(R)-tert-Butyl (1-oxo-1-(pyridin-2-yl)propan-2-yl)carbamate CAS 2743440-29-9

Purity 97%+In StockPharmaceutical Standards
CAS No.2743440-29-9
Molecular FormulaC13H18N2O3
Molecular Weight250.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-tert-Butyl (1-oxo-1-(pyridin-2-yl)propan-2-yl)carbamate CAS 2743440-29-9 chemical structure

Description

As a certified reference material (CRM), (R)-tert-Butyl (1-oxo-1-(pyridin-2-yl)propan-2-yl)carbamate 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.

(R)-tert-Butyl (1-oxo-1-(pyridin-2-yl)propan-2-yl)carbamate (CAS 2743440-29-9), molecular formula C13H18N2O3 and molecular weight 250.29 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, (R)-tert-Butyl (1-oxo-1-(pyridin-2-yl)propan-2-yl)carbamate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 250.29 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 FormulaC13H18N2O3
Molecular Weight250.29 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.)2002
Nitrogen Atoms2

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