KR920002305B1 - Herbicide composition - Google Patents

Herbicide composition

Info

Publication number
KR920002305B1
KR920002305B1 KR1019880006107A KR880006107A KR920002305B1 KR 920002305 B1 KR920002305 B1 KR 920002305B1 KR 1019880006107 A KR1019880006107 A KR 1019880006107A KR 880006107 A KR880006107 A KR 880006107A KR 920002305 B1 KR920002305 B1 KR 920002305B1
Authority
KR
South Korea
Prior art keywords
herbicide
effect
weeds
herbicidal
composition
Prior art date
Application number
KR1019880006107A
Other languages
Korean (ko)
Other versions
KR880013453A (en
Inventor
다까시 미노가이
고오이찌 스즈끼
노부아끼 미또
유우지 후꾸나가
Original Assignee
닛산가가꾸고오교오 가부시기가이샤
니까이 다께오
스미도모 가가꾸고오교오 가부시기가이샤
모리 히데오
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 닛산가가꾸고오교오 가부시기가이샤, 니까이 다께오, 스미도모 가가꾸고오교오 가부시기가이샤, 모리 히데오 filed Critical 닛산가가꾸고오교오 가부시기가이샤
Publication of KR880013453A publication Critical patent/KR880013453A/en
Application granted granted Critical
Publication of KR920002305B1 publication Critical patent/KR920002305B1/en

Links

Images

Classifications

    • 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
    • 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
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/18Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
    • 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
    • A01N47/00Biocides, 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
    • A01N47/08Biocides, 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
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/36Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

내용 없음.No content.

Description

제초제 조성물Herbicide composition

제1도는, 제3표, 제4표의 Cyperus serotinus에 대한 제초 활성을 근거로 90%저해에 소요되는 약량을 등효과 선법에 의해 작도한 것이다. 종축은 브로우부티드의 약량(g/a), 횡축은 화합물(I)의 약량(g/a)를 표시한다. 파선은 상가적(相加的)효과의 경우의 선, 실선은 실측한 성육저해율 90%의 등효과선을 표사한다.In FIG. 1, based on the herbicidal activity against Cyperus serotinus of Tables 3 and 4, the dose required for 90% inhibition was prepared by the iso effect method. The vertical axis represents the amount (g / a) of brobutide and the horizontal axis represents the amount (g / a) of compound (I). The dashed line represents the line in case of additive effect, and the solid line represents the equal effect line of 90% of the estimated growth inhibition rate.

본 발명은 식(I) -The present invention is formula (I)-

Figure kpo00001
Figure kpo00001

로 표시되는 피라졸술포닐요소와 N-(α,α-디메틸벤질)-α-브로모-tert-부틸아세트아미드(이하 브로모부티드라 부른다.)를 유효성분으로서 함유하는 것을 특징으로 하는 제초제 조성물에 관한 것이다.A herbicide composition comprising pyrazolesulfonyl urea and N- (α, α-dimethylbenzyl) -α-bromo-tert-butylacetamide (hereinafter referred to as bromobutydra) represented by It is about.

긴 세월에 걸친 제초제의 연구 개발중에서 다종 다양한 약제가 실용화되고, 이들 제초제는 잡초 방제작업의 생력화나 농원예작물의 생산향상에 기여해 왔다. 오늘날에 있어서도, 보다 뛰어난 제초특성을 가진 신규 약제의 개발이 요망되고, 특히 농원예용 제초제로서는 재배작물에 약해를 미치는 일없이, 대상 잡초만을 선택적으로 또한 저약량(低藥量)으로 방제할 수 있는 것이 바람직하나, 기존의 약제는 반드시 이 요구를 만족시켜 주는 것은 아니었다.In the long years of research and development of herbicides, various kinds of medicines have been put into practical use, and these herbicides have contributed to the improvement of weed control operations and the improvement of the production of agricultural crops. Even today, there is a need for the development of a new drug having more excellent herbicidal properties. Especially, as a horticultural herbicide, only weeds can be selectively and controlled in low doses without harming cultivated crops. Preferably, existing medications do not necessarily meet this requirement.

