5,6-Diaminonaphthalene-1-sulfonamide hydrochloride CAS 1049752-75-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1049752-75-1
Molecular FormulaC10H11N3O2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5,6-Diaminonaphthalene-1-sulfonamide hydrochloride CAS 1049752-75-1 chemical structure

Description

The molecular framework of 5,6-Diaminonaphthalene-1-sulfonamide hydrochloride (C10H11N3O2SHCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 5,6-Diaminonaphthalene-1-sulfonamide hydrochloride (CAS 1049752-75-1), a certified reference material (molecular formula C10H11N3O2SHCl, MW 273.74 g/mol) for analytical method development and quality control.

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

As a certified reference material (CRM), 5,6-Diaminonaphthalene-1-sulfonamide hydrochloride meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC10H11N3O2S HCl
Molecular Weight273.74 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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