L-Phenylalanyl-N-(di-1H-imidazoL-2-ylmethyl)-L-histidinamide CAS 666746-74-3

Purity 97%+In StockPharmaceutical Standards
CAS No.666746-74-3
Molecular FormulaC22H25N9O2
Molecular Weight447.49 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

L-Phenylalanyl-N-(di-1H-imidazoL-2-ylmethyl)-L-histidinamide CAS 666746-74-3 chemical structure

Description

As a certified reference material (CRM), L-Phenylalanyl-N-(di-1H-imidazoL-2-ylmethyl)-L-histidinamide 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.

L-Phenylalanyl-N-(di-1H-imidazoL-2-ylmethyl)-L-histidinamide (CAS 666746-74-3), molecular formula C22H25N9O2 and molecular weight 447.49 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C22H25N9O2, L-Phenylalanyl-N-(di-1H-imidazoL-2-ylmethyl)-L-histidinamide contains a steroid core, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 447.49 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

Physical & Chemical Properties

Molecular FormulaC22H25N9O2
Molecular Weight447.49 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Nitrogen Atoms9

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