MilliporeSigma
All Photos(4)

221937

Sigma-Aldrich

Ammonium iodide

greener alternative

ACS reagent, ≥99%

Linear Formula:
NH4I
CAS Number:
Molecular Weight:
144.94
EC Number:
MDL number:
eCl@ss:
38050607
PubChem Substance ID:

Quality Level

grade

ACS reagent

vapor pressure

1 mmHg ( 210.9 °C)

assay

≥99%

form

crystalline powder

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

impurities

≤0.005% insolubles

ign. residue

≤0.05%

pH

4.5-6.5 (25 °C, 50 g/L)

anion traces

Cl- and Br-: ≤0.005%
phosphate (PO43-): ≤0.001%
sulfate (SO42-): ≤0.05%

cation traces

Ba: ≤0.002%
Fe: ≤5 ppm
heavy metals (as Pb): ≤0.001%

SMILES string

N.I

InChI

1S/HI.H3N/h1H;1H3

Inchi Key

UKFWSNCTAHXBQN-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is used as a ntrogen source for syntheis of many heterocyclic compounds and is also used as a catalyst or redox catalyst in some reactions. Click here for more information.
The high yield and regioselective conversion of an unactivated aziridine to an oxazolidinone using carbon dioxide with ammonium iodide as the catalyst

Application

Catalyst for mild, efficient, and greener dethioacetalization.

Packaging

100, 500 g in poly bottle

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

More Documents

Quotes and Ordering

Jinho Kim et al.
Organic letters, 14(15), 3924-3927 (2012-07-17)
Copper-mediated regioselective cyanation of indoles and 2-phenylpyridines was developed by using ammonium iodide and DMF as the combined source of a cyano unit under "Pd-free" conditions. Mechanistic studies indicate that the reaction of indoles proceeds through a two-step sequence: electrophilic
Simple and regioselective oxyiodination of aromatic compounds with ammonium iodide and Oxone.
Mohan KVVK, et al.
Tetrahedron Letters, 45(43), 8015-8018 (2004)
Xiaofang Gao et al.
Chemical communications (Cambridge, England), 51(1), 210-212 (2014-11-20)
A novel ammonium iodide-induced sulfonylation of alkenes with DMSO and water toward the synthesis of vinyl methyl sulfones is described. The process proceeded smoothly under metal-free conditions with high stereoselectivity and good functional group tolerance. The reaction mechanism was revealed
Low-Frequency Vibrations in Ammonium Iodide and Ammonium Bromide.
Durig JR and Antion DJ.
J. Chem. Phys. , 51(9), 3639-3647 (1969)
Jinho Kim et al.
Journal of the American Chemical Society, 134(5), 2528-2531 (2012-01-28)
The cyanation of aromatic boronic acids, boronate esters, and borate salts was developed under copper-mediated oxidative conditions using ammonium iodide and DMF as the source of nitrogen and carbon atom of the cyano unit, respectively. The procedure was successfully extended

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service