SU586819A3 - Insecticide - Google Patents
InsecticideInfo
- Publication number
- SU586819A3 SU586819A3 SU752149602A SU2149602A SU586819A3 SU 586819 A3 SU586819 A3 SU 586819A3 SU 752149602 A SU752149602 A SU 752149602A SU 2149602 A SU2149602 A SU 2149602A SU 586819 A3 SU586819 A3 SU 586819A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- active substance
- plants
- insecticide
- mortality
- insecticidal
- 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
- A01N37/00—Biocides, 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
- A01N37/44—Biocides, 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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
(54) ИНСЕКТИЦИДНОЕ СРЕДСТВО(54) INSECTICIDE MEANS
Изобретение относитс к химическим средствам защиты растений, а имен но к инсектицидным средствам на основе производных карбаминовой кислоты. Известно использование оксимов кар баматов, а именно 2-метилмеркаптоацетальдегид 0 ( Ы -метилкарбамоил)-окси ма. (Ланат) , flj , 2-этилмеркаптоацеталь дегид-0-( И -метилкарбамоил)-оксима tizj , а также 2-алкилмеркаптоацетальдегид-0- ( 1 -метилкарбамоил)-оксима i3J в качестве инсектицидов системного действи . Однако- известные соединени обла дают высокой токсичностью по отношени к теплокровным. С целью изыскани инсектицидных средств, обладающих высокой инсектицидной активностью и низкой токсич-., ностью дл теплокровных предлагаетс инсектицидное средство на основе про изводных метилкарбаминовой кислоты общей формулы R-S-e N-0-ci-N-S-N d-N d-S-B I 11 I I И I I бНз О Шз №j , -где fij - алкил с 1-5 атомами С, Содержание активно-действующего ещества всредстве составл ет 0,5-95,5 ec.%f остальное добавка. Предложенные соединени получают утем взаимодействи соединени общей ормулы S e- g-c -K o--c-TSH 1 ii 1 . СК5 о СИз где Ь имеет указанное значение, в присутствии основани с хлоридами серы. Средства обычно примен ютс в виде растворов, эмульсий, паст, порошков, готов т их известными методами - общи rипpи изготовлении препаративных форм пестицидов. Пример, Инсектицидное средство кишечного действи . Растени хлопчатника опрыскивают 0, водной эмульсией активного вещества (полученной из 10%-ного эмульгирующего концентрата) После подсыхани покрыти растени заражают личинкаг и Spodoptero uttorofis и Heftothis у|Ре2ОТ5|Процент смертности определ ют .через2,4,24 и 48 ч. В случае 100-ной смертгности через 48 ч растени снова -заражают свежим личинками и оценку смертности производ т через такие .жеThe invention relates to chemical plant protection agents, and specifically insecticidal agents based on carbamic acid derivatives. The use of carbamates' oximes, namely 2-methylmercaptoacetaldehyde 0 (S-methylcarbamoyl) -oxia max, is known. (Lanate), flj, 2-ethylmercaptoacetal dehyd-0- (And-methylcarbamoyl) -oxime tizj, as well as 2-alkylmercaptoacetaldehyde-0- (1-methylcarbamoyl) -oxime i3J as insecticides of systemic action. However, the known compounds are highly toxic to warm-blooded animals. For the purpose of searching for insecticidal agents with high insecticidal activity and low toxicity, warm-blooded insecticides are proposed based on methylcarbamic acid derivatives of the general formula RSe N-0-ci-NSN dN dSB I 11 II & II bN3 O Shz No.j , - where fij is alkyl with 1-5 C atoms, the active substance content of the medium is 0.5-95.5 ec.% f the rest is additive. The proposed compounds are obtained by reacting a compound of the general formula S e-g-c -K o-c-TSH 1 ii 1. CK5 of SIS where b has the indicated value, in the presence of a base with sulfur chlorides. Means are usually applied in the form of solutions, emulsions, pastes, powders, prepared by their known methods — the general process of making preparative forms of pesticides. Example, Insecticidal agent of intestinal action. Cotton plants are sprayed with 0, an aqueous emulsion of the active substance (obtained from a 10% emulsifying concentrate). After drying, the plants are infected with the larvae and Spodoptero uttorofis and Heftothis y | Fe2OT5 | The mortality rate is determined through 2,4,4,24 and 48 hours. After 100 hours, after 48 hours, the plants are again infected with fresh larvae and the mortality is estimated through such plants.
интервалы до 48ч. Если оп ть flOCTH-fгают 100%-ную смертность, то испытание повтор ют ещё через 8 дней. Опыт провид т при и 60%-ной относительной влажности воздуха. Результаты приведены в таблице.intervals up to 48 h. If the flOCTH is again 100% mortality, then the test is repeated after another 8 days. Experience provides with and 60% relative humidity. The results are shown in the table.
