3-Chloro-1-(4-methoxyphenyl)-4-(m-tolylamino)-1H-pyrrole-2,5-dione CAS 61892-19-1

Purity 97%+In StockPharmaceutical Standards
CAS No.61892-19-1
Molecular FormulaC18H15ClN2O3
Molecular Weight342.78 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Chloro-1-(4-methoxyphenyl)-4-(m-tolylamino)-1H-pyrrole-2,5-dione CAS 61892-19-1 chemical structure

Description

3-Chloro-1-(4-methoxyphenyl)-4-(m-tolylamino)-1H-pyrrole-2,5-dione (CAS 61892-19-1), molecular formula C18H15ClN2O3 and molecular weight 342.78 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 3-Chloro-1-(4-methoxyphenyl)-4-(m-tolylamino)-1H-pyrrole-2,5-dione (C18H15ClN2O3) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 12.0, corresponding to approximately 12 ring(s) or double-bond equivalent(s). With a molecular weight of 342.78 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 3-Chloro-1-(4-methoxyphenyl)-4-(m-tolylamino)-1H-pyrrole-2,5-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 FormulaC18H15ClN2O3
Molecular Weight342.78 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Halogen ContentCl-containing
Nitrogen Atoms2

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