JPS6120521B2 - - Google Patents

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Publication number
JPS6120521B2
JPS6120521B2 JP3898477A JP3898477A JPS6120521B2 JP S6120521 B2 JPS6120521 B2 JP S6120521B2 JP 3898477 A JP3898477 A JP 3898477A JP 3898477 A JP3898477 A JP 3898477A JP S6120521 B2 JPS6120521 B2 JP S6120521B2
Authority
JP
Japan
Prior art keywords
nicotinamide
powder
parts
hio
tetrachloroisophthalonitrile
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
JP3898477A
Other languages
Japanese (ja)
Other versions
JPS53124619A (en
Inventor
Shiro Okuda
Ban Sanai
Akira Kawarada
Setsuo Takeuchi
Yasuo Oota
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.)
RIKEN Institute of Physical and Chemical Research
Original Assignee
RIKEN Institute of Physical and Chemical Research
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 RIKEN Institute of Physical and Chemical Research filed Critical RIKEN Institute of Physical and Chemical Research
Priority to JP3898477A priority Critical patent/JPS53124619A/en
Publication of JPS53124619A publication Critical patent/JPS53124619A/en
Publication of JPS6120521B2 publication Critical patent/JPS6120521B2/ja
Granted legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

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

本発明は、3―ヒドロキシ―5―メチルイソオ
キサゾール及びテトラクロロイソフタロニトリル
の併用により生ずる植物薬害の防除剤に関する。 3―ヒドロキシ―5―メチルイソオキサゾール
(以下HIOと略称する)及びテトラクロロイソフ
タロニトル(以下TPNと略称する)は、いずれ
も優れた植物病原菌防除作用を有する物質である
が、両者は抗菌スペクトルを異にしている。たと
えばHIO剤ではリゾープス属菌による病害を防ぐ
ことができず、またTPN剤ではフザリウム属菌
の防除が不完全である。このため稲の苗立枯病な
どの防除には、HIO剤とTPN剤を併用する方法
が用いられ、これによつて卓越した効果が認めら
れている。しかし両者を同時に使用すると、種々
の薬害たとえばモミの立上がり障害、根の生育停
仕及び褐変、冠根異常、発芽抑制、苗の生育障
害、鞘葉褐変、奇形などを起こすことが知られて
いる。従つてこれらの薬害を避けるため両剤を3
〜10日ずらして施用しなければならないが、これ
が実用上の大きな欠点となつている。 本発明者らは、HIO及びTPNの併用により生
ずるこの種の薬害を防除するため種々研究した結
果、ニコチン酸アミドが優れた効果を示すことを
見出した。 本発明はこの知見に基づくもので、ニコチン酸
アミドを有効成分とする、3―ヒドロキシ―5―
メチルイソオキサゾール及びテトラクロロイソフ
タロニトリルの併用により生ずる植物薬害の防除
剤である。 ニコチン酸アミドはビタミンB複合体の一つと
して知られている生理活性物質であつて、植物生
長調節作用ならびに農園芸用殺菌作用を有するこ
とも知られている(特公昭50―26451号及び同51
―34446号各公報参照)。 しかしこの物質が前記の薬害に対して防除作用
を示すことは、全く予想外のことであつた。本発
明者らの研究によれば、この薬害防除作用はニコ
チン酸アミドにきわめて特異的な作用であつて、
他の植物生長調節剤たとえばα―ナフタリン酢
酸、インドール酢酸、カイネチン及びジベレリン
などを用いても、この種の薬害を防除することは
不可能であることが知られた。たとえばジベレリ
ンを用いた場合には、根長の抑制はほとんど回復
されず、また他の薬害も軽減されない。 本発明においてニコチン酸アミドは、遊離塩基
ならびに酸付加塩のいずれの形でも用いることが
できる。塩としては無機酸塩たとえば塩酸塩、硫
酸塩等、有機酸塩としてはたとえば修酸塩等があ
げられる。 本発明の有効成分であるニコチン酸アミドは、
HIO及びTPNが併用されるすべての農園芸用植
物における薬害を防除する作用を有する。対象植
物としては、特に稲が好ましい。 本発明の防除剤はHIO及びTPNが既に施用さ
れ又はこれから使用される農場に適用され、ニコ
チン酸アミド単独の形でも用いられるが、HIO及
び/又はTPNを含有することもできる。しかし
これらの三成分をそれぞれ別個にしておき、同時
に又は任意の順序で使用してもよいことは当然で
ある。後者の場合は、各成分の使用に際し適宜な
間隔をおいてもよい。 本発明の防除剤は、たとえば乳剤、水和剤、粉
剤、粒剤などの製剤として使用することができ、
この際普通の補助材料たとえば各種の担体、溶
剤、界面活性剤等を用いて製剤化することができ
る。さらに本発明の薬害防除剤は、たとえば肥
料、殺虫剤、殺菌剤、除草剤、植物生長調節剤等
を含有し又は併用することもできる。 本防除剤ま目的に応じて、たとえば土壌施用、
葉面散布などの一般施用法に従つて使用される。 ニコチン酸の有効使用量は広い範囲で変えるこ
とができ、対象作物その他の条件によつても異な
るが、通常はそれぞれHIO及びTPNに対して
1/10〜50倍量、好ましくは1〜10倍量(いずれ
も重量)である。 実施例 1 ニコチン酸アミド5部、タルク45部及びクレー
50部をよく混合粉砕して粉剤とする。使用に際し
てはそのまま苗床用土壌に混合する。 実施例 2 ニコチン酸アミド50部を水100部に溶解する。
