KR100449464B1 - Prochloraz Mixtures - Google Patents
Prochloraz Mixtures Download PDFInfo
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- KR100449464B1 KR100449464B1 KR1019960030856A KR19960030856A KR100449464B1 KR 100449464 B1 KR100449464 B1 KR 100449464B1 KR 1019960030856 A KR1019960030856 A KR 1019960030856A KR 19960030856 A KR19960030856 A KR 19960030856A KR 100449464 B1 KR100449464 B1 KR 100449464B1
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
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Abstract
두 화합물, 4,5,6,7-테트라클로로프탈리드 (일반명:프탈리드) 및 1-{N-프로필-N- [2-(2,4,6-트리클로로페녹시)에틸]카르바모일}이미다졸 (프로클로라즈)를 혼합시킴으로써 농업용의 신규 살진균 조성물이 제공된다.(2-ethylhexyl) ethyl] -1,2,3,4-tetrachlorophthalide (generic name: phthalide) and 1- { Carbamoyl} imidazole (proclorase) is mixed to provide a novel fungicidal composition for agricultural use.
Description
본 발명은 농업용 살진균 조성물에 관한 것이다.The present invention relates to an agricultural fungicidal composition.
일반명이 프로클로라즈인 1-{N-프로필-N-[2-(2,4,6-트리클로로페녹시)에틸]카르바모일}이미다졸 및 일반명이 프탈리드인 4,5,6,7-테트라클로로프탈리드는 이미 농업 목적의 살진균제로서 개별적으로 사용되어 오고 있다.(I) wherein the general name is prochloraz, such as 1- {N-propyl-N- [2- (2,4,6-trichlorophenoxy) ethyl] carbamoyl} imidazole, 7-Tetrachlorophthalide has already been used individually as an agricultural fungicide.
프탈리드는 벼의 도열병의 방제에 사용되어 오고 있으며 포유류 뿐만아니라 어류 및 조개에도 아주 안전하고 뛰어난 예방 효과를 갖는다. 그러나, 그의 용도는 예방용 살진균제로 한정되어 있다. 예를 들면, 일단 피리큘라리아 오리재(Pyricularia oryzae)에 의해 감염되게 되면 벼과 식물을 방제하는데 효과가 없다.Phthalide has been used to control rice blast fungus and has a very safe and excellent preventive effect on mammals as well as on fish and shellfish. However, its use is limited to fungicides for prophylaxis. For example, once infected by Pyricularia oryzae, it is ineffective in controlling paddy plants.
한편, 프로클라즈는 볍씨 소독제로써 사용되어 오고 있으나 벼과 식물에 직접 적용되어 사용되지는 않고 있다.On the other hand, Proclaz has been used as a disinfectant for rice seed, but it has not been directly applied to paddy plants.
따라서, 본 발명의 목적은 벼과 식물에 직접 적용할 수 있는 도열병 방제에 효과적인 화합물을 제공하는 것이다.Accordingly, it is an object of the present invention to provide a compound effective for controlling blast fungus which can be directly applied to a plant of a paddy field.
놀랍게도, 본 발명자들에 의해 이 화합물을 온실 및 들판 모두에서 벼과 식물에 직접 살포함으로써 벼의 도열병에 뛰어난 예방 및 방제 효과를 가짐을 발견하였다.Surprisingly, the present inventors have found that this compound has an excellent preventive and control effect on rice blast fungus by directly spraying the compound on a greenhouse in both greenhouse and field.
본 발명자들은 놀랍게도 프탈리드를 프로클로라즈와 조합하여 사용함으로써 프탈리드가 현저한 상승 작용을 나타냄을 발견하였다.The present inventors have surprisingly found that phthalide exhibits remarkable synergism by using phthalide in combination with prochloraz.
