2-(Pentan-2-yl)-2,3-dihydro-1h-isoindol-4-amine CAS 1099643-86-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1099643-86-3
Molecular FormulaC13H20N2
Molecular Weight204.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(Pentan-2-yl)-2,3-dihydro-1h-isoindol-4-amine CAS 1099643-86-3 chemical structure

Description

The occurrence of 2-(Pentan-2-yl)-2,3-dihydro-1h-isoindol-4-amine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

2-(Pentan-2-yl)-2,3-dihydro-1h-isoindol-4-amine (CAS 1099643-86-3) is a high-purity analytical reference standard with the molecular formula C13H20N2 and a molecular weight of 204.31 g/mol.

2-(Pentan-2-yl)-2,3-dihydro-1h-isoindol-4-amine (C13H20N2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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-(Pentan-2-yl)-2,3-dihydro-1h-isoindol-4-amine 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 FormulaC13H20N2
Molecular Weight204.31 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms2

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