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JPS6345365B2 - - Google Patents
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JPS6345365B2 - - Google Patents

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Publication number
JPS6345365B2
JPS6345365B2 JP14636180A JP14636180A JPS6345365B2 JP S6345365 B2 JPS6345365 B2 JP S6345365B2 JP 14636180 A JP14636180 A JP 14636180A JP 14636180 A JP14636180 A JP 14636180A JP S6345365 B2 JPS6345365 B2 JP S6345365B2
Authority
JP
Japan
Prior art keywords
parts
granules
soil
test
methyl
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
JP14636180A
Other languages
Japanese (ja)
Other versions
JPS5770805A (en
Inventor
Hiroshi Kawada
Yasuhisa Kurosu
Haruki Kanasugi
Akio Hosokawa
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 JP14636180A priority Critical patent/JPS5770805A/en
Priority to AU75015/81A priority patent/AU549319B2/en
Priority to NL8104181A priority patent/NL8104181A/en
Priority to GB8127991A priority patent/GB2085301B/en
Priority to DE3140879A priority patent/DE3140879C2/en
Priority to SU813348255A priority patent/SU1419504A3/en
Priority to FR8119614A priority patent/FR2492222A1/en
Priority to IT24553/81A priority patent/IT1140227B/en
Priority to BR8106750A priority patent/BR8106750A/en
Publication of JPS5770805A publication Critical patent/JPS5770805A/en
Priority to US06/462,964 priority patent/US4696947A/en
Publication of JPS6345365B2 publication Critical patent/JPS6345365B2/ja
Granted legal-status Critical Current

