240699
Epichlorohydrin
≥99%
Synonym(s):
(±)-Epichlorohydrin, (±)-2-(Chloromethyl)oxirane, 1-Chloro-2,3-epoxypropane
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About This Item
Empirical Formula (Hill Notation):
C3H5ClO
CAS Number:
Molecular Weight:
92.52
EC Number:
203-439-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
79785
MDL number:
InChI key
BRLQWZUYTZBJKN-UHFFFAOYSA-N
InChI
1S/C3H5ClO/c4-1-3-2-5-3/h3H,1-2H2
SMILES string
ClCC1CO1
vapor density
3.2 (vs air)
vapor pressure
13.8 mmHg ( 21.1 °C)
assay
≥99%
autoignition temp.
779 °F
expl. lim.
21 %
bp
115-117 °C (lit.)
mp
−57 °C (lit.)
density
1.183 g/mL at 25 °C (lit.)
Application
Employed in the preparation of polyglycidyl ethers and as a cross-linking agent for polymers.
Used in the synthesis of a branched heptaglycerol dendrimer.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Carc. 1B - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - Skin Sens. 1
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
82.4 °F
flash_point_c
28 °C
Regulatory Information
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Chromatographia, 37, 603-603 (1993)
Synlett, 2091-2091 (2007)
Synthesis, 487-487 (1993)
Swetha Inturi et al.
ACS nano, 9(11), 10758-10768 (2015-10-22)
Notwithstanding rapid advances of nanotechnology in diagnostic imaging and drug delivery, the engineered nanocarriers still exhibit substantial lack of hemocompatibility. Thus, when injected systemically, nanoparticles are avidly recognized by blood leukocytes and platelets, but the mechanisms of immune recognition are
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.
R J Srám et al.
Mutation research, 87(3), 299-319 (1981-11-01)
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