rel-(1R,2S)-2-Methyl-2,3-dihydro-1H-inden-1-amine CAS 168902-85-0

Purity 97%+In StockPharmaceutical Standards
CAS No.168902-85-0
Molecular FormulaC10H13N
Molecular Weight147.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

rel-(1R,2S)-2-Methyl-2,3-dihydro-1H-inden-1-amine CAS 168902-85-0 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 rel-(1R,2S)-2-Methyl-2,3-dihydro-1H-inden-1-amine.

CATO supplies rel-(1R,2S)-2-Methyl-2,3-dihydro-1H-inden-1-amine (CAS 168902-85-0), a certified reference material (molecular formula C10H13N, MW 147.22 g/mol) for analytical method development and quality control.

The molecular framework of rel-(1R,2S)-2-Methyl-2,3-dihydro-1H-inden-1-amine (C10H13N) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group. 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.

As a certified reference material (CRM), rel-(1R,2S)-2-Methyl-2,3-dihydro-1H-inden-1-amine 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 FormulaC10H13N
Molecular Weight147.22 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2005
Nitrogen Atoms1

Recommended Standards

Why CATO?