PL87666B1 - - Google Patents

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Publication number: PL87666B1
Authority: PL; Poland
Prior art keywords: parts; peroxide; acid; anhydride; formula
Prior art date: 1972-06-24

Application number

PL1973163510A

Other languages

English (en)

Polish (pl)

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.)

1972-06-24

Filing date

1973-06-22

Publication date

1976-07-31

1973-06-22 Application filed filed Critical

1976-07-31 Publication of PL87666B1 publication Critical patent/PL87666B1/pl

Links

PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 10
239000000945 filler Substances 0.000 claims description 9
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 9
229920002554 vinyl polymer Polymers 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 8
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 8
238000000034 method Methods 0.000 claims description 7
239000000178 monomer Substances 0.000 claims description 7
150000008064 anhydrides Chemical class 0.000 claims description 6
230000000749 insecticidal effect Effects 0.000 claims description 6
239000000203 mixture Substances 0.000 claims description 6
229920000728 polyester Polymers 0.000 claims description 6
239000004342 Benzoyl peroxide Substances 0.000 claims description 5
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 5
235000019400 benzoyl peroxide Nutrition 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 5
239000007788 liquid Substances 0.000 claims description 5
239000007787 solid Substances 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
239000002917 insecticide Substances 0.000 claims description 4
150000002978 peroxides Chemical class 0.000 claims description 4
235000004431 Linum usitatissimum Nutrition 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
125000004104 aryloxy group Chemical group 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
230000005855 radiation Effects 0.000 claims description 2
MNRWIFMPVCLIDS-UHFFFAOYSA-N 2,2-dichloroethenyl dihydrogen phosphate Chemical compound OP(O)(=O)OC=C(Cl)Cl MNRWIFMPVCLIDS-UHFFFAOYSA-N 0.000 claims 1
241000208202 Linaceae Species 0.000 claims 1
125000005462 imide group Chemical group 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
230000000052 comparative effect Effects 0.000 description 7
229920006305 unsaturated polyester Polymers 0.000 description 7
NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 6
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
239000004480 active ingredient Substances 0.000 description 4
-1 aromatic dicarboxylic acids Chemical class 0.000 description 4
230000002035 prolonged effect Effects 0.000 description 4
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 3
WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 3
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 3
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000013543 active substance Substances 0.000 description 3
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 3
239000010941 cobalt Substances 0.000 description 3
229910017052 cobalt Inorganic materials 0.000 description 3
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 3
229960001826 dimethylphthalate Drugs 0.000 description 3
239000003365 glass fiber Substances 0.000 description 3
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
239000011976 maleic acid Substances 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
238000006068 polycondensation reaction Methods 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
235000013772 propylene glycol Nutrition 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000004594 Masterbatch (MB) Substances 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
HWVKIRQMNIWOLT-UHFFFAOYSA-L cobalt(2+);octanoate Chemical compound [Co+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O HWVKIRQMNIWOLT-UHFFFAOYSA-L 0.000 description 2
150000001991 dicarboxylic acids Chemical class 0.000 description 2
239000000835 fiber Substances 0.000 description 2
239000001530 fumaric acid Substances 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
230000000149 penetrating effect Effects 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 2
LGRFSURHDFAFJT-UHFFFAOYSA-N phthalic anhydride Chemical compound C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 0.000 description 1
OXYKVVLTXXXVRT-UHFFFAOYSA-N (4-chlorobenzoyl) 4-chlorobenzenecarboperoxoate Chemical compound C1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1 OXYKVVLTXXXVRT-UHFFFAOYSA-N 0.000 description 1
