(S)-N-(2-(4-(tert-Butyl)-1-phenyl-4,5-dihydro-1H-imidazol-2-yl)phenyl)-6-methylpicolinamide CAS 2218516-49-3

Purity 97%+In StockPharmaceutical Standards
CAS No.2218516-49-3
Molecular FormulaC26H28N4O
Molecular Weight412.53 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-N-(2-(4-(tert-Butyl)-1-phenyl-4,5-dihydro-1H-imidazol-2-yl)phenyl)-6-methylpicolinamide CAS 2218516-49-3 chemical structure

Description

CATO supplies (S)-N-(2-(4-(tert-Butyl)-1-phenyl-4,5-dihydro-1H-imidazol-2-yl)phenyl)-6-methylpicolinamide (CAS 2218516-49-3), a certified reference material (molecular formula C26H28N4O, MW 412.53 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, (S)-N-(2-(4-(tert-Butyl)-1-phenyl-4,5-dihydro-1H-imidazol-2-yl)phenyl)-6-methylpicolinamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 412.53 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

As a certified reference material (CRM), (S)-N-(2-(4-(tert-Butyl)-1-phenyl-4,5-dihydro-1H-imidazol-2-yl)phenyl)-6-methylpicolinamide 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 FormulaC26H28N4O
Molecular Weight412.53 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1998
Nitrogen Atoms4

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