JPH0524881B2 - - Google Patents

Info

Publication number
JPH0524881B2
JPH0524881B2 JP59266429A JP26642984A JPH0524881B2 JP H0524881 B2 JPH0524881 B2 JP H0524881B2 JP 59266429 A JP59266429 A JP 59266429A JP 26642984 A JP26642984 A JP 26642984A JP H0524881 B2 JPH0524881 B2 JP H0524881B2
Authority
JP
Japan
Prior art keywords
compound
present
group
composition
granules
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 - Lifetime
Application number
JP59266429A
Other languages
Japanese (ja)
Other versions
JPS61145104A (en
Inventor
Takeo Mogi
Hiroshi Ooshiba
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.)
Hodogaya Chemical Co Ltd
Original Assignee
Hodogaya Chemical Co Ltd
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 Hodogaya Chemical Co Ltd filed Critical Hodogaya Chemical Co Ltd
Priority to JP59266429A priority Critical patent/JPS61145104A/en
Priority to GB08530401A priority patent/GB2169203B/en
Priority to AU51145/85A priority patent/AU568784B2/en
Priority to BR8506361A priority patent/BR8506361A/en
Priority to ZA859661A priority patent/ZA859661B/en
Publication of JPS61145104A publication Critical patent/JPS61145104A/en
Publication of JPH0524881B2 publication Critical patent/JPH0524881B2/ja
Granted legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/24Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、改善された除草組成物であつて、2
−(4−イソプロピル−4−メチル−5−オキソ
−2−イミダゾリン−2−イル)ニコチン酸、そ
のアルリ金属塩、低級アルキル(C1〜C4)エス
テルまたは低級アルキル(C1〜C4)アミン塩
〔以下化合物A群と称す〕とメチルN−(4−アミ
ノフエニルスルホニル)カーバメイトまたはその
アルカリ金属塩〔以下、化合物B群と称す〕とを
含有することを特徴とする除草組成物に関するも
のである。すなわち、本発明の主要な目的は、遅
効性の非農耕地除草剤をその残効性を失うことな
しに連効性とすることにより、非農耕地除草剤と
しての価値を高めることにある。 本発明に係る化合物A群は、非常に低薬量から
除草活性を示す強力な除草剤である。その特徴は
穀草スペクトラムが広く、抑草期間が長く、低薬
量で効果が高いなどであり、非農耕地の除草剤と
して好適な性格をもつている。 ところで、化合物A群は非常に遅効性で、特に
やや生育の進んだ多年草では、完全枯穀に至るま
でに数ケ月を要することが多く、散布目的が散布
当年に達せられないこともあり、これが本化合物
群の欠点とされる。 一方、本発明に係る化合物B群はある種の多年
性雑草に卓効さを示すこと、比較的残効が短かい
ことおよび非常に遅効性であることなどの性質を
有し、牧草地、芝地、サトウキビ畑または樹園地
等で使用されている。ただし、非農耕地、例え
ば、ススキ等の強害草にはかなり多量投入しても
効きにくく、押草期間も短かいため、非農耕地の
除草剤としては適しているとはいいがたい。 非農耕地の雑草防除は通常、雑草が発生して繁
茂するまで放置されてから実施されることが多
く、必しも使用する薬剤の除草活性を最高度に利
用しうる条件で処理されるとは限らない。一方、
非農耕地の除草目的の多くは、環境の美化、防犯
および防火などであり、薬剤処理後、速やかに、
除草効果があらわれることが望まれる。 なお、化合物A群で防除した雑草は、いわゆる
立枯れ状態で枯死するが、これは、防犯、防火上
の目的にそぐわない。 本発明の組成物で防除した場合は、枯死した雑
草は、倒伏し、腐朽するため、非農耕地用除草組
剤としての実用上の価値はさらに高まる。 本発明にかゝる組成物の実用上の使用量は、A
群の化合物、B群の化合物とも、それぞれm2あた
り0.1〜1g(酸換算)が適当であるが、好まし
くは、0.2〜0.6gの範囲である。 本発明の組成物は各々の化合物の持つ物理化学
的性質と散布条件等を照らし合わせ、目的に応じ
た適切な化合物を選ぶが、施用し易い剤型、たと
えば液剤、水和剤、微粒剤、粒剤等にすることが
できる。 なお、本発明の効果は、雑草の薬剤吸収部位の
いかんを問わず発揮される。すなわち、雑草の茎
葉にほとんど付着しない剤型、たとえば、粒剤に
おいても速効化は顕著に認められる。この場合、
化合物B群のA群に対する添加割合は、茎葉散布
として本組成物を使用する場合より、高くするこ
とが必要である。 増量剤としては、水、有機溶媒、不活性な鉱物
粉末や粒状担体があげられ、分剤剤または展着剤
は、陰イオン系、非イオン系の界面活性剤の中か
ら選ぶことができる。 さらに、本発明の組成物に、必要に応じて他の
除草剤などを加えることもできる。 以下、本発明を、試験例、実施例をもつて説明
する。表およびに化合物名を示したが、以
後、各々の化合物は化合物No.で示す。
The present invention provides an improved herbicidal composition comprising: 2
