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SU1079163A3 - Herbecidal composition - Google Patents

Herbecidal composition Download PDF

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Publication number
SU1079163A3
SU1079163A3 SU813247947A SU3247947A SU1079163A3 SU 1079163 A3 SU1079163 A3 SU 1079163A3 SU 813247947 A SU813247947 A SU 813247947A SU 3247947 A SU3247947 A SU 3247947A SU 1079163 A3 SU1079163 A3 SU 1079163A3
Authority
SU
USSR - Soviet Union
Prior art keywords
plants
compounds
compound
parts
composition
Prior art date
Application number
SU813247947A
Other languages
Russian (ru)
Inventor
Иори Синити
Кадзивара Икуо
Дзикихара Казуо
Original Assignee
Кумиаи Кемикал Индастри Ко,Лтд (Фирма)
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.)
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Application granted granted Critical
Publication of SU1079163A3 publication Critical patent/SU1079163A3/en

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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
    • 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
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring

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  • 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

A herbicidal composition is provided which is characterized by the combination use as active ingredients of a thiocarbamate derivative of formula I: <IMAGE> wherein one of X and Y is a hydrogen and the other is a chlorine and 4- amino-3-methyl-6-phenyl-1,2,4-triazin-5(4H)-one of the formula: <IMAGE> Also provided is a process of inhibiting the growth of unwanted plants by applying the herbicidal composition to the plants or to the soil where the plants are grown.

