JPS59212408A - Pest-combatting composition for industrial purpose - Google Patents
Pest-combatting composition for industrial purposeInfo
- Publication number
- JPS59212408A JPS59212408A JP58085532A JP8553283A JPS59212408A JP S59212408 A JPS59212408 A JP S59212408A JP 58085532 A JP58085532 A JP 58085532A JP 8553283 A JP8553283 A JP 8553283A JP S59212408 A JPS59212408 A JP S59212408A
- Authority
- JP
- Japan
- Prior art keywords
- methylisothiazolin
- salt
- heavy metal
- metal complex
- chloro
- 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
Links
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は工業用有害生物防除組成物に係り、更に詳しく
はジチオカルバミン酸重金属地の少なく(但し、Rは水
素又は・・ロゲン原子を′示す。)にて示される2−メ
チルイソチアゾリン−6−オン又はその金属錯塩化合物
を有効成分として含有することを特徴上する工業用有害
生物防除組成物に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an industrial pest control composition, and more particularly to a dithiocarbamic acid heavy metal base represented by 2 (wherein R represents hydrogen or... rogen atom). - An industrial pest control composition characterized by containing methylisothiazolin-6-one or a metal complex compound thereof as an active ingredient.
従来から工業用殺菌殺藻剤は数多く開発されてきたが、
その用途は例えば工業用水、製紙白水。Many industrial bactericides and algaecides have been developed, but
Its uses include, for example, industrial water and white water for paper manufacturing.
塗料、船底塗料、切削加工油および高分子エマルジョン
等の広範囲にわたっているが、その有効性に関して当初
から限度があって効かない生物があったり、また長く使
用する間に生物の優勢様の変遷、あるいは薬剤に対する
生物の抵抗力の獲得等によって期待した効果が得られず
2例えば工業用水にあっては熱交換機能を低下させ、あ
るいは発生電位差により装置の腐触を早めたり、また製
紙白水にあたっては製品の品質低下は勿論、抄紙工程に
おける紙切れ等の障害によって連続運転を阻害し、生産
効率の低下を招くなど経済的にも多大なる損害を与えて
いる。従って安定した持続効果と、かつ巾広い適用性を
有する工業用有害生物の防除対策の確立が強く望まれて
いる。このような現状から、まだ有害生物の変遷と抵抗
性の獲得とその回避の目的でその一つの方法として2次
々と新しい薬剤を施用することが提唱されているが。Paints, ship bottom paints, cutting oils, polymer emulsions, etc. are used in a wide range of products, but there are limits to their effectiveness from the beginning and they may not work against some organisms. Expected effects may not be obtained due to the acquisition of resistance by organisms to chemicals, etc. (2) For example, in the case of industrial water, the heat exchange function may be reduced, or the generated potential difference may accelerate corrosion of the equipment, and in the case of white water used in paper manufacturing, the product may deteriorate. Not only does the quality deteriorate, but continuous operation is obstructed due to paper breakage and other obstacles in the papermaking process, leading to a decline in production efficiency and causing great economic damage. Therefore, there is a strong desire to establish measures for controlling industrial pests that have stable, long-lasting effects and wide applicability. Given this current situation, it is still being proposed to apply new drugs one after another as one method for the purpose of monitoring the evolution of pests, acquiring resistance, and avoiding it.
薬剤の数や種類およびそれらの性能の点でおのずから限
度があり2才だ工業用有害生物の種類の雑多なこと、そ
の上使用しているうちに2種又はそれ以上の薬剤に対し
て同時(/C抵抗性をもつ生物が容易に発生しうろこと
、かつそれが複雑な生物学的な内容を含んでいて容易に
解明することが困難であることなどの理由から未だにP
Iイ決されていない。そこで本発明者等は上記のような
問題を回避し、かつ広範囲の用途に耐え得る工業用有害
生物の防除方法を確立すべく研究を重ねた結果ジテオ(
但し、Rは水素又は・・ロゲン原子を示す。)にて示さ
れる2〜メチルイソチアゾリン−6−オン化合物又はこ
れらの金属錯塩化合物を有効成分とする組成物が、安定
なかつ持続する防除効果を示すことを見い出し1本発明
を完成するに至った。There are natural limits in terms of the number and types of chemicals and their performance, and the variety of types of industrial pests, and on top of that, during use, there is a possibility that two or more types of chemicals may be used at the same time ( /C resistant organisms are easily generated, and because it contains complex biological contents that are difficult to elucidate, P
I haven't decided yet. Therefore, the present inventors conducted repeated research to establish a method for controlling industrial pests that avoids the above-mentioned problems and can withstand a wide range of applications.
