(1S,2S)-Cyclohexane-1,2-dicarboxylic acid CAS 21963-41-7

Purity 97%+In StockPharmaceutical Standards
CAS No.21963-41-7
Molecular FormulaC8H12O4
Molecular Weight172.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1S,2S)-Cyclohexane-1,2-dicarboxylic acid CAS 21963-41-7 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including (1S,2S)-Cyclohexane-1,2-dicarboxylic acid.

CATO supplies (1S,2S)-Cyclohexane-1,2-dicarboxylic acid (CAS 21963-41-7), a certified reference material (molecular formula C8H12O4, MW 172.18 g/mol) for analytical method development and quality control.

The molecular framework of (1S,2S)-Cyclohexane-1,2-dicarboxylic acid (C8H12O4) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional 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).

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), (1S,2S)-Cyclohexane-1,2-dicarboxylic 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 FormulaC8H12O4
Molecular Weight172.18 g/mol
Purity97%+
StorageStore at 2-8°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)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1963

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