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Description

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

本発明は、粒状の有害線虫防除剤に関する。 従来より、果樹、茶樹等の永年作物において、
土壌病害虫の防除は重要な課題であつたが、更に
近年、畑の集約的利用、施設栽培、そ菜の特産地
化が進むにつれ、土壌有害線虫及び病害菌による
連作障害が問題となつてきている。特に忌地とし
て知られる農作物栽培の不適な畑では、その原因
として土壌病害菌の他に、土壌有害線虫が大きく
関与していることが知られている。土壌有害線虫
の被害は、種々の形で発現するが、初期生育の遅
延又は枯死、それに伴なう収量減が一般的で、こ
の他根菜類では奇形を生じたり、表面に傷を付け
たりして商品価値を極度に低下させる。その上、
種々の土壌病害菌の媒介者としての役割も大き
い。更に一旦、線虫の被害をこうむつた畑は、連
作が不可能で、特に日本のような集約型農業では
輪作体系を組むにも余裕がなく、使用上合理的で
安全かつ低価格の殺線虫剤が強く要望されてい
る。 従来殺線虫剤として知られる薬剤は、ハロゲン
化炭化水素系のくん蒸剤が主流で、例えばクロル
ピクリン、臭化メチル、D―D(1,3―ジクロ
ロプロペン)、EDB(エチレンジブロマイド)、
DCIP(ビスクロロイソプロピルエーテル)、
DBCP(1,2―ジブロモ―3―クロロプロパン)
等がある。 これら薬剤のうち、クロルピクリン、臭化メチ
ルはその物性からボンベ詰めの形態で市販され、
主に床土消毒に使用されている。EDB、D―D
は世界的に最も多い使用量の殺線虫剤であるが、
その物性から油剤もしくは乳剤形態で市販されて
いる。また、DBCP、DCIPはその沸点がそれぞ
れ187℃、196℃と高いため、その他のくん蒸剤と
同様乳剤としても使用されるが、主に粒剤型態で
市販されている。 一方、これらのハロゲノ炭化水素系化合物はそ
の特性として粘膜刺激性、金属腐食性といつた取
扱上問題を有するものである。 更に、DBCP、DCIPが一部作物に薬害を生じ
ない以外、ほとんどの薬剤は作物に対して薬害を
生じる。またこれらの薬剤の大部分が液体の剤型
であり、土壌に処理する場合、特別な器具、機械
を必要とする。更にこれら化合物の沸点が例えば
CH3Br:4℃、D―D:119℃、EDB:131℃と
低いため、効果を発現させるために一定期間土壌
表面を水封し、あるいはポリエチレン等で被覆
し、加えて、薬害を避けるため、一定期間後に耕
起して薬剤を大気中に逸散させる(ガス抜き)と
いつた作業を必要とする。このように、使用に際
して、非常な不便さを伴うものである。また、粒
剤化可能なDBCP、DCIPにおいては、DBCP剤
が人体に対する毒性ならびに、土壌、河川水中に
長期に残留するという問題点を有し、製造が中止
されている。DCIP剤は殺線虫活性が低いという
問題を有している。 その他に、米国においては、接触型殺線虫剤も
使用されている。例えばFensulfothion〔o,o―
ジエチル o―(4―メチルスルフイニル)フエ
ニルホスホロチオエート〕、Ethoprop(o―エチ
ルs,s―ジプロピルホスホロジチオエート)、
Phenamiphos〔エチル 3―メチル―4―(メチ
ルチオ)フエニル(1―メチルエチル)ホスホロ
アミデート〕等の有機リン剤、ならびに
Carbofuran(2,3―ジヒドロ―2,2―ジメチ
ル―7―ベンゾフラニルメチルカーバメイト)、
Aldicarb〔2―メチル―2(メチルチオ)プロピ
ルアルデヒドo―(メチルカーバモイル)オキシ
ム〕等のカーバメイト剤である。しかしながら、
これらの接触型殺線虫剤は殺線虫活性が高い反
面、極めて毒性が高く、粒剤型態でのみ、しかも
業者による施用のみが許可されているにすぎな
い。 本発明者らは、このような問題点を解決するた
め、種々研究した結果、本発明を完成させた。本
発明は、S―メチル―N,N―ジメチルチオール
カーバメイトを含有する粒状の有害線虫防除剤で
ある。 本発明にいう「粒状」という言葉には、いわゆ
る粒剤のほかに、いわゆる微粒剤も含まれる。 また本発明に係る、S―メチル―N,N―ジメ
チルチオールカーバメイトの粒状化に際しては、
硅ソウ土など吸油性の高い粒状担体に含浸又は付
着せしめて粒剤、微粒剤を作成できる。これに限
定されるものではなく、その用途に応じて各種担
体と混合し、水等でねりこみ通常広く使用されて
いる農薬製造技術によつて粒状化することも可能
である。使用される担体としては、たとえばベン
トナイト、タルク、カオリンクレー、磋ソウ土な
どがあげられる。更に、製剤に際して乳化性、分
散性を与えるために界面活性剤等を配合すること
ができる。 粒剤中の有効成分量はほぼ5〜40%の範囲で増
減させることができる。 また、本発明に係る薬剤は単独で使用するのみ
でなく、他の農薬、たとえば選択的除草剤、殺菌
剤、殺虫剤もしくは肥料と混合して使用すること
も可能である。 本発明に係る化合物は、ジメチルアミンと硫化
カルボニルを反応させ、生成したカーバメイトの
塩にメチルクロライドまたはジメチル硫酸を反応
させること等によつて、容易に合成しうるもので
ある。その沸点は117℃/90mmHgである。 以下、試験例をあげて本発明に係る有害線虫防
除剤のすぐれた効果について説明する。 試験例 1 トマトを指標としたサツマイモネコブ線虫に対
する試験 サツマイモを寄主として増殖させたサツマイモ
ネコブ線虫(meloidogyne incognita)汚染土壌
を高さ14cmの1/10000aポツトに詰め、実施例1
に準じて作用した粒剤の所定量を混和した。なお
比較目的で使用した市販の殺線虫剤であるDBCP
粒剤、DCIP粒剤も同様に処理した。 粉剤(対照)は有効成分25部、フバサミクレー
(大貫鉱山(株)商標)50部、カープレツクス(塩野
義製薬(株)商標)25部にて混合調整し、粒剤と同様
に土壌に混和処理した。乳剤(対照)は有効成分
10部、キシレン85部、ソルポール800A(東邦化学
(株)商標)5部にて混合し、ポツト表面に1000/
10aとなるよう水で稀釈して潅注処理した。各薬
剤処理後7日間放置し、ポツト当り10粒トマト種
子を播種した。試験はガラス温室内(25〜30℃)
で実施し、播種後1ケ月目に寄生根こぶ程度、薬
害及び茎葉重を調査した。試験は3回繰り返しで
実施し、その結果の平均値は第1表に示す通りで
ある。なお、寄生根こぶ程度及び薬害については
次の数値により表わした。
The present invention relates to a granular harmful nematode control agent. Traditionally, in perennial crops such as fruit trees and tea plants,
Controlling soil pests and diseases has always been an important issue, but in recent years, as fields have become more intensively used, cultivated in facilities, and vegetables have become specialties, problems with continuous cropping caused by soil harmful nematodes and pathogens have become a problem. There is. In particular, it is known that in fields that are unsuitable for crop cultivation, which are known as inhospitable areas, in addition to soil pathogenic bacteria, harmful soil nematodes are largely involved. Damage caused by soil harmful nematodes can occur in a variety of ways, but the most common ones are delayed initial growth or death, and an associated decrease in yield.In addition, root vegetables may be deformed or have their surfaces damaged. and extremely reduce the product value. On top of that,
It also plays a major role as a vector for various soil pathogens. Furthermore, once a field has been damaged by nematodes, continuous cropping is impossible, especially in intensive agriculture like Japan, where there is no room for a crop rotation system. There is a strong demand for nematicides. Conventional drugs known as nematicides are mainly halogenated hydrocarbon fumigants, such as chloropicrin, methyl bromide, DD (1,3-dichloropropene), EDB (ethylene dibromide),
DCIP (bischloroisopropyl ether),
DBCP (1,2-dibromo-3-chloropropane)
etc. Among these drugs, chloropicrin and methyl bromide are commercially available in cylinder form due to their physical properties.
It is mainly used for soil disinfection. EDB, D-D
is the most commonly used nematicide worldwide,