식(I)에서 표시되는 화합물은 종래의 제초제에 비해서 저약량으로 뛰어난 제초효과를 올리고, 또한 벼에 대해서 높은 안전성을 가진다. 또, 1년생 벼과 잡초, 1년생 광엽잡초에 탁효를 나타낼 뿐만 아니라 다년생 잡초에도 강한 효력을 나타내며, 그 유용성은 크다.The compound represented by formula (I) exhibits excellent herbicidal effect in a low dose compared to conventional herbicides, and also has high safety against rice. In addition, it exhibits not only a haze effect on the annual rice and weeds and the annual green leaf weeds but also a strong effect on the perennial weeds, and its usefulness is great.

한편, 브로모부티드는, Scirpus juncoides 등의 Cyperu Stp, 과에 높은 효력을 가진 동시에, Echinochlos Crussgalli, Monochoria vaginalis 등에도 뛰어난 효과를 발휘하고, 유용한 제초제이다. 그러나, 광엽잡초나 괴경(塊莖)으로부터 발생하는 다년생의 Cyperus Stp. 과 잡초, 예를들면 Cyperus Serotinus, Eleocharis Kuroguwai등에는 완전한 효과를 기대하는 것은 어렵고, 개선이 요망되고 있다.Bromobutide, on the other hand, has a high effect on Cyperu Stp, such as Scirpus juncoides, and also has excellent effects on Echinochlos Crussgalli, Monochoria vaginalis and the like, and is a useful herbicide. However, perennial Cyperus Stp. Arising from broadleaf weeds and tubers. And weeds such as Cyperus Serotinus, Eleocharis Kuroguwai, etc., it is difficult to expect full effects and improvements are desired.

본 발명자는, 식(I)에서 표시되는 화합물의 제초효과를 증대시키도록 연구를 행한결과, 식(I)으로 표시되는 화합물에, 브로모부티드를 배합하면, 각각의 제초효과가 단순히 상가적(相加的)으로 얻어질뿐만 아니라, 상승적 살초효과가 나타나, 종래 알려져 있던 혼합제와 비교해서 훨씬 높은 작물에 대한 안전성과 유해잡초에 대한 살초효과를 겸비한 뛰어난 혼합제가 되는 것을 발견하여 본 발명을 완성하였다. 이에의해, 벼에 약해를 주는 일없이, 광범위한 잡초를 저약량으로 방제하는 것이 가능하게 되어 본 발명의 유용성은 극히 높다.MEANS TO SOLVE THE PROBLEM As a result of carrying out research to increase the herbicidal effect of the compound represented by Formula (I), when the bromobutide is mix | blended with the compound represented by Formula (I), each herbicidal effect is simply additive ( The present invention was completed by finding a synergistic herbicidal effect as well as a synergistic herbicidal effect, which is an excellent admixture that combines the safety of a much higher crop and the herbicidal effect against harmful weeds compared to conventionally known admixtures. . This makes it possible to control a wide range of weeds at low doses without harming rice, and the usefulness of the present invention is extremely high.

또, 본 발명 제초제 조성물은, 잡초의 발아전 및 발아후에 처리하여도 효과를 가지며, 토양처리, 줄기잎겸 토양처리로도 높은 효과를 얻을 수 있다. 또 벼이외의 각종 곡류에 대해서도 유용하며, 기타의 발땅, 과수원등의 농원에 분야 및 운동장, 공터, 임야땅, 탱크 지역, 노선가등의 비농경지에서의 각종 잡초의 방제에도 적용할 수 있어, 잡초방제에 있어서 큰 경제적 효과를 나타낸다.Moreover, the herbicide composition of the present invention has an effect even if it is treated before and after germination of weeds, and a high effect can also be obtained by soil treatment, stem leaf and soil treatment. It is also useful for various grains other than rice, and can be applied to the control of various weeds in non-agricultural areas such as fields and playgrounds, vacant lands, forest lands, tank areas, and street roads for farms such as other soils and orchards. It shows a great economic effect in the control.

