(1-Heptyl-5-phenyl-1H-pyrrol-3-yl)-1-naphthalenylmethanone CAS 914458-21-2

Purity 97%+In StockPharmaceutical Standards
CAS No.914458-21-2
Molecular FormulaC28H29NO
Molecular Weight395.54 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1-Heptyl-5-phenyl-1H-pyrrol-3-yl)-1-naphthalenylmethanone CAS 914458-21-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 395.54 g/mol gives (1-Heptyl-5-phenyl-1H-pyrrol-3-yl)-1-naphthalenylmethanone distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

(1-Heptyl-5-phenyl-1H-pyrrol-3-yl)-1-naphthalenylmethanone (CAS 914458-21-2) is a high-purity analytical reference standard with the molecular formula C28H29NO and a molecular weight of 395.54 g/mol.

The molecular framework of (1-Heptyl-5-phenyl-1H-pyrrol-3-yl)-1-naphthalenylmethanone (C28H29NO) 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. 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 FormulaC28H29NO
Molecular Weight395.54 g/mol
AppearancePale yellow to yellow crystalline powder
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)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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