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Merck
CN

89426

3-Sulfo-N-succinimidyl benzoate sodium salt

≥99% (HPLC)

Synonym(s):

1-(Benzoyloxy)-2,5-dioxo-3-pyrrolidinesulfonic acid sodium salt, Benzoic acid (3-sulfo-N-succinimidyl) ester sodium salt, Benzoic acid N-hydroxysulfosuccinimide ester sodium salt

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About This Item

Empirical Formula (Hill Notation):
C11H8NNaO7S
CAS Number:
162823-05-4
Molecular Weight:
321.24
UNSPSC Code:
12352204
NACRES:
NA.25
PubChem Substance ID:
329769731
MDL number:
MFCD22644609
Beilstein/REAXYS Number:
10311265

Key Documents

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Product Name

3-Sulfo-N-succinimidyl benzoate sodium salt, ≥99% (HPLC)

InChI

1S/C11H9NO7S.Na/c13-9-6-8(20(16,17)18)10(14)12(9)19-11(15)7-4-2-1-3-5-7;/h1-5,8H,6H2,(H,16,17,18);/q;+1/p-1

SMILES string

[Na+].[O-]S(=O)(=O)C1CC(=O)N(OC(=O)c2ccccc2)C1=O

InChI key

MDKFDOUBUQSEDS-UHFFFAOYSA-M

assay

≥99% (HPLC)

form

powder

storage temp.

2-8°C

Quality Level

100

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBP5953V
BCBJ9764V
BCBJ9764

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Alexandre Panchaud et al.
Molecular & cellular proteomics : MCP, 7(4), 800-812 (2007-12-18)
Identification and relative quantification of hundreds to thousands of proteins within complex biological samples have become realistic with the emergence of stable isotope labeling in combination with high throughput mass spectrometry. However, all current chemical approaches target a single amino
Involvement of Coenzyme A Esters in the Metabolism of Benzoate and Cyclohexanecarboxylate by Rhodopseudomonas palustris.
Georgina N. Hutber
Microbiology, 129, 2413-2420 (1983)
J V Staros
Biochemistry, 21(17), 3950-3955 (1982-08-17)
We have synthesized and characterized N-hydroxysulfosuccinimide, a new hydrophilic ligand for the preparation of active esters. We have incorporated this ligand into two new protein cross-linking reagents, 3,3'-dithiobis(sulfosuccinimidyl propionate) and bis(sulfosuccinimidyl) suberate. In experiments with rabbit muscle aldolase, it is

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