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22537-49-1

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22537-49-1 Usage

Chemical Description

Indium is a chemical element with the symbol In and atomic number 49.

Check Digit Verification of cas no

The CAS Registry Mumber 22537-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,3 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22537-49:
(7*2)+(6*2)+(5*5)+(4*3)+(3*7)+(2*4)+(1*9)=101
101 % 10 = 1
So 22537-49-1 is a valid CAS Registry Number.

22537-49-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name indium(3+)

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:22537-49-1 SDS

22537-49-1Downstream Products

22537-49-1Relevant articles and documents

Kinetic stability of indium(III) complexes with azaporphyrins in aqueous sulfuric acid

Khelevina,Stuzhin,Migalova,Shukhto

, p. 1647 - 1652 (2001)

Stability of chloro(octaphenyltetraazaporphinato)indium(III) and chloro(2,8,12,18-tetrabutyl-3,7,13,17-tetramethyl-5,15-diazaporphinato)indium(II I) in 90-98 % aqueous sulfuric acid was studied. Kinetic parameters of solvoprotolytic dissociation of the complexes were determined, and a mechanism of the reaction was proposed. Diaza substitution results in more stable complexes than tetraaza substitution. The state of chloro(2,8,12,18-tetrabutyl-3,7,13,17-tetramethyl-5,15-diazaporphinato)indium(II I) in a proton-donor medium was studied to show that the acid-base interaction involves one by one two meso-nitrogen atoms. Dissociation constants of the resulting acid forms were determined.

Convenient preparation and improved stability of aqueous indium(I) solutions used in electron transfer reactions

Chandra, Swapan K.,Gould, Edwin S.

, p. 809 - 810 (1996)

Solutions 0.27 mol dm-3 in InI, prepared by treatment of indium amalgam with silver triflate in dry acetonitrile, are stable for more than 5 days in the absence of oxygen and may be diluted 300-fold with water to give InI(aq) solutions which are stable for over 5 h; kinetic patterns for reactions of [Co(NH3)5X]2+ (X = Cl-, Br-, I-, HC2O4-) with InI point to a pair of consecutive 1 e transactions, the first (slower) of which is predominantly inner sphere.

Extraction of gallium(III) by 1-{[2-(2,4-dichlorophenyl)-4-propyl-1,3- dioxolan-2-yl]methyl}-1H-1,2,4-triazole from hydrochloric acid solutions

Anpilogova,Murinov

, p. 2022 - 2026 (2009)

The extraction of gallium(III) with 1-{[2-(2,4-dichlorophenyl)-4-propyl-1, 3-dioxolan-2- yl]methyl}-1H-1,2,4-triazole from hydrochloric acid solutions into toluene was studied. It was found that gallium( III) was efficiently extracted from 5-10 M solution

Solvent extraction of some trace metals and iron with N-octyl-N,N- bis(dihexylphosphinylmethyl)amine

Cherkasov,Garifzyanov,Bazanova,Leont'eva

, p. 2080 - 2087 (2012/03/12)

The processes were studied of the solvent extraction of the ions of triply-charged trace elements including scandium, indium, gallium, and yttrium, as well as iron, with N-octyl-N,N-bis(dihexylphosphinylmethyl)amine solution in toluene, chloroform or methylene chloride from hydrochloric, nitric or perchloric acids aqueous solutions. The metals extraction dependence on the acid concentration showed that the best results were reached using perchloric acid. The calculation of partition coefficients of metals allowed us to reveal a high selectivity of the scandium extraction. The prospects of using the investigated bisphosphinylamine in the technology of extraction, concentration and separation of the trace metals ions was concluded. Pleiades Publishing, Ltd., 2011.

Reactions of octacyanomolybdate(V) and octacyanotungstate(V) with s 2 metal-ion reducing centers

Yang, Zhiyong,Gould, Edwin S.

, p. 1858 - 1861 (2007/10/03)

The s2 centers, Sn(II), Ge(II), and In(I) reduce Mo v(CN)83- and Wv(CN)8 3- quantitatively to the corresponding octacyanomolybdate(IV) and -tungstate(IV) anions. Reductions by In(I) proceed 103-10 5 times as rapidly as those by Sn(II) and Ge(II). All reactions are triggered by a single electron oxidation, yielding a much more reactive s I intermediate. Reductions by Sn(II) in chloride medium proceed predominantly through the SnCl3- anion. The Ge(II)-W(CN) 83- reaction is initiated by a slow unimolecular heterolysis of the Ge(II) center, yielding very nearly linear profiles when the reductant is in excess. The Royal Society of Chemistry 2004.

KINETICS AND MECHANISM OF THE OXIDATION OF INDIUM (I) BY NITRIC ACID IN AQUEOUS SOLUTION.

Red'kin,Smirnov

, p. 866 - 868 (2008/10/08)

The oxidation of indium (I) by nitrite in aqueous solution was studied. The reaction rate is described by a third-order kinetic equation with constant k//3 equals 1. 5 multiplied by (times) 10**4 liters**2/mole**2 multiplied by (times) sec. The activation energy (E//a) is 72. 2 kj/mole. The end products of the interaction of indium (I) and nitrite are In (III) and N//2O. The reaction mechanism is discussed.

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