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JPH03109303A - crop yield enhancer - Google Patents

crop yield enhancer

Info

Publication number
JPH03109303A
JPH03109303A JP24491989A JP24491989A JPH03109303A JP H03109303 A JPH03109303 A JP H03109303A JP 24491989 A JP24491989 A JP 24491989A JP 24491989 A JP24491989 A JP 24491989A JP H03109303 A JPH03109303 A JP H03109303A
Authority
JP
Japan
Prior art keywords
grain
compound
formula
agent
salt
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
JP24491989A
Other languages
Japanese (ja)
Inventor
Takashi Oritani
折谷 隆志
Shigeo Yoshinaka
吉中 茂生
Takashi Suzuki
隆 鈴木
Takehito Maruyama
岳人 丸山
Toshio Kajita
梶田 敏夫
Masakazu Furushima
古嶋 昌和
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.)
Mitsubishi Gas Chemical Co Inc
Original Assignee
Mitsubishi Gas Chemical Co Inc
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 Mitsubishi Gas Chemical Co Inc filed Critical Mitsubishi Gas Chemical Co Inc
Priority to JP24491989A priority Critical patent/JPH03109303A/en
Priority to EP19900303277 priority patent/EP0390515B1/en
Priority to DE1990606379 priority patent/DE69006379T2/en
Priority to ES90303277T priority patent/ES2062344T3/en
Priority to US07/653,643 priority patent/US5244487A/en
Publication of JPH03109303A publication Critical patent/JPH03109303A/en
Pending legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To provide an agent exhibiting an remarkable yield-increasing activity for grain crops such as rice and beans by containing N<6>-[2-(N-methoxy-N- methylamino)ethyl] adenine or a salt thereof as an active ingredient. CONSTITUTION:The subject agent contains a compound of the formula or its salt with hydrochloric acid, phosphoric acid, acetic acid, etc., as an active ingredient. The compound of the formula is employed in a form of emulsion, water- dispersible powder, powder, solution, etc., together with a liquid diluent such as an alcohol, water or DMF, a solid carrier such as talc, diatomaceous earth or phenolic resin, a surfactant (e.g. alkylbenzene sulfonic acid sodium salt), a dispersing agent, an adhesive agent, etc. The compound of the formula is applied in a rate of 0.01-1g per 10a of the field to a legaminous crop (e.g. soybean, azuki, bean, kidney bean, or peanut) between its flowering time and the grain filling early time of its grain and to the leaf and stem of a gramineous crop (e.g. rice, wheat or corn) between its booting time and its grain filling early time.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は作物増収剤に関し、さらに詳細には新規なアデ
ニン誘導体を有効成分として含有する作物増収剤に関す
る。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a crop yield increasing agent, and more particularly to a crop yield increasing agent containing a novel adenine derivative as an active ingredient.

[従来の技術、発明が解決しようとする問題点]従来、
水稲、マメ等の寂穀類作物の増収をもたらすための多く
の研究がなされている。しかしながら、実用に供されて
いるものは少ない。
[Prior art, problems to be solved by the invention] Conventionally,
Many studies have been conducted to increase the yield of grain crops such as rice and beans. However, few of them are in practical use.

従って、安全で有効な増収効果をもたらす薬剤の開発が
望まれている。
Therefore, it is desired to develop a drug that is safe and effective and has a yield-increasing effect.

さらに従来、カイネチン、ゼアチン、6−ベンジルアミ
ノプリンおよびチジアズロンなどのサイトカイニンがそ
れぞれ細胞の分裂促進、細胞肥大、非分化組織の分化促
進、老化の防止および種子発芽促進等の活性を有するこ
とが知られている。
Furthermore, it has been known that cytokinins such as kinetin, zeatin, 6-benzylaminopurine, and thidiazuron have activities such as promoting cell division, cell hypertrophy, promoting differentiation of undifferentiated tissues, preventing aging, and promoting seed germination, respectively. ing.

近年、前記のごときサイトカイニンで水稲等の穀類作物
の増収をさせる試みがなされている。
In recent years, attempts have been made to increase the yield of cereal crops such as paddy rice using cytokinin as described above.