본 발명의 살진균 조성물은 개개의 성분의 특성으로부터 예측할 수 없는 상승 작용을 나타내는, 특히 피리쿨라리아 오리재의 극히 양호한 방제를 나타낸다. 조성물은 예방 효과 뿐만 아니라 뛰어난 방제 효과를 나타내어 한 성분을 단독으로 사용하는 것에 비하여 두 화합물의 필요량의 감소를 초래한다. 본 발명에 따른 농업용의 살진균 조성물은 또한 벼의 스폿 질병(예, 갈반) 및 푸사리움(Fusarium)의 방제에 특히 효과적이다.The fungicidal compositions of the present invention exhibit an unpreferable synergistic effect from the properties of the individual components, in particular the extremely good control of the pyricularia. The composition exhibits not only a preventive effect but also an excellent controlling effect, resulting in a reduction in the amount of the two compounds required compared with the use of one component alone. The fungicidal compositions for agriculture according to the present invention are also particularly effective for the control of spot diseases (e.g., infestation) and fusarium of rice.
프로클로라즈 대 프탈리드의 비는 상당히 다양하나 일반적으로 4:1 내지 1:4 중량비, 바람직하게는 2:1 내지 1:2 및 특히 바람직하게는 1:1.3 내지 1:1.6이다.The ratio of prochloraz to phthalide varies considerably, but is generally from 4: 1 to 1: 4 by weight, preferably from 2: 1 to 1: 2, and particularly preferably from 1: 1.3 to 1: 1.6.
본 발명에 따른 농업용 살진균제는 분진, 과립, 분진 과립 혼합물, 습윤 분말, 현탁 농축물, 유화 농축물(EC), 유동성인 것 등의 다양한 제제형으로 이러한 제제를 제조하는 공지의 방법에 따라 제공할 수 있다. 이들 제형을 제조하기 위한 보조 물질로서는 예를 들면 규조토, 소성 석회, 탄산 칼슘, 탈크, 화이트 카아본, 탈크, 벤토나이트 및 제올라이트 등의 고체 담체; 톨루엔, 크실렌, 나프타, 에탄올, 디옥산, 아세톤, 이소포론, 메틸 이소부틸케톤, 디메틸포름아미드, 디메틸 술폭시드 및 N-메틸-2-피롤리돈 등의 용매; 알킬술폰산 나트륨, 알킬벤젠술폰산 나트륨, 리그닌 술폰산 나트륨, 폴리옥시에틸렌글리콜 알킬 에테르, 폴리옥시에틸렌 라우릴 에테르, 폴리옥시에틸렌 알킬라우릴 에테르, 폴리옥시에틸렌 소르비탄 지방산 에스테르 등의 습윤제 뿐만 아니라 당업계에 사용되는 기타 다양한 계면 활성제를 예로서 들 수 있다.The agricultural fungicide according to the present invention is provided according to a known method for producing such a preparation in various preparation forms such as dust, granule, dust granule mixture, wet powder, suspension concentrate, emulsion concentrate (EC) can do. As auxiliary substances for preparing these formulations, for example, solid carriers such as diatomaceous earth, calcined lime, calcium carbonate, talc, white carabons, talc, bentonite and zeolite; A solvent such as toluene, xylene, naphtha, ethanol, dioxane, acetone, isophorone, methyl isobutyl ketone, dimethyl formamide, dimethyl sulfoxide and N-methyl-2-pyrrolidone; Wetting agents such as sodium alkylsulfonate, sodium alkylbenzenesulfonate, sodium ligninsulfonate, polyoxyethylene glycol alkyl ether, polyoxyethylene lauryl ether, polyoxyethylene alkylauryl ether, polyoxyethylene sorbitan fatty acid esters, Examples of other various surfactants to be used include surfactants.
본 발명에 따른 농업용의 살진균제 조성물은 포유류 및 어류에 대하여 높은 안정성을 나타내며 작물, 특히 벼에 대해 거의 또는 전혀 식물 독성을 나타내지 않는다.The fungicide composition for agricultural use according to the present invention shows high stability against mammals and fishes and shows little or no phytotoxicity to crops, especially rice.
농업용 살진균제 조성물은 살충제, 제초제 및 식물 성장 조절제 뿐만 아니라 기타 살진균제와 조합하여 사용될 수 있다.The fungicide composition for agricultural use can be used in combination with insecticides, herbicides and plant growth regulators as well as other fungicides.
