SU668565A3 - Herbicide - Google Patents

Herbicide

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Publication number
SU668565A3
SU668565A3 SU772504512A SU2504512A SU668565A3 SU 668565 A3 SU668565 A3 SU 668565A3 SU 772504512 A SU772504512 A SU 772504512A SU 2504512 A SU2504512 A SU 2504512A SU 668565 A3 SU668565 A3 SU 668565A3
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SU
USSR - Soviet Union
Prior art keywords
emergence
plants
treatment
thiol
vessels
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Application number
SU772504512A
Other languages
Russian (ru)
Inventor
Айхен Карл
Теобальд Ханс
Хансен Ханспетер
Вюрцер Бруно
Фет Курт
Original Assignee
Басф Аг (Фирма)
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Application filed by Басф Аг (Фирма) filed Critical Басф Аг (Фирма)
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Publication of SU668565A3 publication Critical patent/SU668565A3/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/10Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon 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
    • 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
    • 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
    • A01N47/16Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof the nitrogen atom being part of a heterocyclic ring
    • 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
    • A01N47/18Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/08Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Agronomy & Crop Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

(54) ГЕРБИЦИДНОЕ СРЕДСТВО(54) HERBICID MEANS

Формы применени  гербицидного средства согласно изобретению обычные: растворы, эмульсии, пасты, rtoрсшки и т.д.The forms of application of the herbicidal agent according to the invention are common: solutions, emulsions, pastes, rtorses, etc.

Их готов т известными способами.They are prepared by known methods.

Рекомендуемые дозы действующих веществ наход тс  в пределах 0,Recommended doses of active ingredients are within 0,

66856546685654

10 кг/га, в зависимости от способа их применени  и вида сорных растений,10 kg / ha, depending on the method of their use and the type of weeds,

В табл.1 представлены соединени  общей формулы и результаты испытани  гербицидного средства согласно изобретению в сравнении с известными гер5 бицидами данного типа.Table 1 shows the compounds of the general formula and the results of testing the herbicidal agent according to the invention in comparison with the known germs of this type of bicides.