-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)nicotinic acid, its allyl metal salt, lower alkyl (C1 - C4 ) ester or lower alkyl ( C1 - C4 ) A herbicidal composition containing an amine salt (hereinafter referred to as compound group A) and methyl N-(4-aminophenylsulfonyl) carbamate or an alkali metal salt thereof (hereinafter referred to as compound group B). It is something. That is, the main object of the present invention is to increase the value of a slow-acting non-agricultural herbicide by making it continuous-acting without losing its residual effectiveness. Compound A group according to the present invention is a powerful herbicide that exhibits herbicidal activity even at very low doses. Its characteristics include a wide spectrum of cereal grasses, a long weed suppression period, and high efficacy at low dosages, making it suitable as a herbicide for non-agricultural land. By the way, compound A group is very slow-acting, and it often takes several months to completely kill the grains, especially for perennial plants that have grown a little. This is considered to be a drawback of this group of compounds. On the other hand, the compound B group according to the present invention has properties such as being highly effective against certain perennial weeds, having a relatively short residual effect, and being extremely slow-acting. Used on lawns, sugarcane fields, orchards, etc. However, it cannot be said to be suitable as a herbicide for non-agricultural land, for example, because it is not effective against harmful grasses such as silver grass, even when applied in large amounts, and the weeding period is short. Weed control in non-agricultural land is usually carried out after weeds are left until they emerge and grow, and it is essential that the weeds are treated under conditions that maximize the herbicidal activity of the chemicals used. is not limited. on the other hand,
Many of the purposes for weeding non-agricultural land include environmental beautification, crime prevention, and fire prevention, and after chemical treatment, immediately
It is hoped that the herbicidal effect will appear. Note that weeds controlled with compound A group die in a so-called damping-off state, but this is not suitable for the purpose of crime prevention and fire prevention. When the composition of the present invention is used to control weeds, dead weeds lie down and rot, which further increases the practical value as a weed killer for non-agricultural land. The practical usage amount of the composition according to the present invention is A
For both the group compound and the group B compound, the amount is suitably 0.1 to 1 g (acid equivalent) per m 2 , and preferably 0.2 to 0.6 g. For the composition of the present invention, an appropriate compound is selected depending on the purpose by comparing the physicochemical properties of each compound and the dispersion conditions. It can be made into granules, etc. Note that the effects of the present invention are exhibited regardless of the drug absorption site of the weed. That is, even in a dosage form that hardly adheres to the leaves and foliage of weeds, such as granules, rapid effects can be clearly observed. in this case,
The addition ratio of compound group B to group A needs to be higher than when the present composition is used as a foliar spray. Extending agents include water, organic solvents, inert mineral powders and granular carriers, and dividing agents or spreading agents can be selected from anionic and nonionic surfactants. Furthermore, other herbicides and the like can be added to the composition of the present invention, if necessary. The present invention will be explained below using test examples and examples. The names of the compounds are shown in the table and in the following, each compound will be referred to as a compound number.

