(5Z,8Z,11Z,14Z)-N-(3-Nitrophenyl)icosa-5,8,11,14-tetraenamide CAS 1175954-87-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1175954-87-6
Molecular FormulaC26H36N2O3
Molecular Weight424.58 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(5Z,8Z,11Z,14Z)-N-(3-Nitrophenyl)icosa-5,8,11,14-tetraenamide CAS 1175954-87-6 chemical structure

Description

CATO manufactures (5Z,8Z,11Z,14Z)-N-(3-Nitrophenyl)icosa-5,8,11,14-tetraenamide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

(5Z,8Z,11Z,14Z)-N-(3-Nitrophenyl)icosa-5,8,11,14-tetraenamide (CAS 1175954-87-6), molecular formula C26H36N2O3 and molecular weight 424.58 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of (5Z,8Z,11Z,14Z)-N-(3-Nitrophenyl)icosa-5,8,11,14-tetraenamide (C26H36N2O3) 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 the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

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 FormulaC26H36N2O3
Molecular Weight424.58 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms2

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