KR950002850B1 - Herbicidal composition - Google Patents

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KR950002850B1
KR950002850B1 KR1019860011112A KR860011112A KR950002850B1 KR 950002850 B1 KR950002850 B1 KR 950002850B1 KR 1019860011112 A KR1019860011112 A KR 1019860011112A KR 860011112 A KR860011112 A KR 860011112A KR 950002850 B1 KR950002850 B1 KR 950002850B1
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weight
parts
weeds
compound
herbicidal composition
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KR870005581A (en
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후미오 기무라
가즈유끼 마에다
쓰네조 요시다
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이시하라 산교 가부시기가이샤
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/561,2-Diazoles; Hydrogenated 1,2-diazoles

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  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
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Abstract

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Description

제초 조성물Herbicidal composition

본 발명은 특정 피라졸계 화합물 및 3, 7-디클로로-8-퀴놀린카르복실산의 2종의 유효성분을 함유하는 제초 조성물, 및 여기에 N-(α, α-디메틸벤질)-α-브로모-tert-부틸아세트아미드, 3-이소프로필-2, 1, 3-벤조티아디아지논-(4)-2, 2-디옥시드 또는 그의 나트륨염을 첨가한 3종의 유효성분을 함유하는 제초조성물에 관한 것이다.The present invention provides a herbicidal composition containing a specific pyrazole compound and two active ingredients of 3,7-dichloro-8-quinolinecarboxylic acid, and N- (α, α-dimethylbenzyl) -α-bromo a herbicidal composition containing three active ingredients added with -tert-butylacetamide, 3-isopropyl-2, 1, 3-benzothiadiazinone- (4) -2, 2-dioxide or its sodium salt It is about.

본 발명에 있어서, 특정한 피라졸 유도체는 일본국 특허출원 공고(소)제56-28,885호, 일본국 특허출원공개(소)제54-70,269호 등에 의하여 벼 재배에 있어서, 화본과 및 광엽류의 잡초에 대하여 양호한 효과를 나타내는 것으로 공지되어 있고, 또한, 3, 7-디클로로-8-퀴눌린카르복실산은 유럽 특허출원 공개 제0060429호에 의하여, N-(α, α-디메틸벤질-α-브로모-tert-부틸아세트아미드는 일본국 특허출원 공개(소)제55-43,014호에 의하여, 또한 3-이소프로필-2, 1, 3-벤조티아디아지논-(4)-2, 2-디옥시드 또는 그의 나트륨염은 일본국 특허출원 공개(소)제49-7,436호에 의하여 벼 재배에 었어서의 제초제로서 적당한 것으로 공지되어 있다.In the present invention, the specific pyrazole derivatives are weeds of flowering plants and broadleaf in rice cultivation according to Japanese Patent Application Publication No. 56-28,885, Japanese Patent Application Publication No. 54-70,269, and the like. It is known to show a good effect for the 3,7-dichloro-8-quinulincarboxylic acid, according to the European Patent Application Publication No. 0060429, N- (α, α-dimethylbenzyl-α-bromo -tert-Butylacetamide is obtained according to Japanese Patent Application Laid-Open No. 55-43,014 and also 3-isopropyl-2, 1, 3-benzothiadiazinone- (4) -2, 2-dioxide. Or its sodium salt is known to be suitable as a herbicide in rice cultivation according to Japanese Patent Application Publication No. 49-7,436.