SINXZUQPXYPKDL-UHFFFAOYSA-N (4-ethyl-5,5-dimethylhexoxy)carbonyloxy (4-ethyl-5,5-dimethylhexyl) carbonate Chemical compound CCC(C(C)(C)C)CCCOC(=O)OOC(=O)OCCCC(CC)C(C)(C)C SINXZUQPXYPKDL-UHFFFAOYSA-N 0.000 description 1
INCCSIKFWGMTDS-OCEACIFDSA-N (E)-2,3-didodecylbut-2-enedioic acid Chemical compound CCCCCCCCCCCC\C(C(O)=O)=C(C(O)=O)\CCCCCCCCCCCC INCCSIKFWGMTDS-OCEACIFDSA-N 0.000 description 1
VPTNWGPGDXUKCY-KHPPLWFESA-N (z)-4-decoxy-4-oxobut-2-enoic acid Chemical compound CCCCCCCCCCOC(=O)\C=C/C(O)=O VPTNWGPGDXUKCY-KHPPLWFESA-N 0.000 description 1
JNPCNDJVEUEFBO-UHFFFAOYSA-N 1-butylpyrrole-2,5-dione Chemical compound CCCCN1C(=O)C=CC1=O JNPCNDJVEUEFBO-UHFFFAOYSA-N 0.000 description 1
BQTPKSBXMONSJI-UHFFFAOYSA-N 1-cyclohexylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1CCCCC1 BQTPKSBXMONSJI-UHFFFAOYSA-N 0.000 description 1
SJLLJZNSZJHXQN-UHFFFAOYSA-N 1-dodecylpyrrole-2,5-dione Chemical compound CCCCCCCCCCCCN1C(=O)C=CC1=O SJLLJZNSZJHXQN-UHFFFAOYSA-N 0.000 description 1
LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
LVYBYRAOZXKVCE-UHFFFAOYSA-N 2-anilinoethane-1,1-diol Chemical compound OC(O)CNC1=CC=CC=C1 LVYBYRAOZXKVCE-UHFFFAOYSA-N 0.000 description 1
GPLIMIJPIZGPIF-UHFFFAOYSA-N 2-hydroxy-1,4-benzoquinone Chemical compound OC1=CC(=O)C=CC1=O GPLIMIJPIZGPIF-UHFFFAOYSA-N 0.000 description 1
SFSBAUGKCFPNCR-UHFFFAOYSA-N 3-anilinopropane-1,1-diol Chemical compound OC(O)CCNC1=CC=CC=C1 SFSBAUGKCFPNCR-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
244000198134 Agave sisalana Species 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
240000006240 Linum usitatissimum Species 0.000 description 1
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
241000257159 Musca domestica Species 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
244000274883 Urtica dioica Species 0.000 description 1
235000009108 Urtica dioica Nutrition 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
125000005396 acrylic acid ester group Chemical group 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
150000007860 aryl ester derivatives Chemical class 0.000 description 1
SSRHZSLSLDOUJB-UHFFFAOYSA-N benzene-1,4-diol;toluene Chemical compound CC1=CC=CC=C1.OC1=CC=C(O)C=C1 SSRHZSLSLDOUJB-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
235000009120 camo Nutrition 0.000 description 1
239000000969 carrier Substances 0.000 description 1
235000005607 chanvre indien Nutrition 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
125000000000 cycloalkoxy group Chemical group 0.000 description 1
BLCKNMAZFRMCJJ-UHFFFAOYSA-N cyclohexyl cyclohexyloxycarbonyloxy carbonate Chemical compound C1CCCCC1OC(=O)OOC(=O)OC1CCCCC1 BLCKNMAZFRMCJJ-UHFFFAOYSA-N 0.000 description 1
230000007547 defect Effects 0.000 description 1
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000011152 fibreglass Substances 0.000 description 1
NKHAVTQWNUWKEO-UHFFFAOYSA-N fumaric acid monomethyl ester Natural products COC(=O)C=CC(O)=O NKHAVTQWNUWKEO-UHFFFAOYSA-N 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000011487 hemp Substances 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
235000013980 iron oxide Nutrition 0.000 description 1
VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
125000005397 methacrylic acid ester group Chemical group 0.000 description 1
OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
NKHAVTQWNUWKEO-IHWYPQMZSA-N methyl hydrogen fumarate Chemical compound COC(=O)\C=C/C(O)=O NKHAVTQWNUWKEO-IHWYPQMZSA-N 0.000 description 1
239000012764 mineral filler Substances 0.000 description 1
GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
PPHQUIPUBYPZLD-UHFFFAOYSA-N n-ethyl-n-methylaniline Chemical compound CCN(C)C1=CC=CC=C1 PPHQUIPUBYPZLD-UHFFFAOYSA-N 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
FEZFGASTIQVZSC-UHFFFAOYSA-N nonanoyl nonaneperoxoate Chemical compound CCCCCCCCC(=O)OOC(=O)CCCCCCCC FEZFGASTIQVZSC-UHFFFAOYSA-N 0.000 description 1
NNBBVUXGGBWVQP-UHFFFAOYSA-N octan-3-yl octan-3-yloxycarbonyloxy carbonate Chemical compound CCCCCC(CC)OC(=O)OOC(=O)OC(CC)CCCCC NNBBVUXGGBWVQP-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
CGEXUOTXYSGBLV-UHFFFAOYSA-N phenyl benzenesulfonate Chemical class C=1C=CC=CC=1S(=O)(=O)OC1=CC=CC=C1 CGEXUOTXYSGBLV-UHFFFAOYSA-N 0.000 description 1
VWSUVZVPDQDVRT-UHFFFAOYSA-N phenylperoxybenzene Chemical compound C=1C=CC=CC=1OOC1=CC=CC=C1 VWSUVZVPDQDVRT-UHFFFAOYSA-N 0.000 description 1
150000003021 phthalic acid derivatives Chemical class 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
235000010215 titanium dioxide Nutrition 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters

