SU651640A3 - Herbicide composition - Google Patents
Herbicide compositionInfo
- Publication number
- SU651640A3 SU651640A3 SU762392645A SU2392645A SU651640A3 SU 651640 A3 SU651640 A3 SU 651640A3 SU 762392645 A SU762392645 A SU 762392645A SU 2392645 A SU2392645 A SU 2392645A SU 651640 A3 SU651640 A3 SU 651640A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- composition
- herbicide composition
- herbicidal
- plants
- mixtures
- Prior art date
Links
Classifications
-
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
- A01N35/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen containing a carbon-to-nitrogen double bond
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Изобретение относитс к химическим средствам дл борьбы с сорной и нежелательной растительностью, а ийе но к гербицидным композици м, содержащим в качестве действующего вещества синергистические смеси органических соединений. Известна гербицидна композици на основе З-алкоксикарбониламинОфенил-N- (метилфенил)карбамата (1. Его эффективность про вл етс S дозе 1 кг/га и недостаточна дл борьбы с некоторыми устойчивыми сорн ками. Известны также гербицидные композиции на основе смесей 3-метоксикарбониламино-N- (3-метилфенил)карбамата с 2-(метахлорфенил)-4Н-3,1-бензоксазин-4-оном 2 и с З-метил-4-амино-6-фенил-1 ,2,4-триазин-5-оном 3. Целый изобретени вл етс нова гербицидна композици на основе 3метоксикарбониламино-N- (3-метилфеНйл карбамата формулы ( в дальнейшем называемого фенмедифамом ) , обладсшвда повьи енной гербицидной активностью. Цель достигаетс тем, что в гербицидную композицию, содержащую фенмедифам , дополнительно ввод т производное циклогександиона-1,3 общей формулы где зтил, пропил; этил, аллил; X - метил, изопропил, метоксикарбонил; п - 1; 2 или 3, или его натриевую соль, причем весовые соотношени компонентов гербицндной композиции наход тс в пределах от 75:25 до 25:75 соответственно. Формы применени композиции согласно изобретению обычные: растворы, эмульсии, пасты, порошки и т.д. Их готов т известными способами, содержание действующих веществ в этих препаративных формах 5-95 вес Л,The invention relates to chemical agents for controlling weeds and undesirable vegetation, and to herbicidal compositions containing, as an active ingredient, synergistic mixtures of organic compounds. Known herbicidal composition based on 3-alkoxycarbonylaminophenyl-N- (methylphenyl) carbamate (1. Its effectiveness is S dose of 1 kg / ha and is insufficient to control some resistant weeds. Herbicidal compositions based on mixtures of N- (3-methylphenyl) carbamate with 2- (methachlorophenyl) -4H-3,1-benzoxazin-4-one 2 and Z-methyl-4-amino-6-phenyl-1, 2,4-triazin-5 -on 3. The whole of the invention is a new herbicidal composition based on 3methoxycarbonylamino-N- (3-methylfeNyl carbamate of the formula (hereinafter referred to as Fenmedipham) possesses superior herbicidal activity. The goal is achieved by addition of a cyclohexanedione-1,3 derivative of the general formula </ BR> where ethyl, propyl; ethyl, allyl; X is methyl, isopropyl, methoxycarbonyl; n is 1; 2 or 3, or its sodium salt, the weight ratios of the components of the herbicidal composition being in the range of 75:25 to 25:75, respectively. The form of application of the composition according to the invention is conventional: solutions, emulsions, pastes, powders, etc. They are prepared by known methods, the content of active substances in these formulations 5-95 weight L,
Предлатаемуго композицию можно нС пользовать как путем довсходовой, так и послевсходоБой обработки. .VB состав этой композици вход т следующие соединени общей формулы {II) - производные циклогександиона-1 ,3: - - -The pre-proposed composition can be used as a pre-emergence and post-emergence treatment. .VB composition of this composition includes the following compounds of general formula {II) - derivatives of cyclohexanedione-1, 3: - - -
2-(1-этоксиамипо)-пропилпден-(5 иэопропилциклогександион- , 3 ( 1)2- (1-ethoxyamipo) -propylpden- (5 isopropylcyclohexanedione-, 3 (1)
2-(1-аллилоксиамнпо)-пропилнден-5 ,5-диметилцнклогексаидиои-1,3 (№ 2);2- (1-allyloxyamnpo) -propyl-inden-5, 5-dimethyl-cyclohexaidio-1,3 (no. 2);
2-(1-аллилокснамиио)-бутйлидён|-5 ,5-диметилциклогександион 1,3 (№ 3) 2- (1-allyloxnamio) -butylidene | -5, 5-dimethylcyclohexanedione 1,3 (№ 3)
2-{-1 аллилоксиамиио)-бутил1щен-4 -мётоксикарбони/ -5,5-лиметилцикЛогек санйион-1,3 (1 4) ; , ; 2 - {- 1 allyloxyamio) butyl-1-4-methoxycarboni / -5,5-methylmethylcycloxy-1,3-1,3 (1 4); ,;
натриева соль 2-(1-аллйлоксиамино ) бутплидеи-4-метоксикарбоннл5,5-днмeтилцнклoгeкcaкднoFia-l f 3 ; (№ 5} /2- (1-allyloxyamino) sodium salt of 4-methoxycarbonyl-5,5-dimethyl-nitrohexacid fia-f 3; (No. 5} /
Приводимые ниже примеры 1 лл острируют эффективность композиции согласно изобретению в сравнении с эффективностью отдельных ее компонептов.The following examples 1 ll rim the effectiveness of the composition according to the invention in comparison with the effectiveness of its individual components.
