4-chloro-5-iodo-6-(2-methylpropyl)pyrimidine CAS 1514650-08-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1514650-08-8
Molecular FormulaC8H10ClIN2
Molecular Weight296.54 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-chloro-5-iodo-6-(2-methylpropyl)pyrimidine CAS 1514650-08-8 chemical structure

Description

Based on its molecular formula C8H10ClIN2, 4-chloro-5-iodo-6-(2-methylpropyl)pyrimidine contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine/iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 296.54 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

4-chloro-5-iodo-6-(2-methylpropyl)pyrimidine (CAS 1514650-08-8) is a high-purity analytical reference standard with the molecular formula C8H10ClIN2 and a molecular weight of 296.54 g/mol.

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.

CATO manufactures 4-chloro-5-iodo-6-(2-methylpropyl)pyrimidine 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.

Physical & Chemical Properties

Molecular FormulaC8H10ClIN2
Molecular Weight296.54 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentCl/I-containing
Nitrogen Atoms2

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