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JPH07196402A - Insecticide, fungicide solvent and insecticide, fungicide - Google Patents

Insecticide, fungicide solvent and insecticide, fungicide

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Publication number
JPH07196402A
JPH07196402A JP34903493A JP34903493A JPH07196402A JP H07196402 A JPH07196402 A JP H07196402A JP 34903493 A JP34903493 A JP 34903493A JP 34903493 A JP34903493 A JP 34903493A JP H07196402 A JPH07196402 A JP H07196402A
Authority
JP
Japan
Prior art keywords
solvent
agent
insecticidal
group
formula
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.)
Pending
Application number
JP34903493A
Other languages
Japanese (ja)
Inventor
Yasuhiro Toida
康宏 戸井田
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.)
Eneos Corp
Original Assignee
Japan Energy Corp
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 Japan Energy Corp filed Critical Japan Energy Corp
Priority to JP34903493A priority Critical patent/JPH07196402A/en
Publication of JPH07196402A publication Critical patent/JPH07196402A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】 【目的】 有機溶剤臭がなく、しかも樹脂系の埋設配管
や断熱材をほとんど損なうことのない殺虫、殺菌剤用溶
剤および殺虫、殺菌剤を提供すること。 【構成】 下記一般式(I) 【化1】 (式中、R1はメチル基、エチル基、プロピル基または
ブチル基、R2はプロピル基またはブチル基、mは1〜
3、nは1〜3で、置換基の位置は問わない)で表され
る少なくとも1種のアルキルナフタレン化合物、特に好
ましくは、下記一般式(II) 【化2】 (式中、R3はメチルまたはエチル基、xは1〜3、y
は1〜3で、置換基の位置は問わない)で表される少な
くとも1種のアルキルナフタレン化合物を主成分とする
殺虫、殺菌剤用溶剤、および前記溶剤に殺虫、殺菌薬
剤、特には、有機リン系薬剤を溶解、乳化もしくは分散
させた殺虫、殺菌剤。
(57) [Abstract] [Purpose] To provide an insecticidal and bactericidal solvent and an insecticidal and bactericidal agent which has no organic solvent odor and which does not substantially damage the resin-based buried pipes and heat insulating materials. [Structure] The following general formula (I): (In the formula, R 1 is a methyl group, an ethyl group, a propyl group or a butyl group, R 2 is a propyl group or a butyl group, and m is 1 to
3, n is 1 to 3, and the position of the substituent is not limited), and at least one alkylnaphthalene compound represented by the following general formula (II) (In the formula, R 3 is a methyl or ethyl group, x is 1 to 3, and y is
Is 1 to 3, and the position of the substituent is not limited) Insecticide containing at least one alkylnaphthalene compound represented by the formula, a fungicide solvent, and an insecticide in the solvent, a fungicide, in particular, organic An insecticidal and bactericidal agent in which a phosphorus-based drug is dissolved, emulsified or dispersed.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、殺虫、殺菌剤用溶剤、
特には、有機リン系の殺虫、殺菌薬剤の溶剤及びその溶
剤を用いた殺虫、殺菌剤に関する。
FIELD OF THE INVENTION The present invention relates to a solvent for insecticides and fungicides,
In particular, the invention relates to a solvent for organic phosphorus insecticides and germicides, and insecticides and germicides using the solvent.

【0002】[0002]

