JPS6157507A - Herbicide composition - Google Patents

Herbicide composition

Info

Publication number
JPS6157507A
JPS6157507A JP17898484A JP17898484A JPS6157507A JP S6157507 A JPS6157507 A JP S6157507A JP 17898484 A JP17898484 A JP 17898484A JP 17898484 A JP17898484 A JP 17898484A JP S6157507 A JPS6157507 A JP S6157507A
Authority
JP
Japan
Prior art keywords
lower alkyl
parts
diisopropyl
methyl
formula
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.)
Pending
Application number
JP17898484A
Other languages
Japanese (ja)
Inventor
Takashi Igai
猪飼 隆
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nissan Chemical Corp filed Critical Nissan Chemical Corp
Priority to JP17898484A priority Critical patent/JPS6157507A/en
Publication of JPS6157507A publication Critical patent/JPS6157507A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide a herbicide composition containing a specific pyrazolesulfonylurea derivative and bensulide, piperophos, etc., exhibiting synergistic activity, and capable of completely controlling cockspur-grass, annual weeds and perennial weeds at a low dose. CONSTITUTION:The objective composition contains (A) the compound of formula (A is lower alkyl; B is halogen or lower alkoxy; R is lower alkyl; X and Y are lower alkyl or lower alkoxy; Z is CH or N) and (B) O,O-diisopropyl-S-(2-benzenesulfonylaminoethyl)-phosphorodithioate (bensulide), N-(O,O-diisopropyl-dithiophosphoryl-acetyl)-2-methyl-piperidine (piperophos), or S-[N-(4-chlorophenyl)-N-isopropylcarbamoylmethyl]-O,O-dimethyl-dithiop hosphate. The amount of the component A is 0.001-50pts., preferably 0.001-10pts. per 1pt. of the component B.

Description

【発明の詳細な説明】 本発明は一般式(I): 〔式中^は低級アルキル基を示す。Bはハロゲン原子ま
たは低級アルコキシ基を示す、Rは低級アルキル基を示
す。XおよびYはそれぞれ独立して、低級アルキル基ま
たは低級アルコキシ基を示す。2はC)I基または窒素
原子を示す。〕 で表されるピラゾールスルボニルウレア誘導体と0.0
−ジイソプロピル−3−(2−ベンゼンスルホニルアミ
ノエチル)−ホスホロジチオエート(以下ベンスリドと
称する)、0−エチル−〇−(2−ニトロ−4−メチル
−フェニル)−N−sec−ブチルホスホロアミドチオ
エート(以下ブタミツオスと称する)、0−エチル−〇
−(2−ニトロ−4−メチル−フェニル)−N−イソプ
ロピルチオノホスホロアミデート(以下アミプロフォス
と称する。)、N−(0,0−ジイソプロピル−ジチオ
ホスホリル−アセチル)−2−メチル−ピペリジン(以
下ピペロフォスと称する)またはS−(N−(4−クロ
ロフェニル)−N−イソプロピルカルバモイルメチル)
−0,0−ジメチル−ジチオホスフェート(以下HOE
574と称する。)のうちの1種とを有効成分として含
有することを特徴とする除草剤組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention is based on the general formula (I): [In the formula, ^ represents a lower alkyl group. B represents a halogen atom or a lower alkoxy group, and R represents a lower alkyl group. X and Y each independently represent a lower alkyl group or a lower alkoxy group. 2 represents a C)I group or a nitrogen atom. ] A pyrazole sulfonylurea derivative represented by and 0.0
-diisopropyl-3-(2-benzenesulfonylaminoethyl)-phosphorodithioate (hereinafter referred to as bensulide), 0-ethyl-〇-(2-nitro-4-methyl-phenyl)-N-sec-butylphosphoro amidothioate (hereinafter referred to as Butamitsuos), 0-ethyl-〇-(2-nitro-4-methyl-phenyl)-N-isopropylthionophosphoroamidate (hereinafter referred to as amiprophos), N-(0, 0-diisopropyl-dithiophosphoryl-acetyl)-2-methyl-piperidine (hereinafter referred to as piperophos) or S-(N-(4-chlorophenyl)-N-isopropylcarbamoylmethyl)
-0,0-dimethyl-dithiophosphate (hereinafter HOE
It is called 574. ) as an active ingredient.

