Iodide ion I-123

Base Information

• Chemical Name: Iodide ion I-123
• CAS No.: 69239-56-1
• Molecular Formula: I-
• Molecular Weight: 123.0005
• UNII: 98QPV8670C
• DSSTox Substance ID: DTXSID40988959
• Wikipedia: Iodine-123
• Wikidata: Q3801335
• RXCUI: 1361657
• Mol file: 69239-56-1.mol

Synonyms:Iodide ion I-123;iodine-123(1-);Iodide (123I(1-));Iodide-123;Iodide I-123;69239-56-1;UNII-98QPV8670C;98QPV8670C;I-123;Iodine 123;IODIDE I-123 ION;IODIDE ION I 123;IODIDE, I-123;IODIDE ION (123 I);DTXSID40988959;DB09420;123I-;Q3801335

Chemical Property of Iodide ion I-123

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: g/cm³
• XLogP3: 0.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 122.90559
• Heavy Atom Count: 1
• Complexity: 0

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: [I-]
• Isomeric SMILES: [123I-]

Technology Process of Iodide ion I-123

There total 239 articles about Iodide ion I-123 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

carbon tetraiodide (507-25-5) → carbonic-acid (463-79-6) + iodide (14362-44-8,20461-54-5,69239-56-1)

Guidance literature:

With potassium hydroxide; water; In methanol; water;

DOI:10.1021/jo01224a009

Reference yield:

hydroxylamine (7803-49-8) + iodine (7553-56-2,12190-71-5,8031-47-8) → iodide (14362-44-8,20461-54-5,69239-56-1) + dinitrogen monoxide (10024-97-2)

Guidance literature:

In water; byproducts: H(1+), H2O; excess of hydroxylamine, in presence of excess I(1-), 25°C, I=0.50 M NaClO4; varying acidity (1.15-9.90 mM HClO4 or acetate or phosphatebuffer or unbuffered soln.; pH=3.44-6.84); not isolated, reaction followed by UV/VIS spectroscopy; Kinetics;

DOI:10.1021/ic00128a021

Reference yield:

hydroxylammonium + iodate (15454-31-6) → iodide (14362-44-8,20461-54-5,69239-56-1) + hydrogen cation + dinitrogen monoxide (10024-97-2)

Guidance literature:

In further solvent(s); in HCl soln.;

upstream raw materials:

4-cyanophenolate

Thiocyanate

iodate

iodine

Downstream raw materials:

4-cyanophenolate

triiodide^(1-)

water

cadmium(II) iodide