SK280990B6 - Rodenticídna mäkká pena - Google Patents
Rodenticídna mäkká pena Download PDFInfo
- Publication number
- SK280990B6 SK280990B6 SK1554-95A SK155495A SK280990B6 SK 280990 B6 SK280990 B6 SK 280990B6 SK 155495 A SK155495 A SK 155495A SK 280990 B6 SK280990 B6 SK 280990B6
- Authority
- SK
- Slovakia
- Prior art keywords
- rodenticidal
- acid
- chain
- foam
- acetophenone
- Prior art date
Links
- 239000006260 foam Substances 0.000 title claims abstract description 39
- 230000001119 rodenticidal effect Effects 0.000 title claims abstract description 18
- 229920000642 polymer Polymers 0.000 claims abstract description 11
- 239000004814 polyurethane Substances 0.000 claims abstract description 8
- 229920002635 polyurethane Polymers 0.000 claims abstract description 8
- 229920001477 hydrophilic polymer Polymers 0.000 claims abstract description 6
- 229920000728 polyester Polymers 0.000 claims abstract description 6
- 239000000194 fatty acid Substances 0.000 claims abstract description 5
- 238000005227 gel permeation chromatography Methods 0.000 claims abstract description 5
- 229920002857 polybutadiene Polymers 0.000 claims abstract description 5
- 229920005906 polyester polyol Polymers 0.000 claims abstract description 5
- 239000004793 Polystyrene Substances 0.000 claims abstract description 4
- 239000005667 attractant Substances 0.000 claims abstract description 4
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 4
- 229920002223 polystyrene Polymers 0.000 claims abstract description 4
- 125000003277 amino group Chemical group 0.000 claims abstract description 3
- 239000003755 preservative agent Substances 0.000 claims abstract description 3
- 239000002904 solvent Substances 0.000 claims abstract description 3
- -1 aliphatic fatty acid Chemical class 0.000 claims description 10
- 239000013543 active substance Substances 0.000 claims description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 4
- 229930195729 fatty acid Natural products 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 7
- 235000021355 Stearic acid Nutrition 0.000 abstract description 6
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract description 6
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract description 6
- 239000008117 stearic acid Substances 0.000 abstract description 6
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 abstract description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 abstract description 4
- 235000021314 Palmitic acid Nutrition 0.000 abstract description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract description 2
- 125000001931 aliphatic group Chemical group 0.000 abstract description 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract description 2
- 150000001340 alkali metals Chemical class 0.000 abstract description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract description 2
- 150000001342 alkaline earth metals Chemical class 0.000 abstract description 2
