(3-methoxynaphthalen-1-yl)(1-pentyl-1H-indol-3-yl)methanone 1696409-36-5 CAS 1696409-36-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1696409-36-5
Molecular FormulaC25H25NO2
Molecular Weight371.47 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3-methoxynaphthalen-1-yl)(1-pentyl-1H-indol-3-yl)methanone
1696409-36-5 CAS 1696409-36-5 chemical structure

Description

(3-methoxynaphthalen-1-yl)(1-pentyl-1H-indol-3-yl)methanone 1696409-36-5 (C25H25NO2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

(3-methoxynaphthalen-1-yl)(1-pentyl-1H-indol-3-yl)methanone 1696409-36-5 (CAS 1696409-36-5), molecular formula C25H25NO2 and molecular weight 371.47 g/mol, is a CATO reference standard with documented purity and traceability.

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), (3-methoxynaphthalen-1-yl)(1-pentyl-1H-indol-3-yl)methanone 1696409-36-5 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 FormulaC25H25NO2
Molecular Weight371.47 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
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Nitrogen Atoms1

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