Skip to Content
Merck

S5799

Suberic acid bis(3-sulfo-N-hydroxysuccinimide ester) sodium salt

≥95% (H-NMR), powder

Synonym(s):

BS3, Bis(sulfosuccinimidyl) suberate sodium salt

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C16H18N2Na2O14S2
CAS Number:
82436-77-9
Molecular Weight:
572.43
NACRES:
NA.22
PubChem Substance ID:
329824554
UNSPSC Code:
12352106
MDL number:
MFCD00054982
Assay:
≥95% (H-NMR)
Form:
powder
Solubility:
H2O: 10 mg/mL, soluble

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

MGJYOHMBGJPESL-UHFFFAOYSA-L

SMILES string

[Na+].[Na+].[O-]S(=O)(=O)C1CC(=O)N(OC(=O)CCCCCCC(=O)ON2C(=O)CC(C2=O)S([O-])(=O)=O)C1=O

InChI

1S/C16H20N2O14S2.2Na/c19-11-7-9(33(25,26)27)15(23)17(11)31-13(21)5-3-1-2-4-6-14(22)32-18-12(20)8-10(16(18)24)34(28,29)30;;/h9-10H,1-8H2,(H,25,26,27)(H,28,29,30);;/q;2*+1/p-2

assay

≥95% (H-NMR)

form

powder

reaction suitability

reagent type: cross-linking reagent

solubility

H2O: 10 mg/mL, soluble

storage temp.

−20°C

Quality Level

300

Related Categories

General description

Suberic acid bis(3-sulfo-N-hydroxysuccinimide ester) sodium salt (BS3) is a water soluble, homobifunctional cross-linking reagent with amine reactivity. It is typically coupled to molecules containing primary amines by amide bonds buffered at pH 7.5 (6.5-8.5). It incorporates 8-atom linker.

Application

Suberic acid bis(3-sulfo-N-hydroxysuccinimide ester) sodium salt (BS3) is useful for the preparation of protein-protein, receptor-ligand and hapten carrier molecule conjugates.

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000483580
0000516538
0000483580
0000516538
0000516540

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Modelling the structure of latexin-carboxypeptidase A complex based on chemical cross-linking and molecular docking.
Mouradov D
Protein engineering, design & selection : PEDS, 19, 9-16 (2006)
Modified apolipoprotein (apo) A-I by artificial sweetener causes severe premature cellular senescence and atherosclerosis with impairment of functional and structural properties of apoA-I in lipid-free and lipid-bound state.
Jang W
Molecular Cell, 31, 461-461 (2011)
Bovine apolipoprotein (apo)A-I displays more enhanced antioxidant and anti-atherosclerotic activity in lipid-free and lipid-bound states than human and porcine apoA-I.
Kim SM
International Journal of Molecular Medicine, 32, 843-843 (2013)
Huawen Lin et al.
PLoS genetics, 9(9), e1003841-e1003841 (2013-10-03)
Whole genome sequencing is a powerful tool in the discovery of single nucleotide polymorphisms (SNPs) and small insertions/deletions (indels) among mutant strains, which simplifies forward genetics approaches. However, identification of the causative mutation among a large number of non-causative SNPs
Hermanson GT
Bioconjugate Techniques (2013)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service