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Ioxilan

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Catalog No. T19377Cas No. 107793-72-6

Ioxilan is a low-osmolar, nonionic, and tri-iodinated diagnostic contrast agent used for excretory urography and contrast-enhanced computed tomographic (CECT) imaging of the head and body. When injected intravascularly, it opacifies vessels, enabling radiographic visualization of internal structures until significant hemodilution occurs.

Ioxilan

Ioxilan

😃Good
Catalog No. T19377Cas No. 107793-72-6
Ioxilan is a low-osmolar, nonionic, and tri-iodinated diagnostic contrast agent used for excretory urography and contrast-enhanced computed tomographic (CECT) imaging of the head and body. When injected intravascularly, it opacifies vessels, enabling radiographic visualization of internal structures until significant hemodilution occurs.
Pack SizePriceAvailabilityQuantity
1 mg$998-10 weeks
1 mL x 10 mM (in DMSO)$2158-10 weeks
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Product Introduction

Bioactivity
Description
Ioxilan is a low-osmolar, nonionic, and tri-iodinated diagnostic contrast agent used for excretory urography and contrast-enhanced computed tomographic (CECT) imaging of the head and body. When injected intravascularly, it opacifies vessels, enabling radiographic visualization of internal structures until significant hemodilution occurs.
In vitro
The development of Ioxilan incorporates a dual methylene structure to act as a hydrophobic region, which is then concealed by a hydrophilic hydroxyl group. This modification reduces osmolality without compromising biological tolerance. As a low-osmolar, nonionic monomer, Ioxilan enhances the safety and tolerability of X-ray contrast agents.
In vivo
Rapid intravenous injection of (water-soluble) X-ray contrast agents (Ioxilan), used in conjunction with dynamic computed tomography, enhances the visualization of liver lesions. These agents, primarily remaining in the extracellular fluid and excreted unchanged by the kidneys, distribute effectively post-injection. The degree of contrast enhancement in a specific region is influenced by the administration method, the delivery of the agent via blood flow, and the resultant iodine concentration in that area.
Chemical Properties
Molecular Weight791.11
FormulaC18H24I3N3O8
Cas No.107793-72-6
Relative Density.1.31g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 250 mg/mL (316.01 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.2640 mL6.3202 mL12.6405 mL63.2023 mL
5 mM0.2528 mL1.2640 mL2.5281 mL12.6405 mL
10 mM0.1264 mL0.6320 mL1.2640 mL6.3202 mL
20 mM0.0632 mL0.3160 mL0.6320 mL3.1601 mL
50 mM0.0253 mL0.1264 mL0.2528 mL1.2640 mL
100 mM0.0126 mL0.0632 mL0.1264 mL0.6320 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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