본 발명에 의한 조성물은, 각 성분의 상대적 활성에도 기인되지만, 일반적으로는 브로모부티드 1중량부당, 식(I)로 표시되는 혼합물을 0.001∼10중량부 함유하고 있다. 적용해야할 혼합물의 양은, 다수의 인자, 예를들면 생육을 저지해야할 특정한 대상 식물의 종류등에 의해 좌우되나, 일반적으로 0.001∼1kg/ha의 양이 보통은 적당하다.Although the composition by this invention originates also in the relative activity of each component, generally, 0.001-10 weight part of mixtures represented by Formula (I) per 1 weight part of bromobutide. The amount of mixture to be applied depends on a number of factors, such as the specific plant to be prevented from growing, but in general amounts of 0.001 to 1 kg / ha are usually suitable.

본 발명 조성물을 제초제로서 사용하는 경우는, 통상고체담체, 액체담체, 계면활성제, 기타의 제제용 보조제와 혼합해서, 유제, 수화제, 현탁제등으로 제제한다.When the composition of the present invention is used as a herbicide, it is usually mixed with a solid carrier, a liquid carrier, a surfactant, and other preparation aids, and then formulated with an emulsion, a hydrating agent, a suspending agent, and the like.

이들 제제에는 유효성분의 합계량이, 중량비로 1∼90%, 바람직하게는 2∼80% 함유된다.These formulations contain 1 to 90% by weight, preferably 2 to 80% by weight, of the total amount of the active ingredients.

고체담지체로서는, 카올리인 클레이, 어터펄자이트클레이, 벤도나이트, 산성백토, 탄산칼슘, 파이로필라이트, 활석, 규조토, 방해석, 호두가루, 뇨소, 황산암모늄, 합성함수산화규소등의 미분말 혹은 입자형상물을 들 수 있으며, 액체담지체로서는 크실렌, 메틸나프탈렌등의 방향족 탄화수소류, 이소프로판올, 에틸렌글리콜, 셀로솔브등의 알코올류, 아세톤시클로헥사논, 이소포론등의 케톤류, 대두유, 면실유등의 식물유, 디메틸술폭시드, 아세트니트릴, 물등을 들수 있다.Examples of solid carriers include kaolin clay, attapulgite clay, bendonite, acidic clay, calcium carbonate, pyrophyllite, talc, diatomaceous earth, calcite, walnut flour, urine, ammonium sulfate, synthetic silicon oxide, etc. And fine powders or particulate matter. Examples of the liquid carrier include aromatic hydrocarbons such as xylene and methylnaphthalene, alcohols such as isopropanol, ethylene glycol and cellosolve, ketones such as acetone cyclohexanone and isophorone, soybean oil and cottonseed oil. Vegetable oils, such as dimethyl sulfoxide, acetonitrile, and water, are mentioned.

유화, 분산, 습전등을 위해서 사용되는 계면활성제로서는 알킬황산에스테르류, 알킬아릴술폰산염, 디알킬술포숙신산염, 폴리옥시에틸렌알킬아릴에테르 인산에스테르염등의 음이온 계면활성제, 폴리옥시에틸렌알킬에테르, 폴리옥시에틸렌폴리옥시프로필렌블록코폴리머, 솔비탄지방산에스테르등의 비이온 계면활성제등을 들 수 있다. 기타의 제제용보조제료로서는, 리그닌술폰산염, 알긴산염, 폴리비닐알코올, 아라비아고무, CMC(카르복시메틸셀루로오즈), PAP(산성인산 이소프로필)등을 들수 있다.Surfactants used for emulsification, dispersion, wet pressing, etc. include anionic surfactants such as alkyl sulfates, alkylaryl sulfonates, dialkyl sulfosuccinates, polyoxyethylene alkylaryl ether phosphate ester salts, polyoxyethylene alkyl ethers, Nonionic surfactants, such as a polyoxyethylene polyoxypropylene block copolymer and a sorbitan fatty acid ester, etc. are mentioned. Examples of other auxiliary additives for preparation include lignin sulfonate, alginate, polyvinyl alcohol, gum arabic, CMC (carboxymethyl cellulose), PAP (acidic phosphate isopropyl), and the like.