たとえば、 「日本作物学会紀事第51巻別号1(19
82年)第147〜148ページ」には、各種植物ホル
モンを直接水稲の穂へ注入する試験を行ないゼアチンお
よびアブサイシン酸のそれぞれに登熟歩合ならびに千粒
重の増加効果があることが報告されている。
For example, “Journal of the Crop Science Society of Japan, Vol. 51, Separate No. 1 (19
1982), pp. 147-148, conducted a test in which various plant hormones were directly injected into rice ears, and it was reported that zeatin and abscisic acid each had the effect of increasing the ripening rate and 1,000-grain weight.

また、特開昭83−181933号公報には、6−(N
−ベンジルアミノ)プリン、チジアズロン、カイネチン
およびゼアチンでイネ科作物の穂を処理することにより
、イネ科作物の増収を計ることが記載されている。
In addition, 6-(N
It has been described that the yield of grass crops can be increased by treating their ears with (benzylamino)purine, thidiazuron, kinetin and zeatin.

前記のような化合物は、たとえば、カイネチンおよびゼ
アチンは天然物であり製造することがきわめて困難であ
るという問題点があり、また、6−(N−ベンジルアミ
ノ)プリンおよびチジアズロンは、製造することは比較
的容易であるが、水に対する溶解度が小さく、かつ、作
物への吸取、移行性が悪いという欠点があり実用上必ず
しも十分なものとは言えない。
The above-mentioned compounds, for example, have the problem that kinetin and zeatin are natural products and are extremely difficult to produce, and 6-(N-benzylamino)purine and thidiazuron are difficult to produce. Although it is relatively easy to use, it has the drawbacks of low solubility in water and poor absorption and transferability to crops, so it is not necessarily sufficient for practical use.

本発明者等は、先に新規なアデニン誘導体であるN6−
[2−(N−メトキシ−N−メチルアミノ)エチル]ア
デニン等が強いサイトカイニン活性を有することを見い
出した(特願平1−73763号)。
The present inventors previously discovered a novel adenine derivative, N6-
It has been found that [2-(N-methoxy-N-methylamino)ethyl]adenine and the like have strong cytokinin activity (Japanese Patent Application No. 1-73763).

本発明者がN6−[2−(N−メトキシ−N−メチルア
ミノ)エチルコアデニンにつき、さらに植物に対する作
用ならびに効果を検討した結果、この化合物は、単にサ
イトカイニン活性を有するのみならず、マメ科およびイ
ネ科等の萩穀類作物の草葉部に施用することにより、作
物の収量が増えることを見い出した。
The present inventor further investigated the action and effect of N6-[2-(N-methoxy-N-methylamino)ethylcoadenine on plants, and found that this compound not only has cytokinin activity but also It was also found that the yield of crops can be increased by applying it to the grass leaves of grass crops such as grasses.

この新知見にもとづいて、本発明に到達した。Based on this new knowledge, we have arrived at the present invention.

[問題を解決するための手段、作IIJ ]本発明は、
N6−[2−(N−メトキシ−N−メチルアミノ)エチ
ルコアデニンまたはその塩を有効成分として含有するこ
とを特徴とする作物増収剤である。N6−[2−(N−
メトキシ−N−メチルアミノ)エチルコアデニン(以下
MOMEAと記すこともある)の構造式は次に示す如く
である。
[Means for solving the problem, made by IIJ] The present invention includes:
This is a crop yield increasing agent characterized by containing N6-[2-(N-methoxy-N-methylamino)ethylcoadenine or a salt thereof as an active ingredient. N6-[2-(N-
The structural formula of methoxy-N-methylamino)ethylcoadenine (hereinafter also referred to as MOMEA) is as shown below.

)fOMEAは塩素、硫酸、硝酸、リン酸、ギ酸および
#酸等の酸と容易に塩をつくる(以下、河OMEAおよ
びその塩を総括してMOMEA類と記すこともある)。
) fOMEA easily forms salts with acids such as chlorine, sulfuric acid, nitric acid, phosphoric acid, formic acid, and #acid (hereinafter, OMEA and its salts may be collectively referred to as MOMEA).

この塩もMOMEAと同様に植物に対しサイトカイニン
活性およびマメ科およびイネ科作物の増収効果を示す。
Like MOMEA, this salt also exhibits cytokinin activity on plants and yield-increasing effects on leguminous and gramineous crops.

