1-Phenyl-2,3,4,9-tetrahydro-1h-pyrido[3,4-b]indole-3-carboxylic acid CAS 82789-18-2

Purity 97%+In StockPharmaceutical Standards
CAS No.82789-18-2
Molecular FormulaC18H16N2O2
Molecular Weight292.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Phenyl-2,3,4,9-tetrahydro-1h-pyrido[3,4-b]indole-3-carboxylic acid CAS 82789-18-2 chemical structure

Description

As a certified reference material (CRM), 1-Phenyl-2,3,4,9-tetrahydro-1h-pyrido[3,4-b]indole-3-carboxylic acid 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.

CATO supplies 1-Phenyl-2,3,4,9-tetrahydro-1h-pyrido[3,4-b]indole-3-carboxylic acid (CAS 82789-18-2), a certified reference material (molecular formula C18H16N2O2, MW 292.33 g/mol) for analytical method development and quality control.

Structurally, 1-Phenyl-2,3,4,9-tetrahydro-1h-pyrido[3,4-b]indole-3-carboxylic acid (C18H16N2O2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 12.0, corresponding to approximately 12 ring(s) or double-bond equivalent(s). With a molecular weight of 292.33 g/mol, it falls into the medium-molecular-weight range. 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.

Physical & Chemical Properties

Molecular FormulaC18H16N2O2
Molecular Weight292.33 g/mol
AppearancePale yellow to yellow crystalline powder
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
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1980
Nitrogen Atoms2

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