【従来の技術】一般に、溶液、分散、乳化タイプの殺
虫、殺菌剤、特には有機リン系殺虫、殺菌剤等において
は、殺虫、殺菌薬剤を灯油やアルキルベンゼン等の有機
溶剤に溶解したもの、あるいはこれに界面活性剤等を添
加し、水で乳化希釈して散布することにより使用されて
いる。このような殺虫、殺菌剤は、灯油やアルキルベン
ゼン等の有機溶剤臭が強く、散布の際に不快感を与え、
更には、この種の溶剤のため、家の周囲や床下等に散布
すると水道等に使用されている硬質塩化ビニル等からな
る埋設配管や発泡ポリスチレン等からなる断熱材を著し
く損傷させる等の欠点があった。
2. Description of the Related Art Generally, solutions, dispersions, emulsion type insecticides, fungicides, particularly organophosphorus insecticides, fungicides, etc., in which the insecticide or fungicide is dissolved in an organic solvent such as kerosene or alkylbenzene, or It is used by adding a surfactant or the like thereto, emulsifying and diluting with water and then spraying. Such insecticides and bactericides have a strong odor of organic solvents such as kerosene and alkylbenzene, which causes discomfort during spraying.
Furthermore, because of this type of solvent, when sprayed around the house or under the floor, there are drawbacks such as serious damage to the buried pipe made of hard vinyl chloride etc. used for water supply etc. and the heat insulating material made of expanded polystyrene etc. there were.

【0003】[0003]

【発明が解決しようとする課題】本発明は、上記課題を
解決するもので、本発明の目的は、有機溶剤臭がなく、
しかも樹脂系の埋設配管や断熱材をほとんど損なうこと
のない殺虫、殺菌剤用溶剤および殺虫、殺菌剤を提供す
ることにある。
SUMMARY OF THE INVENTION The present invention is to solve the above-mentioned problems, and an object of the present invention is to eliminate the smell of organic solvent,
Moreover, it is an object of the present invention to provide a pesticidal and bactericidal solvent and a pesticidal and bactericidal agent that hardly damages resin-based buried pipes and heat insulating materials.

【0004】[0004]

【課題を解決するための手段】本発明者らは、上記課題
を解決するために鋭意研究を進めた結果、アルキルナフ
タレンをプロピル化あるいはブチル化した化合物が有機
リン系の殺虫、殺菌薬剤を溶解するが、臭気がほとんど
なく、しかも硬質塩化ビニル配管や発泡ポリスチレンを
損なわないことを見出した。
Means for Solving the Problems As a result of intensive studies to solve the above problems, the present inventors have found that a compound obtained by propylating or butylating an alkylnaphthalene dissolves an organophosphorus insecticidal or bactericidal agent. However, it has been found that there is almost no odor and that it does not damage the rigid vinyl chloride piping or expanded polystyrene.

【0005】本発明はかかる知見に基づきなされたもの
で、本発明は、下記一般式(I)
The present invention was made on the basis of such findings, and the present invention is based on the following general formula (I):

【化3】 (式中、R1はメチル基、エチル基、プロピル基または
ブチル基、R2はプロピル基またはブチル基、mは1〜
3、nは1〜3で、置換基の位置は問わない)で表され
る少なくとも1種のアルキルナフタレン化合物、特に好
ましくは、下記一般式(II)
[Chemical 3] (In the formula, R 1 is a methyl group, an ethyl group, a propyl group or a butyl group, R 2 is a propyl group or a butyl group, and m is 1 to
3, n is 1 to 3, and the position of the substituent is not limited), and at least one alkylnaphthalene compound represented by the formula (II)

【化4】 (式中、R3はメチルまたはエチル基、xは1〜3、y
は1〜3で、置換基の位置は問わない)で表される少な
くとも1種のアルキルナフタレン化合物を主成分とする
殺虫、殺菌剤用溶剤、および前記溶剤に殺虫、殺菌薬
剤、特には、有機リン系薬剤を溶解、乳化もしくは分散
させた殺虫、殺菌剤からなる。
[Chemical 4] (In the formula, R 3 is a methyl or ethyl group, x is 1 to 3, and y is
Is 1 to 3, and the position of the substituent is not limited) Insecticide containing at least one alkylnaphthalene compound represented by the formula, a fungicide solvent, and an insecticide in the solvent, a fungicide, in particular, organic It consists of insecticides and bactericides in which phosphorus-based drugs are dissolved, emulsified or dispersed.

