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Абамектин
- английское имяAbamectin
- CAS №71751-41-2
- CBNumberCB2258634
- ФормулаC49H74O14
- мольный вес887.11
- EINECS200-096-6
- номер MDLMFCD28010814
- файл Mol71751-41-2.mol
Температура плавления | 150-155°C |
альфа | D +55.7 ±2° (c = 0.87 in CHCl3) |
Температура кипения | 717.52°C (rough estimate) |
плотность | 1.16 |
давление пара | <2 x 10-7 Pa |
показатель преломления | 1.6130 (estimate) |
Fp | 150 °C |
температура хранения | Sealed in dry,Store in freezer, under -20°C |
растворимость | Soluble in DMSO |
форма | Solid |
Растворимость в воде | 0.007-0.01 mg l-1 (20 °C) |
цвет | White to off-white |
Мерк | 13,2 |
ИнЧИКей | GVWIWZFXCGTSLL-MSTMYQEVSA-N |
Справочник по базе данных CAS | 71751-41-2(CAS DataBase Reference) |
Рейтинг продуктов питания EWG | 1 |
FDA UNII | 5U8924T11H |
Предложение 65 Список | Avermectin B1 (Abamectin) |
Пестициды Закон о свободе информации (FOIA) | Abamectin |
Система регистрации веществ EPA | Abamectin (71751-41-2) |
UNSPSC Code | 41116107 |
NACRES | NA.24 |
Коды опасности | T+,N | |||||||||
Заявления о рисках | 20-28-50 | |||||||||
Заявления о безопасности | 36/37/39-45-60-61 | |||||||||
РИДАДР | 2588 | |||||||||
WGK Германия | 3 | |||||||||
RTECS | CL1203000 | |||||||||
Класс опасности | 6.1(a) | |||||||||
Группа упаковки | II | |||||||||
Банк данных об опасных веществах | 71751-41-2(Hazardous Substances Data) | |||||||||
Токсичность | LD50 (technical grade) orally in sesame oil in mouse, rat: 13.5, 10.0 mg/kg; dermally in rabbit: >2000 mg/kg; LD50 in mallard duck, bobwhite quail: 84.6, >2000 mg/kg; LC50 (96 hr) in rainbow trout, bluegill: 3.6, 9.6 mg/l; LC50 (48 hr) in Daphnia magna: 0.34 mg/l (Merck Technical Data Sheet) | |||||||||
NFPA 704: |
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рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
опасность
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вредная бумага
H410:Чрезвычайно токсично для водных организмов с долгосрочными последствиями.
H300:Смертельно при проглатывании.
H332:Вредно при вдыхании.
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оператор предупредительных мер
P261:Избегать вдыхания пыли/ дыма/ газа/ тумана/ паров/ аэрозолей.
P264:После работы тщательно вымыть кожу.
P270:При использовании продукции не курить, не пить, не принимать пищу.
P273:Избегать попадания в окружающую среду.
P301+P310:ПРИ ПРОГЛАТЫВАНИИ: Немедленно обратиться за медицинской помощью. Прополоскать рот.
P304+P340+P312:ПРИ ВДЫХАНИИ: Свежий воздух, покой. Обратиться за медицинской помощью при плохом самочувствии.
Абамектин химические свойства, назначение, производство
Химические свойства
Abamectin is a colorless to yellowish crystalline powder. It is soluble in acetone, methanol, toluene, chloroform, and ethanol, but insoluble in water. It is stable, and incompatible with strong oxidizing agents. Abamectin is a mixture of Abamectins containing about 80% Abamectin B1a and 20% Abamectin B1b. These two components, B1a and B1b, have very similar biological and toxicological properties. The Abamectins are insecticidal/miticidal compounds derived from the soil bacterium Streptomyces avermitilis. Abamectin is used to control insect and mite pests of citrus, pear, and nut tree crops, and is used by homeown- ers to control fi re ants. It acts on the nervous system of insects, causing paralyzing effects. Abamectin is a general use pesticide (GUP). It is grouped as toxicity class IV, meaning practically non-toxic, requiring no precautionary statement on its labelИспользование
Mixture of Abamectins, containing at least 80% of Abamectin B1a (C48H72O14) and not more than 20% of Abamectin B1b (C47H70O14). Used as acaricide, insecticideОпределение
Any of a group of broad spectrum antiparasitic antibiotics produced by the actinomycete, Streptomyces avermitilis.Общее описание
Odorless off-white to yellow crystals from methanol. Does not hydrolyze in water at pH 3, 5, 7. Used as an acaricide and insecticide.Профиль реактивности
A lactone.Опасность
A poison by ingestion. Moderately toxic by inhalation and skin contact.Угроза здоровью
Abamectin is an insecticide and miticide. It is very toxic and causes adverse health effects if swallowed and/or inhaled. Emulsifi able concentrate formulations of Abamectin cause slight to moderate eye irritation and mild skin irritation. The symptoms of poisoning observed in laboratory animals include pupil dilation, vomiting, convulsions and/or trem- ors, and coma. Abamectin acts on insects by interfering with the nervous system. At very high doses, laboratory mammals develop symptoms of nervous system depression, inco- ordination, tremors, lethargy, excitation, and pupil dilation. Very high doses have caused death from respiratory failure in animals. Additionally, Abamectin has been reported to cause reproductive effects. Abamectin blocks the nerval conduct system in insects, caus- ing paralysis and death. Laboratory studies have indicated that abamectin may affect the nervous system in experimental animals. A 1-year study with dogs given oral doses of abamectin (0.5 and 1 mg/kg/day) caused adverse health effects, such as pupil dilation, weight loss, lethargy, tremors, and recumbency.Сельскохозяйственное использование
Acaricide, Miticide, Insecticide, Anthelmentic: Used on fruit, vegetable and ornamental crops; pears, citrus fruits, and nut crops; to control mite and insect pests, and also to control household and lawn insects, including fire ants. Approved by the EPA for use in ash trees for control of emerald ash borer. A U.S. EPA restricted Use Pesticide (RUP).Торговое название
ABACIDE®; AFFIRM®; AVID®, AVID-EC®; AVOMEC®; DYNAMEC®; INJECT-A- CIDE AV®; MK 936®(B 1A ); BOVITIN®; DORATECT®; DUOMECTIN®; DUOTIN®; ENDECTO®; ENZEC®; L 676,863® (B 1A ); MK 0936®; MK 936®; PARAFOIL®; VERTIMEC®, VERTIMIL®; VIVID®; ZECTIN®; ZEPHEYR®; ZEPHYR®Метаболический путь
Abamectin contains the closely related avermectin B1a and B1b as the active ingredients. Avermectin B1a contains a sec-butyl moiety whereas avermectin B1b contains an isopropyl moiety. Chemical degradation and metabolism studies were conducted with avermectin B1a radiolabelled with 3H or 14C at various positions of this large molecule. The overall fates of avermectin B1a and B1b are similar since transformations at the butyl or propyl moiety were not observed.Avermectin B1a is stable to hydrolytic degradation, but it is readily degraded to numerous products in aqueous solutions, soil, glass and plant foliage/fruit surfaces after light irradiation. Isomerisation and O-demethylation appear to the primary degradation reactions. In addition, hydroxylation is a major metabolic reaction in animals. Significant amounts of the residues in plants and animals were characterised as unidentified polar components.
Меры предосторожности
During use of Abamectin, occupational workers should use safety glasses, gloves, and protective clothing to prevent prolonged skin contact, and work in good ventilation.Абамектин запасные части и сырье
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