4-(4-Ethylpiperazin-1-yl)-3-fluorobenzoic acid hydrochloride CAS 1306604-53-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1306604-53-4
Molecular FormulaC13H17FN2O2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(4-Ethylpiperazin-1-yl)-3-fluorobenzoic acid hydrochloride CAS 1306604-53-4 chemical structure

Description

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.

CATO supplies 4-(4-Ethylpiperazin-1-yl)-3-fluorobenzoic acid hydrochloride (CAS 1306604-53-4), a certified reference material (molecular formula C13H17FN2O2HCl, MW 288.75 g/mol) for analytical method development and quality control.

The molecular framework of 4-(4-Ethylpiperazin-1-yl)-3-fluorobenzoic acid hydrochloride (C13H17FN2O2HCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

Physical & Chemical Properties

Molecular FormulaC13H17FN2O2 HCl
Molecular Weight288.75 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF/Cl-containing
Nitrogen Atoms2

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