1,2,3,4-Tetrahydro-1,4-methanoisoquinoline hydrochloride CAS 111635-04-2

Purity 97%+In StockPharmaceutical Standards
CAS No.111635-04-2
Molecular FormulaC10H11N
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,2,3,4-Tetrahydro-1,4-methanoisoquinoline hydrochloride CAS 111635-04-2 chemical structure

Description

CATO manufactures 1,2,3,4-Tetrahydro-1,4-methanoisoquinoline hydrochloride under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

CATO supplies 1,2,3,4-Tetrahydro-1,4-methanoisoquinoline hydrochloride (CAS 111635-04-2), a certified reference material (molecular formula C10H11NHCl, MW 181.66 g/mol) for analytical method development and quality control.

The molecular framework of 1,2,3,4-Tetrahydro-1,4-methanoisoquinoline hydrochloride (C10H11NHCl) 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC10H11N HCl
Molecular Weight181.66 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 chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms1

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