4-Hydroxy-3,5-diiodobenzoic acid

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Reagent Code: #195603
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CAS Number 618-76-8

science Other reagents with same CAS 618-76-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 389.91 g/mol
Formula C₇H₄I₂O₃
badge Registry Numbers
MDL Number MFCD00016532
thermostat Physical Properties
Boiling Point 346.4°C at 760 mmHg
inventory_2 Storage & Handling
Density 2.697g/cm3
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of X-ray contrast media, particularly in the production of iodinated compounds that enhance imaging clarity in radiological procedures. Its high iodine content contributes to effective radiopacity, making it valuable in diagnostic applications such as angiography and urography. Also employed in the development of certain pharmaceuticals where controlled iodine release or specific aromatic substitution patterns are required. Its structural properties allow for further chemical modifications, supporting its role in creating water-soluble contrast agents with low toxicity profiles.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿840.00
inventory 10g
10-20 days ฿1,650.00
inventory 100g
10-20 days ฿16,390.00
inventory 25g
10-20 days ฿4,100.00

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4-Hydroxy-3,5-diiodobenzoic acid
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Used as an intermediate in the synthesis of X-ray contrast media, particularly in the production of iodinated compounds that enhance imaging clarity in radiological procedures. Its high iodine content contributes to effective radiopacity, making it valuable in diagnostic applications such as angiography and urography. Also employed in the development of certain pharmaceuticals where controlled iodine release or specific aromatic substitution patterns are required. Its structural properties allow for furt

Used as an intermediate in the synthesis of X-ray contrast media, particularly in the production of iodinated compounds that enhance imaging clarity in radiological procedures. Its high iodine content contributes to effective radiopacity, making it valuable in diagnostic applications such as angiography and urography. Also employed in the development of certain pharmaceuticals where controlled iodine release or specific aromatic substitution patterns are required. Its structural properties allow for further chemical modifications, supporting its role in creating water-soluble contrast agents with low toxicity profiles.

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