Skip to Content
Merck
All Photos(3)

Key Documents

184489

Sigma-Aldrich

1,3-Dichloro-2-propanol

97%

Synonym(s):

Glycerol-α,γ-dichlorohydrin

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(ClCH2)2CHOH
CAS Number:
Molecular Weight:
128.99
Beilstein:
1732063
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.483 (lit.)

bp

174.3 °C (lit.)

mp

−4 °C (lit.)

solubility

water: soluble 10 part
alcohol: miscible
diethyl ether: miscible

density

1.363 g/mL at 20 °C
1.351 g/mL at 25 °C (lit.)

functional group

chloro

SMILES string

OC(CCl)CCl

InChI

1S/C3H6Cl2O/c4-1-3(6)2-5/h3,6H,1-2H2

InChI key

DEWLEGDTCGBNGU-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

1,3-Dichloro-2-propanol is a food processing contaminant. Biotransformation of 1,3-dichloro-2-propanol to epichlorohydrin by the whole cells of recombinant Escherichia coli via resin-based in situ product removal has been investigated.

1,3-Dichloro-2-propanol is used as a pharmaceutical intermediate and solvent for paints, lacquers, and epoxy resins.

Application

1,3-Dichloro-2-propanol can be used as a reactant to synthesize:
  • Hydroxyl-N-tosylcyclams via sodium ethoxide catalyzed cyclization reaction with di(poly)-N-tosylamides.
  • (R)-Epichlorohydrin using biocatalysts.
  • 1,3-dichloropropene, a soil fumigant, and synthetic glycerol.

It can also be used as an intermediate in the production of epoxy resins, as well as a solvent for hard resins and nitrocellulose.

Pictograms

Skull and crossbonesHealth hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Carc. 1B

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

186.8 °F - closed cup

Flash Point(C)

86 °C - closed cup

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

Customers Also Viewed

Role of mitogen-activated protein kinases and nuclear factor-kappa B in 1, 3-dichloro-2-propanol-induced hepatic injury
Lee In-Chul, et al.
Laboratory Animal Research, 32(1), 24-33 (2016)
Soy-based adhesives with 1, 3-dichloro-2-propanol as a curing agent
Rogers J, et al.
Wood and Fiber Science, 36(2), 186-194 (2004)
Shu-Ping Zou et al.
Biotechnology letters, 35(6), 937-942 (2013-02-23)
Biotransformation of 1,3-dichloro-2-propanol (DCP) to epichlorohydrin (ECH) by the whole cells of recombinant Escherichia coli expressing halohydrin dehalogenase was limited by product inhibition. To solve this problem and improve the ECH yield, a biotransformation strategy using resin-based in situ product
M D Nikolaki et al.
Journal of hazardous materials, 137(2), 1189-1196 (2006-05-19)
The photocatalytic oxidation of 1,3-dichloro-2-propanol (1,3-DCP) was studied by following the target compound degradation, the total organic carbon removal rate and by identifying the oxidation products. The reaction was performed in a batch recycle reactor, at room temperature, using UV
C Crews et al.
Food additives and contaminants, 20(10), 916-922 (2003-11-05)
The results of surveys to investigate the levels of 3-monochloropropane-1,2-diol (3-MCPD) and 1,3-dichloropropanol (1,3-DCP) in UK retail samples of soy sauces and similar products are reported. The products, sampled in 2000 and 2002, were analysed for 3-MCPD using an established

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