Iridium tetrachloride

Catalog Number	ACM10025975-1
CAS	10025-97-5
Structure
Synonyms	Tetrachloroiridium
Molecular Weight	334.03
Molecular Formula	IrCl4
Canonical SMILES	Cl[Ir](Cl)(Cl)Cl
InChI	InChI=1S/4ClH.Ir/h4*1H;/q;+4/p-4
InChI Key	CALMYRPSSNRCFD-UHFFFAOYSA-J
Melting Point	350+ °C
Purity	95%
Appearance	Black crystalline powder
Complexity	19.1
Covalently-Bonded Unit Count	1
Defined Atom Stereocenter Count	0
Exact Mass	334.83538
Heavy Atom Count	5
Hydrogen Bond Acceptor Count	0
Hydrogen Bond Donor Count	0
Monoisotopic Mass	332.83833
Rotatable Bond Count	0
Topological Polar Surface Area	0 Ų

Q&A

What is the CAS number for Iridium tetrachloride?

The CAS number for Iridium tetrachloride is 10025-97-5.

What is the molecular weight of Iridium tetrachloride?

The molecular weight of Iridium tetrachloride is 334.02.

What are some product categories that Iridium tetrachloride belongs to?

Iridium tetrachloride belongs to product categories such as chemical reaction, pharm, electronic, and materials; metal halide.

What is the color of Iridium tetrachloride?

The color of Iridium tetrachloride is dark brown to black.

What is the storage temperature recommended for Iridium tetrachloride?

It is recommended to store Iridium tetrachloride in an inert atmosphere at room temperature.

Can Iridium tetrachloride dissolve in water and ethanol?

Yes, Iridium tetrachloride is soluble in water and ethanol.

What are some synonyms for Iridium tetrachloride?

Some synonyms for Iridium tetrachloride include Iridium chloride(IV) hydrate, Iridium(IV) chloride, and Iridium chloride(IV) hydrate.

What is the HS code for Iridium tetrachloride?

The HS code for Iridium tetrachloride is 2827398590.

How is Iridium tetrachloride classified in terms of toxicity based on the LD50 value for rats?

Iridium tetrachloride is classified as toxic, with an oral LD50 value for rats of 1560mg/kg.

What are some of the uses of Iridium(IV) chloride?

Iridium(IV) chloride is used in chemical analysis for testing nitric acid in the presence of nitrous acid, microscopy, and in plating solutions. It also acts as a catalyst precursor for the stereoselective reduction of cyclohexanones.