IOCETAMIC ACID (200 MG) Chemical Properties

Melting point:

224-225° (NL 6515305); mp range 191-212° (Korver); Consists of 2 isomers having mps 232° and 200-201°

Boiling point:

658.2±55.0 °C(Predicted)

Density 

2.2000 (rough estimate)

refractive index 

1.7400 (estimate)

pka

4.0(at 25℃)

Water Solubility 

5.286g/L(37 ºC)

Stability:

Stable. Incompatible with strong oxidizing agents.

Safety Information

Hazardous Substances Data

16034-77-8(Hazardous Substances Data)

Toxicity

LD50 in rats (g/kg): 7.1 orally; 0.70 i.v. (Janbroers)

IOCETAMIC ACID (200 MG) Usage And Synthesis

Originator

Cholebrine,Nicholas

Uses

Diagnostic aid (radiopaque medium).

Definition

ChEBI: 3-(N-acetyl-3-amino-2,4,6-triiodoanilino)-2-methylpropanoic acid is an aromatic amide.

Manufacturing Process

A mixture of equimolecular amounts of m-nitraniline (69.0 g), methacrylic acid (43.0 g), and pyridine (39.5 g) was heated to 125°C for 20 h, and was then poured into 500 ml water. A semi-crystalline product separated from the liquid. The supernatant liquid was decanted and 500 ml fresh water was added. The pH was adjusted to 7-7.5 by means of sodium hydroxide. The precipitate was filtered with suction and washed with water. When the filtrate was acidified with acetic acid, a precipitate of N-(3-nitrophenyl)-β-aminoisobutyric acid was formed. When filtered, washed with water and dried, it weighed 56.0 g and had a melting point of 130°-131°C (recryst. from alcohol). The yield was 50% based on nitraniline.
0.25 mol (56.0 g) N-(3-nitrophenyl)-β-aminoisobutyric acid, prepared as described above, 160 ml glacial acetic acid, and 40 ml acetic anhydride were heated 48 h to 50°C, and the reaction mixture was poured into 600 ml water. A crystalline precipitate of N-acetyl-N-(3-nitrophenyl)-β-aminoisobutyric acid formed gradually. When recovered, it weighed 56.0 g (84% yield). Melting point 146°-148°C.
100.0 g N-acetyl-N-(3-nitrophenyl)-β-amino-isobutyric acid were dissolved in 1 L water and 40 ml 25% aqueous ammonia, and the solution was hydrogenated in the presence of about 10.0 g Raney nickel at 20°C and about 450 p.s.i. until the pressure drop indicated the complete conversion of the NO2 groups to NH2. Thus N-acetyl-N-(3-aminophenyl)-β-amino-isobutyric acid was obtained.
The solution of N-acetyl-N-(3-aminophenyl)-β-amino-isobutyric acid was filtered after standing overnight, mixed with an equal volume of acetic acid, and there after with a solution of 275.0 g iodine monochloride and 200.0 g sodium chloride in 1 L water. The mixture was kept at 50°C with stirring for 48 h. Light brown crystals of crude N-acetyl-N-(2,4,6-triiodo-3-aminophenyl)- β-amino-isobutyric acid precipitated, were filtered off, washed with water, and dried. They weighed 195.0 g (84.5% yield based on N-acetyl-N 3-nitrophenylp-amino-isobutyric acid).

brand name

Cholebrine (Mallinckrodt).

Therapeutic Function

Diagnostic aid

Hazard

Low toxicity by ingestion.

IOCETAMIC ACID (200 MG)(16034-77-8)Related Product Information

• IOCETAMIC ACID (200 MG)
• 3-(2-IODOPHENYLAMINO)PROPANOIC ACID