【表】【table】

【表】【table】

【表】 試験例 1 100cm2の素焼鉢に、あらかじめ育成したメヒシ
バの5葉期、草丈約20cmのものに、各化合物の希
釈液の単用および混合液を散布処理し、穀草速度
を観察調査した。希釈液濃度は遊離酸換算した濃
度である。散布水量は100ml/m2で、スプレーガ
ンを使用して散布処理した。その結果を表に示
す。 評価基準は下記のようである。 0 :無処理同様 2 :20%防除 4 :40%〃 6 :60%〃 8 :80%〃 10 :完全防除 この結果、おのおのの単用にくらべ、本発明の
混用によつて活性の発現および完成が、はるかに
速まつていることがわかる。
[Table] Test Example 1 In a 100 cm 2 clay pot, a diluted solution or a mixed solution of each compound was sprayed on the 5-leaf stage, approximately 20 cm tall, of crabgrass that had been grown in advance, and the grain speed was observed and investigated. did. The diluent concentration is the concentration converted to free acid. The amount of water sprayed was 100 ml/ m2 , and the spraying treatment was carried out using a spray gun. The results are shown in the table. The evaluation criteria are as follows. 0: Same as no treatment 2: 20% control 4: 40%〃 6: 60%〃 8: 80%〃 10: Complete control As a result, compared to the single application of each, the combined application of the present invention resulted in the expression of activity and It can be seen that completion is much faster.

【表】【table】

【表】【table】

【表】 試験例 2 茎葉処理における添加効果の検討100cm2の素焼
鉢に、あらかじめ4〜5葉期15〜20cmに育成した
メヒシバにNo.2とNo.12の希釈液を単用および混用
で、水量100ml/m2で、スプレーガンを使用して、
散布処理した。処理2週間後の調査結果を第表
に示す。評価基準は試験例1と同様とした。 表の結果から、本発明の除草組成物が相乗効
果を有することは明白である。
[Table] Test Example 2 Examination of the effect of additives in stem and leaf treatment. Diluted solutions No. 2 and No. 12 were used alone or in combination on crabgrass that had been grown in advance to a 4- to 5-leaf stage of 15 to 20 cm in a 100 cm 2 clay pot. , using a spray gun with a water volume of 100ml/ m2 ,
Sprayed. The results of the investigation two weeks after the treatment are shown in Table 1. The evaluation criteria were the same as in Test Example 1. From the results in the table, it is clear that the herbicidal composition of the present invention has a synergistic effect.

【表】 試験例 3 現地試験 非農耕地の代表的強害草であるイネ科多年草の
ススキ、チガヤの優先地および広葉多年草のセイ
タカアワダチソウ、ヨモギの優先地を選び、1区
2.5m×2.5mの試験区を設定し、No.4、No.12の単
用および混用で300ml/m2の水量でジヨロを使つ
て、区内全面に均一散布した。7月5日に散布
し、2週、1ケ月、2ケ月、3ケ用後に観察調査
を行つた。 処理時の雑草の状況は下記のようであつた。草種名 区内占有率 草 丈 (%) (cm) ススキ 50〜80 120〜150 チガヤ 60〜80 60〜80 セイタカアワダチソウ 50〜70 70〜100 ヨモギ 40〜60 40〜70 評価は試験例1と同様の評価基準で行つた。そ
の結果を表−1、−2に示す。 これらの結果から、本発明の組成物が速効性お
いても最終効果においても、おのおのの単用より
はるかにすぐれていることがわかる。
[Table] Test example 3 Field test Select priority areas for grass perennial grasses such as Miscanthus sinensis and Chigaya, which are representative harmful grasses in non-agricultural land, and priority areas for broad-leaved perennials Verbata stingata and Mugwort.
A test area of 2.5 m x 2.5 m was set up, and No. 4 and No. 12, single and mixed, were uniformly sprayed over the entire area using a water sprayer at a water volume of 300 ml/m 2 . The spray was applied on July 5th, and observation and investigation were conducted after 2 weeks, 1 month, 2 months, and 3 applications. The status of weeds at the time of treatment was as follows. Grass species name Area occupancy Plant height (%) (cm) Miscanthus 50-80 120-150 Chigaya 60-80 60-80 Goldenrod 50-70 70-100 Mugwort 40-60 40-70 Evaluations are as in Test Example 1 Similar evaluation criteria were used. The results are shown in Tables-1 and -2. These results show that the composition of the present invention is far superior to each of the compositions used alone, both in terms of immediate effect and final effect.

