Isoquinoline-3-carboxylic Acid Hydrate CAS 203626-75-9

Purity 97%+In StockPharmaceutical Standards
CAS No.203626-75-9
Molecular FormulaC10H7NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Isoquinoline-3-carboxylic Acid Hydrate CAS 203626-75-9 chemical structure

Description

CATO supplies Isoquinoline-3-carboxylic Acid Hydrate (CAS 203626-75-9), a certified reference material (molecular formula C10H7NO2H2O, MW 191.19 g/mol) for analytical method development and quality control.

Isoquinoline-3-carboxylic Acid Hydrate (C10H7NO2H2O) contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; 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), Isoquinoline-3-carboxylic Acid 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 FormulaC10H7NO2 H2O
Molecular Weight191.19 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2015
Nitrogen Atoms1

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