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12050

2-Formylbenzenesulfonic acid sodium salt

≥95.0% (T)

Synonym(s):

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

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About This Item

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

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Product Name

2-Formylbenzenesulfonic acid sodium salt, ≥95.0% (T)

InChI key

ADPUQRRLAAPXGT-UHFFFAOYSA-M

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

SMILES string

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

assay

≥95.0% (T)

form

solid

solubility

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

functional group

aldehyde
sulfonic acid

Quality Level

200

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This Item
239380123579137502
2-Formylbenzenesulfonic acid sodium salt ≥95.0% (T)

Sigma-Aldrich

12050

2-Formylbenzenesulfonic acid sodium salt

2-Formylbenzenesulfonic acid sodium salt hydrate technical grade, 75%

Sigma-Aldrich

239380

2-Formylbenzenesulfonic acid sodium salt hydrate

Benzenesulfinic acid sodium salt 98%

Sigma-Aldrich

123579

Benzenesulfinic acid sodium salt

Sodium 2-bromoethanesulfonate 98%

Sigma-Aldrich

137502

Sodium 2-bromoethanesulfonate

assay

≥95.0% (T)

assay

75%

assay

98%

assay

98%

solubility

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

solubility

-

solubility

-

solubility

water: soluble 100 mg/mL, clear, colorless

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

200

form

solid

form

solid

form

solid

form

-

functional group

aldehyde

functional group

aldehyde, sulfonic acid

functional group

sulfinic acid

functional group

bromo, sulfonic acid

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[1].

General description

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN7261
BCCH0315
BCCF8908
BCCF7414
BCCC7543

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NMR characterization of N-benzyl sulfonated derivatives of chitosan.
Crini G, et al.
Carbohydrate Polymers, 33(2), 145-151 (1997)
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.
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)

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