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iodoxamic acid

Product Name
iodoxamic acid
CAS No.
31127-82-9
Chemical Name
iodoxamic acid
Synonyms
BC-17;B-10610;SQ-21982;Iodoxamic;iodoxamic acid;iodoxamic acid USP/EP/BP;3,3'-[Ethylenebis(oxyethyleneoxyethylenecarbonylimino)]bis(2,4,6-triiodobenzoic acid);3,3'-[(1,16-Dioxo-4,7,10,13-tetraoxahexadecane-1,16-diyl)diimino]bis(2,4,6-triiodobenzoic acid);Benzoic acid, 3,3'-[(1,16-dioxo-4,7,10,13-tetraoxahexadecane-1,16-diyl)diimino]bis[2,4,6-triiodo-;3-[3-[2-[2-[2-[3-(3-carboxy-2,4,6-triiodoanilino)-3-oxopropoxy]ethoxy]ethoxy]ethoxy]propanoylamino]-2,4,6-triiodobenzoic acid
CBNumber
CB6937203
Molecular Formula
C26H26I6N2O10
Formula Weight
1287.92
MOL File
31127-82-9.mol
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iodoxamic acid Property

Boiling point:
977.7±65.0 °C(Predicted)
Density 
2.423±0.06 g/cm3(Predicted)
pka
pKa 1.8/2.8(H2O,t = 25) (Uncertain)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
HCH0137474
Product name
IODOXAMIC ACID
Purity
95.00%
Packaging
5MG
Price
$497.6
Updated
2021/12/16
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iodoxamic acid Chemical Properties,Usage,Production

Originator

Endobil,Bracco

Uses

Diagnostic aid (radiopaque medium).

Definition

ChEBI: Iodoxamic acid is an organic molecular entity.

Manufacturing Process

148.5 g 4,7,10,13-tetraoxahexadecane-1,16-dinitrile (U.S. Patent No. 2,401,607) was added to a solution of 232 g (2.45 mol) concentrate sulfuric acid in 290 ml absolute ethanol at 15°C. The mixture was heated at reflux for 15 hours, cooled and poured into 1000 g ice and 250 g ammonium sulfate. It was extracted with methylene chloride, dried and a solvent was removed in vacuum. The residue was distilled to give 4,7,10,13-tetraoxahexadecane-1,16- dicarbonic acid dimethyl ester; BP: 190°-195°C/0.005 mm Hg.
1 mol above prepared diester was saponificated with equivalent of NaOH in water. The reaction mixture was heated for 90 minutes. On cooling it was extracted with ether and the water layer was evaporated to dryness. The residue was washed with acetone. The obtained disodium salt of 4,7,10,13- tetraoxahexadecane-1,16-dicarbonic acid (yield 100%; MP: 102°-104°C) was acidified with calculated quantity of HCl to give the dicarbonic acid. The solvent was evaporated to dryness. Acetone was added to the residue for removing a by-product (sodium chloride) by filtration. Acetone was evaporated and the residue was extracted with ether, dried and evaporated. The residual liquid was 4,7,10,13-tetraoxahexadecane-1,16-dicarbonic acid.
100 ml thionyl chloride was cautious added to 56 g above prepared diacid and heated at 40°-50°C and excess thionyl chloride was distilled in vacuum. The residue was the 4,7,10,13-tetraoxahexadecane-1,16-dicarbonic acid dichloride. The desired iodoxamic acid was prepared from above dichloride and 3-amino-2,4,6-trijode benzoic acid, in dimethylacetamide

brand name

Endobil (Bracco Industria Chimica S.p.A.,Italy); Endomirabil (Bracco Industria Chimica S.p.A., Italy); Videocolangio (Bracco Industria Chimica S.p.A., Italy).

Therapeutic Function

Diagnostic aid

iodoxamic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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iodoxamic acid Suppliers

2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47

31127-82-9, iodoxamic acidRelated Search:


  • 3-[3-[2-[2-[2-[3-(3-carboxy-2,4,6-triiodoanilino)-3-oxopropoxy]ethoxy]ethoxy]ethoxy]propanoylamino]-2,4,6-triiodobenzoic acid
  • 3,3'-[(1,16-Dioxo-4,7,10,13-tetraoxahexadecane-1,16-diyl)diimino]bis(2,4,6-triiodobenzoic acid)
  • 3,3'-[Ethylenebis(oxyethyleneoxyethylenecarbonylimino)]bis(2,4,6-triiodobenzoic acid)
  • B-10610
  • BC-17
  • SQ-21982
  • Iodoxamic
  • iodoxamic acid
  • Benzoic acid, 3,3'-[(1,16-dioxo-4,7,10,13-tetraoxahexadecane-1,16-diyl)diimino]bis[2,4,6-triiodo-
  • iodoxamic acid USP/EP/BP
  • 31127-82-9
  • C26H26I6N2O10