Date published: 2025-12-5

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(±)-Epichlorohydrin (CAS 106-89-8)

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Alternate Names:
(±)-2-(Chloromethyl)oxirane, 1-Chloro-2,3-epoxypropane
CAS Number:
106-89-8
Purity:
≥99%
Molecular Weight:
92.52
Molecular Formula:
C3H5ClO
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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(±)-Epichlorohydrin is an organic compound. This colorless liquid possesses a pungent odor and exhibits water miscibility. Due to its reactivity, (±)-Epichlorohydrin finds wide-ranging utility in synthesizing an array of products, including polymers, glycerol, and epoxy resins. It also serves as a valuable reagent in organic synthesis. The reactivity of (±)-Epichlorohydrin enables it to engage in diverse chemical reactions. It can undergo dehydration reactions with water, resulting in the formation of glycerol. Additionally, ECH reacts with ammonia to yield glycidol and interacts with alcohols to form epoxides. Furthermore, it partakes in reactions with amines, leading to the creation of amine oxides. These versatile reactions contribute to the compound′s broad utility.


(±)-Epichlorohydrin (CAS 106-89-8) References

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  2. DNA interstrand cross-linking by epichlorohydrin.  |  Romano, KP., et al. 2007. Chem Res Toxicol. 20: 832-8. PMID: 17441735
  3. Flocculation performance of epichlorohydrin-dimethylamine polyamine in treating dyeing wastewater.  |  Wang, Y., et al. 2009. J Environ Manage. 91: 423-31. PMID: 19781846
  4. [Determination of epichlorohydrin in drinking water by isotope dilution gas chromatography-mass spectrometry].  |  Huang, YY., et al. 2013. Zhonghua Yu Fang Yi Xue Za Zhi. 47: 455-8. PMID: 23958132
  5. Adsorption properties of cross-linked cellulose-epichlorohydrin polymers in aqueous solution.  |  Udoetok, IA., et al. 2016. Carbohydr Polym. 136: 329-40. PMID: 26572363
  6. Effect of epichlorohydrin on the wet spinning of carrageenan fibers under optimal parameter conditions.  |  Zhang, W., et al. 2016. Carbohydr Polym. 150: 232-40. PMID: 27312634
  7. Epichlorohydrin crosslinked carboxymethyl cellulose-ethylenediamine imprinted polymer for the selective uptake of Cr(VI).  |  Velempini, T., et al. 2017. Int J Biol Macromol. 101: 837-844. PMID: 28300589
  8. Polymerase bypass of N7-guanine monoadducts of cisplatin, diepoxybutane, and epichlorohydrin.  |  Ye, J., et al. 2018. Mutat Res. 809: 6-12. PMID: 29579534
  9. Biosynthesis of chiral epichlorohydrin using an immobilized halohydrin dehalogenase in aqueous and non-aqueous phase.  |  Zhang, XJ., et al. 2018. Bioresour Technol. 263: 483-490. PMID: 29775904
  10. Preparation and Uses of Chlorinated Glycerol Derivatives.  |  Canela-Xandri, A., et al. 2020. Molecules. 25: PMID: 32481583
  11. Epichlorohydrin and tripolyphosphate-crosslinked chitosan-kaolin composite for Auramine O dye removal from aqueous solutions: Experimental study and DFT calculations.  |  Şenol, ZM., et al. 2022. Int J Biol Macromol. 199: 318-330. PMID: 35026221
  12. Clinical Profile of Patients with Acute Epichlorohydrin Poisoning - An Observational Study.  |  Majumder, B., et al. 2022. J Assoc Physicians India. 70: 11-12. PMID: 35443545
  13. Spectral shift supported epichlorohydrin toxicity and the protective role of sage.  |  Çavuşoğlu, K. and Yalçin, E. 2023. Environ Sci Pollut Res Int. 30: 1374-1385. PMID: 35918582
  14. An evaluation of the genetic toxicity of epichlorohydrin. A report of an expert group of the International Commission for Protection against Environmental Mutagens and Carcinogens.  |  Srám, RJ., et al. 1981. Mutat Res. 87: 299-319. PMID: 7035932

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(±)-Epichlorohydrin, 1 ml

sc-239853
1 ml
$47.00