CA1064513A - And organotin sulfinates as insecticides and acaricides - Google Patents
And organotin sulfinates as insecticides and acaricidesInfo
- Publication number
- CA1064513A CA1064513A CA254,794A CA254794A CA1064513A CA 1064513 A CA1064513 A CA 1064513A CA 254794 A CA254794 A CA 254794A CA 1064513 A CA1064513 A CA 1064513A
- Authority
- CA
- Canada
- Prior art keywords
- compound
- trimethyltin
- organotin
- compounds
- sodium
- 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 description 6
- 239000002917 insecticide Substances 0.000 title description 6
- 239000000642 acaricide Substances 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 67
- 241000238631 Hexapoda Species 0.000 claims abstract description 10
- 238000000034 method Methods 0.000 claims description 22
- -1 p-t-butylphenyl Chemical group 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000005059 halophenyl group Chemical group 0.000 claims description 2
- DFWZRIJQPQOMDV-UHFFFAOYSA-M trimethylstannyl 4-(2-methylbutan-2-yl)benzenesulfinate Chemical compound C[Sn+](C)C.CCC(C)(C)C1=CC=C(S([O-])=O)C=C1 DFWZRIJQPQOMDV-UHFFFAOYSA-M 0.000 claims 2
- KPXUDPMTBQIGOZ-UHFFFAOYSA-M trimethylstannyl 4-bromobenzenesulfinate Chemical compound C[Sn+](C)C.[O-]S(=O)C1=CC=C(Br)C=C1 KPXUDPMTBQIGOZ-UHFFFAOYSA-M 0.000 claims 2
- FIMSUMVLGIAXFW-UHFFFAOYSA-M trimethylstannyl 4-chlorobenzenesulfinate Chemical compound C[Sn+](C)C.[O-]S(=O)C1=CC=C(Cl)C=C1 FIMSUMVLGIAXFW-UHFFFAOYSA-M 0.000 claims 2
- BPESQRQOITZACQ-UHFFFAOYSA-M trimethylstannyl 4-cyclohexylbenzenesulfinate Chemical compound C[Sn+](C)C.C1=CC(S(=O)[O-])=CC=C1C1CCCCC1 BPESQRQOITZACQ-UHFFFAOYSA-M 0.000 claims 2
- BJOJFFOLRNLMMC-UHFFFAOYSA-M trimethylstannyl 4-tert-butylbenzenesulfinate Chemical compound C[Sn+](C)C.CC(C)(C)C1=CC=C(S([O-])=O)C=C1 BJOJFFOLRNLMMC-UHFFFAOYSA-M 0.000 claims 2
- CCRMAATUKBYMPA-UHFFFAOYSA-N trimethyltin Chemical compound C[Sn](C)C.C[Sn](C)C CCRMAATUKBYMPA-UHFFFAOYSA-N 0.000 claims 2
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- SFQLOVJWDLAASO-UHFFFAOYSA-M trimethylstannyl 2,5-dichlorobenzenesulfinate Chemical compound C[Sn+](C)C.[O-]S(=O)C1=CC(Cl)=CC=C1Cl SFQLOVJWDLAASO-UHFFFAOYSA-M 0.000 claims 1
- FUOMIMYBXUCZAO-UHFFFAOYSA-M trimethylstannyl 4-cyclooctylbenzenesulfinate Chemical compound C[Sn+](C)C.C1=CC(S(=O)[O-])=CC=C1C1CCCCCCC1 FUOMIMYBXUCZAO-UHFFFAOYSA-M 0.000 claims 1
- OTKWWIDPFGFAPE-UHFFFAOYSA-M trimethylstannyl 4-cyclopentylbenzenesulfinate Chemical compound C[Sn+](C)C.C1=CC(S(=O)[O-])=CC=C1C1CCCC1 OTKWWIDPFGFAPE-UHFFFAOYSA-M 0.000 claims 1
- MOBOQDDUJMBZKL-UHFFFAOYSA-M trimethylstannyl benzenesulfinate Chemical compound C[Sn](C)(C)OS(=O)C1=CC=CC=C1 MOBOQDDUJMBZKL-UHFFFAOYSA-M 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 28
- 238000012360 testing method Methods 0.000 description 19
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- 239000011734 sodium Substances 0.000 description 17
- 229910052708 sodium Inorganic materials 0.000 description 17
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 16
- 239000007921 spray Substances 0.000 description 14
- 229920000742 Cotton Polymers 0.000 description 12
- 241000219146 Gossypium Species 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000000126 substance Substances 0.000 description 10
- 235000010469 Glycine max Nutrition 0.000 description 9
- 241000256244 Heliothis virescens Species 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 241001124076 Aphididae Species 0.000 description 8
- 244000068988 Glycine max Species 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 241000254175 Anthonomus grandis Species 0.000 description 6
- 229940022682 acetone Drugs 0.000 description 6
- 241000238876 Acari Species 0.000 description 5
- 241000208125 Nicotiana Species 0.000 description 5
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 5
- 231100000674 Phytotoxicity Toxicity 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 241000607479 Yersinia pestis Species 0.000 description 4
