• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    This invention relates to a chemical plant protection agent against the harmful effects of insects and mites. The invention allows to increase the effectiveness of the proposed composition due to the fact that it contains, in wt%: pyrazoline derivatives of the formula @ where X-OCH 2 CF 3 or OCH 2 @, Y-CL or OCHF 2 20 isophorone 75 and a mixture of nonylphenylpolyoxyethylene with calcium dodecylbenzenesulfonate 5. Table 7.
    公开号:SU1612985A3
    申请号:SU864028674
    申请日:1986-12-19
    公开日:1990-12-07
    发明作者:Не Харриберт；Бюманн Ульрих；Вегнер Петер；Йоппиен Хартмут；Джайлес Дэвид；Понт Роусон Грэхэм
    申请人:Шеринг Аг (Фирма)；
    IPC主号:
    专利说明:

    Table 3
    0 "С-МН- Вг
    wanted (3) (1) (2)
    a little
    CFjCH O
    “H. 0-C-NHHQ-OCHF2
    SGS1-C
    6 C-MnnOk-C1
    0,0004 0,00016
    0,0004 0,00016
    0,0004 0,00016
    C-O GuSya I 0,000473
    Y0,0001657
    0 C-NHHQ) -F
    SGSSNO.O-OtTT S oy (3)
    V
    0 "C-4H-Q-OCHr,
    a-f - -r-Oci
    s (y
    0
    Y
    0 C-NH, Compound
    Proposed
    CTjCHjO-O-rT -F
    Y oj
    0 C-NHHQ -Ct
    ci-o-yuT Famous W
    o c-NH-O-ci
    The same
    0 C-NH-F
    Table 4



    100 100
    95 83
    93 70
    Table 5
    2.5
    2.5 2.5
    50
    Table 6
    Concentration of biologically active substance,%

