2,3,4,5-Tetrahydro-1H-benzo[b]azepin-5-amine hydrochloride CAS 1965309-36-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1965309-36-7
Molecular FormulaC10H14N2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,3,4,5-Tetrahydro-1H-benzo[b]azepin-5-amine hydrochloride CAS 1965309-36-7 chemical structure

Description

The molecular framework of 2,3,4,5-Tetrahydro-1H-benzo[b]azepin-5-amine hydrochloride (C10H14N2HCl) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, 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).

CATO supplies 2,3,4,5-Tetrahydro-1H-benzo[b]azepin-5-amine hydrochloride (CAS 1965309-36-7), a certified reference material (molecular formula C10H14N2HCl, MW 198.69 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 2,3,4,5-Tetrahydro-1H-benzo[b]azepin-5-amine 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 FormulaC10H14N2 HCl
Molecular Weight198.69 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
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.)1996
Halogen ContentCl-containing
Nitrogen Atoms2

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