Skip to Content
Merck
All Photos(3)

Key Documents

45340

Sigma-Aldrich

(±)-Epichlorohydrin

purum, ≥99% (GC)

Synonym(s):

(±)-2-(Chloromethyl)oxirane, 1-Chloro-2,3-epoxypropane

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C3H5ClO
CAS Number:
Molecular Weight:
92.52
Beilstein:
79785
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

3.2 (vs air)

Quality Level

vapor pressure

13.8 mmHg ( 21.1 °C)

grade

purum

Assay

≥99% (GC)

autoignition temp.

779 °F

expl. lim.

21 %

impurities

≤0.1% water

color

APHA: ≤20

refractive index

n20/D 1.438 (lit.)
n20/D 1.438

bp

115-117 °C (lit.)

mp

−57 °C (lit.)

density

1.183 g/mL at 25 °C (lit.)

application(s)

agriculture
environmental

storage temp.

room temp

SMILES string

ClCC1CO1

InChI

1S/C3H5ClO/c4-1-3-2-5-3/h3H,1-2H2

InChI key

BRLQWZUYTZBJKN-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

(±)-Epichlorohydrin is an organochlorine compound, used in the manufacturing of epoxy resins, plasticizers, dye stuffs, lubricants, pharmaceuticals, adhesives and oil emulsification products.

Application


  • Pitfalls in the synthesis of fluorescent methotrexate oligopeptide conjugates.: Addresses challenges in synthesizing fluorescent methotrexate conjugates using Fmoc-Lys(Boc)-OH, aiming to optimize peptide-based drug delivery systems (Sebestyén et al., 2016).

  • Fluoreometric behavior of a novel bis-acridine orange bound to double stranded DNA.: Explores the fluorescent properties of a bis-acridine compound integrated with Fmoc-Lys(Boc)-OH for potential applications in DNA interaction studies (Takenaka et al., 2003).

  • Bis-naphthalene diimide exhibiting an effective bis-threading intercalating ability.: Investigates a bis-naphthalene diimide derivative, facilitated by Fmoc-Lys(Boc)-OH, demonstrating significant DNA intercalation, useful for gene therapy and molecular biology research (Nojima et al., 2003).

  • Novel synthesis of a tetra-acridinyl peptide as a new DNA polyintercalator.: Details the synthesis of a new DNA polyintercalator using Fmoc-Lys(Boc)-OH, highlighting its potential to enhance molecular diagnostics and therapeutic strategies (Ueyama et al., 2000).



Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Carc. 1B - Eye Dam. 1 - Flam. Liq. 3 - Repr. 2 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

82.4 °F

Flash Point(C)

28 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Clinical Environmental Health and Toxic Exposures (2001)
Synthesis of (R)-and (S)-epichlorohydrin.
Baldwin JJ, et al.
The Journal of Organic Chemistry, 43(25), 4876-4878 (1978)
Preparation and characterization of water soluble high molecular weight ?-cyclodextrin-epichlorohydrin polymers.
Renard E, et al.
European Polymer Journal, 33(1), 49-57 (1997)
Study of the crosslinking reaction between epichlorohydrin and starch.
Kuniak L and Marchessault RH.
Starch/Staerke, 24(4), 110-116 (1972)
Xing Xu et al.
Journal of colloid and interface science, 440, 219-228 (2014-12-03)
Amine-impregnated cotton stalk (AICS) prepared by the reaction of cotton stalk with epichlorohydrin, pyridine and trimethylamine was used as the effective adsorbent for perchlorate removal. Solid-state (13)C NMR spectra, FT-IR, BET principle and element analysis provided evidence that amine groups

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service