?????? ????
|
|
?????? ???? ??
- ???
- 118-122°C
- ?? ?
- 60 °C
- ??
- 1.55
- ???
- 1.9 x 10-3 Pa (60 °C)
- ?? ??
- APPROX 4°C
- ???
- ?????(?? ???)
- ??? ??
- ??
- ??
- ???
- ???
- 28mg/l(20℃)
- Hydrolytic Sensitivity
- 7: reacts slowly with moisture/water
- Merck
- 14,9745
- CAS ??????
- 900-95-8(CAS DataBase Reference)
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
??? ?? | T+;N,N,T+ | ||
---|---|---|---|
?? ???? ?? | 24/25-26-37/38-40-41-48/23-50/53-63 | ||
????? | 26-28-36/37/39-45-60-61 | ||
????(UN No.) | 3146 | ||
RTECS ?? | WH6650000 | ||
TSCA | Yes | ||
?? ?? | 6.1 | ||
???? | III | ||
?? ?? ??? | 900-95-8(Hazardous Substances Data) | ||
?? | LD50 oral in rabbit: 30mg/kg | ||
???? ?? | KE-34748 | ||
?????? ??? | 97-1-138 | ||
?????? ??? | ??2-82 | ||
?? ? ???? | ????: ????; ???(??)????: ??? ?????? ? ? ??(??????? ??? ???? ????)? ? ? ??? 2% ?? ??? ??? |
????(GHS): | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
?? ?: | Danger | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
??·?? ??: |
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??????: |
|
?????? ???? C??? ??, ??, ??
??
Triphenyltin Acetate is an organotin compound. Triphenyltin Acetate much like its hydroxide analogue is used as a fungicide and antifeeding compound for insect control. Recent studies show that Triphenyltin Acetate may have adverse effects on the reproductive and immune systems and may disrupt the endocrine system.??
ChEBI: An organotin compound that is the O-acetyl derivative of triphenyltin hydroxide. A fungicide used to control blights on potatoes, leaf spot diseases on sugar beet and anthracnose on beans.?? ??
A white crystalline solid. Melting point 123-131°C (253-268°F). Used as a fungicide, algaecide and molluscicide. Controls early and late blight on potatoes.??? ?? ??
Slowly oxidized, hydrolyzed when exposed to air and moisture.?? ???
ACETOXYTRIPHENYLSTANNANE is subject to decomposition when exposed to air, light and moisture [EPA, 1998].????
Very toxic, irritant to skin.????
Avoid air, light and moisture.Safety Profile
Poison by ingestion, intraperitoneal, intravenous, and subcutaneous routes. Moderately toxic by skin contact. Questionable carcinogen with experimental neoplastigenic data. An experimental teratogen. Other experimental reproductive effects. A fungicide and algicide used as a wood preservative. When heated to decomposition it emits acrid smoke and Sn' fumes. See also TIN COMPOUNDS.?? ?? ??
Fentin is degraded in soil and other biological media to give inorganic tin via the di- and mono-phenyltin compounds; often the resulting benzene is liberated. An extensive review on the metabolism and fate and behaviour of triphenyltin and its degradation products was published by Bock (1981). Fentin hydroxide has been the subject of an evaluation by the Pesticide Safety Directorate of UK MAFF (PSD, 1990).?????? ???? ?? ?? ? ???
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???( 117)?? ??
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