長年にわたる除草剤の研究開発のなかから多種多様な薬
剤が実用化され、これら除草剤は雑草防除作業の省力化
や農園芸作物の生産性向上に寄与してきた。今日におい
ても、よ/)優れた除草特性を有する新規薬剤の開発が
要望され、特に農園芸用除草剤としては、栽培作物に薬
害を及ばずことなく、対象雑草のみを選択的にかつ低薬
量で防除しうろことが望ましいが、既存の薬剤は必ずし
もこの要求を満たすものではなかった。
As a result of many years of research and development into herbicides, a wide variety of herbicides have been put into practical use, and these herbicides have contributed to labor-saving weed control operations and improved productivity of agricultural and horticultural crops. Even today, there is a demand for the development of new chemicals with excellent herbicidal properties, and in particular, as herbicides for agriculture and horticulture, they are needed to selectively target only target weeds without causing chemical damage to cultivated crops, and with low chemical It is desirable to be able to control the disease through quantitative control, but existing agents do not necessarily meet this requirement.

一般式(1)で表される化合物は従来の除草剤に比して
低薬量で優れた除草効果をあげ、なおかつイネに対して
高い安全性を有する。また、−年生イネ科雑草、−年生
広葉雑草に卓効を示すのみならず、多年生雑草にも強い
効力を示し、その有用性は大きい。
The compound represented by the general formula (1) exhibits excellent herbicidal effects at lower dosages than conventional herbicides, and has high safety against rice. Moreover, it is highly effective not only against -year-old grass weeds and -year-old broad-leaved weeds, but also against perennial weeds, making it highly useful.

また従来より知られている、ベンスリド、ブタミツオス
、アミプロツメ・ス、ピペロフォスまたはHOE574
はノビエ、−年生雑草に対し、一般式(I)で表される
化合物に比して高薬量で使用されてきたが、その結果こ
れらの薬剤で防除困難な多年生雑草の増加をもたらし、
その改善が望まれている。
In addition, conventionally known benzuride, butamitsuosu, amiprotsumesu, piperofos or HOE574
has been used in higher doses than the compound represented by formula (I) against weeds and annual weeds, but this has resulted in an increase in perennial weeds that are difficult to control with these chemicals.
Improvement is desired.

本発明者は、前記一般式(I)で表される化合物の除草
効果を増大させるべく研究を行った結果、一般式(I)
で表される化合物に、従来使用されている前記除草剤を
配合すると、それぞれの除草効果が単に相加的にえられ
るのみならず、相乗的殺草効果が現れる事を見出し本発
明を完成した。
The present inventor conducted research to increase the herbicidal effect of the compound represented by the general formula (I), and found that the compound represented by the general formula (I)
The present inventors have discovered that when the above-mentioned herbicides conventionally used are combined with the compound represented by the formula, the herbicidal effects of each herbicide are not merely additive, but also a synergistic herbicidal effect appears. .

この相乗効果は大きく、本発明組成物により、イネに対
して薬害を及ぼすこともなく、低薬量でノビエ、−年生
雑草から多年生雑草まで完全に防除でき、本発明の有用
性は非常に大きい。また特にヒエに対する殺草効果の相
乗作用は著しく、上記の混合施用によって、本発明組成
物中に含まれる従来用いられてきた前記除草剤の使用薬
量の低減をも可能とし、極めて有用性が高い。
This synergistic effect is great, and the composition of the present invention does not cause any phytotoxicity to rice, and it is possible to completely control wild weeds, annual weeds, and perennial weeds at a low dose, and the usefulness of the present invention is extremely large. . In addition, the synergistic effect of the herbicidal effect on barnyard grass is particularly remarkable, and by the above-mentioned mixed application, it is possible to reduce the amount of the conventionally used herbicides contained in the composition of the present invention, making it extremely useful. expensive.

