6-((tert-Butoxycarbonyl)amino)-4-chloronicotinic acid CAS 1260670-99-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1260670-99-2
Molecular FormulaC11H13ClN2O4
Molecular Weight272.68 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-((tert-Butoxycarbonyl)amino)-4-chloronicotinic acid CAS 1260670-99-2 chemical structure

Description

The molecular framework of 6-((tert-Butoxycarbonyl)amino)-4-chloronicotinic acid (C11H13ClN2O4) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. 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).

6-((tert-Butoxycarbonyl)amino)-4-chloronicotinic acid (CAS 1260670-99-2) is a high-purity analytical reference standard with the molecular formula C11H13ClN2O4 and a molecular weight of 272.68 g/mol.

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

CATO manufactures 6-((tert-Butoxycarbonyl)amino)-4-chloronicotinic 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.

Physical & Chemical Properties

Molecular FormulaC11H13ClN2O4
Molecular Weight272.68 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms2

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