N-methyl-N-(pyridin-2-ylmethyl)azepan-4-amine trihydrochloride CAS 1803607-55-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1803607-55-7
Molecular FormulaC13H21N3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-methyl-N-(pyridin-2-ylmethyl)azepan-4-amine trihydrochloride CAS 1803607-55-7 chemical structure

Description

Based on its molecular formula C13H21N3HCl, N-methyl-N-(pyridin-2-ylmethyl)azepan-4-amine trihydrochloride contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 255.79 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.

N-methyl-N-(pyridin-2-ylmethyl)azepan-4-amine trihydrochloride (CAS 1803607-55-7), molecular formula C13H21N3HCl and molecular weight 255.79 g/mol, is a CATO reference standard with documented purity and traceability.

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), N-methyl-N-(pyridin-2-ylmethyl)azepan-4-amine trihydrochloride 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 FormulaC13H21N3 3*HCl
Molecular Weight255.79 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentCl-containing
Nitrogen Atoms3

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