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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:
4263-52-9
Molecular Weight:
211.01
Beilstein:
4590828
EC Number:
224-244-4
MDL number:
MFCD00007530
UNSPSC Code:
12352100
PubChem Substance ID:
24848332
NACRES:
NA.22

Assay

98%

mp

283 °C (dec.) (lit.)

solubility

water: soluble 100 mg/mL, clear, colorless

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. 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 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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
Kewei Xu et al.
Bioresource technology, 101(8), 2600-2607 (2009-11-27)
In this study, the microbial response of anaerobic sludge digestion to the addition of two classic methanogenic inhibitors (chloroform, 2-bromoethanesulfonate) was investigated. Both the toxicants showed their effectiveness on CH(4) production, whereas the hydrogen responses and acetate accumulations were elicited
S Venkata Mohan et al.
Bioresource technology, 99(1), 59-67 (2007-01-26)
Influence of different pretreatment methods applied on anaerobic mixed inoculum was evaluated for selectively enriching the hydrogen (H(2)) producing mixed culture using dairy wastewater as substrate. The experimental data showed the feasibility of molecular biohydrogen generation utilizing dairy wastewater as
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