MOMEA類はそれ自体単独でも作物増収剤として用い
られるが、通常は、農薬製剤分野において一般的に用い
られる液体または固体の希釈剤(担体)、さらに必要に
より乳化剤、分散剤および展着剤などとしての界面活性
剤ならびに固着剤などと併用した製剤形態で用いられる
MOMEAs can be used alone as crop yield enhancers, but they are usually used as liquid or solid diluents (carriers) commonly used in the agricultural chemical formulation field, and if necessary, as emulsifiers, dispersants, and spreading agents. It is used in the form of a formulation in combination with a surfactant and a fixing agent.

具体的な形態としては、乳剤、水和剤、粉剤および液剤
などがあげられる。
Specific forms include emulsions, wettable powders, powders, and liquids.

液剤を調整する場合の希釈剤としてはメタノール、エタ
ノールなどのアルコール類、水、ジメチルホルムアミド
およびジメチルスホキシドなどの極性溶剤があげられる
Examples of diluents used in preparing liquid formulations include alcohols such as methanol and ethanol, water, and polar solvents such as dimethylformamide and dimethylsulfoxide.

水和剤、粒剤、粉剤などを調製する場合の固体の希釈剤
(担体)としては、タルク、クレーベントナイト、カオ
リン、モンモリロナイト、珪藻土、フェノール樹脂およ
びホワイトカーボンなどがあげられる。
Examples of solid diluents (carriers) for preparing wettable powders, granules, powders, etc. include talc, clay bentonite, kaolin, montmorillonite, diatomaceous earth, phenolic resin, and white carbon.

界面活性剤としては、アルキルベンゼンスルフオン酸ソ
ーダおよびラウリル硫酸ソーダなどの陰イオン系界面活
性剤、ステアリルトリメチルアンモニウムクロライドな
どの陽イオン系界面活性剤ならびにポリオキシエチレン
アルキルフェニルエーテルなどの非イオン系界面活性剤
などがあげられる。
Examples of surfactants include anionic surfactants such as sodium alkylbenzenesulfonate and sodium lauryl sulfate, cationic surfactants such as stearyltrimethylammonium chloride, and nonionic surfactants such as polyoxyethylene alkylphenyl ether. Examples include drugs.

分散剤として、リグニンスルフオン酸ソーダ、メチルセ
ルロースおよび亜硫酸パルプ廃液があげられる。
Dispersants include sodium ligninsulfonate, methylcellulose and sulfite pulp waste liquor.

固着剤としては、カゼイン石灰、ニカワ、カルボキシメ
チルセルローズ、アルギン酸ソーダおよびポリビニール
アルコールなどがあげられる。
Examples of the fixing agent include casein lime, glue, carboxymethyl cellulose, sodium alginate, and polyvinyl alcohol.

本発明の施用部位、施用量および施用時期などは作物の
種類などによって異なり、−概に特定しえないが、マメ
科作物およびイネ科作物について例示する。
Although the application site, application amount, and application timing of the present invention vary depending on the type of crop and cannot be generally specified, leguminous crops and gramineous crops are exemplified.

すなわち、マメ科作物およびイネ科作物などの寂穀類作
物については茎葉部に施用されるが、薬剤の施用量はM
OMEA換算で10a当り通常は0.003〜3gであ
るが、0.01〜Igが好適である。
In other words, for grain crops such as leguminous crops and gramineous crops, the chemical is applied to the foliage, but the application amount is M
The amount is usually 0.003 to 3 g per 10 a in terms of OMEA, but preferably 0.01 to Ig.

施用時期については、マメ科作物に対しては、通常は着
蕾期から子実の登熟期までの間とされるが、開花始めか
ら子実の登熟初期までの間に施用することが好ましい。
Regarding the timing of application, for leguminous crops, it is usually applied between the bud set stage and the grain ripening stage, but it can be applied from the beginning of flowering to the early stage of grain ripening. preferable.

また、イネ科作物に対しては、通常は幼穂形成期より登
熟期までの間とされるが、穂孕期から登熟初期までの間
が好ましい。
Furthermore, for grass crops, the period from the panicle formation stage to the ripening stage is usually set, but the period from the panicle stage to the early stage of ripening is preferred.

