RU97102726A - COMPOSITIONS BASED ON CYCLIC KETONE PEROXIDES - Google Patents
COMPOSITIONS BASED ON CYCLIC KETONE PEROXIDESInfo
- Publication number
- RU97102726A RU97102726A RU97102726/04A RU97102726A RU97102726A RU 97102726 A RU97102726 A RU 97102726A RU 97102726/04 A RU97102726/04 A RU 97102726/04A RU 97102726 A RU97102726 A RU 97102726A RU 97102726 A RU97102726 A RU 97102726A
- Authority
- RU
- Russia
- Prior art keywords
- ketone
- methyl
- group
- cyclohexanol
- cyclic
- Prior art date
Links
- -1 CYCLIC KETONE PEROXIDES Chemical class 0.000 title claims 19
- 239000000203 mixture Substances 0.000 title claims 15
- HPXRVTGHNJAIIH-UHFFFAOYSA-N Cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 claims 9
- 239000007788 liquid Substances 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 5
- 229920001577 copolymer Polymers 0.000 claims 5
- 150000002148 esters Chemical class 0.000 claims 5
- KWOLFJPFCHCOCG-UHFFFAOYSA-N methylphenylketone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 5
- 239000003795 chemical substances by application Substances 0.000 claims 4
- 239000003085 diluting agent Substances 0.000 claims 4
- 150000001451 organic peroxides Chemical class 0.000 claims 4
- 239000007787 solid Substances 0.000 claims 4
- 239000002904 solvent Substances 0.000 claims 4
- 150000001298 alcohols Chemical class 0.000 claims 3
- 239000000969 carrier Substances 0.000 claims 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- 150000002576 ketones Chemical class 0.000 claims 3
- 239000003921 oil Substances 0.000 claims 3
- 235000019198 oils Nutrition 0.000 claims 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 3
- 239000000758 substrate Substances 0.000 claims 3
- 125000006651 (C3-C20) cycloalkyl group Chemical group 0.000 claims 2
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-Trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 claims 2
- CVBUKMMMRLOKQR-UHFFFAOYSA-N 1-phenylbutane-1,3-dione Chemical compound CC(=O)CC(=O)C1=CC=CC=C1 CVBUKMMMRLOKQR-UHFFFAOYSA-N 0.000 claims 2
- NKXMBTKMOVMBPH-UHFFFAOYSA-N 1-phenylpentane-1,3-dione Chemical compound CCC(=O)CC(=O)C1=CC=CC=C1 NKXMBTKMOVMBPH-UHFFFAOYSA-N 0.000 claims 2
- NROOHYGFTHTDFF-UHFFFAOYSA-N 1-phenylpentane-2,4-dione Chemical compound CC(=O)CC(=O)CC1=CC=CC=C1 NROOHYGFTHTDFF-UHFFFAOYSA-N 0.000 claims 2
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2,6-dimethylheptan-4-one Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 claims 2
- CEGGECULKVTYMM-UHFFFAOYSA-N 2,6-dimethylheptane-3,5-dione Chemical compound CC(C)C(=O)CC(=O)C(C)C CEGGECULKVTYMM-UHFFFAOYSA-N 0.000 claims 2
- CATSNJVOTSVZJV-UHFFFAOYSA-N 2-Heptanone Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 claims 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims 2
- IGMOYJSFRIASIE-UHFFFAOYSA-N 6-methylheptane-2,4-dione Chemical compound CC(C)CC(=O)CC(C)=O IGMOYJSFRIASIE-UHFFFAOYSA-N 0.000 claims 2
- VQFAIAKCILWQPZ-UHFFFAOYSA-N Bromoacetone Chemical compound CC(=O)CBr VQFAIAKCILWQPZ-UHFFFAOYSA-N 0.000 claims 2
- BULLHNJGPPOUOX-UHFFFAOYSA-N Chloroacetone Chemical compound CC(=O)CCl BULLHNJGPPOUOX-UHFFFAOYSA-N 0.000 claims 2
- KSMVZQYAVGTKIV-UHFFFAOYSA-N Decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 claims 2
- NZZIMKJIVMHWJC-UHFFFAOYSA-N Dibenzoylmethane Chemical compound C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 claims 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N Isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 claims 2
- QCCDLTOVEPVEJK-UHFFFAOYSA-N Phenylacetone Chemical compound CC(=O)CC1=CC=CC=C1 QCCDLTOVEPVEJK-UHFFFAOYSA-N 0.000 claims 2
- KRIOVPPHQSLHCZ-UHFFFAOYSA-N Propiophenone Chemical compound CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 claims 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 2
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims 2
- 125000003368 amide group Chemical group 0.000 claims 2
- 230000000111 anti-oxidant Effects 0.000 claims 2
