JPS60237007A - Granular composition of agricultural chemical - Google Patents

Granular composition of agricultural chemical

Info

Publication number
JPS60237007A
JPS60237007A JP9018284A JP9018284A JPS60237007A JP S60237007 A JPS60237007 A JP S60237007A JP 9018284 A JP9018284 A JP 9018284A JP 9018284 A JP9018284 A JP 9018284A JP S60237007 A JPS60237007 A JP S60237007A
Authority
JP
Japan
Prior art keywords
water
granules
parts
esoprophos
ethoprophos
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
JP9018284A
Other languages
Japanese (ja)
Inventor
Kaoru Chiba
馨 千葉
Shinji Yonemura
伸二 米村
Yukinobu Murata
村田 行信
Yoshihiko Nabeya
鍋谷 桂彦
Satoru Moriyama
森山 知
Chiyuki Hori
堀 千之
Shoji Tanaka
正二 田中
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.)
Hokko Chemical Industry Co Ltd
Original Assignee
Hokko Chemical Industry 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 Hokko Chemical Industry Co Ltd filed Critical Hokko Chemical Industry Co Ltd
Priority to JP9018284A priority Critical patent/JPS60237007A/en
Publication of JPS60237007A publication Critical patent/JPS60237007A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:A granular composition for agricultural purposes that is obtained by coating granules of agricultural chemicals including ethoprophos with a water- soluble high polymer, thus showing reduced percutaneous toxicity. CONSTITUTION:Granules for agricultural purposes which contains, as an active ingredient, ethoprophos: O-ethyl S,S-dipropyl phosphorodithioate, being active as a soil insecticide and nematocide against a variety of nematodes, gold beetles and scale insects are coated with more than 0.1wt%, preferably 0.1-5wt% of a water-soluble high polymer such as alginic acid, methyl cellulose or PVA. The granules are obtained by spraying granules of mineral support previously sprayed with ethoprophos with a solution of the water-soluble high polymer in water or an organic solvent and drying them.

Description

【発明の詳細な説明】 (イ)発明の目的 上の1 本発明は、農業上、特に農薬粒剤の製造業の分野におい
て利用しうる新規な発明に関する。より詳しくは、本発
明は有効成分として、以下に示すエソプロホスを含有す
る粒状農薬組成物において、哺乳動物に対する経皮毒性
を軽減化する改良技術に関するものである。
DETAILED DESCRIPTION OF THE INVENTION (A) OBJECTS OF THE INVENTION 1. The present invention relates to a novel invention that can be used in agriculture, particularly in the field of manufacturing agricultural chemical granules. More specifically, the present invention relates to an improved technique for reducing transdermal toxicity to mammals in a granular agricultural chemical composition containing esoprophos shown below as an active ingredient.

エソプロホス 〇−エチル S、S−ジプロピルホスホ
ロジチオエート 従JLEDJL術 エソプロホスを含有する粒剤の経皮毒性を軽減する方法
として、アマニ油を添加する方法が知られている(特公
昭57−5201号公報)。
Esoprophos 〇-Ethyl S,S-dipropyl phosphorodithioate (JLEDJL) A method of adding linseed oil to reduce the dermal toxicity of granules containing esoprophos is known (Japanese Patent Publication No. 57-5201 Publication No.).

が しようと る。 占 エソプロホスは、既に、ジャガイモシストセンチュウ、
サツマイモネコブセンチュウをはじめとする各種センチ
ュウ類、コガネムシ、ハリガネムシ、カイガラムシ類な
どに効果を有することが公知の土壌殺虫殺線虫剤である
。しかし、エソプロホスは哺乳動物に対する経皮毒性が
非常に強く、この製剤の取扱いには厳重な注意が必要で
ある。
is trying to do it. Zhan Esoprophos has already been used in potato cyst nematode,
It is a soil insecticide and nematocide that is known to be effective against various nematodes including the sweet potato knot nematode, scarab beetles, hedge beetles, scale insects, and the like. However, esoprofos has very strong dermal toxicity to mammals, and strict care is required when handling this preparation.

このような現状に対し、満足のい〈経皮毒性の軽減化技
術はないのが実状である。したがって、本発明は、従来
の技術に代り、経皮毒性のない新しいタイプのエソプロ
ホス粒剤を提供することにある。
Under these circumstances, the reality is that there is no satisfactory technique for reducing dermal toxicity. Therefore, the object of the present invention is to provide a new type of esoprofos granules without transdermal toxicity, instead of the conventional technology.

