ChemicalBook--->CAS DataBase List--->83-73-8

83-73-8

83-73-8 Structure

83-73-8 Structure
IdentificationMore
[Name]

5,7-Diiodo-8-quinolinol
[CAS]

83-73-8
[Synonyms]

5,7-DIIODO-8-HYDROXYQUINOLINE
5,7-DIIODO-8-QUINOLINOL
5,7-DIIODOOXINE
DIIODOHYDROXYQUIN
DIIODOHYDROXYQUINOLINE
EMBEQUIN
IODOQUINOL
10doquinol
5,7-diiodo-8-quinolino
5,7-dilodo-8-hydroxyquinoline
5,7-Diodo-8-quinolinol
8-Hydroxy-5,7-diiodoquinoline
8-Hydroxy-5,7-diiod-oquinoline
8-Quinolinol, 5,7-diiodo-
8-quinolinol,5,7-diiodo-
component of Vytone
Diamoebin
diidoquin
Diiodohydroxyguinoline
Diiodo-oxyquinoline
[EINECS(EC#)]

201-497-9
[Molecular Formula]

C9H5I2NO
[MDL Number]

MFCD00006789
[Molecular Weight]

396.95
[MOL File]

83-73-8.mol
Chemical PropertiesBack Directory
[Melting point ]

>200 °C (dec.) (lit.)
[Boiling point ]

370.95°C (rough estimate)
[density ]

2.3013 (estimate)
[storage temp. ]

Refrigerator
[solubility ]

DMSO (Slightly, Heated), Ethyl Acetate (Slightly, Heated)
[form ]

Solid
[pka]

pKa 8.0 (Uncertain)
[color ]

Pale Yellow to Light Beige
[Water Solubility ]

1g/L at 26℃
[Merck ]

5042
[InChIKey]

UXZFQZANDVDGMM-UHFFFAOYSA-N
[LogP]

0.602 at 26℃
[CAS DataBase Reference]

83-73-8(CAS DataBase Reference)
[NIST Chemistry Reference]

5,7-Diiodo-8-hydroxyquinoline(83-73-8)
[EPA Substance Registry System]

83-73-8(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R22:Harmful if swallowed.
R41:Risk of serious damage to eyes.
[Safety Statements ]

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 .
[RIDADR ]

3249
[WGK Germany ]

3
[RTECS ]

VC5775000
[HazardClass ]

6.1(b)
[PackingGroup ]

III
[HS Code ]

29334900
[Safety Profile]

Poison by ingestion and intravenous routes. Human systemic effects by ingestion: eye effects. Mutation data reported. When heated to decomposition it emits very toxic fumes of Iand Nox
[Hazardous Substances Data]

83-73-8(Hazardous Substances Data)
[Toxicity]

LD50 intravenous in mouse: 56mg/kg
Raw materials And Preparation ProductsBack Directory
[Raw materials]

8-Hydroxyquinoline-->Potassium iodate-->Potassium iodide-->Salicylic acid-->1,2-Benzenedicarboxylic acid, 1-[2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl] ester-->[2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl] hydrogen succinate-->Metronidazole-->Water-->Phthalic acid-->Iodine monochloride-->Hydrochloric acid-->Succinic acid
[Preparation Products]

5-iodo-8-quinolinol-->5,7-Dichloro-8-hydroxyquinoline
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

5,7-Diiodo-8-quinolinol(83-73-8).msds
Hazard InformationBack Directory
[Originator]

Diiodohydroxyquinoline,Adco Co.
[Uses]

Antiamebic.
[Uses]

GABA prodrug
[Uses]

It acts as an amoebicidal and so used in the treatment of amoebiasis, balantidiasis (an infection caused by protozoa).
[Definition]

ChEBI: Iodoquinol is a monohydroxyquinoline that is quinolin-8-ol in which the hydrogens at positions 5 and 7 are replaced by iodine. It is considered the drug of choice for treating asymptomatic or moderate forms of amoebiasis. It has a role as an antiamoebic agent, an antibacterial agent, an antiseptic drug and an antiprotozoal drug. It is a monohydroxyquinoline and an organoiodine compound.
[Indications]

