137502
Sodium 2-bromoethanesulfonate
98%
Synonym(s):
2-Bromoethanesulfonic acid sodium salt
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About This Item
Linear Formula:
BrCH2CH2SO3Na
CAS Number:
Molecular Weight:
211.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-244-4
Beilstein/REAXYS Number:
4590828
MDL number:
Assay:
98%
InChI key
HNFOAHXBHLWKNF-UHFFFAOYSA-M
InChI
1S/C2H5BrO3S.Na/c3-1-2-7(4,5)6;/h1-2H2,(H,4,5,6);/q;+1/p-1
SMILES string
[Na+].[O-]S(=O)(=O)CCBr
assay
98%
mp
283 °C (dec.) (lit.)
solubility
water: soluble 100 mg/mL, clear, colorless
functional group
bromo, sulfonic acid
Quality Level
Related Categories
General description
Sodium 2-bromoethanesulfonate acts as methanogenesis inhibitor during anaerobic digestion. It reacts with lithium sulfinated polysulfones(PSU) to yield sulfoethylated PSU.
Application
Sodium 2-bromoethanesulfonate(BES) was used to investigate the effect of BES on inhibition of bacterial growth.
Storage Class
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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J Sipma et al.
Applied microbiology and biotechnology, 64(3), 421-428 (2003-10-14)
The conversion routes of carbon monoxide (CO) at 55 degrees C by full-scale grown anaerobic sludges treating paper mill and distillery wastewater were elucidated. Inhibition experiments with 2-bromoethanesulfonate (BES) and vancomycin showed that CO conversion was performed by a hydrogenogenic
Polysulfone ionomers for proton-conducting fuel cell membranes: sulfoalkylated polysulfones.
Karlsson LE and Jannasch P.
Journal of Membrane Science, 230(1), 61-70 (2004)
Jeffrey M Boyd et al.
Journal of bacteriology, 188(23), 8062-8069 (2006-09-26)
Bacterial growth with short-chain aliphatic alkenes requires coenzyme M (CoM) (2-mercaptoethanesulfonic acid), which serves as the nucleophile for activation and conversion of epoxide products formed from alkene oxidation to central metabolites. In the present work the CoM analog 2-bromoethanesulfonate (BES)
Meike Goenrich et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 9(6), 691-705 (2004-09-15)
Methyl-coenzyme M reductase (MCR) catalyses the reduction of methyl-coenzyme M (CH(3)-S-CoM) with coenzyme B (HS-CoB) to methane and CoM-S-S-CoB. It contains the nickel porphyrinoid F(430) as prosthetic group which has to be in the Ni(I) oxidation state for the enzyme
F J Cervantes et al.
Applied microbiology and biotechnology, 64(5), 702-711 (2004-02-06)
The impact of humic acids and the humic model compound, anthraquinone-2,6-disulfonate (AQDS), on the biodegradation of carbon tetrachloride (CT) by anaerobic granular sludge was studied. Addition of both humic acids and AQDS at sub-stoichiometric levels increased the first-order rate of
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