- 150000003863 ammonium salts Chemical class 0.000 abstract description 2
- 125000002843 carboxylic acid group Chemical group 0.000 abstract description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract description 2
- 239000011976 maleic acid Substances 0.000 abstract description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 abstract description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 241000700159 Rattus Species 0.000 description 21
- 241001465754 Metazoa Species 0.000 description 11
- 241000283984 Rodentia Species 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 230000004071 biological effect Effects 0.000 description 7
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 208000005374 Poisoning Diseases 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 239000003146 anticoagulant agent Substances 0.000 description 4
- 229940127219 anticoagulant drug Drugs 0.000 description 4
- 239000001282 iso-butane Substances 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 231100000572 poisoning Toxicity 0.000 description 4
- 230000000607 poisoning effect Effects 0.000 description 4
- 239000003128 rodenticide Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 208000024891 symptom Diseases 0.000 description 4
- VXIXUWQIVKSKSA-UHFFFAOYSA-N 4-hydroxycoumarin Chemical class C1=CC=CC2=C1OC(=O)C=C2O VXIXUWQIVKSKSA-UHFFFAOYSA-N 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Natural products CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 3
- 239000005058 Isophorone diisocyanate Substances 0.000 description 3
- 241000699670 Mus sp. Species 0.000 description 3
- 239000001361 adipic acid Substances 0.000 description 3
- 235000011037 adipic acid Nutrition 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 235000021551 crystal sugar Nutrition 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 239000012875 nonionic emulsifier Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000003549 soybean oil Substances 0.000 description 3
- 235000012424 soybean oil Nutrition 0.000 description 3
- 239000008399 tap water Substances 0.000 description 3
- 235000020679 tap water Nutrition 0.000 description 3
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000004970 Chain extender Substances 0.000 description 2
- ULSLJYXHZDTLQK-UHFFFAOYSA-N Coumatetralyl Chemical group C1=CC=CC2=C1OC(=O)C(C1C3=CC=CC=C3CCC1)=C2O ULSLJYXHZDTLQK-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229960002887 deanol Drugs 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 239000012972 dimethylethanolamine Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
- 235000014593 oils and fats Nutrition 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- IWKHKRWVNCYEOR-UHFFFAOYSA-N 1,1,3,3-tetraphenylpropan-2-one Chemical class C=1C=CC=CC=1C(C=1C=CC=CC=1)C(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 IWKHKRWVNCYEOR-UHFFFAOYSA-N 0.000 description 1
- WQXCZSOYNVLDCJ-UHFFFAOYSA-N 1-(2-phenoxyphenyl)-2-piperidin-2-ylethanone Chemical compound C=1C=CC=C(OC=2C=CC=CC=2)C=1C(=O)CC1CCCCN1 WQXCZSOYNVLDCJ-UHFFFAOYSA-N 0.000 description 1
