JPS61233604A - Herbicide composition - Google Patents

Herbicide composition

Info

Publication number
JPS61233604A
JPS61233604A JP60074961A JP7496185A JPS61233604A JP S61233604 A JPS61233604 A JP S61233604A JP 60074961 A JP60074961 A JP 60074961A JP 7496185 A JP7496185 A JP 7496185A JP S61233604 A JPS61233604 A JP S61233604A
Authority
JP
Japan
Prior art keywords
parts
compound
benzyl
alkyl
lower alkyl
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.)
Granted
Application number
JP60074961A
Other languages
Japanese (ja)
Other versions
JPH0477721B2 (en
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 JP60074961A priority Critical patent/JPS61233604A/en
Priority to KR1019860001105A priority patent/KR930002954B1/en
Publication of JPS61233604A publication Critical patent/JPS61233604A/en
Publication of JPH0477721B2 publication Critical patent/JPH0477721B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To provide the titled composition containing a pyrazolesulfonylurea dericative and S-benzyl-N-ethyl-N-(1,2-dimethylpropyl)-thiolcarbamate, etc., having synergistic activity and capable of selectively and completely controlling the objective weeds at a low rate of application. CONSTITUTION:The objective herbicide composition contains (A) a pyrazolesulfonylurea derivative of formula (A is alkyl; B is H, alkyl, halogen or alkoxy; R is alkyl; X and Y are alkyl or alkoxy; Z is CH or N) and (B) S-benzyl-N-ethyl-N-(1,2-dimethylpropyl)-thiolcarbamate or S-benzyl-N-di-n- propyltiolcarbamate. The amount of the compound of formula is preferably 0.001-50 pts. wt., especially 0.001-10 pts. wt. per 1 pt. wt. of the compound B.

Description

【発明の詳細な説明】 本発明は一般式(I): 〔式中Aは低級アルキル基を示す。Bは水素原子、低級
アルキル基、ハロゲン原子または低級アルコキシ基を示
す。P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C11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S−ヘンシル−N
−エチル−N−(1,2−ジメチルプロピル)−チオー
ルカーバメート(以下化合物Aと称する)またはS−ベ
ンジル−N−ジ−n−プロピルチオールカーバメート(
以下化合物Bと称する)のいずれかをとを有効成分とし
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, A represents a lower alkyl group. B represents a hydrogen atom, a lower alkyl group, a halogen atom, or a lower alkoxy group. P represents a lower alkyl group. X and Y each independently represent a lower alkyl group or a lower alkoxy group. 2 represents a C11 group or a nitrogen atom. ] pyrazolesulfonylurea derivative and S-hensyl-N
-ethyl-N-(1,2-dimethylpropyl)-thiol carbamate (hereinafter referred to as compound A) or S-benzyl-N-di-n-propylthiol carbamate (
The present invention relates to a herbicidal composition containing any one of the following (hereinafter referred to as compound B) 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/r
薬剤が実用化され、これら除草剤は5KI(草防除作業
の省力化や農園芸作物の生産性向にに寄りしてきた。今
日においても、より優れた除#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G剤、として4:I:
、 i、’j、培作物に薬害を及はずごとlζく、対象
Xf草のめを選択的にかつ仙薬Mで防除しうるごとか望
ましいが、既存の薬剤は必ずしもこの要ン1〈を満たず
ものではなかった。
A wide variety of herbicide research and development over many years /r
As herbicides have been put into practical use, these herbicides have focused on the 5KI (labor saving in weed control work and productivity of agricultural and horticultural crops).Even today, there is a demand for the development of new herbicides with better weed control properties. , especially as a G remover for agriculture and horticulture, 4:I:
, i, 'j, It is desirable that the target Xf grass can be selectively controlled with the herbal medicine M, as it is unlikely to cause phytotoxicity to cultivated crops, but existing drugs do not necessarily meet this requirement 1. It wasn't a joke.

−・般r((1)で表される化合物は従来の除債剤にI
t L、て低薬量で1yれた除草効果をあ(J、なおか
つイネ1こり・1して高い安全性を有する。また、−年
生イネ11雑ηl、−年生広葉雑草に小効を示すのみな
らず、多年生jft草にも強い効力を示し、その有用性
番;1大きい。
-・General r (The compound represented by (1) is used as a conventional debt relief agent.
tL has a weeding effect of 1y at a low dose (J, and has a high safety level of 1.1 in rice plants. It also shows a small effect on 11 miscellaneous ηl of -year-old rice and -year-old broad-leaved weeds. It also shows strong efficacy against perennial JFT grass, and its usefulness is number 1.

