(1-(2,4-Dimethylphenyl)-1H-1,2,3-triazol-4-yl)methanamine CAS 1250784-51-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1250784-51-0
Molecular FormulaC11H14N4
Molecular Weight202.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1-(2,4-Dimethylphenyl)-1H-1,2,3-triazol-4-yl)methanamine CAS 1250784-51-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 202.26 g/mol gives (1-(2,4-Dimethylphenyl)-1H-1,2,3-triazol-4-yl)methanamine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

(1-(2,4-Dimethylphenyl)-1H-1,2,3-triazol-4-yl)methanamine (CAS 1250784-51-0) is a high-purity analytical reference standard with the molecular formula C11H14N4 and a molecular weight of 202.26 g/mol.

(1-(2,4-Dimethylphenyl)-1H-1,2,3-triazol-4-yl)methanamine (C11H14N4) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

As a certified reference material (CRM), (1-(2,4-Dimethylphenyl)-1H-1,2,3-triazol-4-yl)methanamine meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H14N4
Molecular Weight202.26 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms4

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