4-Benzyl-1-piperazineacetic Acid Hydrazide CAS 24632-70-0

Purity 97%+In StockPharmaceutical Standards
CAS No.24632-70-0
Molecular FormulaC13H20N4O
Molecular Weight248.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Benzyl-1-piperazineacetic Acid Hydrazide CAS 24632-70-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 248.32 g/mol gives 4-Benzyl-1-piperazineacetic Acid Hydrazide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 4-Benzyl-1-piperazineacetic Acid Hydrazide (CAS 24632-70-0), a certified reference material (molecular formula C13H20N4O, MW 248.32 g/mol) for analytical method development and quality control.

The molecular framework of 4-Benzyl-1-piperazineacetic Acid Hydrazide (C13H20N4O) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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 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).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

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 FormulaC13H20N4O
Molecular Weight248.32 g/mol
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1964
Nitrogen Atoms4

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