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JPS5919081B2 - Herbicide composition for paddy fields - Google Patents

Herbicide composition for paddy fields

Info

Publication number
JPS5919081B2
JPS5919081B2 JP5078575A JP5078575A JPS5919081B2 JP S5919081 B2 JPS5919081 B2 JP S5919081B2 JP 5078575 A JP5078575 A JP 5078575A JP 5078575 A JP5078575 A JP 5078575A JP S5919081 B2 JPS5919081 B2 JP S5919081B2
Authority
JP
Japan
Prior art keywords
weeds
parts
herbicides
compound
paddy
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
Application number
JP5078575A
Other languages
Japanese (ja)
Other versions
JPS51128425A (en
Inventor
良夫 高沢
修 森川
耐介 呉地
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP5078575A priority Critical patent/JPS5919081B2/en
Publication of JPS51128425A publication Critical patent/JPS51128425A/en
Publication of JPS5919081B2 publication Critical patent/JPS5919081B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は、α−(β−ナフトキシ)プロピオンアニリド
(以下N0PAと略称する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to α-(β-naphthoxy)propionanilide (hereinafter abbreviated as N0PA).

)と一般式(式中、Rは−OCH3、−0CH2CH2
X または−COOCH3を、ここでXは、塩素原子、
または、フッ素原子を表わす。
) and the general formula (wherein, R is -OCH3, -0CH2CH2
X or -COOCH3, where X is a chlorine atom,
Or it represents a fluorine atom.

)で示されるジフェニルエーテル系化合物とを有効成分
として含有する水田用除草剤組成物に関するものである
The present invention relates to a herbicide composition for paddy fields containing a diphenyl ether compound represented by the following as an active ingredient.

更に詳しくは、Rが−CH2CH2Fで示される新規化
合物を含む前記一般式(1)で示される化合物と公知化
合物N0PAとを混用することにより、従来の水田除草
剤よりも、その使用適期幅および殺草スペクトラムの著
しく拡大された、すなわち、水田雑草の発芽期から生育
期までのいずれの時期でも使用でき、かつ従来の除草剤
では防除困難であった多年生雑草をも防除できる優れた
除草剤組成物を提供するものである。
More specifically, by mixing the compound represented by the general formula (1), including a new compound in which R is -CH2CH2F, with the known compound N0PA, the range of suitable use period and the killing of the herbicide are improved compared to conventional paddy field herbicides. An excellent herbicide composition that has a significantly expanded grass spectrum, that is, can be used at any time from the germination period to the growth period of paddy weeds, and can also control perennial weeds that are difficult to control with conventional herbicides. It provides:

わが国の水田用除草剤は、使用時期の面から初期用除草
剤、中期用除草剤および後期用除草剤の3つに大別され
るが、前二者で使用量の大半を占めている。
Herbicides for paddy fields in Japan are roughly divided into three categories based on the timing of use: early-season herbicides, mid-season herbicides, and late-season herbicides, and the first two account for the majority of the amount used.

初期用除草剤としては、GNP(2・4・6−ドリクロ
ルフエニルー4−ニトロフェニルエーテル)およびNL
P(2・4−ジクロルフェニル−4−ニトロフェニルエ
ーテル)で代表され、中期用除草剤としては、スエップ
M〔メチル−N−(3・4−ジクロルフェニル)カーバ
メートト2=メチルー4−クロルフェノキシ酢酸エチル
エステルとの混合剤〕、サターン5C8−(4−クロル
ベンジル)−N−N−ジエチルチオールカーバメートと
2−メチルチオ−4・6−ピスエチルアミノーs−hリ
アジンとの混合剤〕等がある。
Initial herbicides include GNP (2,4,6-dolychlorophenyl-4-nitrophenyl ether) and NL.
P (2,4-dichlorophenyl-4-nitrophenyl ether), and as a medium-term herbicide, SWEP M [methyl-N-(3,4-dichlorophenyl) carbamate 2=methyl-4- Mixture with chlorophenoxyacetic acid ethyl ester], Mixture with Saturn 5C8-(4-chlorobenzyl)-N-N-diethylthiol carbamate and 2-methylthio-4,6-pisethylamino-s-h riazine] etc.

