TYROPANOATE SODIUM Property

Melting point:

208-210°

storage temp. 

Refrigerator

solubility 

Methanol (Slightly)

form 

Solid

color 

Off-White to Pale Pink

Safety

Toxicity

LD50 i.v. in mice: 720 mg/kg (Hoppe)

Hazard and Precautionary Statements (GHS)

TYROPANOATE SODIUM Chemical Properties,Usage,Production

Originator

Bilopaque,Winthrop,US,1972

Uses

Tyropanoate Sodium is used for radiographic analysis of the gallbladder via oral cholecystography. Iodinated contrast agent.

Definition

ChEBI: Tyropanoate sodium is a member of benzenes and a monocarboxylic acid.

Manufacturing Process

A solution of 5.0 g of α-ethyl-β-(aminophenyl)propionic acid in 100 ml of water containing 5 ml of concentrated hydrochloric acid was added over a period of ? hour to a stirred solution of 3.2 ml of iodine monochloride in 25 ml of water and 25 ml of concentrated hydrochloric acid heated to 60°C. After addition was complete, the heating was continued for ? hour longer at 60° to 70°C. A black oil separated which gradually solidified. The mixture was then cooled and sodium bisulfite was added to decolorize. Recrystallization of the product from methanol gave about 8 g of α-ethyl-β-(2,4,6-triiodo-3- aminophenyl)-propionic acid, MP 147° to 150°C. The product could be further purified by precipitation of its morpholine salt from ether solution and regeneration of the free amino acid by treatment of a methanol solution of the morpholine salt with sulfur dioxide. The pure amino acid had the MP 155° to 156.5°C (corr).
A mixture of 57.1 g (0.1 mol) of α-ethyl-β-(3-amino-2,4,6- triiodophenyl)propionic acid, 250 ml of butyric anhydride and 1 ml of 70% perchloric acid was heated at 105°C for 5 hours. After cooling, the reaction mixture was poured onto ice, diluted to a volume of 3 liters with water, and heated on a steam bath with addition of solid sodium carbonate to keep the mixture basic. After all the excess butyric anhydride had been hydrolyzed, the mixture was made acid with dilute hydrochloric acid, the aqueous layer decanted from the resulting gummy solid, and the latter was then washed several times with water. The product was dissolved in acetic acid, decolorized with activated charcoal, and the solution while hot diluted with water to the point of turbidity. The product was collected by filtration and dried, giving 40 g of α-ethyl-β-(3-dibutyramido-2,4,6-triiodophenyl)propionic acid, MP 166° to 169.5°C (corr.) when recrystallized from acetic acid. Reaction with sodium hydroxide gives the final product.

brand name

Bilopaque (GE Healthcare).

Therapeutic Function

Diagnostic aid (radiopaque medium)