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Ioversol CAS NO 133442-32-7


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CAS No.:133442-32-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Ioversol is a non-ionic, water-soluble, tri-iodinated contrast agent belonging to the class of low-osmolar radiographic media. Its primary value lies in its excellent safety profile and diagnostic efficacy for visualizing vascular structures and organs during radiographic procedures. This compound is essential for manufacturers and formulators in the pharmaceutical and diagnostic imaging industries, where it is used to produce injectable contrast solutions for computed tomography (CT), angiography, and urography.

Application

  • Diagnostic Imaging Contrast Media: Primary component in formulations for intravenous and intra-arterial injection.
  • Computed Tomography (CT) Enhancement: Used for body cavity and vascular imaging to improve soft tissue contrast and lesion detection.
  • Angiography: Critical for visualizing blood vessels in coronary, cerebral, and peripheral angiography procedures.
  • Urography/Excretory Urography: Employed to assess the structure and function of the kidneys, ureters, and bladder.
  • Pharmaceutical Intermediates: Serves as a key starting material or intermediate in the synthesis of specialized contrast agents.
  • Research & Development: Utilized in academic and industrial R&D for developing new imaging protocols and contrast formulations.

Basic Information

Product Name Ioversol
CAS No. 133442-32-7
Molecular Formula C24H36I3N3O9
Molecular Weight 807.28 g/mol
Synonyms Ioversol; Optiray; 5-[N-(2-Hydroxyethyl)acetamido]-2,4,6-triiodo-N,N'-bis(2,3-dihydroxypropyl)isophthalamide; Ioversolum; ZK 35760; Ioversolum [Latin]; (OC-6-11)-5-(Acetylmethylamino)-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1,3-benzenedicarboxamide
EINECS Contact for details

Quality Control

Our Ioversol is manufactured under strict quality management systems, targeting specifications suitable for pharmaceutical applications. Quality is assured through comprehensive analytical testing, including HPLC for assay and impurity profiling, residual solvent analysis, and tests for related substances. We provide full traceability and support our products with Certificates of Analysis (COA) that detail compliance with agreed specifications. Our quality commitment aligns with cGMP principles to ensure batch-to-batch consistency and reliability for our global B2B partners.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture. Keep away from incompatible materials.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water (KF) ≤ 5.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any individual impurity ≤ 1.0%
Residual Solvents (GC) Complies with ICH Q3C
Heavy Metals ≤ 20 ppm
pH (5% Solution) 5.5 - 7.5
Specific Rotation Contact for details

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

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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