Таблица1 В табл.1-12 представлены результ ты испытани  гербицидной активности соединений. Номера соединений в эти таблицах соответствуют их номерам в табл.1. I.Испытани  в теплицах. Бумажные стаканы, пропитанные па рафином, емкостью 200 см, .служат сосудами дл  культивировани ,а глини та  песчана  почва, приблизительно с 1,5 вес.% аерегно  - в качестве субстрата. В них поверхностно засевают семена испытуемых растений, ра деленные по видам. Непосредственно после этого внос т действующее вещество (прёдвсходова  обработка). Дл  этого его суспендируют или эмул гируют в воде и при помощи тонких сопел разбрызгивают на поверхность почвы. Перед химической обработкой сосуды слегка орошеиот дл  того, что средство имело контакт с влажной землей. После внесени  средства сос ды накрывают прозрачным пластиковым колпачком до тех пор, пока не вырастут растени . Это покрытие преп тствует испарению воды и легко летучи веществ. В то же врем  это способствует равномерному всходу испытуемых растений, если последние не под вержены действию химикалиев. При послевсходовой обработке растени м дают расти в зависимости от их вида в вегетационных сосудах до 3-10 см и затем обрабатывают. Их не накрывают . Б соответствии с температурой котора  требуетс  дл  испытуемых растений, испытани  производ т в хо лодной части теплицы (IC-ZO C) или в теплой (18-30 С) . Исгитани  продолжаютс  до 2,5 до 6 нед. В течение этого времени за растени ми ухаживаю и оценивают их реакцию на отдельные виды обработки. Испытуемые вещества нормы расхода активного вещества в кг/га в каждом случае и виды испытуемых растений приведены в табл.212 . Оценку производ т по шкале ОтЮО При этом О означает, что нет повреждений или всходы, нормальны, а 100 полное умерщвление или же нет всходо II.Опыты на открытом грунте. 1 ып(т об испытани х на помощью снабженного мотором, смонтированного на носителе устройства дл  разбрызгивани  на отдельных дел нках. Чаще всего примен ют методы предпосевного внесени  в почву и способ предвсходовой обработки. При некоторых испытани х провер ли и действие, оказываемое средством при опрыскивании во врем  всходов культурных и сорных трав, а в послевсходовом способе - после образовани нескольких истинных ЛИСьев. Все испытани  протекали в течение нескольких мес цев и в это врем  производили оценку в различных интервалах времени по шкале от О до 100. III. Гербицидное действие через паровую фазу. Исход  из этого значительного гербицидного действи  изоксазолил - метилтиолкарбаматов, даже в том случае , если эти вещества не внесены в почву, что необходимо при известных тиолкарбаматах, можно предположить, что потери действующего начала изза испарени  у этих соединений очень незначительны. Чтобы доказать это превосходство, были проведены следующие испытани : нежный сорт культурного овса засевают , как описано в разделе 1, и обрабатывают гербицидными действующими веществами в различной дозировке. После этого сосуды, однако, не покрывают пластиковыми колпачками, а став т их попарно в цилиндры емкостью 5л. Пары состо т из одного обработанного и одного необработанного сосуда . Приготавливают и контрольные цилиндры с необработанными горшками дл  сравнени . Дл  предотвращени  обмена газами с внешней средой кра  цилиндра смазывают вазелином и покрывают отверсти  стекл нной пластинкой . Легко испар ющиес  действую11№1е вещества могут таким образом улетучиватьс  с.поверхности почвы обработанных сосудов в пространство цилиндра и вли ть на прорастание и развитие испытуемых растений в пероначально свободных от действующего ачала р дом сто щих сосудах. Темпеатура Б стекл нных цилиндрах колебетс  от 11 С по утрам до 30°С к по- .rt г-ппнечной 7668565 Действие на сорные травы в теплицах при 8 Таблица 2 предвсходовой обработкеTable 1 Tables 1-12 present the results of testing the herbicidal activity of the compounds. The numbers of the compounds in these tables correspond to their numbers in Table 1. I. Tests in greenhouses. Paper cups, impregnated with paraffin, with a capacity of 200 cm, serve as vessels for cultivation, and clay from sandy soil, with approximately 1.5 wt.% Of aeregne, as a substrate. Seeds of test plants divided by species are sown superficially in them. Immediately thereafter, the active substance is applied (pre-emergence treatment). For this, it is suspended or emulsified in water and sprayed onto the surface of the soil with the help of thin nozzles. Before chemical treatment, the vessels are lightly irrigated in order for the product to come into contact with wet soil. After the addition is made, the sump is covered with a transparent plastic cap until the plants grow. This coating prevents the evaporation of water and easily volatile substances. At the same time, it contributes to the uniform germination of the test plants, if the latter are not exposed to the action of chemicals. During the post-emergence treatment, plants are allowed to grow, depending on their species, in vegetative vessels up to 3-10 cm and then treated. They are not covered. In accordance with the temperature required for the test plants, the tests are carried out in the cold part of the greenhouse (IC-ZO C) or in the warm part (18-30 C). Ishitani continue to 2.5 to 6 weeks. During this time, I take care of the plants and evaluate their response to individual treatments. The test substances of the consumption rate of the active substance in kg / ha in each case and the types of test plants are listed in Table 222. The assessment is made on the scale of OJU. At the same time, O means that there are no damages or shoots, they are normal, and 100 are completely killed, or not shoots II. Experiments on open ground. 1 sp (test about using a sprinkling device mounted on a carrier for spraying on separate cases. Mostly used are pre-sowing methods and a pre-emergence treatment method. For some tests, the effect exerted by the spray agent during the sprouting of cultivated and weed grasses, and in the post-emergence method - after the formation of several true LISIs. All tests were carried out for several months and at this time they were evaluated at various intervals x on a scale from 0 to 100. III. Herbicidal action through the vapor phase. Based on this significant herbicidal action of isoxazolyl methylthiolcarbamate, even if these substances are not applied to the soil, which is necessary with the known thiolcarbamate, it can be assumed that The losses of active substance due to evaporation of these compounds are very insignificant.To prove this superiority, the following tests were carried out: a delicate variety of cultivated oats is sown as described in section 1 and treated with herbicidal active and substances in different dosage. After that, however, the vessels are not covered with plastic caps, but placed in pairs in 5-liter cylinders. The vapors consist of one treated and one untreated vessel. Control cylinders are also prepared with untreated pots for comparison. To prevent the exchange of gases with the external environment, the edges of the cylinder are smeared with petroleum jelly and covered the openings with a glass plate. Easily evaporating active substances can thus volatilize the soil surfaces of the treated vessels into the cylinder space and affect the germination and development of the test plants in the initially free from the active vessels of the standing vessels. Tempeatura B of glass cylinders ranges from 11 ° C in the mornings to 30 ° C to – .rt g-purge 7668565 Effect on weeds in greenhouses at 8 Table 2 pre-emergence treatment

