Methyl 1-amino-2,3-dihydro-1h-indene-1-carboxylate CAS 90104-36-2

Purity 97%+In StockPharmaceutical Standards
CAS No.90104-36-2
Molecular FormulaC11H13NO2
Molecular Weight191.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 1-amino-2,3-dihydro-1h-indene-1-carboxylate CAS 90104-36-2 chemical structure

Description

The molecular framework of Methyl 1-amino-2,3-dihydro-1h-indene-1-carboxylate (C11H13NO2) is characterized by an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. 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).

Methyl 1-amino-2,3-dihydro-1h-indene-1-carboxylate (CAS 90104-36-2), molecular formula C11H13NO2 and molecular weight 191.23 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), Methyl 1-amino-2,3-dihydro-1h-indene-1-carboxylate 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 FormulaC11H13NO2
Molecular Weight191.23 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Nitrogen Atoms1

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