326089
Ammonium hexachloroiridate(IV)
98%
Synonym(s):
Iridium(IV)-ammonium chloride
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About This Item
Linear Formula:
(NH4)2IrCl6
CAS Number:
Molecular Weight:
441.01
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23
Assay
98%
form
powder
density
2.86 g/mL at 25 °C (lit.)
SMILES string
[H][N+]([H])([H])[H].[H][N+]([H])([H])[H].Cl[Ir--](Cl)(Cl)(Cl)(Cl)Cl
InChI
1S/6ClH.Ir.2H3N/h6*1H;;2*1H3/q;;;;;;+4;;/p-4
InChI key
LWNOUTCTZQNGEN-UHFFFAOYSA-J
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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L D Kwiatkowski et al.
Journal of inorganic biochemistry, 14(3), 209-222 (1981-06-01)
The steady-state kinetics of four redox reactions catalyzed by galactose oxidase have been determined. The alcohol substrate used in each case was galactose; the four oxidant substrates used were O2, IrCl6(2)-, porphyrexide, and Fe(CN)6(3)-. With the exception of the last
Edward P Randviir et al.
Nanoscale, 4(20), 6470-6480 (2012-09-11)
A newly synthesised type of graphene, Q-Graphene, has been physically and electrochemically characterised with Scanning and Transmission Electron Microscopy (SEM, TEM), X-ray Photoelectron Spectroscopy (XPS) and Cyclic Voltammetry (CV). Interpretation of SEM, TEM and XPS data reveal the material to
Olga Kornyushyna et al.
Biochemistry, 41(51), 15304-15314 (2002-12-18)
The low redox potential of 8-oxo-7,8-dihydroguanine (OG), a molecule regarded as a marker of oxidative damage in cells, makes it an easy target for further oxidation. Using a temperature-dependent method of synthesis, the oxidation products of OG, guanidinohydantoin (Gh) and/or
J G Muller et al.
Nucleic acids research, 26(9), 2247-2249 (1998-06-20)
Two gel electrophoretic methods are described for detection of 7, 8-dihydro-8-oxoguanine and 7,8-dihydro-8-oxoadenine based on their further oxidation with one-electron oxidants including IrCl62-and IrBr62-. The products of nucleobase oxidation lead to enhanced piperidine-sensitive cleavage and to highly visible stop points
Na Song et al.
Inorganic chemistry, 47(24), 11458-11460 (2008-11-14)
One-electron oxidation of phenol, 2,4,6-trimethylphenol, and 2,6-dimethylphenol by [IrCl(6)](2-) in aqueous solution has a simple pH dependence, indicating slow bimolecular oxidation of ArOH and faster oxidation of ArO(-). H/D kinetic isotope effects as large as 3.5 for oxidation of ArOH
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