【0006】上記式(I)のアルキルナフタレン化合
物、つまりナフタレン環に1〜3個のメチル基、エチル
基、プロピル基またはブチル基のいずれかが付加したも
のに、1〜3個のイソプロピル基またはブチル基のいず
れかが付加したものである。これらの化合物としては、
メチルイソプロピルナフタレン、ジメチルイソプロピル
ナフタレン、トリメチルイソプロピルナフタレン、メチ
ルジイソプロピルナフタレン、ジメチルジイソプロピル
ナフタレン、トリメチルジイソプロピルナフタレン、メ
チルトリイソプロピルナフタレン、ジメチルトリイソプ
ロピルナフタレン、トリメチルトリイソプロピルナフタ
レン、エチルイソプロピルナフタレン、ジエチルイソプ
ロピルナフタレン、トリエチルイソプロピルナフタレ
ン、エチルジイソプロピルナフタレン、ジエチルジイソ
プロピルナフタレン、トリエチルジイソプロピルナフタ
レン、エチルトリイソプロピルナフタレン、ジエチルト
リイソプロピルナフタレン、トリエチルトリイソプロピ
ルナフタレン、メチルエチルイソプロピルナフタレン、
ジメチルエチルイソプロピルナフタレン、メチルジエチ
ルイソプロピルナフタレン、メチルエチルジイソプロピ
ルナフタレン、ジメチルエチルジイソプロピルナフタレ
ン、メチルジエチルジイソプロピルナフタレン、メチル
エチルトリイソプロピルナフタレン、ジメチルエチルト
リイソプロピルナフタレン、メチルジエチルトリイソプ
ロピルナフタレン等を例示できる。
To the alkylnaphthalene compound of the above formula (I), that is, a compound obtained by adding 1 to 3 methyl groups, ethyl groups, propyl groups or butyl groups to a naphthalene ring, 1 to 3 isopropyl groups or One of the butyl groups is added. These compounds include
Methylisopropylnaphthalene, dimethylisopropylnaphthalene, trimethylisopropylnaphthalene, methyldiisopropylnaphthalene, dimethyldiisopropylnaphthalene, trimethyldiisopropylnaphthalene, methyltriisopropylnaphthalene, dimethyltriisopropylnaphthalene, trimethyltriisopropylnaphthalene, ethylisopropylnaphthalene, diethylisopropylnaphthalene, triethylisopropylnaphthalene , Ethyldiisopropylnaphthalene, diethyldiisopropylnaphthalene, triethyldiisopropylnaphthalene, ethyltriisopropylnaphthalene, diethyltriisopropylnaphthalene, triethyltriisopropylnaphthalene, methylethylisopropylnaphthalene,
Examples thereof include dimethylethylisopropylnaphthalene, methyldiethylisopropylnaphthalene, methylethyldiisopropylnaphthalene, dimethylethyldiisopropylnaphthalene, methyldiethyldiisopropylnaphthalene, methylethyltriisopropylnaphthalene, dimethylethyltriisopropylnaphthalene, and methyldiethyltriisopropylnaphthalene.

【0007】上記化合物において、メチル基、エチル
基、イソプロピル基、ブチル基は、ナフタレン環上のど
の位置に付加していてもよく、またこれらのアルキルナ
フタレン化合物は、単独であっても、2種以上が混合し
た状態であってもよい。
In the above compound, a methyl group, an ethyl group, an isopropyl group and a butyl group may be added at any position on the naphthalene ring, and these alkylnaphthalene compounds may be used alone or in combination of two kinds. The above may be in a mixed state.

【0008】本発明は、上記アルキルナフタレン化合物
を殺虫、殺菌剤用溶剤として用いるものであるが、この
溶剤にはこの化合物以外にも、他の有機化合物、例え
ば、ベンゼン、ナフタレン、インダン、インデンあるい
はこれらの環にアルキル基等が付加した化合物が混合し
ていても特に支障とはならない。しかし、本発明の顕著
な効果のためには上記アルキルナフタレン化合物が当該
溶剤中に50重量%以上、好ましくは70重量%以上、
特には90重量%含まれているものがよい。
The present invention uses the above-mentioned alkylnaphthalene compound as a solvent for insecticides and bactericides. In addition to this compound, other organic compounds such as benzene, naphthalene, indane, indene or Even if a compound in which an alkyl group or the like is added to these rings is mixed, there is no particular problem. However, for the remarkable effect of the present invention, the above-mentioned alkylnaphthalene compound is contained in the solvent in an amount of 50% by weight or more, preferably 70% by weight or more,
In particular, 90% by weight is preferable.