본 발명의 제초제조성물은, 보다 뛰어난 제초효과를 얻기 위하여, 또 다른 제초제와 배합할 수도 있다. 이와같은 제초제로서는 예를들면, 2,4,6-트리클로로페닐-4'-니트로페닐에테르, 2,4-디클로로페닐-3'-메톡시카르보닐-4'-니트로페닐에테르, 2,4-디클로로페닐-3'-메톡시-4'-니트로로페닐에테르, S-(4-클로로벤질)-N,N-디에틸티올 카아바메이트, S-에틸-N,N-헥사메틸렌티올카아바메이트, S-벤질-N-(1,2-디메틸프로필)-N-에틸-티올카아바메이트, S-(1-메틸-1-페닐에틸)-피페리딘-1-카르보티오에이트, 2-클로로-2',6'-디에틸-N-(부톡시메틸) 아세트아닐리드, 2-클로로-2',6'-디에틸-N-(2-프로폭시에틸)아세트 아닐리드, N-[2'-(3'-메톡시)-티에닐메틸]-N-클로로아세트-2,6-디메틸아닐리드, 2',3'-디클로로-4-에톡시메톡시벤즈 아닐리드, 2-벤조티아졸-2-일옥시-N-메틸아세트 아닐리드, 3,7-디클로로-8-퀴놀린카르복시산, 0-(3-tert-부틸페닐)-N-(6-메톡시-2-피리딜)-N-메틸티오 카아바에이트, 3(2,4-디클로로-5-이소프로폭시페닐)-5-tert-부틸-1,3,4-옥사디아졸-2(3H)-온등을 들 수 있다. 개개의 활성화물은, 그 제초활성에 각각 결점을 나타내는 경우가 많이 있으나, 그 경우 2종의 활성화합물을 조합시킨 경우의 제초활성이, 그 2종의 화합물의 각각의 활성의 단순한 합계(기대되는 활성)보다도 크게 되는 경우에 이것을 상승 작용이라 한다. 2종의 제초제의 특정조합에 의해 기대되는 활성은, 다음과 같이해서 계산할 수 있다. (Colby S. R. 제초제 조합의 상승(相乘) 및 길항작용 반응의 계산「Weed」15권 20∼22페이지, 1967년을 참조)The herbicidal composition of the present invention may be blended with another herbicide in order to obtain more excellent herbicidal effect. As such herbicides, for example, 2,4,6-trichlorophenyl-4'-nitrophenyl ether, 2,4-dichlorophenyl-3'-methoxycarbonyl-4'-nitrophenyl ether, 2,4 -Dichlorophenyl-3'-methoxy-4'-nitrolophenylether, S- (4-chlorobenzyl) -N, N-diethylthiol carbamate, S-ethyl-N, N-hexamethylenethiolka Abamate, S-benzyl-N- (1,2-dimethylpropyl) -N-ethyl-thiolcarbamate, S- (1-methyl-1-phenylethyl) -piperidine-1-carbothioate , 2-chloro-2 ', 6'-diethyl-N- (butoxymethyl) acetanilide, 2-chloro-2', 6'-diethyl-N- (2-propoxyethyl) acet anilide, N -[2 '-(3'-methoxy) -thienylmethyl] -N-chloroacet-2,6-dimethylanilide, 2', 3'-dichloro-4-ethoxymethoxybenz anilide, 2-benzo Thiazol-2-yloxy-N-methylacet anilide, 3,7-dichloro-8-quinolinecarboxylic acid, 0- (3-tert-butylphenyl) -N- (6-methoxy-2-pyridyl)- N-methylthio carbaate, 3 (2,4-di Chloro-5-isopropoxyphenyl) -5-tert-butyl-1,3,4-oxadiazole-2 (3H) -one and the like. Although individual activators often exhibit drawbacks in their herbicidal activity, in this case, the herbicidal activity in the case of combining two active compounds is a simple sum of the activities of each of the two compounds. Active), this is called synergism. The activity expected by the specific combination of two herbicides can be calculated as follows. (Calculation of synergistic and antagonistic reactions of the Colby S. R. herbicide combination, see Weed 15, pages 20-22, 1967)