However, R represents hydrogen or... rogen atom. The present invention has been completed based on the discovery that compositions containing the 2-methylisothiazolin-6-one compounds shown in ) or their metal complex salt compounds as active ingredients exhibit stable and long-lasting pesticidal effects.
ジチオカルバミン酸型金属塩I″i+農園芸用の分野に
殺菌剤等として広く使用されており、優れた作用効果を
示すものとして知られている。そして人畜に対して低毒
性であることから、工業用としても殺菌、殺藻、スライ
ムコントロール剤等の水処理剤として巾広く使用されて
いるが、その効果において持続性があるものの効果が若
干緩慢であるので、その点に関して難点が存在する。一
方。Dithiocarbamate type metal salt I''i+ is widely used as a fungicide in the fields of agriculture and horticulture, and is known to exhibit excellent effects.And because it has low toxicity to humans and livestock, it is used industrially. It is widely used as a water treatment agent such as disinfectant, algaecide, and slime control agent, but although its effect is long-lasting, the effect is somewhat slow, so there are some drawbacks in this regard. .
2−メチルイノチアゾリン−6−オン化合物又はその金
属錯塩化合物は、静菌力の優れた化合物で活性があり、
かつ持続性があるものとして知られている。しかし、生
物の種類によって有効な濃度に差があり、また持続効果
も例えば1ケ月乃至3ヶ月と差があり、効果の安定性と
いう点で問題がある。更に上述した如く使用していると
2発生する耐性生物や生物の種類の変遷による問題があ
る。2-Methylinothiazolin-6-one compound or its metal complex salt compound is a compound with excellent bacteriostatic activity and is active.
It is also known to be sustainable. However, the effective concentration varies depending on the type of organism, and the duration of the effect also varies, for example, from 1 month to 3 months, which poses a problem in terms of the stability of the effect. Furthermore, as mentioned above, when used, there are problems due to the occurrence of resistant organisms and changes in the types of organisms.
本発明の組成物は1本発明の化合物の単独使用では活性
を示さない低濃度において著しく増強され。The compositions of the present invention are significantly potentiated at low concentrations where one compound of the present invention exhibits no activity when used alone.
また持続性においても改良されている。本発明のジチオ
カルバミン酸塩の酸部としては、アルキレンビスジチオ
カルバミン酸、単官能モノアルキルジチオカルバミン酸
、単官能ジアルキルジチオカルバミン酸が挙げられ、ま
た重金属塩部としては亜鉛、マンガン、銅、鉄が挙けら
れる。そしてこれらの重金属塩に対し他の重金A71S
塩が配位せるもの例えばエチンンビスジチオ力ルバミン
酸マンガンに亜鉛や銅が配位したものであっても本発明
に含まれる。更にアルキ7ンビスジチオ力ルバミン酸部
位と(又は)単官能モノ又はンアルキルジチオ力ルバミ
ン酸部位とか亜鉛等の重金属を介して結合せる混成塩で
あってもよい。具体的には7 エチレンビスジチオカル
バミン酸部位及び(又は)ジメチルジチオカルバミン酸
部位とが亜鉛を介して結合せる混成塩である。また、前
記一般にて示される2−メチルイソチアゾリン−3−オ
ン化合物としては5−クロル−2−メチルイソチアゾリ
ン−3−オン、2−メチルイソチアゾリン−3−オンが
挙げられ、またこれらと金属錯塩を形成せる金属塩とし
ては塩化亜鉛、塩化カルシウム、塩化マグネンウム、硝
酸マグネシウム、塩化鉄、塩化す) IJウム、硝酸銅