그러나, 상기 화합물을 단독으로 제초제로서 사용하는 경우, 사용자가 충분히 만족할 수 있는 효과를 얻을 수는 없다. 종래, 논의 잡초 중 가장 문제가 되는 강피(nobie), 물달개비(konagi), 1년생 광엽 잡초 및 다년생 잡초의 쇠털골(matsubai)등의 방제를 위하여, 여러가지 우수한 제초제가 개발되었고, 단제(單劑), 혼합제로서 사용되어 왔다. 이 결과, 근년 상기 논의 잡초가 방제됨에 따라, 잡초 상호간의 경합 밸런스가 무너지고, 상기 잡초뿐만 아니라, 종래의 약제로서는 충분히 방제할 수 없었던 잡초, 예를들면 올챙이 고랭이(Hotarui), 올미(urikawa), 너도방동산이(mizugayatsuri)등의 다년생 잡초가 우세하게 되어, 벼에 해를 끼치게 되었다. 또한, 이들 논의 잡초는 동일 지역에 있어서 공존 생육하고, 또한 각 개체의 발아 및 생육시기는 같지 않다. 따라서, 제초제의 산포는 다년성을 포함하는 다종류의, 더구나 생육 단계가 다른 논의 잡초를 대상으로 행하여지는 것이 되고, 1회의 제초제 산포로 모든 잡초를 방제한다는 것은 사실상 약간 곤란한 상태에 있다. 제초제 산포를 행하여도 혹시 잔존 잡초가 있으면 그것들은 뒤늦게 발아하게 되고, 지상부가 일단 고사한 후 재생하여 무성하게 됨으로써 제조체 산포의 효과는 반감하게 된다. 이런 결점을 보충하기 위하여, 종래보다 여러차례에 걸쳐서 산포하는, 소위 체계 산포가 행하여져 왔다. 그러나, 근래, 잡초방제에 필요한 비용, 노력이나, 환경오염 등이 문제로 되어 오고 있는 것에서, 1회의 산포로 생육 단계가 다른 광범위한 잡초를 방제할 수 있고, 그러고 잡초 억제 효과가 장기간에 걸쳐서 지속되고, 더구나, 벼에 약품 피해를 주지않는 제초제의 출현이 강력하게 요망되고 있다.However, when the compound is used alone as a herbicide, it is not possible to obtain an effect that the user can be sufficiently satisfied with. Conventionally, various excellent herbicides have been developed for the control of nobies, konagi, annual broadleaf weeds, and matsubai of perennial weeds, which are the most problematic of the weeds. ), Has been used as a mixing agent. As a result, in recent years, as the weeds of the above-mentioned rice fields are controlled, the contention balance between weeds is broken, and not only the weeds but also weeds that could not be sufficiently controlled by conventional medicines, for example, tadpoles (Hotarui) and snares (urikawa) ), Perennial weeds, such as mizugayatsuri, became dominant and harmed rice. In addition, these rice weeds coexist and grow in the same region, and germination and growth time of each individual are not the same. Therefore, the spread of herbicides is to be carried out for different types of weeds, including the perennial variety, and the growing stage, and it is actually a little difficult to control all the weeds with one herbicide spread. Even if the herbicide is spread, if there is any residual weeds, they germinate late, and once the ground part dies, it regenerates and becomes lush, so that the effect of the production spread is halved. In order to make up for this drawback, so-called system scattering, which has been distributed more than once, has been performed. However, in recent years, the cost, effort, environmental pollution, etc. required for weed control have become a problem, and one spread can control a wide range of weeds with different growth stages, and the weed suppression effect lasts for a long time. Moreover, the emergence of herbicides that does not cause chemical damage to rice is strongly desired.

본 발명자들은, 상기 특정 피라졸 유도체의 제초 효과를 증대시키기 위한 연구를 행한 결과, 특정 피라졸 유도체 및 3, 7-디클로로-8-퀴놀린카르복실산의 2종의 유효성분을 배합하여 시용(施用)한 경우, 및 여기에, N-(α, α-디메틸벤질)-α-브로모-tert-부틸아세트아미드, 3-이소프로필-2, 1, 3-벤조티아디아지논-(4)-2, 2-디옥시드 또는 그의 나트륨염을 첨가한 3종의 유효성분을 배합하여 시용한 경우에, 각각의 단독 시용에 비해서 우수한 제초 효과를 얻음, 즉 논에 있어서, 1회의 약제 산포로 벼에 전혀 악영향을 주는 일없이, 그러고 유해 잡초인 강피, 올챙이 고랭이, 물달개비, 올미, 너도방동산이 등, 실질적으로 모든 유해 잡초의 생육을 억제하고, 또한 약제 산포 이후의 제초 작업을 필요로 하지 않을 만큼 장기간에 걸쳐서 잡초 억제 효과가 지속되며, 사용자가 오랫동안 기다리고 바랐던 실용적 효과를 가짐을 발견하고, 본 발명을 완성하였다.The present inventors conducted a study to increase the herbicidal effect of the specific pyrazole derivatives, and as a result, a combination of two active ingredients of a specific pyrazole derivative and 3,7-dichloro-8-quinolinecarboxylic acid was applied. , And here, N- (α, α-dimethylbenzyl) -α-bromo-tert-butylacetamide, 3-isopropyl-2, 1, 3-benzothiadiazinone- (4)- When three kinds of active ingredients added with 2, 2-dioxide or its sodium salt are combined and applied, excellent herbicidal effect is obtained compared to each application alone, that is, in the rice paddy, rice is used as a single chemical dispersion. It does not adversely affect at all, and substantially inhibits the growth of all harmful weeds such as bark, tadpoles, water canes, snares and beetles, and also requires weeding after drug spread. Long lasting weed suppression effect It found that has a practical effect wanted for a long time waiting for, and have completed the present invention.