Due to its physical properties, it is commercially available in oil or emulsion form. In addition, DBCP and DCIP have high boiling points of 187°C and 196°C, respectively, so they are used as emulsions like other fumigants, but they are mainly commercially available in granule form. On the other hand, these halogeno-hydrocarbon compounds have problems in handling, such as mucous membrane irritation and metal corrosiveness. Furthermore, most drugs cause phytotoxicity to crops, except for DBCP and DCIP, which do not cause phytotoxicity to some crops. Additionally, most of these chemicals are in liquid form, and require special equipment and machinery when applied to soil. Furthermore, the boiling points of these compounds are e.g.
CH 3 Br: 4℃, DD: 119℃, EDB: 131℃, which are low, so in order to develop the effect, the soil surface is sealed with water for a certain period of time or covered with polyethylene, etc., and in addition, to avoid chemical damage. Therefore, it is necessary to plow after a certain period of time to dissipate the chemicals into the atmosphere (degassing). As described above, it is very inconvenient to use. Furthermore, production of DBCP and DCIP, which can be made into granules, has been discontinued due to the problems that the DBCP agent is toxic to the human body and remains in soil and river water for a long time. DCIP agents have a problem of low nematicidal activity. In addition, contact nematicides are also used in the United States. For example, Fensulfothion [o, o-
Diethyl o-(4-methylsulfinyl) phenyl phosphorothioate], Ethoprop (o-ethyl s,s-dipropyl phosphorodithioate),
Organic phosphorus agents such as Phenamiphos [ethyl 3-methyl-4-(methylthio)phenyl(1-methylethyl)phosphoramidate], and
Carbofuran (2,3-dihydro-2,2-dimethyl-7-benzofuranyl methyl carbamate),
It is a carbamate agent such as Aldicarb [2-methyl-2(methylthio)propylaldehyde o-(methylcarbamoyl)oxime]. however,
Although these contact-type nematicides have high nematicidal activity, they are extremely toxic and are only permitted in granule form, and moreover, only for application by a professional. In order to solve these problems, the present inventors completed the present invention as a result of various studies. The present invention is a granular harmful nematode control agent containing S-methyl-N,N-dimethylthiol carbamate. The term "granular" as used in the present invention includes not only so-called granules but also so-called fine granules. Furthermore, when granulating S-methyl-N,N-dimethylthiol carbamate according to the present invention,
Granules and fine granules can be prepared by impregnating or adhering it to a highly oil-absorbing granular carrier such as diatomaceous earth. The present invention is not limited to this, but it is also possible to mix it with various carriers depending on the use, mix it with water, etc., and granulate it by a commonly used agricultural chemical production technique. Examples of carriers used include bentonite, talc, kaolin clay, and clay. Furthermore, surfactants and the like may be added to impart emulsifying and dispersing properties during formulation. The amount of active ingredient in the granules can be increased or decreased by approximately 5-40%. Furthermore, the agent according to the present invention can be used not only alone, but also in combination with other agricultural chemicals, such as selective herbicides, fungicides, insecticides, or fertilizers. The compound according to the present invention can be easily synthesized by reacting dimethylamine with carbonyl sulfide and reacting the resulting carbamate salt with methyl chloride or dimethyl sulfate. Its boiling point is 117°C/90mmHg. The excellent effects of the harmful nematode control agent according to the present invention will be explained below with reference to test examples. Test Example 1 Test against sweet potato knot nematode using tomatoes as an indicator Sweet potato knot nematode (meloidogyne incognita) contaminated soil grown using sweet potatoes as a host was packed in a 1/10000a pot with a height of 14 cm, and Example 1
A predetermined amount of granules that acted according to the method was mixed. DBCP, a commercially available nematicide, was used for comparison purposes.
Granules and DCIP granules were also treated in the same way. The powder (control) was mixed with 25 parts of the active ingredient, 50 parts of Fubasami Clay (trademark of Onuki Mining Co., Ltd.), and 25 parts of Carplex (trademark of Shionogi & Co., Ltd.), and mixed into the soil in the same manner as the granules. . Emulsion (control) is the active ingredient
10 parts, xylene 85 parts, Solpol 800A (Toho Chemical
Co., Ltd. Trademark) Mix at 5 parts and apply 1000/ml on the surface of the pot.
It was diluted with water to a concentration of 10a and then irrigated. After each chemical treatment, the pots were left for 7 days, and 10 tomato seeds were sown per pot. The test was conducted in a glass greenhouse (25-30℃)
One month after sowing, the degree of parasitic root galls, chemical damage, and stem and leaf weight were investigated. The test was repeated three times, and the average values of the results are shown in Table 1. The degree of parasitic root galls and chemical damage were expressed by the following values.

