2-Methyl-1-[(4-methylphenyl)methyl]-1h-indole-3-carbaldehyde CAS 592550-44-2

Purity 97%+In StockPharmaceutical Standards
CAS No.592550-44-2
Molecular FormulaC18H17NO
Molecular Weight263.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Methyl-1-[(4-methylphenyl)methyl]-1h-indole-3-carbaldehyde CAS 592550-44-2 chemical structure

Description

The occurrence of 2-Methyl-1-[(4-methylphenyl)methyl]-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.

CATO supplies 2-Methyl-1-[(4-methylphenyl)methyl]-1h-indole-3-carbaldehyde (CAS 592550-44-2), a certified reference material (molecular formula C18H17NO, MW 263.33 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, 2-Methyl-1-[(4-methylphenyl)methyl]-1h-indole-3-carbaldehyde is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 263.33 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC18H17NO
Molecular Weight263.33 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.)1984
Nitrogen Atoms1

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