Description

чh

соwith

00

со эквивалентной 500 л/га. Через 25 д после разбрызгивани  измер ют вес испытуемых растений и из него рассч тывают ингибирование роста по формуле . Ингибирование роста, % вес растений, выросших в обработанном контейнере. 100 вес растений, выросших в необработанном контейнере Полученные результаты представлены в табл. 1. Дл  сравнени  проводили такие же испытани , в которых соединени , используемые в композиции, примен ли по отдельност в указанных услови х. Результаты также представлены в табл. 1„ Пример 7. Он иллюстрирует гербицидную активность композиции против различных сорн ков и фитоток сичность по отношению к свекле при обработке после прорастани . В каждом и полиэтиленовых контейнеров площадью 2000 см, наполненных землей из питомника выращивают свеклу (стади  1,5-2 листа), курино просо (стади  2-2,5 листа), м тлик однолетний (стади  1,5-2 листа), вод ной перец (стади  1-2 листа) и марь (стади  1,5-2 листа). Смачивающийс  порошок, содержащий 40 ч. соединени  А и 20 ч. соединений С, приготовленный по примеру 2, или смачивающийс  порошок, содержащий 40 ч, соединени  А и 10 ч, соединени  С, приготовленный по примеру илн смачивающийс  порошок, содержа:ший 40 ч. соединени  В и 20 ч. соединени  С, приготовленный по примеру 2, или смачивающийс  порошо содержащий 40 ч. соединени  В и 10 соединени  С, приготовленный по примеру 4, раствор ют в воде с полу чением таких концентраций активных соединений, которые обеспечивают надлежащие соотношени , показанные Гербицидна  активность к свекле при об в табл. 2. Приготовленные таким образом водные растворы (или водные дисперсии) равномерно разбрызгивают на стебли и листь  проросших растений при концентрации нанесени  500 л/га. Через 20 дней после опрыскивани  измер ют вес растений, из которого в соответствии с указанной выше форму : лой рассчитывают ингибирование роста (%), Результаты представлены в табл. 2. Пример 8. Иллюстрирует гер бицидную активность композиции про тив желтого щетинника и ширицы при обработке до и после прорастани . Семена испытуемых видов размещают на поверхности почвы, наход щейс  в полиэтиленовом контей-нере площадью 2000 см, и присыпают сверху слоем почвы толщиной 0,5 см Смачивающийс  порошок, содержаший 30 ч. соединени  А и 30 ч. соединени  С, приготовленный по примеру 5, или смачивающийс  nopoiiiOK, содержащий 40 ч. соединени  А и 10 ч. соединени  С, приготовленный по примеру 4, или смачивающийс  порошок, содержащий 30 ч. соедине-. ни  В и 30 ч. соединени  С, приготовленный по примеру 5, или смачивающийс  порошок, содержащий 40 ч, соединени  В и 10 частей соединени  С, приготовленный по примеру 4, раствор ют в воде с получением таких концентраций активных соединений, которые обеспечивают отисхиени  активных соединений, приведенные в табл. 3 . Приготовленные предлагаемым способом водные растворы (или водные дисперсии) равномерно разбрызгивают на почву при испытании до прорастани  и на стебли и листь  растущих растений при испытании после прорастани  с концентрацией 500 л/га. Через 20 дней после обработки определ ют степень ингибировани  растений, как показано вьше. Таблица 1 токсичиость по отношению е до прорастани with an equivalent of 500 l / ha. After 25 d after spraying, the weights of the test plants are measured and the growth inhibition calculated by it is calculated from it. Inhibition of growth,% weight of plants grown in the treated container. 100 weight plants grown in an unprocessed container The results obtained are presented in Table. 1. For comparison, the same tests were carried out in which the compounds used in the composition were used separately under the conditions indicated. The results are also presented in table. 1 Example 7. It illustrates the herbicidal activity of the composition against various weeds and its phytotoxicity with respect to beets during processing after germination. In each and polyethylene containers with an area of 2000 cm, filled with ground from the nursery, beets are grown (stage 1.5-2 leaves), chicken millet (stage 2-2.5 leaves), one-year meter (stage 1.5-2 leaves), water pepper (stage 1-2 of the sheet) and mar (stage 1.5-2 of the sheet). A wettable powder containing 40 parts of compound A and 20 parts of compounds C prepared according to example 2, or a wettable powder containing 40 hours, compounds A and 10 hours, compounds C prepared by example or a wettable powder, containing: 40 hours Compounds B and 20 parts of Compound C prepared according to Example 2 or a wettable powder containing 40 parts of Compounds B and 10 Compounds C prepared as described in Example 4 are dissolved in water to obtain concentrations of the active compounds that ensure proper ratios shown herbicide Activity to beets when about in tab. 2. The aqueous solutions (or aqueous dispersions) prepared in this way are uniformly sprayed on the stems and leaves of the sprouted plants at a deposition concentration of 500 l / ha. 20 days after spraying, the weight of the plants is measured, from which growth inhibition (%) is calculated according to the above form: The results are presented in Table. 2. Example 8. Illustrates the germicidal activity of the composition against the yellow bristle and the width of the seedlings during processing before and after germination. Seeds of test species are placed on the soil surface in a 2000 cm polyethylene container and sprinkled on top with a 0.5 cm thick layer of soil with a wettable powder containing 30 parts of compound A and 30 hours of compound C prepared in example 5, or wettable nopoiiiOK, containing 40 parts of compound A and 10 parts of compound C, prepared according to example 4, or a wettable powder, containing 30 hours of compound-. Neither B and 30 parts of Compound C prepared according to Example 5 or a wettable powder containing 40 hours, Compounds B and 10 parts of Compound C prepared as described in Example 4 is dissolved in water to obtain concentrations of the active compounds that ensure the active compounds listed in Table. 3 Prepared by the proposed method, aqueous solutions (or aqueous dispersions) are uniformly sprayed on the soil when tested before germination and on the stems and leaves of growing plants when tested after germination with a concentration of 500 l / ha. 20 days after treatment, the degree of inhibition of the plants is determined, as shown above. Table 1 toxicity with respect to e to germination

ОABOUT

3 3 23 3 2

о о оLtd

1one

19 20 100 19 20 100

23 25 100 23 25 100

86 83 63 20 79 80 Гербицидна  активность и фитотоксичность стеблей и листвы на стадии роста86 83 63 20 79 80 Herbicidal activity and phytotoxicity of stems and foliage at the growth stage

АBUT

+ С+ C

Продолжение табл. 1 100 Continued table. 1,100

8686

100100

93 Таблица 2 при обработке ЧОО Гербицидна  активностт при обработке на различных93 Table 2 in the processing of ORT Herbicidal activity in the processing of various