    80
    0.1 0.1
    20
    20
    g g Proposed (1) X „)
    CHjO
     same (2).
    SGSSN About
    The same (3)
    0-C-NH-O CI
    CTjCH o-Q -O-f
    O-C-NH- -OCHFj
    Known
    Table 7
    0.1
    98
    O -0 C-KOOSNG7
    m:
    0.1
    100
    0.1
    100
    0.1
    thirty
    权利要求:
    Claims (1)
    [1]
    Claim
    Insehtoacaricidal composition comprising a pyrazoline derivative as an active principle, a liquid carrier and a surfactant, characterized in that, in order to increase the effectiveness, it contains a compound of the formula as a pyrazoline derivative
    Isophorone is used as a liquid carrier, and a mixture of nonylphenylpolyoxyethylene with calcium dodecylbenzenesulfonate in the following ratio of components, wt.%, as a surfactant in the following ratio of components:
    Pyrazoline derivative '20
    Isoforoc 75
    A mixture of nonylphenylpolyoxyethylene with calcium dodecyl benzene sulfonate 5
    five
    1612985
    6
    T a gb l and c a 1
    Compound X Υ T, pl., ° C YY one osn 2 - ^ osng 154-155 2 OCH ^ SGS C1 180 3 est r cr 3Osng 2153-154
    table 2
    Compound
    Concentration Death, biolo% of active substance,%
    Proposed
    e cr 3 en 2 0-O ^^ yO-g
    0.1 to
    Known
    about "s- ~ w- £ usng g
    '-H ^ a
    Ο = ΟΝΗ40-Γ
    ο, ι о
    Table 3
    Compound Concentration Act, biologically % active substances,%
    Proposed
    os-sh-o-osnb
    0 "С-УН-ф-Вг
    Known
    : o - ^ - in-f-osng,
    0.040 thirty 0.016 25 0.040 thirty 0.016 0 0.040 20 0.016 ten 0.040 0 0.016 0
    7
    1612985 '8
    Table 4
    Compound Concentration Act biologically later 7 active substance,% 48 h, 7,
    Proposed
    The same (1)
    TC same (2)
    (3)
    OS-UN-0-G
    Gg
    About "C-KK-0-OCHD 2
    0.0004
    0,00016
    0.0004
    0,00016
    100
    100
    95
    83
    Known
    Compound
    <* 3 g of CH <2> ^ C> -r
    0 = С-Ш ~ О-С1
    I
    Ο "€ -ΝΗ-0-Γ
    0.0004
    0,00016
    0.0004
    0,00016
    73
    57
    93
    70
    Table 5
    The concentration of biologically active substances, million ~ 1Act,7a
    oneProposed СГзСН г 0-О ^ уО-Г. Ο'-Ο-ΝΗ-θ-ΟΟΗΓ, 2.5 50 Known ΟΟ-ΝΗ-θ-Βη 2.5 0 ο = ς-ΝΗ-θ-Γ 2.5 0
    Table 6
    .Compound
    The concentration of biologically active substances,%
    Ovicidal
    act,
    7, with
    Proposed
    Known
    • Also
    p / o 1
    ι „ υ » 1
    0 = C-MN- {US1
    “O ^ gu-Os, 0> |
    o = c-in £ £ Us1
    ABOUT,,
    OS-ΝΗ-θ-τ "
    80
    20
    20
    9
    1612985
    ten
    Compound
    .3.
    Table 7
    The concentration of biologically active substances,%
    • η
    Ovicidal action,%
    Proposed About "S-YN-0-OSNG 70.1 98 The same (2). 0 “С-МН-О-С1 0.1 100 The same (3) OzNGO-O ^ r-yO-g O-C-YN-0-OSNG g ν 4γ Ο'ό-ΝΗ - ^ - εΐ 0.1 100 Known 0.1 thirty
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    同族专利:
    公开号 | 公开日
    IL81002A|1991-07-18|
    EP0227055A1|1987-07-01|
    JPS62228064A|1987-10-06|
    US4888340A|1989-12-19|
    DD259996A5|1988-09-14|
    DK611686D0|1986-12-18|
    DK166208C|1993-08-16|
    CA1283111C|1991-04-16|
    ZA869269B|1987-07-29|
    IE59522B1|1994-03-09|
    CS960586A2|1988-01-15|
    MX168494B|1993-05-27|
    CN86108628A|1987-07-01|
    AT65994T|1991-08-15|
    HUT45021A|1988-05-30|
    ZW24786A1|1987-06-17|
    PH24969A|1990-12-26|
    DE3545786A1|1987-06-25|
    GR3003067T3|1993-02-17|
    AU600688B2|1990-08-23|
    IE863330L|1987-06-21|
    KR940008289B1|1994-09-10|
    FI87773B|1992-11-13|
    FI87773C|1993-02-25|
    MW8086A1|1987-12-09|
    BR8606336A|1987-10-06|
    KR870006001A|1987-07-08|
    DK611686A|1987-06-22|
    PT83961B|1989-05-12|
    PT83961A|1987-01-01|
    CS258495B2|1988-08-16|
    OA08455A|1988-06-30|
    ES2040208T3|1993-10-16|
    EG18334A|1992-11-30|
    CN1013671B|1991-08-28|
    NZ218642A|1990-02-26|
    FI865233A0|1986-12-19|
    HU204790B|1992-02-28|
    DK166208B|1993-03-22|
    IL81002D0|1987-03-31|
    EP0227055B1|1991-08-07|
    DE3680772D1|1991-09-12|
    AU6680586A|1987-06-25|
    FI865233A|1987-06-22|
    引用文献:
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    DE4218745A1|1992-06-04|1993-12-09|Schering Ag|1-pyrazoline|NL158178B|1974-07-12|1978-10-16|Philips Nv|METHOD OF PREPARING INSECTICIDE PREPARATIONS CONTAINING A PYRAZOLINE DERIVATIVE, SO PREPARED PREPARATIONS, AND METHOD OF PREPARING PYRAZOLINE DERIVATIVES WITH INSECTICIDE ACTION.|
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    EP0004733A3|1978-03-31|1979-10-31|Imperial Chemical Industries Plc|Diaryl substituted pyrazoline carboxanilides, processes for preparing them, insecticidal compositions and uses thereof, and intermediates therefor|
    EP0021506B1|1979-07-03|1983-09-07|Duphar International Research B.V|New pyrazoline derivatives, method of preparing the new compounds, as well as insecticidal composition on the basis of these new compounds|
    US4540706A|1981-02-17|1985-09-10|Nissan Chemical Industries Ltd.|Insecticidal 1-N-phenylcarbamoyl-3--4-phenyl-2-pyrazoline derivatives|
    GB2093836B|1981-02-17|1984-09-05|Nissan Chemical Ind Ltd|Insecticidal pyrazoline derivatives|
    JPH0143748B2|1981-02-17|1989-09-22|Nissan Chemical Ind Ltd|
    US4407813A|1981-02-17|1983-10-04|Nissan Chemical Industries Ltd.|Insecticidal pyrazoline derivatives and composition|
    JPS57209275A|1981-06-19|1982-12-22|Nissan Chem Ind Ltd|Novel pyrazoline derivative, its preparation, and vermin-controlling agent containing said derivative as active component|
    JPH0339060B2|1982-01-14|1991-06-12|Nissan Chemical Ind Ltd|
    JPS58128374A|1982-01-26|1983-07-30|Nissan Chem Ind Ltd|Novel pyrazoline derivative, its preparation and agent for controlling noxious life containing said derivative as active component|
    EP0113213B1|1982-12-30|1988-04-06|Schering Agrochemicals Limited|Pyrazoline insecticides|
    JPS59137462A|1983-01-28|1984-08-07|Nissan Chem Ind Ltd|Novel pyrazoline derivative and insecticide|
    US4663341A|1984-02-16|1987-05-05|Rohm And Haas Company|Insecticidal n-aryl-3-aryl-4,5-dihydro-1h-pyrazole-1-carboxamides|
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    ZA858002B|1984-10-25|1987-04-29|Fmc Corp|Pyrazoline insecticides|
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    US5116850A|1987-11-30|1992-05-26|E. I. Du Pont De Nemours And Co.|Heterocyclic pyrazoline carboxanilides|
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    ES2143459T3|1990-07-13|2000-05-16|Rohm & Haas|4,5-DIHIDRO-1H-PIRAZOL-1-CARBOXAMIDAS N-ARIL-3-ARIL-4 SUBSTITUTED AND PROCEDURES FOR ITS PRODUCTION.|
    US5250532A|1991-04-11|1993-10-05|Dowelanco|3,4,N-trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insecticides|
    US5493024A|1991-04-11|1996-02-20|Dowelanco|3,4,N-trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insectioides|
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    US5338856A|1992-08-17|1994-08-16|Dowelanco|3,4-N,trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insecticides|
    DE4318938A1|1993-05-27|1994-12-01|Schering Ag|Substituted pyrazolines|
    DE4403788C1|1994-02-03|1995-10-26|Hoechst Schering Agrevo Gmbh|Substituted pyrazoline|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DE19853545786|DE3545786A1|1985-12-21|1985-12-21|Pyrazoline derivatives, their preparation, and their use as insecticides|
    DE19863628647|DE3628647A1|1986-08-22|1986-08-22|Pyrazoline derivatives, their preparation, and their use as insecticides and acaricides|
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