本発明剤が適用される作物の代表例としては、マメ科作
物では大豆、小豆、インゲン豆、シカク豆および落花生
などがあり、イネ科作物では、稲、小麦、大麦、ライ麦
、ハト麦、エンバクおよびトウモロコシなどがある。
Typical examples of crops to which the present invention is applied include leguminous crops such as soybeans, adzuki beans, kidney beans, shikaku beans, and peanuts, and grass crops such as rice, wheat, barley, rye, pigeon wheat, and oats. and corn.

[実施例] 実施例I HOMEA 0.1gおよびツルポール−8222(ノ
ニオン系界面活性剤東邦化学工業株式会社製品)10.
0gを水89.9gに溶解してMOMEA液剤を調製し
た。
[Examples] Example I HOMEA 0.1 g and Trupol-8222 (nonionic surfactant manufactured by Toho Chemical Industry Co., Ltd.) 10.
A MOMEA solution was prepared by dissolving 0g in 89.9g of water.

実施例2 MOMEA 2gおよびニアロールCT−1(ttsイ
オン系界面活性剤東邦化学工業株式会社製品)38gを
ジメチルスフオキシド60gに溶解して乳剤を調製した
Example 2 An emulsion was prepared by dissolving 2 g of MOMEA and 38 g of Nearol CT-1 (tts ionic surfactant manufactured by Toho Chemical Industries, Ltd.) in 60 g of dimethylsulfoxide.

実施例3 HOMEAlog、ホワイトカーボン15g、リグニン
スルフオン酸カルシウム3g、ポリオキシエチレンノニ
ルフェニルエーテル1g、珪藻土5gおよびクレー88
gを粉砕して均一に混合して、水和剤を調製した。
Example 3 HOMEAlog, 15 g of white carbon, 3 g of calcium lignin sulfonate, 1 g of polyoxyethylene nonylphenyl ether, 5 g of diatomaceous earth, and 88 g of clay
A wettable powder was prepared by pulverizing and uniformly mixing g.

試験例1 4月20日水稲(品種コシヒカリ)の幼苗を水田に植え
、穂孕期に当たる8月4日および登熟初期に当たる8月
19日のそれぞれの時期に実施例1で調整されたMOM
EA液剤を、第1表に示す所定の濃度になるよう水で希
釈し、10a当り1009を茎葉散布した。
Test Example 1 Seedlings of paddy rice (variety Koshihikari) were planted in a paddy field on April 20th, and the MOM prepared in Example 1 was planted on August 4th, which is the heading stage, and August 19th, which is the early stage of ripening.
The EA solution was diluted with water to a predetermined concentration shown in Table 1, and 1009 mg/10a was sprayed on the foliage.

また、比較剤として6−(N−ベンジルアミノ)プリン
2gおよびニアロールCT−1(陰イオン系界面活性剤
東邦化学工業株式会社製品)38gをジメチルスルフオ
キシド60gに溶解して乳剤(以下BA乳剤と記す)を
調整し、MOMEA液剤と同様な時期、濃度、液量で施
用した。
In addition, as a comparison agent, 2 g of 6-(N-benzylamino)purine and 38 g of Nyalol CT-1 (anionic surfactant manufactured by Toho Chemical Industry Co., Ltd.) were dissolved in 60 g of dimethyl sulfoxide to form an emulsion (hereinafter referred to as BA emulsion). ) was prepared and applied at the same timing, concentration, and volume as the MOMEA solution.

なお、1区は6II12で3反復とし試験を行なった。In addition, the test was conducted with 3 repetitions of 6II12 in 1st section.

出穂後41日0に当たる9月19日に数種を行ない、玄
米重および玄米千粒重を測定した。
Several tests were conducted on September 19, 41 days after heading, and the weight of brown rice and the weight of 1,000 grains of brown rice were measured.

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

第1表 以下余白 無処理区の玄米重は536kg/10a、玄米千粒重は
21.0gであった。
The weight of brown rice in the untreated area in Table 1 was 536 kg/10a, and the weight of 1,000 grains of brown rice was 21.0 g.

