221937
Ammonium iodide
ACS reagent, ≥99%
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About This Item
Linear Formula:
NH4I
CAS Number:
Molecular Weight:
144.94
PubChem Substance ID:
eCl@ss:
38050607
UNSPSC Code:
12352300
EC Number:
234-717-7
MDL number:
Assay:
≥99%
Grade:
ACS reagent
Form:
powder or crystals
grade
ACS reagent
Quality Level
vapor pressure
1 mmHg ( 210.9 °C)
assay
≥99%
form
powder or crystals
greener alternative product characteristics
Catalysis
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sustainability
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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%
greener alternative category
SMILES string
N.I
InChI
1S/HI.H3N/h1H;1H3
InChI key
UKFWSNCTAHXBQN-UHFFFAOYSA-N
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
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.
Catalyst for mild, efficient, and greener dethioacetalization.
Chemoselective Bromination of Active Methylene and Methyne Compounds by Potassium Bromide, Hydrochloric Acid and Hydrogen Peroxide
Chemoselective Bromination of Active Methylene and Methyne Compounds by Potassium Bromide, Hydrochloric Acid and Hydrogen Peroxide
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signalword
Danger
hcodes
Hazard Classifications
STOT RE 1 Oral
target_organs
Thyroid
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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)
Low-Frequency Vibrations in Ammonium Iodide and Ammonium Bromide.
Durig JR and Antion DJ.
J. Chem. Phys. , 51(9), 3639-3647 (1969)