4-Amino-N-(4-methoxyphenyl)benzenesulfonamide hydrochloride CAS 1047620-36-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1047620-36-9
Molecular FormulaC13H14N2O3S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Amino-N-(4-methoxyphenyl)benzenesulfonamide hydrochloride CAS 1047620-36-9 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

4-Amino-N-(4-methoxyphenyl)benzenesulfonamide hydrochloride (CAS 1047620-36-9) is a high-purity analytical reference standard with the molecular formula C13H14N2O3SHCl and a molecular weight of 314.78 g/mol.

Structurally, 4-Amino-N-(4-methoxyphenyl)benzenesulfonamide hydrochloride (C13H14N2O3SHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 314.78 g/mol, it falls into the moderately-high-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO manufactures 4-Amino-N-(4-methoxyphenyl)benzenesulfonamide hydrochloride under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC13H14N2O3S HCl
Molecular Weight314.78 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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