| | Identification | More |  | [Name] 
 (S)-(+)-Epichlorohydrin
 |  | [CAS] 
 67843-74-7
 |  | [Synonyms] 
 1-CHLORO-2,3-EPOXYPROPANE
 2,3-EPOXYPROPYL CHLORIDE
 (+/-)-2-(CHLOROMETHYL)OXIRANE
 2-(CHLOROMETHYL)OXIRANE
 3-Chloro-1,2-epoxypropane
 3-CHLOROPROPYLENE OXIDE
 AKOS BBS-00004288
 ALPHA-EPICHLOROHYDRIN
 CHLOROMETHYLOXIRANE
 EPICHLORHYDRIN
 (+/-)-EPICHLOROHYDRIN
 EPICHLOROHYDRIN
 EPICHLOROHYDRINE
 G-CHLOROPROPYLENE OXIDE
 OXIRANE, (CHLOROMETHYL)-, (2S)-
 (S)-(+)-1-CHLORO-2,3-EPOXYPROPANE
 (S)-1-CHLORO-2,3-EPOXYPROPANE
 S(+)-2-(CHLOROMETHYL)OXIRANE
 (S)-3-CHLOROPROPYLENE OXIDE
 (S)-(+)-CHLOROMETHYLOXIRANE
 |  | [EINECS(EC#)] 
 203-439-8
 |  | [Molecular Formula] 
 C3H5ClO
 |  | [MDL Number] 
 MFCD00005132
 |  | [Molecular Weight] 
 92.52
 |  | [MOL File] 
 67843-74-7.mol
 | 
 | Chemical Properties | Back Directory |  | [Appearance] 
 Colorless to light yellow liqui
 |  | [Melting point ] 
 −57 °C(lit.)
 
 |  | [alpha ] 
 34 º (589nm, c=1, MeOH)
 |  | [Boiling point ] 
 92-93 °C360 mm Hg(lit.)
 
 |  | [density ] 
 1.183 g/mL at 25 °C(lit.)
 
 |  | [vapor density ] 
 3.2 (vs air)
 
 |  | [vapor pressure ] 
 13.8 mm Hg ( 21.1 °C)
 
 |  | [refractive index ] 
 n20/D 1.438(lit.)
 
 |  | [Fp ] 
 93 °F
 
 |  | [storage temp. ] 
 2-8°C
 
 |  | [solubility ] 
 Chloroform, Methanol (Slightly)
 |  | [form ] 
 Liquid
 |  | [color ] 
 Clear colorless to very pale yellow
 |  | [explosive limit] 
 21%
 |  | [Optical Rotation] 
 [α]20/D +35°, c = 1 in methanol
 |  | [Water Solubility ] 
 insoluble
 |  | [BRN ] 
 1420784
 |  | [Dielectric constant] 
 22.9(20℃)
 |  | [CAS DataBase Reference] 
 67843-74-7(CAS DataBase Reference)
 | 
 | Safety Data | Back Directory |  | [Hazard Codes ] 
 T
 |  | [Risk Statements ] 
 R45:May cause cancer.
 R10:Flammable.
 R23/24/25:Toxic by inhalation, in contact with skin and if swallowed .
 R34:Causes burns.
 R43:May cause sensitization by skin contact.
 |  | [Safety Statements ] 
 S53:Avoid exposure-obtain special instruction before use .
 S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
 |  | [RIDADR ] 
 UN 2023 6.1/PG 2
 
 |  | [WGK Germany ] 
 3
 
 |  | [RTECS ] 
 TX4900000
 
 |  | [Autoignition Temperature] 
 1421 °F
 |  | [HazardClass ] 
 6.1
 |  | [PackingGroup ] 
 II
 |  | [HS Code ] 
 29103000
 | 
 | Hazard Information | Back Directory |  | [Chemical Properties] 
 Colorless to light yellow liqui
 |  | [Uses] 
 S-enantiomer of Epichlorohydrin, (S)-Epichlorohydrin), an important industrial chemical, is a bifunctional alkylating agent with the potential to form DNA cross-links. It is used as a solvent for natural and synthetic resins, gums, cellulose esters and ethers, paints, varnishes, nail enamels and lacquers, cement for Celluloid. Also, it is used as stabilizer.
 |  | [Definition] 
 ChEBI: (S)-epichlorohydrin is an epichlorohydrin. It is functionally related to a (R)-1,2-epoxypropane. It is an enantiomer of a (R)-epichlorohydrin.
 |  | [Synthesis] 
 
 The general procedure for the synthesis of (S)-(+)-epichlorohydrin from 1-chloro-2,3-epoxypropane is as follows: first, 463 kg of racemic epichlorohydrin was mixed with 19.2 kg of the catalyst [(1-RR)-(dibenzoyl-LLA)] made from Example 1 of the Preparation and the mixture was cooled to 5 °C. Subsequently, 49.5 kg of water was slowly added and the reaction continued at 20°C for 7 hours. Upon completion of the reaction, the reaction mixture was subjected to reduced-pressure thin-film evaporation at less than 30 °C to afford 190 kg of (S)-epichlorohydrin with an optical purity of 99.8% ee and a yield of 82%. The above reaction process was repeated by adding new racemic epichlorohydrin and water to the evaporated residue to again obtain (S)-epichlorohydrin with an optical purity of more than 99.0%ee. |  | [References] 
 [1] Patent: WO2008/153280,  2008,  A1. Location in patent: Page/Page column 41
 [2] Patent: WO2008/153280,  2008,  A1. Location in patent: Page/Page column 28
 [3] Tetrahedron Asymmetry,  2003,  vol. 14,  # 22,  p. 3633 - 3638
 [4] Journal of the American Chemical Society,  1995,  vol. 117,  # 21,  p. 5897 - 5898
 [5] Journal of the American Chemical Society,  1999,  vol. 121,  # 17,  p. 4147 - 4154
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