JPS608209A - Stabilized solid agricultural chemical composition - Google Patents

Stabilized solid agricultural chemical composition

Info

Publication number
JPS608209A
JPS608209A JP11549183A JP11549183A JPS608209A JP S608209 A JPS608209 A JP S608209A JP 11549183 A JP11549183 A JP 11549183A JP 11549183 A JP11549183 A JP 11549183A JP S608209 A JPS608209 A JP S608209A
Authority
JP
Japan
Prior art keywords
parts
carbosulfan
calcium
clay
calcium carbonate
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
JP11549183A
Other languages
Japanese (ja)
Inventor
Shiro Kamaki
鎌木 史朗
Muneo Wada
和田 宗生
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.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical 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 Nissan Chemical Corp filed Critical Nissan Chemical Corp
Priority to JP11549183A priority Critical patent/JPS608209A/en
Publication of JPS608209A publication Critical patent/JPS608209A/en
Pending legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To suppress decomposition of carbosulfan, by blending a solid preparation of carbosulfan with calcium oxide, calcium hydroxide, or calcium carbonate. CONSTITUTION:In supporting carbosulfan: 2,3-dihydro-2,2-dimethyl-7-benzofuranyl- N-dibutylaminothio-N-methyl carbamate shown by the formula, well-known as an improved insecticide having excellent effect on various kinds of insect pests in paddy rice plants and crops in plowed fields, showing wide insecticidal spectrum on a powdery or granular mineral carrier (e.g., bentonite, or clay), the insecticide is blended with >=5wt% calcium oxide, calcium hydroxide, or calcium carbonate. Addition of another stabilizer such as epoxydized soybean oil, etc. further raises stabilizing effect.

Description

【発明の詳細な説明】 本発明は2,3−ジヒドロ−2,2−ジメチル−7−ベ
ンゾフラニル−N−ジブチルアミノチオ−N−メチルカ
ーハメ−1−(以下、単にカルボスルフアンと称す。)
の固体服薬製剤に、カルシウムの酸化物、水酸化物また
は炭酸塩の1種または2種以上を配合することを特徴と
する安定化させた固体農薬組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to 2,3-dihydro-2,2-dimethyl-7-benzofuranyl-N-dibutylaminothio-N-methylcarhame-1- (hereinafter simply referred to as carbosulfan).
The present invention relates to a stabilized solid agrochemical composition characterized in that one or more of calcium oxides, hydroxides, or carbonates are blended into a solid pharmaceutical preparation.

カルボスルフアンは、市販されている殺虫剤の白゛す」
成分化合物であり、水稲及び畑作におりる各種害虫に対
し卓効を有し幅広い殺虫スペクトラノ・を有する優れた
殺虫剤として知られている。しかし、カルボスルフアン
は極めて不安定であり通常使用される鉱物質担体(例え
ば、ヘン1−ナイト。
Carbosulfan is one of the most commercially available insecticides.
It is a component compound and is known as an excellent insecticide with a wide range of insecticidal spectra and is extremely effective against various pests in paddy rice and field crops. However, carbosulfan is extremely unstable and commonly used mineral carriers (e.g. hennite).

クレー、ゼオライト、ケイソウ上等)またはポリイトカ
ーボン(例えば、カープレックス#1120、#80.
ジオツギ製薬θ菊製)の15)末法または粒状のものに
担持させて製剤化した場合、カル7沢スルフアンは著し
く分解し2時には50℃で1力月後の分解率が100%
(全部分解)になる場合もあり、また分解過程で毒性の
高いカルボフランの生成も認められ、安全性の観点から
もこの分解を極力抑制することが強く要望され′ζいる
clay, zeolite, diatomaceous, etc.) or polyitocarbon (e.g. Carplex #1120, #80.
15) of Geotsugi Pharmaceutical (manufactured by θ Kiku) or when formulated by being supported on granules, Cal7sawa sulfan was significantly decomposed and the decomposition rate was 100% after 1 month at 50°C.
In some cases, highly toxic carbofuran is also produced during the decomposition process, and there is a strong desire to suppress this decomposition as much as possible from a safety standpoint.

0=C−N−3−N =(n=Bu)z H O= C−N−CH3 (カルボフラン) 本発明者らは、固体農薬製剤化されたカルボスルフアン
の分解抑制について種々検討を重ねた結果。
0=C-N-3-N = (n=Bu)z H O= C-N-CH3 (carbofuran) The present inventors have repeatedly conducted various studies on suppressing the decomposition of carbosulfan made into a solid agricultural chemical formulation. The result.