Figure kpo00002
Figure kpo00002

α : 제초제 A를 akg/ha의 양으로 처리했을때의 억제율α: inhibition rate when the herbicide A is treated in akg / ha

β : 제초제 B를 bkg/ha의 양으로 처리했을때의 억제율β: inhibition rate when the herbicide B was treated with the amount of bkg / ha

E : 제초제 A를 akg/ha, 제초제 B를 bkg/ha의 양으로 처리했을 경우에 기대되는 억제율E: Inhibition rate expected when herbicide A was treated with akg / ha and herbicide B with bkg / ha

즉, 실제의 억제율이 상기 계산보다 크면 조합에 의한 활성은 상승작용을 나타낸다고 말할 수 있다.In other words, if the actual inhibition rate is greater than the above calculation, it can be said that the activity by the combination is synergistic.

이하 본 발명은 실시예에 의해서 더욱 구체적으로 설명하나, 본 발명에 있어서의 화합물, 제제량, 제형(劑形)등은 실시예에만 한정되는 것은 아니다. 또한 「부」는 모두 중량부를 의미한다.Hereinafter, although an Example demonstrates further more concretely by the Example, the compound, formulation amount, a dosage form, etc. in this invention are not limited only to an Example. In addition, all "parts" mean a weight part.

[배합예1 : 입제(粒劑)][Combination example 1: granulation]

화합물(I); 0.07부Compound (I); 0.07part

브로모부티드; 3부Bromobutide; Part Three

벤도나이트; 20부Bendonite; Part 20

활석; 76.93부talc; Part 76.93

이상을 균일하게 혼합분쇄한 후 소량의 물을 첨가해서 교반혼합반죽하여 뭉쳐서, 압출식조립기에 의해서 조립(造粒)하여, 건조시켜서 입제로 한다.After uniformly mixing and grinding the above, a small amount of water is added, the mixture is stirred and kneaded together, granulated by an extrusion granulator, dried and granulated.

[배합예2 : 입제][Combination Example 2]

화합물(I); 0.05부Compound (I); 0.05 parts

브로모부티드; 5부Bromobutide; Part 5

벤도나이트; 20부Bendonite; Part 20

활석; 74.95부talc; Part 74.95

이상을 균일하게 혼합분쇄한후 소량의 물을 첨가해서 교반혼합반죽하여 뭉쳐서, 압출식 조립기에 의해서 조립하여, 건조시켜서 입제로 한다.After uniformly mixing and grinding the above, a small amount of water is added, the mixture is stirred and kneaded together, granulated by an extrusion granulator, dried and granulated.

[배합예3 : 유동성(Flowable)제][Composition Example 3: Flowable Agent]

화합물(I); 0.4부Compound (I); 0.4 part

브로모부티드; 2.5부Bromobutide; Part 2.5

아그리졸 S-710; 10부Agrisol S-710; Part 10

(비이온성 계면활성제 : 일본국, 카오아토라스(주)회사 상품명)르녹스 1000; 0.5부(Nonionic surfactant: Japan, Kao Atlas Co., Ltd.) Renox 1000; 0.5 part

(음이온성계면활성제 : 일본국, 토오호카가꾸(주)회사 상품명)1%로도폴수; 20부(Anionic surfactant: Japan, Tohoka Chemical Co., Ltd.) 1% Rhodopolsu; Part 20

(증점(增粘)제 : 론푸우란회사 상품명)(Thickener: Lonpuran Company)

에틸렌글리콜; 10부Ethylene glycol; Part 10

물; 56.6부water; Part 56.6

원체(原體)를 미분쇄하여, 상기다른 성분과 균일하게 혼합해서 액제로 한다.The original body is pulverized, mixed with the other components homogeneously to obtain a liquid.

