Iron(3+);trichloride;hydrate

Base Information

• Chemical Name: Iron(3+);trichloride;hydrate
• CAS No.: 10025-77-1
• Molecular Formula: Cl₃Fe*2H₂O
• Molecular Weight: 198.237
• Hs Code.: 28273300
• Mol file: 10025-77-1.mol

Synonyms:

Chemical Property of Iron(3+);trichloride;hydrate

Chemical Property:

• Appearance/Colour: yellow solid
• Vapor Pressure: 1 mm Hg ( 194 °C)
• Melting Point: 37 °C
• Boiling Point: 280 °C decomp.
• Flash Point: 280-285°C
• PSA: 55.38000
• Density: 1,82 g/cm3
• LogP: -9.37630
• Storage Temp.: Store at RT
• Sensitive.: Hygroscopic
• Solubility.: 920g/l
• Water Solubility.: 920 g/L (20 ºC)
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 178.852058
• Heavy Atom Count: 5
• Complexity: 0

Purity/Quality:

99% ^*data from raw suppliers

Iron(III) chloride hexahydrate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn,C
• Hazard Codes: Xn,C
• Statements: 22-38-41-34
• Safety Statements: 26-39-45-36/37/39

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: O.[Cl-].[Cl-].[Cl-].[Fe+3]
• Description: Ferric Chloride is the chloride of the Iron (III) form. It has various kinds of applications. In industry, it can be used in sewage treatment and drinking water production (for example, used for arsenic removal); used as a leaching agent in chloride hydrometallurgy; for etching copper in two-step redox reactions to copper (I) chloride and then to copper chloride during production of printed circuit boards; as the catalyst for the synthesis of ethylene dichloride from the reaction of ethylene with chlorine. In laboratory, it is commonly employed as a Lewis acid for catalysing reactions such as chlorination of aromatic compounds and Friedel–Crafts reaction of aromatics. The ferric chloride test can be used as a traditional colorimetric test for phenols. Ferric chloride can also be applied for the determination of total cholesterol and cholesterol esters. In disease field, it can be used to induce arterial thrombosis for thrombosis research. It can also be used for decolorization of disperse and reactive dye solutions.
• Uses: :Iron chloride hexahydrate can be used in clinical reagents (amino acids in urine). Iron(III) chloride hexahydrate is used to prepare organically templated iron phosphates. It is used for sewerage treatment of industrial wastes, chloride hydrometallurgy (Silgarin process for the production of silicon), drinking water production, production of precursors for polyvinyl chloride (PVC) and copper-based metals in printed circuit boards. It plays an important role in photoengraving and photography as an etching agent. It is useful as a mordant in dyeing and printing textiles. It is useful in the detection of phenols and phenolic derivatives; gamma-hydroxybutyric acids and also in the Trinder spot test for detecting salicylic acids. Iron(III) chloride hexahydrate (FeCl3.6H2O) may be employed as an oxidant for the following conversions: Synthesis of 2-substituted 4(3H)-quinazolinones (yield = 77-93%). Oxidation of 1,4-dihydropyridines (1,4-DHPs) to corresponding pyridines. Oxidation of 4-isopropyl-1,4-DHP to dealkylated pyridine.

Technology Process of Iron(3+);trichloride;hydrate

There total 28 articles about Iron(3+);trichloride;hydrate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

iron(III) chloride (7705-08-0) → iron(III) chloride hexahydrate (121714-78-1,24290-40-2,58694-80-7,10025-77-1,64333-00-2)

Guidance literature:

In water; concd. soln. of FeCl3 cooled;;

Reference yield:

iron(III) chloride * 2.5 H2O (121714-78-1,24290-40-2,58694-80-7,10025-77-1,64333-00-2) → iron(III) trichloride dihydrate (121714-78-1,24290-40-2,58694-80-7,10025-77-1,64333-00-2)

Guidance literature:

With H₂SO₄; In neat (no solvent); was not built when kept over concd. H2SO4 at room temp.;;

Reference yield:

iron(III) chloride hexahydrate (121714-78-1,24290-40-2,58694-80-7,10025-77-1,64333-00-2) → iron(III) chloride * 2.5 H2O (121714-78-1,24290-40-2,58694-80-7,10025-77-1,64333-00-2)

Guidance literature:

In neat (no solvent); byproducts: H2O; loss of water above H2SO4 with deliquescence;; crystn.;;

upstream raw materials:

water

chlorine

iron

iron(III) chloride

Downstream raw materials:

((C₆H₅)2CCC(CH₃)COOC₂H₅)Fe(CO)4

((C₆H₅)2CCHC(CH₂)COOC₂H₅)Fe(CO)3

α-methyl-γ,γ-diphenylallenecarboxylic acid ethyl ester

7,8-dicarba-nido-undecaborane⁽¹¹⁾ * 4-stilbazole

Refernces

Fe₃O₄ magnetic nanoparticles in the layers of montmorillonite as a valuable heterogeneous nanocatalyst for the one-pot synthesis of indeno[1,2-b]indolone derivatives in aqueous media

10.1007/s11164-018-3659-7

This study presents the synthesis of montmorillonite (MMT) supported Fe3O4 magnetic nanoparticles, which were used as heterogeneous nanocatalysts for the one-pot synthesis of indeno[1,2-b]indolone derivatives in aqueous media. The MMT@Fe3O4 nanocomposites were characterized using various techniques including X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), vibrating sample magnetometer (VSM), thermogravimetric analysis (TGA), and Fourier transform infrared spectroscopy (FT-IR). The catalyst exhibited high efficiency in promoting the cyclocondensation of ninhydrin, 1,3-diketone compounds, and amine derivatives to generate the desired indeno[1,2-b]indolone derivatives in excellent yields under mild conditions. This study highlights the advantages of using MMT@Fe3O4 as an environmentally friendly, cost-effective, and recyclable catalyst, providing a green and efficient approach for the synthesis of these heterocyclic compounds of biological and pharmacological importance.

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