また、本発明除草剤組成物は、雑草の発芽前および発芽
後に処理しても効果を有し、土壌処理、茎葉兼土壌処理
でも高い効果が得られる。又、イネ以外の各種穀類に対
してもを用であり、その他の畑地、果樹園などの農園芸
分野及び運動場、空き地、林地、タンクヤード、線路端
などの非農JJF地における各種雑草の防除にも適用で
き、雑草防除にあたって大きな経済的効果を示す。
Furthermore, the herbicidal composition of the present invention is effective even when treated before and after weed germination, and is highly effective when treated with soil or with both foliage and soil. It can also be used for various grains other than rice, and can be used to control various weeds in agricultural and horticultural fields such as fields and orchards, as well as non-agricultural JJF areas such as playgrounds, vacant lots, forest lands, tank yards, and railway edges. It can also be applied to plants and shows great economic effects in weed control.

本発明による組成物は、各成分の相対的活性にもよるが
、一般にはベンスリド、ブタミツオス、アミプロフォス
、ピベロフォスまたはHOE574を1重量部当たり一
般式(I)で表される化合物0.001〜50重■部、
好適には0.001〜10重景部含ん重量る。多くの場
合、本発明の配合除草剤の最高の利点は式・(’r )
で表される化合物の割合が他の除草剤よりも比較的低い
時、例えば他の除草剤1重量部当たり一般式(1)で表
される化合物が0.001〜0.1重量部のときに得ら
れる。
The composition according to the present invention generally contains 0.001 to 50 parts by weight of the compound represented by formula (I) per part by weight of bensuride, butamitsuosu, amiprofos, piverofos or HOE574, depending on the relative activity of each component. ■ Department,
The weight is preferably 0.001 to 10 times. In many cases, the greatest advantage of the combined herbicide of the invention is the formula ('r)
When the proportion of the compound represented by formula (1) is relatively lower than that of other herbicides, for example, when the compound represented by formula (1) is 0.001 to 0.1 part by weight per 1 part by weight of other herbicides. can be obtained.

適用すべき混合物の量は、多数の因子、例えば生育を阻
止すべき特定の対象植物の種類などにより左右されるが
、一般に0.001〜10Kg/haの量が普通は適当
である。当業者であれば標準化された通常のテストによ
り特に多数の実験を行わなくても適当な使用割合が容易
に決定出来る。
The amount of mixture to be applied will depend on a number of factors, such as the particular species of target plant to be inhibited, but generally amounts of 0.001 to 10 Kg/ha are usually adequate. Those skilled in the art can readily determine appropriate usage rates by routine, standardized tests without the need for extensive experimentation.

本発明組成物は、活性成分を固体または液体希釈剤から
なるキャリヤーと混合した組成物の形態で使用するのが
好ましい。組成物は更に界面活性剤を含むのが好ましい
The compositions of the invention are preferably used in the form of a composition in which the active ingredient is mixed with a carrier consisting of a solid or liquid diluent. Preferably, the composition further comprises a surfactant.

次ぎに本発明における一般式(Nで表される化合物の代
表例を第1表に示す。以下の化合物は一般式(I)で表
される化合物に包含されるものではあるが、一般式(1
)で表される化合物はこれらに限定されるものではない
Next, representative examples of compounds represented by the general formula (N) in the present invention are shown in Table 1. Although the following compounds are included in the compounds represented by the general formula (I), 1
) The compounds represented by these are not limited to these.

第1表 Me:メチル基 1ミL:エチル基 個々の活性化合物は、その除草活性にそれぞれ欠点を示
す場合が多くあるが、その場合2種の活性化合物を組合
せた場合の除草活性が、その2種の化合物の各々の活性
の華純な合計(期待される活性)よりも大きくなる場合
にこれを相乗作用という。2種の除草剤の特定組合せに
より期待される活性は、次のようにして計算することが
できる。
Table 1 Me: Methyl group 1 miL: Ethyl group In many cases, individual active compounds exhibit drawbacks in their herbicidal activity, but in such cases, the herbicidal activity when two types of active compounds are combined is When the activity of two compounds is greater than the pure sum of their respective activities (expected activities), this is called synergism. The expected activity of a particular combination of two herbicides can be calculated as follows.