一力化合物△J−夕よび化合物BLJノヒエ、−・年生
雑草に対し一般式(1)で表される化合物に比して高薬
陀で使用されるがその結果これらの薬剤で防除田デ1r
な多年生jiff、 47jの増加をもたらし改善が望
まれている。
The compound △J-Yuyo and the compound BLJ Nohie are used at a higher drug dose than the compound represented by the general formula (1) against annual weeds, but as a result, these drugs can be used to control rice fields.
This has led to an increase in perennial jiff, 47j, and improvements are desired.

本発明者圓、前記一般式(1)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(1)
で表される化合物に、化合物Aまたは化合物Bを配合す
ると、それぞれの除醒効果か単に相加的にえられるのみ
ならず、相乗的殺草効果か現れる事を見出し本発明を完
成した。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はずこともなく、低薬量でノヒエ、
−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極めて有用性が高い。
The present inventor, En, conducted research to increase the herbicidal effect of the compound represented by the general formula (1), and found that the compound represented by the general formula (1)
The present invention was completed by discovering that when Compound A or Compound B is blended with the compound represented by the formula, not only the respective agronomic effects are obtained additively, but also a synergistic herbicidal effect appears. This synergistic effect is large, and the composition of the present invention does not cause any phytotoxicity to rice;
- The present invention is extremely useful as it can completely control both annual and perennial weeds. In particular, the synergistic herbicidal effect on barnyard grass is extremely useful.

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、草葉兼土壌処理
でも高い効果か得られる。又、イネ以外の各種穀類に対
しても有用であり、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
などの非農耕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 high effects can be obtained even when treated with soil or when treated with grass and soil. It is also useful for various grains other than rice, and can also be used to control various weeds in agricultural and horticultural fields such as fields and orchards, as well as in non-agricultural areas such as playgrounds, vacant lots, forest areas, tank yards, and railway edges. applicable,
Shows great economic effect in weed control.

本発明による組成物は、各成分の相対的活性にも、J、
るか、−・般には化合物Aまたは化合物131重量部当
たり一般式(1)で表される化合物を0.001へ50
屯量部、好適には0.001〜10重量部含んでいる。
Compositions according to the invention also have the relative activity of each component, J.
or - Generally, the compound represented by the general formula (1) is added to 0.001 to 50 parts by weight of compound A or compound (131 parts by weight).
It contains 0.001 to 10 parts by weight, preferably 0.001 to 10 parts by weight.

適用ず−、き混合物の量は、多数の因子、例えば生育を
fill +l−ずべき時定の対象植物の種類などによ
り左右されるか、一般に0.001〜1Kg/haの量
か昔11TIは適当である。当業者であれば標準化され
た通常のテスI〜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。
However, the amount of the mixture depends on a number of factors, such as the type of plant to be filled and the amount of time the growth should be adjusted. Appropriate. A person skilled in the art can easily determine an appropriate usage rate using a standardized ordinary test I without performing a large number of experiments.

不発明組酸物番J、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。
Preferably, the active ingredient is 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.

次きに本発明におiJる一般式(1)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か、−fr
t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, Table 1 shows representative examples of the compounds represented by the general formula (1) according to the present invention. The following compounds have general formula (I)
Is it included in the compound represented by -fr?
The compounds represented by formula (1) are not limited to these.

第1表 Me二メチル)l;:[:t:エチル基個々の活性化合
物シ31、その除草活性にそれぞ狛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3.目金ゼた場
合の除争活性が、その2種の化合物の各々の活性の11
1純な合口(3!JI持される活性)、[、リノ)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・Uにより期待される活1ノ目11、次のように
して計算することができる。
Table 1 Medimethyl)l;:[:t:Ethyl group Individual active compounds 31 In many cases, their herbicidal activity shows some drawbacks, but in such cases, two types of active compounds are combined. The elimination activity in case of blindness is 11 of the activity of each of the two types of compounds.
1. When the pure aguchi (3! JI retained activity), [, Reno) increases, this is called synergism. The expected activity of a specific combination of two herbicides/U can be calculated as follows.

