10225-77-1

Usage

Uses

Used in Chemical Synthesis:
Iron(III) chloride hexahydrate is used as a catalyst in organic synthesis for facilitating various chemical reactions. Its catalytic properties enable it to speed up the reaction process, making it an essential component in the production of numerous organic compounds.
Used in Water Treatment:
In the water treatment industry, iron(III) chloride hexahydrate is used as a flocculant and coagulant. It helps in the aggregation of suspended particles and impurities, which can then be easily removed from water, thus improving water quality and safety.
Used in Electronics Manufacturing:
Iron(III) chloride hexahydrate is used as an etchant for copper-based metals in the production of printed circuit boards. Its etching properties allow for the precise removal of copper layers, which is crucial for the manufacturing of intricate circuitry.
Used in Pharmaceutical Industry:
Iron(III) chloride hexahydrate has applications in the pharmaceutical industry, where it is utilized in the synthesis of various iron-based compounds used for medical purposes, such as treating iron deficiency.
Used in Dye Industry:
In the dye industry, iron(III) chloride hexahydrate is used in the production of various dyes and pigments. Its ability to interact with different chemical compounds makes it a valuable component in creating a wide range of colors and shades.
Overall, iron(III) chloride hexahydrate is a multifaceted chemical with applications spanning across various industries, including chemical synthesis, water treatment, electronics manufacturing, pharmaceuticals, and dye production. Its unique properties and wide-ranging uses make it an indispensable component in numerous processes.

Upstream product

• 98-88-4 benzoyl chloride 
• 91-09-8 (2S,3S,4R,5R)-2-Methoxy-tetrahydro-pyran-3,4,5-triol 
• 67-56-1 methanol 
• 40010-17-1 2,3,4-tri-O-benzoyl-β-D-arabinopyranosyl bromide 
• 28697-53-2 D-arabinopyranose 
• 7702-26-3 2-O-(methylsulfonyl)-1,3,5-tri-O-benzoyl-α-D-ribofuranose 
• 30319-42-7 1,2,3,4-tetra-O-benzoyl-α-D-arabinopyranose 
• 22434-99-7 1,2,3,4-tetra-O-benzoyl-β-D-arabinopyranose 
• 3068-29-9 2,3,4-tri-O-acetyl-β-D-arabinosyl bromide 
• 22224-41-5 1,3,5-tri-O-benzoyl-α-D-ribofuranoside 
• 122999-79-5 O¹,O³,O⁵-tribenzoyl-O²-methanesulfonyl-β-D-arabinofuranose 
• 110-86-1 pyridine 
• 124-41-4 sodium methylate 
• 91-09-8 methyl β-D-ribopyranoside 

Downstream Products

• 91-09-8 (2S,3S,4R,5R)-2-Methoxy-tetrahydro-pyran-3,4,5-triol 
• 102448-76-0 methyl-(O³,O⁴-dibenzoyl-O²-methanesulfonyl-α-D-arabinopyranoside) 
• 4782-99-4 methyl-(O³,O⁴-isopropyliden-α-D-arabinopyranoside) 
• 50447-01-3 methyl 2-O-methanesulfonyl-α-D-arabinopyranoside 
• 863998-29-2 methyl 3,4-O-isopropylidene-2-O-methanesulfonyl-α-D-arabinopyranoside 
• 91-09-8 methyl β-D-ribopyranoside 

Relevant academic research and scientific papers

Metal complexation of a D -ribose-based ligand decoded by experimental and theoretical studies

A combination of experimental and theoretical methods have been used to elucidate the complexation properties of a new sugar-derived hexadentate ligand, namely methyl 2,3,4-tri-O-(2-picolyl)-β-D-ribopyranoside (L). The coordination bond lengths in the complexes with MnII, Co II, NiII, and ZnII show substantial deviations from ideal octahedra with deformation towards trigonal-prismatic geometries, which is indicative of a conformationally constrained ligand. The metal-cation-ligand interactions were studied for L and the acyclic analogue L' [1,2,3-tri-O-(2-picolyl)-1,2,3-propanetriol] by spectroscopic methods and isothermal calorimetric titrations for the series MnII, Co II, NiII, ZnII, and CuII. The results indicate a stabilization of the complexes obtained with L compared with L', depending on the nature of the metal. Molecular modeling studies showed that the presence of the sugar moiety strongly favors conformations compatible with metal binding, which suggests an entropic origin of the stabilization of L complexes with regards to L' complexes. Moreover, the differences in the metal chelation profiles of L and L' are related to the constraints in the sugar group in the metal-bound structures. This study shows that foreseeing the degree of preorganization of flexible ligands may drive the design of a new generation of chelating compounds. A new sugar-derived ligand, with its coordination site embedded in a pyranoside cycle in the chair conformation, has been designed. Its transition-metal complexes were characterized by experimental and complexation methods and revealed a dramatic impact of the preorganization and complementarity of the carbohydrate scaffold on the metal binding.

Sinularioside, a triacetylated glycolipid from the Indonesian soft coral Sinularia sp., is an inhibitor of NO release

Chemical analysis of the Indonesian soft coral Sinularia sp. (order Alcyonacea, family Alcyoniidae) afforded a known glucosylcerebroside of the sarcoehrenoside-type and sinularioside (2), a new naturally triacetylated glycolipid containing two α-d-arabinopyranosyl residues and a myristyl alcohol unit. Their complete stereostructures were solved by interpretation of MS and NMR data along with CD analysis of degradation products. Sinularioside proved to moderately inhibit LPS-induced NO release, providing interesting clues into the poorly understood structure-activity relationships for anti-inflammatory glycolipids.

Vesparioside from the marine sponge Spheciospongia vesparia, the first diglycosylceramide with a pentose sugar residue

The marine sponge Spheciospongia vesparia produces vesparioside (1a), a diglycosylated glycosphingolipid which is the first example of a natural diglycosylceramide with a pentose sugar residue. The structure of vesparioside was mostly determined by extensive spectroscopic analysis but determination of the nature of the alkyl chains and elucidation of the absolute stereochemistry of the sugars and of the ceramide required chemical degradation. In this respect, an improved and simplified procedure for the microscale chemical degradation of glycosphingolipids was employed here for the first time. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.