2,3,4,5-Tetrahydro-1H-1,5-methanobenzo[d]azepine CAS 69718-72-5

Purity 97%+In StockPharmaceutical Standards
CAS No.69718-72-5
Molecular FormulaC11H13N
Molecular Weight159.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,3,4,5-Tetrahydro-1H-1,5-methanobenzo[d]azepine CAS 69718-72-5 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 2,3,4,5-Tetrahydro-1H-1,5-methanobenzo[d]azepine.

2,3,4,5-Tetrahydro-1H-1,5-methanobenzo[d]azepine (CAS 69718-72-5) is a high-purity analytical reference standard with the molecular formula C11H13N and a molecular weight of 159.23 g/mol.

Based on its molecular formula C11H13N, 2,3,4,5-Tetrahydro-1H-1,5-methanobenzo[d]azepine contains a nitrogen-containing heterocyclic scaffold, a nitrile group; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 159.23 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

CATO manufactures 2,3,4,5-Tetrahydro-1H-1,5-methanobenzo[d]azepine 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.

Physical & Chemical Properties

Molecular FormulaC11H13N
Molecular Weight159.23 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1976
Nitrogen Atoms1

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