【0009】本発明にかかるアルキルナフタレン化合物
は、石炭タール油中やナフサ、灯油等の留分を接触改質
生成油中に含まれるメチルナフタレン、ジメチルナフタ
レンあるいはエチルナフタレン等を蒸留操作等により分
離、回収し、これらをプロピル化することにより簡便に
得ることができる。
The alkylnaphthalene compound according to the present invention is obtained by separating methyl naphthalene, dimethylnaphthalene or ethylnaphthalene contained in a catalytically reformed product oil from a fraction such as coal tar oil, naphtha or kerosene by a distillation operation or the like, It can be easily obtained by collecting and propylating these.

【0010】上記殺虫、殺菌剤用溶剤は、殺虫、殺菌薬
剤、特には有機リン系殺虫、殺菌薬剤、例えば、CYA
P(シアノホス)剤(サイアノックス、ギボシム)、M
PP(フェンチオン)剤、MEP(フェニトロチオン)
剤、ECP(ジクロフェンチオン)剤、ピリミホスメチ
ル剤、ダイアジノン剤、エトリムホス剤、イソキサチオ
ン剤、ピリダフェンチオン剤、クロルピリホスメチル
剤、クロルピリホス剤(ダーズバン)、ESP剤(エス
トックス)、バンドチオン剤、マラソン剤、PAP(フ
ェントエート)剤、ジメトエート剤、ホルモチオン剤、
メカルバム剤、チオメトン剤、エチルチオメトン剤、ホ
サロン剤、PMP(ホスメット)剤、DMTP(メチダ
チオン)剤、プロチオホス剤、DDVP剤、モノクロト
ホス剤、BRP剤、CVMP剤、ジメチルビンホス剤、
CVP(クロルフェンビンホス)剤、プロパホス剤、ア
セフェート剤、サリチオン剤、DEP剤、EPN剤、テ
トラクロルビンホス剤、フェニトロチオン剤、プロペタ
ンホス剤、ホキシム剤、IBP剤、EDDP剤等に溶剤
として好適であるが、このうちでも特に、蟻駆除用の防
蟻剤の薬効成分であるクロルピリホス剤に好適である。
The above-mentioned insecticidal and bactericidal solvent includes insecticidal and bactericidal agents, especially organophosphorus-based insecticidal and bactericidal agents such as CYA.
P (cyanophos) agent (Cyanox, Gibosim), M
PP (fenthion) agent, MEP (fenitrothion)
Agent, ECP (diclofenthion) agent, pirimiphos-methyl agent, diazinon agent, etrimphos agent, isoxathion agent, pyridafenthion agent, chlorpyrifos-methyl agent, chlorpyrifos agent (dazban), ESP agent (estox), bandthione agent, marathon agent, PAP (fentoate) agent , Dimethoate, formothione,
Mecarbam agent, thiomethone agent, ethylthiomethone agent, fosalone agent, PMP (phosmet) agent, DMTP (methidathion) agent, prothiophos agent, DDVP agent, monocrotophos agent, BRP agent, CVMP agent, dimethylvinphos agent,
Suitable as a solvent for CVP (chlorphenvinphos) agents, propaphos agents, acephate agents, salicion agents, DEP agents, EPN agents, tetrachlorvinphos agents, fenitrothion agents, propetanephos agents, phoxime agents, IBP agents, EDDP agents, etc. However, among these, it is particularly suitable as a chlorpyrifos agent which is a medicinal component of an ant exterminating agent for controlling ants.