- 239000003963 antioxidant agent Substances 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- DGCTVLNZTFDPDJ-UHFFFAOYSA-N heptane-3,5-dione Chemical compound CCC(=O)CC(=O)CC DGCTVLNZTFDPDJ-UHFFFAOYSA-N 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N n-butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 2
- 150000002825 nitriles Chemical class 0.000 claims 2
- GJYXGIIWJFZCLN-UHFFFAOYSA-N octane-2,4-dione Chemical compound CCCCC(=O)CC(C)=O GJYXGIIWJFZCLN-UHFFFAOYSA-N 0.000 claims 2
- PJEPOHXMGDEIMR-UHFFFAOYSA-N octane-3,5-dione Chemical compound CCCC(=O)CC(=O)CC PJEPOHXMGDEIMR-UHFFFAOYSA-N 0.000 claims 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 2
- 150000002978 peroxides Chemical class 0.000 claims 2
- 239000004014 plasticizer Substances 0.000 claims 2
- 229920000642 polymer Polymers 0.000 claims 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 2
- 239000000377 silicon dioxide Substances 0.000 claims 2
- 235000012239 silicon dioxide Nutrition 0.000 claims 2
- OVRRJBSHBOXFQE-UHFFFAOYSA-N 1,1,2,2-tetrabromoethene Chemical group BrC(Br)=C(Br)Br OVRRJBSHBOXFQE-UHFFFAOYSA-N 0.000 claims 1
- CPXZPNOXVRUBHI-UHFFFAOYSA-N 1,1-dibromo-2,2-dichloroethane Chemical compound ClC(Cl)C(Br)Br CPXZPNOXVRUBHI-UHFFFAOYSA-N 0.000 claims 1
- IKAACYWAXDLDPM-UHFFFAOYSA-N 1,2,3,4,4a,5-hexahydronaphthalene Chemical compound C1=CCC2CCCCC2=C1 IKAACYWAXDLDPM-UHFFFAOYSA-N 0.000 claims 1
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 claims 1
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 claims 1
- WQONPSCCEXUXTQ-UHFFFAOYSA-N 1,2-dibromobenzene Chemical compound BrC1=CC=CC=C1Br WQONPSCCEXUXTQ-UHFFFAOYSA-N 0.000 claims 1
- UNEATYXSUBPPKP-UHFFFAOYSA-N 1,3-bis(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC(C(C)C)=C1 UNEATYXSUBPPKP-UHFFFAOYSA-N 0.000 claims 1
- HILAULICMJUOLK-UHFFFAOYSA-N 1,3-diethyl-5-methylbenzene Chemical compound CCC1=CC(C)=CC(CC)=C1 HILAULICMJUOLK-UHFFFAOYSA-N 0.000 claims 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-Butanediol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims 1
- SWJPEBQEEAHIGZ-UHFFFAOYSA-N 1,4-Dibromobenzene Chemical compound BrC1=CC=C(Br)C=C1 SWJPEBQEEAHIGZ-UHFFFAOYSA-N 0.000 claims 1
- ULTHEAFYOOPTTB-UHFFFAOYSA-N 1,4-dibromobutane Chemical compound BrCCCCBr ULTHEAFYOOPTTB-UHFFFAOYSA-N 0.000 claims 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N 1,5-Pentanediol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 claims 1
- UMVMVEZHMZTUHD-UHFFFAOYSA-N 1-(benzoyloxy)propan-2-yl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C)COC(=O)C1=CC=CC=C1 UMVMVEZHMZTUHD-UHFFFAOYSA-N 0.000 claims 1
- WLPXNBYWDDYJTN-UHFFFAOYSA-N 1-bromo-2,3-dimethylbenzene Chemical group CC1=CC=CC(Br)=C1C WLPXNBYWDDYJTN-UHFFFAOYSA-N 0.000 claims 1
- YSFLQVNTBBUKEA-UHFFFAOYSA-N 1-bromo-2,4-dimethylbenzene Chemical group CC1=CC=C(Br)C(C)=C1 YSFLQVNTBBUKEA-UHFFFAOYSA-N 0.000 claims 1
- LMFRTSBQRLSJHC-UHFFFAOYSA-N 1-bromo-3,5-dimethylbenzene Chemical group CC1=CC(C)=CC(Br)=C1 LMFRTSBQRLSJHC-UHFFFAOYSA-N 0.000 claims 1
- VMKOFRJSULQZRM-UHFFFAOYSA-N 1-bromooctane Chemical compound CCCCCCCCBr VMKOFRJSULQZRM-UHFFFAOYSA-N 0.000 claims 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims 1
- OWBTYPJTUOEWEK-UHFFFAOYSA-N 2,3-Butanediol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 claims 1
- GFWVDQCGGDBTBS-UHFFFAOYSA-N 2,6,8-trimethylnonan-4-one Chemical compound CC(C)CC(C)CC(=O)CC(C)C GFWVDQCGGDBTBS-UHFFFAOYSA-N 0.000 claims 1
- XXJWXESWEXIICW-UHFFFAOYSA-N 2-(2-Ethoxyethoxy)ethanol Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 claims 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 claims 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-Butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-Ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims 1
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-Methyl-2,4-pentanediol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims 1
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-Methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 claims 1
- XNLICIUVMPYHGG-UHFFFAOYSA-N 2-Pentanone Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 claims 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N 2-Pyrrolidone Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 1
