Gatifloxacin USP RC E HCI CAS 1219097-41-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1219097-41-2
Molecular FormulaC19H22FN3O4
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Gatifloxacin USP RC E HCI CAS 1219097-41-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 411.86 g/mol gives Gatifloxacin USP RC E HCI distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Gatifloxacin USP RC E HCI (CAS 1219097-41-2) is a high-purity analytical reference standard with the molecular formula C19H22FN3O4HCl and a molecular weight of 411.86 g/mol.

The molecular framework of Gatifloxacin USP RC E HCI (C19H22FN3O4HCl) is characterized by a flavonoid core, an amide group, a hydroxyl group, an ether linkage, fluorine/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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

As a certified reference material (CRM), Gatifloxacin USP RC E HCI 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 FormulaC19H22FN3O4 HCl
Molecular Weight411.86 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF/Cl-containing
Nitrogen Atoms3

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