[배합예4 : 유제]Formulation Example 4: Emulsion

화합물(I); 0.5부Compound (I); 0.5 part

브로모부티드; 6부Bromobutide; Part 6

크실렌; 72.5부xylene; Part 72.5

디메틸포름아미도; 15부Dimethylformamido; Part 15

대두유; 1부Soybean oil; chapter 1

솔포올 2680; 5부Solfool 2680; Part 5

(비이온성계면활성제와 음이온성계면활성제와의 혼합물 : 일본국, 토오호카가꾸(주)회사 상품명) 이상을 균일하게 혼합해서 유제로 한다.(The mixture of a nonionic surfactant and anionic surfactant: Japan, Tohoka Chemical Co., Ltd. make) The above is mixed uniformly and is made into an emulsion.

[배합예5 : 수화제]Formulation Example 5: Hydrating Agent

화합물(I); 2부Compound (I); Part Two

브로모부티드; 24부Bromobutide; Part 24

디-클라이트A; 64부Di-crite A; Part 64

(카올리인계클레이 : 일본국, 디-클라이트코오교(주)회사 상품명)(Kaolin-based clay: Japan, D-Clite Kogyo Co., Ltd. product name)

솔포올 5039; 2부Solfool 5039; Part Two

(알킬에테르황산염 : 일본국, 토오호카가꾸(주)회사 상품명)(Alkyl ether sulfate: Japan, Tohoka Chemical Co., Ltd.)

솔포올 5050; 2부Solfool 5050; Part Two

(디옥틸술포숙신산의 백색카아본 50%희석품 : 일본국, 토오호카가꾸(주)회사 상품명(50% diluent of dioctyl sulfosuccinic acid white carbon: Japan, Tohoka Chemical Co., Ltd.)

대두유; 2부Soybean oil; Part Two

카아플렉스(고결방지제); 4부Carplex (antifreeze); Part 4

(백색카아본 : 일본국, 시오노기세이야꾸(주)회사 상품명)(White Carbon: Japan, Shionogi Seiyaku Co., Ltd.)

이상을 균일하게 혼합분쇄하여 수화제로 한다.The above is mixed and pulverized uniformly to obtain a hydrate.

시험예 1 : 담수(湛水)조건에 있어서의 제초효과시험 1/5000아아르의 바그너포트중에 충적(沖積)토양을 넣은후, 물을 넣어서 혼화(混和)하여 수심 4cm의 담수조건으로 한다.Test Example 1: Herbicide Effect Test in Freshwater Condition An alluvial soil is placed in a Wagner pot of 1/5000 ar, mixed with water to obtain a fresh water condition of 4 cm.

Echinochloa oryzicola 광옆잡초(monochoria, Lindernia Procumbens, Rotala indica의 각각의 종자를, 상기한 포트에 혼파(混播)하고, 또 Sagittarria pygmaea, Cyperus Serotinus의 괴경을 치상(置床)하였다. 또 2.5옆기의 quay를 이식하였다. 포트를 25∼30℃의 온실내에 놓고 식물을 육성하고, 파종후 10일째, Echinochloa oryzicola가 1.5옆기의 시기에 수면에 소정의 약량이 되도록, 약제희석액을 눈금피펫으로 적하처리하였다.Seeds of Echinochloa oryzicola broad weeds (monochoria, Lindernia Procumbens, Rotala indica) were mixed in the above-mentioned ports, and the tubers of Sagittarria pygmaea and Cyperus Serotinus were wounded. The pots were placed in a greenhouse at 25 to 30 ° C., and the plants were grown, and on the 10th day after sowing, the chemical diluent was dropwise treated with a graduated pipette so that Echinochloa oryzicola had a predetermined amount on the surface at the time of 1.5 side period.

