Skip to Content
Merck
All Photos(1)

Documents

12050

Sigma-Aldrich

2-Formylbenzenesulfonic acid sodium salt

≥95.0% (T)

Synonym(s):

2-Sulfobenzaldehyde sodium salt, Benzaldehyde-2-sulfonic acid sodium salt, Sodium 2-formyl-benzolsulfonate

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C7H5NaO4S
CAS Number:
1008-72-6
Molecular Weight:
208.17
Beilstein:
4040884
EC Number:
213-758-4
MDL number:
MFCD00007478
UNSPSC Code:
12352100
PubChem Substance ID:
57646966
NACRES:
NA.22

Quality Level

200

Assay

≥95.0% (T)

form

solid

solubility

H2O: soluble 1 g/10 mL, clear, colorless to faintly brownish-yellow

SMILES string

[Na+].[O-]S(=O)(=O)c1ccccc1C=O

InChI

1S/C7H6O4S.Na/c8-5-6-3-1-2-4-7(6)12(9,10)11;/h1-5H,(H,9,10,11);/q;+1/p-1

InChI key

ADPUQRRLAAPXGT-UHFFFAOYSA-M

General description

2-Formylbenzenesulfonic acid sodium salt reacts with chitosan in the presence of sodium cyanoborohydride to yield N-benzyl derivatives.

Application

2-Formylbenzenesulfonic acid sodium salt was used as precursor to test the ability of fungal strains for transformation of phenolic and non-phenolic precursors into stable and non-toxic dyes.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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’.

Already Own This Product?

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

Visit the Document Library

Hao-Xuan Guo et al.
Polymers, 12(2) (2020-02-08)
In this study, water-soluble, narrow-band-gap polymers containing reactive groups were prepared by the addition-condensation of pyrrole (Pyr), benzaldehyde-2-sulfonic acid sodium salt (BS), and terephthalaldehydic acid (TPA) or p-hydroxybenzaldehyde (p-HB). TPA and p-HB were used for the post-crosslinking reaction between polymers.
NMR characterization of N-benzyl sulfonated derivatives of chitosan.
Crini G, et al.
Carbohydrate Polymers, 33(2), 145-151 (1997)
Jolanta Polak et al.
Microbial cell factories, 9, 51-51 (2010-07-06)
Chemical methods of producing dyes involve extreme temperatures and unsafe toxic compounds. Application of oxidizing enzymes obtained from fungal species, for example laccase, is an alternative to chemical synthesis of dyes. Laccase can be replaced by fungal biomass acting as
Sonja Rittchen et al.
Biochemical pharmacology, 182, 114277-114277 (2020-10-11)
Life-threatening inflammatory conditions such as acute respiratory distress syndrome or sepsis often go hand in hand with severe vascular leakage. During inflammation, endothelial cell integrity and intact barrier function are crucial to limit leukocyte and plasma extravasation. Prostaglandin D2 (PGD2)

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