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МЕТИДАТИОН

МЕТИДАТИОН структура
950-37-8
CAS №
950-37-8
Химическое название:
МЕТИДАТИОН
английское имя:
Methidathion
Синонимы:
DMTP;faat;sphat;oms844;NC2964;gs13005;hionate;OMS 844;Somonil;gs-13005
CBNumber:
CB4160797
Формула:
C6H11N2O4PS3
молекулярный вес:
302.33
MOL File:
950-37-8.mol

МЕТИДАТИОН атрибут

Температура плавления: 39-40°C
Температура кипения: 347.7±52.0 °C(Predicted)
плотность: 1.51 g/cm3
давление пара: 2.5×10-4 Pa (20 °C)
Fp: 100 °C
температура хранения: 0-6°C
растворимость: ДМСО (Мало растворим), метанол (Мало растворим)
пка: -4.17±0.40(Predicted)
форма: Твердый
цвет: Бесцветный
Растворимость в воде: 0,024 г/100 мл
БРН: 619915
Стабильность:: Чувствительный к воздуху, чувствительный к влаге
Справочник по базе данных CAS: 950-37-8(CAS DataBase Reference)
Рейтинг продуктов питания EWG: 9
FDA UNII: Y2P145U7KK
Справочник по химии NIST: Methidathion(950-37-8)
Система регистрации веществ EPA: Methidathion (950-37-8)
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
Коды опасности T+;N,N,T+
Заявления о рисках 21-28-50/53-41-26-24
Заявления о безопасности 22-28-36/37-45-60-61-39-26
РИДАДР UN 2811
WGK Германия 3
RTECS TE2100000
Класс опасности 6.1(a)
Группа упаковки II
Банк данных об опасных веществах 950-37-8(Hazardous Substances Data)
Токсичность LD50 in adult male, female rats (mg/kg): 31, 32 orally (Gaines, Linder)
символ(GHS) GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
сигнальное слово Danger
Заявление об опасности
пароль Заявление об опасности Класс опасности категория сигнальное слово пиктограмма предупреждение
H300+H310+H330 Смертельно при проглатывании, при контакте с кожей или при вдыхании.
H318 При попадании в глаза вызывает необратимые последствия. Серьезное повреждение/раздражение глаз Категория 1 Опасность GHS hazard pictograms P280, P305+P351+P338, P310
H410 Чрезвычайно токсично для водных организмов с долгосрочными последствиями. Опасность для водной среды, долгосрочная опасность Категория 1 Предупреждение GHS hazard pictograms P273, P391, P501
Внимание
P262 Избегать попадания в глаза, на кожу или одежду.
P273 Избегать попадания в окружающую среду.
P280 Использовать перчатки/ средства защиты глаз/ лица.
P302+P352+P310 ПРИ ПОПАДАНИИ НА КОЖУ: Промыть большим количеством воды. Немедленно обратиться за медицинской помощью.
P304+P340+P310 ПРИ ВДЫХАНИИ: Свежий воздух, покой. Немедленно обратиться за медицинской помощью.
P305+P351+P338 ПРИ ПОПАДАНИИ В ГЛАЗА: Осторожно промыть глаза водой в течение нескольких минут. Снять контактные линзы, если Вы ими пользуетесь и если это легко сделать. Продолжить промывание глаз.

МЕТИДАТИОН MSDS


Methidathion

МЕТИДАТИОН химические свойства, назначение, производство

Описание

Methidation is used as an insecticide. Cross-sensitivity was described to dichlorvos.

Химические свойства

Methidathion is a colorless crystalline pesticide at room temperature. It is sparingly soluble in water, but very soluble in octanol, ethanol, xylene, acetone, and cyclohexane. Methidathion is a non-systemic organophosphorous insecticide and acaricide with stomach and contact action. It is used to control a variety of insects and mites on crops and fruit plants. Methidathion is highly toxic to animals and humans. The US EPA grouped methidathion as a class I toxic substance and as an RUP.

Использование

Methidathion is an organophosphate insecticide and was examined for human health and toxicological concerns.

Общее описание

Methidathion is a colourless crystalline pesticide at room temperature. It is sparingly soluble in water but very soluble in octanol, ethanol, xylene, acetone, and cyclohexane.

Реакции воздуха и воды

Stable in neutral or weak acid solution. Hydrolyzed by alkali. [EPA, 1998].

Профиль реактивности

Organophosphates, such as Methidathion, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

Опасность

Toxic by ingestion, a cholinesterase inhibitor.

Угроза здоровью

Methidathion is poisonous to humans. Its toxic effects are by action on the nervous system. Human volunteers ingesting 0.11 mg/kg/day for 6 weeks had no clinical effects.

Пожароопасность

(Non-Specific -- Organophosphorus Pesticide, n.o.s.) Container may explode in heat of fire. Fire and runoff from fire control water may produce irritating or poisonous gases. Stable in neutral or weak acid solution. Hydrolyzed by alkali.