初期用除草剤は、雑算メ発生始期での使用は極めて効果
的であるが、発生盛期で使用すると、その効果は著しく
低下する。
Early stage herbicides are extremely effective when used at the beginning of the outbreak, but their effectiveness decreases significantly when used during the peak bloom stage.

中期用除草剤は、雑草の発芽期から生育期まで有効であ
るが、発芽期の使用では、水稲に対する薬害が著しく、
その使用時期が水稲の生育がかなり進んだ時期に限定さ
れる。
Mid-season herbicides are effective from the weed germination stage to the growth stage, but if used during the germination stage, they cause significant chemical damage to paddy rice.
Its use is limited to the period when the growth of paddy rice is considerably advanced.

また、温度や土壌条件によっては、薬害の発生や効果の
低下を来たす場合もしばしばある。
Furthermore, depending on the temperature and soil conditions, phytotoxicity may occur or the effectiveness may decrease.

さらに、これらの除草剤は多年生雑草に対する効果が充
分でなく、かえって多年生雑草の発生を促す結果となっ
ている。
Furthermore, these herbicides are not sufficiently effective against perennial weeds, and instead encourage the growth of perennial weeds.

最近は、農作業省力化の点からも、1回の処理ですべて
の雑草を防除できるような、使用適期幅の広い除草剤の
出現が望まれているにもかかわらず、前記のように、既
存除草剤には、水稲に対してその全生育期間を通じて薬
害がなく、かつ、この要求を満足させるものがない。
Recently, there has been a desire for herbicides that can control all weeds in a single treatment and can be used over a wide range of periods to save labor in agricultural work. There is no herbicide that does not cause any phytotoxicity to paddy rice during its entire growing period and that satisfies this requirement.

本発明者らは、田植直後の雑草の発芽始期から生育期ま
での任意の時期に使用して適確な防除効果を示し、かつ
、水稲に無害な除草剤の開発を目標に研究を重ねた結果
、前記一般式(1)で示される化合物とN0PAとの適
当な割合の混合物が、予想を大きく上まわる極めて顕著
な殺草効果を境わし、各成分単独では防除することので
きないような少量の薬量で1年生雑草はもちろん、最近
、多発化してきている多年生雑草のウリカワ、ホタルイ
、ヘラオモダカに対しても顕著な防除効果があり、しか
も水稲に対しては全く薬害のないことを見い出し、本発
明を完成した。
The present inventors have conducted extensive research with the goal of developing a herbicide that can be used at any time from the beginning of weed germination to the growing season immediately after rice transplantation, exhibiting an appropriate control effect, and is harmless to paddy rice. As a result, a mixture of the compound represented by the general formula (1) and N0PA in an appropriate ratio had an extremely significant herbicidal effect that far exceeded expectations, and a small amount that could not be controlled by each component alone. It was discovered that at a dosage of 1, it has a remarkable control effect not only on annual weeds, but also on the perennial weeds that have recently become more prevalent, such as porcupine, firefly, and snail, and that it has no phytotoxic effects on paddy rice. The invention has been completed.

前記一般式(1)で表わされる本発明組成物の有効成分
の例示化合物として次の化合物がある。
The following compounds are exemplified as active ingredients of the composition of the present invention represented by the general formula (1).

2・4−ジクロルフェニル−3−、、!)キシ−4−二
トロフェニルエーテル(以下化合物Aといつ)2・4−
ジクロルフェニル−3−(β−クロルエトキシ)−4−
ニトロフェニルエーテル(以下化合物Bとい5 )、’
2・4−ジクロルフェニル−3−(β−フルオルエトキ
シ)−4−−40フエニルエーテル(以下化合物Cとい
う)、2・4−ジクロルフェニル−3−カルポキシメf
#−4−=トロフェニルエーテル(以下化合物りといつ
)。
2,4-dichlorophenyl-3-,,! ) xy-4-nitrophenyl ether (hereinafter referred to as compound A) 2,4-
Dichlorophenyl-3-(β-chloroethoxy)-4-
Nitrophenyl ether (hereinafter referred to as compound B5),'
2,4-dichlorophenyl-3-(β-fluoroethoxy)-4-40 phenyl ether (hereinafter referred to as compound C), 2,4-dichlorophenyl-3-carpoxime f
#-4-=trophenyl ether (hereinafter referred to as the compound).

