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IOXITALAMIC ACID

CAS No.
28179-44-4
Chemical Name:
IOXITALAMIC ACID
Synonyms
AG-58107;Telebrix;Vasobrix;Ioxitalamic;IoxitalaMate;IOXITALAMIC ACID;iooxitalamic acid;Acidum Joxitalamicum;IOXITALAMIC ACID USP/EP/BP;3-Acetamido-5-(2-hydroxyethylcarbamoyl)-2,4,6-triiodobenzoic acid
CBNumber:
CB6406686
Molecular Formula:
C12H11I3N2O5
Molecular Weight:
643.94
MDL Number:
MFCD00867942
MOL File:
28179-44-4.mol
Last updated:2023-09-20 16:43:00

IOXITALAMIC ACID Properties

Melting point 253-255?C
Boiling point 582.8±50.0 °C(Predicted)
Density 2.519±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,2-8°C
solubility DMSO (Slightly, Heated), Methanol (Slightly)
form Solid
pka 0.85±0.10(Predicted)
color Off-White to Pale Brown
FDA UNII 967RDI7Z6K
ATC code V08AA05

IOXITALAMIC ACID price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC I738100 IoxitalamicAcid 28179-44-4 1g $1065 2021-12-16 Buy
American Custom Chemicals Corporation CHM0069200 IOXITALAMIC ACID 95.00% 28179-44-4 10MG $2009.7 2021-12-16 Buy
Matrix Scientific 099667 3-Acetamido-5-((2-hydroxyethyl)carbamoyl)-2,4,6-triiodobenzoic acid 95+% 28179-44-4 1g $775 2021-12-16 Buy
Matrix Scientific 099667 3-Acetamido-5-((2-hydroxyethyl)carbamoyl)-2,4,6-triiodobenzoic acid 95+% 28179-44-4 250mg $327 2021-12-16 Buy
AK Scientific Z3684 Ioxitalamicacid 28179-44-4 250mg $491 2021-12-16 Buy
Product number Packaging Price Buy
I738100 1g $1065 Buy
CHM0069200 10MG $2009.7 Buy
099667 1g $775 Buy
099667 250mg $327 Buy
Z3684 250mg $491 Buy

IOXITALAMIC ACID Chemical Properties,Uses,Production

Chemical Properties

White Solid

Originator

Oxilan,Cook Imaging Corporation

Uses

A substituted 2,4,6-triiodobenzoic acid, an excellent contrast media for ventriculography, radiculography, lumbar myelography and x-rays of the cardiovascular system.

Definition

ChEBI: An organoiodine compound that is 2,4,6-triiodobenzoic acid substituted by an acetylamino group at position 3 and a (2-hydroxyethyl)carbamoyl group at position 5. It is used as a contrast medium.

Manufacturing Process

3-Methoxycarboxyl-5-nitrobenzoic acid (25 g) was hydrogenated in methanol (500 ml) using palladium oxide on charcoal (2.5 g 10%) at atmospheric pressure. When the exothermic reaction was completed the catalyst was fluttered off. After cooling the solution at -20°C for 2.5 h, 12.7 g of 3-amino- 5-methoxycarbonylbenzoic acid was isolated. An additional 6.5 g of it was isolated by concentrating the mother liquor.
The 3-amino-5-methoxycarbonylbenzoic acid (12.0 g) was suspended in water (280 ml), dissolved by addition of concentrated hydrochloric acid (7.1 ml) and glacial acetic acid (28.5 ml). At 60°-70°C NaICl2 solution (73 ml, 58.7 g ICl/100 ml) was added dropwise while stirring in the course of about 3 h. The reaction mixture was heated at 80°-90°C for additional 3 h while stirring.
After cooling to room temperature the mother liquor was decanted and the residue dissolved as ammonium salt in water (80 ml). The ammonium salt was precipitated by adding ammonium chloride (2.4 g) and cooling to 0°C. The ammonium salt was filtered off and dissolved in water (140 ml), charcoaled twice at 80°C and the acid was precipitated at room temperature by addition of hydrochloric acid and was filtered off. The crude product was dissolved in ethyl acetate (100 ml) and the solution was washed 3 times with hydrochloric acid (2 N). By evaporating the solvent, 19 g of 3-amino-5- methoxycarbonyl-2,4,6-triiodobenzoic acid was isolated. Melting point 170°- 176°C.
A mixture of 3-amino-5-methoxycarbonyl-2,4,6-triiodobenzoic acid (198 g) and thionyl chloride (400 ml) was heated while stirring at 70°C for 16 h. The solid material dissolved slowly. Thionyl chloride was evaporated in vacuo, the residue dissolved in chloroform (1000 ml), the solution washed with water (80 ml each), twice with saturated sodium bicarbonate, then 5 times with 2 N sodium hydroxide solution and finally with water to neutral. The solution was dried with CaCl2 filtered and evaporated to dryness. The 3-amino-5- methoxycarbonyl-2,4,6-triiodobenzoyl chloride was dried at 50°C in vacuo. Yield: 203.0 g. Melting point 55°-60°C.
To the 3-amino-5-methoxycarbonyl-2,4,6-triiodobenzoyl chloride (53.0 g) was added acetic anhydride (106 ml). After stirring at room temperature for 20 min then insoluble material was filtered off (3-4 g). To the filtrate was added concentrated sulfuric acid (0.3 ml) whereby a yellowish product started to precipitate. The temperature reached about 50°C. The 3-acetamido-5- methoxycarbonyl-2,4,6-triiodobenzoyl chloride was isolated after storing in refrigerator overnight. Yield: 39.0 g. Melting point 210°-215°C.
The 3-acetamido-5-methoxycarbonyl-2,4,6-triiodobenzoyl chloride was dissolved in a mixture of dioxan and dimethylformamide. In the course of 2 h this solution was added dropwise to a solution of ethanolamine and triethylamine in dioxan. The stirring was continued. A sticky precipitate was filtered off. The filtrate was evaporated to dryness in vacuo. The residue was triturated with aqueous sodium bicarbonate, filtered off and mixed with first fraction. The combined solids were then suspended in aqueous sodium bicarbonate filtered off washed with water and dried in vacuo to give methyl 5-acetamido-2,4,6-triiodo-(N-β-hydroxyethyl)-isophthalamate.
The methyl 5-acetamido-2,4,6-triiodo-(N-β-hydroxyethyl)-isophthalamate was mixed with fresh distilled ethanolamine and stirred. The excess ethanolamine was removed in vacuo at 50°-60°C. The residue was dissolved in water, and charcoaled at pH 5.5. The crude product was precipitated with hydrochloric acid (pH 0.5) and filtered after stirring at 0°C. 5-Acetamido-2,4,6-triiodo-(N- β-hydroxyethyl)isophthalamic acid was suspended in ethanol and dissolved by addition of concentrated ammonia. The ammonium salt started to precipitate in the course and was isolated after stirring. The salt was dissolved in water, filtered and the acid was precipitated with hydrochloric acid (pH 0.5). After stirring the product was filtered off and dried in vacuo.

