Gatifloxacin hydrate CAS 614751-80-3

Purity 97%+In StockPharmaceutical Standards
CAS No.614751-80-3
Molecular FormulaC19H22FN3O4
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Gatifloxacin hydrate CAS 614751-80-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 393.41 g/mol gives Gatifloxacin hydrate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Gatifloxacin hydrate (CAS 614751-80-3), a certified reference material (molecular formula C19H22FN3O4H2O, MW 393.41 g/mol) for analytical method development and quality control.

Structurally, Gatifloxacin hydrate (C19H22FN3O4H2O) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 393.41 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 hydrate 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 H2O
Molecular Weight393.41 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°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.)1985
Halogen ContentF-containing
Nitrogen Atoms3

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