Приме чание; .-NyЫ-диэтил-З-(4-хлорбензил)тиолкарбамат -N, Ы-дипропил-5.-этйлтиолкарбамат , Уничтожение нежелательных растений и совместимость культурных растений по отнс иению к тиодкарбаматам в теплице при предвсходовом применении Т а б л и ц а 3Note; . -NyY-diethyl-3- (4-chlorobenzyl) thiol-carbamate-N, Y-dipropyl-5.-etyl-thiol carbamate, Destruction of undesirable plants and compatibility of cultivated plants in relation to thiodocarbamate in a greenhouse during pre-emergence T b b and c 3

Продолжение табл.3 ПримечаниContinued Table 3 Notes

Продолжение табл. 3 е -З-этилгексаметилениьданотиолкарбамат, , Ы-диизопропил-5-2, 3-дихлораллилтиолкарбамат.Continued table. 3 e-3-ethylhexamethylene yldanothiolcarbamate, N-diisopropyl-5-2, 3-dichloroallylthiolcarbamate

1313

Таблица 4Table 4

Пример гербицидного действи  изоксаэолилтиолкарбаматов при предвсхоловом и послевсходовом примемеиии в теплице П р и м An example of a herbicidal action of isoxaolylthiolcarbamate with pre-hollow and post-emergence primetium in a greenhouse.

6685651466856514

Таблица 5Table 5

Селективна  борьба с произрастанием сорных трав в культурах свеклы посредством различных тиолкарбаматов на открытом грунте при предпосевноЯ обработке е ч а н и е: А - предвсходо- Примечание: -N ,К-диизова  обработка; Б - после- ,- пропил-5-2,3,3-трихлораллилвсходова  обработка. тиолкарбамат Совместимость некоторых тиолкарбаматов по отношению к fpancy и пшенице летней на открытом грунте при предпосевной обработке Таблица 6Selective control of weed plants in beet cultures by means of various thiol-carbamates on open ground during pre-sowing treatment. Part: A - pre-emergence Note: -N, K-di-dize treatment; B - after-, propyl-5-2,3,3-trichloroallyl-seed treatment. thiol carbamate Compatibility of some thiol carbamate with respect to fpancy and summer wheat on open ground for presowing treatment Table 6

J5668565J5668565

Действие некоторых тиолкарбаматов от метода применени  по отношению открытом грунтеThe effect of some thiol carbamates on the method of application to open ground

Примечание. Метод применени : 1 - внесение в почву, перед посевом; II - предвсходова  обработка после посева; III - опрыскивание во врем  всходов; IV - послевсходова  обработка.Note. Method of application: 1 - introduction into the soil, before sowing; II - pre-emergence treatment after sowing; III - spraying during germination; IV - post-harvest processing.

