Chlorobutanol
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Names | |||
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IUPAC name
1,1,1-Trichloro-2-methylpropan-2-ol | |||
Other names
1,1,1-Trichloro-2-methyl-2-propanol; Chlorbutol; Chloreton; Chloretone; Chlortran; Trichloro-tert-butyl alcohol; 1,1,1-Trichloro-tert-butyl alcohol; 2-(Trichloromethyl)propan-2-ol, 1,1,1-trichloro-2-methyl-2-propanol; tert-Trichlorobutyl alcohol; Trichloro-tert-butanol; Trichlorisobutylalcohol; 2,2,2-Trichloro-1,1-dimethylethanol | |||
Identifiers | |||
3D model (JSmol) |
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ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.000.288 | ||
EC Number | 200-317-6 | ||
KEGG | |||
PubChem CID |
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UNII | |||
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Properties | |||
C4H7Cl3O | |||
Molar mass | 177.45 g·mol−1 | ||
Appearance | White solid | ||
Odor | Menthol | ||
Melting point | 95–99 °C (203–210 °F; 368–372 K) | ||
Boiling point | 167 °C (333 °F; 440 K) | ||
Slightly soluble | |||
Solubility in acetone | Soluble | ||
Pharmacology | |||
A04AD04 (WHO) | |||
Hazards | |||
Main hazards | Xn | ||
NFPA 704 | |||
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 | |||
Chlorobutanol (trichloro-2-methyl-2-propanol) is a preservative, sedative, hypnotic and weak local anesthetic similar in nature to chloral hydrate. It has antibacterial and antifungal properties. Chlorobutanol is typically used at a concentration of 0.5% where it lends long term stability to multi-ingredient formulations. However, it retains antimicrobial activity at 0.05% in water. Chlorobutanol has been used in anesthesia and euthanasia of invertebrates and fishes.[1][2] It is a white, volatile solid with a menthol-like odor.
Synthesis
Chlorobutanol is formed by the reaction of chloroform and acetone in the presence of potassium or sodium hydroxide.
Toxicity
Chlorobutanol is highly toxic to the liver, is a skin irritant and a severe eye irritant.[3]
Parthenogenesis
Chlorobutanol has proven effective at stimulating parthenogenesis in sea urchin eggs up to the pluteus stage, possibly by increasing irritability to cause stimulation. For the eggs of the fish Oryzias latipes, however, chlorobutanol only acted as an anesthetic.[4]
Pharmacology
It is an anesthetics with effects related to isoflurane and halothane.[5]
References
- ↑ W. N. McFarland & G. W. Klontz (1969). "Anesthesia in fishes". Federation Proceedings. 28 (4): 1535–1540. PMID 4894939.
- ↑ John E. Cooper (2011). "Anesthesia, analgesia, and euthanasia of invertebrates". ILAR Journal. 52 (2): 196–204. PMID 21709312.
- ↑ MSDS
- ↑ Embryologia 1956
- ↑ Nicholas P. Franks (2006). "Molecular targets underlying general anaesthesia". British Journal of Pharmacology. 147 Suppl 1: S72–S81. doi:10.1038/sj.bjp.0706441. PMC 1760740. PMID 16402123.