- 240000008042 Zea mays Species 0.000 description 4
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 4
- 239000000443 aerosol Substances 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 235000005822 corn Nutrition 0.000 description 4
- 235000005911 diet Nutrition 0.000 description 4
- 230000037213 diet Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- UKHQRARQNZOXRL-UHFFFAOYSA-N trimethyltin Chemical compound C[SnH](C)C UKHQRARQNZOXRL-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 244000070406 Malus silvestris Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 244000105624 Arachis hypogaea Species 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000726103 Atta Species 0.000 description 2
- 240000007124 Brassica oleracea Species 0.000 description 2
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
- 241001388466 Bruchus rufimanus Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 241001163743 Perlodes Species 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 235000021016 apples Nutrition 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 235000015110 jellies Nutrition 0.000 description 2
- 239000008274 jelly Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000020232 peanut Nutrition 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- CAZDDRMAVQSBDV-UHFFFAOYSA-N 2,5-dichlorobenzenesulfinic acid Chemical compound OS(=O)C1=CC(Cl)=CC=C1Cl CAZDDRMAVQSBDV-UHFFFAOYSA-N 0.000 description 1
- VNDWQCSOSCCWIP-UHFFFAOYSA-N 2-tert-butyl-9-fluoro-1,6-dihydrobenzo[h]imidazo[4,5-f]isoquinolin-7-one Chemical compound C1=2C=CNC(=O)C=2C2=CC(F)=CC=C2C2=C1NC(C(C)(C)C)=N2 VNDWQCSOSCCWIP-UHFFFAOYSA-N 0.000 description 1
- 241000219498 Alnus glutinosa Species 0.000 description 1
- XUKUURHRXDUEBC-KAYWLYCHSA-N Atorvastatin Chemical compound C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CC[C@@H](O)C[C@@H](O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=CC=C1 XUKUURHRXDUEBC-KAYWLYCHSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 1
- 241000254171 Curculionidae Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241000283014 Dama Species 0.000 description 1
- 240000002024 Gossypium herbaceum Species 0.000 description 1
- 235000004341 Gossypium herbaceum Nutrition 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 101100027968 Penicillium canescens olcL gene Proteins 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 241000208422 Rhododendron Species 0.000 description 1
- 101100137826 Streptococcus pneumoniae (strain ATCC BAA-255 / R6) prsA gene Proteins 0.000 description 1
- 241000159959 Takecallis sasae Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000001856 aerosol method Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 210000001217 buttock Anatomy 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 230000005058 diapause Effects 0.000 description 1
- JNSGIVNNHKGGRU-JYRVWZFOSA-N diethoxyphosphinothioyl (2z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetate Chemical compound CCOP(=S)(OCC)OC(=O)C(=N/OC)\C1=CSC(N)=N1 JNSGIVNNHKGGRU-JYRVWZFOSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- PWEVMPIIOJUPRI-UHFFFAOYSA-N dimethyltin Chemical compound C[Sn]C PWEVMPIIOJUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 235000014105 formulated food Nutrition 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical compound [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- CSHCPECZJIEGJF-UHFFFAOYSA-N methyltin Chemical compound [Sn]C CSHCPECZJIEGJF-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 238000005580 one pot reaction Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FJSOUHVHPWODGS-UHFFFAOYSA-M sodium;4-bromobenzenesulfinate Chemical compound [Na+].[O-]S(=O)C1=CC=C(Br)C=C1 FJSOUHVHPWODGS-UHFFFAOYSA-M 0.000 description 1
- UDHFNWMINVBZNA-UHFFFAOYSA-M sodium;5-bromonaphthalene-1-sulfinate Chemical compound [Na+].C1=CC=C2C(S(=O)[O-])=CC=CC2=C1Br UDHFNWMINVBZNA-UHFFFAOYSA-M 0.000 description 1
