(1R,3s,5S)-9-(tert-butoxycarbonyl)-9-azabicyclo[3.3.1]Nonane-3-carboxylic acid CAS 2231663-92-4

Purity 97%+In StockPharmaceutical Standards
CAS No.2231663-92-4
Molecular FormulaC14H23NO4
Molecular Weight269.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1R,3s,5S)-9-(tert-butoxycarbonyl)-9-azabicyclo[3.3.1]Nonane-3-carboxylic acid CAS 2231663-92-4 chemical structure

Description

(1R,3s,5S)-9-(tert-butoxycarbonyl)-9-azabicyclo[3.3.1]Nonane-3-carboxylic acid (C14H23NO4) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

(1R,3s,5S)-9-(tert-butoxycarbonyl)-9-azabicyclo[3.3.1]Nonane-3-carboxylic acid (CAS 2231663-92-4), molecular formula C14H23NO4 and molecular weight 269.34 g/mol, is a CATO reference standard with documented purity and traceability.

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

As a certified reference material (CRM), (1R,3s,5S)-9-(tert-butoxycarbonyl)-9-azabicyclo[3.3.1]Nonane-3-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 FormulaC14H23NO4
Molecular Weight269.34 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1998
Nitrogen Atoms1

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