使用に際しては水で希釈して床上に潅注する。 実施例 3 ニコチン酸アミド40部、ヒドロキシイソキサゾ
ール2.4部、テトラクロロイソフタニトリル7.5
部、ソルポール7080(東邦化学製界面活性剤)1
部及びホワイトカーボン10部にクレーを加えて
100部とし、よく混合粉砕して水和剤とする。使
用に際しては水で希釈して床上に潅注する。 実施例 4 タチガレン粉剤(有効成分:ヒドロキシイソオ
キサゾール4%、三共製)0.24g及び第1表に示
す量のニコチン酸アミド50%粉剤を、クレハ水稲
用培土(呉羽化学製)200mlによく混合し、水稲
種子(品種:日本晴)30粒を播種したのち、ダコ
ニール水和剤(有効成分:テトラクロロイソフタ
ロニトリル75%、クミアイ化学製)の500倍液200
mlを潅注した。次いで5000ルツクス及び30℃で生
育させ、13日後に薬害防除作用を調査した。その
結果を第1表に示す。
The present invention relates to an agent for controlling plant damage caused by the combination of 3-hydroxy-5-methylisoxazole and tetrachloroisophthalonitrile. 3-Hydroxy-5-methylisoxazole (hereinafter abbreviated as HIO) and tetrachloroisophthalonitrile (hereinafter abbreviated as TPN) are both substances that have excellent plant pathogen control effects, but both have a limited antibacterial spectrum. are different. For example, HIO agents cannot prevent diseases caused by Rhizopus spp., and TPN agents are incomplete in controlling Fusarium spp. For this reason, to control rice seedling damping off, etc., a method is used in which HIO agents and TPN agents are used in combination, and this method has been shown to be highly effective. However, when both are used at the same time, it is known that various chemical injuries may occur, such as failure of fir to stand up, growth failure and browning of roots, crown and root abnormalities, suppression of germination, growth problems of seedlings, browning of coleoptiles, and malformations. . Therefore, in order to avoid these drug-induced harms, both drugs should be administered at 3 doses.
Applications must be applied at intervals of ~10 days, which is a major practical drawback. The present inventors have conducted various studies to control this type of drug damage caused by the combination of HIO and TPN, and have found that nicotinamide exhibits excellent effects. The present invention is based on this knowledge, and consists of a 3-hydroxy-5-
This is a control agent for plant damage caused by the combined use of methylisoxazole and tetrachloroisophthalonitrile. Nicotinic acid amide is a physiologically active substance known as one of the vitamin B complexes, and is also known to have plant growth regulating effects and bactericidal effects for agriculture and horticulture (Japanese Patent Publication No. 50-26451 and the same). 51
-Refer to each publication No. 34446). However, it was completely unexpected that this substance exhibited a controlling effect against the above-mentioned chemical damage. According to the research conducted by the present inventors, this drug damage control effect is extremely specific to nicotinamide.
It has been found that it is impossible to control this type of phytotoxicity even by using other plant growth regulators such as α-naphthalene acetic acid, indole acetic acid, kinetin, and gibberellin. For example, when gibberellin is used, inhibition of root length is hardly recovered, and other chemical damages are not alleviated. In the present invention, nicotinamide can be used in either the form of a free base or an acid addition salt. Examples of the salt include inorganic acid salts such as hydrochloride and sulfate, and examples of organic acid salts include oxalate. Nicotinic acid amide, which is the active ingredient of the present invention, is
