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FENBUCONAZOLE
- русский язык имя
- английское имяFENBUCONAZOLE
- CAS №114369-43-6
- CBNumberCB7405237
- ФормулаC19H17ClN4
- мольный вес336.82
- EINECS406-140-2
- номер MDLMFCD01632336
- файл Mol114369-43-6.mol
химическое свойство
Температура плавления | 125.0℃ |
Температура кипения | 507.14°C (rough estimate) |
плотность | 1.1288 (rough estimate) |
давление пара | 5 x l0-6 Pa (20 °C) |
показатель преломления | 1.6110 (estimate) |
температура хранения | 0-6°C |
растворимость | Chloroform (Slightly), DMSO (Slightly) |
Растворимость в воде | 0.2 mg l-1 (25 °C) |
пка | 2.34±0.10(Predicted) |
БРН | 8333667 |
LogP | 3.79 at 20℃ |
FDA UNII | P9P3C2AL0Z |
Система регистрации веществ EPA | Fenbuconazole (114369-43-6) |
Пестициды Закон о свободе информации (FOIA) | Fenbuconazole |
UNSPSC Code | 41116107 |
NACRES | NA.24 |
Коды опасности | N |
Заявления о рисках | 50/53 |
Заявления о безопасности | 60-61 |
РИДАДР | UN 3077 9/PG 3 |
WGK Германия | 2 |
RTECS | XZ5257500 |
Токсичность | LD50 in rats (mg/kg): >2000 orally; >5000 dermally (Driant) |
рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
предупреждение
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вредная бумага
H410:Чрезвычайно токсично для водных организмов с долгосрочными последствиями.
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оператор предупредительных мер
P273:Избегать попадания в окружающую среду.
P391:Ликвидировать просыпания/проливы/утечки.
P501:Удалить содержимое/ контейнер на утвержденных станциях утилизации отходов.
FENBUCONAZOLE химические свойства, назначение, производство
Использование
Fenbuconazole is a conazole based fungicide used as a spray for the control of leaf spot, yellow and brown rust, powdery mildew and net blotch on wheat and barley and apple scab, pear scab and apple p owdery mildew on apples and pears.Метаболический путь
A number of sites in the fenbuconazole molecule are susceptible to enzymic attack. Consequently, a large variety of metabolites may be formed by oxidative attack on the phenolic rings or the aliphatic benzylic carbon atom adjacent to the 4-chlorophenyl ring. In mammals, oxidation at the benzylic carbon atom is an important pathway, which gives rise to the corresponding alcohol or ketone. This pathway also leads to lactone formation via hydrolysis of the nitrile group and elimination of a molecule of water. The alcohol may also form conjugates with glucuronic or sulfuric acid. Additional reactions in mammals involve hydroxylation of the phenolic rings.In plants, oxidation at the benzylic carbon is an important step to further metabolites and cleavage of the linkage to the triazole ring generates triazole, which is subsequently incorporated in a number of metabolic products. Information presented in this entry is based on the PSD Evaluation (PSD, 1995).
Деградация
Fenbuconazole is thermally stable up to 150 °C and there was no observed degradation when fenbuconazole was incubated in the dark in aqueous solutions at pH 5,7 and 9 for up to 30 days at 25 °C.When an aqueous solution of fenbuconazole (concentration 1.5μg ml-1, pH 7) was irradiated with a xenon arc lamp (filtered to remove wavelengths below 290 nm), the overall radioactivity was 105% of the original amount and the only compound detected was fenbuconazole.
FENBUCONAZOLE поставщик
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