(R)-3-(1-tert-Butoxycarbonylamino-ethyl)-benzoic acid CAS 193150-14-0

Purity 97%+In StockPharmaceutical Standards
CAS No.193150-14-0
Molecular FormulaC14H19NO4
Molecular Weight265.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-3-(1-tert-Butoxycarbonylamino-ethyl)-benzoic acid CAS 193150-14-0 chemical structure

Description

As a certified reference material (CRM), (R)-3-(1-tert-Butoxycarbonylamino-ethyl)-benzoic acid 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)-3-(1-tert-Butoxycarbonylamino-ethyl)-benzoic acid (CAS 193150-14-0) is a high-purity analytical reference standard with the molecular formula C14H19NO4 and a molecular weight of 265.30 g/mol.

The molecular framework of (R)-3-(1-tert-Butoxycarbonylamino-ethyl)-benzoic acid (C14H19NO4) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC14H19NO4
Molecular Weight265.30 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 methanol, acetonitrile, DMSO, water (slightly soluble)
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.)2012
Nitrogen Atoms1

Recommended Standards

Why CATO?