[1,2,3]Triazolo[1,5-a]pyridine-7-carbaldehyde CAS 169888-58-8

Purity 97%+In StockPharmaceutical Standards
CAS No.169888-58-8
Molecular FormulaC7H5N3O
Molecular Weight147.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[1,2,3]Triazolo[1,5-a]pyridine-7-carbaldehyde CAS 169888-58-8 chemical structure

Description

The occurrence of [1,2,3]Triazolo[1,5-a]pyridine-7-carbaldehyde is closely related to an amide group, a hydroxyl group, an ether linkage, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies [1,2,3]Triazolo[1,5-a]pyridine-7-carbaldehyde (CAS 169888-58-8), a certified reference material (molecular formula C7H5N3O, MW 147.13 g/mol) for analytical method development and quality control.

Owing to an amide group, a hydroxyl group, an ether linkage, an aromatic ring system, [1,2,3]Triazolo[1,5-a]pyridine-7-carbaldehyde is typically off-white to pale yellow liquid. Its solid-state physicochemical attributes — including a molecular weight of 147.13 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 FormulaC7H5N3O
Molecular Weight147.13 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.)2005
Nitrogen Atoms3

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