(11bS)-3,5-Dihydro-4H-dinaphtho[2,1-c:1′,2′-e]phosphepin-4-ethanamine CAS 1092064-06-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1092064-06-6
Molecular FormulaC24H22NP
Molecular Weight355.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(11bS)-3,5-Dihydro-4H-dinaphtho[2,1-c:1′,2′-e]phosphepin-4-ethanamine CAS 1092064-06-6 chemical structure

Description

CATO supplies (11bS)-3,5-Dihydro-4H-dinaphtho[2,1-c:1′,2′-e]phosphepin-4-ethanamine (CAS 1092064-06-6), a certified reference material (molecular formula C24H22NP, MW 355.41 g/mol) for analytical method development and quality control.

(11bS)-3,5-Dihydro-4H-dinaphtho[2,1-c:1′,2′-e]phosphepin-4-ethanamine (C24H22NP) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, organophosphorus functionality. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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), (11bS)-3,5-Dihydro-4H-dinaphtho[2,1-c:1′,2′-e]phosphepin-4-ethanamine 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 FormulaC24H22NP
Molecular Weight355.41 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
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)14.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms1

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