上記化合物のうち、化合物Cは、特願昭49−1467
89にかかわる新規化合物である。
Among the above compounds, compound C is
This is a new compound related to No. 89.

これらの化合物はいずれも接触的殺草作用を示す除草剤
で発芽始期のイネ科雑草に対する抑制力が強いので、雑
草の発芽する前後の時期に、たとえば水田においては田
植3日前ころから田植後6日ころまでに、使用しなげれ
ばならない。
All of these compounds are herbicides that exhibit contact herbicidal action and have a strong suppressive power against grass weeds at the beginning of germination, so they can be used before and after weed germination, for example in paddy fields, from about 3 days before rice planting to 6 days after rice planting. It must be used by the end of the day.

これらの化合物の殺草力は、雑草の成長に従ってその効
力が低下し、特にコナギ等の広葉雑草や多年生雑草のウ
リカワ、ホタルイ等に対する除草効果が低下して(る。
The herbicidal power of these compounds decreases as the weeds grow, and in particular, their herbicidal effects against broad-leaved weeds such as the grasshopper and perennial weeds such as the weeds and fireflies decrease.

従ってこれらの化合物はその適用雑草の種類および適用
時期が限定されるという実用上の欠点を有している。
Therefore, these compounds have practical drawbacks in that the types of weeds to which they can be applied and the timing of application are limited.

一方N0PAは発生始期の雑草を抑制するもので、特に
たん水条件下において、その作用発現が強力であり、ま
た生育中の雑草に; 対して接触による殺草作用が極め
て強く、とくにたん水状態の広葉雑草に対して卓効を示
すが、イネ科雑草、たとえば、タイヌビエに対しては抑
制力が小さいという欠点を有する。
On the other hand, N0PA suppresses weeds at the beginning of their emergence, and its effect is particularly strong under stagnant conditions.It also has an extremely strong herbicidal effect on contact with growing weeds; Although it is highly effective against broad-leaved weeds, it has the disadvantage of low suppressive power against grass weeds, such as Japanese millet.

しかし従来のフェノキシ系除草剤の24−D、MCPA
に較べて、水稲に対しては奇形葉、その他の薬害はまっ
たく認められないというすぐれた特徴をもっている。
However, the conventional phenoxy herbicides 24-D and MCPA
It has the superior feature of not causing any malformed leaves or other chemical damage to paddy rice.

本発明(気前記のような欠点を有するN0PAと前記一
般式(1)で示される化合物とを適当に混合することに
よって各単独で施用する場合の欠点を; 補うのみなら
ず、相乗効果により雑草に対する適用中および使用時期
中を著しく増大させることを可能にするものである。
The present invention (by appropriately mixing N0PA, which has the above-mentioned drawbacks, and the compound represented by the general formula (1) above, not only compensates for the drawbacks of applying each alone, but also suppresses weeds due to the synergistic effect) This makes it possible to significantly increase the application and usage period for

すなわちNoPAl重量部と本発明の一般式(1)で示
される化合物の0.5〜2重量部との混合物を: 施用
することにより、発芽時の雑草はもちろん、ある程度成
長したイネ科雑草、広葉雑草およびウリカワ、ホタルイ
等の多年生雑草に対しても強い抑制力を発現させるもの
であり、このことは前記一般式(1)の化合物とN0P
Aの混合によって始めて完成された画期的な除草効果で
ある。
That is, by applying a mixture of parts by weight of NoPA1 and 0.5 to 2 parts by weight of the compound represented by the general formula (1) of the present invention, it is possible to not only weeds at the time of germination but also gramineous weeds and broad-leaved weeds that have grown to some extent. It exhibits a strong suppressive power against weeds and perennial weeds such as weeds and fireflies, and this indicates that the compound of general formula (1) and N0P
This is an epoch-making herbicidal effect that was first achieved by mixing A.

本発明の除草剤組成物は、いろいろな型に製剤して水田
用除草剤として使用できるが、特に粒剤としてたん水状
態の水田に施用すると実用価値は一段と高まるものであ
る。
The herbicidal composition of the present invention can be formulated into various forms and used as a herbicide for paddy fields, but its practical value is particularly enhanced when it is applied as granules to stagnant paddy fields.