- RCZKMQBZMANREZ-UHFFFAOYSA-M sodium;5-cyclopentylnaphthalene-1-sulfinate Chemical compound [Na+].C1=CC=C2C(S(=O)[O-])=CC=CC2=C1C1CCCC1 RCZKMQBZMANREZ-UHFFFAOYSA-M 0.000 description 1
- SBXOOHSFFYHREV-UHFFFAOYSA-M sodium;5-decylnaphthalene-1-sulfinate Chemical compound [Na+].C1=CC=C2C(CCCCCCCCCC)=CC=CC2=C1S([O-])=O SBXOOHSFFYHREV-UHFFFAOYSA-M 0.000 description 1
- SGMYUXKXDMERTA-UHFFFAOYSA-M sodium;5-fluoronaphthalene-1-sulfinate Chemical compound [Na+].C1=CC=C2C(S(=O)[O-])=CC=CC2=C1F SGMYUXKXDMERTA-UHFFFAOYSA-M 0.000 description 1
- XAPAGHGHFQGMNF-UHFFFAOYSA-M sodium;5-octylnaphthalene-1-sulfinate Chemical compound [Na+].C1=CC=C2C(CCCCCCCC)=CC=CC2=C1S([O-])=O XAPAGHGHFQGMNF-UHFFFAOYSA-M 0.000 description 1
- ILLWTNFMIIPBGN-UHFFFAOYSA-M sodium;8-(2,4,4-trimethylpentan-2-yl)naphthalene-2-sulfinate Chemical compound [Na+].C1=C(S([O-])=O)C=C2C(C(C)(C)CC(C)(C)C)=CC=CC2=C1 ILLWTNFMIIPBGN-UHFFFAOYSA-M 0.000 description 1
- SFBWRGDPMDPIKZ-UHFFFAOYSA-M sodium;8-dodecylnaphthalene-2-sulfinate Chemical compound [Na+].C1=C(S([O-])=O)C=C2C(CCCCCCCCCCCC)=CC=CC2=C1 SFBWRGDPMDPIKZ-UHFFFAOYSA-M 0.000 description 1
- VDUGOCJVMLFBSW-UHFFFAOYSA-M sodium;8-ethylnaphthalene-2-sulfinate Chemical compound [Na+].C1=C(S([O-])=O)C=C2C(CC)=CC=CC2=C1 VDUGOCJVMLFBSW-UHFFFAOYSA-M 0.000 description 1
- ACZRTLXTFHGGCF-UHFFFAOYSA-M sodium;8-phenylnaphthalene-2-sulfinate Chemical compound [Na+].C12=CC(S(=O)[O-])=CC=C2C=CC=C1C1=CC=CC=C1 ACZRTLXTFHGGCF-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 150000003738 xylenes Chemical class 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/02—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing metal atoms
- A01N55/04—Tin
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2224—Compounds having one or more tin-oxygen linkages
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/691,186 US4089972A (en) | 1976-05-28 | 1976-05-28 | Organotin sulfinates as insecticides and acaricides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1064513A true CA1064513A (en) | 1979-10-16 |
Family
ID=24775495
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA254,794A Expired CA1064513A (en) | 1976-05-28 | 1976-06-14 | And organotin sulfinates as insecticides and acaricides |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4089972A (ref) |
| JP (1) | JPS52148052A (ref) |
| CA (1) | CA1064513A (ref) |
| DE (1) | DE2724089C3 (ref) |
| FR (1) | FR2352822A1 (ref) |
| GB (2) | GB1548853A (ref) |
| IL (1) | IL52185A0 (ref) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3031483A (en) * | 1957-11-18 | 1962-04-24 | Philips Corp | Method of producing organic tin compounds and preparations containing such compoundsfor combating noxious micro-organisms |
| NL96805C (ref) * | 1957-11-18 | 1900-01-01 | ||
| US3976672A (en) * | 1974-12-26 | 1976-08-24 | Uniroyal Inc. | (Hydrocarbylphenylsulfonyl)alkyltrimethylstannanes |
-
1976
- 1976-05-28 US US05/691,186 patent/US4089972A/en not_active Expired - Lifetime
- 1976-06-14 CA CA254,794A patent/CA1064513A/en not_active Expired
-
1977
- 1977-05-27 DE DE2724089A patent/DE2724089C3/de not_active Expired
- 1977-05-27 FR FR7716376A patent/FR2352822A1/fr active Granted
- 1977-05-27 IL IL52185A patent/IL52185A0/xx unknown
- 1977-05-28 JP JP6269777A patent/JPS52148052A/ja active Pending
- 1977-05-30 GB GB22747/77A patent/GB1548853A/en not_active Expired
- 1977-05-30 GB GB39441/78A patent/GB1548854A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2352822B1 (ref) | 1979-03-09 |
| JPS52148052A (en) | 1977-12-08 |
| US4089972A (en) | 1978-05-16 |
| DE2724089B2 (de) | 1979-05-23 |
| GB1548853A (en) | 1979-07-18 |
| GB1548854A (en) | 1979-07-18 |
| DE2724089A1 (de) | 1977-12-08 |
| IL52185A0 (en) | 1977-07-31 |
| FR2352822A1 (fr) | 1977-12-23 |
| DE2724089C3 (de) | 1980-01-10 |
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