Chloralose
From Self-sufficiency
Revision as of 03:07, 28 March 2010 by حسن علي البط (Talk) (Quick-adding category Acetals (using HotCat))
| Chloralose | |
|---|---|
| File:Chloralose.svg | |
| (5ξ)-1,2-O-[(1R)-2,2,2-trichloroethylidene]-α-D-xylo-hexofuranose | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 15879-93-3 |
| PubChem | 27525 |
| ChemSpider | 21442036 |
| SMILES | Script error: No such module "collapsible list". |
| InChI | Script error: No such module "collapsible list". |
| InChI key | OJYGBLRPYBAHRT-UQOKZTPDBF |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
| Molecular formula | C8H11Cl3O6 |
| Molar mass | 309.53 g mol−1 |
| Melting point |
176-182 °C |
| style="background: #F8EABA; text-align: center;" colspan="2" | Hazards | |
| R-phrases | R22 |
| S-phrases | (S1/2), S16, S24/25, S28 |
| style="background: #F8EABA; text-align: center;" colspan="2" | Related compounds | |
| Related compounds | Chloral hydrate |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
Chloralose is an avicide, rodenticide used to kill mice in temperatures below 15 °C, and bird repellent. It is also widely used in neuroscience and veterinary medicine as an anesthetic and sedative.
Chemically, it is a chlorinated acetal derivative of glucose.
It is listed in Annex I of Directive 67/548/EEC with the classification Harmful (Xn)
External links
- Data Sheet - including structural diagram
- European Chemicals Bureau
- Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
| 25px | This article about an organic halide is a stub. You can help ssf by expanding it. |