次にたん水状態の水田に施用した場合の効果を試験例に
よって説明する。
Next, the effects when applied to stagnant rice fields will be explained using test examples.

試験例 1 水田一般雑草の種子が自然混在している土壌3、3 k
gを5000分の1アールのワグネルポットに充テンシ
テ、これKN、P2O5、K20各々0.8グを化成肥
料で全層に施肥し、適量の水を加えて充分かきまぜ、た
ん水状態とした。
Test example 1 Soil 3,3k where seeds of common weeds in paddy fields are naturally mixed
Fill a 1/5000th area Wagner pot with 0.8 g of each of KN, P2O5, and K20 and fertilize the entire layer with chemical fertilizers, add an appropriate amount of water, and stir thoroughly to create a water-filled state.

次に、温室内で育苗した水稲苗(葉令3.0)の2本を
1株とし、ポット当りその2株を3crrLの深さにそ
う苗したのち、これにノビエ種子2001n9を表層に
は種混合し、温室で生育させた。
Next, two paddy rice seedlings (leaf age 3.0) grown in a greenhouse were used as one plant, and the two plants were planted per pot at a depth of 3 crrL. The seeds were mixed and grown in a greenhouse.

移植3日後または8日後に供試化合物の所定量を用いて
≧・これにたん水土壌処理を行なった。
3 or 8 days after transplantation, a predetermined amount of the test compound was used to treat the soil with stamina.

薬剤処理1力月後に、残草量および水稲に対する薬害を
調査して、第1表に示す結果を得た。
One month after the chemical treatment, the amount of remaining grass and the chemical damage to paddy rice were investigated, and the results shown in Table 1 were obtained.

第1表の結果かられかるように、N0PAは移植3日後
および8日後の画処理とも、タイヌビエに対して除草効
果が小さく、コナギ、ウリカワ、ヘラオモダカ等の広葉
雑草およびタマガヤツリ、ホタルイに対して効果が高い
As can be seen from the results in Table 1, N0PA has a small herbicidal effect on Japanese grasshopper when treated 3 days and 8 days after transplantation, and is effective against broad-leaved weeds such as Japanese grasshopper, Japanese grasshopper, and grasshopper, as well as on Japanese cypress and firefly. is high.

一方化合物A、 B、CおよびDは、移植3日後処理で
は多年生のウリカワ、ヘラオモダカ、ホタルイを除き全
般的に効果が高いが、移植8日後処理では、全般に効果
が低下し、タイヌビエ等のイネ科雑草に対しては、比較
的効果が高いが、広葉雑草に対してはやや効果不足、多
年生のホタルイ、ウリカワに対しては、はとんど効果が
ない。
On the other hand, Compounds A, B, C, and D were generally highly effective when treated 3 days after transplantation, except for perennials such as Prunus japonicum, Helaomodaca, and Firefly, but when treated 8 days after transplantation, the effects decreased overall, and It is relatively effective against family weeds, but it is slightly less effective against broad-leaved weeds, and it is hardly effective against perennial fireweeds and weeds.

これに対してN0PAと化合物A、 B、 CまたはD
と混合した薬剤は、移植3日後および8日後処理とも、
タイヌビエに対して充分な生長抑制力を示すとともに、
コナギ、タマガヤツリ、多年生ジく雑草のウリカワ、ヘ
ラオモダカ、ホタルイに対しても車効を示した。
In contrast, N0PA and compounds A, B, C or D
The drug mixed with
In addition to showing sufficient growth suppressing power against Japanese millet,
It was also shown to be effective against the common weeds, Japanese cypress, and perennial weeds such as porcupine weeds, staghorn weeds, and firefly.

しかも、水稲に対しては、はとんど薬害を与えずすぐれ
た実用性を示した。
Moreover, it showed excellent practicality with no phytotoxicity to paddy rice.

試験例 2 水田一般雑草種子が自然混在しているは場を通常の方法
により耕起施肥しく N、 P205、K20各a当り
1 kg )、荒代および整地を行ない、1区Iom2
(2,5mX4m)に区画し、これに葉令5.0の水稲
苗2本を1株として、あぜ間30へ株間15Crnに移
植した。
Test Example 2 A paddy field where common weed seeds are naturally mixed was tilled and fertilized using the usual method (1 kg per a of N, P205, K20), roughage and land leveling, 1 area Iom2
(2.5 m x 4 m), and two paddy rice seedlings with leaf age of 5.0 were transplanted into this as one plant with a furrow spacing of 30 and a plant spacing of 15 cr.

