N-Benzyl-6-chloropyrimidin-4-amine CAS 61667-16-1

Purity 97%+In StockPharmaceutical Standards
CAS No.61667-16-1
Molecular FormulaC11H10ClN3
Molecular Weight219.67 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Benzyl-6-chloropyrimidin-4-amine CAS 61667-16-1 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 219.67 g/mol gives N-Benzyl-6-chloropyrimidin-4-amine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies N-Benzyl-6-chloropyrimidin-4-amine (CAS 61667-16-1), a certified reference material (molecular formula C11H10ClN3, MW 219.67 g/mol) for analytical method development and quality control.

The molecular framework of N-Benzyl-6-chloropyrimidin-4-amine (C11H10ClN3) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.

CATO manufactures N-Benzyl-6-chloropyrimidin-4-amine 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 FormulaC11H10ClN3
Molecular Weight219.67 g/mol
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Halogen ContentCl-containing
Nitrogen Atoms3

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