n-(1-(Furan-2-yl)propan-2-yl)pivalamide CAS 1210193-14-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1210193-14-8
Molecular FormulaC12H19NO2
Molecular Weight209.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(1-(Furan-2-yl)propan-2-yl)pivalamide CAS 1210193-14-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 209.28 g/mol gives n-(1-(Furan-2-yl)propan-2-yl)pivalamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

n-(1-(Furan-2-yl)propan-2-yl)pivalamide (CAS 1210193-14-8) is a high-purity analytical reference standard with the molecular formula C12H19NO2 and a molecular weight of 209.28 g/mol.

Owing to an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage, n-(1-(Furan-2-yl)propan-2-yl)pivalamide is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 209.28 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

As a certified reference material (CRM), n-(1-(Furan-2-yl)propan-2-yl)pivalamide 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 FormulaC12H19NO2
Molecular Weight209.28 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms1

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