【表】【table】

【表】【table】

【表】【table】

【表】 試験例 2 ゴボウを指標とするキタネグサレ線虫に対する
防除試験 インゲン豆を寄主として増殖させたキタネグサ
レ線虫(pratylenchus penetrans)汚染土壌を高
さ14cmの1/10000aポツトに詰め、実施例1に準
じて作成した粒剤の所定量を混和した。なお
DBCP粒剤ならびに試験例1と同様に調整した粉
剤も同様に処理した。7日間放置後、ポツト当り
5粒のゴボウ種子を播種した。試験はガラス温室
内(25〜30℃)で実施し、播種後50日目に根部加
害程度、薬害及び総重量を調査した。試験は3回
繰り返しで実施し、その結果の平均値を第2表に
示す。根部の加害程度は根部褐変部位数により不
記の通り判定した。薬害の表示は試験例1に準じ
て行つた。
[Table] Test Example 2 Control test against Pratylenchus penetrans using burdock as an indicator. Soil contaminated with Pratylenchus penetrans, which was grown using kidney beans as a host, was packed in a 1/10000a pot with a height of 14 cm, and the same method as in Example 1 was carried out. A predetermined amount of granules prepared in the same manner were mixed. In addition
DBCP granules and powders prepared in the same manner as in Test Example 1 were also treated in the same manner. After standing for 7 days, 5 burdock seeds were sown per pot. The test was conducted in a glass greenhouse (25-30°C), and the degree of root damage, chemical damage, and total weight were investigated 50 days after sowing. The test was repeated three times, and the average value of the results is shown in Table 2. The degree of damage to the roots was determined by the number of browned parts of the roots (not specified). The labeling of drug damage was carried out in accordance with Test Example 1.

【表】【table】

【表】 試験例 3 キユウリを対象とした圃場におけるサツマイモ
ネコブ線虫の防除試験 前作にサツマイモを植付けてあつた、サツマイ
モネコブ線虫汚染圃場に、実施例2に準じて作成
した粒剤、及び試験例1と同様に調整した粉剤を
圃場の全面に散布し、直ちに耕起混層した。なお
DBCP粒剤も同様に処理した。5日間放置後、本
葉5枚が展開したキユウリ苗を1区2m2当り8本
定植した。試験は3回繰り返しで、6月中旬から
8月上旬にかけて行い、その間の潅水、病害虫防
除は慣行に従つた。側枝を含む草丈及び試験例1
に準じた根こぶ程度、薬害の調査結果の平均値は
第3表に示す通りである。
[Table] Test Example 3 Control test of sweet potato knot nematode in the field targeting cucumbers Granule prepared according to Example 2 and test in a field contaminated with sweet potato knot nematode where sweet potatoes had been planted in the previous crop. A powder prepared in the same manner as in Example 1 was spread over the entire surface of the field, and the field was immediately mixed with plowing. In addition
DBCP granules were treated in the same way. After being left for 5 days, 8 cucumber seedlings with 5 true leaves developed were planted per 2 m 2 of each plot. The test was repeated three times from mid-June to early August, during which irrigation and pest control practices were followed. Plant height including lateral branches and test example 1
Table 3 shows the average values of the root gall level and chemical damage survey results.

