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10378-50-4

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10378-50-4 Usage

Chemical Properties

Blue/Black Crystals

Uses

Potassium perruthenate(VII) is used in the production of carbon nanotubes for flexible solid-state supercapacitors. It is also used as an oxidizing agent in the synthesis of 5-formylcytosine from 5-hydroxymethylcytosine.

Check Digit Verification of cas no

The CAS Registry Mumber 10378-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,7 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10378-50:
(7*1)+(6*0)+(5*3)+(4*7)+(3*8)+(2*5)+(1*0)=84
84 % 10 = 4
So 10378-50-4 is a valid CAS Registry Number.
InChI:InChI=1/K.4O.Ru/q+1;;;;-1;/rK.O4Ru/c;1-5(2,3)4/q+1;-1

10378-50-4 Well-known Company Product Price

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  • Aldrich

  • (334537)  Potassiumperruthenate  

  • 10378-50-4

  • 334537-500MG

  • 1,205.10CNY

  • Detail

10378-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name POTASSIUM PERRUTHENATE

1.2 Other means of identification

Product number -
Other names Potassiumperruthenate

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:10378-50-4 SDS

10378-50-4Downstream Products

10378-50-4Relevant articles and documents

Structural and Magnetic Studies of ABO4-Type Ruthenium and Osmium Oxides

Avdeev, Maxim,Brand, Helen E. A.,Injac, Sean,Kennedy, Brendan J.,Turner, Peter,Wang, Chun-Hai,Yuen, Alexander K. L.

, p. 2791 - 2802 (2020)

Oxides of the form ABO4 with A = K, Rb, Cs and B = Ru and Os have been synthesized and characterized by diffraction and magnetic techniques. For A = K the oxides adopted the tetragonal (I41/a) scheelite structure. RbOsO4, which crystallizes as a scheelite at room temperature, underwent a continuous phase transition to I41/amd near 550 K. RbRuO4 and CsOsO4 were found to crystallize in the orthorhombic (Pnma) pseudoscheelite structure, and both displayed discontinuous phase transitions to I41/a at high temperatures. CsOsO4 was determined to undergo a phase transition to a P21/c structure below 140 K. CsRuO4 crystallizes with a baryte-type structure at room temperature. Upon heating CsRuO4 a first order phase transition to the scheelite structure in I41/a is observed at 400 K. A continuous phase transition is observed to P212121 below 140 K. DC magnetic susceptibility data is consistent with long-range antiferromagnetic ordering at low temperatures for all compounds except for CsOsO4, which is paramagnetic to 2 K. The effective magnetic moments are in agreement with the spin only values for an S = 1/2 quantum magnet. Effective magnetic moments calculated for Os compounds were lower than their Ru counterparts, reflective of an enhanced spin orbit coupling effect. A magnetic structure is proposed for RbRuO4 consisting of predominately antiferromagnetic (AFM) ordering along the 001 direction, with canting of spins in the 100 plane. A small ordered magnetic moment of 0.77 μB was determined.

Oxo Complexes of Ruthenium(VI) and (VII) as Organic Oxidants

Green, Graham,Griffith, William P.,Hollinshead, David M.,Ley, Steven V.,Schroeder, Martin

, p. 681 - 686 (2007/10/02)

Oxidation of a variety of saturated and unsaturated primary and secondary alcohols by tetraoxoruthenate(VI), 2-, tetraoxoruthenate(VII), -, barium trans-trioxodihydroxoruthenium(VI), trans-Ba, dioxotrichlororuthenate(VI), -, and dioxodichlorobipyridylruthenate(VI),, has been studied; 2- may be used catalytically in conjunction with 2- under basic aqueous conditions.For some of these systems, the oxidation of several aldehydes and amines were also examined.Both 2- and - oxidise primary alcohols to carboxylic acids and secondary alcohols to ketones; the reactivity of these reagents towards unsaturated alcohols was studied in particular.The new species and also cleanly oxidise a wide range of alcohols to aldehydes and ketones without attack of double bonds.Ba functions as a heterogeneous oxidant in dichloromethane, oxidising only the most reactive alcohols to aldehydes.

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