5-(4-Tert-butylphenyl)-1H-indole-3-carbaldehyde CAS 893738-42-6

Purity 97%+In StockPharmaceutical Standards
CAS No.893738-42-6
Molecular FormulaC19H19NO
Molecular Weight277.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(4-Tert-butylphenyl)-1H-indole-3-carbaldehyde CAS 893738-42-6 chemical structure

Description

The occurrence of 5-(4-Tert-butylphenyl)-1H-indole-3-carbaldehyde is closely related to a steroid core, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

5-(4-Tert-butylphenyl)-1H-indole-3-carbaldehyde (CAS 893738-42-6), molecular formula C19H19NO and molecular weight 277.36 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 5-(4-Tert-butylphenyl)-1H-indole-3-carbaldehyde (C19H19NO) is characterized by a steroid core, 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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), 5-(4-Tert-butylphenyl)-1H-indole-3-carbaldehyde 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 FormulaC19H19NO
Molecular Weight277.36 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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