2,4-Diamino-6-((4-iodophenyl)amino)pyrimidine-5-carboxamide CAS 7254-18-4

Purity 97%+In StockPharmaceutical Standards
CAS No.7254-18-4
Molecular FormulaC11H11IN6O
Molecular Weight370.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,4-Diamino-6-((4-iodophenyl)amino)pyrimidine-5-carboxamide CAS 7254-18-4 chemical structure

Description

CATO manufactures 2,4-Diamino-6-((4-iodophenyl)amino)pyrimidine-5-carboxamide 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.

2,4-Diamino-6-((4-iodophenyl)amino)pyrimidine-5-carboxamide (CAS 7254-18-4) is a high-purity analytical reference standard with the molecular formula C11H11IN6O and a molecular weight of 370.15 g/mol.

Structurally, 2,4-Diamino-6-((4-iodophenyl)amino)pyrimidine-5-carboxamide (C11H11IN6O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 370.15 g/mol, it falls into the moderately-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 FormulaC11H11IN6O
Molecular Weight370.15 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1959
Halogen ContentI-containing
Nitrogen Atoms6

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