(Colby S、R,除草剤の糾合−Uの相乗及び拮
抗作用反応の51算r Weed 、、I 15巻20
〜22頁、1967年を参照)(χ:除草剤AをaKg
/haの量で処理した時の1丁11制率 β:除草剤BをbKg/haの量で処理した時の抑制率 E:除草剤AをaKg/ha、除草剤Bをbkg/ha
の量で処理した場合に101持される抑制率即ち、実際
の抑制率が−1−記計算より大きいならば組合セによる
活性は相乗作用を示すということができる。
(Colby S, R, 51 Calculations of Synergistic and Antagonistic Reactions of Herbicide Combinations-U Weed,, I Vol. 15, 20
~22, 1967) (χ: aKg of herbicide A)
1/11 control rate β when treated at an amount of /ha: Suppression rate E when treated with herbicide B at an amount of bKg/ha: aKg/ha of herbicide A, bkg/ha of herbicide B
If the inhibition rate maintained by 101 when treated with an amount of 101, that is, the actual inhibition rate is greater than the calculated value of −1−, then it can be said that the activity by the combination 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」ば全て重量部を意味する。In addition, all "parts" mean parts by weight.

配5介例−1−粒剤 化合物Na1−−−−0.07部 化合物A       −−−−−7部ヘントナイト 
    −−50部 タルク       −−−42,93部以上を均一に
混合わ)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。
Example 5 - Granules Compound Na1 --- 0.07 parts Compound A --- 7 parts Hentonite
--- 50 parts of talc --- 42.93 parts or more are mixed uniformly) After crushing, add a small amount of water, mix and knead, granulate with an extrusion type granulator, and dry to form granules. Make it.

俣治・例−?−粒剤 化合動歯2     −−−−−−−0.05部化合物
A       −−−−−10部ヘントナイト   
 〜 −−50部 タルク            39.95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。
Osamu Mata/Example-? - Granule Compound Moving Tooth 2 -------0.05 parts Compound A ----10 parts Hetonite
~ --50 parts of talc 39.95 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. .

配涜例−?−粒剤 化合物No3     −     (1,03部化合
物A      ’−−−−一一−6部ヘントナイt 
    −−−−中−43,97部タルク      
  −−一=−、50部以上を均一に混合わ)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。
Example of sacrilege? - Granule Compound No. 3 - (1,03 parts Compound A'---11-6 parts Hentonite
----- Medium-43,97 parts talc
--1=-, 50 parts or more are uniformly mixed) After crushing, a small amount of water is added, stirred and kneaded, granulated with an extrusion type granulator, and dried to form granules.

促合例−4−粒剤 化合動歯4     =−−〜−−−−−0、]部部会
合物       −−−−8部 ヘントナ・イト    −−−−−−41,9部タルク
            50  部以」−を均一にl
■L合↑5)砕して後生h↓の氷を加えて攪拌混合捏和
し、押し出し式潰粒機−(造簿カし、乾燥して粒剤にす
る。
Promotion example - 4 - Granule compound moving tooth 4 =--~------0,] parts association substance --- 8 parts hentonaite --- 41,9 parts talc 50 parts uniformly
■L ↑ 5) Crush, add ice of raw h↓, stir, mix and knead, crush with extrusion type crusher (roller), and dry to make granules.

遭d合−例−へ−rl剤 化合物1t、5          0.07部化合物
A       −9部 −・ン]・ナイト     −−50部タルク    
        40.93部以−1−を均一に混合粉
砕して後少量の水を加えて攪拌混合)1p和し、押し出
し式造粒機で造粒し、乾燥して粒剤にする。
Example: 1 ton of RL agent compound, 5 0.07 parts Compound A - 9 parts Night - 50 parts Talc
After 40.93 parts or more are uniformly mixed and pulverized, a small amount of water is added and the mixture is stirred and mixed to 1p, granulated using an extrusion granulator, and dried to form granules.

筒「1例」ト 粒剤 化合物No、6     −−−0.05部化合物B 
      −6部 ヘントナイ1〜   −−28.95部タルク    
   −    (i5  部以上を均一に混合わ)砕
して後少量の水を加えて)脣拌混合程和し、押し出し式
造)1“1機−(造’l+7 シ、乾燥して粒剤にする
Cylinder "1 example" G Granule Compound No. 6 --- 0.05 part Compound B
-6 parts Hentonai 1~--28.95 parts Talc
- (Mix 15 parts or more evenly) Crush and add a small amount of water) Stir gently to soften, extrusion method) do.

