2-Methylamino-pyridine-3-carbaldehyde, hydrochloride CAS 67295-24-3

Purity 97%+In StockPharmaceutical Standards
CAS No.67295-24-3
Molecular FormulaC7H8N2O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Methylamino-pyridine-3-carbaldehyde, hydrochloride CAS 67295-24-3 chemical structure

Description

As a certified reference material (CRM), 2-Methylamino-pyridine-3-carbaldehyde, hydrochloride 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.

CATO supplies 2-Methylamino-pyridine-3-carbaldehyde, hydrochloride (CAS 67295-24-3), a certified reference material (molecular formula C7H8N2OHCl, MW 172.61 g/mol) for analytical method development and quality control.

Based on its molecular formula C7H8N2OHCl, 2-Methylamino-pyridine-3-carbaldehyde, hydrochloride contains an amide group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 172.61 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

Physical & Chemical Properties

Molecular FormulaC7H8N2O HCl
Molecular Weight172.61 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1976
Halogen ContentCl-containing
Nitrogen Atoms2

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