(5-Aminoindolin-1-yl)(pyrrolidin-1-yl)methanone CAS 1538056-69-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1538056-69-7
Molecular FormulaC13H17N3O
Molecular Weight231.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(5-Aminoindolin-1-yl)(pyrrolidin-1-yl)methanone CAS 1538056-69-7 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 231.29 g/mol gives (5-Aminoindolin-1-yl)(pyrrolidin-1-yl)methanone distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

(5-Aminoindolin-1-yl)(pyrrolidin-1-yl)methanone (CAS 1538056-69-7), molecular formula C13H17N3O and molecular weight 231.29 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of (5-Aminoindolin-1-yl)(pyrrolidin-1-yl)methanone (C13H17N3O) is characterized by a nitrogen-containing heterocyclic scaffold, 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), (5-Aminoindolin-1-yl)(pyrrolidin-1-yl)methanone 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 FormulaC13H17N3O
Molecular Weight231.29 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Nitrogen Atoms3

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Why CATO?