Description

Ioxilan (400 Mg) is a non-ionic, low-osmolar contrast medium used in diagnostic imaging. This compound is critical for enhancing radiographic visualization in various medical procedures, ensuring clear and precise diagnostic results. It is primarily required by manufacturers in the pharmaceutical and diagnostic imaging industries for formulating injectable contrast agents.

Application

• X-ray Contrast Media: Key active pharmaceutical ingredient (API) in formulations for intravascular injection.
• Computed Tomography (CT) Scans: Used to improve image contrast for detailed visualization of internal organs, blood vessels, and tissues.
• Angiography: Essential for imaging the blood vessels and chambers of the heart.
• Urography: Employed in procedures to examine the urinary tract, including the kidneys, ureters, and bladder.
• Pharmaceutical Intermediates: Serves as a high-purity building block in the synthesis of specialized diagnostic agents.
• Research & Development: Used in preclinical and clinical studies for developing new imaging protocols and contrast formulations.

Basic Information

Product Name	Ioxilan (400 Mg)
CAS No.	107793-72-6
Molecular Formula	C23H28I3N3O8
Molecular Weight	791.10 g/mol
Synonyms	Ioxilan; 5-[N-(2,3-Dihydroxypropyl)acetamido]-2,4,6-triiodo-N,N'-bis(2,3-dihydroxypropyl)isophthalamide; ZK 39482; Ioxilano; Ioxilanum; Optiray 350 (Brand Name Formulation); Ioversol analog (structural)
EINECS	Contact for details

Quality Control

Our Ioxilan is manufactured under strict quality systems to meet the exacting standards required for pharmaceutical APIs. Each batch is tested against comprehensive specifications, including identity, purity, and impurity profiles, to ensure compliance with ICH guidelines and relevant pharmacopeial standards. A detailed Certificate of Analysis (COA) is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

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	< 1.0 EU/mg (as applicable for grade)

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