- XCIMYWGFLXCNAY-UHFFFAOYSA-N 1-(4-fluorophenyl)-1-phenyl-3-piperidin-2-ylpropan-2-one Chemical compound C1=CC(F)=CC=C1C(C=1C=CC=CC=1)C(=O)CC1NCCCC1 XCIMYWGFLXCNAY-UHFFFAOYSA-N 0.000 description 1
- CTSJGSOPMYSZDR-UHFFFAOYSA-N 1-(4-methylphenyl)-1-phenyl-3-piperidin-2-ylpropan-2-one Chemical compound C1=CC(C)=CC=C1C(C=1C=CC=CC=1)C(=O)CC1NCCCC1 CTSJGSOPMYSZDR-UHFFFAOYSA-N 0.000 description 1
- OHWCOJAVWWLSMS-UHFFFAOYSA-N 1-(4-phenylphenyl)-2-pyrrolidin-2-ylethanone Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1C(=O)CC1CCCN1 OHWCOJAVWWLSMS-UHFFFAOYSA-N 0.000 description 1
- BAZHNJAVUCQWDE-UHFFFAOYSA-N 1-[2-(2-phenylethoxy)phenyl]-2-piperidin-2-ylethanol Chemical compound C=1C=CC=C(OCCC=2C=CC=CC=2)C=1C(O)CC1CCCCN1 BAZHNJAVUCQWDE-UHFFFAOYSA-N 0.000 description 1
- IQFCVTZPLJMZDQ-UHFFFAOYSA-N 1-[3-(4-phenoxybutoxy)phenyl]-2-piperidin-1-ylethanol Chemical compound C=1C=CC(OCCCCOC=2C=CC=CC=2)=CC=1C(O)CN1CCCCC1 IQFCVTZPLJMZDQ-UHFFFAOYSA-N 0.000 description 1
- GZUUSPUYZCSRMS-UHFFFAOYSA-N 1-[4-(3-phenoxypropoxy)phenyl]-2-piperidin-2-ylethanone Chemical compound C=1C=C(OCCCOC=2C=CC=CC=2)C=CC=1C(=O)CC1CCCCN1 GZUUSPUYZCSRMS-UHFFFAOYSA-N 0.000 description 1
- UQFLOPRZLDDOQK-UHFFFAOYSA-N 1-[4-(4-bromophenoxy)phenyl]-2-(6-methylpiperidin-2-yl)ethanol Chemical compound N1C(C)CCCC1CC(O)C(C=C1)=CC=C1OC1=CC=C(Br)C=C1 UQFLOPRZLDDOQK-UHFFFAOYSA-N 0.000 description 1
- WTQSVJXCCQVOKO-UHFFFAOYSA-N 1-[4-(4-butoxyphenoxy)phenyl]-2-pyrrolidin-2-ylethanone Chemical compound C1=CC(OCCCC)=CC=C1OC1=CC=C(C(=O)CC2NCCC2)C=C1 WTQSVJXCCQVOKO-UHFFFAOYSA-N 0.000 description 1
- UOUGXQFEYARLCX-UHFFFAOYSA-N 1-[4-(4-butoxyphenyl)phenyl]-2-(4-tert-butylpiperidin-2-yl)ethanone Chemical compound C1=CC(OCCCC)=CC=C1C1=CC=C(C(=O)CC2NCCC(C2)C(C)(C)C)C=C1 UOUGXQFEYARLCX-UHFFFAOYSA-N 0.000 description 1
- AQFLFYVIIFGCNY-UHFFFAOYSA-N 1-[4-(4-chlorophenoxy)phenyl]-2-piperidin-2-ylethanone Chemical compound C1=CC(Cl)=CC=C1OC1=CC=C(C(=O)CC2NCCCC2)C=C1 AQFLFYVIIFGCNY-UHFFFAOYSA-N 0.000 description 1
- CZNPDHOSNNIGBB-UHFFFAOYSA-N 1-[4-(4-phenylbutyl)phenyl]-2-piperidin-2-ylethanone Chemical compound C=1C=C(CCCCC=2C=CC=CC=2)C=CC=1C(=O)CC1CCCCN1 CZNPDHOSNNIGBB-UHFFFAOYSA-N 0.000 description 1
- ZASXCTCNZKFDTP-UHFFFAOYSA-N 1-ethynyl-3-methoxybenzene Chemical group COC1=CC=CC(C#C)=C1 ZASXCTCNZKFDTP-UHFFFAOYSA-N 0.000 description 1
- LLDBWBLRNOTXLL-UHFFFAOYSA-N 1-ethynyl-4-methylsulfanylbenzene Chemical group CSC1=CC=C(C#C)C=C1 LLDBWBLRNOTXLL-UHFFFAOYSA-N 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- XUCDGUUOHCXLKR-UHFFFAOYSA-N 2-(3,5-diethylpiperidin-2-yl)-1-[4-(2-phenylethyl)phenyl]ethanone Chemical compound CCC1CC(CC)CNC1CC(=O)C(C=C1)=CC=C1CCC1=CC=CC=C1 XUCDGUUOHCXLKR-UHFFFAOYSA-N 0.000 description 1
- RIEBKPLCULBJGM-UHFFFAOYSA-N 2-(5,5-dimethylpyrrolidin-2-yl)-1-(4-phenylphenyl)ethanone Chemical compound N1C(C)(C)CCC1CC(=O)C1=CC=C(C=2C=CC=CC=2)C=C1 RIEBKPLCULBJGM-UHFFFAOYSA-N 0.000 description 1
