Tacrolimus impurity 67 CAS CATO-C4X-130067

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-130067
Molecular FormulaC44H69NO12
Molecular Weight804.02 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Tacrolimus impurity 67 CAS CATO-C4X-130067 chemical structure

Description

As a certified reference material (CRM), Tacrolimus impurity 67 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.

CATO supplies Tacrolimus impurity 67 (CAS CATO-C4X-130067), a pharmacopoeial impurity reference standard (molecular formula C44H69NO12, MW 804.02 g/mol) used for the identification and quantification of trace impurities in APIs.

Tacrolimus impurity 67 (C44H69NO12) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

Physical & Chemical Properties

Molecular FormulaC44H69NO12
Molecular Weight804.02 g/mol
Purity97%+
StorageStore at room temperature, 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
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms1

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