試験例2 10月20日秋播小麦(品種農林61号)の種子を畑に
播種し、伸長最盛期に当たる4月20日および登熟初期
に当たる5月10日のそれぞれに実施例1で調製された
MOMEA液剤および比較剤として試験例1で調製され
たBA乳剤と第2表に示す所定の濃度になるようにそれ
ぞれを水で希釈し、10a当り100Qを茎菜散布した
Test Example 2 Seeds of autumn sown wheat (variety Norin No. 61) were sown in a field on October 20th, and the seeds prepared in Example 1 were sown on April 20th, which is the peak elongation period, and May 10th, which is the early stage of ripening. The MOMEA solution and the BA emulsion prepared in Test Example 1 as a comparative agent were each diluted with water to the predetermined concentrations shown in Table 2, and 100Q per 10a was sprayed on stem vegetables.

播種235日後、収穫を行ない子実型を測定した。235 days after sowing, the seeds were harvested and the grain type was measured.

その結果を第2表に示す。The results are shown in Table 2.

第2表 試験例3 5月15日大豆(品種エンレイ)の種子を畑に播種し、
開花始めに当たる7月3日および登熟初期に当たる8月
7日のそれぞれに実施伊Hで調製されたMOMEA液剤
および比較剤として試験例1で得られたBA乳剤を第3
表に示す所定濃度になるようにそれぞれを水で希釈し、
loa当り1009を茎葉散布した。
Table 2 Test Example 3 On May 15th, soybean (variety Enrei) seeds were sown in the field.
On July 3rd, the beginning of flowering, and August 7th, the beginning of ripening, the MOMEA solution prepared in Experiment IH and the BA emulsion obtained in Test Example 1 as a comparison agent were added to the third experiment.
Dilute each with water to the specified concentration shown in the table,
1009 per loa was sprayed on the foliage.

なお、1区は12m2で、4反復として試験を行なった
In addition, 1 area was 12 m2, and the test was conducted in 4 repetitions.

播種132日後子実重を測定した。Grain weight was measured 132 days after sowing.

その結果を第3表に示す。The results are shown in Table 3.

以下余白 無処理区のlOa当りの子実型は470kgであった。Margin below The grain size per lOa in the untreated plot was 470 kg.

第3表 無処理区の子実型は10a当り372kgであった。Table 3 The grain size in the untreated plot was 372 kg per 10 a.

[発明の効果] 本発明剤は作物の特に寂穀類作物に対して顕著な増収作
用を示す。
[Effects of the Invention] The agent of the present invention exhibits a remarkable yield-increasing effect on crops, especially grain crops.

Claims (1)

【特許請求の範囲】[Claims] N^6−[2−(N−メトキシ−N−メチルアミノ)エ
チル]アデニンまたはその塩を有効成分として含有する
ことを特徴とする作物増収剤。
A crop yield increasing agent characterized by containing N^6-[2-(N-methoxy-N-methylamino)ethyl]adenine or a salt thereof as an active ingredient.
JP24491989A 1989-03-28 1989-09-22 crop yield enhancer Pending JPH03109303A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP24491989A JPH03109303A (en) 1989-09-22 1989-09-22 crop yield enhancer
EP19900303277 EP0390515B1 (en) 1989-03-28 1990-03-28 Novel adenine derivatives and their use as agents for increasing crop yields
DE1990606379 DE69006379T2 (en) 1989-03-28 1990-03-28 Adenine derivatives and their use to increase the crop yield of plants.
ES90303277T ES2062344T3 (en) 1989-03-28 1990-03-28 NEW ADENINE DERIVATIVES AND THEIR USE AS AGENTS TO INCREASE CROP YIELDS.
US07/653,643 US5244487A (en) 1989-03-28 1991-02-11 Adenine derivatives and their use as agents for increasing yield of crops

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP24491989A JPH03109303A (en) 1989-09-22 1989-09-22 crop yield enhancer

Publications (1)

Publication Number Publication Date
JPH03109303A true JPH03109303A (en) 1991-05-09

Family

ID=17125926

Family Applications (1)

Application Number Title Priority Date Filing Date
JP24491989A Pending JPH03109303A (en) 1989-03-28 1989-09-22 crop yield enhancer

Country Status (1)

Country Link
JP (1) JPH03109303A (en)

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