Therapeutic Function

Diagnostic aid

IOXITALAMIC ACID Suppliers

Global( 57)Suppliers
Supplier Tel Email Country ProdList Advantage
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070 product@chemlin.com.cn CHINA 3012 60
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17367 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9409 58
Hebei Lingding Biotechnology Co., Ltd.
+86-18031140164 +86-19933155420 erin@hbldbiotech.com China 878 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29322 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
LEAP CHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 24738 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49999 58

View Lastest Price from IOXITALAMIC ACID manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
IoxitalaMic Acid pictures 2021-10-20 IoxitalaMic Acid
28179-44-4
US $350.00 / KG 1KG 99% 9000kg/per week Hebei Lingding Biotechnology Co., Ltd.
IOXITALAMIC ACID USP/EP/BP pictures 2021-08-14 IOXITALAMIC ACID USP/EP/BP
28179-44-4
US $1.10 / g 1g 0.999 100 Tons min Dideu Industries Group Limited
IOXITALAMIC ACID pictures 2020-01-05 IOXITALAMIC ACID
28179-44-4
US $1.00 / KG 1KG 95--99% 1ton Career Henan Chemical Co
  • IoxitalaMic Acid pictures
  • IoxitalaMic Acid
    28179-44-4
  • US $350.00 / KG
  • 99%
  • Hebei Lingding Biotechnology Co., Ltd.

IOXITALAMIC ACID Spectrum

Ioxitalamic Acidum Joxitalamicum 2,4,6-Triiodo-3-(acetylamino)-5-(2-hydroxyethylcarbamoyl)benzoic acid 3-(Acetylamino)-2,4,6-triiodo-5-[[(2-hydroxyethyl)amino]carbonyl]benzoic acid IOXITALAMIC ACID 3-(AcetylaMino)-5-[[(2-hydroxyethyl)aMino]carbonyl]-2,4,6-triiodobenzoic Acid 3-AcetaMido-2,4,6-triiodo-(N-β-hydroxyethyl)isophthalic Acid MonoaMide IoxitalaMate Benzoic acid,3-(acetylaMino)-5-[[(2-hydroxyethyl)aMino]carbonyl]-2,4,6-triiodo- iooxitalamic acid 5-(Acetylamino)-3-[(2-hydroxyethyl)carbamoyl]-2,4,6-triiodobenzoic acid 5-Acetylamino-3-[N-(2-hydroxyethyl)carbamoyl]-2,4,6-triiodobenzoic acid AG-58107 3-Acetamido-5-(2-hydroxyethylcarbamoyl)-2,4,6-triiodobenzoic acid sodium 3-acetamido-5-[(2-hydroxyethylamino)-oxomethyl]-2,4,6-triiodobenzoate IOXITALAMIC ACID USP/EP/BP Telebrix Vasobrix 28179-44-4 C12H11I3N2O5 Amines Aromatics Diagnostic Isotope Labelled Compounds Intermediates & Fine Chemicals Pharmaceuticals