移植後ばたん水深3〜5crrLに保ち、移植3日後お
よび移植8日後に供試化合物の粒剤アール当り300グ
をたん水面に散布した。
After transplanting, the water depth was maintained at 3 to 5 crrL, and 300 g of the test compound per granule area was sprayed on the water surface 3 days after transplantation and 8 days after transplantation.

散布1力月後に残草量を測定し、併せて水稲に対する薬
害を観察調査し第2表の結果を得た。
One month after spraying, the amount of remaining grass was measured, and the chemical damage to paddy rice was also observed and the results shown in Table 2 were obtained.

試験例2の結果によると、各単剤区は、3日後処理では
効果が高いが、8日後処理では全般に効果が低下し、薬
剤によっては、タイヌビエ、ウリカワ、ヘラオモダカ、
ホタルイなどには効果がほとんどない。
According to the results of Test Example 2, each single drug group was highly effective after 3 days of treatment, but the overall effect decreased after 8 days of treatment.
It has little effect on firefly etc.

ところが混合区では、処理時期や草種に関係なく効果高
く、水稲に対する薬害もまったくないことがわかる。
However, in the mixed area, it is highly effective regardless of the treatment time or grass type, and it is clear that there is no chemical damage to paddy rice at all.

本発明除草剤組成物の有効成分の配合割合は広範囲に適
用し得るが、NoPAI重量部に対して一般式(1)で
示される化合物の0.5〜2重量部を配合することが望
ましい。
Although the blending ratio of the active ingredients in the herbicidal composition of the present invention can be applied over a wide range, it is desirable to blend 0.5 to 2 parts by weight of the compound represented by general formula (1) to parts by weight of NoPAI.

本発明除草剤組成物は、使用目的に応じて固体担体、例
えば、希釈剤、増量剤と混合して使用するが、その際必
要に応じて補助剤として安定剤、分散剤、懸濁剤、展着
剤、浸透剤、湿展剤などを添加することにより、水和剤
、粒剤、または粉剤の剤型として使用することができる
The herbicidal composition of the present invention is used by mixing with a solid carrier such as a diluent or a filler depending on the purpose of use. At that time, if necessary, auxiliary agents such as stabilizers, dispersants, suspending agents, etc. By adding a spreading agent, penetrating agent, wetting agent, etc., it can be used as a wettable powder, granule, or powder.

また、本発明の除草剤組成物は、殺菌剤、殺虫剤、他の
除草剤等の農薬、尿素、硫安、リン安、カリ塩なとの肥
効性物質、およびまたは土壌改良剤との混合使用はもち
ろん、これ等との混合製剤も可能である。
Further, the herbicidal composition of the present invention can be mixed with pesticides such as fungicides, insecticides, and other herbicides, fertilizing substances such as urea, ammonium sulfate, ammonium phosphorus, and potassium salts, and/or soil conditioners. Not only can they be used, but also mixed preparations with these are possible.

本発明除草剤組成物中の有効成分総合有量は粒剤で1〜
20%、水利剤で30〜60%が望ましい。
The total amount of active ingredients in the herbicide composition of the present invention is 1 to 1 in granules.
20%, and 30-60% for irrigation agents is desirable.

次に本発明組成物の実施例を示す。Next, examples of the composition of the present invention will be shown.

実施例 1 粒剤 NoPAI部、化合物A7部、ベントナイト60部、タ
ルク23部、ポリオキシエチレングライコールモノラウ
リレート2部、およびナフタレンスルホン酸縮合物1部
を混合し造粒機を用いて通常の方法により造粒し、粒剤
100部を得る。
Example 1 Parts of NoPAI granules, 7 parts of compound A, 60 parts of bentonite, 23 parts of talc, 2 parts of polyoxyethylene glycol monolaurylate, and 1 part of naphthalene sulfonic acid condensate were mixed and processed using a granulator in a conventional manner. Granulate according to the method to obtain 100 parts of granules.

