{1-[amino(phenyl)methyl]cyclopent-3-en-1-yl}methanol hydrochloride CAS 1909336-69-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1909336-69-1
Molecular FormulaC13H17NO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

{1-[amino(phenyl)methyl]cyclopent-3-en-1-yl}methanol hydrochloride CAS 1909336-69-1 chemical structure

Description

The molecular framework of {1-[amino(phenyl)methyl]cyclopent-3-en-1-yl}methanol hydrochloride (C13H17NOHCl) 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

{1-[amino(phenyl)methyl]cyclopent-3-en-1-yl}methanol hydrochloride (CAS 1909336-69-1), molecular formula C13H17NOHCl and molecular weight 239.74 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.

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 FormulaC13H17NO HCl
Molecular Weight239.74 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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.)1995
Halogen ContentCl-containing
Nitrogen Atoms1

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