33626
Sulfanilamide
≥98% (calc. to the dried substance), solid, purum p.a.
Synonym(s):
p-Aminobenzenesulfonamide
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About This Item
Product Name
Sulfanilamide, puriss. p.a., ≥98% (calc. to the dried substance)
grade
puriss. p.a.
Quality Segment
assay
≥98% (calc. to the dried substance)
form
solid
impurities
≤0.002% heavy metals (as Pb)
ign. residue
≤0.1% (as SO4)
loss
≤0.5% loss on drying, 105 °C
color
white to faint beige
mp
163-166 °C, 164-166 °C (lit.)
anion traces
chloride (Cl-): ≤100 mg/kg, sulfate (SO42-): ≤200 mg/kg
antibiotic activity spectrum
Gram-negative bacteria, Gram-positive bacteria
mode of action
DNA synthesis | interferes, enzyme | inhibits
SMILES string
Nc1ccc(cc1)S(N)(=O)=O
InChI
1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)
InChI key
FDDDEECHVMSUSB-UHFFFAOYSA-N
Gene Information
human ... CA1(759), CA2(760), CA5A(763), CA5B(11238), CA9(768)
mouse ... Car13(71934), Car5a(12352)
General description
Application
- Study of new azo-azomethine derivatives of sulfanilamide: synthesis, characterization, spectroscopic, antimicrobial, antioxidant and anticancer activity: This study explores new derivatives of sulfanilamide synthesized through diazonium salt reactions and coupling with 2-hydroxy-3-methoxybenzaldehyde, providing insights into their potential antimicrobial, antioxidant, and anticancer activities (HS Al-Atbi, IJ Al-Assadi, et al., 2020).
Packaging
Other Notes
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Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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