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D43050

Sigma-Aldrich

2,3-Dibromo-1-propanol

98%

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About This Item

Linear Formula:
BrCH2CH(Br)CH2OH
CAS Number:
Molecular Weight:
217.89
Beilstein:
1719127
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.559 (lit.)

bp

95-97 °C/10 mmHg (lit.)

density

2.12 g/mL at 25 °C (lit.)

SMILES string

OCC(Br)CBr

InChI

1S/C3H6Br2O/c4-1-3(5)2-6/h3,6H,1-2H2

InChI key

QWVCIORZLNBIIC-UHFFFAOYSA-N

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Related Categories

Application

Synthetic building block, fire-proofing agent, and carcinogen.

Pictograms

Skull and crossbonesHealth hazard

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 1B - Repr. 2

Storage Class Code

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

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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R Benigni
Mutagenesis, 6(5), 423-425 (1991-09-01)
A QSAR model based on the combination of two molecular descriptors--estimated electrophilic reactivity and Ashby's structural alerts--was used to predict the carcinogenicity of 44 chemicals currently bioassayed by the US National Toxicology Program. These predictions will be compared with the
Ijaz Gul et al.
Analytical biochemistry, 609, 113971-113971 (2020-09-27)
Enzyme immobilization using inorganic membranes has enticed increased attention as they not only improve enzyme stability, but also furnish user-friendly biodevices that can be tailored to different applications. Herein, we explored the suitability of the glass fiber membrane for enzyme
2,3-Dibromopropan-1-ol.
IARC monographs on the evaluation of carcinogenic risks to humans, 77, 439-453 (2000-12-02)
Journal of Heterocyclic Chemistry, 28, 891-891 (1991)
G K Hemakanthi De Alwis et al.
Archives of environmental contamination and toxicology, 53(1), 134-139 (2007-03-31)
2,3-Dibromo-1-propanol (DBP) was used as an active flame retardant in the 1970s. It was also used as an intermediate in the preparation of insecticide formulations, pharmaceuticals and the flame retardants tris(2,3-dibromopropyl) phosphate (Tris-BP) and tetrabromobisphenol A bis (2,3-dibromopropyl ether). DBP

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