It has the effect of controlling phytotoxicity in all agricultural and horticultural plants where HIO and TPN are used together. Rice is particularly preferred as the target plant. The pest control agent of the present invention is applied to farms where HIO and TPN have already been applied or will be used, and can be used in the form of nicotinamide alone, but can also contain HIO and/or TPN. However, it is of course possible to keep these three components separate and use them simultaneously or in any order. In the latter case, each component may be used at appropriate intervals. The pesticidal agent of the present invention can be used as a formulation such as an emulsion, a wettable powder, a powder, or a granule.
At this time, the formulation can be prepared using conventional auxiliary materials such as various carriers, solvents, surfactants, etc. Furthermore, the phytotoxicity control agent of the present invention may contain or be used in combination with, for example, fertilizers, insecticides, fungicides, herbicides, plant growth regulators, and the like. Depending on the purpose of this pest control agent, for example, soil application,
Used according to common application methods such as foliar spraying. The effective amount of nicotinic acid can be varied over a wide range and varies depending on the target crop and other conditions, but it is usually 1/10 to 50 times the amount of HIO and TPN, preferably 1 to 10 times. amount (both weight). Example 1 5 parts of nicotinamide, 45 parts of talc and clay
Mix and grind 50 parts thoroughly to make a powder. When using it, mix it directly into seedbed soil. Example 2 50 parts of nicotinamide are dissolved in 100 parts of water.
To use, dilute with water and sprinkle on the floor. Example 3 40 parts of nicotinamide, 2.4 parts of hydroxyisoxazole, 7.5 parts of tetrachloroisophthanitrile
Part, Solpol 7080 (Toho Chemical surfactant) 1
and 10 parts of white carbon with clay added.
Make 100 parts, mix well and grind to make a wettable powder. To use, dilute with water and sprinkle on the floor. Example 4 0.24 g of Tachigaren powder (active ingredient: 4% hydroxyisoxazole, manufactured by Sankyo) and 50% nicotinic acid amide powder in the amount shown in Table 1 were thoroughly mixed with 200 ml of Kureha rice cultivation soil (manufactured by Kureha Chemical). After sowing 30 rice seeds (variety: Nipponbare), add 200 times a 500 times solution of Daconyl hydrating agent (active ingredient: 75% tetrachloroisophthalonitrile, manufactured by Kumiai Chemical Co., Ltd.)
ml was irrigated. The plants were then grown at 5,000 lux and 30°C, and the phytotoxicity control effect was investigated after 13 days. The results are shown in Table 1.