Iodoquinol (diiodohydroxyquin, Yodoxin, Moebiquin) is a halogenated 8-hydroxyquinoline derivative whose precise mechanism of action is not known but is thought to involve an inactivation of essential parasite enzymes. Iodoquinol kills the trophozoite forms of E. histolytica, B. coli, B. hominis, and Dientamoeba fragilis.
Iodoquinol is absorbed from the gastrointestinal tract and is excreted in the urine as glucuronide and sulfate conjugates. Most of an orally administered dose is excreted in the feces. Iodoquinol has a plasma half-life of about 12 hours.
Iodoquinol is the drug of choice in the treatment of asymptomatic amebiasis and D. fragilis infections. It is also used in combination with other drugs in the treatment of other forms of amebiasis and as an alternative to tetracycline in the treatment of balantidiasis.
Adverse reactions are related to the iodine content of the drug; the toxicity is often expressed as skin reactions, thyroid enlargement, and interference with thyroid function studies. Headache and diarrhea also occur. Chronic use of clioquinol, a closely related agent, has been linked to a myelitislike illness and to optic atrophy with permanent loss of vision.
[Manufacturing Process]

5,7-Diiodo-8-quinolinol widely used as an intestinal antiseptic, especially as an antiamebic agent. It is also used topically in other infections and may cause CNS and eye damage. It is known by very many similar trade names worldwide.
0.01 mol 8-oxychinoline and 0.01 mol salicylic acid were dissolved in 500 ml of water and then 0.05 mol potassium iodide was added. The mixture was heated to temperature 90°-100°C. After that 0.01 mol of KIO3 by little tiles was added. The next tile was added after a disappearence of discharging iodine. Then 10 ml 2 N HCl was added. The solid product was fallen, filtered off, washed with hot water and in 0.25 N NaOH dissolved. The solution was filtered and the clear filtrate precipitated with a very little excess of HCl. The product 5,7-diiodo-8-quinolinol was filtered, washed with hot water and dried. MP: 200°-250°C (with decomposition).
[Brand name]

Quinadome (Bayer); Yodoxin (Glenwood).
[Therapeutic Function]

Antibacterial
[Flammability and Explosibility]

Nonflammable
[Clinical Use]

5,7-Diiodo-8-quinolinol, 5,7-diiodo-8-hydroxyquinoline,or diiodohydroxyquin (Yodoxin, Diodoquin, Diquinol) is ayellowish to tan microcrystalline, light-sensitive substancethat is insoluble in water. It is recommended for acute andchronic intestinal amebiasis but is not effective in extraintestinaldisease. Because a relatively high incidence of topicneuropathy has occurred with its use, iodoquinol should notbe used routinely for traveler’s diarrhea.
[Synthesis]

Iodoquinol, 5,7-diiodo-8-quinolinol (37.2.2), is made by iodination of 8-oxyquinoline (37.2.1) using a mixture of potassium iodide/potassium iodate. The initial 8-hydroxyquinolin (37.2.1) is made from 2-aminophenol and glycerol in the presence of sulfuric acid and nitrobenzene (Skraup synthesis).

Synthesis_83-73-8

[storage]

Store at -20°C
[Purification Methods]

It crystallises from xylene and is dried at 70o in a vacuum. [Beilstein 21 II 58.]
Spectrum DetailBack Directory
[Spectrum Detail]

5,7-Diiodo-8-quinolinol(83-73-8)MS
5,7-Diiodo-8-quinolinol(83-73-8)1HNMR
5,7-Diiodo-8-quinolinol(83-73-8)13CNMR
5,7-Diiodo-8-quinolinol(83-73-8)IR1
5,7-Diiodo-8-quinolinol(83-73-8)IR2
5,7-Diiodo-8-quinolinol(83-73-8)Raman
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

83-73-8(sigmaaldrich)
[TCI AMERICA]

5,7-Diiodo-8-hydroxyquinoline,>98.0%(T)(83-73-8)
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