trans-Cyclohexane-1,3,5-tricarboxylic acid CAS 16526-69-5

Purity 97%+In StockPharmaceutical Standards
CAS No.16526-69-5
Molecular FormulaC9H12O6
Molecular Weight216.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

trans-Cyclohexane-1,3,5-tricarboxylic acid CAS 16526-69-5 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 trans-Cyclohexane-1,3,5-tricarboxylic acid.

CATO supplies trans-Cyclohexane-1,3,5-tricarboxylic acid (CAS 16526-69-5), a certified reference material (molecular formula C9H12O6, MW 216.19 g/mol) for analytical method development and quality control.

Structurally, trans-Cyclohexane-1,3,5-tricarboxylic acid (C9H12O6) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 216.19 g/mol, it falls into the medium-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC9H12O6
Molecular Weight216.19 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.)1961

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