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301930

Sigma-Aldrich

2,2-Bis(bromomethyl)-1,3-propanediol

98%

Synonym(s):

1,3-Dibromo-2,2-bis(hydroxymethyl)propane, Dibromoneopentyl glycol, Pentaerythritol dibromide, Pentaerythritol dibromohydrin

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About This Item

Linear Formula:
HOCH2C(CH2Br)2CH2OH
CAS Number:
3296-90-0
Molecular Weight:
261.94
EC Number:
221-967-7
MDL number:
MFCD00004688
UNSPSC Code:
12162002
PubChem Substance ID:
24858219
NACRES:
NA.23

vapor pressure

10 mmHg ( 178 °C)

Assay

98%

form

solid

mp

112-114 °C (lit.)

SMILES string

OCC(CO)(CBr)CBr

InChI

1S/C5H10Br2O2/c6-1-5(2-7,3-8)4-9/h8-9H,1-4H2

InChI key

CHUGKEQJSLOLHL-UHFFFAOYSA-N

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H340,H350

Hazard Classifications

Carc. 1B - Muta. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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K A Treinen et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 13(2), 245-255 (1989-08-01)
The effect of 2,2-bis(bromomethyl)-1,3-propanediol (BMP) on reproduction in Swiss CD-1 mice was evaluated by use of a continuous breeding protocol. BMP was administered in the feed at 0.1, 0.2, and 0.4% concentrations. Both male and female F0 mice (20 pairs
Weixi Kong et al.
Toxicology letters, 222(3), 273-279 (2013-08-21)
2,2-Bis(bromomethyl)-1,3-propanediol (BMP) is a brominated flame retardant used in urethane foams and polyester resins. In a two year dietary study, BMP caused neoplastic lesions at multiple sites including the urinary bladder of both rats and mice. However, liver was not
Shai Ezra et al.
Journal of contaminant hydrology, 86(3-4), 195-214 (2006-05-13)
This study investigates the mechanisms controlling the distribution of 3-bromo-2,2-bis(bromomethyl)propanol (TBNPA) and 2,2-bis(bromomethyl)propan-1,3-diol (DBNPG) in a fractured chalk aquitard. An extensive monitoring program showed a systematic decrease in the TBNPA/DBNPG ratio with distance from the contamination source. Sorption of TBNPA
Shai Ezra et al.
Chemosphere, 79(4), 476-481 (2010-03-02)
The mechanism and kinetics of the spontaneous decomposition of 2,2-bis(bromomethyl)propan-1,3-diol (DBNPG) and its decomposition daughter products were determined in aqueous solution at a temperatures range between 30 and 70 degrees C and pH from 7.0 to 9.5. DBNPG decomposition in
J Sun
Biometrics, 55(4), 1273-1276 (2001-04-21)
Historical control data are often available in carcinogenicity studies and are included for testing dose effects in current studies. A new method is developed for incorporating the historical control information into a dose effect test. The method generalizes the test
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