Mn(III) meso-Tetra (4-carboxyphenyl) porphine chloride CAS 55266-18-7

Purity 97%+In StockPharmaceutical Standards
CAS No.55266-18-7
Molecular FormulaC48H27N4O8
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Mn(III) meso-Tetra (4-carboxyphenyl) porphine chloride CAS 55266-18-7 chemical structure

Description

CATO manufactures Mn(III) meso-Tetra (4-carboxyphenyl) porphine chloride 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.

Mn(III) meso-Tetra (4-carboxyphenyl) porphine chloride (CAS 55266-18-7) is a high-purity analytical reference standard with the molecular formula C48H27N4O8MnHCl and a molecular weight of 879.16 g/mol.

Structurally, Mn(III) meso-Tetra (4-carboxyphenyl) porphine chloride (C48H27N4O8MnHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 36.5, corresponding to approximately 36 ring(s) or double-bond equivalent(s). With a molecular weight of 879.16 g/mol, it falls into the high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC48H27N4O8 Mn HCl
Molecular Weight879.16 g/mol
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)36.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1972
Halogen ContentCl-containing
Nitrogen Atoms4

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