(Colby S、R,除草剤の組合せの相乗及び拮抗
作用反応の計算rWeedJ 15巻20〜22頁、1
967年を参照)α:除草剤AをaKg/haの量で処
理した時の抑制率 β:除草剤BをbKc/haの量で処理した時の抑制率 E:除草剤Aをa K g / h a %除草剤Bを
bKg/haO量で処理した場合に期待される抑制率即
ち、実際の抑制率が上記計算より大きいならば組合せに
よる活性は相乗作用を示すということができる。
(Colby S, R, Calculation of synergistic and antagonistic responses of herbicide combinations rWeedJ vol. 15, pp. 20-22, 1
967) α: Inhibition rate when herbicide A is treated at a Kg/ha amount β: Suppression rate when herbicide B is treated at bKc/ha amount E: Herbicide A at a Kg/ha /ha% If the expected inhibition rate when herbicide B is treated at bKg/haO, that is, the actual inhibition rate is greater than the above calculation, it can be said that the combined activity exhibits a synergistic effect.

以下本発明を実施例によりさらに具体的に説明するが、
本発明における化合物、製剤量、剤型等は実施例のみに
限定されるものではない。
Hereinafter, the present invention will be explained in more detail with reference to Examples.
The compounds, dosage amounts, dosage forms, etc. in the present invention are not limited to the examples.

尚、「部」は全て重量部を意味する。In addition, all "parts" mean parts by weight.

配合例1 粒剤 化合物点4    −・−−−−−−−−0,2部HO
E574        1部 ベントナイト   −・・・−−−−−−−・  50
部タルク      −・・−・−−−−−−・−・4
8.8部以上を均一に混合粉砕して後少量の水を加えて
撹拌混合捏和し、押し出し式造粒機で造粒し、乾燥して
粒剤にする。
Formulation example 1 Granule compound point 4 -・---------0.2 parts HO
E574 1 part bentonite ------- 50
Part talc −・・−・−−−−−−・−・4
8.8 parts or more are uniformly mixed and pulverized, then a small amount of water is added, stirred and kneaded, granulated with an extrusion granulator, and dried to form granules.

配合例2 粒剤 化合物点5     −−−−−・−・−・・ 0.1
部アミプロフォス         3部ベントナイト
   −・−・−・−・−・−49,9部タルク   
   ・・−−−−−・〜−−−−−−−47部以上を
均一に混合粉砕して後少量の水を加えて攪拌混合捏和し
、押し出し式造粒機で造粒し、乾燥して粒剤にする。
Formulation example 2 Granule compound point 5 -------・-・-・・0.1
Part Amiprophos 3 parts Bentonite -・-・--・--・--49, 9 parts Talc
・・・・・−−−−・〜−−−−−−− After uniformly mixing and pulverizing 47 parts or more, adding a small amount of water, stirring and kneading, granulating with an extrusion granulator, and drying. and make into granules.

皿豆炎主 粒剤 化合物NcL1      ・・・・−・−・−・−・
 0.1部ピベロフォス    −・曲面−4,4部ベ
ントナイト   −・・−・−・・−50部タルク  
    −・−・・−・・−45,5部以上を均一に混
合粉砕して後少量の水を加えて攪拌混合捏和し、押し出
し式造粒機で造粒し、乾燥して粒剤にする。
Granule compound NcL1 ・・・・−・−・−・−・
0.1 part Piberophos - Curved surface - 4,4 parts Bentonite - 50 parts Talc
−・−・・−・・−45. After uniformly mixing and pulverizing 5 parts or more, adding a small amount of water, stirring and kneading, granulating with an extrusion type granulator, and drying to form granules. do.

配合例4 粒剤 化合物阻7     ・−・−・−0,1部HOE57
4   −・・・・−−−−−−・ 1.5部ベントナ
イト   −・−・・・−・・−・  50部タルク 
     −・−・・−−−−−・−・−47,5耶以
上を均一に混合粉砕して後少量の水を加えて攪拌混合捏
和し、押し出し式造粒機で造粒し、乾燥して粒剤にする
Formulation example 4 Granule compound compound 7 ・-・-・-0, 1 part HOE57
4 −・・・−−−−−・ 1.5 parts bentonite −・−・・・−・・−・ 50 parts talc
−・−・・−−−−−・−・−47, 5 or more are mixed and pulverized uniformly, then a small amount of water is added, stirred and kneaded, granulated with an extrusion type granulator, and dried. and make into granules.