、硫酸亜鉛等が挙げられる。It also has improved durability. Examples of the acid moiety of the dithiocarbamate of the present invention include alkylene bisdithiocarbamic acid, monofunctional monoalkyldithiocarbamate, and monofunctional dialkyldithiocarbamate, and examples of the heavy metal salt moiety include zinc, manganese, copper, and iron. . And for these heavy metal salts, other heavy metals A71S
Even salts in which zinc or copper is coordinated to manganese bisdithiorubamate are included in the present invention. Furthermore, it may be a mixed salt that is bonded to an alkyl-7-bisdithio-rubamate moiety and/or a monofunctional mono- or alkyl-dithio-rubamate moiety via a heavy metal such as zinc. Specifically, 7 is a mixed salt in which an ethylenebisdithiocarbamate site and/or a dimethyldithiocarbamate site are bonded via zinc. In addition, examples of the 2-methylisothiazolin-3-one compounds generally indicated above include 5-chloro-2-methylisothiazolin-3-one and 2-methylisothiazolin-3-one, and also form metal complex salts with these. Examples of metal salts that can be used include zinc chloride, calcium chloride, magnesium chloride, magnesium nitrate, iron chloride, aluminum chloride, copper nitrate, and zinc sulfate.
本発明の活性成分は所望に応じて任意の割合で配合する
ことができるが、好ましくは1.5o乃至1°0.02
の範囲が望ましい。本発明の組成物はその丑ま使用して
もよいし、更にこれを通常使用する担体と同時に用いる
こともできる。形態としては例えば水溶剤、乳剤、マイ
クロカプセル剤、ペース!・剤2粒剤、粉剤等のいずれ
としても使ハ:することができ、使用される担体として
は例えば水。The active ingredients of the present invention can be blended in any ratio as desired, but preferably 1.5° to 1°0.02
range is desirable. The composition of the present invention may be used alone or may be used simultaneously with a commonly used carrier. Forms include aqueous solutions, emulsions, microcapsules, and PACE! - It can be used as either granules or powder, and the carrier used is, for example, water.
有機溶剤、無機化合物等が利用されうる。これらの活性
成分とともに他の活性成分2例えば殺菌剤。Organic solvents, inorganic compounds, etc. can be used. Together with these active ingredients there may be other active ingredients 2, such as fungicides.
殺虫剤、殺礫剤、除草剤とともに混用することも可能で
あり、更に補助剤1例えば界面活性剤、乳化剤、防錆剤
、顔料、展着剤等を添加することも可能である。また活
性成分を安定化せしめる安定剤をも添加してもよい。It is also possible to use them in combination with insecticides, gravel killers, and herbicides, and it is also possible to add auxiliary agents such as surfactants, emulsifiers, rust preventives, pigments, and spreading agents. Stabilizers may also be added to stabilize the active ingredient.
次に以下の実施例をもって具体的に本発明を説明する。Next, the present invention will be specifically explained with reference to the following examples.