4 4 4 1 44 4 4 1 4

4 44 4

1 414

брабонныйbrabone

Продолжение табл. 2Continued table. 2

1ТаблицаЗ 1Table3

стади х ростаstages of growth

50 52 92 8850 52 92 88

86 88 О О86 88 O O

53 58 О О53 58 O O

100 100

100 100

100 100 100100 100 100

9696

100100

100100

100100

100100

100 100

9898

Claims (1)

ГЕРБИЦИДНАЯ КОМПОЗИЦИЯ, содержащая производное тиокарбаминовой кислоты общей формулы где один из X и У - водород, а другой - хлор, отличающаяся тем, что, с целью усиления гербицидной активности, она дополнительно содержит производноеA HERBICIDAL COMPOSITION containing a thiocarbamic acid derivative of the general formula where one of X and Y is hydrogen and the other is chlorine, characterized in that, in order to enhance the herbicidal activity, it further comprises a derivative 1,2,4-триазина формулы π 5 '1,2,4-triazine of the formula π 5 ' ЮЬтГ'т’-кНг '—' к.уЛсНз при массовом соотношении: 1-4:1 соответственно.UTG't’-kNg '-' k.uLsNz with a mass ratio of 1-4: 1, respectively.
SU813247947A 1980-02-22 1981-02-20 Herbecidal composition SU1079163A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2059880A JPS56118004A (en) 1980-02-22 1980-02-22 Herbicidal composition

Publications (1)

Publication Number Publication Date
SU1079163A3 true SU1079163A3 (en) 1984-03-07

Family

ID=12031702

Family Applications (1)

Application Number Title Priority Date Filing Date
SU813247947A SU1079163A3 (en) 1980-02-22 1981-02-20 Herbecidal composition

Country Status (10)

Country Link
JP (1) JPS56118004A (en)
CS (1) CS219947B2 (en)
DE (1) DE3106407A1 (en)
FR (1) FR2477837B1 (en)
GB (1) GB2072507B (en)
IT (1) IT1167832B (en)
NL (1) NL8100829A (en)
PL (1) PL126706B1 (en)
RO (1) RO81509B (en)
SU (1) SU1079163A3 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3833801A1 (en) * 1988-10-05 1990-04-12 Bayer Ag SELECTIVE HERBICIDE AGENT, CONTAINING METAMITRON IN COMBINATION WITH CERTAIN TRIAZOLINONES
EP4295686A1 (en) * 2022-06-22 2023-12-27 Adama Agan Ltd. Agrochemical herbicidal composition
EP4295684A1 (en) * 2022-06-22 2023-12-27 Adama Agan Ltd. Agrochemical herbicidal composition
EP4295687A1 (en) * 2022-06-22 2023-12-27 Adama Agan Ltd. Agrochemical herbicidal composition
EP4295685A1 (en) * 2022-06-22 2023-12-27 Adama Agan Ltd. Method of application of herbicidal active ingredients in different stages

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5521004B1 (en) * 1968-10-31 1980-06-06
DE2413298A1 (en) * 1974-03-20 1975-09-25 Bayer Ag Means for selective weed control in turnips
DE2528302A1 (en) * 1975-06-25 1977-01-13 Bayer Ag Selective herbicide for beet and soya beans - contg. 3-methyl 4 amino 6 phenyl 1,2,4 triazin 5 one and 4 methoxy benzyl diethyl thiolcarbamate

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
1. Патент JP 48-33369, кл. 30 F 371.217.2, 1973 . (прототип). 2. Патент СССР 728687, кл. А 01 N 43/64, 1972. г. /J *

Also Published As

Publication number Publication date
DE3106407A1 (en) 1982-02-11
GB2072507B (en) 1983-06-02
CS219947B2 (en) 1983-03-25
GB2072507A (en) 1981-10-07
NL8100829A (en) 1981-09-16
PL126706B1 (en) 1983-08-31
FR2477837B1 (en) 1985-06-07
IT8109340A0 (en) 1981-02-20
PL229716A1 (en) 1981-10-16
RO81509B (en) 1983-04-30
RO81509A (en) 1983-04-29
JPS56118004A (en) 1981-09-16
IT1167832B (en) 1987-05-20
FR2477837A1 (en) 1981-09-18

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