1-(3-Fluoro-4-nitrophenyl)-1H-tetrazole CAS 1922148-30-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1922148-30-8
Molecular FormulaC7H4FN5O2
Molecular Weight209.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(3-Fluoro-4-nitrophenyl)-1H-tetrazole CAS 1922148-30-8 chemical structure

Description

CATO supplies 1-(3-Fluoro-4-nitrophenyl)-1H-tetrazole (CAS 1922148-30-8), a certified reference material (molecular formula C7H4FN5O2, MW 209.14 g/mol) for analytical method development and quality control.

The molecular framework of 1-(3-Fluoro-4-nitrophenyl)-1H-tetrazole (C7H4FN5O2) is characterized by an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. 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 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.

CATO manufactures 1-(3-Fluoro-4-nitrophenyl)-1H-tetrazole 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 FormulaC7H4FN5O2
Molecular Weight209.14 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1996
Halogen ContentF-containing
Nitrogen Atoms5

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