Rodent repellent powders and preparation thereof
    14.
    发明授权
    Rodent repellent powders and preparation thereof 失效
    啮齿动物驱避粉末及其制备方法

    公开(公告)号:US4025643A

    公开(公告)日:1977-05-24

    申请号:US543638

    申请日:1975-01-23

    申请人: Paul F. Warner

    发明人: Paul F. Warner

    IPC分类号: A01N47/24 A01N9/12 A01N9/20

    摘要: Free-flowing rodent repellent powders are provided in which a rodent repellent effective N,N-dialkyl-sulfenyl dithiocarbamate is admixed with a chemically inert grinding aid having a density of 5 pounds per cubic foot or less to form a non-caking composition. A solids suspending agent, inert to the N,N-dialkyl-sulfenyl dithiocarbamate, and a wetting agent are admixed with the rodent repellent and the grinding agent to produce a water-dispersible, free-flowing powder. The composition is an effective rodent repellent as a dry powder of two components, as a dispersible powder of four components, or as an aqueous disperson. A method is provided for preparing the free-flowing powder which entails grinding crystals of the N,N-dialkyl-sulfenyl dithiocarbamate with the low-density grinding aid or in combination with the solids suspending agent and the wetting agent for up to about 15 minutes.

    摘要翻译: 提供了自由流动的灭鼠剂,其中将具有驱虫能力的有效N,N-二烷基 - 亚磺酰基二硫代氨基甲酸盐与密度为5磅/立方英尺或更小的化学惰性研磨助剂混合以形成非结块组合物。 将与N,N-二烷基 - 亚磺酰基二硫代氨基甲酸盐惰性的固体悬浮剂和润湿剂与啮齿动物驱避剂和研磨剂混合以产生水分散性自由流动的粉末。 该组合物是作为两种组分的干粉末的有效的啮齿动物驱避剂,作为四种组分的可分散粉末,或作为水性分散体。 提供了一种制备自由流动粉末的方法,其需要用低密度研磨助剂研磨N,N-二烷基 - 亚磺酰基二硫代氨基甲酸盐的晶体,或与固体悬浮剂和润湿剂组合研磨长达约15分钟 。

    Carbamates
    15.
    发明授权
    Carbamates 失效
    氨基甲酸酯

    公开(公告)号:US4012435A

    公开(公告)日:1977-03-15

    申请号:US762144

    申请日:1968-09-24

    申请人: Erwin Nikles

    发明人: Erwin Nikles

    IPC分类号: C07C125/06

    摘要: The invention comprises [5,8-dihydro-5,8-endomethylene-1-naphthyl]-carbamates and their use in pesticides.

    摘要翻译: 本发明包括[5,8-二氢-5,8-亚甲基-1-萘基] - 氨基甲酸酯及其在农药中的用途。

    Chrysanthemic acid esters
    18.
    再颁专利

    公开(公告)号:USRE28110E

    公开(公告)日:1974-08-13

    申请号:US28110D

    IPC分类号: A01N53/10

    摘要: THE INVENTION COMPRISES CHRYSANTHEMIC ACID ESTER COMPOUNDS OF THE FORMULA 1,1-DI(H3C-),2-(Y-OOC-),3-((H3C)2-C=CH-)-CYCLOPROPANE WHEREIN Y IS THE MOIETY R2-C(-R3)=C(-R1)-CH2-C*C-CH2(R5-C(-R6)=C(-R4)-CH2-CH=CH-CH2)HC*C-CH2-C*C-CH2- OR (R7)-(R4-1,2-PHENYLENE)-CH2-C*C-CH2WHEREIN R1-R4(R7) IS HYDROGEN OR AN ALKYL GROUP. THE COMPOUNDS OF FORMULA 1 ARE USEFUL AS INSECTICIDES AND ARE PREPARED BY REACTING AN ACID CHLORIDE WITH ALCOHOL OR BY REACTING A HALIDE WITH A SALT OF A CHRYSANTHEMUM CARBOXYLIC ACID.