カルボスルフアンの固体製剤にカルシウムの酸化物、水
酸化物、または炭酸塩の一種または二種以上を配合する
ことによりカルボスルフアンの安定性を著しく高めるこ
と、即ち分解を著しく抑制することを見いだし本発明を
完成した。
It has been discovered that by incorporating one or more calcium oxides, hydroxides, or carbonates into a solid preparation of carbosulfan, the stability of carbosulfan can be significantly increased, that is, decomposition can be significantly inhibited. The invention has been completed.

本発明において、固体農薬製剤とは、粉剤1粒剤。In the present invention, the solid agricultural chemical formulation refers to one powder.

微粒剤、水和剤のような製剤形態を意味するものであり
、担体として用いられる鉱物質担体或いはホワイトカー
ボンの形状は破砕した粉末状2粒状。
This refers to formulations such as fine granules and wettable powders, and the mineral carrier or white carbon used as the carrier is in the form of two crushed powder particles.

微粒状、塊状のいずれでも良く、また粉末状のものをバ
インダー、界面活性剤、水などを用いて造粒したもので
も良い。
It may be in the form of fine particles or blocks, or it may be granulated from a powder using a binder, a surfactant, water, etc.

カルシウムの酸化物としては酸化カルシウムCab。Calcium oxide Cab is an oxide of calcium.

過酸化カルシウムCa%があり、水酸化カルシウムとし
てはCa (Oll)2があげられる。また炭酸塩とし
てはCaC01があげられる。添加量は特に限定されな
いが、5%以上添加するのが効果的である。また他の安
定剤9例えばエポキシ化大豆油等を添加することで更に
高い効果を示すこともある。
Calcium peroxide is Ca%, and calcium hydroxide includes Ca(Oll)2. Moreover, CaC01 is mentioned as a carbonate. Although the amount added is not particularly limited, it is effective to add 5% or more. Furthermore, even higher effects may be obtained by adding other stabilizers 9, such as epoxidized soybean oil.

以下実施例をあげて本発明の方法及び効果について説明
するが9本発明の内容はこれらに限定されるものではな
い。 : 遺」1例」−粉剤 カルボスルフアン原体(エポキシ化大豆油4%含有iF
Mc社製)3部、添加剤10部、タレ−(埼玉県産)粉
末品87部をあらかじめ混合した後ハンマーミル(不ニ
バウダル社製)で混合粉砕し3%粉剤を得た。この粉剤
をガラス瓶にいれて密栓し、40℃恒温器に1力月間保
存した後カルボスルフアンの含量を分析し、初期含量に
対する分解率をめた。結果は第1表に示す。
The method and effects of the present invention will be described below with reference to Examples, but the content of the present invention is not limited thereto. : ``1 case'' - Powder carbosulfan drug substance (iF containing 4% epoxidized soybean oil)
Mc), 10 parts of additives, and 87 parts of powdered tare (produced in Saitama Prefecture) were mixed in advance and mixed and pulverized in a hammer mill (manufactured by Fuji Baudal) to obtain a 3% powder. This powder was placed in a glass bottle, sealed tightly, and stored in a 40°C incubator for one month.The content of carbosulfan was analyzed to determine the decomposition rate relative to the initial content. The results are shown in Table 1.

以下余白 第1表 添加剤 力ルホスルファン分解率 1 無添加(対照)34% 2 Ca0z 10% 3 Ca0 13% 4 Ca (OH)2 、 15% 5 CaCO317% 6 CaO1/CaC03(1: 1) 12%7Na
OH(対照)100% 第1表に示した通り2本発明による粉剤はカルボスルフ
アンの安定性が対照に比べ1/2以下に抑制されている
ことが明らかである。また苛性ソーダでは安定効果がな
(逆に分解を促進することがキする。
Table 1 with blank space below Additives Decomposition rate of rufosulfan 1 No additive (control) 34% 2 Ca0z 10% 3 Ca0 13% 4 Ca(OH)2, 15% 5 CaCO3 17% 6 CaO1/CaC03 (1: 1) 12% 7Na
OH (control) 100% As shown in Table 1, it is clear that the stability of carbosulfan in the powder formulation according to the present invention is suppressed to 1/2 or less compared to the control. Also, caustic soda has no stabilizing effect (on the contrary, it promotes decomposition).