(ロ)発明の構成 ロ るための 本発明者らは、エソプロホスを含有する粒剤の哺乳動物
に対する経皮毒性を軽減化する技術について鋭意研究し
た。その結果、エソプロホス含有粒剤を水溶性高分子の
1種で被覆することにより、経皮毒性を顕著に軽減化す
ることを見出し、本発明に至った。
(B) Structure of the Invention The present inventors have conducted extensive research into techniques for reducing the transdermal toxicity of granules containing esoprophos to mammals. As a result, it was discovered that transdermal toxicity can be significantly reduced by coating esoprophos-containing granules with one type of water-soluble polymer, leading to the present invention.

すなわち、エソプロホスが水溶性高分子で被覆された状
態となり、哺乳動物の皮膚に直接触れることが避けられ
、その結果、経皮毒性が顕著に軽減される。また添加物
が水溶性のため、施用されると土壌中の水分で簡単に溶
解または破損してエンプロホスの溶出が容易となり、高
い生物効果を発現するものと考えられる。
That is, esoprofos is coated with a water-soluble polymer, avoiding direct contact with mammalian skin, and as a result, transdermal toxicity is significantly reduced. Furthermore, since the additive is water-soluble, when applied, it is easily dissolved or damaged by moisture in the soil, facilitating the elution of Enprophos, and is thought to exhibit high biological effects.

本発明に使用する水溶性高分子としては、たとえば次の
ようなものが挙げられる。
Examples of water-soluble polymers used in the present invention include the following.

■)天然高分子系 グアーカ′ム、ローカストど−ン刀゛ム、アラビアガム
、トラガントガム、カラギーナン、アルギン酸、寒天、
ペクチン、デンプン、デキストリン、α−サイクロデキ
ストリン、β−サイクロデキストリン、ザンサンガム、
プルラン、ゼラチンなど。
■) Natural polymer guarcum, locust dragonfly, gum arabic, gum tragacanth, carrageenan, alginic acid, agar,
Pectin, starch, dextrin, α-cyclodextrin, β-cyclodextrin, xanthan gum,
pullulan, gelatin, etc.

2)半合成高分子系 メチルセルロース、エチルセルロース、ヒドロキシエチ
ルセルロース、ヒドロキシプロピルセルロース、カルボ
キシメチルセルロース、アルギン酸ナトリウム、アルギ
ン酸アンモニウムなど。
2) Semi-synthetic polymeric methylcellulose, ethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, sodium alginate, ammonium alginate, etc.

3)合成高分子系 ポリビニルアルコール、ポリアクリル酸ナトリウム、ポ
リエチレンオキサイド、ポリエチレングリコール、ポリ
プロピレングリコールなど。
3) Synthetic polymeric polyvinyl alcohol, sodium polyacrylate, polyethylene oxide, polyethylene glycol, polypropylene glycol, etc.

本発明で使用する水溶性高分子の添加量は、粒剤中に0
.1%(重量%)以上あれば効果を発揮するが、効果と
経済性の両面から考えると0.1〜5%が望ましい。
The amount of water-soluble polymer used in the present invention is 0.
.. If the content is 1% (wt%) or more, the effect will be exhibited, but from the viewpoint of both effectiveness and economy, 0.1 to 5% is desirable.

艶月 本発明の水溶性高分子でエソプロホス粒剤を被覆すると
、経皮毒性を顕著に軽減化することができる。また、水
溶性高分子を添加しても、エソプロホスの前記した本来
有する生物効果を損なうこともない。
When esoprophos granules are coated with the water-soluble polymer of the present invention, transdermal toxicity can be significantly reduced. Furthermore, even if a water-soluble polymer is added, the biological effects that esoprofos originally has are not impaired.

本発明の調製法は、特に限定されることはなく、通常の
農薬粒剤を調製する方法でよい。例えば、次の方法で調
製できる。
The preparation method of the present invention is not particularly limited, and may be a method for preparing ordinary pesticide granules. For example, it can be prepared by the following method.

調製法l あらかじめエソプロホスを噴霧吸着させた粒
状鉱物質担体に、水溶性高 分子の水または有機溶剤溶液を噴霧 し、乾燥して粒剤を得る。
Preparation method 1 A water or organic solvent solution of a water-soluble polymer is sprayed onto a granular mineral carrier onto which esoprophos has been sprayed and adsorbed in advance, and dried to obtain granules.

調製法2 エソプロホス、鉱物質担体に結合剤を加えて
混合し、水を加えて混線 後、押し出し造粒機または転勤造粒 機などで造粒し、乾燥、整粒する。
Preparation method 2 Esoprofos and a mineral carrier are mixed with a binder, water is added, mixed, and then granulated using an extrusion granulator or transfer granulator, dried, and sized.

