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Sigma-Aldrich

Potassium iodide

ACS reagent, ≥99.0%

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About This Item

Linear Formula:
KI
CAS Number:
Molecular Weight:
166.00
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

vapor pressure

1 mmHg ( 745 °C)

Assay

≥99.0%

form

crystals

impurities

≤0.001% N compounds
≤0.005% insolubles

loss

≤0.2% loss on drying

pH

6.0-9.2 (25 °C, 5%)

mp

681 °C (lit.)

anion traces

chloride, bromide (as Cl)-: ≤0.01%
iodate (IO3-): ≤3 ppm
phosphate (PO43-): ≤0.001%
sulfate (SO42-): ≤0.005%

cation traces

Ba: ≤0.002%
Ca: ≤0.002%
Fe: ≤3 ppm
Mg: ≤0.001%
Na: ≤0.005%
heavy metals (as Pb): ≤5 ppm

SMILES string

[K+].[I-]

InChI

1S/HI.K/h1H;/q;+1/p-1

InChI key

NLKNQRATVPKPDG-UHFFFAOYSA-M

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General description

Potassium iodide is a water soluble inorganic salt that can be prepared by reacting hydrogen iodide and potassium bicarbonate.

Application

Potassium iodide may be used as a catalyst in the following processes: Conversion of aromatic primary amines to the corresponding nitro compounds in the presence of tert-butyl hydroperoxide as oxidant. Conversion of aryl halide to aryl iodides in the presence of nickel catalysts. Preparation of sulfonated oxindoles from activated alkenes and sulfonylhydrazides in water and in the presence of 8-crown-6 and tert-butyl hydroperoxide.

Legal Information

Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

STOT RE 1 Oral

Target Organs

Thyroid

Storage Class Code

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Synthesis of Aryl Iodides from Aryl Halides and Potassium Iodide by Means of Nickel Catalyst
Takagi K, et al
Chemistry Letters (Jpn), 7(2), 191-192 (1978)
Synthesis of sulfonated oxindoles by potassium iodide catalyzed arylsulfonylation of activated alkenes with sulfonylhydrazides in water.
<BIG>Li X, et al. </BIG>
The Journal of Organic Chemistry, 78(14), 7343-7348 (2013)
Selective Oxidation of Aromatic Amines to Nitro Derivatives using Potassium Iodide-tert-Butyl Hydroperoxide Catalytic System
Reddy KR, et al
Advanced Synthesis & Catalysis, 351(1-2), 93-96 (2009)
Eagleson M.
Concise Encyclopedia Chemistry, 889-889 (1994)
Alumina-supported potassium iodide as a heterogeneous catalyst for biodiesel production from soybean oil.
Xie W and Li H.
J. Mol. Catal. A: Chem., 255(1), 1-9 (2006)

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