본 발명에 따른 농업용 살진균제 제형은 일반적으로 두 유효 화합물의 총량으로서 1.0 내지 95.0%, 바람직하게는 유효 화합물의 3.0 내지 70%를 포함한다. 제형의 살포 용량은 일반적으로 헥타아르 당 조합된 유효 화합물의 150 내지 600 g, 바람직하게는 250 내지 400 g이다.The agricultural fungicide formulations according to the invention generally comprise from 1.0 to 95.0%, preferably from 3.0 to 70% of the active compound, of the total amount of the two active compounds. The dosage of the formulation is generally from 150 to 600 g, preferably from 250 to 400 g, of the active compound combined per hectare.
다음의 실시예는 본 발명에 따른 농업용의 살진균제 조성물의 제조를 설명하기 위해 나타낸 것이다.The following examples are presented to illustrate the preparation of fungicide compositions for agriculture according to the present invention.
제형 1(비유동 분진)Formulation 1 (non-flux dust)
분진은 프로클로라즈 1.5 중량부, 프탈리드 1.5 중량부, 화이트 카아본 1.0 중량부, 응집제 0.5 중량부 및 점토 95.5 중량부를 균일하게 혼합시킴으로서 얻었다.The dust was obtained by uniformly mixing 1.5 parts by weight of prochloraz, 1.5 parts by weight phthalide, 1.0 part by weight of white carabons, 0.5 part by weight of flocculant and 95.5 parts by weight of clay.
제형 2(습윤 분말)Formulation 2 (wet powder)
습윤 분말은 프로클로라즈 15.0 중량부, 프탈리드 15.0 중량부, 리그닌 설페이트 나트륨 5.0 중량부, 화이트 카아본 15.0 중량부 및 카올린 50.0 중량부를 균일하게 혼합시킴으로서 얻었다.The wet powder was obtained by homogeneously mixing 15.0 parts by weight of prochloraz, 15.0 parts by weight of phthalide, 5.0 parts by weight of sodium lignin sulfate, 15.0 parts by weight of white carabine and 50.0 parts by weight of kaolin.
제형 3(과립)Formulation 3 (granule)
과립은 프로클로라즈 1.5 중량부, 프탈리드 1.5 중량부, 벤토나이트 30.0 중량부 및 점토 67.0 중량부를 통상의 방법에 따라 균일하게 혼합시킴으로서 얻었다.The granules were obtained by uniformly mixing 1.5 parts by weight of prochloraz, 1.5 parts by weight of phthalide, 30.0 parts by weight of bentonite and 67.0 parts by weight of clay according to a conventional method.
본 발명에 따른 조성물의 피리큘라리아 오리재(Pyricularia oryzae)에 대한 살진균 작용은 다음의 실시예에서 설명한다.The fungicidal action of the composition according to the present invention on the Pyricularia oryzae is illustrated in the following examples.
<실시예 1>≪ Example 1 >
피리큘라리아 오리재(Pyricularia oryzae)의 방제Control of Pyricularia oryzae
직경이 9 ㎝인 플라스틱 폿에서 고상 재배하여 성장시킨 3-4잎 단계의 벼(품종:니혼바레(Nihonbare))를 시험에 사용하여 예방 및 방제 효과 모두를 알아보았다.3-4 leaf stage rice (variety: Nihonbare) cultivated in solid pots in a plastic pot with a diameter of 9 ㎝ was used for the test, and both prevention and control effects were examined.
유효 성분은 그들의 상업적으로 입수되는 제형; 프탈리드를 20% 현탁 농축액 및 프로클로라즈를 25% EC로서 사용하고 이들을 예정된 농도로 희석하였다. 희석된 제형을 매 3 폿트마다 30 ㎖의 양으로 식물에 분무하였다.The active ingredients may be in the form of their commercially available formulations; Phthalide was used as the 20% suspension concentrate and procollase as 25% EC and diluted to the predetermined concentration. The diluted formulations were sprayed to the plants in an amount of 30 ml per 3 pots.