1)5−クロル−2−メチルインデアゾリン−6−オン
・塩化マグネ/ラム塩とエチレンビスジチオカルバミン
酸マンガンを11にしたもの
2)5−クロル−2−メチルイノチアゾリン−6−オン
・塩化マグネシウム塩と亜鉛配位エチレンビスジチオカ
ルバミン酸マンガンを1:1にしたもの
3)5−クロル−2−メチルイノチアゾリン−6−オン
・塩化マグネシウム塩とエチレンビスジチオカルバミン
酸及び(又は)ジメチルジチオカルバミン酸とが亜鉛を
介して結合ぜる混成塩を11にしたもの
4)5−クロル−2−メチルイノチアゾリン−6′−オ
ン・塩化マグネシウム塩とモノメチルジチオカルバミン
酸亜鉛を11にしたもの5)2−メチルイソチアゾリン
−6−オン・塩化マグネシウム塩とエチレンビスジチオ
カルバミン酸亜鉛を11にしだもの
6)2−メチルイソチアゾリン−6・−オン・塩化マグ
ネシウム塩と亜鉛配位エチレンビスジチオカルバミン酸
マンガンを11にしたもの
7)5−クロル−2−メチルイソチアゾリン−6−オン
・硝酸マグネシウム塩とエチレンビスジチオカルバミン
酸マンガンヲ1:2にしたもの
8)5−クロル−2−メチルイソチアゾリン−3−オン
・硝酸マグネシウム塩とジメチルジチオカルバミン酸亜
鉛1.2にしたもの9)5−クロル−2−メチルイソチ
アゾリン−3−オン・塩化マグネシウム塩及び2−メチ
ルイノチアゾリン−3−オン・塩化マグネ/ラム塩(1
:1)とエチレンビスジチオカルバミン酸マンガンf:
2 :: 1にしたもの10)5−クロル−2−メチル
イソチアゾリン−6−オン・塩化マグネシウム塩
11)2−メチルイソチアゾリン−3−オン 塩化マグ
ネシウム塩
12)エチンンビスシチオカルノくミン酸マンガン16
)エチレンビスジチオカルノくミン酸及び(又は)ジメ
チルジチオカルバミン酸とが亜鉛を介して結合せる混成
塩
実施例2
ガラス製1oz水槽に原液(Chlorella sp
p。1) 5-chloro-2-methylinothiazolin-6-one, magnesium chloride/rum salt and manganese ethylenebisdithiocarbamate 11 2) 5-chloro-2-methylinothiazolin-6-one, chloride Magnesium salt and zinc-coordinated manganese ethylene bisdithiocarbamate in a 1:1 ratio 3) 5-chloro-2-methylinothiazolin-6-one magnesium chloride salt and ethylene bisdithiocarbamic acid and/or dimethyldithiocarbamic acid 4) 5-chloro-2-methylinothiazolin-6'-one magnesium chloride salt and zinc monomethyldithiocarbamate (11) 5) 2-methyl 6) 2-Methylisothiazolin-6-one, magnesium chloride salt and zinc-coordinated manganese ethylenebisdithiocarbamate in 11 7) ) 5-chloro-2-methylisothiazolin-6-one, magnesium nitrate and manganese ethylenebisdithiocarbamate in a ratio of 1:2 8) 5-chloro-2-methylisothiazolin-3-one, magnesium nitrate and dimethyldithiocarbamine 9) 5-chloro-2-methylisothiazolin-3-one, magnesium chloride salt and 2-methylinothiazolin-3-one, magnesium chloride/rum salt (1.2)
:1) and manganese ethylene bisdithiocarbamate f:
2:: 10) 5-chloro-2-methylisothiazolin-6-one magnesium chloride salt 11) 2-methylisothiazolin-3-one magnesium chloride salt 12) Manganese ethynebiscythiocarnocuminate 16
) Mixed salt in which ethylene bisdithiocarnocumic acid and/or dimethyldithiocarbamic acid are bonded via zinc Example 2 Add the stock solution (Chlorella sp.
p.
Scendesmus sppを主体とするcompl
ex )を加え。compl mainly composed of Scendesmus spp.
Add ex).
窒素源として尿素を1を当p 0.59の割合でこれに
添加した。これに所定の濃度で薬剤を施用し、藻類の生
育を経時的に副食した。その結果を下表に示す。Urea was added thereto as a nitrogen source in a ratio of 1:0.59. Chemicals were applied at a predetermined concentration to this, and the algae growth was fed as a side dish over time. The results are shown in the table below.
注)表中−は藻類の発育を認めない。Note) - in the table indicates no growth of algae.
士は藻類の一部の発育を認める。The inspector found some algae growth.
+は藻類の生育を認める。+ indicates growth of algae.
を示す。shows.
実施例6 工業用水中に発生して有害なる作用を示すかび。Example 6 Mold that occurs in industrial water and exhibits harmful effects.
