| Identification | More | [Name]
Iopanoic acid | [CAS]
96-83-3 | [Synonyms]
2-(3-AMINO-2,4,6-TRIIODOBENZYL)BUTYRIC ACID
2-ETHYL-3-(3-AMINO-2,4,6-TRIIODOPHENYL)PROPIONIC ACID
3-[3-AMINO-2,4,6-TRIIODOPHENYL]-2-ETHYLPROPANOIC ACID
3-(3-AMINO-2,4,6-TRIIODOPHENYL)-2-ETHYLPROPIONIC ACID
3-AMINO-ALPHA-ETHYL-2,4,6-TRIIODOHYDROCINNAMIC ACID
COPANOIC
IODOPANOIC ACID
IOPANOIC ACID
JOPANOIC ACID
3-amino-alpha-ethyl-2,4,6-triiodo-benzenepropanoicaci
3-amino-alpha-ethyl-2,4,6-triiodobenzenepropanoicacid
3-amino-alpha-ethyl-2,4,6-triiodo-hydrocinnamicaci
3-Amino-ethyl-2,4,6-triiodobenaenepropanoicacid
3-Amino-ethyl-2,4,6-triiodohydrocinnamicacid
beta-(3-amino-2,4,6-triiodophenyl)-alpha-ethylpropionicacid
bilijodon
choladine
cholevid
cistobil
colepax | [EINECS(EC#)]
202-539-9 | [Molecular Formula]
C11H12I3NO2 | [MDL Number]
MFCD00038687 | [Molecular Weight]
570.93 | [MOL File]
96-83-3.mol |
| Safety Data | Back Directory | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed . | [Safety Statements ]
S22:Do not breathe dust .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [WGK Germany ]
1 | [RTECS ]
NW5075000 | [HS Code ]
2922.49.3700 | [Hazardous Substances Data]
96-83-3(Hazardous Substances Data) |
| Hazard Information | Back Directory | [Chemical Properties]
Light Brown Solid | [Originator]
Telepaque,Winthrop,US,1952 | [Uses]
antiulcer | [Uses]
Iodopanoic Acid is an iodine-containing radiocontrast medium used in cholecystography. Iodopanoic Acid is a potent inhibitor of thyroid hormone release from thyroid gland. | [Definition]
ChEBI: Iopanoic acid is a monocarboxylic acid. | [Manufacturing Process]
(A) Preparation of α-Ethyl-m-Nitrocinnamic Acid: This acid is prepared from
100 g of m-nitrobenzaldehyde, 210 g of butyric anhydride and 73 g of sodium
butyrate. The crude α-ethyl-m-nitrocinnamicacid is crystallized from ethanol
giving about 105 g, MP 140° to 142°C. From the filtrates there may be
isolated a small amount of a stereoisomer, which when pure melts at 105° to
106°C.
(B) Preparation of m-Amino-α-Ethylhydrocinnamic Acid: A mixture of 50 g of
α-ethyl-m-nitrocinnamic acid, 9.1 g of sodium hydroxide, 600 cc of water and
5 teaspoons of Raney nickel catalyst is shaken at 32°C in an atmosphere ofhydrogen at an initial pressure of 450 psi until the calculated amount of
hydrogen is absorbed. The filtered solution is acidified with hydrochloric acid,
made basic with ammonium hydroxide and again acidified with acetic acid.
Upon concentration of this solution, an oil separates which crystallizes upon
standing, giving about 20 g, MP 60° to 68°C. Complete evaporation of the
filtrate and extraction of the residue of inorganic salts with ether gives about
20 g of additional material, MP 54° to 59°C. Recrystallization of the combined
product from benzene petroleum ether gives about 35 g of m-amino-α-
ethylhydrocinnamic acid, MP 67° to 70°C.
(C) Preparation of β-(3-Amino-2,4,6-Triiodophenyll-α-Ethylpropionic Acid: A
solution of 5.0 g of m-amino-α-ethylhydrocinnamic acid in 100 cc of water
containing 5 cc of concentrated hydrochloric acid is added over a period of ?
hour to a stirred solution of 3.2 cc of iodine monochloride in 25 cc of water
and 25 cc of concentrated hydrochloric acid heated to 60°C. After addition is
complete, the heating is continued for one hour longer at 60° to 70°C. A black
oil separates which gradually solidifies.
The mixture is then cooled and sodium bisulfite added to decolorize.
Recrystallization of the product from methanol gives about 8 g, MP 147° to
150°C. The β-(3-amino-2,4,6-triiodophenyl)-α-ethylpropionic acid may be
purified further by precipitation of the 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 has the MP 155° to
156.5°C. | [Therapeutic Function]
Diagnostic aid (radiopaque medium) | [storage]
Store at -20°C |
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