약액적하후 3주째에 각종 잡초에 대한 제초효과를 하기의 판정기준에 따라서 조사하였다. 단제(單劑)의 제초효과시험의 결과를 제1표에 2가지의 약제를 혼합하였을 경우의 제초효과시험의 결과를 제2표에 표시하였다.At 3 weeks after dropping, the herbicidal effects on the various weeds were examined according to the following criteria. The results of the herbicidal effect test of single herb are shown in the second table when the two herbicides are mixed in the first table.

판정기준Criteria

5 : 살초율 90%이상(거의 완전고사)5: 90% or more kill rate (nearly complete test)

4 : 살초율 70∼89%4: 70-89% of the herbicide rate

3 : 살초율 40∼69%3: 40-69% of the herbicide rate

2 : 살초율 20∼39%2: 20 ~ 39% kill rate

1 : 살초율 5∼19% - 살초율 5%이하(거의 효력없음)1: 5 ~ 19% of the herbicide-5% or less of the herbicide (almost no effect)

[표 1]TABLE 1

Figure kpo00003
Figure kpo00003

[표 2]TABLE 2

Figure kpo00004
Figure kpo00004

시험예 2 : Cyperus Serotinus에 대한 상승효과시험 1/1000아아르의 노이바우어 포트에논의 토양을 충전하여 논상태로하고, 최아(催芽)한 flet sedge의 괴경을 심었다. 심은지 3일째, 물속에 소정 농도의 약제 희석액 1ml를 눈금피펫으로 적하처리하였다. 온실내에서 30일 성육시킨후, Cyperus Serotinus의 지상부분생체무게를 측정하여, 하기의 방법으로 저해율을 구하였다.Test Example 2: Synergistic effect test on Cyperus Serotinus The soil of Neubauer Fort-Enon of 1 / 1000are was filled with rice paddy, and the tuber of flet sedge was planted. On the third day of planting, 1 ml of the drug diluent of a predetermined concentration was added dropwise to the water in a scale pipette. After 30 days of incubation in the greenhouse, the ground portion biomass of Cyperus Serotinus was measured, and the inhibition rate was determined by the following method.

Figure kpo00005
Figure kpo00005

단제의 시험결과를 제3표에, 2가지의 약제를 혼합했을 경우의 시험 결과를 제4표에 표시하였다.The test result of a single agent was shown to the 3rd table, and the test result at the time of mixing two drugs is shown to the 4th table.

[표 3]TABLE 3

flat sedge의 지상부분 생체무게의 저해율(단제)Inhibition rate of biomass on the ground of flat sedge (single)

Figure kpo00006
Figure kpo00006

[표 4]TABLE 4

flat sedge의 지상부분 생체무게의 저해율(혼제)Inhibition rate of ground weight biomass of flat sedge (mixed)

Figure kpo00007
Figure kpo00007

표중, 기대치는 상기 콜베이식으로부터 구한 계산치를 표시한다. 이상과 같이, 지상부분 생체무게의 저해율은 기대치를 상회하는 것이였다.In a table | surface, an expectation value shows the calculated value calculated | required from the said Colbay's formula. As mentioned above, the inhibition rate of the ground part bio weight exceeded expectations.

본 발명 조성물의 상승효과는 등효과선법에 의한 해것에 의해서도, 더욱 명확하게 나타나 있다.The synergistic effect of the composition of the present invention is more clearly shown by the solution by the equal effect line method.