- MYMYVYZLMUEVED-UHFFFAOYSA-N 2-bromo-1,3-dimethylbenzene Chemical group CC1=CC=CC(C)=C1Br MYMYVYZLMUEVED-UHFFFAOYSA-N 0.000 claims 1
- WMEDSSFYIKNTNG-UHFFFAOYSA-N 3,6-dimethyloctane-3,6-diol Chemical compound CCC(C)(O)CCC(C)(O)CC WMEDSSFYIKNTNG-UHFFFAOYSA-N 0.000 claims 1
- FDPIMTJIUBPUKL-UHFFFAOYSA-N 3-Pentanone Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 claims 1
- QOGHRLGTXVMRLM-UHFFFAOYSA-N 4-bromo-1,2-dimethylbenzene Chemical group CC1=CC=C(Br)C=C1C QOGHRLGTXVMRLM-UHFFFAOYSA-N 0.000 claims 1
- LCLCVVVHIPPHCG-UHFFFAOYSA-N 5,5-dimethylhexane-2,4-dione Chemical compound CC(=O)CC(=O)C(C)(C)C LCLCVVVHIPPHCG-UHFFFAOYSA-N 0.000 claims 1
- FFWSICBKRCICMR-UHFFFAOYSA-N 5-Methyl-2-hexanone Chemical compound CC(C)CCC(C)=O FFWSICBKRCICMR-UHFFFAOYSA-N 0.000 claims 1
- PSBKJPTZCVYXSD-UHFFFAOYSA-N 5-methylheptan-3-one Chemical compound CCC(C)CC(=O)CC PSBKJPTZCVYXSD-UHFFFAOYSA-N 0.000 claims 1
- KHZGUWAFFHXZLC-UHFFFAOYSA-N 5-methylhexane-2,4-dione Chemical compound CC(C)C(=O)CC(C)=O KHZGUWAFFHXZLC-UHFFFAOYSA-N 0.000 claims 1
- YRKCREAYFQTBPV-UHFFFAOYSA-N Acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 239000004709 Chlorinated polyethylene Substances 0.000 claims 1
- NNBZCPXTIHJBJL-UHFFFAOYSA-N Decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 claims 1
- 229940113120 Dipropylene Glycol Drugs 0.000 claims 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N Dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 claims 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N Dodecanol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims 1
- 239000001692 EU approved anti-caking agent Substances 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 240000008528 Hevea brasiliensis Species 0.000 claims 1
- 229920002681 Hypalon Polymers 0.000 claims 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 claims 1
- 229940117969 NEOPENTYL GLYCOL Drugs 0.000 claims 1
- PJGSXYOJTGTZAV-UHFFFAOYSA-N Pinacolone Chemical compound CC(=O)C(C)(C)C PJGSXYOJTGTZAV-UHFFFAOYSA-N 0.000 claims 1
- 239000005062 Polybutadiene Substances 0.000 claims 1
- 229920001748 Polybutylene Polymers 0.000 claims 1
- 229920002367 Polyisobutene Polymers 0.000 claims 1
- 229960004063 Propylene glycol Drugs 0.000 claims 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N Tetrahydro-2-furanmethanol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 claims 1
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 claims 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 claims 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical class [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- 239000002216 antistatic agent Substances 0.000 claims 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 claims 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 claims 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
- 150000001860 citric acid derivatives Chemical class 0.000 claims 1
- 229940075614 colloidal silicon dioxide Drugs 0.000 claims 1
- 230000001268 conjugating Effects 0.000 claims 1
- 150000003950 cyclic amides Chemical class 0.000 claims 1
- 150000001991 dicarboxylic acids Chemical class 0.000 claims 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 claims 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 229920001971 elastomer Polymers 0.000 claims 1
- 150000002118 epoxides Chemical class 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000004088 foaming agent Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 230000000855 fungicidal Effects 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 150000008282 halocarbons Chemical class 0.000 claims 1
- FJPGAMCQJNLTJC-UHFFFAOYSA-N heptane-2,3-dione Chemical compound CCCCC(=O)C(C)=O FJPGAMCQJNLTJC-UHFFFAOYSA-N 0.000 claims 1
- ILPNRWUGFSPGAA-UHFFFAOYSA-N heptane-2,4-dione Chemical compound CCCC(=O)CC(C)=O ILPNRWUGFSPGAA-UHFFFAOYSA-N 0.000 claims 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims 1
- NDOGLIPWGGRQCO-UHFFFAOYSA-N hexane-2,4-dione Chemical compound CCC(=O)CC(C)=O NDOGLIPWGGRQCO-UHFFFAOYSA-N 0.000 claims 1