본 원의 제1 발명은 하기 일반식The first invention of the present application is the following general formula

Figure kpo00001
Figure kpo00001

[식중, R1은 수소원자 또는 메틸기이고, R2[Wherein, R 1 is a hydrogen atom or a methyl group, and R 2 is

Figure kpo00002
기(
Figure kpo00003
은 0 또는 1임)]으로 표시되는 피라졸계 화합물 적어도 1종 및 3, 7-디클로로-8-퀴놀린카르복실산을 유효성분으로서 함유하는 것을 특징으로 하는 제초 조성물이고, 본 원의 제2발명은 상기 제1발명의 제초 조성물에 N-(α, α-디메틸벤질)-α-브로모-tert-부틸아세트아미드, 3-이소프로필-2, 1, 3-벤조티아디아지논-(4)-2, 2-디옥시드 또는 그의 나트륨염으로 이루어진 군에서 선택된 1종의 화합물을 유효성분으로 첨가하는 것을 특징으로 하는 제초 조성물이다.
Figure kpo00002
group(
Figure kpo00003
Is 0 or 1), and is a herbicidal composition comprising at least one pyrazole-based compound and 3, 7-dichloro-8-quinolinecarboxylic acid as an active ingredient. In the herbicidal composition of the first invention, N- (α, α-dimethylbenzyl) -α-bromo-tert-butylacetamide, 3-isopropyl-2, 1, 3-benzothiadiazinone- (4)- It is a herbicidal composition characterized by adding one compound selected from the group consisting of 2, 2-oxide or its sodium salt as an active ingredient.

본 발명에 관계되는 유효성분의 대표적인 예를 이하에 기재한다.Representative examples of the active ingredient according to the present invention are described below.

화합물 번호 A-1 : 1,3-디메틸-4-(2, 4-디클로로벤조일)-5-페나실옥시피라졸Compound No. A-1: 1,3-dimethyl-4- (2, 4-dichlorobenzoyl) -5-phenacyloxypyrazole

화합물 번호 A-2 : 1, 3-디메틸-4-(2, 4-디클로로벤조일)-5-(4-메틸페르나실옥시)피라졸Compound No. A-2: 1, 3-dimethyl-4- (2, 4-dichlorobenzoyl) -5- (4-methylfernasiloxy) pyrazole

화합물 번호 B : 3, 7-디클로로-8-퀴놀린카르복실산Compound No. B: 3, 7-dichloro-8-quinolinecarboxylic acid

화합물 번호 C : N-(α, α-디메틸벤질)-α-브로모-tert-부틸아세트아미드Compound No. C: N- (α, α-dimethylbenzyl) -α-bromo-tert-butylacetamide

화합물 번호 D-1 : 3-이소프로필-2, 1, 3-벤조티아디아지논-(4)-2, 2-디옥시드Compound No. D-1: 3-Isopropyl-2, 1, 3-benzothiadiazinone- (4) -2, 2-dioxide

화합물번호 D-2 : 3-이소프로필-2, 1, 3-벤조티아디아지논-(4)-2, 2-디옥시드나트륨염Compound No. D-2: 3-Isopropyl-2, 1, 3-benzothiadiazinone- (4) -2, 2-dioxide sodium salt

