Chloralose
Names | |
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IUPAC name
(5ξ)-1,2-O-[2,2,2-Trichloroethylidene]-α-xylo-hexofuranose | |
Identifiers | |
3D model (JSmol) |
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85418 | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.036.363 |
EC Number | 240-016-7 |
KEGG | |
MeSH | Chloralose |
PubChem CID |
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RTECS number | FM9450000 |
UNII | |
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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EU classification (DSD) (outdated) |
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R-phrases (outdated) | R20/22 |
S-phrases (outdated) | (S2) S16 S24/25 S28 |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). | |
Infobox references | |
Chloralose (also known as α-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)
Chloralose exerts barbiturate-like actions on synaptic transmission in the brain, including potent effects at inhibitory γ-aminobutyric acid type A (GABAA) receptors.[2][3] A structural isomer of chloralose, β-chloralose (also called parachloralose in older literature), is inactive as a GABAA modulator and also as a general anesthetic.[4]
References
- ↑ Silverman J, Muir WW (Jun 1993). "A review of laboratory animal anesthesia with chloral hydrate and chloralose". Lab Anim Sci. 43 (3): 210–6. PMID 8355479.
- ↑ R. A. Nicoll & J. M. Wojtowicz (1980). "The effects of pentobarbital and related compounds on frog motoneurons". Brain Research. 191 (1): 225–237. PMID 6247012.
- ↑ K. M. Garrett & J. Gan (1998). "Enhancement of gamma-aminobutyric acidA receptor activity by alpha-chloralose". The Journal of Pharmacology and Experimental Therapeutics. 285 (2): 680–686. PMID 9580613.
- ↑ M. D. Krasowski & N. L. Harrison (2000). "The actions of ether, alcohol and alkane general anaesthetics on GABAA and glycine receptors and the effects of TM2 and TM3 mutations". British Journal of Pharmacology. 129 (4): 731–743. doi:10.1038/sj.bjp.0703087. PMC 1571881. PMID 10683198.
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