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

Altretamine Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Altretamine-d18 Stable Isotopes CS-T-103339 65886-69-3 Enquire


API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Altretamine API CS-T-01768 645-05-6 Enquire


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
4,6-dichloro-N,N-dimethyl-1,3,5-triazin-2-amine Impurity CS-ED-00530 2401-64-1 Enquire


Fine Chemicals

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
6-chloro-N2,N2,N4,N4,-tetramethyl-1,3,5-triazine-2,4-diamine Fine Chemicals CS-T-93525 3140-74-7 Enquire