18204-93-8

Basic information

• Product Name: DI-N-HEXYLDICHLOROSILANE
• Synonyms: LS 4460;dichlorodihexyl-silan;DI-N-HEXYLDICHLOROSILANE;DIHEXYLDICHLOROSILANE;DICHLORODI-N-HEXYLSILANE;DICHLORODIHEXYLSILANE;Dichlorodi-n-hexysilane
• CAS NO: 18204-93-8
• Molecular Formula: C₁₂H₂₆Cl₂Si
• Molecular Weight: 269.33
• EINECS: 242-093-2
• Product Categories: Dichlorosilanes;Dichlorosilanes (for Polysilanes);Functional Materials;Reagent for High-Performance Polymer Research;Si (Classes of Silicon Compounds);Si-Cl Compounds
• Mol File: 18204-93-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: <0°C
• Boiling Point: 111 °C
• Flash Point: 88°C
• Appearance: /
• Density: 0.962
• Vapor Pressure: 0.00685mmHg at 25°C
• Refractive Index: 1.4104
• Storage Temp.: below 5° C
• CAS DataBase Reference: DI-N-HEXYLDICHLOROSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: DI-N-HEXYLDICHLOROSILANE(18204-93-8)
• EPA Substance Registry System: DI-N-HEXYLDICHLOROSILANE(18204-93-8)

Safety Data

• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: 2987
• TSCA: No
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 18204-93-8(Hazardous Substances Data)

Usage

General Description

DI-N-HEXYLDICHLOROSILANE is an organosilicon compound with the chemical formula C12H28Cl2Si. It is a colorless liquid with a strong irritating odor that is highly reactive and flammable. DI-N-HEXYLDICHLOROSILANE is primarily used as a precursor in the production of silicone polymers and resins, as well as in the development of various silicone-based materials and products. It is a versatile chemical with applications in the automotive, construction, electronics, and pharmaceutical industries. However, it is important to handle DI-N-HEXYLDICHLOROSILANE with caution due to its hazardous nature and potential health risks if not used properly.

InChI:InChI=1/C12H26Cl2Si/c1-3-5-7-9-11-15(13,14)12-10-8-6-4-2/h3-12H2,1-2H3

Upstream product

• 10026-04-7 tetrachlorosilane 
• 3761-92-0 n-hexylmagnesium bromide 
• 1002-78-4 (1-hexyl)(hexyl)silane 
• 592-41-6 1-hexene 

Downstream Products

• 811433-79-1 1,2-bis[2-(ethoxydihexylsilyl)-5-fluorophenyl]acetylene 
• 811433-67-7 1,2-bis[2-(ethoxydihexylsilyl)-5-methoxyphenyl]acetylene 
• 906372-08-5 4,4-dihexyl-4H-silolo[3,2-b:4,5-b']dithiophene 
• 122916-53-4 C₁₈H₃₁ClSi 
• 852138-91-1 (2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan)-9,9-dihexyl)silafluorene 
• 852138-90-0 3,7-dibromo-5,5-dihexyl-5H-dibenzo-[b,d]-silole 
• 18407-13-1 di-n-hexyldiethoxysilane 
• 126990-43-0 di-n-hexyldimethoxysilane 
• 283157-77-7 allyl-di-n-hexylphenylsilane 

Relevant articles and documents

SYNTHESIS OF ORGANO CHLOROSILANES FROM ORGANOSILANES

The invention relates to a process for the production of chlorosilanes by subjecting one or more hydndosilanes to the reaction with hydrogen chloride in the presence of at least one ether compound, and a process for the production of such hydndosilanes serving as starting materials.

Macrocyclic polyether compounds

Macrocyclic polyether "crown" compounds of the formula EQU1 WHEREIN T is a C2 -C3 alkylene, A is EQU2 R being H or C1 -C18 alkyl, R2 and R3 being independently C1 -C18 alkyl, C2 -C4 alkenyl, or C6 -C14 aryl; Q and Z are independently 1,2-arylene (or saturated derivatives thereof) or substituted 1,2-arylene (or saturated derivatives thereof); a is 0, 1, 2, or 3; b is an integer from 3 to 20; y is 1 or zero; x1, x2, x3, and x4 are integers independently selected to give a 15-60 atom ring. Such crown compounds are generally useful in the formation of complexes with ionic metal compounds, thus making it possible to use certain chemical reagents in media wherein they are normally insoluble.