Trimethyltin acetate
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| Names | |
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| IUPAC name
Trimethylstannyl acetate[1]
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| Other names | |
| Identifiers | |
3D model (JSmol)
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| ECHA InfoCard | Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). |
| E number | Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| CH 3COOSn(CH 3) 3 | |
| Molar mass | 222.859 g·mol−1 |
| Appearance | White crystalline solid |
| Melting point | 193 °C (379 °F; 466 K)[2] |
| Solubility | Sparingly soluble in chloroform and carbon tetrachloride. |
| Hazards | |
| Main hazards | Highly toxic |
| GHS pictograms | 
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| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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9 mg/kg (rat, oral) |
| Related compounds | |
Related compounds
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Trimethyltin acetate is an organotin compound with the chemical formula CH
3COOSn(CH
3)
3. It is a white crystalline solid. It is a poison.
Preparation
Trimethyltin acetate can be prepared by reaction between tetramethyltin and mercury(I) acetate in methanol at room temperature.[3]
Safety
Triorganyltin compounds, like trimethyltin acetate, are poisonous. They are highly toxic if swallowed and harmful in contact with skin. Cause serious skin and eye irritation. They can cause serious eye damage. Cause serious damages to organs and nerves. They are highly toxic to aquatic life, with long-lasting effects.[4][5]
References
- ↑ 1.0 1.1 1.2 1.3 "Trimethyltin acetate".
- ↑ "CAS Common Chemistry".
- ↑ Plazzogna, Gualtiero; Peruzzo, Valerio; Tagliavini, Giuseppe (1969). "A new method of preparing a soluble form of trimethyltin acetate". Journal of Organometallic Chemistry. 16 (3): 500–502. doi:10.1016/S0022-328X(00)89777-6. Retrieved 2026-01-05.
- ↑ https://www.rewe-group.com/content/uploads/2020/12/FS-Organotin-Compounds.pdf [bare URL PDF]
- ↑ Barbosa, Carolina Monteiro de Lemos; Ferrão, Fernanda Magalhães; Graceli, Jones B. (2018). "Organotin Compounds Toxicity: Focus on Kidney". Frontiers in Endocrinology. 9. doi:10.3389/fendo.2018.00256. PMC 5972511. PMID 29872423. Unknown parameter
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