3,4-Diamino-N-(4-((4-methylpiperazin-1-yl)methyl)phenyl)benzamide CAS 936940-89-5

Purity 97%+In StockPharmaceutical Standards
CAS No.936940-89-5
Molecular FormulaC19H25N5O
Molecular Weight339.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Diamino-N-(4-((4-methylpiperazin-1-yl)methyl)phenyl)benzamide CAS 936940-89-5 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3,4-Diamino-N-(4-((4-methylpiperazin-1-yl)methyl)phenyl)benzamide.

3,4-Diamino-N-(4-((4-methylpiperazin-1-yl)methyl)phenyl)benzamide (CAS 936940-89-5) is a high-purity analytical reference standard with the molecular formula C19H25N5O and a molecular weight of 339.43 g/mol.

3,4-Diamino-N-(4-((4-methylpiperazin-1-yl)methyl)phenyl)benzamide (C19H25N5O) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. Its physicochemical properties are representative of its class; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC19H25N5O
Molecular Weight339.43 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms5

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