次いで、水溶性高分子の水または有 機溶剤溶液を噴霧し、乾燥して粒剤 を得る。Next, the water-soluble polymer is dissolved in water or Spray the organic solvent solution and dry it to form granules. get.

本発明で使用する鉱物質担体としては、農薬製剤で通常
用いられるものはいずれも使用できる。
As the mineral carrier used in the present invention, any carrier commonly used in agricultural chemical formulations can be used.

例えば、クレー、珪藻土、タルク、ベントナイト、アタ
パルジャイト、バーミキュライト、ゼオライト、軽石、
セルロースパウダー、ホワイトカーボンなどが挙げられ
、粒状鉱物質担体を使用する場合は、これら鉱物質を適
当な粒径に揃えたものでもよく、通常の造粒法によって
調製した有効成分の含有されない空粒剤でもよい。
For example, clay, diatomaceous earth, talc, bentonite, attapulgite, vermiculite, zeolite, pumice,
Examples include cellulose powder, white carbon, etc. If a granular mineral carrier is used, these mineral carriers may be prepared in an appropriate particle size, and empty granules containing no active ingredients prepared by normal granulation methods may be used. It may also be a drug.

また、本発明の粒状組成物の効果を失わない分解防止剤
、界面活性剤などを必要により併用することができる。
Furthermore, decomposition inhibitors, surfactants, and the like that do not impair the effects of the granular composition of the present invention may be used in combination, if necessary.

なお、水溶性高分子をあらかじめエソプロホス、鉱物質
担体等を混合し、水を加えて造粒しても経皮毒性の軽減
効果は得られない。
Note that even if a water-soluble polymer is mixed with esoprophos, a mineral carrier, etc. in advance and granulated by adding water, the effect of reducing transdermal toxicity cannot be obtained.

以下に、本発明を具体的に説明するために実施例を挙げ
るが、本発明はこれらの例示のみに限定されるものでは
ない。なお、実施例中で部とあるのはすべて重量部であ
る。
Examples are given below to specifically explain the present invention, but the present invention is not limited to these examples. In addition, all parts in the examples are parts by weight.

l11」(調製法l) 粒状アタパルジャイト(14〜48メツシユ)94.8
部にエソプロホス5部を噴霧吸着させたのち、カルボキ
シメチルセルロース0.5%水溶液40部を噴霧する。
111'' (Preparation method 1) Granular attapulgite (14-48 mesh) 94.8
After adsorbing 5 parts of esoprophos by spraying onto the sample, 40 parts of a 0.5% carboxymethylcellulose aqueous solution is sprayed onto the sample.

流動乾燥機で乾燥して、工ソプロホスとして5%含有す
る粒剤を得る。
Dry in a fluidized fluid dryer to obtain granules containing 5% of soprophos.

支庭潰」(調製法l) 粒状アタパルジャイト(14〜48メツシユ)94.5
%にエソプロホス5部を噴霧吸着させたのち、メチルセ
ルロース1%水溶液50部を噴霧する。流動乾燥機で乾
燥して、エソプロホスとして5%含有する粒剤を得る。
Granular attapulgite (14-48 mesh) 94.5
After adsorbing 5 parts of esoprophos by spraying onto the sample, 50 parts of a 1% aqueous solution of methylcellulose was sprayed onto the sample. Dry in a fluidized fluid dryer to obtain granules containing 5% esoprophos.

支意涜」(調製法1) 粒状ゼオライト(14〜48メツシユ)94部にエソプ
ロホス5部を噴霧吸着させたのち、ポリビニルアルコー
ル3%水溶液33部を噴霧する。
(Preparation method 1) After 5 parts of esoprophos is sprayed and adsorbed on 94 parts of granular zeolite (14 to 48 mesh), 33 parts of a 3% aqueous solution of polyvinyl alcohol is sprayed.

流動乾燥機で乾燥して、エンプロホスとして5%含有す
る粒剤を得る。
Dry in a fluidized fluid dryer to obtain granules containing 5% enprofos.

1隻1(iS1製法1) 粒状珪藻±(14〜48メツシユ)94.8部にエソプ
ロホス5部を噴霧吸着させる。アルギン酸ナトリウム1
%水溶液20部を噴霧する。i動乾燥機で乾燥して、エ
ソプロホスとして5%含有する粒剤を得る。
1 ship 1 (iS1 manufacturing method 1) 94.8 parts of granular diatoms (14 to 48 mesh) are sprayed and adsorbed with 5 parts of esoprophos. Sodium alginate 1
% aqueous solution. Dry in a dynamic dryer to obtain granules containing 5% esoprophos.