Пример 1. Опытныерастени , выращенные в услови х теплицы до стадии 4 листьев, обрабатывают вод( эмульсией действ тощих веществ (смес мй и отдельными компонентами смесей ) .Example 1. Pilot plants grown in greenhouse conditions up to the 4-leaf stage are treated with water (emulsion of lean substances (mixtures and individual components of the mixtures).
Гербицидмую активность определ ют через три недели после обработки и одекпвают путем взвешивани растений Г олуче1|ные результаты представлены 3 табл. 1 (где номера соединений - производных: цйклогександиона-- ,3 соответствуют их номерам, указанным вьаие) . . ,Herbicidal activity is determined three weeks after treatment and is prepared by weighing the plants. The best results are presented in Table 3. 1 (where the numbers of the compounds are derivatives: cyclohexanedione--, 3 correspond to their numbers indicated above). . ,
Пример 2. Опыу провод т в услоЕк х примера .1, но с другими тест-растени ми.Example 2. The experiment was carried out in the conditions of example .1, but with other test plants.
Гербидидную активность оценивают путем взвешивани опытн5лх растений и.выражают в относительных величинах по сравнению с весом необработанных растений.Результаты опыта представле ны в табл. 2. Gerbididal activity is assessed by weighing the experimental plants and I. express in relative values compared to the weight of untreated plants. The results of the experiment are presented in Table. 2
Представленныев табл. 1 и 2 результаты свидетельствуют о значительно более высокой .эффективности гербицидной композиции на основе сйесей по сравнению с отдельными ее компонентами , т.е. о наличии эффекта синергизма . Presented in table. 1 and 2, the results indicate a significantly higher efficacy of the herbaceous composition based on seysey compared to its individual components, i.e. about the presence of synergies.
+ +
0,50+0,50 4,70.50 + 0.50 4.7
Фенмедифам + соединение 2 0,50+0,50 5,5Fenmedifam + Compound 2 0.50 + 0.50 5.5
Таблица 1Table 1
4,34.3
9,09.0
3,93.9
9,49.4
Та б л и ц а 2Table 2
Продолжение табл.2Continuation of table 2
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP49107654A JPS5931481B2 (en) | 1974-09-20 | 1974-09-20 | Cyclohexanedione herbicide composition |
Publications (1)
Publication Number | Publication Date |
---|---|
SU651640A3 true SU651640A3 (en) | 1979-03-05 |
Family
ID=14464651
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU752173209A SU628799A3 (en) | 1974-09-20 | 1975-09-19 | Herbicide composition |
SU762392645A SU651640A3 (en) | 1974-09-20 | 1976-08-10 | Herbicide composition |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU752173209A SU628799A3 (en) | 1974-09-20 | 1975-09-19 | Herbicide composition |
Country Status (30)
Country | Link |
---|---|
JP (1) | JPS5931481B2 (en) |
AR (1) | AR218213A1 (en) |
AT (1) | AT347174B (en) |
AU (1) | AU477150B2 (en) |
BE (1) | BE833488A (en) |
BG (1) | BG27049A3 (en) |
BR (1) | BR7506049A (en) |
CA (1) | CA1044912A (en) |
CH (1) | CH619113A5 (en) |
CS (1) | CS191946B2 (en) |
DD (1) | DD119700A5 (en) |
DE (1) | DE2541702A1 (en) |
DK (2) | DK421775A (en) |
EG (1) | EG11973A (en) |
FI (1) | FI752645A (en) |
FR (1) | FR2285070A1 (en) |
GB (1) | GB1481389A (en) |
HU (1) | HU176584B (en) |
IL (1) | IL48010A (en) |
IN (1) | IN144613B (en) |
IT (1) | IT1060068B (en) |
NL (1) | NL7510946A (en) |
NZ (1) | NZ178624A (en) |
OA (1) | OA05112A (en) |
PL (1) | PL101883B1 (en) |
RO (1) | RO71395A (en) |