- QEIORKFSXOMORK-UHFFFAOYSA-N 2-(5,5-dimethylpyrrolidin-2-yl)-1-[4-(4-fluorophenoxy)phenyl]ethanone Chemical compound N1C(C)(C)CCC1CC(=O)C(C=C1)=CC=C1OC1=CC=C(F)C=C1 QEIORKFSXOMORK-UHFFFAOYSA-N 0.000 description 1
- YGUIWALGTFPWIU-ZHACJKMWSA-N 2-(azepan-2-yl)-1-[4-[(e)-2-phenylethenyl]phenyl]ethanone Chemical compound C=1C=C(\C=C\C=2C=CC=CC=2)C=CC=1C(=O)CC1CCCCCN1 YGUIWALGTFPWIU-ZHACJKMWSA-N 0.000 description 1
- CLUFCWZMZURGAI-UHFFFAOYSA-N 2-[1-[(2,5-dimethylphenyl)-phenylmethyl]piperidin-2-yl]ethanol Chemical compound CC1=CC=C(C)C(C(N2C(CCCC2)CCO)C=2C=CC=CC=2)=C1 CLUFCWZMZURGAI-UHFFFAOYSA-N 0.000 description 1
- OSIDMAJZERBPOJ-UHFFFAOYSA-N 2-hydroxythiochromen-4-one Chemical class C1=CC=C2SC(O)=CC(=O)C2=C1 OSIDMAJZERBPOJ-UHFFFAOYSA-N 0.000 description 1
- BBKBCALFZXONPG-UHFFFAOYSA-N 2-piperidin-2-yl-1-[4-[3-(trifluoromethyl)phenoxy]phenyl]ethanone Chemical compound FC(F)(F)C1=CC=CC(OC=2C=CC(=CC=2)C(=O)CC2NCCCC2)=C1 BBKBCALFZXONPG-UHFFFAOYSA-N 0.000 description 1
- KRHDZSDICYBXDT-UHFFFAOYSA-N 2-piperidin-2-yl-1-[4-[4-(trifluoromethyl)phenyl]phenyl]ethanone Chemical compound C1=CC(C(F)(F)F)=CC=C1C1=CC=C(C(=O)CC2NCCCC2)C=C1 KRHDZSDICYBXDT-UHFFFAOYSA-N 0.000 description 1
- LQDOTCPMIROXBT-UHFFFAOYSA-N 3,3-diphenyl-1-piperidin-2-ylbutan-2-ol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C)C(O)CC1CCCCN1 LQDOTCPMIROXBT-UHFFFAOYSA-N 0.000 description 1
- TYVVCTHKBQJCEM-UHFFFAOYSA-N 3,3-diphenyl-1-piperidin-2-ylbutan-2-one Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(C)C(=O)CC1CCCCN1 TYVVCTHKBQJCEM-UHFFFAOYSA-N 0.000 description 1
- HXGAYKDDYLXIHH-UHFFFAOYSA-N 3,3-diphenyl-1-pyrrolidin-2-ylpentan-2-ol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(CC)C(O)CC1CCCN1 HXGAYKDDYLXIHH-UHFFFAOYSA-N 0.000 description 1
- CJAZCKUGLFWINJ-UHFFFAOYSA-N 3,4-dihydroxybenzene-1,2-disulfonic acid Chemical compound OC1=CC=C(S(O)(=O)=O)C(S(O)(=O)=O)=C1O CJAZCKUGLFWINJ-UHFFFAOYSA-N 0.000 description 1
- DACWTUJVICQWIX-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-3-phenyl-1-piperidin-2-ylheptan-2-one Chemical compound C=1C=CC=CC=1C(C=1C(=CC(Cl)=CC=1)Cl)(CCCC)C(=O)CC1CCCCN1 DACWTUJVICQWIX-UHFFFAOYSA-N 0.000 description 1
- SNSJAZLBMADDQL-UHFFFAOYSA-N 3-(5,5-dimethylpyrrolidin-2-yl)-1-(4-methylsulfanylphenyl)-1-phenylpropan-2-one Chemical compound C1=CC(SC)=CC=C1C(C=1C=CC=CC=1)C(=O)CC1NC(C)(C)CC1 SNSJAZLBMADDQL-UHFFFAOYSA-N 0.000 description 1
- NTMNWGSFYJKQDJ-UHFFFAOYSA-N 3-(5-methylpyrrolidin-2-yl)-1,1-diphenylpropan-2-one Chemical compound N1C(C)CCC1CC(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 NTMNWGSFYJKQDJ-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- WFFZGYRTVIPBFN-UHFFFAOYSA-N 3h-indene-1,2-dione Chemical class C1=CC=C2C(=O)C(=O)CC2=C1 WFFZGYRTVIPBFN-UHFFFAOYSA-N 0.000 description 1
- ZWHGRROQOQMNEW-UHFFFAOYSA-K 4-aminobenzenesulfonate;cerium(3+) Chemical compound [Ce+3].NC1=CC=C(S([O-])(=O)=O)C=C1.NC1=CC=C(S([O-])(=O)=O)C=C1.NC1=CC=C(S([O-])(=O)=O)C=C1 ZWHGRROQOQMNEW-UHFFFAOYSA-K 0.000 description 1