1竃1](調製法l) 軽石(14〜48メツシユ)94.8部にエソプロホス
5部を噴霧吸着させる。ポリアクリル酸ナトリウム1%
水溶液20部を噴霧する。流動乾燥機で乾燥して、エソ
プロホスとして5%含有する粒剤を得る。
1 pot 1] (Preparation method 1) 5 parts of esoprophos is sprayed and adsorbed onto 94.8 parts of pumice (14 to 48 mesh). Sodium polyacrylate 1%
Spray with 20 parts of aqueous solution. Dry in a fluidized fluid dryer to obtain granules containing 5% esoprophos.

支胤潰」(調製法2) エソプロホス5部、ホワイトカーボン3部、リグニンス
ルホン酸ソーダ5部、クレー86.8部を混合し、水1
5部を加えて混線後、押し出し造粒機にて造粒する。乾
燥、整粒(14〜48メツシユ)後、プルラン1%水溶
液20部を噴霧する。流動乾燥機で乾燥して、エソプロ
ホスとして5%含有する粒剤を得る。
(Preparation method 2) Mix 5 parts of esoprophos, 3 parts of white carbon, 5 parts of sodium lignin sulfonate, and 86.8 parts of clay, and add 1 part of water.
After adding 5 parts and mixing, the mixture is granulated using an extrusion granulator. After drying and sizing (14 to 48 meshes), 20 parts of a 1% pullulan aqueous solution is sprayed. Dry in a fluidized fluid dryer to obtain granules containing 5% esoprophos.

(ハ)発明の効果 本発明の有用性を証するために試験例をあげる。(c) Effects of the invention Test examples will be given to prove the usefulness of the present invention.

なお、実施例1〜6より本発明の水溶性高分子を除いて
調製したものを対照例1〜6とし、以下 □の方法で調
製した試料を対照例7.8とした。
In addition, samples prepared by removing the water-soluble polymer of the present invention from Examples 1 to 6 were designated as Control Examples 1 to 6, and samples prepared by the method described below were designated as Control Examples 7 and 8.

〔対照例7の調製法〕 エソプロホス5部、ホワイトカーボン3部、リグニンス
ルホン酸ナトリウム5部、クレー86部にカルボキシメ
チルセルロース1部を加え混合したのち、水15部を加
えて混線後、押し出し造粒機にて造粒する。乾燥、整粒
(14〜48メツシユ)して、エソプロホスとして5%
含有する粒剤を得る。
[Preparation method of Comparative Example 7] Add 1 part of carboxymethyl cellulose to 5 parts of esoprophos, 3 parts of white carbon, 5 parts of sodium ligninsulfonate, and 86 parts of clay, mix, then add 15 parts of water, mix, and extrude granulation. Granulate using a machine. Dry and size (14 to 48 mesh) and 5% as esoprophos.
Obtain granules containing:

〔対照例8の調製法〕 特公昭57−5201号公報記
載のエソプロホス粒剤 エソプロホス5部、アマニ油1部およびプロピレングリ
コール2.5部を相溶させたものを、粒状アタパルジャ
イト(14〜48メツシユ)91.5部に噴霧吸着させ
、エソプロホスとして5%含有する粒剤を得る。
[Preparation method of Comparative Example 8] Esoprophos granules described in Japanese Patent Publication No. 57-5201 A mixture of 5 parts of esoprophos, 1 part of linseed oil and 2.5 parts of propylene glycol was mixed with granular attapulgite (14 to 48 mesh). ) to obtain granules containing 5% of esoprophos.

試]1例」エ マウスによる パッチテスト絆創膏のガーゼ部(直径1.5cm)を蒸
留水で湿し、実施例に準じて調製した試料(マウス1k
gに対しエソプロホスとして5゜mg)を塗布する。そ
して、これをマウスの脱毛した皮膚に貼付し、経時的に
死亡数を観察した。
Trial] Example 1 Patch test with mice Moisten the gauze part (diameter 1.5 cm) of a bandage with distilled water, and prepare a sample according to the example (mouse 1k).
5 mg of esoprophos) per g. This was then applied to the depilated skin of mice, and the number of deaths was observed over time.

本試験に供したマウスはl試料当り5匹である。Five mice were used in this test per sample.

結果を第1表に示す。The results are shown in Table 1.