O 配−合例ユ li:L斉11 化合物No、7          0.03部化fj
物B           5 部−\ントナイ1. 
   、、、、、、、−、、、、 25   部タルク
       −−、69,97部以上を均一に混合粉
砕して後少量の水を加えて撹↑1:混合程和し、押し7
出し式造粒機で造粒し、乾燥して粒剤にずろ。
O Combination Example Yu li:L 11 Compound No., 7 0.03 part fj
Item B 5 parts-\Toni 1.
, , , , , , - , , 25 parts talc --, 69,97 parts or more are mixed and crushed uniformly, then a small amount of water is added and stirred ↑ 1: Mix and soften, press 7
It is granulated using a dispensing type granulator, dried and made into granules.

配合インII 、Ej−粒剤 化合物No、8     −−−−0.07部化合物I
3     −−− 7 部 ヘントナイ1   −−−−−−−20 部タルク  
     −−−−72.93部以」−を均一に混合わ
]砕して後少量の水を加えて撹拌混合捏和し、押し7出
し式造粒機で造粒し、乾燥して粒剤にする。
Blend In II, Ej-Grain Compound No. 8 ----0.07 part Compound I
3 ---- 7 parts hentai 1 ----------20 parts talc
--- 72.93 parts or more''-- is crushed, then a small amount of water is added, stirred and kneaded, granulated using a push-out granulator, and dried to form granules. Make it.

配合−例−9−粒剤 化合動歯!1     −−  0 、1部化合物r3
      −一一一−−−7部ヘントナイl    
 −−−−−20部タルク       −−−−−−
−−−12,9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。
Formulation - Example - 9 - Granule compound moving teeth! 1 -- 0, 1 part compound r3
-111---Part 7 Hentai l
−−−−−20 parts talc −−−−−−
---After uniformly mixing and pulverizing 12.9 parts or more, adding a small amount of water, stirring and kneading, and granulating with an extrusion granulator,
Dry and make into granules.

配治−(夕uCi  粒剤 化合物1tio、10     −−−−−−−  0
.05部化合物B       −−−−−−−−−8
部ヘントナイト     −−−−−−50部タルク 
      −−−−−−41,95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。
Treatment - (YuCi granule compound 1tio, 10 ------- 0
.. Part 05 Compound B ----------------------8
part hentonite --------50 parts talc
------- 41.95 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.

配イH舛月1 粒剤 化合動歯15     −−−−−−  0.2部化合
物B       −−−−−−−−8部ヘンI・ナイ
l−−−−−−−−40部タルク       =−−
−−−51,8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。
Distribution H Masuzuki 1 Granule compound moving tooth 15 --------- 0.2 parts Compound B --- 8 parts Hen I/Nyl --- 40 parts Talc =--
---After uniformly mixing and pulverizing 51.8 parts or more, adding a small amount of water, stirring and kneading, and granulating with an extrusion type granulator,
Dry and make into granules.

配合例12 粒剤 化合物No17−0.15部 化合物■3     −−一−−6部 ・\ン1リーイ]・−−50部 タルク        −一−−43.85部以−にを
均一に混合粉砕して後少量の水を加えて攪拌混合程1n
シ、押し出し式造粒機で造i;ll、、乾燥して粒剤に
する。
Formulation Example 12 Granule Compound No. 17 - 0.15 parts Compound ■ 3 - - 1 - - 6 parts /\n 1 Lee] - - 50 parts Talc - 1 - - 43.85 parts or more - were uniformly mixed and pulverized. After that, add a small amount of water and stir for 1n.
Then, it is made into granules using an extrusion granulator and dried.

試−験−例、、1−  湛水条件におりる除草効果試験
115000アールのワグネルボソ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、キカシグ!
))ホタルイのそれぞれの種子を、」−記のボットに混
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2醒を移植した。
Test Examples, 1- Weeding effect test under flooded conditions After putting alluvial soil in a 115,000 are Wagner Bosoto, water is added and mixed to create a freshwater condition with a water depth of 2 cm. Japanese millet, broad-leaved weeds (Japanese azalea, azalea, kikasig!
)) Seeds of each species of firefly were mixedly sown in the bots described above, and tubers of urikawa, cypress, and black bream were also placed on the bed. Furthermore, I2Ki at the 2.5-leaf stage was transplanted.