즉, 제초제제 A와 제초제 B의 다른 혼합비로 이루어지는 조성물로서 90% 성육저해율을 나타내는 것을 수점구하고, 이것을 제1도에 표시한 바와같이 도시하면, 상승효과, 상가효과, 길항효과를 요이하게 해석할 수 있다(일본국, 후카미중이찌, 우에스기야스히꼬, 이즈까코오조, 토미사와 초오지로 편, 농약실험법 제8권 제초제편 제1판 제109∼111페이지(1981)년 소프트사이언스사 발행참조). 즉 등효과선이 상가 효과선을 기준으로 해서, 그 아래에 오면 상승효과를 나타낸다. 제1도에 표시한 바와같이 본 발명 조성물의 등효과선을 상가 효과선의 아래에 와 있으며, 진정한 상승효과를 나타내고 있다는 사실이 명확하게 표시되어 있다.In other words, as a composition consisting of different mixture ratios of herbicide A and herbicide B, several scores showing 90% growth inhibition rate and shown as shown in FIG. 1 show synergistic effects, additive effects, and antagonistic effects. (Japan, Fukami-jungichi, Uesugiyasuhiko, Izukako-jo, Tomisawa Chooji-ro, Pesticides, Volume 8, First Herb, First Edition, pages 109-111 (1981), published by Soft Science, Inc.) ). In other words, when the equal effect line is below the additive effect line, the synergistic effect is obtained. As shown in FIG. 1, it is clearly shown that the isoline of the composition of the present invention is below the additive effect line and shows a true synergistic effect.

Claims (1)

식(I) :Formula (I):
Figure kpo00008
Figure kpo00008
로 표시되는 피라졸술포닐요소 0.001∼10중량부와 N-(α,α-디메틸벤질)-α-브로 모-tert-부틸아세트아미드 1중량부를 유효성분으로서 함유하는 것을 특징으로 하는 제초제 조성물.A herbicide composition comprising 0.001 to 10 parts by weight of pyrazolesulfonyl urea and 1 part by weight of N- (α, α-dimethylbenzyl) -α-bromo-tert-butylacetamide as an active ingredient.
KR1019880006107A 1987-05-27 1988-05-25 Herbicide composition KR920002305B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP62127968A JPS63295503A (en) 1987-05-27 1987-05-27 Herbicide composition
JP62-127968 1987-05-27

Publications (2)

Publication Number Publication Date
KR880013453A KR880013453A (en) 1988-12-21
KR920002305B1 true KR920002305B1 (en) 1992-03-21

Family

ID=14973140

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019880006107A KR920002305B1 (en) 1987-05-27 1988-05-25 Herbicide composition

Country Status (2)

Country Link
JP (1) JPS63295503A (en)
KR (1) KR920002305B1 (en)

Also Published As

Publication number Publication date
JPS63295503A (en) 1988-12-01
KR880013453A (en) 1988-12-21
JPH0580443B2 (en) 1993-11-09

Similar Documents

Publication Publication Date Title
PL110361B1 (en) Herbicide
KR100276932B1 (en) Herbicide composition
KR0166095B1 (en) Herbicidal composition for paddy fields
KR920002305B1 (en) Herbicide composition
JPH02160706A (en) Herbicidal composition
JPS6045503A (en) Herbicide
KR100415595B1 (en) Power herbicide composition
KR930007406B1 (en) Herbicidal composition
JPH04257503A (en) Herbicide composition
WO2022118272A1 (en) Synergistic ternary herbicidal composition
JPS62185003A (en) Herbicidal composition
KR0169136B1 (en) A weed killer
JPH05186306A (en) Herbicide composition
KR930002954B1 (en) Hebicidal composition
WO2022023911A1 (en) Synergistic ternary herbicidal composition
KR100336318B1 (en) Herbicide composition
CN104904743B (en) Pesticidal combination
JPH0655650B2 (en) Herbicide composition
JPH05139921A (en) Granule for control of noxious organism
JPH0597614A (en) Herbicide composition
KR810002007B1 (en) Herbicide composition
JPH0617287B2 (en) Herbicide
JPS6351304A (en) Herbicide composition
HU204662B (en) Herbicidal composition having synergetic effect and comprising n-(substituted phenyl)-tetrahydrophthalimide derivative and n-(substituted phenyl)-n&#39;,n&#39;-dimethylurea derivative, as well as utilization of the composition for exterminating wheeds
JPS63179806A (en) Herbicide composition

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
G160 Decision to publish patent application
E701 Decision to grant or registration of patent right
GRNT Written decision to grant
FPAY Annual fee payment

Payment date: 20080311

Year of fee payment: 17

EXPY Expiration of term