配合例5 粒剤。Formulation example 5 Granules.

化合動磁2    −・・−−一−−−−−・0.15
部ベンスリド            9部ベントナイ
ト   −・・・・−−−−−−−−−−50部タルク
      −−−−−−−〜・−・40.85部以上
を均一に混合粉砕して後少量の水を加えて攪拌混合捏和
し、押し出し式造粒機で造粒し、乾燥して粒剤にする。
Combined dynamic magnetism 2 −・・−−−−−−−−・0.15
Part bensuride 9 parts Bentonite ------50 parts Talc------------- Mix and grind at least 40.85 parts uniformly, then add a small amount of water. The mixture is stirred and kneaded, granulated using an extrusion granulator, and dried to form granules.

基1信」−粒剤 化合動磁3     ・−−−−−−−−−・・ 0.
1部ブタミフォス    −・−・・−・−・   3
部ベントナイト   −・−・−−−−−−・−50部
タルク      −・−・−・−・−・46.9部以
上を均一に混合粉砕して後少量の水を加えて攪拌混合捏
和し、押し出し式造粒機で造粒し、乾燥して粒剤にする
``Basic 1 Shin'' - Granule Compound Dynamic Magnetism 3 ・---------------... 0.
Part 1 Butamiphos −・−・・−・−・ 3
Part bentonite -・-・---- Then, it is granulated using an extrusion type granulator and dried to form granules.

配合例7 粒剤 化合動磁9     −−−−−−−−−−−・0.1
5部ベンスリド     ・−・−−−−−−1,5部
ベントナイト   ・・・−・・・・・・・−・−・ 
 50部タルク      ・−・−・−・・48.3
5部以上を均一に混合粉砕して後少量の水を加えて攪拌
混合捏和し、押し出し式造粒機で造粒し、乾燥して粒剤
にする。
Formulation example 7 Granule compound dynamic magnetic 9 ----------・0.1
5 parts Bensuride ・−・−−−−−−1, 5 parts Bentonite ・・・−・・・・・・・−・−・
50 parts talc ・−・−・−・48.3
At least 5 parts are uniformly mixed and pulverized, then a small amount of water is added, stirred and kneaded, granulated using an extrusion granulator, and dried to form granules.

皿金五l 粒剤 化合物N16     −−−−−−−−−−−・ 0
.1部ピペロフォス    −・・・−−−−−−4,
4sベントナイト   ・・−・−・・・・・・−・ 
 50部タルク      ・−・−・−・ 45.5
部以上を均一に混合粉砕して後少量の水を加えて攪拌混
合捏和し、押し出し式造粒機で造粒し、乾燥して粒剤に
する。
Plate 5l Granule Compound N16 -------------・0
.. 1 part piperophos −・・・−−−−−−4,
4s bentonite ・・・-・-・・・・・・-・
50 parts talc ・−・−・−・ 45.5
After uniformly mixing and pulverizing more than one part, a small amount of water is added, the mixture is stirred and kneaded, and the mixture is granulated using an extrusion granulator and dried to form granules.

配合例9 水和剤 化合物111t18      ・・−・−・−・−・
−・0.3部ブタミフォス    ・・−一−−−−・
・−・−・−・40ジ−クライトA  −・・−・・−
−−−−・55.7部(カオリン系クレー:シーク・ラ
イト工業a零商品名)ツルポール5039 ・−−−−
−−−一・−一−−−−−・ 2部(非イオン性界面活
性剤とアニオン性界面活性剤との混合物:東邦化学9部
商品名) カープレックス(固結防止剤)−・2部(ホワイトカー
ボン:塩野義製薬■商品名)以上を均一に混合粉砕して
水和剤とする。
Formulation example 9 Wettable powder compound 111t18 ・・−・−・−・−・
−・0.3 parts Butamiphos・・−1−−−・
・−・−・−・40 Zikrite A −・・−・・−
-----・55.7 parts (Kaolin clay: Seek Light Kogyo A Zero product name) Tsurupol 5039・---
---1.--1--2 parts (Mixture of nonionic surfactant and anionic surfactant: Toho Chemical 9 Part brand name) Carplex (anti-caking agent)--2 (white carbon: Shionogi & Co., Ltd. trade name) or more is mixed and ground uniformly to make a wettable powder.