【表】【table】

【表】【table】

【表】 試験例 4 粒剤による効果 洪積火山灰畑土をつめた100cm2の素焼鉢にメヒ
シバを4葉期、約15cmに育成し、鉢体の土壌表面
にNo.6の1%粒剤をNo.12の2%粒剤を、それぞれ
の単用および混用で、均一に手撒き処理した。粒
剤処理後は、土壌の乾湿に応じ1日に1〜3回の
人工降雨を与え、やや土壌水分の多い状態で生育
管理し、処理20日後に視察調査した。評価基準は
試験例1と同様とした。結果を表に示す。この
結果から、本発明の除草組成物が、一般にはむず
かしいといわれる、粒剤による速効性においても
すぐれていることがわかる。
[Table] Test example 4 Effect of granules Grow crabgrass to the 4-leaf stage and approximately 15 cm in a 100 cm 2 clay pot filled with soil from a volcanic ash field, and apply No. 6 1% granules on the soil surface of the pot. No. 12 2% granules were uniformly distributed by hand, both alone and in combination. After the granule treatment, artificial rain was applied 1 to 3 times a day depending on the dryness and humidity of the soil, and growth was controlled in a state with slightly high soil moisture, and an inspection was conducted 20 days after the treatment. The evaluation criteria were the same as in Test Example 1. The results are shown in the table. This result shows that the herbicidal composition of the present invention is also excellent in quick-acting properties when used in granules, which is generally said to be difficult.

【表】 試験例 5 粒剤による現地試験 スギナの多い造成地に1区2m×2mの試験区を
設け、本発明の組成物および各々の単剤の粒剤を
手撒で区内に均一に散布した。散布は8月2日で
以後、2週、1ケ月、2ケ月後に視察による調査
を行つた。評価基準は試験例1と同様とした。結
果は表に示す。この結果、粒剤の一体製剤で
も、すぐれた速効性と相乗効果を示すことが証明
された。
[Table] Test Example 5 On-site test using granules A test plot of 2 m x 2 m was set up in a cultivated area with many horsetails, and the composition of the present invention and each single agent granule were distributed uniformly within the plot by hand. Spread. The spraying took place on August 2nd, and inspections were conducted two weeks, one month, and two months later. The evaluation criteria were the same as in Test Example 1. The results are shown in the table. As a result, it was demonstrated that even the integrated formulation of granules exhibits excellent fast-acting properties and synergistic effects.

【表】 試験例 6 微粒剤による現地試験 梅雨明け前に刈払いを行い、再生してきたスス
キ、チガヤ、メドハギ、ヨモギ等の多年草とブタ
クサ、エノコログサの繁茂地に7m×7mの試験区
を設け、化合物No.4を2%とNo.12を3%含有する
本発明の組成物の微粒剤を、m2当り10g、20g、
区内に均一に手撒きした。8月2日に散布し、1
ケ月、2ケ月後に観察による調査を行つた。評価
基準は試験例1と同様とした。その結果を表に
示す。本発明の除草組成物は多種類の雑草に対し
て、1ケ月後には確実に除草効果を発揮した。し
かも、枯死した雑草は立枯れ状態ではなく倒伏し
た状態であり、満足な結果であつた。
[Table] Test example 6 Field test using fine grains A 7m x 7m test plot was set up in a flourishing area of perennial grasses such as pampas grass, Japanese grass, Japanese grass, and mugwort, which had been mowed down and regenerated before the end of the rainy season, as well as ragweed and hackberry. Microgranules of the composition of the present invention containing 2% of Compound No. 4 and 3% of No. 12 were prepared at 10 g, 20 g,
They were evenly distributed by hand within the ward. Sprayed on August 2nd, 1
An observational investigation was conducted after a month or two. The evaluation criteria were the same as in Test Example 1. The results are shown in the table. The herbicidal composition of the present invention reliably exhibited herbicidal effects against a wide variety of weeds after one month. In addition, the dead weeds were not in a standing state but in a lodging state, which was a satisfactory result.