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)
Macromonomer-Based Addition Polymer (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Polymerisation Methods In General (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

PL1973163510A 1972-06-24 1973-06-22 PL87666B1 (2)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2231099A DE2231099C3 (de)	1972-06-24	1972-06-24	Geruchsanne Formkörper mit insekticider Depotgas-Wirkung

Publications (1)

Publication Number	Publication Date
PL87666B1 true PL87666B1 (2)	1976-07-31

Family

ID=5848754

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL1973163510A PL87666B1 (2)	1972-06-24	1973-06-22

Country Status (20)

Country	Link
US (1)	US3932612A (2)
JP (1)	JPS572745B2 (2)
AT (1)	AT326414B (2)
AU (1)	AU5725073A (2)
BE (1)	BE801333A (2)
CA (1)	CA1001552A (2)
CH (1)	CH583762A5 (2)
DD (2)	DD110888A5 (2)
DE (1)	DE2231099C3 (2)
DK (1)	DK131882C (2)
FR (1)	FR2189435B1 (2)
GB (1)	GB1398825A (2)
IE (1)	IE37836B1 (2)
IL (1)	IL42577A (2)
IT (1)	IT989412B (2)
NL (1)	NL7308650A (2)
PL (1)	PL87666B1 (2)
SU (1)	SU469233A3 (2)
TR (1)	TR17232A (2)
ZA (1)	ZA734243B (2)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4935232A (en) *	1983-08-16	1990-06-19	Interface Research Corporation	Microbiocidal composition and method of preparation thereof
US5474739A (en) *	1978-02-04	1995-12-12	Interface, Inc.	Microbiocidal composition
US5032310A (en) *	1983-08-16	1991-07-16	Interface, Inc.	Microbiocidal cleansing and disinfecting formulations and preparation thereof
US4908209A (en) *	1983-08-16	1990-03-13	Interface, Inc.	Biocidal delivery system of phosphate ester and method of preparation thereof
US5024840A (en) *	1984-03-08	1991-06-18	Interface, Inc.	Antimicrobial carpet and carpet tile
US5453275A (en) *	1988-05-05	1995-09-26	Interface, Inc.	Biocidal polymeric coating for heat exchanger coils
US4957948A (en) *	1988-05-05	1990-09-18	Interface, Inc.	Biocidal protective coating for heat exchanger coils
AU2001262559A1 (en) *	2000-05-18	2001-11-26	Eva Honti	Sustained release composition comprising an active agent in a plastic carrier and shaped articles made therefrom
WO2015071890A1 (en)	2013-11-18	2015-05-21	0903608 B.C. Ltd.	Compositions, devices and methods for control of pests using vapor activity
JP6600262B2 (ja)	2016-02-19	2019-10-30	株式会社ジェイテクト	転がり摺動部材とこれを利用した転がり軸受、及び転がり摺動部材の製造方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3318769A (en) *	1963-05-31	1967-05-09	Shell Oil Co	Resin compositions comprising organo-phosphorus pesticides
CH496399A (de) *	1967-12-29	1970-09-30	Geigy Ag J R	Geformter Festkörper zur Bekämpfung von Insekten in Räumen
DE1694240C3 (de) *	1968-01-16	1973-11-29	Bayer Ag, 5090 Leverkusen	Verfahren zur Herstellung von insektizid wirksamen Formkorpern

1972
- 1972-06-24 DE DE2231099A patent/DE2231099C3/de not_active Expired
1973
- 1973-06-12 SU SU1939669A patent/SU469233A3/ru active
- 1973-06-15 US US05/370,512 patent/US3932612A/en not_active Expired - Lifetime
- 1973-06-21 IL IL7342577A patent/IL42577A/en unknown
- 1973-06-21 DD DD178126*A patent/DD110888A5/xx unknown
- 1973-06-21 NL NL7308650A patent/NL7308650A/xx not_active Application Discontinuation
- 1973-06-21 DD DD171742A patent/DD104800A5/xx unknown
- 1973-06-22 BE BE132628A patent/BE801333A/xx not_active IP Right Cessation
- 1973-06-22 CH CH912973A patent/CH583762A5/xx not_active IP Right Cessation
- 1973-06-22 JP JP6994173A patent/JPS572745B2/ja not_active Expired
- 1973-06-22 CA CA174,810A patent/CA1001552A/en not_active Expired
- 1973-06-22 GB GB2978273A patent/GB1398825A/en not_active Expired
- 1973-06-22 FR FR7322893A patent/FR2189435B1/fr not_active Expired
- 1973-06-22 DK DK349373A patent/DK131882C/da active
- 1973-06-22 IE IE1037/73A patent/IE37836B1/xx unknown
- 1973-06-22 AT AT549973A patent/AT326414B/de not_active IP Right Cessation
- 1973-06-22 ZA ZA734243A patent/ZA734243B/xx unknown
- 1973-06-22 IT IT25756/73A patent/IT989412B/it active
- 1973-06-22 AU AU57250/73A patent/AU5725073A/en not_active Expired
- 1973-06-22 TR TR17232A patent/TR17232A/xx unknown
- 1973-06-22 PL PL1973163510A patent/PL87666B1/pl unknown

