9-Methoxy-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole hydrochloride CAS 15918-69-1

Purity 97%+In StockPharmaceutical Standards
CAS No.15918-69-1
Molecular FormulaC13H17N2O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

9-Methoxy-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole hydrochloride CAS 15918-69-1 chemical structure

Description

9-Methoxy-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole hydrochloride (CAS 15918-69-1), molecular formula C13H17N2OCl and molecular weight 252.74 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 9-Methoxy-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole hydrochloride (C13H17N2OCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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), 9-Methoxy-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole hydrochloride 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 FormulaC13H17N2O Cl
Molecular Weight252.74 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Halogen ContentCl-containing
Nitrogen Atoms2

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