Details
Stereochemistry | ACHIRAL |
Molecular Formula | IO3.K |
Molecular Weight | 214.001 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[K+].[O-]I(=O)=O
InChI
InChIKey=JLKDVMWYMMLWTI-UHFFFAOYSA-M
InChI=1S/HIO3.K/c2-1(3)4;/h(H,2,3,4);/q;+1/p-1
Molecular Formula | IO3 |
Molecular Weight | 174.9027 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | K |
Molecular Weight | 39.0983 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
The iodate ion is an oxoanion of iodine bearing a negative charge and containing three oxygen atoms. Because it is more stable than iodide, most health authorities preferentially recommend iodate as an additive to salt for correcting iodine deficiency. In humans and rats, oral bioavailability of iodine from iodate is virtually equivalent to that from iodide. When given intravenously to rats, or when added to whole blood or tissue homogenates in vitro or to foodstuff, iodate is quantitatively reduced to iodide by nonenzymatic reactions, and thus becomes available to the body as iodide. Therefore, except perhaps for the gastrointestinal mucosa, exposure of tissues to iodate might be minimal. At much higher doses given intravenously (i.e., above 10 mg/kg), iodate is highly toxic to the retina. Ocular toxicity in humans has occurred only after exposure to doses of 600 to 1,200 mg per individual. Oral exposures of several animal species to high doses, exceeding the human intake from fortified salt by orders of magnitude, pointed to corrosive effects in the gastrointestinal tract, hemolysis, nephrotoxicity, and hepatic injury.
Approval Year
PubMed
Title | Date | PubMed |
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Diagnosis and management of lymphoceles after renal transplantation. | 1988 Apr |
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[Current problems in the pathogenesis and treatment of endemic goiter]. | 1990 |
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The inactivation of sodium channels in the node of Ranvier and its chemical modification. | 1990 |
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[A volumetric increase in the submandibular glands due to an organic iodate contrast medium. A case report]. | 1993 Jan-Feb |
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Regeneration of mammalian retinal pigment epithelium. | 1994 |
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Iodine deficiency disorders in South Africa. | 1998 Mar |
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[The possibilities of using the newest experimental results in the progressive myopia treatment]. | 1999 |
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The toxicology of iodate: a review of the literature. | 2001 May |
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Iodised salt for preventing iodine deficiency disorders. | 2002 |
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Ozonation of drinking water: part II. Disinfection and by-product formation in presence of bromide, iodide or chlorine. | 2003 Apr |
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Iodine supplementation for preventing iodine deficiency disorders in children. | 2004 |
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Exploiting genotypic variation in plant nutrient accumulation to alleviate micronutrient deficiency in populations. | 2005 |
|
Fifty-five-year personal experience with human nutrition worldwide. | 2007 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:04:31 GMT 2023
by
admin
on
Fri Dec 15 16:04:31 GMT 2023
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Record UNII |
I139E44NHL
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Record Status |
Validated (UNII)
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Record Version |
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CFR |
21 CFR 184.1635
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NCI_THESAURUS |
C797
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EPA PESTICIDE CODE |
75703
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C039693
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100000079419
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1231
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m9033
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PRIMARY | Merck Index | ||
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I139E44NHL
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C87200
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215201
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231-831-9
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DTXSID5058480
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POTASSIUM IODATE
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23665710
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34312
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7758-05-6
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I139E44NHL
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SUB14984MIG
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Related Record | Type | Details | ||
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ACTIVE MOIETY |