【表】【table】

【表】 実施例 1 水和剤 化合物A群およびB群の原体にカオリンクレー
とホワイトカーボンを加え、擂潰機を使用した
後、粉末の界面活性剤を加えて、良く撹拌混合
し、化合物No.1の25%および化合物No.11の20%を
含有する水和剤を得た。 化合物No.1 25重量部 〃 No.11 20 〃 カオリンクレー 45 〃 ホワイトカーボン 5 〃 ソルポール5039(東邦化学商標・陰イオン系界
面活性剤) 4 〃 ラビゾールBB−75(日本油脂商標・陰イオン
系界面活性剤) 1 〃 実施例 2 液剤 化合物A群およびB群の原体と界面活性剤をイ
オン交換処理した水に溶解して、化合物No.4を12
%と化合物No.12を18%を含有する本発明の組成物
の液剤を得た。 化合物No.4 12重量部 〃 No.12 18 〃 ポリオキシエチレンアリールエーテル 5 〃 イオン交換処理した水 65 〃 実施例 3 粒剤 化合物A群およびB群の原体にベントナイテ、
クレーおよび界面活性剤を混合し、水を加えてニ
ーダーで均一に練り、造粒機にかけて造粒した
後、送風乾燥して、化合物No.6の1%および化合
物No.11の2%を含有する本発明の組成物の粒剤を
得た。 化合物No.6の原体 1重量部 〃 No.11の原体 2 〃 ジオクチルスルホサクシネート 1 〃 ベントナイト 40 〃 クレー 56 〃 実施例 4 微粒剤 化合物A群およびB群の原体を水で希釈し、ス
ピードニーダー中で、撹拌中の微粒ゼオライト
(48〜150メツシユ)に注入し、さらに界面活性剤
の水希釈液を注加して、撹拌を続けた後にホワイ
トカーボンを加えてから取り出し、送風乾燥して
化合物No.4の2%と化合物No.12の3%を含有する
本発明の組成物の微粒剤を得た。 化合物No.4の原体 2重量部 〃 No.12の原体 3 〃 微粒ゼオライト 90 〃 ポリオキシエチレンドデシルエーテル 2 〃 ホワイトカーボン 3 〃 発明の効果 本発明の除草組成物は、おのおのの単用をはる
かに越えた速効性と相乗効果を有し、非農耕地で
の強害草は1ケ月後には確実に枯死する。また、
以上のように速効性でありながら、残効性をも合
わせて有する。しかも枯死した雑草は立故れ状態
ではなく、倒伏した状態であり、環境美化、防
犯、防災上の利点を有する。
[Table] Example 1 Wettable powder Kaolin clay and white carbon were added to the raw materials of compounds A and B, and after using a crusher, a powdered surfactant was added, and the mixture was thoroughly stirred and mixed. A wettable powder containing 25% of No. 1 and 20% of Compound No. 11 was obtained. Compound No. 1 25 parts by weight 〃 No. 11 20 〃 Kaolin clay 45 〃 White carbon 5 〃 Solpol 5039 (Toho Chemical trademark, anionic surfactant) 4 〃 Ravisol BB-75 (NOF trademark, anionic surfactant) Active agent) 1 〃 Example 2 Liquid agent The active ingredients of compound A group and B group and a surfactant were dissolved in ion-exchanged water, and compound No. 4 was dissolved in 12
A solution of the composition of the present invention containing 18% of Compound No. 12 was obtained. Compound No. 4 12 parts by weight 〃 No. 12 18 〃 Polyoxyethylene aryl ether 5 〃 Ion-exchange treated water 65 〃 Example 3 Granules Bentonite, the active substance of compound group A and group B
Clay and surfactant are mixed, water is added, kneaded uniformly with a kneader, granulated using a granulator, and dried with air to create a product containing 1% of Compound No. 6 and 2% of Compound No. 11. Granules of the composition of the present invention were obtained. Raw material of compound No. 6 1 part by weight 〃 Raw material of No. 11 2 〃 Dioctylsulfosuccinate 1 〃 Bentonite 40 〃 Clay 56 〃 Example 4 Microgranules The raw materials of compound group A and group B were diluted with water. In a speed kneader, pour into the fine zeolite particles (48 to 150 mesh) being stirred, add a diluted surfactant solution in water, continue stirring, add white carbon, take out, and dry with air. Fine granules of the composition of the present invention containing 2% of Compound No. 4 and 3% of Compound No. 12 were obtained. Raw material of compound No. 4 2 parts by weight Raw material of No. 12 3 Fine zeolite 90 Polyoxyethylene dodecyl ether 2 White carbon 3 Effect of the invention The herbicidal composition of the present invention can be used individually. It has far superior fast-acting and synergistic effects, and will surely wilt harmful grasses in non-agricultural land within a month. Also,
As mentioned above, it is fast-acting, but also has a residual effect. Moreover, the dead weeds are not in a standing state but in a fallen state, which has advantages in environmental beautification, crime prevention, and disaster prevention.

