Furo[2,3-b]pyridin-6-ylmethanamine CAS 193750-81-1

Purity 97%+In StockPharmaceutical Standards
CAS No.193750-81-1
Molecular FormulaC8H8N2O
Molecular Weight148.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Furo[2,3-b]pyridin-6-ylmethanamine CAS 193750-81-1 chemical structure

Description

The molecular framework of Furo[2,3-b]pyridin-6-ylmethanamine (C8H8N2O) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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 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).

CATO supplies Furo[2,3-b]pyridin-6-ylmethanamine (CAS 193750-81-1), a certified reference material (molecular formula C8H8N2O, MW 148.16 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), Furo[2,3-b]pyridin-6-ylmethanamine 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 FormulaC8H8N2O
Molecular Weight148.16 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2012
Nitrogen Atoms2

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