3-(tert-Butyl)-7-iodo-[1,2,4]triazolo[4,3-a]pyridine CAS 1057393-45-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1057393-45-9
Molecular FormulaC10H12IN3
Molecular Weight301.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(tert-Butyl)-7-iodo-[1,2,4]triazolo[4,3-a]pyridine CAS 1057393-45-9 chemical structure

Description

CATO manufactures 3-(tert-Butyl)-7-iodo-[1,2,4]triazolo[4,3-a]pyridine 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.

3-(tert-Butyl)-7-iodo-[1,2,4]triazolo[4,3-a]pyridine (CAS 1057393-45-9) is a high-purity analytical reference standard with the molecular formula C10H12IN3 and a molecular weight of 301.13 g/mol.

Structurally, 3-(tert-Butyl)-7-iodo-[1,2,4]triazolo[4,3-a]pyridine (C10H12IN3) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 301.13 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC10H12IN3
Molecular Weight301.13 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
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentI-containing
Nitrogen Atoms3

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