14883-34-2

Basic information

• Product Name: tripotassium trioxalatoferrate
• Synonyms: tripotassium trioxalatoferrate;Kalium-Eisen(III)-oxalat-3-hydrat;PotassiumIron(III)oxalatetrihydrate;Ferrate(3-), tris(oxalato)-, tripotassium;Ferrate(3-), tris(oxalato)-, tripotassium, tris(oxalato)-, tripotassium;Ferrate(3-), tris[ethanedioato(2-)-o,o']-, tripotassium, (oc-6-11)-;Iron potassium oxalate, K3fe(C2o4)3;Nsc2915
• CAS NO: 14883-34-2
• Molecular Formula: C4H6FeKO11
• Molecular Weight: 325.02714
• EINECS: 238-954-7
• Mol File: 14883-34-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 365.1°C at 760 mmHg
• Flash Point: 188.8°C
• Appearance: /
• Density: 2.13 g/cm³
• Vapor Pressure: 2.51E-06mmHg at 25°C
• CAS DataBase Reference: tripotassium trioxalatoferrate(CAS DataBase Reference)
• NIST Chemistry Reference: tripotassium trioxalatoferrate(14883-34-2)
• EPA Substance Registry System: tripotassium trioxalatoferrate(14883-34-2)

Safety Data

• RIDADR: 3288
• HazardClass: 6.1(b)
• PackingGroup: III
• Hazardous Substances Data: 14883-34-2(Hazardous Substances Data)

Usage

General Description

Tripotassium trioxalatoferrate, also known as potassium ferrioxalate, is a chemical compound with the formula K3[Fe(C2O4)3]. It is an orange-red crystalline solid that is soluble in water. Potassium ferrioxalate is used in analytical chemistry as a primary standard for standardizing potassium permanganate solutions. It is also used in photography as a reducing agent and in the manufacturing of pigments and dyes. Additionally, potassium ferrioxalate has been studied for its potential applications in solar energy conversion processes and as a catalyst in organic synthesis reactions. Overall, tripotassium trioxalatoferrate has a variety of industrial and scientific uses due to its unique chemical properties.

InChI:InChI=1/3C2H2O4.Fe/c3*3-1(4)2(5)6;/h3*(H,3,4)(H,5,6);

Upstream product

• 583-52-8 potassium oxalate 

Relevant articles and documents

Visible Light Copper Photoredox-Catalyzed Aerobic Oxidative Coupling of Phenols and Terminal Alkynes: Regioselective Synthesis of Functionalized Ketones via C C Triple Bond Cleavage

Direct oxidative coupling of phenols and terminal alkynes was achieved at room temperature by a visible-light-mediated copper-catalyzed photoredox process. This method allows regioselective synthesis of hydroxyl-functionalized aryl and alkyl ketones from simple phenols and phenylacetylene via C C triple bond cleavage. 47 examples were presented. From a synthetic perspective, this protocol offers an efficient synthetic route for the preparation of pharmaceutical drugs, such as pitofenone and fenofibrate.