JPS5839129B2 - 殺昆虫または殺ダニ剤 - Google Patents
殺昆虫または殺ダニ剤Info
- Publication number
- JPS5839129B2 JPS5839129B2 JP50109044A JP10904475A JPS5839129B2 JP S5839129 B2 JPS5839129 B2 JP S5839129B2 JP 50109044 A JP50109044 A JP 50109044A JP 10904475 A JP10904475 A JP 10904475A JP S5839129 B2 JPS5839129 B2 JP S5839129B2
- Authority
- JP
- Japan
- Prior art keywords
- active compound
- weight
- compounds
- insects
- solvent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 230000000895 acaricidal effect Effects 0.000 title claims description 7
- 239000000642 acaricide Substances 0.000 title claims description 3
- 239000002917 insecticide Substances 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 61
- -1 ethylmercapto-ethyl Chemical group 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 239000011593 sulfur Chemical group 0.000 claims description 2
- 229910052717 sulfur Chemical group 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 28
- 239000002904 solvent Substances 0.000 description 17
- 241000238631 Hexapoda Species 0.000 description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- 241000607479 Yersinia pestis Species 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 239000003995 emulsifying agent Substances 0.000 description 10
- 238000009472 formulation Methods 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 241000238876 Acari Species 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 241001124076 Aphididae Species 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 241001454293 Tetranychus urticae Species 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000003085 diluting agent Substances 0.000 description 6
- 241000255925 Diptera Species 0.000 description 5
- 241000256251 Spodoptera frugiperda Species 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 241001425390 Aphis fabae Species 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 125000002877 alkyl aryl group Chemical group 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 241000238657 Blattella germanica Species 0.000 description 3
- 241000254173 Coleoptera Species 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 241000721623 Myzus Species 0.000 description 3
- 241000721621 Myzus persicae Species 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 241001608567 Phaedon cochleariae Species 0.000 description 3
- 241000500437 Plutella xylostella Species 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000005907 alkyl ester group Chemical group 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 125000004494 ethyl ester group Chemical group 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000000575 pesticide Substances 0.000 description 3
- 229920000151 polyglycol Polymers 0.000 description 3
- 239000010695 polyglycol Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 241001143309 Acanthoscelides obtectus Species 0.000 description 2
- 241001136249 Agriotes lineatus Species 0.000 description 2
- 241001674044 Blattodea Species 0.000 description 2
- 241000042459 Byturus aestivus Species 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000483001 Euproctis chrysorrhoea Species 0.000 description 2
- 241000257303 Hymenoptera Species 0.000 description 2
- 241000257159 Musca domestica Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 241001491877 Operophtera brumata Species 0.000 description 2
- 241000488583 Panonychus ulmi Species 0.000 description 2
- 241000257149 Phormia Species 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000255969 Pieris brassicae Species 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 241000722238 Pseudococcus maritimus Species 0.000 description 2
- 240000001890 Ribes hudsonianum Species 0.000 description 2
- 235000016954 Ribes hudsonianum Nutrition 0.000 description 2
- 235000001466 Ribes nigrum Nutrition 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 230000002147 killing effect Effects 0.000 description 2
- 239000000865 liniment Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 201000004792 malaria Diseases 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 230000009885 systemic effect Effects 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- 241000238818 Acheta domesticus Species 0.000 description 1
- 241000253994 Acyrthosiphon pisum Species 0.000 description 1
- 241000256111 Aedes <genus> Species 0.000 description 1
- 241001136265 Agriotes Species 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241001414900 Anopheles stephensi Species 0.000 description 1
- 241000239290 Araneae Species 0.000 description 1
- 206010004194 Bed bug infestation Diseases 0.000 description 1
- 241000238805 Blaberus Species 0.000 description 1
- 241001510109 Blaberus giganteus Species 0.000 description 1
- 241000238658 Blattella Species 0.000 description 1
- 241000167854 Bourreria succulenta Species 0.000 description 1
- 241000256593 Brachycaudus schwartzi Species 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 241001444260 Brassicogethes aeneus Species 0.000 description 1
