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Merck
CN

93792

Benzenesulfonic acid

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About This Item

Linear Formula:
C6H5SO3H
CAS Number:
Molecular Weight:
158.18
NACRES:
NA.21
UNSPSC Code:
12352005
Beilstein/REAXYS Number:
742513
MDL number:
Assay:
≥99.8% (area, HPLC)
Concentration:
≥98.0 % (w/w) (T)
Form:
solid
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biological source

synthetic

Quality Level

assay

≥99.8% (area, HPLC)

form

solid

concentration

≥98.0 % (w/w) (T)

impurities

≤0.05% phenyl p-tolylsulfone (area), ≤0.1% any not specified impurity (area), ≤1% water (Karl Fischer), ≤2 mg/kg residual solvents (benzene) (GC), ≤5000 mg/kg residual solvents (heptane) (GC), ≤890 mg/kg residual solcents (toluene) (GC)

ign. residue

≤0.2%

solubility

H2O: 0.1 g/10 mL, clear, colorless

anion traces

chloride (Cl-): ≤500 mg/kg, sulfate (SO42-): ≤600 mg/kg

suitability

corresponds for identity (IR) (ATR)

SMILES string

OS(=O)(=O)c1ccccc1

InChI

1S/C6H6O3S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H,7,8,9)

InChI key

SRSXLGNVWSONIS-UHFFFAOYSA-N

Analysis Note

white/colorless to slightly beige crystals; powder with lumps


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pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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Snehlata Yadav et al.
European journal of medicinal chemistry, 45(12), 5985-5997 (2010-10-26)
A series of 4-[1-(substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzene sulphonic acids (1-20) was synthesized and evaluated, in vitro, for their antimicrobial activity and the results indicated that compounds 4-[1-(4-Nitrobenzoyl)-1H-benzoimidazol-2-yl]-benzenesulfonic acid (9) and 4-(1-octadec-9-enoyl-1H-benzoimidazol-2-yl)-benzenesulfonic acid (18) were found to be the most active ones.
Wenyi Huang et al.
ACS nano, 6(11), 10178-10185 (2012-10-27)
High-performance graphene nanopapers are prepared from an aqueous solution of functional graphenes with benzenesulfonic acid groups via covalent bonds. The formed hydrophobic graphene nanopapers showed the highest tensile strength of 360 MPa and Young's modulus of 102 GPa for samples
Ramasubbu Ramani et al.
Biomacromolecules, 9(5), 1390-1397 (2008-04-19)
We present lamellar self-assembly of cationic poly(L-histidine) (PLH) stoichiometrically complexed with an anionic surfactant, dodecyl benzenesulfonic acid (DBSA), which allows a stabilized conformation reminiscent of polyproline type II (PPII) left-handed helices. Such a conformation has no intrapeptide hydrogen bonds, and



Global Trade Item Number

SKUGTIN
93792-500G04061833283240
93792-1KG04061826002391