11-09

Country Status (12)

Country	Link
US (1)	US4174297A (xx)
JP (1)	JPS5928226B2 (xx)
AU (1)	AU1949376A (xx)
BE (1)	BE848155A (xx)
DE (1)	DE2651294A1 (xx)
DK (1)	DK504376A (xx)
FI (1)	FI763208A (xx)
FR (1)	FR2330710A1 (xx)
NL (1)	NL7612489A (xx)
NO (1)	NO763800L (xx)
SE (1)	SE7612530L (xx)
ZA (1)	ZA766718B (xx)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2823161A1 (de) *	1978-05-26	1979-11-29	Bayer Ag	Weichgemachte vinylchloridpolymerisate
DE3918405A1 (de) *	1989-06-06	1990-12-13	Bayer Ag	Polymerisatmischungen fuer flexible folien
US6824711B2 (en)	2001-03-02	2004-11-30	Dover Chemical Corporation	Phosphite ester additive composition

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1177517A (fr) *	1956-11-21	1959-04-27	Albert Ag Chem Werke	Procédé de préparation d'esters thermoplastiques à partir d'acides dicarboxyliques et de diphénols
BE570530A (xx)	1957-08-22
BE570531A (xx) *	1957-08-22
US3030331A (en) *	1957-08-22	1962-04-17	Gen Electric	Process for preparing copolyesters comprising reacting a carbonyl halide with a dicarboxylic acid and a dihydroxy compound in the presence of a tertiary amine
GB898775A (en)	1958-01-13	1962-06-14	Bexford Ltd	Improvements in or relating to polymeric materials
US3030335A (en) *	1959-01-02	1962-04-17	Gen Electric	Aromatic polycarbonate reaction products
DE1495626B1 (de)	1960-03-30	1971-06-09	Bayer Ag	Verfahren zum herstellen von polyestern
US4032510A (en) *	1975-07-18	1977-06-28	Exxon Research And Engineering Company	Novel polycarbon stabilizers

1975
- 1975-11-10 JP JP50134971A patent/JPS5928226B2/ja not_active Expired
1976
- 1976-11-09 NO NO763800A patent/NO763800L/no unknown
- 1976-11-09 ZA ZA766718A patent/ZA766718B/xx unknown
- 1976-11-09 BE BE172211A patent/BE848155A/xx unknown
- 1976-11-09 FI FI763208A patent/FI763208A/fi not_active Application Discontinuation
- 1976-11-09 DK DK504376A patent/DK504376A/da unknown
- 1976-11-09 US US05/740,110 patent/US4174297A/en not_active Expired - Lifetime
- 1976-11-10 AU AU19493/76A patent/AU1949376A/en not_active Expired
- 1976-11-10 NL NL7612489A patent/NL7612489A/xx unknown
- 1976-11-10 FR FR7633894A patent/FR2330710A1/fr not_active Withdrawn
- 1976-11-10 SE SE7612530A patent/SE7612530L/xx unknown
- 1976-11-10 DE DE19762651294 patent/DE2651294A1/de not_active Withdrawn

Also Published As

Publication number	Publication date
FI763208A (xx)	1977-05-11
JPS5258747A (en)	1977-05-14
NL7612489A (nl)	1977-05-12
US4174297A (en)	1979-11-13
AU1949376A (en)	1978-05-18
BE848155A (fr)	1977-05-09
FR2330710A1 (fr)	1977-06-03
SE7612530L (sv)	1977-05-11
DE2651294A1 (de)	1977-05-18
JPS5928226B2 (ja)	1984-07-11
DK504376A (da)	1977-05-11
ZA766718B (en)	1977-10-26

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US4255301A (en)	1981-03-10	Glycol carbonate ester stabilizers for synthetic resins
GB2257141A (en)	1993-01-06	Thiomethylated benzofuran-2-ones and their use as stabilizer for organic materials
FR2460943A1 (fr)	1981-01-30	Derives de la benzofuranne-2-one et de l'indoline-2-one
US4321218A (en)	1982-03-23	Phosphite stabilizer
US5169925A (en)	1992-12-08	Polymeric polyalkyl-1-oxa-diazaspirodecanes
CA1295619C (en)	1992-02-11	1,3,2-oxazaphospholidine stabilizers
TW201348227A (zh)	2013-12-01	含１，１－二甲基肼型安定劑及其組成物
US4812501A (en)	1989-03-14	1,3,2-oxazaphospholidine stabilizers
KR100292209B1 (ko)	2001-11-22	가수분해안정성3가인화합물의제조방법,이를사용한열가소성수지의안정화방법및이를포함하는열가소성성형조성물
US4104217A (en)	1978-08-01	Carbonate ester stabilizers for polymers
US4743640A (en)	1988-05-10	Alpha, beta-unsaturated carbonyl-containing carbonate stabilizers for chlorinated polymers
US4960863A (en)	1990-10-02	Polycarbonate cross-linked resin
TWI513762B (zh)	2015-12-21	雙官能型安定劑及其組成物
NO763800L (xx)	1977-05-11
JPS5890545A (ja)	1983-05-30	メルカプトフエノ−ル誘導体および該化合物を含有する材料組成物
KR100286115B1 (ko)	2001-04-16	2,4-디알킬-6-이차알킬페놀 및 이를 함유하는 조성물
US4617333A (en)	1986-10-14	Stabilized polyolefinic compositions and stabilizer compounds suitable to that purpose
JP2553846B2 (ja)	1996-11-13	置換４ーヒドロキシフェニル化合物及び有機材料用安定剤
JPS59176256A (ja)	1984-10-05	オリゴマーエステル及び有機ポリマーの安定化方法
JPH0678310B2 (ja)	1994-10-05	ヒンダードアミン基を持つ新規なジヒドロピリジン
JPS5813577B2 (ja)	1983-03-14	安定化合成重合体組成物
BE1006547A5 (fr)	1994-10-11	Esters d'acides carboxyliques d'hydroxyphenylalcanols comme stabilisants.
US4960839A (en)	1990-10-02	Method of making a polycarbonate cross-linked resin
US4107136A (en)	1978-08-15	Synthetic resin stabilizer comprising an organic phosphite and a carbonate
US4107137A (en)	1978-08-15	Phenolic antioxidants for synthetic polymers