(1E)-N-[(4-Methoxyphenyl)methoxy]-2,3,4,9-tetrahydro-1H-carbazol-1-imine CAS 860612-35-7

Purity 97%+In StockPharmaceutical Standards
CAS No.860612-35-7
Molecular FormulaC20H20N2O2
Molecular Weight320.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1E)-N-[(4-Methoxyphenyl)methoxy]-2,3,4,9-tetrahydro-1H-carbazol-1-imine CAS 860612-35-7 chemical structure

Description

(1E)-N-[(4-Methoxyphenyl)methoxy]-2,3,4,9-tetrahydro-1H-carbazol-1-imine (CAS 860612-35-7), molecular formula C20H20N2O2 and molecular weight 320.39 g/mol, is a CATO reference standard with documented purity and traceability.

(1E)-N-[(4-Methoxyphenyl)methoxy]-2,3,4,9-tetrahydro-1H-carbazol-1-imine (C20H20N2O2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, 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. 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), (1E)-N-[(4-Methoxyphenyl)methoxy]-2,3,4,9-tetrahydro-1H-carbazol-1-imine 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 FormulaC20H20N2O2
Molecular Weight320.39 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2

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