식물들을 미리 도열병으로 감염시킨 벼로부터 얻은 피리큘라리아 오리재(Pyricularia oryzae)의 포자 현탁액(5-6 x 106/㎖)로 분무하였다.Plants were sprayed with spore suspension (5-6 x 10 6 / ml) of Pyricularia oryzae obtained from rice infected with blast flame in advance.
예방 시험에 있어서, 식물들을 시험 화합물을 가한지 하루 후에 접종하고 이어서 25±2 ℃의 습실에서 24시간 동안 위치시킨 다음, 온실에 방치하여 질병의 효과를 기다렸다.In the preliminary test, plants were inoculated one day after the test compound was added, then placed in a wet room at 25 ± 2 ° C for 24 hours, then left in the greenhouse to await the effect of the disease.
방제 시험에 있어서, 시험 물질을 진균으로 접종시킨지 24 시간 후에 가하였다. 식물들을 이어서 온실에 방치하여 질병의 효과를 기다렸다.In the control test, 24 hours after the test substance was inoculated with the fungi, the test substance was added. The plants were then placed in the greenhouse to await the effects of the disease.
감염의 정도는 접종후 7일까지의 손실을 측정함으로서 방어값은 다음의 식에 따라 계산될 수 있다.The degree of infection can be calculated according to the following equation by measuring the loss up to 7 days after inoculation.
방어값 = ━━━━━━━━━━━━━━━━━━━━━━━ x 100Defensive value = ━━━━━━━━━━━━━━━━━━━━━━━━ x 100
미처리 폿 중 손상 정도Degree of damage in untreated pot
시험의 결과Results of the test
1. 예방 효과1. Prevention effect
2. 방제 효과2. Control effect
<실시예 2>≪ Example 2 >
고지대 벼 묘상에서 피리큘라리아 오리재(Pyricularia oryzae)의 방제Control of Pyricularia oryzae in highland rice seedlings
볍씨(품종: 니혼바레)를 관개되지 않은 벼 묘상에서 조파기로 파종하였다. 질병의 발생을 촉진시키기 위하여 균일한 잎들을 피리큘라리아 오리재(Pyricularia oryzae)로 공격하고 약 1㎝의 길이로 절단하여, 접종원으로서 포장에 골고루 흩뿌렸다. 그 결과 포장의 벼들은 도열병으로 감염된 상태에 놓이게 되었다.Rice seeds (cultivar: Nihonbare) were sown on rice seedlings that had not been irrigated. To promote disease development, uniform leaves were attacked with Pyricularia oryzae, cut to a length of about 1 cm, and spread evenly on the packaging as an inoculum. As a result, the paddy rice was infected with blast.
시험하고자 하는 제형은 실시예 1에 따라 제조되었으며 소형 분무기로 플롯 당 100 ㎖의 속도로 2회 분무시킴으로써 예정된 농도로 적용하였다.The formulation to be tested was prepared according to Example 1 and applied at the predetermined concentration by spraying twice with a small atomizer at a rate of 100 ml per plot.
첫번째 분무는 3-4잎 단계에서 수행함으로써 상흔이 2 잎, 3 잎 단계에서 나타나고 두번째 분무는 7일 후에 나타났다.The first spray was performed at the 3-4 leaf stage and the scars appeared at the 2 leaf, 3 leaf stage and the second spray appeared after 7 days.
질병의 발발의 검사는 3회에 걸쳐서 수행하였다. 즉, 처음 분무후 7일후 두번째 분무의 바로 전(첫번째), 두번째 분무한 2일후(두번째) 및 두번째 분무후 8일(세번째)에 수행하여 제형의 방제 효과를 평가하였다.Examination of the outbreak of the disease was carried out three times. That is, the effect of controlling the formulation was evaluated by performing 7 days after the first spraying, immediately before (first), 2 days after the second spray (second), and 8 days (third) after the second spray.
도열병에 기인하여 %로 나타낸 손상의 정도는 각각 처리된 플롯에서 평가하였으며 각각의 제형의 방어값은 실시예 1의 식에 따라 계산하였다. 시험 결과는 다음과 같다.The degree of damage due to blast damage in% was evaluated on each treated plot, and the defensive value of each formulation was calculated according to the formula of Example 1. [ The test result is as follows.
