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Key Documents

221929

Sigma-Aldrich

Iodic acid

ACS reagent, ≥99.5%

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About This Item

Empirical Formula (Hill Notation):
HIO3
CAS Number:
Molecular Weight:
175.91
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

assay

≥99.5%

form

crystals or chunks

impurities

≤0.01% insolubles
≤0.1% N compounds

ign. residue

≤0.02%

solubility

water: soluble

density

4.63 g/cm3

anion traces

Cl- and Br-: ≤0.02%
iodide (I-): ≤0.01%
sulfate (SO42-): ≤0.015%

cation traces

Fe: ≤0.002%
heavy metals (as Pb): ≤0.001%

SMILES string

OI(=O)=O

InChI

1S/HIO3/c2-1(3)4/h(H,2,3,4)

InChI key

ICIWUVCWSCSTAQ-UHFFFAOYSA-N

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pictograms

Flame over circleCorrosion

signalword

Danger

hcodes

Hazard Classifications

Ox. Sol. 2 - Skin Corr. 1B

Storage Class

5.1B - Oxidizing hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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Glass formation and unusual hygroscopic growth of iodic acid solution droplets with relevance for iodine oxide particles in the coastal marine boundary layer.
Murray BJ, et al.
Atmospheric Chemistry and Physics Discussions, 12(3), 7879-7908 (2012)
Manometric carbon determination.
Van Slyke DD and Folch J.
The Journal of Biological Chemistry, 136(2), 509-541 (1940)
Raman studies of iodic acid and sodium iodate.
Durig JR, et al.
The Journal of Physical Chemistry, 69(11), 3886-3892 (1965)
The rate of the reaction between iodic and hydriodic acids.
Dushman S.
The Journal of Physical Chemistry, 8(7), 453-482 (1904)
K J Hill et al.
Biochimica et biophysica acta, 1326(1), 37-46 (1997-05-22)
Liposomes were prepared from phospholipid mixtures of dipalmitoylphosphatidylcholine (DPPC) and phosphatidylinositol (PI), encapsulating the enzymes glucose oxidase (GO) and GO in combination with horse radish peroxidase (HRP) by both extrusion (VET) and reverse-phase evaporation (REV). The optimum level of PI

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