3-(1,4-Diazepane-1-carbonyl)-1h-indole hydrochloride CAS 1235439-36-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1235439-36-7
Molecular FormulaC14H17N3O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(1,4-Diazepane-1-carbonyl)-1h-indole hydrochloride CAS 1235439-36-7 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 3-(1,4-Diazepane-1-carbonyl)-1h-indole hydrochloride.

3-(1,4-Diazepane-1-carbonyl)-1h-indole hydrochloride (CAS 1235439-36-7) is a high-purity analytical reference standard with the molecular formula C14H17N3OHCl and a molecular weight of 279.77 g/mol.

The molecular framework of 3-(1,4-Diazepane-1-carbonyl)-1h-indole hydrochloride (C14H17N3OHCl) 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 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC14H17N3O HCl
Molecular Weight279.77 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms3

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