3-Amino-2-(3-((tert-butoxycarbonyl)amino)propyl)isonicotinic acid CAS 1393550-11-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1393550-11-2
Molecular FormulaC14H21N3O4
Molecular Weight295.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Amino-2-(3-((tert-butoxycarbonyl)amino)propyl)isonicotinic acid CAS 1393550-11-2 chemical structure

Description

CATO supplies 3-Amino-2-(3-((tert-butoxycarbonyl)amino)propyl)isonicotinic acid (CAS 1393550-11-2), a certified reference material (molecular formula C14H21N3O4, MW 295.33 g/mol) for analytical method development and quality control.

3-Amino-2-(3-((tert-butoxycarbonyl)amino)propyl)isonicotinic acid (C14H21N3O4) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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), 3-Amino-2-(3-((tert-butoxycarbonyl)amino)propyl)isonicotinic 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 FormulaC14H21N3O4
Molecular Weight295.33 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 DMSO, DMF, methanol
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.)1991
Nitrogen Atoms3

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