- 229940051250 hexylene glycol Drugs 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 230000002209 hydrophobic Effects 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 239000006193 liquid solution Substances 0.000 claims 1
- 239000000314 lubricant Substances 0.000 claims 1
- 229940094933 n-dodecane Drugs 0.000 claims 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N n-heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims 1
- SECXISVLQFMRJM-UHFFFAOYSA-N n-methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims 1
- 229920001194 natural rubber Polymers 0.000 claims 1
- 239000012188 paraffin wax Substances 0.000 claims 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims 1
- 235000021317 phosphate Nutrition 0.000 claims 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
- 125000005498 phthalate group Chemical class 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims 1
- 229920000058 polyacrylate Polymers 0.000 claims 1
- 229920002857 polybutadiene Polymers 0.000 claims 1
- 229920001610 polycaprolactone Polymers 0.000 claims 1
- 239000004632 polycaprolactone Substances 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 229920001195 polyisoprene Polymers 0.000 claims 1
- 229920000098 polyolefin Polymers 0.000 claims 1
- 229920002635 polyurethane Polymers 0.000 claims 1
- 239000004814 polyurethane Substances 0.000 claims 1
- UOHMMEJUHBCKEE-UHFFFAOYSA-N prehnitene Chemical compound CC1=CC=C(C)C(C)=C1C UOHMMEJUHBCKEE-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 239000005060 rubber Substances 0.000 claims 1
- 229920002545 silicone oil Polymers 0.000 claims 1
- 229920002379 silicone rubber Polymers 0.000 claims 1
- 239000004945 silicone rubber Substances 0.000 claims 1
- 235000012424 soybean oil Nutrition 0.000 claims 1
- 239000003549 soybean oil Substances 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 claims 1
- 239000000454 talc Substances 0.000 claims 1
- 229910052623 talc Inorganic materials 0.000 claims 1
- 0 *CC1(**)OOC(*)OO1 Chemical compound *CC1(**)OOC(*)OO1 0.000 description 1
Claims (9)
в которых R1-R10 независимо выбирают из группы, состоящей из водорода, C1-20-алкила, C3-20-циклоалкила, C6-20-арила, C7-20-аралкила и C7-20-алкарила, которые (группы) могут включать линейные или разветвленные алкильные остатки, и каждый из R1-R10 может быть необязательно замещен одной или более группами, выбранными из гидрокси, C1-20-алкокси, линейного или разветвленного C1-20-алкила, C6-20-арилокси, галогена, сложного эфира, карбокси, нитрила и амидо,
и 10-99 мас.% одного или более разбавителей, выбранных из группы, состоящей из жидких флегматизаторов для циклических перекисей кетона, пластификаторов, твердых полимерных носителей, неорганических подложек, органических перекисей и их смесей, при условии, что когда указанный разбавитель содержит нециклическую перекись кетона, то не менее 20% общего содержания активного кислорода рецептуры должно приходиться на одну или более циклических перекисей кетона общих формул I-III.1. Transportable shelf-stable peroxide composition, which contains 1.0 to 90% by weight of one or more cyclic ketone peroxides selected from peroxides represented by general formulas I-III:
in which R 1 -R 10 are independently selected from the group consisting of hydrogen, C 1-20 alkyl, C 3-20 cycloalkyl, C 6-20 aryl, C 7-20 aralkyl and C 7-20 alkaryl which (groups) may include linear or branched alkyl residues, and each of R 1 -R 10 may be optionally substituted with one or more groups selected from hydroxy, C 1-20 alkoxy, linear or branched C 1-20 alkyl , C 6-20 -aryloxy, halogen, ester, carboxy, nitrile and amido,
and 10-99% by weight of one or more diluents selected from the group consisting of liquid phlegmatizers for cyclic ketone peroxides, plasticizers, solid polymer carriers, inorganic substrates, organic peroxides and mixtures thereof, provided that the specified diluent contains non-cyclic peroxide ketone, then at least 20% of the total active oxygen of the formulation must fall on one or more cyclic ketone peroxides of the general formulas I-III.