상기 본 발명에 관계되는 유효성분 A, B, C 및 D의 실용적인 배합 중량비는, 제제 100중량부에 있어서의 비로 나타내면, A : B=2-20 : 0.1-5이고, 바람직하기로는 5-10 : 0.5-2이고, A : B : C=2-20 : 0.1-5 : 2-20이고, 바람직하기로는 5-10 : 0.5-2 : 4-10이고, A : B : D=2-20 : 0.1-5 : 2-20이고, 바람직하기로는5-10 : 0.5-2 : 5-10이다.The practical compounding weight ratios of the active ingredients A, B, C, and D according to the present invention are A: B = 2-20: 0.1-5, preferably 5-10, when expressed by the ratio in 100 parts by weight of the formulation. : 0.5-2, A: B: C = 2-20: 0.1-5: 2-20, preferably 5-10: 0.5-2: 4-10, A: B: D = 2-20 : 0.1-5: 2-20, preferably 5-10: 0.5-2: 5-10.

본 발명의 제조 조성물의 바람직한 시용량은 기상조건, 토양조건, 약제의 조제형태, 시용시기, 시용방법 등에 따라서 달라지나, 일반적으로, 1아르당의 총 유효성분량은 6.0-150g이고, 바람직하기로는 15-70g이다. 본 발명의 제초 조성물의 적당한 시용시기는, 잡초 발생기로부터 4엽기의 사이이고, 이식 논의 경우에는 일반적으로 논 이식 전부터 이식 후 20일 사이이다.The preferred dosage of the preparation of the present invention will vary depending on weather conditions, soil conditions, the type of preparation of the medicament, the time of application, the method of application, and the like, but in general, the total effective amount per argan is 6.0-150 g, preferably 15- 70 g. The suitable application time of the herbicidal composition of the present invention is between the weed generator and the 4-leaf stage, and in the case of transplant discussion, it is generally between the rice transplantation and the 20 days after transplantation.

또한, 본 발명의 제초 조성물의 시용에 있어서, 상기 유효성분 A, B, C 및 D는 통상의 농약 제제법에 준해서 각종 보조제와 배합하고, 예를들면 유제, 수화제, 입제 등의 형태로 제제되지만, 유효성분을 함께 혼합, 제제하여도 좋으며, 또는 따로따로 제제한 것을 다시 혼합하여도 좋다.In addition, in the application of the herbicidal composition of the present invention, the active ingredients A, B, C and D are blended with various auxiliaries according to the conventional pesticide preparation method, for example, formulations in the form of emulsions, hydrating agents, granules and the like. However, the active ingredients may be mixed and formulated together or separately formulated separately.

제제에 사용하는 보조제로서는, 규조토, 소석회, 탄산칼슘, 활석, 화이트카아본, 활석, 카올린, 벤토나이트, 지클라이트, 점토, 전분 등의 고형 담체 ; 물, 톨루엔, 크실렌, 솔벤트납사, 디옥산, 아세톤, 이소포론, 메틸이소부틸케톤, 클로로벤젠, 시클로헥산, 디메틸술폭시드, 디메틸포름아미드, N-메틸-2-피롤리돈, 알코올 등의 용제 ; 알킬 황산소다, 알킬벤젠술폰산소다, 리그닐술폰산소다, 폴리옥시에틸렌글리코올알킬에테르, 폴리옥시에틸렌라우릴에테르,, 폴리옥시에틸렌알킬아릴에테르, 폴리옥시에틸렌 지방산에스테르, 폴리옥시에틸렌소르비탄 지방산 에스테르 등의 전착제 ; 계면활성제 등이 열거되지만, 상기 보조제는 물론 이것에만 한정되는 것은 아니다.As an adjuvant to be used for the preparation, solid carriers such as diatomaceous earth, slaked lime, calcium carbonate, talc, white carbon, talc, kaolin, bentonite, zircite, clay, and starch; Solvents such as water, toluene, xylene, solvent naphtha, dioxane, acetone, isophorone, methyl isobutyl ketone, chlorobenzene, cyclohexane, dimethyl sulfoxide, dimethylformamide, N-methyl-2-pyrrolidone, and alcohols ; Alkyl sodium sulfate, sodium alkylbenzene sulfonic acid, sodium lignyl sulfonic acid, polyoxyethylene glycol alkyl ether, polyoxyethylene lauryl ether, polyoxyethylene alkylaryl ether, polyoxyethylene fatty acid ester, polyoxyethylene sorbitan fatty acid ester Electrodeposition agents, such as; Although surfactant etc. are enumerated, the said adjuvant is not limited to this, of course.

