Telmisartan Impurity 101 CAS 1338830-39-9

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.1338830-39-9
Molecular FormulaC33H29N5
Molecular Weight495.62 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Telmisartan Impurity 101 CAS 1338830-39-9 chemical structure

Description

Telmisartan Impurity 101 (CAS 1338830-39-9) is a certified pharmaceutical impurity reference standard with the molecular formula C33H29N5 and a molecular weight of 495.62 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, Telmisartan Impurity 101 is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 495.62 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures Telmisartan Impurity 101 under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC33H29N5
Molecular Weight495.62 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)22.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms5

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