Amoxicillin EP Impurity J(See C4X-11489) CAS CATO-C4X-114810

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Amoxicillin EP Impurity J(See C4X-11489).

Amoxicillin EP Impurity J(See C4X-11489) (CAS CATO-C4X-114810) is a certified pharmaceutical impurity reference standard with the molecular formula C33H39N5O10S2 and a molecular weight of 729.82 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, Amoxicillin EP Impurity J(See C4X-11489) is typically pale yellow to yellow amorphous powder. Its solid-state physicochemical attributes — including a molecular weight of 729.82 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 Amoxicillin EP Impurity J(See C4X-11489) 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

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