尖施皿(粉剤 過酸化カルシウム0〜50%、鉱物質担体の粉末品また
はホワイトカーボン97〜47部を混合しカルボスルフ
アン原体(エポキシ化大豆油4%含有i FMC社製)
3部をスプレー混合した後、ハンマーミル(不ニバウダ
ル社製)で混合わ)砕し3%粉剤を得た。この粉剤をガ
ラス)1ルにいれて密栓し、40℃恒温器に1力月間保
存した後カルボスルフアンの含量を分析し、初期含量に
対する分解率をめた。結果は第2表に示す。
A sharp dish (0 to 50% powdered calcium peroxide, 97 to 47 parts of powdered mineral carrier or white carbon mixed together to form carbosulfan raw material (containing 4% epoxidized soybean oil, manufactured by FMC)
After spray-mixing 3 parts, the mixture was crushed in a hammer mill (manufactured by Fuji Baudal) to obtain a 3% powder. This powder was placed in a glass container, sealed tightly, and stored in a 40° C. incubator for one month, and then the carbosulfan content was analyzed to determine the decomposition rate relative to the initial content. The results are shown in Table 2.

以下余白 第2表 担体(部) CaO1添加量 カルボスルフアン分解率 ヘン1−ナイト(97部) 0部 100%ヘントナイ
I−(87部)10部 33%クレー (97都) 0
93 34% クレー (96部) 1部 15% クレー (92部) 5部 8% クレー (87部)10部 10% クレー (62部)35部 12% クレー (47部)50部 11% カープレックス(97部)0部 100%#1120 カープレックス(87部)10部 6%#1120 炭酸カルシウム(97部)0部 6% へントナイト(群馬産)、クレー(埼玉産)、カープレ
ックス#1120 (ホワイトカーボン、ジオツギ製薬
製)、炭酸カルシウム(山口産)を使用。
Table 2 with blank space below Carrier (parts) Amount of CaO1 added Carbosulfan decomposition rate Hentonite (97 parts) 0 parts 100% Hentonite I- (87 parts) 10 parts 33% Clay (97 parts) 0
93 34% Clay (96 parts) 1 part 15% Clay (92 parts) 5 parts 8% Clay (87 parts) 10 parts 10% Clay (62 parts) 35 parts 12% Clay (47 parts) 50 parts 11% Carplex (97 parts) 0 parts 100% #1120 Carplex (87 parts) 10 parts 6% #1120 Calcium carbonate (97 parts) 0 parts 6% Hentonite (produced in Gunma), Clay (produced in Saitama), Carplex #1120 ( Uses white carbon (manufactured by Geotsugi Pharmaceutical) and calcium carbonate (produced in Yamaguchi).

第2表より担体にかかわらず2本発明はカルボスルフア
ンの分解を抑制していることが判る。
Table 2 shows that the present invention suppresses the decomposition of carbosulfan regardless of the carrier.

尖廠皿主 粉剤 実施例2と同様にして以下の組成の3%粉剤を(nた。Sharp plate main powder A 3% powder having the following composition was prepared in the same manner as in Example 2.

この粉剤をガラス)1ハにいれて密栓し、40”C恒温
器に1力月間保存した後カルボスルフアンの含量を分析
し、初期含量に対する分解率をめた。
This powder was placed in a glass jar, sealed tightly, and stored in a 40"C thermostat for one month. The content of carbosulfan was analyzed to determine the decomposition rate relative to the initial content.

結果は第3表に示す。The results are shown in Table 3.

第3表 組 成 カルボスルフアン 分解率 ベン1−ナイト97部 100% ベントナイト95部、8502部 50%CaCO58
5部、Ca0210部、ESO2部 2%ESOはエポ
キシ化大豆油(竹本油脂製)を示す。
Table 3 Composition Carbosulfan decomposition rate Ben1-Nite 97 parts 100% Bentonite 95 parts, 8502 parts 50% CaCO58
5 parts, 10 parts of Ca0, 2 parts of ESO 2% ESO indicates epoxidized soybean oil (manufactured by Takemoto Yushi).

