Description

Iomeron 350-D3 is a high-purity, non-ionic, iodinated contrast agent used in diagnostic imaging. Its optimized formulation ensures excellent radiographic opacity and patient safety during medical procedures. This product is essential for manufacturers in the pharmaceutical and medical device industries, particularly for producing injectable solutions used in X-ray, CT (Computed Tomography), and angiography.

Application

• Primary component in injectable contrast media for diagnostic radiology.
• Used in CT (Computed Tomography) scans for enhanced visualization of blood vessels, organs, and tissues.
• Formulation of contrast agents for angiography and cardiac catheterization procedures.
• Key ingredient in specialized contrast solutions for urological imaging (e.g., intravenous urography).
• Manufacturing of sterile, apyrogenic finished dosage forms for hospital and clinical use.
• Research and development of novel diagnostic imaging formulations and delivery systems.

Basic Information

Product Name	Iomeron 350-D3
CAS No.	1185146-41-1
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Iomeprol; Iomeron; Iomeprol 350; Iopamiron; Iopamiro; Niopam; 1-N,3-N-Bis(2,3-dihydroxypropyl)-5-[(hydroxyacetyl)methylamino]-2,4,6-triiodo-1,3-benzenedicarboxamide; Iodinated contrast medium 350
EINECS	Contact for details

Quality Control

Our Iomeron 350-D3 is manufactured under strict quality systems to meet the exacting standards required for pharmaceutical active ingredients. Quality assurance includes comprehensive testing for identity, purity, potency, and safety profiles. A Certificate of Analysis (COA) is provided with each batch, detailing compliance with relevant pharmacopoeial monographs (e.g., Ph. Eur., USP) and internal specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); ensure the original container is kept sealed in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Bacterial Endotoxins	< 0.5 EU/mg
Sterility (for sterile grade)	Sterile

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