Сельскохозяйственное использование

Insecticide: A U.S. EPA restricted Use Pesticide (RUP). Not approved for use in EU countries . There are no residential uses for methidathion. Methidathion is a non-systemic organophosphate insecticide and acaricide with stomach and contact action. The compound is used to control a variety of insects and mites in many crops such as nuts, artichokes, olives, cotton, fruits, vegetables, tobacco, alfalfa, and sunflowers, and also in greenhouses and on rose cultures. It is especially useful against scale insects.

Торговое название

CIBA-GEIGY® GS 13005®; COBRACIDE®; FISONS NC® 2964; GEIGY® 13005; GS-13005®; SOMONIC®; SOMONIL®; SURPRACIDE®; SUPRATHION®; ULTRACID®; ULTRACIDE®

Контактные аллергены

Methidation is an organophosphorus compound used as an insecticide. Cross-sensitivity was described to Dichlorvos.

Профиль безопасности

Poison by ingestion and skin contact. Moderately toxic by inhalation. Human mutation data reported. Human systemic effects: coma, lachrymation, miosis. A severe eye irritant. An insecticide. When heated to decomposition it emits very toxic fumes of NOx, POx, and SOx

Канцерогенность

In a chronic toxicity/carcinogenicity study, rats were fed diets with 0, 4, 40, or 100 ppm methidathion (equivalent to 0, 0.16, 1.72, or 4.91 mg/kg/day (males) and 0, 0.22, 2.20, or 6.93 mg/kg/day (females)) for 2 years, and there was no evidence of carcinogenicity in either males or females . Body weight decreases occurred in both sexes at the highest dose throughout the study.

Экологическая судьба

Photolytic. When methidathion in an aqueous buffer solution (25°C and pH 7.0) was exposed to filtered UV light (l >290 nm) for 24 hours, 17% decomposed to 5-methoxy- 3H-1,3,4-thiadiazol-2-one. At 50°C, 56% was degraded after 24 hours. Degradation occurred via hydrolysis of the thiol bond of the phosphorodithioic ester. Under acidic and alkaline conditions, hydrolytic cleavage occurred at the C-S and P-S bonds, respectively (Burkhard and Guth, 1979). Smith et al. (1978) demonstrated that methidathion degraded to methidathion oxon at a faster rate in six air-dried soils than in moist soils. Half-lives for methidathion in the air-dried soils ranged from 19 to 110 days. In addition, methidathion degraded faster in an air-dried soil exposed to ozone (half-lives 2.5 to 7.0 days).
Chemical/Physical. Emits toxic fumes of phosphorus, nitrogen and sulfur oxides when heated to decomposition (Sax and Lewis, 1987). Methidathion oxon was also found in fogwater collected near Parlier, CA (Glotfelty et al., 1990). It was suggested

Метаболический путь

The main route of methidathion metabolism in animals and plants is via hydrolysis or oxidation (or hydrolysis of the oxon) to yield the 3- thiomethyl-5-methoxy-1,3,4-thiadiazoldee rivative. This may either lose methanethiol to yield the methoxy-1,3,4thiadiazolinone or be conjugated as the cysteine derivative via a route involving desmethylmethidathion (in plants). In plants and mammals an additional route involves the methylation of the thiomethyl methoxy-1,3,4-thiadiazolinone derivative by S-adenosylmethionine followed by oxidation to the corresponding sulfoxide and sulfone which are excreted in the urine in mammals. Another route of detoxification in insects, plants and mammals is via demethylation of the 5-methoxy group of the 1,3,4-thiadiazolinone ring to form a metabolite which may be conjugated in plants. As is common with many phosphorothioates, the active acetylcholinesterase inhibitor, methidaoxon, is usually detected in metabolism studies but at very low concentration due to its rapid rate of hydrolysis.

Метаболизм

The principal degradation route is similar both in animals and plants, that is, cleavage of the P?S bond via oxidative desulfuration (activation) to the oxon followed by hydrolysis to O,O-dimethyl hydrogen phosphorothioate and the 3-thiomethyl-5-methoxythiadiazole derivative, which is further degraded or conjugated. Methidathion is rapidly degraded in soil; DT50 in soil is 3–18 d.

Перевозки

Color code—Blue: Health Hazard/Poison: Store in a secure poison location. Prior to working with this chemical, personnel should be trained on its proper handling and storage. Store in tightly closed containers in a cool, wellventilated area

Утилизация отходов

Treat with strong alkali, mix with soil and bury in the case of small quantities. For large quantities, use incineration with effluent gas scrubbing

Меры предосторожности

Occupational workers should be very careful during use and chemical management of methidathion. As this chemical substance is a highly toxic pesticide, it has been grouped by the US EPA as toxicity class I. The containers and labels of the products should bear the signal word DANGER. Methidathion is an RUP, except for use in nurseries, and on saffl ower and sunfl owers.

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