iocarmic acid Chemical Properties

Melting point:

302° (dec)

Boiling point:

868.1±65.0 °C(Predicted)

Density 

2.4238 (estimate)

pka

0.56±0.10(Predicted)

iocarmic acid Usage And Synthesis

Originator

Myelotrast,Winthrop

Uses

Diagnostic aid (radiopaque medium, cholecystographic).

Definition

ChEBI: Iocarmic acid is an organic molecular entity.

Manufacturing Process

5-Amino-2,4,6-triiodo-N-methylisophthalamic acid (228.0 g, 4 mole) was added to stirred, heated dimethylacetamide (400 ml). When the temperature reached 95°C, adipoyl chloride (27.5 g, 0.15 mole) was added all at once, followed by an equal amount added slowly over a period of 15 min (a total of 55.0 g). After addition of the adipoyl chloride the solution was stirred at about 95°C for another 15 min, then poured into 2 L of hot water. As the above mixture cooled to room temperature a gum separated. The mother liquor was discarded and the gum was dissolved in water (2 L) with sufficient sodium hydroxide to complete solution. The solution was acidified with hydrochloric and acetic acids, treated with decolorizing charcoal and filtered. The filtrate was then strongly acidified with hydrochloric acid, which caused the separation of an apparently amorphous granular solid. This was filtered off, digested 0.5 h with hot ethanol (500 ml) collected, washed with ethanol and dried at 110°C. Yield of crude 5,5-(adipoyldiimino)-bis[2,4,6-triiodo-Nmethylisophthalamic acid].
The 5,5-(adipoyldiimino)-bis[2,4,6-triiodo-N-methylisophthalamic acid] was precipitated a second and third time from its sodium salt solution. The third precipitate was then dissolved in hot dimethylformamide (400 ml), and water (1.5 L) was slowly added. The mixture was digested and the hot mixture filtered, yielding a crystalline product which, after drying at 110°C, weighed 126.0 g (neutral equivalent, 724). This product was dissolved in dilute sodium hydroxide solution (1 L) and the solution was acidified (pH 5) and filtered into a hot stirred solution of hydrochloric acid (25 ml of concentrated acid in 75 ml water). The mixture was chilled and the solid collected, washed with water and dried at 110°C. Yield of 5,5-(adipoyldiimino)-bis[2,4,6-triiodo-Nmethylisophthalamic acid] 114.0 g (45%). Melting point, 302°C (corrected), with decomposition.

brand name

Dimeray (Mallinckrodt).

Therapeutic Function

Diagnostic aid

iocarmic acid (10397-75-8)Related Product Information

• BISMUTH OXYIODIDE
• 4-Iodobenzoic acid
• 5-Amino-2,4,6-triiodo-N-methylisophthalamic Acid
• 2-IODO-3-METHYLBENZOIC ACID
• iocarmic acid
• IODIPAMIDE
• 2-IODO-5-METHYLBENZOIC ACID
• 4-IODO-3-METHYLBENZOIC ACID
• Iotalamic acid
• 5-AMINO-N-METHYLISOPHTHALAMIC ACID
• 3,5-DIMETHYL-4-IODOANILINE
• ADIPIC DIANILIDE
• iocarmic acid meglumate salt
• 2,4-DIIODO-3,5-DIMETHYLANILINE
• 3-(N-butyrylamino)benzamide
• 3,5-DIMETHYL-4-IODO-ACETANILIDE
• 1,3-DIIODO-2,4-DIMETHYLBENZENE