【0011】本出願の他の発明である殺虫、殺菌剤は、
上記殺虫、殺菌薬剤の1種あるいは数種を本発明の上記
殺虫、殺菌剤用溶剤に0.5〜90重量%溶解、分散、
あるいは乳化させたもの、あるいはこれを水、その他の
溶媒で1〜10000倍に希釈したものである。この場
合、殺虫、殺菌薬剤以外に、アニオン、カリオン、ノニ
オン、さらには両性界面活性剤等の乳化剤、その他、効
力増強剤、共力剤等の殺虫、殺菌剤に通常用いられる添
加剤、あるいは防腐剤などを添加してもよい。
The insecticidal and bactericidal agent according to another invention of the present application is
One or several kinds of the above insecticidal and bactericidal agents are dissolved and dispersed in the above insecticidal and bactericidal solvent of the present invention in an amount of 0.5 to 90% by weight.
Alternatively, it is an emulsified product or a product obtained by diluting this with water or another solvent 1 to 10000 times. In this case, in addition to insecticides and bactericides, anions, carions, nonions, and also emulsifiers such as amphoteric surfactants, other potentiating agents, insecticides such as synergists, additives usually used for bactericides, or antiseptics Agents and the like may be added.

【0012】[0012]

【実施例】溶剤の調製 表1の中央欄に示した組成を有する原料留分をプロピル
化し、蒸留により290〜310℃の沸点範囲の留分を
回収し、表1の右欄に示した組成を有するプロピル化油
を得た。
EXAMPLES Preparation of Solvent A raw material fraction having the composition shown in the center column of Table 1 was propylated, and a fraction in the boiling range of 290 to 310 ° C. was recovered by distillation. The composition shown in the right column of Table 1 was obtained. A propylated oil having

【0013】[0013]

【表1】 [Table 1]

【0014】このプロピル化油は、全くナフタレン臭、
その他の有機溶剤臭は認められず、表2に示す一般性状
を有していた。
This propylated oil has a naphthalene odor,
No other organic solvent odor was observed, and it had the general properties shown in Table 2.

【0015】[0015]

【表2】 [Table 2]

【0016】溶解試験 上記で調製したプロピル化油50mlを200mlのビーカ
ーに取り、23℃で、マグネチックスタラーで撹拌しな
がら不溶分が出るまで、クロルピリホスを加え、24時
間放置後、不溶分の重量を測定し、加えた量から差引
き、溶解量を求めた。また、参考までに、従来殺虫、殺
菌剤用溶剤として用いられているキシレン、カクタスソ
ルベントP−150(以下「P-150」と略記、日鉱石油化
学(株)製;ナフサの改質油から蒸留分離された留分で炭
素数8〜9のアルキルベンゼンを主成分とするもの)及
び白灯油についても同様の試験を行った。なお、これら
のキシレン、P−150及び白灯油は、強い有機溶剤臭
がある。これらの結果を表3に示した。
Dissolution test 50 ml of the propylated oil prepared above was placed in a 200 ml beaker, and while stirring with a magnetic stirrer, chlorpyrifos was added until an insoluble matter appeared, and after standing for 24 hours, the weight of the insoluble matter was measured. Was measured and subtracted from the added amount to obtain the dissolved amount. For reference, xylene and Cactus Solvent P-150 (hereinafter abbreviated as "P-150", which has been conventionally used as a solvent for insecticides and fungicides, manufactured by Nikko Petrochemical Co., Ltd .; distilled from naphtha modified oil) Similar tests were conducted for the separated fractions containing alkylbenzene having 8 to 9 carbon atoms as the main component) and white kerosene. In addition, these xylene, P-150, and white kerosene have strong organic solvent odor. The results are shown in Table 3.

【0017】[0017]

【表3】 [Table 3]

【0018】これらの結果から、本発明のアルキルナフ
タレン化合物であるプロピル化油は、従来の溶剤等に比
べて、溶解力にはほとんど差がないことが分かる。
From these results, it is understood that the propylated oil which is the alkylnaphthalene compound of the present invention has almost no difference in the dissolving power as compared with the conventional solvent and the like.