芙j劉性t 粒剤 破砕後篩別して粒度を14〜42ノソシユに揃えたヘン
トナイト ゼオライト(宮城共産)、ケイソウ土(岡山共産)及び
炭酸カルシウム(山口共産)を粒状担体として,各粒状
担体95部にカルボスルフアン原体(エポキシ化大Ij
油4%含有iFMC社!!り 5部をピペットでゆっく
り;商工しながら混合攪拌し5%粒剤を調製した。この
粒剤をガラス)1■にいれて密栓し,40℃恒温器に1
力月間保存した後カルボスルフアンの含量を分析し,初
期含量に対する分解率をめた。結果は第4表に示す。
Hentonite zeolite (Miyagi Co., Ltd.), diatomaceous earth (Okayama Co., Ltd.), and calcium carbonate (Yamaguchi Co., Ltd.), which were crushed and sieved to have a particle size of 14 to 42 mm, were used as granular carriers, each granular carrier 95 In the part, carbosulfan drug substance (epoxidized large Ij
iFMC containing 4% oil! ! 5 parts of the mixture were mixed and stirred slowly with a pipette to prepare 5% granules. Put this granule in a glass), seal it tightly, and place it in a 40℃ thermostat.
After storage for one month, the carbosulfan content was analyzed and the decomposition rate relative to the initial content was determined. The results are shown in Table 4.

第4表 担体 カルボスルフアン分解率 ヘントナイト 98% クレー 30% ゼオライト 100% ケイソウ上 38% 炭酸カルシウム 3% 実施1 造粒品 鉱物質担体と過酸化カルシウムを第5表の如き配合割合
で混合し,この混合物97部にリグニンスルボン酸カル
シウム1部,ゴーセノール05S(日本合成@製ポリビ
ニルアルコール)1部,ツルポール5060 (東邦化
学製界面活性剤)1部及び水15部を加えて混練し+ 
0 、 8mmφのスクリーンを装着したエソクペレッ
タ−(不二パウダル社製)で造粒した。上記操作を速や
かに行いかつ得られた含水造粒物を流動乾燥機(不二パ
ウダル社M)にて速やかに乾燥し,粒状担体を得た。得
られた造粒空球95部にカルボスルフアン原体(エポキ
シ化大豆油4%含有i FMC社111) 5部をスプ
レー混合して5%粒剤を得た。この粒剤をガラスllH
にいれて密栓し40℃恒温器に1力月間保存した後カル
ボスルフアンの含量を分析し,初期含量に対する分11
+T率をめた。結果は第5表に示す。
Table 4 Support Carbosulfan decomposition rate Hentonite 98% Clay 30% Zeolite 100% Diatomite 38% Calcium carbonate 3% Example 1 Granulated mineral support and calcium peroxide were mixed in the proportions shown in Table 5, To 97 parts of this mixture, 1 part of calcium lignin sulfonate, 1 part of Gohsenol 05S (polyvinyl alcohol manufactured by Nippon Gosei@), 1 part of Tsurupol 5060 (surfactant manufactured by Toho Chemical) and 15 parts of water were added and kneaded.
Pelletization was carried out using an Esoku pelleter (manufactured by Fuji Paudal Co., Ltd.) equipped with a screen of 0.0 and 8 mmφ. The above operation was quickly carried out, and the resulting water-containing granules were quickly dried in a fluidized dryer (manufactured by Fuji Paudal Co., Ltd.) to obtain a granular carrier. 95 parts of the resulting granulated empty spheres were spray-mixed with 5 parts of carbosulfan raw material (i FMC Co., Ltd. 111 containing 4% epoxidized soybean oil) to obtain 5% granules. Glass llH of this granule
After storing it in a thermostat at 40℃ for 1 month, the content of carbosulfan was analyzed, and the amount of 11 minutes relative to the initial content was analyzed.
Achieved +T rate. The results are shown in Table 5.

