6-(Tert-butyl)-N-propylpyrimidin-4-amine CAS 1247552-72-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1247552-72-2
Molecular FormulaC11H19N3
Molecular Weight193.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(Tert-butyl)-N-propylpyrimidin-4-amine CAS 1247552-72-2 chemical structure

Description

The occurrence of 6-(Tert-butyl)-N-propylpyrimidin-4-amine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

6-(Tert-butyl)-N-propylpyrimidin-4-amine (CAS 1247552-72-2), molecular formula C11H19N3 and molecular weight 193.29 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, 6-(Tert-butyl)-N-propylpyrimidin-4-amine is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 193.29 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 6-(Tert-butyl)-N-propylpyrimidin-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 FormulaC11H19N3
Molecular Weight193.29 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms3

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