【0019】埋設配管に対する影響試験 上記プロピル化油52重量部、クロルピリホス40重量
部、乳化剤であるポリオキシエチレンノニルフェニルエ
ーテル(EO付加モル数7.5)8重量部からなる乳化タ
イプの防蟻剤原液を調製し、この150mlに硬質塩化ビ
ニル配管(JISK 6742規格品:内径25mm、外径32mm、
肉厚3.5mm、長さ50mm)を30℃の温度下に、72
時間浸漬した。水洗した後、室温で一昼夜乾燥し、浸漬
前後の硬質塩化ビニル配管の重量変化率を測定した。ま
た、比較のために、プロピル化油に代えて、キシレン、
P−150及び白灯油を用いて同様の防蟻剤原液を調製
し、同様の試験を行った。この結果を表4に示した。
Effect test on buried pipes Emulsion type termiticide consisting of 52 parts by weight of the above-mentioned propylated oil, 40 parts by weight of chlorpyrifos, and 8 parts by weight of polyoxyethylene nonylphenyl ether (7.5 moles of EO addition) as an emulsifier. Prepare an undiluted solution, and add to this 150 ml rigid vinyl chloride piping (JIS K 6742 standard product: inner diameter 25 mm, outer diameter 32 mm,
(Thickness: 3.5 mm, length: 50 mm) at a temperature of 30 ° C
Soak for hours. After washing with water, it was dried at room temperature for a whole day and night, and the weight change rate of the hard vinyl chloride pipe before and after immersion was measured. For comparison, instead of propylated oil, xylene,
Using P-150 and white kerosene, a similar ant-preventive stock solution was prepared and the same test was conducted. The results are shown in Table 4.

【0020】[0020]

【表4】 [Table 4]

【0021】これらの結果から、キシレンやP−150
は硬質塩化ビニル配管を膨潤させるが、プロピル化油は
ほとんど影響ないことが分かる。
From these results, xylene and P-150
Swells the hard vinyl chloride pipe, but it can be seen that the propylated oil has little effect.

【0022】断熱剤に対する影響試験 上記と同様の防蟻剤原液150mlに、住宅用断熱材とし
て使用されている発泡ポリスチレン(JIS A 9511 B類 3
種規格品;50mm×50mm×30mm)を25.5℃の温度
下に、5分間浸漬した。水洗した後、室温で一昼夜、続
いて40℃で6時間乾燥し、浸漬前後のポリスチレンの
寸法変化率を測定した。また、比較のために、上記と同
様にキシレン、P−150及び白灯油についても試験し
た。この結果を表5に示した。
Impact test on heat insulation agent In 150 ml of the same stock solution of termite control agent as described above, expanded polystyrene (JIS A 9511 B 3
Specified product: 50 mm × 50 mm × 30 mm) was immersed at a temperature of 25.5 ° C. for 5 minutes. After washing with water, it was dried overnight at room temperature and then at 40 ° C. for 6 hours, and the dimensional change rate of polystyrene before and after immersion was measured. For comparison, xylene, P-150 and white kerosene were also tested as above. The results are shown in Table 5.

【0023】[0023]

【表5】 [Table 5]

【0024】寸法変化率から、キシレンやP−150は
発泡ポリスチレンを著しく溶解し、灯油も若干溶解する
が、プロピル化油はほとんど影響ないことが分かる。
From the dimensional change rate, it can be seen that xylene and P-150 dissolve the expanded polystyrene remarkably and the kerosene slightly, but the propylated oil has almost no effect.

【0025】以上の結果から、本発明のアルキルナフタ
レン化合物からなるものが殺虫、殺菌剤の溶剤として優
れていることが分かる。
From the above results, it can be seen that the alkylnaphthalene compound of the present invention is excellent as a solvent for insecticides and bactericides.

