5,6,7,8-Tetrahydro-1,6-naphthyridine, oxalic acid CAS 1193388-00-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1193388-00-9
Molecular FormulaC8H10N2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5,6,7,8-Tetrahydro-1,6-naphthyridine, oxalic acid CAS 1193388-00-9 chemical structure

Description

CATO manufactures 5,6,7,8-Tetrahydro-1,6-naphthyridine, oxalic acid 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.

CATO supplies 5,6,7,8-Tetrahydro-1,6-naphthyridine, oxalic acid (CAS 1193388-00-9), a certified reference material (molecular formula C8H10N2C2H2O4, MW 224.22 g/mol) for analytical method development and quality control.

Based on its molecular formula C8H10N2C2H2O4, 5,6,7,8-Tetrahydro-1,6-naphthyridine, oxalic acid contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 224.22 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

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

Physical & Chemical Properties

Molecular FormulaC8H10N2 C2H2O4
Molecular Weight224.22 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms2

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