4-(tert-Butoxy)-5-cyclopropoxy-N,N-dimethylnicotinamide CAS 1243312-77-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1243312-77-7
Molecular FormulaC15H22N2O3
Molecular Weight278.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(tert-Butoxy)-5-cyclopropoxy-N,N-dimethylnicotinamide CAS 1243312-77-7 chemical structure

Description

As a certified reference material (CRM), 4-(tert-Butoxy)-5-cyclopropoxy-N,N-dimethylnicotinamide 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.

CATO supplies 4-(tert-Butoxy)-5-cyclopropoxy-N,N-dimethylnicotinamide (CAS 1243312-77-7), a certified reference material (molecular formula C15H22N2O3, MW 278.35 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 4-(tert-Butoxy)-5-cyclopropoxy-N,N-dimethylnicotinamide is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 278.35 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC15H22N2O3
Molecular Weight278.35 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.)1990
Nitrogen Atoms2

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