【0026】[0026]

【発明の効果】本発明の殺虫、殺菌剤用溶剤および殺
虫、殺菌剤は、有機溶剤臭がなく、しかも樹脂系の埋設
配管や断熱材をほとんど損なうことがないという格別の
効果を奏する。
INDUSTRIAL APPLICABILITY The insecticidal and bactericidal solvent and the insecticidal and bactericidal agent of the present invention have a particular effect that there is no odor of an organic solvent and that the resin-based buried pipe and the heat insulating material are hardly damaged.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 下記一般式(I) 【化1】 (式中、R1はメチル基、エチル基、プロピル基または
ブチル基、R2はプロピル基またはブチル基、mは1〜
3、nは1〜3で、置換基の位置は問わない)で表され
る少なくとも1種のアルキルナフタレン化合物を主成分
とする殺虫、殺菌剤用溶剤。
1. The following general formula (I): (In the formula, R 1 is a methyl group, an ethyl group, a propyl group or a butyl group, R 2 is a propyl group or a butyl group, and m is 1 to
3, n is 1 to 3 and the position of the substituent does not matter), and is a solvent for insecticides and bactericides containing at least one alkylnaphthalene compound as a main component.
【請求項2】 請求項1に記載の一般式(I)の化合物
が下記一般式(II) 【化2】 (式中、R3はメチルまたはエチル基、xは1〜3、y
は1〜3で、置換基の位置は問わない)で表される少な
くとも1種のアルキルナフタレン化合物であることを特
徴とする殺虫、殺菌剤用溶剤。
2. The compound of general formula (I) according to claim 1 is represented by the following general formula (II): (In the formula, R 3 is a methyl or ethyl group, x is 1 to 3, and y is
Is 1 to 3 and the position of the substituent is not limited), and it is at least one kind of alkylnaphthalene compound.
【請求項3】 請求項1に記載の殺虫、殺菌剤用溶剤に
殺虫、殺菌薬剤を溶解、乳化もしくは分散させたことを
特徴とする殺虫、殺菌剤。
3. An insecticidal or bactericidal agent, which comprises dissolving, emulsifying or dispersing an insecticidal or bactericidal agent in the insecticidal or bactericidal solvent according to claim 1.
【請求項4】 請求項3に記載の殺虫、殺菌薬剤が有機
リン系薬剤であることを特徴とする殺虫、殺菌剤。
4. An insecticidal or bactericidal agent, wherein the insecticidal or bactericidal agent according to claim 3 is an organophosphorus agent.
JP34903493A 1993-12-28 1993-12-28 Insecticide, fungicide solvent and insecticide, fungicide Pending JPH07196402A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP34903493A JPH07196402A (en) 1993-12-28 1993-12-28 Insecticide, fungicide solvent and insecticide, fungicide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP34903493A JPH07196402A (en) 1993-12-28 1993-12-28 Insecticide, fungicide solvent and insecticide, fungicide

Publications (1)

Publication Number Publication Date
JPH07196402A true JPH07196402A (en) 1995-08-01

Family

ID=18401050

Family Applications (1)

Application Number Title Priority Date Filing Date
JP34903493A Pending JPH07196402A (en) 1993-12-28 1993-12-28 Insecticide, fungicide solvent and insecticide, fungicide

Country Status (1)

Country Link
JP (1) JPH07196402A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09143002A (en) * 1995-11-17 1997-06-03 Hokko Chem Ind Co Ltd Aqueous suspension pesticide formulation and suspension stabilizer
JPH09143007A (en) * 1995-11-17 1997-06-03 Hokko Chem Ind Co Ltd Aqueous suspension pesticide formulation and suspension stabilizer

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09143002A (en) * 1995-11-17 1997-06-03 Hokko Chem Ind Co Ltd Aqueous suspension pesticide formulation and suspension stabilizer
JPH09143007A (en) * 1995-11-17 1997-06-03 Hokko Chem Ind Co Ltd Aqueous suspension pesticide formulation and suspension stabilizer

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