- VEUZZDOCACZPRY-UHFFFAOYSA-N Brodifacoum Chemical compound O=C1OC=2C=CC=CC=2C(O)=C1C(C1=CC=CC=C1C1)CC1C(C=C1)=CC=C1C1=CC=C(Br)C=C1 VEUZZDOCACZPRY-UHFFFAOYSA-N 0.000 description 1
- 239000005966 Bromadiolone Substances 0.000 description 1
- OWNRRUFOJXFKCU-UHFFFAOYSA-N Bromadiolone Chemical compound C=1C=C(C=2C=CC(Br)=CC=2)C=CC=1C(O)CC(C=1C(OC2=CC=CC=C2C=1O)=O)C1=CC=CC=C1 OWNRRUFOJXFKCU-UHFFFAOYSA-N 0.000 description 1
- UDHXJZHVNHGCEC-UHFFFAOYSA-N Chlorophacinone Chemical compound C1=CC(Cl)=CC=C1C(C=1C=CC=CC=1)C(=O)C1C(=O)C2=CC=CC=C2C1=O UDHXJZHVNHGCEC-UHFFFAOYSA-N 0.000 description 1
- 239000006010 Difenacoum Substances 0.000 description 1
- JYGLAHSAISAEAL-UHFFFAOYSA-N Diphenadione Chemical compound O=C1C2=CC=CC=C2C(=O)C1C(=O)C(C=1C=CC=CC=1)C1=CC=CC=C1 JYGLAHSAISAEAL-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 102100027378 Prothrombin Human genes 0.000 description 1
- 108010094028 Prothrombin Proteins 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- MECHNRXZTMCUDQ-UHFFFAOYSA-N Vitamin D2 Natural products C1CCC2(C)C(C(C)C=CC(C)C(C)C)CCC2C1=CC=C1CC(O)CCC1=C MECHNRXZTMCUDQ-UHFFFAOYSA-N 0.000 description 1
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 238000002144 chemical decomposition reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- HENZOLWOIZODCT-UHFFFAOYSA-N coumachlor Chemical compound OC=1OC2=CC=CC=C2C(=O)C=1C(CC(=O)C)C1=CC=C(Cl)C=C1 HENZOLWOIZODCT-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- NZOWVZVFSVRNOR-UHFFFAOYSA-N difenacoum Chemical compound OC=1OC2=CC=CC=C2C(=O)C=1C(C1=CC=CC=C1C1)CC1C(C=C1)=CC=C1C1=CC=CC=C1 NZOWVZVFSVRNOR-UHFFFAOYSA-N 0.000 description 1
- VSVAQRUUFVBBFS-UHFFFAOYSA-N difethialone Chemical compound OC=1SC2=CC=CC=C2C(=O)C=1C(C1=CC=CC=C1C1)CC1C(C=C1)=CC=C1C1=CC=C(Br)C=C1 VSVAQRUUFVBBFS-UHFFFAOYSA-N 0.000 description 1
- 229960000267 diphenadione Drugs 0.000 description 1
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229960002061 ergocalciferol Drugs 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- OWUZCVPRFKSBRG-UHFFFAOYSA-N flocoumafen Chemical compound OC=1OC2=CC=CC=C2C(=O)C=1C(C1=CC=CC=C1C1)CC1C(C=C1)=CC=C1OCC1=CC=C(C(F)(F)F)C=C1 OWUZCVPRFKSBRG-UHFFFAOYSA-N 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 125000001207 fluorophenyl group Chemical group 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 235000012631 food intake Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- QNXSIUBBGPHDDE-UHFFFAOYSA-N indan-1-one Chemical compound C1=CC=C2C(=O)CCC2=C1 QNXSIUBBGPHDDE-UHFFFAOYSA-N 0.000 description 1
- 239000008011 inorganic excipient Substances 0.000 description 1
- 230000009191 jumping Effects 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N n-propyl alcohol Natural products CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920003255 poly(phenylsilsesquioxane) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229940039716 prothrombin Drugs 0.000 description 1
- WSWCOQWTEOXDQX-MQQKCMAXSA-N sorbic acid group Chemical group C(\C=C\C=C\C)(=O)O WSWCOQWTEOXDQX-MQQKCMAXSA-N 0.000 description 1