実施例 2 粒剤 NoPAI部、化合物B5部、ドデシルベンゼンスルホ
ン酸ソーダ2部、リグニンスルホン酸ソーダ1部、タル
ク35部、およびベントナイト50部を混合し、造粒機
を用いて通常の方法により造粒し、粒剤100部を得る
Example 2 Parts of granules NoPAI, 5 parts of compound B, 2 parts of sodium dodecylbenzenesulfonate, 1 part of sodium ligninsulfonate, 35 parts of talc, and 50 parts of bentonite were mixed, and granulated by a normal method using a granulator. Granulate to obtain 100 parts of granules.

実施例 3 水和剤 N0PA25部、化合物C20部、ベントナイト50部
、およびドデシルベンゼンスルホン酸ソーダ5部を混合
して水和剤100部を得る。
Example 3 25 parts of wettable powder N0PA, 20 parts of compound C, 50 parts of bentonite, and 5 parts of sodium dodecylbenzenesulfonate are mixed to obtain 100 parts of wettable powder.

以上述べたように、本発明組成物は、田植直後の雑草の
発芽始期から最盛期までのいずれの時期に使用しても、
水稲に対しては無害で、しかも1回の散布ですべての雑
草を防除することができ、従来多く使用されている除草
剤に較べて著しく優れている。
As mentioned above, the composition of the present invention can be used at any time from the beginning of weed germination to the peak of weed germination immediately after rice transplantation.
It is harmless to paddy rice and can control all weeds with a single application, making it significantly superior to conventionally used herbicides.

従来、除草剤は殺菌剤や殺虫剤と異なり、田植時期が3
〜4日前後しても雑草の生育に差が生ずるため、その散
布の時期をずらさなければならないという事情から、広
範囲にわたる機械化散布が不可能で、農作業の省力化を
はばんでいるのが実情である。
Conventionally, herbicides differ from fungicides and insecticides in that the rice planting period is
Because there are differences in the growth of weeds even after ~4 days, the timing of spraying has to be staggered.The reality is that mechanized spraying over a wide area is not possible and labor-saving in agricultural work is hindered. It is.

本発明組成物は、その使用適期幅が著しく長いため、田
植時期が10〜20日前後しても、田植と同時に散布す
ることができ、従って広範囲にわたる共同散布も可能と
なり、労力の節減に貢献するところは大きい。
Since the composition of the present invention has a significantly long suitable period of use, it can be applied at the same time as rice planting even if the rice planting period is around 10 to 20 days. Therefore, joint application over a wide range is possible, contributing to labor savings. There's a lot to do.

Claims (1)

【特許請求の範囲】 1 α−(β−ナフトキシ)プロピオンアニリドと一般
式 (式中、Rは一0CH3、0CH2CH2X または−
COOCH3を、ここでXは、塩素原子または、フッ素
原子を表わす。 )で示されるジフェニルエーテル系化合物とを有効成分
として含有する水田用除草剤組成物。
[Scope of Claims] 1 α-(β-naphthoxy)propionanilide and the general formula (wherein R is -0CH3, 0CH2CH2X or -
COOCH3, where X represents a chlorine atom or a fluorine atom. ) as an active ingredient.
JP5078575A 1975-04-28 1975-04-28 Herbicide composition for paddy fields Expired JPS5919081B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5078575A JPS5919081B2 (en) 1975-04-28 1975-04-28 Herbicide composition for paddy fields

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5078575A JPS5919081B2 (en) 1975-04-28 1975-04-28 Herbicide composition for paddy fields

Publications (2)

Publication Number Publication Date
JPS51128425A JPS51128425A (en) 1976-11-09
JPS5919081B2 true JPS5919081B2 (en) 1984-05-02

Family

ID=12868462

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5078575A Expired JPS5919081B2 (en) 1975-04-28 1975-04-28 Herbicide composition for paddy fields

Country Status (1)

Country Link
JP (1) JPS5919081B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1129665A (en) * 1978-12-21 1982-08-17 James L. Glasgow Method of combating weeds in cereal crops and herbicidal formulation therefor
JPS5679607A (en) * 1979-12-03 1981-06-30 Schering Ag Herbicidal composition
JPS5785303A (en) * 1980-11-17 1982-05-28 Hodogaya Chem Co Ltd Herbicidal composition for paddy rice field

Also Published As

Publication number Publication date
JPS51128425A (en) 1976-11-09

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