拭呈炭上 湛水条件における除草効果試験115000
アールのフグネルポット中に沖積土壌を入れた後、水を
入れて混和し水深2cmの淡水条件とする。タイヌビエ
、広葉雑草(コナギ、アゼナミキカシグサ)ホタルイの
それぞれの種子を、上記のポットに混播し、さらにウリ
カワ、ミズガヤツリ、クログワイの塊茎を置床した。さ
らに2.5葉期のイネ苗を移植した。ポットを25〜3
0℃の温室内において植物を育成し、播種後10日口重
タイヌビエが1.5葉期の時期に水面へ所定の薬量にな
るように、薬剤希釈液をメスピペットで滴下処理した。
Weeding effect test under flooded conditions on charcoal 115000
After putting alluvial soil in Earl's Hugner pot, water is added and mixed to create a freshwater condition with a water depth of 2 cm. Seeds of Japanese grasshopper, broad-leaved weeds (Japanese grasshopper, Japanese aphrodisiac), and firefly were mixedly sown in the above-mentioned pots, and tubers of Japanese grasshopper, Japanese cypress, and black bream were also placed in the beds. Furthermore, rice seedlings at the 2.5 leaf stage were transplanted. 25-3 pots
Plants were grown in a greenhouse at 0° C., and 10 days after sowing, at the 1.5-leaf stage, a diluted drug solution was dropped onto the water surface using a volumetric pipette at a predetermined dose.

 薬液滴下後3週目に各種雑草に対する除草効果を下記
の判定基準に従って調査した。
Three weeks after dropping the chemical solution, the herbicidal effect on various weeds was investigated according to the following criteria.

結果は第2表及び第3表に示す。The results are shown in Tables 2 and 3.

判定基準 5・−・殺草率 90%以上(はとんど完全枯死)4−
・殺草率 70〜89% 3− 殺草率 40〜69% 2・−・・殺草率 20〜39% 1 ・−・殺草率  5へ19% 0−・殺草率  5%以下(はとんど効力なし)但し、
上記の殺草率は、薬剤処理区の地上部生草重および無処
理区の地上部生草重を測定して下記の式により求めたも
のである。
Judgment Criteria 5: Weed killing rate 90% or more (almost complete death) 4-
・Weed killing rate 70-89% 3- Weed killing rate 40-69% 2--Weed killing rate 20-39% 1--Weed killing rate 5 to 19% 0--Weed killing rate 5% or less None) However,
The above-mentioned weed killing rate was determined by the following formula by measuring the weight of above-ground plants in the chemically treated area and the weight of above-ground plants in the non-treated area.

第3表(続き) 広狂聞1 ヒエに対する相乗効果試験 内径8cmのポリエチレン製ボットに水田土壌を充填し
、水田状態でタイヌビエを育成し、ヒエの2葉期に粒剤
に製剤した各所定の薬剤を湛水土壌処理した。ポットは
25〜30℃の温室内に置いて管理育成し、処理後30
日口重残存しているヒエの地上部生草重及び無処理区の
地上部生草重を測定し、殺草率を算出し下記の判定基準
に従って判定した。結果を第4表及び第5表に示す。
Table 3 (Continued) Kokyomon 1 Synergistic effect test on barnyard millet A polyethylene bot with an inner diameter of 8 cm was filled with paddy soil, and Japanese millet was grown in the paddy field. The drug was applied to flooded soil. The pots are placed in a greenhouse at 25-30℃ for controlled cultivation, and after treatment
The above-ground fresh grass weight of the barnyard grass remaining in the daily harvest and the above-ground fresh grass weight of the untreated area were measured, and the weed killing rate was calculated and judged according to the following criteria. The results are shown in Tables 4 and 5.

