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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Lorlatinib, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Lorlatinib impurity reference standards are invaluable for pharmaceutical research, supporting product development, ANDA and DMF submissions, quality control (QC), method validation, and stability studies. They also aid in identifying unknown impurities and assessing genotoxic potential.
Our Lorlatinib-related products undergo thorough characterization and are supplied with detailed Certificates of Analysis (COA) and analytical data that meet regulatory requirements. All supplied products are re-tested at regular intervals to ensure ongoing quality and compliance.

Lorlatinib Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Deulorlatinib Stable Isotopes CS-O-59446 2131126-33-3 Enquire
Lorlatinib 13C,d3 Stable Isotopes CS-CX-00760 1454846-35-5 (Unlabeled) Enquire
Lorlatinib-d6 Stable Isotopes CS-O-59447 2541062-00-2 Enquire


API Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Lorlatinib API Standards CS-T-84754 1454846-35-5 Enquire


Impurities

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
(S)-Lorlatinib Impurities CS-O-57760 1454847-76-7 Enquire
Lorlatinib Impurity 2 Impurities CS-O-57139 1455009-85-4 Enquire
Lorlatinib Methyl ester impurity Impurities CS-O-56954 1454848-04-4 Enquire
N-Nitroso Lorlatinib impurity-4 Impurities CS-EO-02671 Not Available Enquire