【表】 以上の通り、本発明粒剤は、作物に大きな被害
を与えるサツマイモネコブ線虫、キタネグサレ線
虫に対して高い防除効果を示す。しかもトマト、
キユウリ及びゴボウに対して薬害もなく安全性の
高いすぐれた殺線虫剤である。 以下に製剤の例を示す。なお文中において部と
あるのは、いずれも重量部を示す。 実施例 1 S―メチル―N,N―ジメチルチオールカーバ
メイト 25部 粒状ケイソウ土 75部 以上有効成分を粒状ケイソウ土に含浸させて粒
剤とした。 実施例 2 S―メチル―N,N―ジメチルチオールカーバ
メイト 25部 ニユーコール565(分散剤、日本乳化剤(株)商標)
5部 粒状ケイソウ土 70部 以上有効成分と活性剤を混合したものを粒状ケ
イソウ土に含浸させ粒剤とした。 実施例 3 S―メチル―N,N―ジメチルチオールカーバ
メイト 25部 カープレツクス(シリカ、塩野義製薬(株)商標)
15部 ベントナイト 55部 サーフイノールTGE(非イオン界面活性剤、
Air Products and Chemicals,Inc商標)
2部 ラピゾールB―80(分散剤、日本油脂(株)商標)
3部 以上を混合粉砕して、水とねり粒剤とした。
[Table] As described above, the granules of the present invention exhibit a high control effect against sweet potato knot nematodes and northern red cabbage nematodes that cause great damage to crops. And tomatoes,
It is an excellent nematocide that is highly safe and has no chemical harm to cucumbers and burdock. Examples of formulations are shown below. In addition, all parts in the text indicate parts by weight. Example 1 S-methyl-N,N-dimethylthiol carbamate 25 parts Granular diatomaceous earth 75 parts The above active ingredients were impregnated into granular diatomaceous earth to prepare granules. Example 2 S-methyl-N,N-dimethylthiol carbamate 25 parts Newcol 565 (dispersant, Nippon Nyukazai Co., Ltd. trademark)
5 parts granular diatomaceous earth 70 parts A mixture of the above active ingredient and activator was impregnated into granular diatomaceous earth to form a granule. Example 3 S-methyl-N,N-dimethylthiol carbamate 25 parts Carplex (silica, trademark of Shionogi & Co., Ltd.)
15 parts bentonite 55 parts Surfinol TGE (nonionic surfactant,
Air Products and Chemicals, Inc. Trademark)
2 parts Rapizole B-80 (dispersant, NOF Corporation trademark)
Three parts or more were mixed and ground to form granules by mixing with water.

Claims (1)

【特許請求の範囲】[Claims] 1 S―メチル―N,N―ジメチルチオールカー
バメートを含有する粒状の有害線虫防除剤。
1. A granular harmful nematode control agent containing S-methyl-N,N-dimethylthiol carbamate.
JP14636180A 1980-10-21 1980-10-21 Controlling agent against harmful nematode Granted JPS5770805A (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
JP14636180A JPS5770805A (en) 1980-10-21 1980-10-21 Controlling agent against harmful nematode
AU75015/81A AU549319B2 (en) 1980-10-21 1981-09-08 Nematocide
NL8104181A NL8104181A (en) 1980-10-21 1981-09-10 THE INVENTION RELATES TO A NEMATOCIDE.
GB8127991A GB2085301B (en) 1980-10-21 1981-09-16 Nematocide
DE3140879A DE3140879C2 (en) 1980-10-21 1981-10-14 nematicide
SU813348255A SU1419504A3 (en) 1980-10-21 1981-10-19 Versions of chematocid composition
FR8119614A FR2492222A1 (en) 1980-10-21 1981-10-19 NEMATOCIDAL AGENTS COMPRISING THIOLCARBAMATE
IT24553/81A IT1140227B (en) 1980-10-21 1981-10-19 NEMATOCIDE FOR THE CONTROL OF NEMATODES IN AGRICULTURAL LAND
BR8106750A BR8106750A (en) 1980-10-21 1981-10-20 NEMATOCIDE
US06/462,964 US4696947A (en) 1980-10-21 1983-02-01 Nematocide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14636180A JPS5770805A (en) 1980-10-21 1980-10-21 Controlling agent against harmful nematode

Publications (2)

Publication Number Publication Date
JPS5770805A JPS5770805A (en) 1982-05-01
JPS6345365B2 true JPS6345365B2 (en) 1988-09-09

Family

ID=15405973

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14636180A Granted JPS5770805A (en) 1980-10-21 1980-10-21 Controlling agent against harmful nematode

Country Status (2)

Country Link
JP (1) JPS5770805A (en)
SU (1) SU1419504A3 (en)

Also Published As

Publication number Publication date
JPS5770805A (en) 1982-05-01
SU1419504A3 (en) 1988-08-23

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