301930
2,2-二(溴甲基)-1,3-丙二醇
98%
别名:
1,3-二溴-2,2-双（羟甲基）丙烷, 二溴新戊二醇, 戊四醇二溴化物, 戊四醇二溴水合物
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关于此项目
线性分子式:
HOCH2C(CH2Br)2CH2OH
化学文摘社编号:
分子量:
261.94
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
221-967-7
MDL number:
产品名称
2,2-二(溴甲基)-1,3-丙二醇, 98%
InChI key
CHUGKEQJSLOLHL-UHFFFAOYSA-N
InChI
1S/C5H10Br2O2/c6-1-5(2-7,3-8)4-9/h8-9H,1-4H2
SMILES string
OCC(CO)(CBr)CBr
vapor pressure
10 mmHg ( 178 °C)
assay
98%
form
solid
mp
112-114 °C (lit.)
Quality Level
signalword
Danger
hcodes
Hazard Classifications
Carc. 1B - Muta. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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
Simone I Hoehle et al.
Drug metabolism and disposition: the biological fate of chemicals, 37(2), 408-416 (2008-11-26)
2,2-Bis(bromomethyl)-1,3-propanediol (BMP) is a brominated flame retardant, previously shown to be a multisite carcinogen in experimental animals. Studies were performed to characterize the dispositional and metabolic fate of BMP after oral or intravenous administration to male Fischer-344 rats. After a
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
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
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
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