다음에 본 발명의 제초 조성물의 식물 시험예를 기재한다.Next, a plant test example of the herbicidal composition of the present invention will be described.

시험예Test Example

1/10,000아르 자기제 포트에 논의 토양을 채워넣고, 강피, 올챙이 고랭이, 물달개비, 올미 및 너도방동산이의 종자 또는 괴경(塊莖)을 파종하거나, 또는 한곳에 많이 심어 놓고, 담수(擔水) 조건하에서 생육시켰다. 각각의 풀씨가, 소정의 엽기에 달한 때에, 각 유효성분을 후기 배합예 4에 준해서, 제제한 소정량의 수화제(단제는 그대로, 혼제는 적당히 배합)를 현탁액으로서 피팻으로 적하 처리하였다. 약제 처리후 4주간째에 잔존 잡초를 뽑고, 풍건중(風乾重)을 측정하여, 하기의 제초 효과 표시기준에 의하여, 무처리 구역에 대한 백분율을 생육 억제정도로서 나타내고, 제1-1표 및 제2-1표의 결과를 얻었다.Fill the rice paddy soil in a pot of 1 / 10,000 algae, sowing seeds or tubers of bark, tadpoles, water squirrels, snares and beetles, or planting a lot in one place, fresh water Growing under conditions. When each grass seed reached the predetermined leaf period, each active ingredient was treated dropwise with a fiat as a suspension of a predetermined amount of a hydrating agent (a mixture is mixed as appropriate) as a suspension in accordance with the later formulation example 4. After 4 weeks of treatment, the remaining weeds were pulled and the air dry weight was measured, and the percentage of the untreated zone was expressed as the growth inhibition degree according to the following herbicidal labeling criteria. The result of Table 2-1 was obtained.

제초 효과 표시기준Herbicide Effect Criteria

10 잡초의 잔존율 10% 이하 5 잡초의 잔존율 51-60%Survival rate of less than 10 weeds 10% or less Survival rate 51-60% of 5 weeds

9 잡초의 잔존율 11-20% 4 잡조의 잔존율 61-70%9 Remaining rate of weeds 11-20% Remaining rate of 4 weeds 61-70%

8 잡초의 잔존율 21-30% 3 잡초의 잔존율 71-80%8 Weeding Survival Rate 21-30% 3 Weeding Survival Rate 71-80%

7 잡초의 잔존율 31-40% 2 잡초의 잔존율 81-90%7 Weeding Survival Rate 31-40% 2 Weeding Survival Rate 81-90%

6 잡초의 잔존율 41-50% 1 잡초의 잔존율 91-100%Survival Rate of 6 Weeds 41-50% Survival Rate of 1 Weeds 91-100%

제1-1표Table 1-1

Figure kpo00004
Figure kpo00004

Figure kpo00005
Figure kpo00005

다음에 본 발명의 제조 조성물의 배합예를 기재한다.Next, the compounding example of the manufacturing composition of this invention is described.

배합예 1Formulation Example 1

(1) 화합물 번호 A-1 8중량부(1) 8 parts by weight of compound number A-1

(2) 화합물 번호 B 0.7중량부(2) 0.7 parts by weight of compound number B

(3) 벤토나이트 20중량부(3) 20 parts by weight of bentonite

(4) 알킬아릴술포네이트 및 폴리옥시에틸렌 알킬아릴에테르술페이트의 혼합물 1.5중량부(4) 1.5 parts by weight of a mixture of alkylarylsulfonate and polyoxyethylene alkylarylethersulfate

[상품명 : 솔포올 5146, 도호가가꾸고오교 가부시끼가이샤(東邦化學工業株式會社)제품][Product name: Solfool 5146, Toho Kagaku Kogyo Kabuki Kiisha Co., Ltd.]