SE (1) | SE426772B (en) |
SU (2) | SU628799A3 (en) |
TR (1) | TR18679A (en) |
ZA (1) | ZA755662B (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3032259A1 (en) | 1980-08-27 | 1982-04-08 | Basf Ag, 6700 Ludwigshafen | HERBICIDES BASED ON CYCLOHEXANE-1,3-DION DERIVATIVES AND 3,6-DICHLOR-2-PICOLINE ACID DERIVATIVES |
DE3047924A1 (en) * | 1980-12-19 | 1982-07-15 | Basf Ag, 6700 Ludwigshafen | 5-ARYL-CYCLOHEXAN-1,3-DION DERIVATIVES, HERBICIDES THAT CONTAIN THESE COMPOUNDS, AND METHOD FOR THE PRODUCTION THEREOF |
DE3121355A1 (en) * | 1981-05-29 | 1982-12-16 | Basf Ag, 6700 Ludwigshafen | CYCLOHEXANDION DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND HERBICIDES CONTAINING THEM |
NZ204160A (en) * | 1982-05-24 | 1985-07-31 | Imp Chemical Ind Australia Ltd | Heterocyclic compounds and herbicidal compositions |
GB8313774D0 (en) * | 1983-05-18 | 1983-06-22 | Ici Plc | Herbicidal compositions |
US4511391A (en) * | 1983-05-24 | 1985-04-16 | Ici Australia Limited | Cyclohexane-1,3-dione derivatives and their herbicidal compositions and methods |
EP0350079B1 (en) * | 1985-12-30 | 1993-09-01 | Stauffer Chemical Company | Synergistic herbicide combinations and method of application |
CA2780142C (en) * | 2009-11-16 | 2018-07-17 | Centre National De La Recherche Scientifique - Cnrs | Compounds and methods for purifying peptides produced by solid phase peptide synthesis |
-
1974
- 1974-09-20 JP JP49107654A patent/JPS5931481B2/en not_active Expired
-
1975
- 1975-08-28 IL IL48010A patent/IL48010A/en unknown
- 1975-09-02 AU AU84475/75A patent/AU477150B2/en not_active Expired
- 1975-09-04 SE SE7509840A patent/SE426772B/en not_active IP Right Cessation
- 1975-09-04 ZA ZA00755662A patent/ZA755662B/en unknown
- 1975-09-04 CA CA234,775A patent/CA1044912A/en not_active Expired
- 1975-09-08 FR FR7527459A patent/FR2285070A1/en active Granted
- 1975-09-08 NZ NZ178624A patent/NZ178624A/en unknown
- 1975-09-09 CH CH1167575A patent/CH619113A5/en not_active IP Right Cessation
- 1975-09-15 IN IN1765/CAL/1975A patent/IN144613B/en unknown
- 1975-09-16 HU HU75NI192A patent/HU176584B/en unknown
- 1975-09-16 TR TR18679A patent/TR18679A/en unknown
- 1975-09-17 BE BE160097A patent/BE833488A/en not_active IP Right Cessation
- 1975-09-17 BG BG031005A patent/BG27049A3/en unknown
- 1975-09-17 NL NL7510946A patent/NL7510946A/en not_active Application Discontinuation
- 1975-09-18 DD DD188421A patent/DD119700A5/xx unknown
- 1975-09-18 OA OA55612A patent/OA05112A/en unknown
- 1975-09-18 PL PL1975183476A patent/PL101883B1/en unknown
- 1975-09-18 DE DE19752541702 patent/DE2541702A1/en active Pending
- 1975-09-18 GB GB38348/75A patent/GB1481389A/en not_active Expired
- 1975-09-19 SU SU752173209A patent/SU628799A3/en active
- 1975-09-19 BR BR7506049*A patent/BR7506049A/en unknown
- 1975-09-19 CS CS756364A patent/CS191946B2/en unknown
- 1975-09-19 AT AT719475A patent/AT347174B/en active
- 1975-09-19 IT IT51405/75A patent/IT1060068B/en active
- 1975-09-19 RO RO7583429A patent/RO71395A/en unknown
- 1975-09-19 AR AR260460A patent/AR218213A1/en active
- 1975-09-19 DK DK421775A patent/DK421775A/en unknown
- 1975-09-20 EG EG562/75A patent/EG11973A/en active
- 1975-09-22 FI FI752645A patent/FI752645A/fi not_active Application Discontinuation
-
1976
- 1976-08-10 SU SU762392645A patent/SU651640A3/en active
- 1976-08-19 DK DK374276AA patent/DK141642B/en not_active IP Right Cessation
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