- 241000907225 Bruchidius Species 0.000 description 1
- 241000257163 Calliphora vicina Species 0.000 description 1
- 241001519020 Cassia brewsteri Species 0.000 description 1
- 241000255579 Ceratitis capitata Species 0.000 description 1
- 241000254137 Cicadidae Species 0.000 description 1
- 241001414836 Cimex Species 0.000 description 1
- 241001414835 Cimicidae Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241001415288 Coccidae Species 0.000 description 1
- 241001465977 Coccoidea Species 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000256059 Culex pipiens Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241000289763 Dasygaster padockina Species 0.000 description 1
- 241000255601 Drosophila melanogaster Species 0.000 description 1
- 241001581006 Dysaphis plantaginea Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000630736 Ephestia Species 0.000 description 1
- 241000953886 Fannia canicularis Species 0.000 description 1
- 241000255896 Galleria mellonella Species 0.000 description 1
- 241000199026 Gyptis <bristle worm> Species 0.000 description 1
- 241000258937 Hemiptera Species 0.000 description 1
- 241001659688 Hercinothrips femoralis Species 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 241001251909 Hyalopterus pruni Species 0.000 description 1
- 241000256602 Isoptera Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000255777 Lepidoptera Species 0.000 description 1
- 241000258916 Leptinotarsa decemlineata Species 0.000 description 1
- 241000406668 Loxodonta cyclotis Species 0.000 description 1
- 241000721703 Lymantria dispar Species 0.000 description 1
- 241000721714 Macrosiphum euphorbiae Species 0.000 description 1
- 241000254071 Melolontha Species 0.000 description 1
- 241000254099 Melolontha melolontha Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000257229 Musca <genus> Species 0.000 description 1
- 241000257226 Muscidae Species 0.000 description 1
- 241001508687 Mustela erminea Species 0.000 description 1
- 241000810465 Myzus cerasi cerasi Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000131101 Oryzaephilus surinamensis Species 0.000 description 1
- 241001246312 Otis Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241001548358 Parapiesma quadratum Species 0.000 description 1
- 241000238675 Periplaneta americana Species 0.000 description 1
- 229930046231 Phaseol Natural products 0.000 description 1
- 241001396980 Phytonemus pallidus Species 0.000 description 1
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- 235000005805 Prunus cerasus Nutrition 0.000 description 1
- 241001509970 Reticulitermes <genus> Species 0.000 description 1
- 241001509967 Reticulitermes flavipes Species 0.000 description 1
- 241000722249 Rhodnius prolixus Species 0.000 description 1
- 241000125167 Rhopalosiphum padi Species 0.000 description 1
- 241001510241 Rhyparobia Species 0.000 description 1
- 241001510236 Rhyparobia maderae Species 0.000 description 1
- 241000254179 Sitophilus granarius Species 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- 241000985245 Spodoptera litura Species 0.000 description 1
- 241001177161 Stegobium paniceum Species 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 241000254109 Tenebrio molitor Species 0.000 description 1
- 241001454295 Tetranychidae Species 0.000 description 1
- 241001454294 Tetranychus Species 0.000 description 1
- 241001414989 Thysanoptera Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 241001238452 Tortrix Species 0.000 description 1
- 241001414831 Triatoma infestans Species 0.000 description 1
- 241000267822 Trogoderma granarium Species 0.000 description 1
- 241000219873 Vicia Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical group ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 241001466337 Yponomeuta Species 0.000 description 1
- 241000064240 Yponomeuta padellus Species 0.000 description 1
- 241000209149 Zea Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- AVKUERGKIZMTKX-NJBDSQKTSA-N ampicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=CC=C1 AVKUERGKIZMTKX-NJBDSQKTSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 125000005228 aryl sulfonate group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- 230000001055 chewing effect Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000003958 fumigation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 210000004013 groin Anatomy 0.000 description 1
- 239000007954 growth retardant Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 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
- 101150085091 lat-2 gene Proteins 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- OAQWWRSICWQQSE-UHFFFAOYSA-N octan-2-yl 16-methylheptadecanoate Chemical compound CCCCCCC(C)OC(=O)CCCCCCCCCCCCCCC(C)C OAQWWRSICWQQSE-UHFFFAOYSA-N 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000003090 pesticide formulation Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000003128 rodenticide Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2454—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2458—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic of aliphatic amines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/505,440 US3940457A (en) | 1972-04-06 | 1974-09-12 | N-(N,N-disubstituted-aminomethylidene)-(thiono)thiol-phosphoric acid esters amides |
