2-[2-(tert-Butoxycarbonyl)hydrazino]nicotinic acid CAS 1027808-61-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1027808-61-2
Molecular FormulaC11H15N3O4
Molecular Weight253.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[2-(tert-Butoxycarbonyl)hydrazino]nicotinic acid CAS 1027808-61-2 chemical structure

Description

Based on its molecular formula C11H15N3O4, 2-[2-(tert-Butoxycarbonyl)hydrazino]nicotinic 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 253.25 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).

CATO supplies 2-[2-(tert-Butoxycarbonyl)hydrazino]nicotinic acid (CAS 1027808-61-2), a certified reference material (molecular formula C11H15N3O4, MW 253.25 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), 2-[2-(tert-Butoxycarbonyl)hydrazino]nicotinic acid 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 FormulaC11H15N3O4
Molecular Weight253.25 g/mol
AppearanceOff-white to pale yellow crystalline powder
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.)1988
Nitrogen Atoms3

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