2-(3-Methoxypropyl)-1H-thioxantheno[2,1,9-def]isoquinoline-1,3(2H)-dione CAS 14121-47-2

Purity 97%+In StockPharmaceutical Standards
CAS No.14121-47-2
Molecular FormulaC22H33NO3S
Molecular Weight391.57 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3-Methoxypropyl)-1H-thioxantheno[2,1,9-def]isoquinoline-1,3(2H)-dione CAS 14121-47-2 chemical structure

Description

2-(3-Methoxypropyl)-1H-thioxantheno[2,1,9-def]isoquinoline-1,3(2H)-dione (CAS 14121-47-2) is a high-purity analytical reference standard with the molecular formula C22H33NO3S and a molecular weight of 391.57 g/mol.

Structurally, 2-(3-Methoxypropyl)-1H-thioxantheno[2,1,9-def]isoquinoline-1,3(2H)-dione (C22H33NO3S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 391.57 g/mol, it falls into the moderately-high-molecular-weight range. 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.

As a certified reference material (CRM), 2-(3-Methoxypropyl)-1H-thioxantheno[2,1,9-def]isoquinoline-1,3(2H)-dione 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 FormulaC22H33NO3S
Molecular Weight391.57 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Nitrogen Atoms1
Sulfur Atoms1

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