Description

Gadoversetamide (200 Mg) is a paramagnetic gadolinium-based contrast agent used in magnetic resonance imaging (MRI). This compound is critical for enhancing the contrast and diagnostic clarity of vascular structures and lesions during medical imaging procedures. It is primarily required by pharmaceutical manufacturers, diagnostic imaging centers, and research institutions developing advanced contrast media.

Application

• Primary component in the formulation of non-ionic, low-osmolar MRI contrast agents.
• Used in clinical diagnostics for contrast-enhanced magnetic resonance angiography (CE-MRA).
• Essential for research and development of next-generation gadolinium-based contrast agents (GBCAs).
• Applied in preclinical studies to evaluate organ perfusion and vascular integrity.
• Utilized in the quality control and analytical testing of finished pharmaceutical products.
• Serves as a reference standard in regulatory submissions and pharmacopeial testing.

Basic Information

Product Name	Gadoversetamide (200 Mg)
CAS No.	131069-91-5
Molecular Formula	C20H34GdN5O10
Molecular Weight	661.77 g/mol
Synonyms	Gadoversetamide; OptiMARK; Gd-DTPA-BMEA; Gadolinium diethylenetriaminepentaacetate bismethoxyethylamide; (OC-6-21)-[N,N-Bis[2-[bis(carboxymethyl)amino]ethyl]glycinato(5-)]gadolinate(2-); Gd-DTPA-BMA; B-19036; Gadoversetamide (USP)
EINECS	Contact for details

Quality Control

Our Gadoversetamide is manufactured and tested to meet stringent pharmaceutical standards. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) verifying identity, purity, and absence of critical impurities, including free gadolinium. We adhere to relevant pharmacopeial guidelines (e.g., USP monographs) and GMP principles to ensure product integrity and traceability for our global B2B clients.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference standard
Assay (HPLC)	NLT 98.0%
Free Gadolinium	NMT 0.1%
Related Substances (HPLC)	Total impurities NMT 2.0%
Water Content (KF)	NMT 5.0%
Residue on Ignition	NMT 0.5%
Bacterial Endotoxins	< 0.5 EU/mg

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.