CAS 67843-74-7

(S)-(+)-epichlorohydrin

Description:

(S)-(+)-epichlorohydrin is a chiral organic compound characterized by its three-membered epoxide ring, which contributes to its reactivity and utility in various chemical applications. It is a colorless to pale yellow liquid with a distinctive odor and is soluble in water and organic solvents. The compound is primarily used as an intermediate in the synthesis of epoxy resins, which are valued for their strong adhesive properties and chemical resistance. Additionally, (S)-(+)-epichlorohydrin serves as a building block in the production of pharmaceuticals and agrochemicals. Its chirality is significant in applications where stereochemistry plays a crucial role in biological activity. The compound is also known to be a potential irritant and should be handled with care, following appropriate safety protocols. Overall, (S)-(+)-epichlorohydrin is an important chemical in both industrial and research settings, with diverse applications stemming from its unique structural properties.

Formula: C₃H₅ClO

InChI: InChI=1/C3H5ClO/c4-1-3-2-5-3/h3H,1-2H2/t3-/m1/s1

InChI key: InChIKey=BRLQWZUYTZBJKN-GSVOUGTGSA-N

SMILES: C(Cl)[C@@H]1CO1

Synonyms:

• (+)-2-(Chloromethyl)oxirane
• (+)-Epichlorohydrin
• (2S)-2-(chloromethyl)oxirane
• (S)-(Chloromethyl)oxirane
• (S)-1-Chloro-2,3-epoxypropane
• (S)-2-Chloromethyloxirane
• (S)-Epichlorhydrin
• 2(S)-Epichlorohydrin
• Oxirane, (chloromethyl)-, (2S)-
• Oxirane, (chloromethyl)-, (S)-
• Oxirane, 2-(chloromethyl)-, (2S)-
• (S)-Epichlorohydrin
• (S)-Epichlorohydrin
• (S)-(+)Epichlorohydrin
• S(+)-2-(CHLOROMETHYL)OXIRANE
• G-CHLOROPROPYLENE OXIDE
• AKOS BBS-00004288
• 1-CHLORO-2,3-EPOXYPROPANE
• 3-CHLOROPROPYLENE OXIDE
• EPICHLOROHYDRINE
• (S)-(+)-CHLOROMETHYLOXIRANE
• CHLOROMETHYLOXIRANE
• 2,3-EPOXYPROPYL CHLORIDE
• ALPHA-EPICHLOROHYDRIN
• EPICHLORHYDRIN
• (S)-3-CHLOROPROPYLENE OXIDE

(S)-Epichlorohydrin

CAS: 67843-74-7

Formula: C₃H₅ClO

Purity: >98.0%(GC)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 92.52

Ref: 3B-E0533

(S)-(+)-Epichlorohydrin, 98+%

CAS: 67843-74-7

(S)-(+)-Epichlorohydrin is utilized for the synthesis of macquarimicins and hydroxyisoxazolidines and (+)-cis-sylvaticin, which is a potential antitumor agent. It is used to synthesize inhibitors of fatty acid oxidation as potential metabolic modulators. It acts as a solvent for natural and syntheti

Formula: C₃H₅ClO

Purity: 98+%

Color and Shape: Clear colorless, Liquid

Molecular weight: 92.52

Ref: 02-L14298

(2S)-2-(chloromethyl)oxirane

CAS: 67843-74-7

Formula: C₃H₅ClO

Purity: 98%

Color and Shape: Liquid

Molecular weight: 92.5242

Ref: IN-DA0032H3

(2S)-(+)-3-Chloro-1,2-propenoxide

CAS: 67843-74-7

(2S)-(+)-3-Chloro-1,2-propenoxide

Formula: C₃H₅ClO

Purity: ≥95%

Color and Shape: clear. almost colourless liquid

Molecular weight: 92.5242g/mol

Ref: 54-OR28971

(S)-(+)-Epichlorohydrin

CAS: 67843-74-7

Formula: C₃H₅ClO

Purity: 99.0%

Color and Shape: Liquid

Molecular weight: 92.52

Ref: 10-F023907

(S)-(+)-Epichlorohydrin - 96%

CAS: 67843-74-7

Formula: C₃H₅ClO

Purity: 96.0%

Molecular weight: 92.52

Ref: 10-F546508

Ornidazole Impurity 34 ((S)-Epichlorohydrin)

CAS: 67843-74-7

Formula: C₃H₅ClO

Molecular weight: 92.52

Ref: 4Z-O-1947

(S)-Epichlorohydrin

Controlled Product

CAS: 67843-74-7

Applications S-enantiomer of 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.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Romano, K.P. et al.: Chem. Res. Toxicol., 20, 832 (2007); Smyth, H.F., et al.: J. Ind. Hyg. Toxicol., 30, 63 (1948);

Formula: C₃H₅ClO

Color and Shape: Neat

Molecular weight: 92.52

Ref: TR-E582310

(S)-(+)-Epichlorohydrin

CAS: 67843-74-7

(S)-(+)-Epichlorohydrin is a chlorohydrin that is used as an industrial chemical. It can be synthesized by reacting benzyl chloride with sodium hydroxide in the presence of water. The reaction mechanism for this process involves nucleophilic addition of the chlorine atom to the carbonyl group, followed by protonation and elimination of hydrogen chloride. The stereoselective synthesis of (S)-(+)-epichlorohydrin is based on asymmetric induction by enantiomers of the reactant. This product has been shown to have a constant pressure kinetic study at 0.1 M in acetonitrile and 0.2 M in dichloromethane with a turnover number of 1.4 × 10 mol/L/s, which is comparable to other synthetic methods for epichlorohydrin. Pharmacokinetic data for this product has been shown to show good bioavailability in rats, with a half-life of 0.

Formula: C₃H₅ClO

Purity: Min. 95%

Color and Shape: Colorless Powder

Molecular weight: 92.52 g/mol

Ref: 3D-FE10798