【表】 実施例 5 タチガレン粉剤6gを苗床用土壌(水田土壌2
部対クレハ水稲用培土1部)5に混合し、(30
×60×3cm)に入れ、これに水稲種子(品種:日
本晴)200gを播種した。次いでダコニール水和
剤の500倍液500ml及び第2表に示す量のニコチン
酸アミド50%水和剤の混合物をそれぞれ潅注し、
3000ルツクス及び30℃で育成し、14日後に薬害防
除作用を調査した。その結果を第2表に示す。な
お表中の記号は前記の意味を有する。
[Table] Example 5 6g of Tachigaren powder was added to seedbed soil (paddy soil 2
Mix 5 parts of Kureha paddy rice cultivation soil (1 part) and (30
x 60 x 3 cm), and 200 g of paddy rice seeds (variety: Nipponbare) were sown therein. Next, 500 ml of a 500 times solution of Daconyl hydrating powder and a mixture of 50% nicotinamide hydrating powder in the amount shown in Table 2 were irrigated, respectively.
The plants were grown at 3000 lux and 30°C, and their phytotoxicity control effect was investigated after 14 days. The results are shown in Table 2. In addition, the symbols in the table have the above-mentioned meanings.

【表】 実施例 6 フスマ培地でリゾープス菌及びフザリウム菌を
培養し、この培養物100g及び床土5を育苗箱
(30×60×3cm)中で混合し、さらにタチガレン
粉剤6g及びニコチン酸アミド10%粉剤40gをよ
く混和した。これに水稲種子(品種:日本晴)
200gを播種し、覆土したのち、ダコニール水和
剤の500倍液500mlを潅注した。30℃で48時間出芽
させたのち菌の発生状況及び薬害除作用を調査し
た。その結果を、無処理及びニコチン酸ミド無添
加の場合と併せて第3表に示す。表中の記号は前
記の意味を有する。
[Table] Example 6 Rhizopus bacteria and Fusarium bacteria were cultured in a bran medium, and 100 g of this culture and bed soil 5 were mixed in a seedling box (30 x 60 x 3 cm), and then 6 g of Tachigaren powder and 10 nicotinic acid amide were added. % powder was mixed well. Paddy rice seeds (variety: Nipponbare)
After 200 g of seeds were sown and covered with soil, 500 ml of a 500 times solution of Daconyl hydrating agent was irrigated. After sprouting at 30°C for 48 hours, the status of bacterial development and the effect of controlling chemical damage were investigated. The results are shown in Table 3 together with the cases without treatment and without the addition of nicotinic acid amide. The symbols in the table have the meanings given above.

【表】 これらの結果から明らかなように、ニコチン酸
アミドの使用により、HIO及びTPOの土壌病菌
に対する効果は悪影響を全く受けず、しかもこれ
らの併用により生ずる薬害が完全に防除されたこ
とが認められる。
[Table] As is clear from these results, the effects of HIO and TPO against soil pathogens were not adversely affected at all by the use of nicotinamide, and furthermore, the phytotoxicity caused by the combination of these was completely controlled. It will be done.

Claims (1)

【特許請求の範囲】 1 ニコチン酸アミドを有効成分とする、3―ヒ
ドロキシ―5―メチルイソオキサゾール及びテト
ラクロロイソフタロニトリルの併用により生ずる
植物薬害の防除剤。 2 3―ヒドロキシ―5―メチルイソオキサゾー
ル及び/又はテトラクロロイソフタロニトリルと
ニコチン酸アミドとを含有することを特徴とす
る、特許請求の範囲第1項に記載の薬害防除剤。
[Scope of Claims] 1. An agent for controlling plant damage caused by a combination of 3-hydroxy-5-methylisoxazole and tetrachloroisophthalonitrile, which contains nicotinamide as an active ingredient. 2. The chemical damage control agent according to claim 1, which contains 3-hydroxy-5-methylisoxazole and/or tetrachloroisophthalonitrile and nicotinic acid amide.
JP3898477A 1977-04-07 1977-04-07 Agent for preventing plant phytotoxicity Granted JPS53124619A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3898477A JPS53124619A (en) 1977-04-07 1977-04-07 Agent for preventing plant phytotoxicity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3898477A JPS53124619A (en) 1977-04-07 1977-04-07 Agent for preventing plant phytotoxicity

Publications (2)

Publication Number Publication Date
JPS53124619A JPS53124619A (en) 1978-10-31
JPS6120521B2 true JPS6120521B2 (en) 1986-05-22

Family

ID=12540401

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3898477A Granted JPS53124619A (en) 1977-04-07 1977-04-07 Agent for preventing plant phytotoxicity

Country Status (1)

Country Link
JP (1) JPS53124619A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0261905U (en) * 1988-10-28 1990-05-09
EP3447319A1 (en) 2017-08-22 2019-02-27 Topcon Corporation Structure for applying pre-load to rolling bearing and three-dimensional survey device having the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0261905U (en) * 1988-10-28 1990-05-09
EP3447319A1 (en) 2017-08-22 2019-02-27 Topcon Corporation Structure for applying pre-load to rolling bearing and three-dimensional survey device having the same

Also Published As

Publication number Publication date
JPS53124619A (en) 1978-10-31

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