| DE2517101A DE2517101C2 (de) | 1974-09-12 | 1975-04-18 | N-[O-Alkyl-S-aliphatische(thiono)thiolphosphoryl]-iminoameisensäurealkylester, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Insektizide und Akarizide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5154930A JPS5154930A (en) | 1976-05-14 |
| JPS5839129B2 true JPS5839129B2 (ja) | 1983-08-27 |
Family
ID=25768783
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50109044A Expired JPS5839129B2 (ja) | 1974-09-12 | 1975-09-10 | 殺昆虫または殺ダニ剤 |
Country Status (12)
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4913336A (US08063081-20111122-C00044.png) * | 1972-04-06 | 1974-02-05 |
-
1975
- 1975-09-04 RO RO7583322A patent/RO65820A/ro unknown
- 1975-09-09 NL NL7510627A patent/NL7510627A/xx not_active Application Discontinuation
- 1975-09-10 DD DD18826975A patent/DD123266A5/xx unknown
- 1975-09-10 CH CH1171775A patent/CH617706A5/de not_active IP Right Cessation
- 1975-09-10 LU LU73360A patent/LU73360A1/xx unknown
- 1975-09-10 IT IT2711375A patent/IT1042444B/it active
- 1975-09-10 JP JP50109044A patent/JPS5839129B2/ja not_active Expired
- 1975-09-11 BR BR7505869A patent/BR7505869A/pt unknown
- 1975-09-11 ES ES440884A patent/ES440884A1/es not_active Expired
- 1975-09-11 GB GB3741475A patent/GB1509618A/en not_active Expired
- 1975-09-11 DK DK405575A patent/DK140062B/da not_active IP Right Cessation
- 1975-09-12 FR FR7528114A patent/FR2284612A1/fr active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4913336A (US08063081-20111122-C00044.png) * | 1972-04-06 | 1974-02-05 |
Also Published As
| Publication number | Publication date |
|---|---|
| RO65820A (ro) | 1980-06-15 |
| DK405575A (US08063081-20111122-C00044.png) | 1976-03-13 |
| GB1509618A (en) | 1978-05-04 |
| DD123266A5 (US08063081-20111122-C00044.png) | 1976-12-12 |
| IT1042444B (it) | 1980-01-30 |
| ES440884A1 (es) | 1977-03-16 |
| DK140062C (US08063081-20111122-C00044.png) | 1979-11-12 |
| FR2284612B1 (US08063081-20111122-C00044.png) | 1979-06-29 |
| NL7510627A (nl) | 1976-03-16 |
| CH617706A5 (en) | 1980-06-13 |
| JPS5154930A (en) | 1976-05-14 |
| LU73360A1 (US08063081-20111122-C00044.png) | 1976-08-13 |
| FR2284612A1 (fr) | 1976-04-09 |
| BR7505869A (pt) | 1976-08-03 |
| DK140062B (da) | 1979-06-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3763160A (en) | Phosphorus containing esters of 2-hydroxyquinoxaline | |
| EP0100528A2 (de) | Neue (Di)-thiophosphor- und -phosphonsäure-Derivate, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung im Pflanzenschutz | |
| US3775517A (en) | 1-phenyl-2-cyano-2-methylvinyl-thiono-phosphoric(phosphonic)acid esters | |
| US3914243A (en) | O-alkyl-o-{8 7-substituted-benzisoxazol(3)yl{9 -(thiono)-phosphoric (phosphonic) acid esters | |
| US3888951A (en) | O-aryl-thiono alkanephosphonic acid ester-formamidines | |
| EP0065216A1 (de) | Pestizide S-(1.2.4-Triazol-5-ylmethyl)-(di)-thiophosph(on)ate und Verfahren zu ihrer Herstellung | |
| JPS598277B2 (ja) | 置換されたエチル−りん酸（ホスホン酸）エステル、それらの製造方法並びに殺昆虫剤、殺ダニ剤及び殺線虫剤としてのそれらの使用 | |
| GB1560712A (en) | Phosphoruscontaining isoxazole derivatives useful as pesticides | |
| US3911055A (en) | O-alkyl-O-(1-cyano-1-tert.-butylketonoxime)-thionophosphoric (phosphonic) acid esters | |
| DE2523324A1 (de) | Pyrimidin(4,6)diyl-bis-(thiono) (thiol)phosphor-(phosphon)-saeureester, verfahren zu ihrer herstellung sowie ihre verwendung als insektizide und akarizide | |
| JPS5839129B2 (ja) | 殺昆虫または殺ダニ剤 | |
| JPS5838439B2 (ja) | トリアゾロチアゾリル−（チオノ）−リン酸（ホスホン酸）エステルの製造方法 | |
| US3749720A (en) | Pyridazinothionophosphoric (phosphonic) acid esters | |
| US3733376A (en) | Phosphoric acid esters | |
| US4426379A (en) | Insecticidal 2-oxo-3-dialkoxyphosphoro-5-cyclopropyl-1,3,4-oxadiazoline | |
| US4086239A (en) | Thiazole bis-phosphates and phosphonates, intermediates, and insecticidal compositions and methods | |
| HU183194B (en) | Insecticide compositions containing substituted ester of5-pyrimidino-phosphoric acid as active agent, and process for producing the active agent | |
| US3420829A (en) | 3,4 - dihydro - 4 - oxo - 1,2,3 - benzotriazine-3-yl-ethyl phosphoric and phosphonic acid esters | |
| US3644598A (en) | 1 - alkoxy(-alkenyloxy -phenoxy) - 1-thiono-3-chloro(3-alkyl)phospholines | |
| US3880997A (en) | Insecticidal and acaricidal phosphorous-containing esters of 2-hydroxyquinoxaline | |
| US3808227A (en) | Pyrazolo(thiono)phosphoric(phosphonic)acid esters | |
| JPS5811404B2 (ja) | 殺虫、殺ダニおよび殺線虫剤 | |
| US3839355A (en) | Pyrazolo-(thiono)-phosphoric(phosphonic)acid esters | |
| PL88487B1 (US08063081-20111122-C00044.png) | ||
| US3828063A (en) | Benzisoxazolo(thiono)phosphoric(phosphonic)acid esters |
