ChemicalBook--->CAS DataBase List--->96-83-3

96-83-3

96-83-3 Structure

96-83-3 Structure
IdentificationMore
[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
Chemical PropertiesBack Directory
[Melting point ]

153 °C
[Boiling point ]

529.1±50.0 °C(Predicted)
[density ]

2.2567 (estimate)
[storage temp. ]

2-8°C
[solubility ]

DMSO, Methanol
[form ]

neat
[pka]

4.8(at 25℃)
[color ]

Light Brown
[Water Solubility ]

348.3mg/L(37 ºC)
[Merck ]

5058
[BCS Class]

2
[CAS DataBase Reference]

96-83-3(CAS DataBase Reference)
[EPA Substance Registry System]

96-83-3(EPA Substance)
Safety DataBack 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)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Aluminum-->Dichloroethane-->Ethylbenzene-->KAOLIN-->3-Nitrobenzaldehyde-->Aluminium-nickel-->Butyric anhydride-->Iodic acid-->Sodium Butyrate-->3-Phenylpropionic acid-->Iodine monochloride-->Hydrogen
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

2-Ethyl-3-(3-amino-2,4,6-triiodophenyl)propionic acid(96-83-3).msds
Hazard InformationBack 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
Spectrum DetailBack Directory
[Spectrum Detail]

Iopanoic acid(96-83-3)MS
Iopanoic acid(96-83-3)1HNMR
Iopanoic acid(96-83-3)13CNMR
Iopanoic acid(96-83-3)IR1
Iopanoic acid(96-83-3)IR2
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

96-83-3(sigmaaldrich)
[TCI AMERICA]

Iopanoic Acid,>98.0%(T)(96-83-3)
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