1-(4-(tert-Butyl)cyclohexyl)-1H-1,2,3-triazole-4-carboxylic acid CAS 1710674-55-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1710674-55-7
Molecular FormulaC13H21N3O2
Molecular Weight251.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-(tert-Butyl)cyclohexyl)-1H-1,2,3-triazole-4-carboxylic acid CAS 1710674-55-7 chemical structure

Description

The molecular framework of 1-(4-(tert-Butyl)cyclohexyl)-1H-1,2,3-triazole-4-carboxylic acid (C13H21N3O2) 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).

CATO supplies 1-(4-(tert-Butyl)cyclohexyl)-1H-1,2,3-triazole-4-carboxylic acid (CAS 1710674-55-7), a certified reference material (molecular formula C13H21N3O2, MW 251.32 g/mol) for analytical method development and quality control.

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), 1-(4-(tert-Butyl)cyclohexyl)-1H-1,2,3-triazole-4-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 FormulaC13H21N3O2
Molecular Weight251.32 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 DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Nitrogen Atoms3

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