词条 | Propylene chlorohydrin |
释义 |
| ImageFile = 2-hydroxy-1-chloropropane.png | ImageSize = | ImageAlt = | PIN = 1-Chloropropan-2-ol | OtherNames = 1-Chloro-2-hydroxypropane |Section1={{Chembox Identifiers | CASNo = 127-00-4 (isomer: 78-89-7) | PubChem = 31370 | ChemSpiderID = 29103 | SMILES = CC(CCl)O | StdInChI = 1S/C3H7ClO/c1-3(5)2-4/h3,5H,2H2,1H3 | StdInChIKey = YYTSGNJTASLUOY-UHFFFAOYSA-N }} |Section2={{Chembox Properties | C = 3| H = 7| Cl = 1| O = 1 | MolarMass = 94.54 | Appearance = colorless liquid | Density = 1.1154 g/mL | MeltingPt = | BoilingPt = 127 | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}Propylene chlorohydrin usually refers to the organic compound with the formula CH3CH(OH)CH2Cl. A related compound, an isomer, is CH3CH(Cl)CH2OH. Both isomers are colorless liquids that are soluble in organic solvents. They are classified as chlorohydrins. Both are generated on a large scale as intermediates in the production of propylene oxide.[1] The reaction of aqueous solution of chlorine with propene gives a 10:1 ratio of CH3CH(OH)CH2Cl and CH3CH(Cl)CH2OH. These compounds are treated with lime to give propylene oxide, which is useful in the production of plastics and other polymers. References1. ^Gordon Y. T. Liu, W. Frank Richey, Joanne E. Betso, Brian Hughes, Joanna Klapacz, and Joerg Lindner "Chlorohydrins" in Ullmann's Encyclopedia of Industrial Chemistry, 2014, Wiley-VCH, Weinheim. {{DOI|10.1002/14356007.a06_565.pub2}} 2 : Organochlorides|Commodity chemicals |
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