Chemistry:Propylene chlorohydrin
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Names | |
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Preferred IUPAC name
1-Chloropropan-2-ol | |
Other names
1-Chloro-2-hydroxypropane
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
EC Number |
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PubChem CID
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UNII | |
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Properties | |
C3H7ClO | |
Molar mass | 94.54 |
Appearance | colorless liquid |
Density | 1.1154 g/mL |
Boiling point | 127°C |
Hazards | |
GHS pictograms | ![]() ![]() |
GHS Signal word | Warning |
H226, H302, H315, H319, H332, H335 | |
P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P280, P301+312, P302+352, P303+361+353, P304+312, P304+340, P305+351+338, P312, P321, P330, P332+313, P337+313, P362, P370+378, P403+233 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
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.
References
- ↑ 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
![]() | Original source: https://en.wikipedia.org/wiki/Propylene chlorohydrin.
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