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185744

Sigma-Aldrich

2-Chloroethanol

99%

Synonym(s):

Ethylene chlorohydrin

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About This Item

Linear Formula:
ClCH2CH2OH
CAS Number:
Molecular Weight:
80.51
Beilstein:
878139
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

2.78 (vs air)

Quality Level

vapor pressure

5 mmHg ( 20 °C)

Assay

99%

form

liquid

autoignition temp.

797 °F

expl. lim.

16 %

refractive index

n20/D 1.441 (lit.)

bp

129 °C (lit.)

mp

−89 °C (lit.)

solubility

alcohol: miscible
water: miscible

density

1.201 g/mL at 25 °C (lit.)

SMILES string

OCCCl

InChI

1S/C2H5ClO/c3-1-2-4/h4H,1-2H2

InChI key

SZIFAVKTNFCBPC-UHFFFAOYSA-N

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General description

2-Chloroethanol is a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Photodissociation of 2-chloroethanol in a molecular beam at 193nm has been investigated. It is widely used as an industrial solvent.

Application

2-Chloroethanol was used in the synthesis of the polyethylene terepthalate model substrate, bis(benzoyloxyethyl)terephthalate.

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

131.0 °F - closed cup

Flash Point(C)

55 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Photodissociation of 2-bromoethanol and 2-chloroethanol at 193 nm.
Hintsa EJ, et al.
J. Chem. Phys. , 92(4), 2280-2286 (1990)
Stereoregular poly(methyl methacrylate) with double-clickable ?-end: synthesis and click reaction
Y Kohsaka, et al.
Polymer Chemistry: Introduction to an Indispensable Science, 6, 3601-3607 (2015)
Bacterial degradation of 2-chloroethanol proceeds via 2-chloroacetic acid.
Stucki G and Leisinger T.
FEMS Microbiology Letters, 16(1), 123-126 (1983)
New enzymes with potential for PET surface modification.
Fischer-Colbrie G, et al.
Biocatalysis and Biotransformation, 22(5-6), 341-346 (2004)
Apryl Bronley-DeLancey et al.
Environmental health perspectives, 114(8), 1237-1242 (2006-08-03)
Trichloroethylene (TCE) is a suspected human carcinogen and a common groundwater contaminant. Chloral hydrate (CH) is the major metabolite of TCE formed in the liver by cytochrome P450 2E1. CH is metabolized to the hepatocarcinogen trichloroacetate (TCA) by aldehyde dehydrogenase

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