バクテリヤについてその殺滅力を試験した。Its killing power against bacteria was tested.
供試薬剤の濃度(5ppm )の有効成分を加えたPo
teto Dextrose Agar平面培地に下表
に示した各種の浮遊液(約106Ce I Is/d
)を噴霧して接種し。Po containing the active ingredient at the concentration of the test drug (5 ppm)
Various suspensions shown in the table below (approximately 106Ce I Is/d
) to inoculate by spraying.
25℃の定温器内に24時間培養し、それぞれの生育の
有無を調査した。The cells were cultured in an incubator at 25° C. for 24 hours, and the presence or absence of growth was examined.
注)表中−は完全阻止。Note) - in the table means complete inhibition.
土はほぼ阻止。Soil is almost blocked.
十は生育。Ten is growth.
を示す。shows.
実施例4
工場の冷却水用のパイプ内に耐着している凝集体を採取
し、これを培養液(o、i%の尿素水)中に一定量ずつ
加え2次いで1記の濃度で本発明組成物を加え攪拌し、
20〜30℃で1o日間培養して調査した。Example 4 Aggregates stuck in the cooling water pipes of a factory were collected, and a certain amount of this was added to a culture solution (o, i% urea water) at the concentration listed in 1. Add the invention composition and stir,
The cells were cultured at 20-30°C for 10 days and investigated.
主)表中−は完全阻止。Main) - in the table is completely blocked.
士は殆んど阻止。Most of the masters prevented it.
十は一部生育。Ten is partially grown.
十十は生育。Ten is growing up.
を示す。shows.
特許出願人 東京有機化学工業株式会社patent applicant Tokyo Organic Chemical Industry Co., Ltd.
Claims (1)
Rは水素又はハロゲン原子を示す。)にて示される2−
メチルイノチアシリ/−3−オノ又はその金属錯塩化合
物を有効成分として含有することを特徴とする工業用有
害生物防除組成物。At least one dithiorubamic acid heavy metal salt (provided that
R represents hydrogen or a halogen atom. ) shown in 2-
An industrial pest control composition comprising methylinothiacyly/-3-ono or a metal complex salt thereof as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58085532A JPS59212408A (en) | 1983-05-16 | 1983-05-16 | Pest-combatting composition for industrial purpose |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58085532A JPS59212408A (en) | 1983-05-16 | 1983-05-16 | Pest-combatting composition for industrial purpose |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59212408A true JPS59212408A (en) | 1984-12-01 |
JPH0373521B2 JPH0373521B2 (en) | 1991-11-22 |
Family
ID=13861494
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58085532A Granted JPS59212408A (en) | 1983-05-16 | 1983-05-16 | Pest-combatting composition for industrial purpose |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59212408A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6210003A (en) * | 1985-07-05 | 1987-01-19 | Katayama Chem Works Co Ltd | Industrial fungicidal and algicidal agent |
JPS63316702A (en) * | 1987-06-19 | 1988-12-26 | Somar Corp | Antimicrobial agent |
JP2007254296A (en) * | 2006-03-20 | 2007-10-04 | Bayer Cropscience Kk | Controlling agent for algae |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101399018B1 (en) * | 2013-02-04 | 2014-05-27 | 허승환 | Execising device |
-
1983
- 1983-05-16 JP JP58085532A patent/JPS59212408A/en active Granted
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6210003A (en) * | 1985-07-05 | 1987-01-19 | Katayama Chem Works Co Ltd | Industrial fungicidal and algicidal agent |
JPH0563445B2 (en) * | 1985-07-05 | 1993-09-10 | Katayama Chemical Works Co | |
JPS63316702A (en) * | 1987-06-19 | 1988-12-26 | Somar Corp | Antimicrobial agent |
JP2007254296A (en) * | 2006-03-20 | 2007-10-04 | Bayer Cropscience Kk | Controlling agent for algae |
Also Published As
Publication number | Publication date |
---|---|
JPH0373521B2 (en) | 1991-11-22 |
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