П р и м е р 2. Действие против Chile вup e5saUsPRI mme R 2. Action against Chile wup e5saUs
В пластмассовых гориочках выращивают по 6 рисовых ростков сорта Калоро таким образом, что их корнеёа система переплелась в виде диска. Корни погружают в раствор с 0,08%, 0,02%In plastic gorochki grow 6 rice shoots of the variety Caloro in such a way that their roots are intertwined in the form of a disk. The roots are immersed in a solution with 0.08%, 0.02%
и 0,01% активного вещества, которому затем дают стечь. Каждый грршочек заражают 5 личинками Chile dppre saLis и в него сажают растени . Процент смертности определ ют через 5 дней. Соединени 1-4 дают 100%-ную смертность при всех трех концентраци хand 0.01% of the active substance, which is then allowed to drain. Each group is infected with 5 Chile dppre saLis larvae and plants are planted in it. The mortality rate is determined after 5 days. Compounds 1-4 give 100% mortality at all three concentrations.
П р и м е р 3. Сравнение токсичности (ЛЛ) предложенных и известных соединений дл крыс в дозе, мг/кг Соединение № 1 300 № 2 320 № 3 17-24 № 4 15 , Фомину л а изобретени Инсектицидное средство, содержащее производные метилкарбаминовой кислоты как активное вещество, а также добавку, выбранную из группы - раство ритель, диспер атор, эмульгатор, о тличающеес тем, что, с целью усилени инсектицидной активности и уменьшени токсичности дл теплокро ных, оно содержит в качестве производ ного метилкарбаминовой кислоты соединение общей формулы ft-S-C«N-0-C-N-S-N - 0-N 3-S-R I где - алкил с 1-5 атомами углерода , причем содержание активно действующего вещества в средстве составл ет 0,5-95,5 вес.%. Источники информации, прин тые во внимание при экспертизе; 1.Мельников Н. Н. Хими и технологи пестицидов. М., Хими ,1974, с. 318., 2.Патент Франции 1521784, кл. С U7 С, 1968. 3. Патент СССР 275896, кл. А 01 Я ,9/20, 1966,Example 3: Comparison of Toxicity (LL) of Proposed and Known Compounds for Rats at a dose, mg / kg Compound No. 1 300 No. 2 320 No. 3 17-24 No. 4 15, Fominu of the Invention Insecticide containing derivatives methylcarbamic acid as an active substance, as well as an additive selected from the group of: solvent, dispersion, emulsifier, which, in order to enhance the insecticidal activity and reduce toxicity for heat energy, it contains as a derivative of methylcarbamic acid Formulas ft-SC "N-0-CNSN - 0 -N 3-S-R I where is alkyl with 1-5 carbon atoms, and the content of the active substance in the medium is 0.5-95.5 wt.%. Sources of information taken into account in the examination; 1.Melnikov N.N. Chemistry and pesticide technology. M., Himi, 1974, p. 318., 2. The patent of France 1521784, cl. C U7 C, 1968. 3. Patent of the USSR 275896, cl. A 01 I, 9/20, 1966,
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH960874A CH596757A5 (en) | 1974-07-11 | 1974-07-11 | N,N'-thiobis(O-(1-alkylthioethylimino)-N-methyl-carbamates) |
Publications (1)
Publication Number | Publication Date |
---|---|
SU586819A3 true SU586819A3 (en) | 1977-12-30 |
Family
ID=4353757
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU752149602A SU586819A3 (en) | 1974-07-11 | 1975-07-02 | Insecticide |
Country Status (6)
Country | Link |
---|---|
BE (1) | BE831212A (en) |
CH (1) | CH596757A5 (en) |
DO (1) | DOP1977002600A (en) |
GT (1) | GT198065796A (en) |
SU (1) | SU586819A3 (en) |
ZA (1) | ZA754421B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4382957A (en) | 1975-12-01 | 1983-05-10 | Union Carbide Corporation | Symmetrical insecticidal bis-carbamate compounds |
-
1974
- 1974-07-11 CH CH960874A patent/CH596757A5/en not_active IP Right Cessation
-
1975
- 1975-07-02 SU SU752149602A patent/SU586819A3/en active
- 1975-07-10 ZA ZA00754421A patent/ZA754421B/en unknown
- 1975-07-10 BE BE158162A patent/BE831212A/en not_active IP Right Cessation
-
1977
- 1977-09-02 DO DO1977002600A patent/DOP1977002600A/en unknown
-
1980
- 1980-10-13 GT GT198065796A patent/GT198065796A/en unknown
Also Published As
Publication number | Publication date |
---|---|
DOP1977002600A (en) | 1989-06-09 |
CH596757A5 (en) | 1978-03-15 |
ZA754421B (en) | 1976-06-30 |
BE831212A (en) | 1976-01-12 |
GT198065796A (en) | 1982-04-06 |
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