以下余白 第5表 担体(部) CaO□添加量 カルボスルフアン分解率 ヘントナイI−100部 0部 95%ヘントナイト クレー 100部 0部 32% クレー 80部 20部 11% 炭酸カルシウム100部 0部 6% 炭酸カルシウム 80部 20部 7%実実施直立水和
剤 カルボスルフアン原体(エポキシ化大豆油4%含有; 
1? M C社製)10部,鉱物質担体の粉末品,リグ
ニンスルポン酸す1す1シム3部,ツルポール5080
(東邦化学製界面活性剤)5部,カープレックス#11
20 (ジオツギ製薬製ホワイトカーボン)5部,過酸
化カルシウムを第6表の如き配合割合で混合した後ジェ
ット・オー・マイザー(セイシン企業製)で微,粉砕し
ぞ10%水和剤を得た。この水和剤をガラス瓶にいれて
密栓し40℃恒温器に1力月間保存した後カルボスルフ
アンの含量を分析し,初期含量に対する分解率をめた。
Table 5 with blank space below Carrier (parts) Addition amount of CaO□ Carbosulfan decomposition rate Hentoni I-100 parts 0 parts 95% hentonite clay 100 parts 0 parts 32% Clay 80 parts 20 parts 11% Calcium carbonate 100 parts 0 parts 6 % Calcium carbonate 80 parts 20 parts 7% Practical erect wettable powder Carbosulfan raw material (contains 4% epoxidized soybean oil;
1? (manufactured by MC) 10 parts, powdered mineral carrier, 1 part lignin sulfonic acid 1 part 1 shim, 3 parts Tsurupol 5080
(Toho Chemical surfactant) 5 parts, Carplex #11
20 5 parts of White Carbon (manufactured by Geotsugi Pharmaceutical Co., Ltd.) and calcium peroxide were mixed in the proportions shown in Table 6, and then finely ground with a Jet-O-Miser (manufactured by Seishin Enterprises) to obtain a 10% hydrating powder. . This hydrating powder was placed in a glass bottle, sealed and stored in a 40°C thermostat for one month, and then the carbosulfan content was analyzed to determine the decomposition rate relative to the initial content.

結果は第6表に示す。The results are shown in Table 6.

第6表 担体(部) Ca%添加量 カルボスルフアン分解率 ジ−クライトPPP 77部 0部 35%ジークライ
トPPP 72部 5部 11%ネオキャリア0277
部 0部 31%ネオキャリア0272部 5部 12
%重質炭酸カルシウム 77部 0部 11%重質炭酸
カルシウム 72部 5部 9%特許出願人 日産化学
工業株式会邑7
Table 6 Support (parts) Ca% addition amount Carbosulfan decomposition rate Zicraite PPP 77 parts 0 parts 35% Ziecrite PPP 72 parts 5 parts 11% Neocarrier 0277
Part 0 part 31% Neocarrier 0272 part 5 part 12
% heavy calcium carbonate 77 parts 0 parts 11% heavy calcium carbonate 72 parts 5 parts 9% Patent applicant Nissan Chemical Industries, Ltd.

Claims (1)

【特許請求の範囲】[Claims] 2.3−ジヒドロ−2,2−ジメチル−7−ベンゾフラ
ニル−N−ジブチルアミノチオ−N=メチルカーバメー
トの固体農薬製剤に、カルシウムの酸化物、水酸化物ま
たは炭酸塩の1種または2種以上を配合することを特徴
とする安定化さ・ヒた固体農薬組成物
2. One or more calcium oxides, hydroxides, or carbonates are added to the solid pesticide formulation of 2.3-dihydro-2,2-dimethyl-7-benzofuranyl-N-dibutylaminothio-N=methylcarbamate. A stabilized solid agricultural chemical composition characterized by containing
JP11549183A 1983-06-27 1983-06-27 Stabilized solid agricultural chemical composition Pending JPS608209A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11549183A JPS608209A (en) 1983-06-27 1983-06-27 Stabilized solid agricultural chemical composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11549183A JPS608209A (en) 1983-06-27 1983-06-27 Stabilized solid agricultural chemical composition

Publications (1)

Publication Number Publication Date
JPS608209A true JPS608209A (en) 1985-01-17

Family

ID=14663826

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11549183A Pending JPS608209A (en) 1983-06-27 1983-06-27 Stabilized solid agricultural chemical composition

Country Status (1)

Country Link
JP (1) JPS608209A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6351306A (en) * 1986-08-20 1988-03-04 Otsuka Chem Co Ltd Stable solid agricultural chemical composition
US4824864A (en) * 1984-07-14 1989-04-25 Basf Aktiengesellschaft Stabilization of zineb

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57156402A (en) * 1981-03-24 1982-09-27 Nissan Chem Ind Ltd Mineral carrier for agricultural chemicals

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57156402A (en) * 1981-03-24 1982-09-27 Nissan Chem Ind Ltd Mineral carrier for agricultural chemicals

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4824864A (en) * 1984-07-14 1989-04-25 Basf Aktiengesellschaft Stabilization of zineb
JPS6351306A (en) * 1986-08-20 1988-03-04 Otsuka Chem Co Ltd Stable solid agricultural chemical composition
JPH0788284B2 (en) * 1986-08-20 1995-09-27 大塚化学株式会社 Stable pesticide composition

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