- 235000000891 standard diet Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 235000001892 vitamin D2 Nutrition 0.000 description 1
- 239000011653 vitamin D2 Substances 0.000 description 1
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
- 235000005282 vitamin D3 Nutrition 0.000 description 1
- 239000011647 vitamin D3 Substances 0.000 description 1
- QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
- 229940021056 vitamin d3 Drugs 0.000 description 1
- 229960005080 warfarin Drugs 0.000 description 1
- PJVWKTKQMONHTI-UHFFFAOYSA-N warfarin Chemical compound OC=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 PJVWKTKQMONHTI-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/16—Foams
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Polyesters Or Polycarbonates (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4444261A DE4444261A1 (de) | 1994-12-13 | 1994-12-13 | Rodentizide Schäume |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK155495A3 SK155495A3 (en) | 1997-01-08 |
| SK280990B6 true SK280990B6 (sk) | 2000-10-09 |
Family
ID=6535623
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK1554-95A SK280990B6 (sk) | 1994-12-13 | 1995-12-12 | Rodenticídna mäkká pena |
Country Status (22)
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4549027B2 (ja) * | 2002-02-04 | 2010-09-22 | アース製薬株式会社 | ネズミ用毒餌剤及びその安定化方法 |
| MY143382A (en) * | 2005-11-18 | 2011-05-13 | Basf Se | Aqueous rodenticide formulations |
| RU2289925C1 (ru) * | 2006-02-26 | 2006-12-27 | Алексей Юрьевич Похолков | Родентицидное средство |
| BRPI0817718A2 (pt) * | 2007-10-01 | 2015-10-13 | Basf Se | mistura rondenticida, formulação de isca rodenticida, uso de uma formulação de isca rodenticida, método para combater pestes de roedores, e, caixa de isca |
| WO2013003946A1 (en) * | 2011-07-04 | 2013-01-10 | Contech Enterprises Inc. | Compositions and methods for attracting and stimulating feeding by mice and rats |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES312702A1 (es) * | 1964-06-02 | 1966-02-16 | Mcneil Laboratories Incorporated | Un procedimiento para preparar un cebo raticida. |
| US3816610A (en) * | 1969-04-25 | 1974-06-11 | Westinghouse Electric Corp | Palatable foamed rodent control material |
| CH592189B5 (enrdf_load_stackoverflow) * | 1972-06-21 | 1977-10-14 | Ciba Geigy Ag | |
| DE2633834A1 (de) * | 1975-08-19 | 1977-03-03 | Lipha | Nagetierbekaempfungsmittel und dessen verwendung |
| US4207335A (en) * | 1975-09-23 | 1980-06-10 | Beecham Group Limited | Indan-1,3-diones |
| EP0098629B1 (en) * | 1982-06-14 | 1987-08-26 | Shell Internationale Researchmaatschappij B.V. | Anti-coagulants of the 4-hydroxycoumarin type, the preparation thereof, and rodenticidal compositions (baits) comprising such anti-coagulants |
| US4836939A (en) * | 1986-07-25 | 1989-06-06 | Rockwood Systems Corporation | Stable expandable foam & concentrate & method |
-
1994
- 1994-12-13 DE DE4444261A patent/DE4444261A1/de not_active Withdrawn
-
1995
- 1995-10-13 TR TR95/01266A patent/TR199501266A2/xx unknown
