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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Phenyltoloxamine, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Phenyltoloxamine 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 Phenyltoloxamine-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.

Phenyltoloxamine Related Compounds

Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
N-Desmethyl Phenyltoloxamine Hydrochloride Impurity CS-T-16416 75859-72-2 Enquire


Intermediate

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Phenyltoloxamine Intermediate CS-O-59352 92-12-6 Enquire


Nitrosamine

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
N-Nitroso N-Desmethyl Phenyltoloxamine Nitrosamine CS-O-57937 --- Enquire


Secondary Standards

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Phenyltoloxamine Citrate Secondary Standards CS-SS-25786-200MG 1176-08-05 Enquire


Analytical Standard

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
N-Nitroso N-Desmethyl Phenyltoloxamine Analytical Standard CS-O-57937-10MG --- Enquire
N-nitroso-desmethyl-phenyltoloxamine-100 PPM in Acetonitrile Analytical Standard CS-O-57937-1.5ML --- Enquire