ポットを25〜30℃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。 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。
Grow plants in pots in a greenhouse at 25 to 30°C,
Ten days after sowing, when the Japanese millet was at the 1.5-leaf stage, a diluted solution of the drug was dropped onto the water surface using a volumetric pipette in a predetermined amount. 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% ■ −殺草率  5〜19% 〇 −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」二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% ■ - Weed killing rate 5-19% 〇 - Weed killing rate 5% or less (hardly effective) However,
The above-mentioned weed killing rate was determined by measuring the weight of above-ground grass in the chemically treated plot and the weight of bipartite grass in the non-treated plot using the following formula.

第2表 第  3 表(続き) 第  3 表(続き) 第  3 表(続き) 第  3 表(続き) 第  3 表(続き) 第   3 表(続き) 越駈例−?−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[に水ITI土壌を充填し、水田状態
でクイヌビエを育成し、ヒエの2葉期に粒剤に製剤した
各所定の薬剤を湛水上If(処理した。ボットは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−1一部生草重及び無処理区の地
上部生傅止を測定し7、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 2 Table 3 (continued) Table 3 (continued) Table 3 (continued) Table 3 (continued) Table 3 (continued) Table 3 (continued) Example of canter -? - Synergistic effect test on barnyard millet A polyethylene container with an inner diameter of 8 cm was filled with water ITI soil, and the common millet was grown in a paddy field. I did.The bot is 25~
The barnyard grass was grown under control in a greenhouse at 30°C, and the residual weight of millet plants was measured for 30 days after treatment.The weight of some fresh grass and the growth of above-ground parts in the untreated area were measured. It was calculated and judged according to the following criteria. The results are shown in Tables 4 and 5.

評点    殺草率 0   0〜9% 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% 以下余白 第4表 第4表(続き) 第4表(続き) 以下余白 第  5  表 第 5 表(続き) 第5表(続き) 第 5 表(続き) 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。
Score Weed killing rate 0 0-9% 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% Margin below Table 4 Table 4 (continued) Table 4 (continued) Margin below Table 5 Table 5 (continued) Table 5 (continued) Table 5 (continued) Table 5 ( (Continued) Table 5 (Continued) In the table, the calculated values indicate the expected values obtained from the Colby equation.

Z 以上の表から明らかなように、本発明組成物は、一般式
(1)で表される化合物及び従来公知の除草剤それぞれ
の活性の単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。
Z As is clear from the above table, the composition of the present invention exhibits not only the simple sum of the activities of the compound represented by general 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 dose.

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は水素原子、低級
アルキル基、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S−ベ
ンジル−N−エチル−N−(1,2−ジメチルプロピル
)−チオールカーバメートまたはS−ベンジル−N−ジ
−n−プロピルチオールカーバメートのいずれかを有効
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 hydrogen atom, a lower alkyl group, a halogen atom, or a lower alkoxy group. 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. ] A pyrazolesulfonylurea derivative represented by and either S-benzyl-N-ethyl-N-(1,2-dimethylpropyl)-thiol carbamate or S-benzyl-N-di-n-propylthiol carbamate as active ingredients. A herbicide composition comprising:
JP60074961A 1985-02-19 1985-04-09 Herbicide composition Granted JPS61233604A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP60074961A JPS61233604A (en) 1985-04-09 1985-04-09 Herbicide composition
KR1019860001105A KR930002954B1 (en) 1985-02-19 1986-02-18 Hebicidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60074961A JPS61233604A (en) 1985-04-09 1985-04-09 Herbicide composition

Publications (2)

Publication Number Publication Date
JPS61233604A true JPS61233604A (en) 1986-10-17
JPH0477721B2 JPH0477721B2 (en) 1992-12-09

Family

ID=13562414

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60074961A Granted JPS61233604A (en) 1985-02-19 1985-04-09 Herbicide composition

Country Status (1)

Country Link
JP (1) JPS61233604A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009057310A (en) * 2007-08-31 2009-03-19 Hodogaya Chem Co Ltd Herbicide composition

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61191602A (en) * 1985-02-19 1986-08-26 Nissan Chem Ind Ltd Herbicide composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61191602A (en) * 1985-02-19 1986-08-26 Nissan Chem Ind Ltd Herbicide composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009057310A (en) * 2007-08-31 2009-03-19 Hodogaya Chem Co Ltd Herbicide composition

Also Published As

Publication number Publication date
JPH0477721B2 (en) 1992-12-09

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