Also Published As

Publication number	Publication date
ATA549973A (de)	1975-02-15
CH583762A5 (2)	1977-01-14
DE2231099C3 (de)	1981-01-22
DE2231099A1 (de)	1974-01-03
NL7308650A (2)	1973-12-28
FR2189435B1 (2)	1976-07-23
TR17232A (tr)	1976-08-03
JPS4952888A (2)	1974-05-22
CA1001552A (en)	1976-12-14
ZA734243B (en)	1974-05-29
AU5725073A (en)	1975-01-09
AT326414B (de)	1975-12-10
IE37836L (en)	1973-12-24
US3932612A (en)	1976-01-13
IT989412B (it)	1975-05-20
DK131882C (da)	1976-02-16
SU469233A3 (ru)	1975-04-30
BE801333A (fr)	1973-12-26
DD110888A5 (2)	1975-01-12
DE2231099B2 (de)	1980-05-08
FR2189435A1 (2)	1974-01-25
DK131882B (da)	1975-09-22
IE37836B1 (en)	1977-10-26
IL42577A (en)	1976-12-31
IL42577A0 (en)	1973-08-29
DD104800A5 (2)	1974-03-20
GB1398825A (en)	1975-06-25
JPS572745B2 (2)	1982-01-18

Publication	Publication Date	Title
PL87666B1 (2)	1976-07-31
DE1694240C3 (de)	1973-11-29	Verfahren zur Herstellung von insektizid wirksamen Formkorpern
US4129524A (en)	1978-12-12	Radiation shielding material and a process for producing the same
US4189365A (en)	1980-02-19	Photopolymerizable compositions based on acrylic or methacrylic acid esters containing organic phosphites
IL116442A (en)	1997-06-10	Preparation of e-oxime ethers of phenylglyoxylic acids
JP2015174822A (ja)	2015-10-05	ハチ忌避方法
Roos et al.	1985	Biochemical studies on cell fusion. II. Control of fusion response by lipid alteration.
GB1529095A (en)	1978-10-18	Polymerization products based on polycarbodiimides and radically polymerizable carboxylic acids
TW200715051A (en)	2007-04-16	Colored alkali-developable photosensitive resin composition and color filters made by using the same
Loucas et al.	1994	Initial damage in human interphase chromosomes from alpha particles with linear energy transfers relevant to radon exposure
DE59302956D1 (de)	1996-07-25	Verfahren zur Herstellung von E-Oximethern von Phenylglyoxylsäureestern
Abraham et al.	1992	Identification of surrogate rodent hosts for larval Onchocerca lienalis and induction of protective immunity in a model system
DE1694149C2 (de)	1976-01-02	Polyester-Form- und Überzugsmassen
US3754006A (en)	1973-08-21	Esters and amides of substituted glyoxylic acids
ES475189A1 (es)	1979-04-16	Procedimiento para la obtencion de sales de acidos-isociano-carboxilicos.
EP0395982A3 (de)	1991-08-14	Beta,gamma-Ungesättigte Nitrile, deren Herstellung und Verwendung als Riechstoffe
JPS5738765A (en)	1982-03-03	Isolating method of 4,4'-dihydroxydiphenyl sulfone from dihydroxydiphenyl sulfone isomeric mixture
DE2261577B2 (de)	1974-05-30	Di-(2-phenoxyäthyl)-peroxydicarbonat und dessen Verwendung als Polymerisationsinitiator und als Härtungskatalysator
US2809182A (en)	1957-10-08	Use of hydroxytetronic acid as an accelerator of polymerization
FR2254328A1 (en)	1975-07-11	Antirhinoviral benzofuranyl ethylidene carbazic acid esters - prepd. from (substd.) 2-acetylbenzofuran and alkyl carbazate ester
ES8106286A1 (es)	1981-08-01	Un procedimiento para la preparacion de sulfuros de carbamoilo fluorados.
Davis et al.	1975	In vitro analysis of experimental avian viral myocarditis
DE1902930C2 (de)	1977-10-13	Durch UV-Bestrahlen härtbare Polyesterform- und Überzugsmassen
JPS5588051A (en)	1980-07-03	Forming method for positive type resist pattern
Hardt	1974	Triggered luminescences in chloroplasts reflecting primary photoacts in photosynthesis