в которых R1-R10 независимо выбираются из группы, состоящей из водорода, C1-20-алкила, C3-20-циклоалкила, C6-20 -арила, C7-20-аралкила и C7-20-алкарила, которые (группы) могут включать линейные или разветвленные алкильные остатки, и каждый из R1-R10 может быть необязательно замещен одной или более группами, выбранными из гидрокси, C1-20-алкокси, линейного или разветвленного C1-20-алкила, C6-20-арилокси, галогена, сложного эфира, карбокси, нитрила и амидо,
и 10-99 мас.% одного или более разбавителей, выбранных из группы, состоящей из жидких флегматизаторов для циклических перекисей кетона, пластификаторов, твердых полимерных носителей, неорганических подложек, органических перекисей и их смесей, при условии, что, когда указанный разбавитель содержит нециклическую перекись кетона, не менее 20% общего содержания активного кислорода композиции должно приходиться на одну или более циклических перекисей кетона общих формул I-III.9. Copolymers modified with an organic peroxide composition, which is transportable and storage-stable organic peroxide composition, and which contains 1.0 - 90% by weight of one or more cyclic ketone peroxides, selected from the general formulas I-III:
in which R 1 -R 10 are independently selected from the group consisting of hydrogen, C 1-20 alkyl, C 3-20 cycloalkyl, C 6-20 aryl, C 7-20 aralkyl and C 7-20 alkaryl which (groups) may include linear or branched alkyl residues, and each of R 1 -R 10 may be optionally substituted with one or more groups selected from hydroxy, C 1-20 alkoxy, linear or branched C 1-20 alkyl , C 6-20 -aryloxy, halogen, ester, carboxy, nitrile and amido,
and 10-99% by weight of one or more diluents selected from the group consisting of liquid phlegmatizers for cyclic ketone peroxides, plasticizers, solid polymer carriers, inorganic substrates, organic peroxides and mixtures thereof, provided that when the specified diluent contains non-cyclic ketone peroxide, not less than 20% of the total active oxygen content of the composition should fall on one or more cyclic ketone peroxides of the general formulas I-III.
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- 1995-07-14 MX MX9700535A patent/MX9700535A/en unknown
- 1995-07-14 RU RU97102726/04A patent/RU2154649C2/en not_active IP Right Cessation
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- 1995-07-14 KR KR1019970700294A patent/KR100441557B1/en not_active IP Right Cessation
- 1995-07-14 CA CA002195537A patent/CA2195537C/en not_active Expired - Fee Related
- 1995-07-14 AU AU36437/95A patent/AU686466B2/en not_active Ceased
- 1995-07-14 BR BR9508409A patent/BR9508409A/en not_active Application Discontinuation
- 1995-07-14 AT AT95926943T patent/ATE176910T1/en not_active IP Right Cessation
- 1995-07-14 HU HUP9700172A patent/HU216142B/en not_active IP Right Cessation
- 1995-07-14 JP JP50543796A patent/JP3794701B2/en not_active Expired - Fee Related
- 1995-07-14 CN CN95194239A patent/CN1068323C/en not_active Expired - Fee Related
- 1995-07-14 CZ CZ97184A patent/CZ18497A3/en unknown
- 1995-07-14 DE DE69507956T patent/DE69507956T2/en not_active Expired - Fee Related
- 1995-09-05 TW TW084109263A patent/TW414709B/en not_active IP Right Cessation
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