(4-Methylcyclohexyl)(pyridin-4-yl)methanamine CAS 1343816-09-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1343816-09-0
Molecular FormulaC13H20N2
Molecular Weight204.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-Methylcyclohexyl)(pyridin-4-yl)methanamine CAS 1343816-09-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 204.31 g/mol gives (4-Methylcyclohexyl)(pyridin-4-yl)methanamine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

(4-Methylcyclohexyl)(pyridin-4-yl)methanamine (CAS 1343816-09-0), molecular formula C13H20N2 and molecular weight 204.31 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, (4-Methylcyclohexyl)(pyridin-4-yl)methanamine is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 204.31 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC13H20N2
Molecular Weight204.31 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms2

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