- 1995-10-20 TW TW084111065A patent/TW290429B/zh not_active IP Right Cessation
- 1995-11-21 AR AR33431795A patent/AR000174A1/es unknown
- 1995-11-30 EP EP95118834A patent/EP0719498B1/de not_active Expired - Lifetime
- 1995-11-30 ES ES95118834T patent/ES2132499T3/es not_active Expired - Lifetime
- 1995-11-30 AT AT95118834T patent/ATE180384T1/de not_active IP Right Cessation
- 1995-11-30 DE DE59506027T patent/DE59506027D1/de not_active Expired - Lifetime
- 1995-11-30 DK DK95118834T patent/DK0719498T3/da active
- 1995-12-06 AU AU40268/95A patent/AU696810B2/en not_active Ceased
- 1995-12-08 CA CA002164788A patent/CA2164788C/en not_active Expired - Fee Related
- 1995-12-11 FI FI955937A patent/FI110052B/fi active
- 1995-12-11 PL PL95311777A patent/PL185220B1/pl unknown
- 1995-12-11 JP JP34542395A patent/JP3498159B2/ja not_active Expired - Fee Related
- 1995-12-12 UA UA95125272A patent/UA40620C2/uk unknown
- 1995-12-12 CZ CZ19953279A patent/CZ290972B6/cs not_active IP Right Cessation
- 1995-12-12 ZA ZA9510543A patent/ZA9510543B/xx unknown
- 1995-12-12 NO NO955021A patent/NO305461B1/no unknown
- 1995-12-12 SK SK1554-95A patent/SK280990B6/sk unknown
- 1995-12-12 BR BR9505761A patent/BR9505761A/pt not_active IP Right Cessation
- 1995-12-13 HU HU9503559A patent/HU222007B1/hu not_active IP Right Cessation
- 1995-12-13 RU RU95120581/13A patent/RU2143803C1/ru not_active IP Right Cessation
-
1999
- 1999-06-09 GR GR990401522T patent/GR3030435T3/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101019652B1 (ko) | 살서성 미끼 시스템 | |
| CA2754434C (en) | Microencapsulated insecticide formulations | |
| AU626561B2 (en) | Terrestrial delivery compositions | |
| EP0285404B1 (en) | Improved insecticidal delivery compositions and methods for controlling a population of insects in an aquatic environment | |
| AU608597B2 (en) | Insecticidal bait composition for control of household infestations of cockroaches | |
| KR20110069168A (ko) | 상승적 살서제 | |
| JPWO2019111839A1 (ja) | 揮発性物質放散用組成物 | |
| SK280990B6 (sk) | Rodenticídna mäkká pena | |
| US6036970A (en) | Rodenticidal foams | |
| WO2001014478A1 (fr) | Composition de resine moulee sous forme de gel, produit chimique sous forme de gel volatil emballe, et processus de production de celui-ci. | |
| JPS61268602A (ja) | ゴキブリ抑制用新規組成物および方法 | |
| DE19837064B4 (de) | Rodentizide Köder | |
| JPH09278604A (ja) | 殺齧歯動物性フオーム | |
| NZ280650A (en) | Flexible foams containing rodenticide; premixes | |
| EP0789998B1 (de) | Rodentizide Schäume | |
| EP0478578A1 (en) | Water-soluble stable arthropodicidally-active foam matrix and method of manufacture | |
| JPH10506625A (ja) | 殺鼠毒餌系 | |
| WO2002023989A1 (en) | Insecticidal microcrystalline dry aerosol spray | |
| JP4938940B2 (ja) | 害虫誘引性駆除剤 | |
| EP2019584B1 (fr) | Produit composite apte a diffuser un agent actif | |
| JPH0610125B2 (ja) | 衛生害虫防除組成物 | |
| AU718028B2 (en) | Cockroach bait | |
| WO2007069796A1 (en) | Insecticidal composition containing boric acid | |
| JPS6289605A (ja) | ピレスロイド系農薬組成物 |