2-(Piperazin-1-yl)-n-[4-(trifluoromethoxy)phenyl]acetamide CAS 901271-83-8

Purity 97%+In StockPharmaceutical Standards
CAS No.901271-83-8
Molecular FormulaC13H16F3N3O2
Molecular Weight303.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(Piperazin-1-yl)-n-[4-(trifluoromethoxy)phenyl]acetamide CAS 901271-83-8 chemical structure

Description

As a certified reference material (CRM), 2-(Piperazin-1-yl)-n-[4-(trifluoromethoxy)phenyl]acetamide 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 2-(Piperazin-1-yl)-n-[4-(trifluoromethoxy)phenyl]acetamide (CAS 901271-83-8), a certified reference material (molecular formula C13H16F3N3O2, MW 303.28 g/mol) for analytical method development and quality control.

Structurally, 2-(Piperazin-1-yl)-n-[4-(trifluoromethoxy)phenyl]acetamide (C13H16F3N3O2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 303.28 g/mol, it falls into the moderately-high-molecular-weight range. 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.

Physical & Chemical Properties

Molecular FormulaC13H16F3N3O2
Molecular Weight303.28 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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; 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.)1987
Halogen ContentF-containing
Nitrogen Atoms3

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