    N-phenylsuccinimides
    19.
    发明授权
    N-phenylsuccinimides 失效
    N-PHENYLSUCCINIMIDES

    公开(公告)号:US3804856A

    公开(公告)日:1974-04-16

    申请号:US17671371

    申请日:1971-08-31

    CPC分类号: C07D207/416 Y10S514/949

    摘要: A NOVEL N-PHENYLSUCCINIMIDE DERIVATIVE HAVING THE FORMULA,

    1-(2-R,6-R'',(X)N-PHENYL),3-(R"-S(=O)M-)PYRROLIDINE-2,5-

    DIONE

    WHEREIN R AND R'' ARE INDIVIDUALLY HALOGEN OR A LOWER ALKYL, X IS HALOGEN, A LOWER ALKYL, A LOWER ALKOXY OR NITRO, R" IS AN ALKYL HAVING 1 TO 10 CARBON ATOMS, AN ALKENYL, A GROUP OF THE FORMULA,

    (Q-PHENYL)-(CH2)L-

    WHEREIN Q IS HYDROGEN, HALOGEN, A LOWER ALKYL, A LOWER ALKOXY OR NITRO, AND L IS 1, 2, 3 OR 4, A GROUP OF THE FORMULA,

    Z-PHENYL

    WHEREIN Z IS HYDROGEN, HALOGEN, A LOWER ALKYL, A LOWER ALKOXY OR NITRO, A-FURFURYL OR A GROUP OF THE FORMULA, -CH2COOR'''''' WHEREIN R'''''' IS A LOWER ALKYL, N IS 0, 1, 2 OR 3, AND M IS 0, 1 OR 2, EXHIBITS AND EXTREMELY STRONG MICROBICIDAL ACTIVITY ON A MARKEDLY WIDE SCOPE OF MICROORGANISMS AND HAS A LOW TOXICITY. THE ABOVE-MENTIONED COMPOUND CAN BE PREPARED BY THE ADDITION REACTION OF AN N-PHENYLMALEIMIDE DERIVATIVE REPRESENTED BY THE FORMULA,

    1-(2-R,6-R'',(X)N-PHENYL)-3-PYRROLINE-2,5-DIONE

    WITH A COMPOUND REPRESENTED BY THE FORMULA

    R''''SH

    OR BY THE OXIDATION OF A COMPOUND OF THE FORMULA,

    1-(2-R,6-R'',(X)N-PHENYL),3-(R"-S-)PYRROLIDINE-2,5-DIONE

    WHICH IS OBTAINED BY THE ABOVE-MENTIONED REACTION. ALTERNATIVELY, THE SAID NOVEL N-PHENYLSUCCINIMIDE DERIVATIVE CAN BE PREPARED BY DEHYDRATING AND RING-CLOSING A COMPOUND OF THE FORMULA,

    (2-R,6-R'',(X)N-PHENYL)-NH-CO-CH(-S(=O)M-R")-CH2-COOH OR

    (2-R,6-R'',(X)N-PHENYL)-NH-CO-CH2-CH(-S(=O)M-R")-COOH

    N-phenylmaleimide derivatives
    20.
    发明授权
    N-phenylmaleimide derivatives 失效
    N-苯甲酰亚胺衍生物

    公开(公告)号:US3743654A

    公开(公告)日:1973-07-03

    申请号:US3743654D

    申请日:1969-09-11

    摘要: NOVEL N-PHENYLMALEIMIDE DERIVATIVES PREFERABLE AS MICROBICIDES WHICH ARE REPRESENTED BY THE FORMULA

    1-(2,5-DI(O=),4-R1-1,5-DIHYDRO-2H-PYRROL-1-YL),3,5-DI(X-),

    4-R2-BENZENE

    WHEREIN R1 REPRESENTS A HYDROGEN ATOM, A HALOGEN ATOM, A LOWER ALKYL GROUP OR A PHENYL GROUP, WHICH MAY HAVE BEEN SUBSTITUTED BY A HALOGEN ATOM; R2 REPRESENTS A HYDROGEN ATOM, A LOWER ALKYL GROUP OR A HALOGEN ATOM; AND X REPRESENTS A HALOGEN ATOM, PROVIDED THAT IN CASE R1 AND R2 ARE HYDROGEN ATOMS, X REPRESENTS OTHER HALOGEN ATOM THAN A CHLORINE ATOM. EXAMPLES OF SUCH DERIVATIVES ARE: N-(3'',5''-DI-BROMO OR IODO-PHENYL) MALEIMIDES, N-(3'',4'',5''-TRIHALOGENOPHENYL) MALEIMIDES, N-(3'',5''-DIHALOGENO-4''-ALKYLPHENYL) MALEIMIDES, N-(3'',5''-DIHALOGENOPHENYL)-3-METHYLMALEIMIDES, N-(3'',5''-DIHALOGENOPHENYL)-3-PHENYLMALEIMIDES, AND N-(3'',5''-DIHALOGENOPHENYL)-3-(HALOGENOPHENYL) MALEIMIDES. THESE COMPOUNDS ARE PREPARED BY CYCLIZING CORRESPONDING MALEIC ACID MONOANILIDES UNDER DEHYDRATION CONDITIONS.