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137502

Sigma-Aldrich

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
Beilstein:
4590828
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level

Assay

98%

mp

283 °C (dec.) (lit.)

solubility

water: soluble 100 mg/mL, clear, colorless

functional group

bromo
sulfonic acid

SMILES string

[Na+].[O-]S(=O)(=O)CCBr

InChI

1S/C2H5BrO3S.Na/c3-1-2-7(4,5)6;/h1-2H2,(H,4,5,6);/q;+1/p-1

InChI key

HNFOAHXBHLWKNF-UHFFFAOYSA-M

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General description

Sodium 2-bromoethanesulfonate acts as methanogenesis inhibitor during anaerobic digestion[1]. It reacts with lithium sulfinated polysulfones(PSU) to yield sulfoethylated PSU[2].

Application

Sodium 2-bromoethanesulfonate(BES) was used to investigate the effect of BES on inhibition of bacterial growth[3].

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

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
Oleg R Kotsyurbenko et al.
Environmental microbiology, 6(11), 1159-1173 (2004-10-14)
Sites in the West Siberian peat bog 'Bakchar' were acidic (pH 4.2-4.8), low in nutrients, and emitted CH4 at rates of 0.2-1.5 mmol m(-2) h(-1). The vertical profile of delta13CH4 and delta13CO2 dissolved in the porewater indicated increasing isotope fractionation
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
Sam D Molenaar et al.
ChemSusChem, 11(13), 2171-2178 (2018-04-26)
Detailed studies of microbial growth in bioelectrochemical systems (BESs) are required for their suitable design and operation. Here, we report the use of optical coherence tomography (OCT) as a tool for in situ and noninvasive quantification of biofilm growth on electrodes
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)

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