(Z)-4-(4-methylpiperazin-1-yl)-4-oxobut-2-enoic acid CAS 42574-70-9

Purity 97%+In StockPharmaceutical Standards
CAS No.42574-70-9
Molecular FormulaC9H14N2O3
Molecular Weight198.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(Z)-4-(4-methylpiperazin-1-yl)-4-oxobut-2-enoic acid CAS 42574-70-9 chemical structure

Description

CATO supplies (Z)-4-(4-methylpiperazin-1-yl)-4-oxobut-2-enoic acid (CAS 42574-70-9), a certified reference material (molecular formula C9H14N2O3, MW 198.22 g/mol) for analytical method development and quality control.

The molecular framework of (Z)-4-(4-methylpiperazin-1-yl)-4-oxobut-2-enoic acid (C9H14N2O3) is characterized by an amino-acid-derived structure, 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.

CATO manufactures (Z)-4-(4-methylpiperazin-1-yl)-4-oxobut-2-enoic acid 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 FormulaC9H14N2O3
Molecular Weight198.22 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1969
Nitrogen Atoms2

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