(5) 리그닌술폰산 칼슘 50% 수용액 2중량부(5) 2 parts by weight of calcium lignin sulfonate 50% aqueous solution

[상품명 : 산에끼스 C, 산요고꾸사꾸 펄프 가부시끼가이샤(山陽國第 パルペ株式會社)제품][Product Name: Sanekisu C, Sanyo Kokusaku Pulp, Kabushiki Kaisha Co., Ltd.]

(6) 입상 탄산칼슘 68.8중량부(6) 68.8 parts by weight of granular calcium carbonate

이상 (1)-(6)의 각 성분을 혼합, 분쇄하고, 적당량의 조립 소요수를 첨가하여 압출 조립하여 압출 조립시킴으로써 입제를 얻었다.The granules were obtained by mixing and pulverizing each component of the above (1)-(6), adding the required quantity of granulation water, extrusion granulating, and extruding granulation.

배합예 2Formulation Example 2

(1) 화합물 번호 A-1 7중량부(1) 7 parts by weight of compound number A-1

(2) 화합물 번호 B 0.7중량부(2) 0.7 parts by weight of compound number B

(3) 화합물 번호 C 5중량부(3) Compound No. C 5 parts by weight

(4) 알킬아릴술포네이트 및 폴리옥시에틸렌 알킬아릴에테르술페이트의 혼합물(4) mixtures of alkylarylsulfonates and polyoxyethylene alkylarylethersulfates

6중량부6 parts by weight

[상품명 : 솔포올 5146, 도호가가꾸고오교 가부시끼가이샤제품][Product name: Solfool 5146, Toho Kagaku Kogyo Kabushiki Kaisha]

(5) 폴리옥시에틸렌옥틸페닐에테르 2중량부(5) 2 parts by weight of polyoxyethylene octylphenyl ether

[상품명 : 노이겐 EA-112, 다이이찌고오교 세이야꾸 가부시끼가이샤(第一工業製藥株式會社)제품][Product name: Neugen EA-112, Daiichigo Gyo Seiyaku Kabushiki Kaisha Co., Ltd.]

(6) 지클라이트 25중량부(6) Zicklite 25 parts by weight

(7) 벤토나이트 54.3중량부(7) 54.3 parts by weight of bentonite

이상 (1)-(7)의 각 성분을 혼합, 분쇄하고, 적당량의 조립 소요수를 첨가해서 압출 조립시킴으로 입제를 얻었다.The granules were obtained by mixing and pulverizing each component of the above (1)-(7), and adding an appropriate quantity of granulation required and carrying out extrusion granulation.

배합예 3Formulation Example 3

(1) 화합물 번호 A-1 6중량부(1) 6 parts by weight of compound number A-1

(2) 화합물 번호 B 1중량부(2) 1 part by weight of compound number B

(3) 화합물 번호 D-1(50% 수용액) 12중량부(3) 12 parts by weight of compound number D-1 (50% aqueous solution)

(4) 지클라이트 25중량부(4) 25 parts by weight of Zicklite

(5) 알킬아릴술포네이트 및 폴리옥시에틸렌 알킬아릴에테르술페이트의 혼합물(5) mixtures of alkylarylsulfonates and polyoxyethylene alkylarylethersulfates

6중량부6 parts by weight

(상품명 : 솔포올 5146, 도호가가꾸고오교 가부시끼가이샤제품)(Product name: Solfool 5146, Toho Kagaku Kogyo Kabuki Kaisha)

(6) 폴리옥시에틸렌옥틸페닐에테르 2중량부(6) 2 parts by weight of polyoxyethylene octylphenyl ether

(상품명 : 노이겐 EA-112, 다이이찌고오교 세이야꾸 가부시끼가이샤제품)(Product name: Neugen EA-112, Daiichi Gogyo Seiyaku Kabushiki Kaisha)

(7) 벤토나이트 54중량부(7) Bentonite 54 parts by weight

이상 (1)-(7)의 각 성분을 혼합, 분쇄하고 적당량의 조립 소요수를 첨가해서 압출 조립시킴으로써 입제를 얻었다.Each granule of (1)-(7) mentioned above was mixed and grind | pulverized, and granulation was obtained by adding an appropriate quantity of granulation water, and extruding granulation.

