Gadobutrol

Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Gadobutrol reference materials. Our portfolio includes both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine derivatives (N-NO products). These reference standards play a crucial role in pharmaceutical R&D, aiding in formulation development, ANDA/DMF submissions, quality control, method validation, stability studies, and impurity profiling—including the identification and assessment of potentially genotoxic impurities.

Each Gadobutrol-related product is rigorously characterized and delivered with a detailed Certificate of Analysis (COA) and comprehensive analytical data to ensure regulatory compliance. Upon request, we also offer EP/USP traceable standards. To maintain the highest quality standards, all materials are subject to periodic re-testing and continuous quality monitoring.

Gadobutrol Monohydrate

Picture of Gadobutrol Monohydrate
CAT No: VS-G003001
CAS No: 198637-52-4
Mol.F.: C18H31GdN4O9 : H2O
Mol.Wt.: 604.7 : 18.0
Status: Custom Synthesis

Gadobutrol EP Impurity A

Picture of Gadobutrol EP Impurity A
CAT No: VS-G003002
CAS No: 2514736-58-2
Mol.F.: C20H40N4O10
Mol.Wt.: 496.6
Status: Custom Synthesis

Gadobutrol EP Impurity B

Picture of Gadobutrol EP Impurity B
CAT No: VS-G003003
CAS No: 138168-36-2
Mol.F.: C18H34N4O9
Mol.Wt.: 450.5
Status: Custom Synthesis

Gadobutrol EP Impurity C

Picture of Gadobutrol EP Impurity C
CAT No: VS-G003004
CAS No: 112188-16-6
Mol.F.: C14H23GdN4O6
Mol.Wt.: 500.6
Status: Custom Synthesis

Contact

040-23076623, 040-4852 9278

E-Mail

info@venkatasailifesciences.com