Chloralose
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Names | |
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IUPAC name
(5ξ)-1,2-O-[2,2,2-Trichloroethylidene]-α-xylo-hexofuranose | |
Identifiers | |
15879-93-3 ![]() | |
85418 | |
ChEMBL | ChEMBL2104181 ![]() |
ChemSpider | 5414376 ![]() |
EC Number | 240-016-7 |
Jmol interactive 3D | Image |
KEGG | C18707 ![]() |
MeSH | Chloralose |
PubChem | 7057995 40467114 (2R,3aR,5R,6R)-6-hydroxy-2-methyl-furo-5-yl 27525 (2R,5R,6S,6aR)-6-hydroxy-2-methyl-furo-5-yl 16211632 (1R)-dioxol, (2R,5R,6S,6aR)-6-hydroxy-2-methyl-furo-5-yl 186624 (1R)-dioxol, (3aR,5R,6S,6aR)-6-hydroxy-furo-5-yl 2723807 (2R,3aR,5R,6S,6aR)-6-hydroxy-2-methyl-furo-5-yl 85991 |
RTECS number | FM9450000 |
UNII | 238BZ29MUE ![]() |
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Properties | |
C8H11Cl3O6 | |
Molar mass | 309.52 g·mol−1 |
Melting point | 176 to 182 °C (349 to 360 °F; 449 to 455 K) |
Hazards | |
Main hazards | Harmful if swallowed Harmful if inhaled |
EU classification (DSD) |
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R-phrases | R20/22 |
S-phrases | (S2) S16 S24/25 S28 |
Related compounds | |
Related compounds |
Chloral hydrate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Infobox references | |
Chloralose is an avicide, and a rodenticide used to kill mice in temperatures below 15 °C. It is also widely used in neuroscience and veterinary medicine as an anesthetic and sedative.[1]
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)
References
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