본 발명의 살진균 조성물은 개개의 성분의 특성으로부터 예측할 수 없는 상승작용을 나타내는, 특히 피리쿨라리아 오리재의 극히 양호한 방제를 나타낸다. 조성물은 예방 효과 뿐만 아니라 뛰어난 방제 효과를 나타내어 한 성분을 단독으로 사용하는 것에 비하여 두 화합물의 필요량의 감소를 초래한다. 본 발명에 따른 농업용의 살진균 조성물은 또한 벼의 스폿 질병(예, 갈반) 및 푸사리움(Fusarium)의 방제에 특히 효과적이다.The fungicidal compositions of the present invention exhibit an unpreferable synergistic effect from the properties of the individual components, in particular the extremely good control of the pyricularia. The composition exhibits not only a preventive effect but also an excellent controlling effect, resulting in a reduction in the amount of the two compounds required compared with the use of one component alone. The fungicidal compositions for agriculture according to the present invention are also particularly effective for the control of spot diseases (e.g., infestation) and fusarium of rice.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7193684A JPH0940513A (en) | 1995-07-28 | 1995-07-28 | Agricultural fungicide |
JP95-193684 | 1995-07-28 |
Publications (2)
Publication Number | Publication Date |
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KR970005058A KR970005058A (en) | 1997-02-19 |
KR100449464B1 true KR100449464B1 (en) | 2004-12-17 |
Family
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Application Number | Title | Priority Date | Filing Date |
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KR1019960030856A KR100449464B1 (en) | 1995-07-28 | 1996-07-27 | Prochloraz Mixtures |
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JP (1) | JPH0940513A (en) |
KR (1) | KR100449464B1 (en) |
BR (1) | BR9603178A (en) |
TW (1) | TW360497B (en) |
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CN103798290A (en) * | 2014-02-18 | 2014-05-21 | 中国水稻研究所 | Compound pesticide containing bismerthiazol and application of compound pesticide |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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KR940008571A (en) * | 1992-10-21 | 1994-05-16 | 다께다 구니오 | Foot blight control composition |
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Publication number | Priority date | Publication date | Assignee | Title |
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GB1469772A (en) * | 1973-06-21 | 1977-04-06 | Boots Co Ltd | Fungicidal imidazole derivatives |
JPS6027642B2 (en) * | 1977-07-20 | 1985-06-29 | 日本特殊農薬製造株式会社 | Fungicide for agriculture and horticulture |
JPS5978108A (en) * | 1982-09-22 | 1984-05-04 | シェーリング・アグロケミカルズ・リミテッド | Bactericidal composition |
JPS6041603A (en) * | 1983-08-15 | 1985-03-05 | Hokko Chem Ind Co Ltd | Fungicide for agricultural and horticultural use |
GB8328061D0 (en) * | 1983-10-20 | 1983-11-23 | Fbc Ltd | Anti-microbial composition |
JPH0436830A (en) * | 1990-05-31 | 1992-02-06 | Sharp Corp | Remainder converter for natural number |
JPH04257506A (en) * | 1991-02-08 | 1992-09-11 | Sumitomo Chem Co Ltd | Fungicidal composition for agricultural and horticultural use |
-
1995
- 1995-07-28 JP JP7193684A patent/JPH0940513A/en active Pending
-
1996
- 1996-07-26 BR BR9603178-6A patent/BR9603178A/en not_active IP Right Cessation
- 1996-07-27 KR KR1019960030856A patent/KR100449464B1/en not_active IP Right Cessation
- 1996-08-09 TW TW085109682A patent/TW360497B/en not_active IP Right Cessation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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KR940008571A (en) * | 1992-10-21 | 1994-05-16 | 다께다 구니오 | Foot blight control composition |
Also Published As
Publication number | Publication date |
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JPH0940513A (en) | 1997-02-10 |
KR970005058A (en) | 1997-02-19 |
TW360497B (en) | 1999-06-11 |
BR9603178A (en) | 2005-10-04 |
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