3-[(tert-Butoxy)carbonyl]bicyclo[1.1.1]pentane-1-carboxylic acid CAS 1638765-30-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1638765-30-6
Molecular FormulaC11H16O4
Molecular Weight212.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[(tert-Butoxy)carbonyl]bicyclo[1.1.1]pentane-1-carboxylic acid CAS 1638765-30-6 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

3-[(tert-Butoxy)carbonyl]bicyclo[1.1.1]pentane-1-carboxylic acid (CAS 1638765-30-6), molecular formula C11H16O4 and molecular weight 212.24 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 3-[(tert-Butoxy)carbonyl]bicyclo[1.1.1]pentane-1-carboxylic acid (C11H16O4) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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).

As a certified reference material (CRM), 3-[(tert-Butoxy)carbonyl]bicyclo[1.1.1]pentane-1-carboxylic 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.

Physical & Chemical Properties

Molecular FormulaC11H16O4
Molecular Weight212.24 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993

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