評点    殺草率 OO〜 9% 1  10〜19% 2  20〜29% 3  30〜39% 4  40〜49% 5   50〜59% 6  60〜69% 7  70〜79% 8   80〜89% 9  90〜99% 10     100% 第4表 第5表 第5表(続き) 第5表(続き) 表中、計算値は前記Co1byの式より求めた期待値を
示す。
Rating Weed killing rate OO ~ 9% 1 10-19% 2 20-29% 3 30-39% 4 40-49% 5 50-59% 6 60-69% 7 70-79% 8 80-89% 9 90- 99% 10 100% Table 4 Table 5 Table 5 (Continued) Table 5 (Continued) In the table, the calculated values indicate the expected values obtained from the Co1by formula.

以上の表から明らかなように、本発明組成物は、−i式
(1)で表される化合物及び従来公知の除草剤それぞれ
の活性のii1純な合計にとどまらず、より大きな相乗
的除草活性を有しており更にかつ低薬量で対象雑草を選
択的に完全に防除することができる。
As is clear from the above table, the composition of the present invention has not only the pure sum of the activities of the compound represented by formula (1) and the conventionally known herbicides, but also a greater synergistic herbicidal activity. Furthermore, target weeds can be selectively and completely controlled with a low dosage.

Claims (1)

【特許請求の範囲】 一般式( I ): ▲数式、化学式、表等があります▼( I ) 〔式中Aは低級アルキル基を示す。Bはハロゲン原子ま
たは低級アルコキシ基を示す、Rは低級アルキル基を示
す。XおよびYはそれぞれ独立して、低級アルキル基ま
たは低級アルコキシ基を示す。ZはCH基または窒素原
子を示す。〕 で表されるピラゾールスルホニルウレア誘導体とO,O
−ジイソプロピル−S−(2−ベンゼンスルホニルアミ
ノエチル)−ホスホロジチオエート、O−エチル−O−
(2−ニトロ−4−メチル−フェニル)−N−sec−
ブチルホスホロアミドチオエート、O−エチル−O−(
2−ニトロ−4−メチル−フェニル)−N−イソプロピ
ルチオノホスホロアミデート、N−(O,O−ジイソプ
ロピル−ジチオホスホリル−アセチル)−2−メチル−
ピペリジンまたはS−〔N−(4−クロロフェニル)−
N−イソプロピルカルバモイルメチル〕−O,O−ジメ
チル−ジチオホスフェートのうちの1種を有効成分とし
て含有することを特徴とする除草剤組成物。
[Claims] General formula (I): ▲There are numerical formulas, chemical formulas, tables, etc.▼(I) [In the formula, A represents a lower alkyl group. B represents a halogen atom or a lower alkoxy group, and R represents a lower alkyl group. X and Y each independently represent a lower alkyl group or a lower alkoxy group. Z represents a CH group or a nitrogen atom. ] Pyrazole sulfonylurea derivative represented by O, O
-diisopropyl-S-(2-benzenesulfonylaminoethyl)-phosphorodithioate, O-ethyl-O-
(2-nitro-4-methyl-phenyl)-N-sec-
Butyl phosphoramidothioate, O-ethyl-O-(
2-Nitro-4-methyl-phenyl)-N-isopropylthionophosphoroamidate, N-(O,O-diisopropyl-dithiophosphoryl-acetyl)-2-methyl-
piperidine or S-[N-(4-chlorophenyl)-
1. A herbicidal composition comprising one of N-isopropylcarbamoylmethyl]-O,O-dimethyl-dithiophosphate as an active ingredient.
JP17898484A 1984-08-28 1984-08-28 Herbicide composition Pending JPS6157507A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17898484A JPS6157507A (en) 1984-08-28 1984-08-28 Herbicide composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17898484A JPS6157507A (en) 1984-08-28 1984-08-28 Herbicide composition

Publications (1)

Publication Number Publication Date
JPS6157507A true JPS6157507A (en) 1986-03-24

Family

ID=16058078

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17898484A Pending JPS6157507A (en) 1984-08-28 1984-08-28 Herbicide composition

Country Status (1)

Country Link
JP (1) JPS6157507A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988002598A1 (en) * 1986-10-10 1988-04-21 E.I. Du Pont De Nemours And Company Herbicidal mixtures

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988002598A1 (en) * 1986-10-10 1988-04-21 E.I. Du Pont De Nemours And Company Herbicidal mixtures

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