5,6,7,8-Tetrahydro-1,2,4-triazolo[4,3-a]pyridin-8-amine CAS 1307237-49-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1307237-49-5
Molecular FormulaC6H10N4
Molecular Weight138.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5,6,7,8-Tetrahydro-1,2,4-triazolo[4,3-a]pyridin-8-amine CAS 1307237-49-5 chemical structure

Description

The occurrence of 5,6,7,8-Tetrahydro-1,2,4-triazolo[4,3-a]pyridin-8-amine is closely related to a nitrile group, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 5,6,7,8-Tetrahydro-1,2,4-triazolo[4,3-a]pyridin-8-amine (CAS 1307237-49-5), a certified reference material (molecular formula C6H10N4, MW 138.17 g/mol) for analytical method development and quality control.

The molecular framework of 5,6,7,8-Tetrahydro-1,2,4-triazolo[4,3-a]pyridin-8-amine (C6H10N4) is characterized by a nitrile group, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.

As a certified reference material (CRM), 5,6,7,8-Tetrahydro-1,2,4-triazolo[4,3-a]pyridin-8-amine 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 FormulaC6H10N4
Molecular Weight138.17 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms4

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