Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

36295

Sigma-Aldrich

2,3-Dichloro-1-propanol

≥97.0% (GC)

Synonym(s):

Glycerol-α,β-dichlorohydrin

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
ClCH2CHClCH2OH
CAS Number:
616-23-9
Molecular Weight:
128.99
Beilstein:
1732060
EC Number:
210-470-0
MDL number:
MFCD00040446
UNSPSC Code:
12352100
PubChem Substance ID:
57649508
NACRES:
NA.22
Pricing and availability is not currently available.

Assay

≥97.0% (GC)

density

1.360 g/mL at 20 °C (lit.)

functional group

chloro
hydroxyl

SMILES string

OCC(Cl)CCl

InChI

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

InChI key

ZXCYIJGIGSDJQQ-UHFFFAOYSA-N

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
184489292087189316
2,3-Dichloro-1-propanol ≥97.0% (GC)

36295

2,3-Dichloro-1-propanol

1,3-Dichloro-2-propanol 97%

184489

1,3-Dichloro-2-propanol

1-Chloro-2-propanol 70%

292087

1-Chloro-2-propanol

3-Chloro-2,2-dimethyl-1-propanol 99%

189316

3-Chloro-2,2-dimethyl-1-propanol

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

100

density

1.360 g/mL at 20 °C (lit.)

density

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

density

1.111 g/mL at 25 °C (lit.)

density

-

functional group

chloro

functional group

chloro, hydroxyl

functional group

chloro, hydroxyl

functional group

chloro, hydroxyl

General description

2,3-Dichloro-1-propanol belongs to the group of chloropropanols.[1] Inhibitory effects of 2,3-dichloro-1-propanol on T cell both in vivo and in vitro is reported.[1] Improved enantioselective resolution of (R,S)-2,3-dichloro-1-propanol to (S)-2, 3-dichloro-1-propanol by whole cells of a recombinant Escherichia coli in n-heptane-aqueous biphasic system is reported.[2]

Application

2,3-Dichloro-1-propanol may be employed as carbon and energy supplement for the growth of Pseudomonas putida strain (MC4).[3]

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301,H310,H319

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Eye Irrit. 2

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

199.4 °F

Flash Point(C)

93 °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
BCCL9038
BCCK3499
BCCG1239
BCCF2801
BCCC9003

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Jing Lu et al.
International immunopharmacology, 17(2), 321-328 (2013-07-16)
2,3-Dichloro-1-propanol (2,3-DCP) is a member of a group of chemicals known as chloropropanols. Currently, immunotoxicity of 2,3-DCP has not been reported. In the present study, we studied its inhibitory effects on T cell both in vivo and in vitro. The
K Fujishiro et al.
Fukuoka igaku zasshi = Hukuoka acta medica, 85(8), 247-250 (1994-08-01)
The toxicity of dichloropropanols (DCPs) was investigated by hematological and blood chemical examination. Solutions of two isomers of DCPs, 1,3-dichloro-2-propanol (DC2P) and 2,3-dichloro-1-propanol (DC1P) were dissolved in saline at a concentration of 100 mg/ml and 0.1 ml of each was
Shu-Ping Zou et al.
Journal of biotechnology, 188, 42-47 (2014-08-26)
The enantioselective resolution of (R,S)-2,3-dichloro-1-propanol ((R,S)-DCP) to (S)-DCP by whole cells of a recombinant Escherichia coli expressing halohydrin dehalogenase (HHDH) activity was limited by product inhibition. To solve this problem to improve the productivity of (S)-DCP, an n-heptane-aqueous biphasic system
Ijaz Gul et al.
Biotechnology and applied biochemistry, 67(4), 685-692 (2020-02-18)
Epoxides are widely used chemicals, the determination of which is of paramount importance. Herein, we present an enzyme-based approach for noninstrumental detection of epoxides in standard solution and environmental samples. Halohydrin dehalogenase (HheC) as a biological recognition element and epichlorohydrin
K Imazu et al.
Journal of UOEH, 14(1), 73-76 (1992-03-01)
We investigated the toxicity of dichloropropanols (DCPs) in hematological findings and serum chemistry. The solutions of two isomers of DCPs, 1,3-dichloro-2-propanol (DC2P) and 2,3-dichloro-1-propanol (DC1P) were dissolved in saline at the concentration of 100 mg/ml, and 0.1 ml of each
View All Related Papers

Questions

Reviews

No rating value

Active Filters

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