16650-11-6

Basic information

• Product Name: (2R,3S)-2,3-dichlorooxirane
• Synonyms: (2R,3S)-2,3-Dichlorooxirane; oxirane, 2,3-dichloro-, (2R,3S)-
• CAS NO: 16650-11-6
• Molecular Formula: C₂H₂Cl₂O
• Molecular Weight: 112.9427
• Mol File: 16650-11-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 139°C at 760 mmHg
• Flash Point: 153.2°C
• Density: 1.54g/cm³
• Vapor Pressure: 8.17mmHg at 25°C
• Refractive Index: 1.477
• CAS DataBase Reference: (2R,3S)-2,3-dichlorooxirane(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-2,3-dichlorooxirane(16650-11-6)
• EPA Substance Registry System: (2R,3S)-2,3-dichlorooxirane(16650-11-6)

Safety Data

• Hazardous Substances Data: 16650-11-6(Hazardous Substances Data)

Upstream product

• 156-60-5 trans-1,2-dichloroethylene 
• 156-59-2 cis-1,2-Dichloroethylene 

Relevant articles and documents

Cometabolism of cis-1,2-dichloroethene by aerobic cultures grown on vinyl chloride as the primary substrate.

An aerobic enrichment culture was grown on vinyl chloride (VC) as the sole source of carbon and energy. In the absence of VC, the enrichment culture cometabolized cis-1,2-dichloroethene (cDCE) and, to a lesser extent, trans1,2-dichloroethene (tDCE), beginning with oxidation to the corresponding DCE-epoxides. When provided with VC (1.3 mM) and cDCE (0.2-0.3 mM), the enrichment culture cometabolized repeated additions of cDCE for over 85 days. Cometabolism of repeated additions of tDCE was also demonstrated but at a lower ratio of nongrowth substrate to VC. VC-grown Pseudomonas aeruginosa MF1 (previously isolated from the enrichment culture) also readily cometabolizes cDCE, with an observed transformation capacity (Tc,obs) of 0.82 micromol of cDCE/mg of total suspended solids (TSS). When provided with VC and cDCE, MF1 did not begin cometabolizing cDCE until nearly all of the VC was consumed. The presence of cDCE reduces the maximum specific rate of VC utilization. A kinetic model was developed that describes these phenomena via Monod parameters for substrate and nongrowth substrate, plus inactivation and inhibition coefficients. MF1 did not show any cometabolic activity on tDCE or trichloroethene and very limited activity on 1,1-DCE (Tc,obs = 2 x 10(-5) micromol/mg TSS). Above 40 microM, tDCE and TCE noticeably increased the maximum specific rate of VC utilization, even though neither compound was consumed during or after VC consumption. High concentrations of 1,1-DCE (950 microM) completely inhibited VC biodegradation. As there is currently no evidence for aerobic biodegradation of cDCE as a sole source of carbon and energy, the results of this study provide a potential explanation for in situ disappearance of cDCE when the only other significant substrate available is VC. It is fortuitous that the VC-grown cultures tested exhibit their highest cometabolic activity toward cDCE, because it is the predominant DCE isomer formed during anaerobic reductive dechlorination of trichloroethene and tetrachloroethene.

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