4-Fluoro-5-methylbenzene-1,2-diamine CAS 97389-11-2

Purity 97%+In StockPharmaceutical Standards
CAS No.97389-11-2
Molecular FormulaC7H9FN2
Molecular Weight140.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Fluoro-5-methylbenzene-1,2-diamine CAS 97389-11-2 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 4-Fluoro-5-methylbenzene-1,2-diamine.

CATO supplies 4-Fluoro-5-methylbenzene-1,2-diamine (CAS 97389-11-2), a certified reference material (molecular formula C7H9FN2, MW 140.16 g/mol) for analytical method development and quality control.

4-Fluoro-5-methylbenzene-1,2-diamine (C7H9FN2) contains a nitrile group, fluorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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), 4-Fluoro-5-methylbenzene-1,2-diamine 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 FormulaC7H9FN2
Molecular Weight140.16 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, 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
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentF-containing
Nitrogen Atoms2

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