0 に鼓1」 トマトのサツマイモネコブセンチュ実施例に
準じて調製した試料の所定量を、115000アールポ
ツトに入れたサツマイモネコブセンチュウ汚染土壌に施
用し、均一に混和した。
A predetermined amount of the sample prepared according to Example 1 was applied to sweet potato knot nematode contaminated soil placed in a 115,000 are pot and mixed uniformly.

混和後、トマト種子5粒を播種して散水し、温室内に放
置した。播種20日後に発芽して生育したトマト苗を抜
き取り、根部のネコブ発現程度を調べ、防除価(%)を
めた。
After mixing, five tomato seeds were sown, watered, and left in a greenhouse. 20 days after sowing, the tomato seedlings that had germinated and grown were taken out, the degree of Nekobu expression in the roots was examined, and the control value (%) was determined.

なお、ネコブ程度評価および防除価は以下の方法でめた
。また、本試験は1区1ボツト、5反復で行った。結果
を第2表に示す。
In addition, the evaluation of the degree of staghorn and the control value were determined by the following method. In addition, this test was conducted with 1 bottle per group and 5 repetitions. The results are shown in Table 2.

ネコブ発現程度 O:無 l:僅 2:少3:中 4:
多 5:激 (%) 無処理区の平均ネコブ発現程度100 8 なお、薬剤無処理区のネコブ発現程度は4.7であった
Degree of Nekobu expression O: None L: Slight 2: Slight 3: Medium 4:
High 5: Severe (%) The average degree of Nekobu expression in the untreated area was 100 8 The degree of Nekobu expression in the drug-untreated area was 4.7.

特許出願人 北興化学工業株式会社 1 47−Patent applicant: Hokuko Chemical Industry Co., Ltd. 1 47-

Claims (1)

【特許請求の範囲】[Claims] 有効成分として〇−エチルS、S−ジプロピルホスホロ
ジチオエートを含有する粒状農薬を、水溶性高分子の1
種で被覆することを特徴とする、経皮毒性の軽減された
粒状農薬組成物。
A granular pesticide containing 〇-ethyl S, S-dipropyl phosphorodithioate as an active ingredient is added to one of the water-soluble polymers.
A granular agricultural chemical composition with reduced transdermal toxicity, characterized in that it is coated with seeds.
JP9018284A 1984-05-08 1984-05-08 Granular composition of agricultural chemical Pending JPS60237007A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9018284A JPS60237007A (en) 1984-05-08 1984-05-08 Granular composition of agricultural chemical

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9018284A JPS60237007A (en) 1984-05-08 1984-05-08 Granular composition of agricultural chemical

Publications (1)

Publication Number Publication Date
JPS60237007A true JPS60237007A (en) 1985-11-25

Family

ID=13991342

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9018284A Pending JPS60237007A (en) 1984-05-08 1984-05-08 Granular composition of agricultural chemical

Country Status (1)

Country Link
JP (1) JPS60237007A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63198602A (en) * 1986-11-24 1988-08-17 アメリカン・サイアナミド・カンパニー Detoxicated vermicidal composition for controlling vermins present in soil
US4971796A (en) * 1988-10-05 1990-11-20 Sjogren Robert D Slow release pest control granule composition
US5643590A (en) * 1986-11-24 1997-07-01 American Cyanamid Company Safened pesticidal resin composition for controlling soil borne pests and process for the preparation thereof
WO1998016105A1 (en) * 1996-10-11 1998-04-23 Basf Aktiengesellschaft Solid phytosanitary agent
CN104798776A (en) * 2014-01-28 2015-07-29 中国科学院大连化学物理研究所 Method for alleviating toxicity of herbicides to crops

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63198602A (en) * 1986-11-24 1988-08-17 アメリカン・サイアナミド・カンパニー Detoxicated vermicidal composition for controlling vermins present in soil
US5643590A (en) * 1986-11-24 1997-07-01 American Cyanamid Company Safened pesticidal resin composition for controlling soil borne pests and process for the preparation thereof
US5650163A (en) * 1986-11-24 1997-07-22 American Cyanamid Company Safened pesticidal resin compositions for controlling soil borne pests and process for the preparation thereof
US5650161A (en) * 1986-11-24 1997-07-22 American Cyanamid Company Safened pesticidal resin compositions for controlling soil borne pests and process for the preparation thereof
US4971796A (en) * 1988-10-05 1990-11-20 Sjogren Robert D Slow release pest control granule composition
WO1998016105A1 (en) * 1996-10-11 1998-04-23 Basf Aktiengesellschaft Solid phytosanitary agent
CN104798776A (en) * 2014-01-28 2015-07-29 中国科学院大连化学物理研究所 Method for alleviating toxicity of herbicides to crops

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