Фитотоксичность паровой фазы некоторых тиолкарбаматов против культурного овса в модельном опытеPhytotoxicity of the vapor phase of some thiol-carbamates against cultured oats in a model experiment

Т T

ТаблицаTable

Селективное гербицидное действие в рисовых культурах при предвсходовом применении в теплицеSelective herbicidal action in rice crops with pre-emergence application in the greenhouse

Гербицидное действие и совместимость культурных растений по отношению к некоторым тиолкарбаматам в теплице . при довсходовом применении Примечание:Herbicidal action and compatibility of cultivated plants in relation to some thiol-carbamate in the greenhouse. for pre-emergence note:

Действие З-метил-5-изоксазолилметил-Ы ,Ы-диизопропилтиолкарбамата при предвсходовом применении без внесени  в почву на открытом грунтеEffect of 3-methyl-5-isoxazolylmethyl-S, L-diisopropylthiol carbamate in pre-emergence application without soil application on open ground

1818

668565668565

Т а б л и t; а 9T and b and t; a 9

ТаблицаTable

10 Ы-этил-Ы-циклогексил-З-этилтиолкарбамат, таблица 1110 S-ethyl-S-cyclohexyl-3-ethylthiolcarbamate, table 11

19nineteen

Гербицидкое действие и совместимость культурных растений с некоторыми тиапкарбаматами в теплице при послевсходовомHerbicidal action and compatibility of cultivated plants with some tiapcarbamates in a greenhouse with post-emergence

примененииapplication

Claims (3)

1. Патент ФРГ WH42464, 45 е 9/12, 1972.1. The patent of Germany WH42464, 45 e 9/12, 1972. кл с , .C with. 2.Патент Японии № 48-8812, кл. 30 F 371.221, 1973.2. Japanese Patent No. 48-8812, cl. 30 F 371.221,1973. 3.Патент СШЙ 3175897, кл. 71-2.6, 1965.3. The patent of US 3175897, cl. 71-2.6, 1965.
SU772504512A 1976-07-28 1977-07-25 Herbicide SU668565A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19762633790 DE2633790A1 (en) 1976-07-28 1976-07-28 ISOXAZOLYLMETHYLTHIOLCARBAMATE

Publications (1)

Publication Number Publication Date
SU668565A3 true SU668565A3 (en) 1979-06-15

Family

ID=5984086

Family Applications (1)

Application Number Title Priority Date Filing Date
SU772504512A SU668565A3 (en) 1976-07-28 1977-07-25 Herbicide

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JP (1) JPS5315369A (en)
AT (1) AT355862B (en)
AU (1) AU511197B2 (en)
BE (1) BE857260A (en)
BR (1) BR7704931A (en)
CA (1) CA1108133A (en)
CH (1) CH629080A5 (en)
DD (1) DD131068A5 (en)
DE (1) DE2633790A1 (en)
DK (1) DK145717C (en)
FR (1) FR2359833A1 (en)
GB (1) GB1581767A (en)
HU (1) HU177166B (en)
IE (1) IE45532B1 (en)
IL (1) IL52365A (en)
IT (1) IT1079363B (en)
NL (1) NL7707697A (en)
PL (1) PL102149B1 (en)
SU (1) SU668565A3 (en)
ZA (1) ZA774535B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2943965A1 (en) * 1979-10-31 1981-05-27 Basf Ag, 6700 Ludwigshafen 1,2-OXAZOLYLALKYLCARBAMATE, A METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS HERBICIDES

Also Published As

Publication number Publication date
DK145717B (en) 1983-02-07
IT1079363B (en) 1985-05-08
JPS5315369A (en) 1978-02-13
ZA774535B (en) 1978-07-26
NL7707697A (en) 1978-01-31
PL102149B1 (en) 1979-03-31
AT355862B (en) 1980-03-25
DE2633790A1 (en) 1978-02-02
GB1581767A (en) 1980-12-17
CA1108133A (en) 1981-09-01
IE45532B1 (en) 1982-09-22
BE857260A (en) 1978-01-30
IL52365A (en) 1980-07-31
AU511197B2 (en) 1980-07-31
FR2359833B1 (en) 1981-02-20
IL52365A0 (en) 1977-08-31
HU177166B (en) 1981-08-28
DK145717C (en) 1983-08-01
IE45532L (en) 1978-01-28
AU2633377A (en) 1979-01-04
CH629080A5 (en) 1982-04-15
DK338577A (en) 1978-01-29
ATA543077A (en) 1979-08-15
PL199854A1 (en) 1978-03-13
DD131068A5 (en) 1978-05-31
FR2359833A1 (en) 1978-02-24
BR7704931A (en) 1978-03-28

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