배합예 4Formulation Example 4

(1) 화합물 번호 A, B, C 또는 D 10중량부(1) 10 parts by weight of compound number A, B, C or D

(2) 함수 무정형 이산화 규소 8중량부(2) 8 parts by weight of hydrous amorphous silicon dioxide

[상품명 : 커플렉스 SO, 시오노기 세이야꾸 가부시끼가이샤(鹽野義製藥株式會社)제품][Product Name: Couple Rex SO, Shionogi Seiyaku Kabushiki Kaisha Co., Ltd.]

(3) 폴리옥시에틸렌알킬아릴에테르술페이트 4중량부(3) 4 parts by weight of polyoxyethylene alkylaryl ether sulfate

(상품명 : 솔포올 5039, 도호가가꾸고오교 가부시끼가이샤제품)(Product Name: Solfool 5039, Toho Chemical Co., Ltd.)

(4) 나프탈린 술폰산 소다 포르말린 축합물 1중량부(4) 1 part by weight of naphthalin sulfonic acid soda formalin condensate

(상품명 : 라베린 FA-N, 다이이찌고요고 세이야꾸 가부시끼가이샤제품)(Product name: Laberine FA-N, Daiichi Goyogo Seiyaku Kabuki Kaisha)

(5) 지클라이트 77중량부(5) Zicklite 77 parts by weight

이상 (1)-(5)의 각 성분을 혼합, 분쇄하여 수화제를 얻었다.Each component of above (1)-(5) was mixed and grind | pulverized and the hydration agent was obtained.

Claims (2)

유효성분으로서 하기 일반식의 피라졸계 화합물 적어도 1종 및 3, 7-디클로로-8-퀴놀린카르복실산을 함유하는 것을 특징으로 하는 제초 조성물.A herbicidal composition comprising at least one pyrazole compound of the following general formula and 3,7-dichloro-8-quinolinecarboxylic acid as an active ingredient.
Figure kpo00006
Figure kpo00006
상기 식중, R1은 수소원자 또는 메틸기이고, R2
Figure kpo00007
(
Figure kpo00008
은 0 또는 1임)이다.
Wherein R 1 is a hydrogen atom or a methyl group, R 2 is
Figure kpo00007
(
Figure kpo00008
Is 0 or 1).
유효성분으로서 하기 일반식의 피라졸계 화합물 적어도 1종, 3, 7-디클로로--8-퀴놀린카르복실산, 및 N-(α, α-디메틸벤질)-α-브로모-tert-부틸아세트아미드, 3-이소프로필-2, 1, 3-벤조니아디아지논-(4)-2, 2, -디옥시드 및 그의 나트륨염으로 이루어진 군 중에서 선택된 화합물 적어도 1종을 함유하는 것을 특징으로 하는 제조 조성물.As an active ingredient, at least one pyrazole compound of the following general formula, 3, 7-dichloro-8-quinolinecarboxylic acid, and N- (α, α-dimethylbenzyl) -α-bromo-tert-butylacetamide , 3-isopropyl-2, 1, 3-benzoniadiazinone- (4) -2, 2, -dioxide and at least one compound selected from the group consisting of sodium salts thereof .
Figure kpo00009
Figure kpo00009
상기 식중, R1은 수소원자 또는 메틸기이고, R2Wherein R 1 is a hydrogen atom or a methyl group, R 2 is
Figure kpo00010
(
Figure kpo00011
은 0 또는 1임)이다.
Figure kpo00010
(
Figure kpo00011
Is 0 or 1).
KR1019860011112A 1985-12-24 1986-12-23 Herbicidal composition KR950002850B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP85-290948 1985-12-24
JP60290948A JPS62149602A (en) 1985-12-24 1985-12-24 Herbicide composition
JP290948 1985-12-24

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KR870005581A KR870005581A (en) 1987-07-06
KR950002850B1 true KR950002850B1 (en) 1995-03-27

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