1-Ethyl-3-(pyrrolidin-3-yl)-1H-indole CAS 804443-56-9

Purity 97%+In StockPharmaceutical Standards
CAS No.804443-56-9
Molecular FormulaC14H18N2
Molecular Weight214.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Ethyl-3-(pyrrolidin-3-yl)-1H-indole CAS 804443-56-9 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 1-Ethyl-3-(pyrrolidin-3-yl)-1H-indole.

CATO supplies 1-Ethyl-3-(pyrrolidin-3-yl)-1H-indole (CAS 804443-56-9), a certified reference material (molecular formula C14H18N2, MW 214.31 g/mol) for analytical method development and quality control.

Structurally, 1-Ethyl-3-(pyrrolidin-3-yl)-1H-indole (C14H18N2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 214.31 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 1-Ethyl-3-(pyrrolidin-3-yl)-1H-indole 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 FormulaC14H18N2
Molecular Weight214.31 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Nitrogen Atoms2

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