5-Dodecylpyrimidine-2,4,6-triamine CAS 94087-76-0

Purity 97%+In StockPharmaceutical Standards
CAS No.94087-76-0
Molecular FormulaC16H31N5
Molecular Weight293.45 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Dodecylpyrimidine-2,4,6-triamine CAS 94087-76-0 chemical structure

Description

The occurrence of 5-Dodecylpyrimidine-2,4,6-triamine 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.

5-Dodecylpyrimidine-2,4,6-triamine (CAS 94087-76-0) is a high-purity analytical reference standard with the molecular formula C16H31N5 and a molecular weight of 293.45 g/mol.

5-Dodecylpyrimidine-2,4,6-triamine (C16H31N5) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its physicochemical properties are representative of its class; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 5-Dodecylpyrimidine-2,4,6-triamine 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 FormulaC16H31N5
Molecular Weight293.45 g/mol
AppearanceOff-white to pale yellow crystalline powder
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.)1983
Nitrogen Atoms5

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