Claims (1)

【特許請求の範囲】[Claims] 1 2−(4−イソプロピル−4−メチル−5−
オキソ−2−イミダゾリン−2−イル)ニコチン
酸、そのアルカリ金属塩、低級アルキル(C1
C4)エステルまたは低級アルキル(C1〜C4)ア
ミン塩とメチルN−(4−アミノフエニルスルホ
ニル)カーバメイトまたはそのアルカリ金属塩と
を含有することを特徴とする除草組成物。
1 2-(4-isopropyl-4-methyl-5-
oxo-2-imidazolin-2-yl) nicotinic acid, its alkali metal salts, lower alkyl (C 1 -
A herbicidal composition comprising a C4 ) ester or a lower alkyl ( C1 to C4 ) amine salt and methyl N-(4-aminophenylsulfonyl)carbamate or an alkali metal salt thereof.
JP59266429A 1984-12-19 1984-12-19 Herbicidal composition Granted JPS61145104A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP59266429A JPS61145104A (en) 1984-12-19 1984-12-19 Herbicidal composition
GB08530401A GB2169203B (en) 1984-12-19 1985-12-10 Herbicidal composition
AU51145/85A AU568784B2 (en) 1984-12-19 1985-12-12 Herbicidal composition
BR8506361A BR8506361A (en) 1984-12-19 1985-12-18 HERBICIDE COMPOSITION AND PROCESS TO COMBAT WEED
ZA859661A ZA859661B (en) 1984-12-19 1985-12-18 Herbicidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59266429A JPS61145104A (en) 1984-12-19 1984-12-19 Herbicidal composition

Publications (2)

Publication Number Publication Date
JPS61145104A JPS61145104A (en) 1986-07-02
JPH0524881B2 true JPH0524881B2 (en) 1993-04-09

Family

ID=17430810

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59266429A Granted JPS61145104A (en) 1984-12-19 1984-12-19 Herbicidal composition

Country Status (5)

Country Link
JP (1) JPS61145104A (en)
AU (1) AU568784B2 (en)
BR (1) BR8506361A (en)
GB (1) GB2169203B (en)
ZA (1) ZA859661B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2243160B (en) * 1990-02-13 1994-08-10 Honda Motor Co Ltd A method of producing a moulded article
DE10160139A1 (en) * 2001-12-07 2003-06-18 Bayer Cropscience Gmbh Synergistic herbicidal compositions containing certain herbicides from the group of benzoylcylohexanediones
CN103907613B (en) * 2014-04-15 2016-01-20 山东潍坊润丰化工股份有限公司 A kind of Herbicidal combinations and application thereof containing hexazinone and imazapyr

Also Published As

Publication number Publication date
AU5114585A (en) 1986-06-26
BR8506361A (en) 1986-09-02
GB8530401D0 (en) 1986-01-22
AU568784B2 (en) 1988-01-07
JPS61145104A (en) 1986-07-02
GB2169203A (en) 1986-07-09
ZA859661B (en) 1986-08-27
GB2169203B (en) 1987-11-18

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