Revision as of 20:35, 27 April 2007 edit217.198.224.168 (talk) lv: interwiki← Previous edit | Revision as of 21:21, 9 July 2007 edit undoChem-awb (talk | contribs)Bots12,956 edits Removed {{ChemicalSources}} as obsoleteNext edit → | ||
Line 40: | Line 40: | ||
* | * | ||
* Allyl alcohol from ] and ] in ], Coll. Vol. 1, p.42 (1941); Vol. 1, p.15 (1921). | * Allyl alcohol from ] and ] in ], Coll. Vol. 1, p.42 (1941); Vol. 1, p.15 (1921). | ||
{{ChemicalSources}} | |||
] | ] |
Revision as of 21:21, 9 July 2007
Allyl alcohol or 2-propen-1-ol is an organic compound with the formula CH2=CHCH2OH. It is a water soluble, colourless liquid with an ethanol like odour at low concentrations and a mustard-like pungent odour at higher concentration. Allyl alcohol is used as a pesticide and as a raw material for the production of many chemical compounds.
Allyl alcohol can be obtained by many methods: hydrolysis of allyl chloride, by oxidation of propylene oxide with potassium alum at high temperature, dehydrogenation of propanol, and the by reaction of glycerol and formic acid. Allyl alcohol is the smallest representative of the allylic alcohols. Allyl alcohols in general can be prepared by allylic oxidation of allyl compounds by for instance selenium dioxide.
Safety
The compound is toxic and flammable, see MSDS.
External links
- International Chemical Safety Card 0095
- NIOSH Pocket Guide to Chemical Hazards. "#0017". National Institute for Occupational Safety and Health (NIOSH).
- Institut national de recherche et de sécurité (2004). "Alcool allylique." Fiche toxicologique n° 156. Paris:INRS. (in French)
- State of Michigan public information on allyl alcohol
- Occupational exposure guidelines
- MSDS for allyl alcohol
- Datasheet regulatory information
- Allyl alcohol from glycerol and formic acid in Organic Syntheses, Coll. Vol. 1, p.42 (1941); Vol. 1, p.15 (1921). Online Article