13083-94-8

Basic information

• Product Name: 1,6-BIS(TRICHLOROSILYL)HEXANE
• Synonyms: BIS(TRICHLOROSILYL)HEXANE;1,6-BIS(TRICHLOROSILYL)HEXANE;1,6-hexanediylbis[trichloro-silan;1,6-hexanediylbis[trichlorosilane];1,6-BIS(TRICHLOROSILYL)HEXANE 97%;Hexamethylenebis(trichlorosilane);1,6-Bis(trichlorosilyl)hexane,97%;trichloro(6-trichlorosilylhexyl)silane
• CAS NO: 13083-94-8
• Molecular Formula: C₆H₁₂Cl₆Si₂
• Molecular Weight: 353.05
• EINECS: 253-994-7
• Product Categories: Industrial/Fine Chemicals;Bridged MonomersOrganic Electronics and Photonics;Dielectric MaterialsSelf Assembly&Contact Printing;Organic Conductors and Photovoltaics: OFET and OPV Materials;POSS? Precursors and Intermediates;Self-Assembly Materials;Silanes;Silsesquioxanes: POSS? Nanohybrids
• Mol File: 13083-94-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: <25°C
• Boiling Point: 281 °C(lit.)
• Flash Point: 167 °F
• Appearance: light brown liquid
• Density: 1.327 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.00406mmHg at 25°C
• Refractive Index: n20/D 1.475(lit.)
• BRN: 1768655
• CAS DataBase Reference: 1,6-BIS(TRICHLOROSILYL)HEXANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6-BIS(TRICHLOROSILYL)HEXANE(13083-94-8)
• EPA Substance Registry System: 1,6-BIS(TRICHLOROSILYL)HEXANE(13083-94-8)

Safety Data

• Hazard Codes: C
• Statements: 14-34
• Safety Statements: 26-36/37/39-43-45
• RIDADR: UN 2987 8/PG 2
• WGK Germany: 3
• F: 10-21
• TSCA: Yes
• Hazardous Substances Data: 13083-94-8(Hazardous Substances Data)

Usage

Description

1,6-BIS(TRICHLOROSILYL)HEXANE, also known as a silane-based cross-linking agent, is a light brown liquid with unique chemical properties that make it suitable for various applications in the field of polymer science and organic electronics. It is characterized by its ability to form cross-links within polymeric structures, enhancing their overall performance and stability.

Uses

Used in Organic Electronics Industry:
1,6-BIS(TRICHLOROSILYL)HEXANE is used as a cross-linking agent for the synthesis of polymeric blended films. These films serve as dielectrics in organic electronic-based devices, such as organic field-effect transistors (OFETs) and organic thin-film transistors (OTFTs). The cross-linking ability of 1,6-BIS(TRICHLOROSILYL)HEXANE improves the dielectric properties of the films, leading to enhanced performance and stability in these electronic devices.

InChI:InChI=1/C6H12Cl6Si2/c7-13(8,9)5-3-1-2-4-6-14(10,11)12/h1-6H2

Upstream product

• 592-42-7 1,5-Hexadien 
• 10025-78-2 trichlorosilane 
• 2163-00-0 1,6-dichlorohexane 
• 693-02-7 hex-1-yne 
• 13095-00-6 E-1-trichlorosilylhex-1-ene 

Relevant articles and documents

Process for Preparing Polysilylalkane

Polysilylalkane according to the present invention is represented by following formula. The present invention has an advantage that bis(silyl)alkanes or tri(silyl)alkanes can be manufactured in a high yield by dehydrochlorination with a small amount of catalyst by using a silane compound having a dichloro organic matter or a dichloromethyl group.COPYRIGHT KIPO 2020

Process for Preparing Polysilylalkane

A polysilyalkane according to the present invention is presented by a formula. Here, m=n=0, R^3 is chloro, and methyl group; when R^4 is H, -SiMe_2Cl, -SiMe_3,-SiMeCl_2, -SiCl_3, R^3=-SiCl_3; R^4 is H, R^5=R^6=Me or R^5=Me, when R6=Et, R^3-SiCl_3; R^4 is H, R^5= -CH_2SiCl_3, when R^6 is Me, R^3=-SiCl_3; R^4 is H, when R5=R6=-CH_2SiCl_3, R^3=Et, SiMe_2Cl, -SiMeCl_2, -SiCl_3, and m is integer number of 0-9.COPYRIGHT KIPO 2015

PREPARATION OF A HALOSILYLATED CHAIN HYDROCARBON

A method for the preparation of a chain hydrocarbon halosilylated at its terminal carbon atom or terminal carbon atoms by subjecting a diene-type compound and a hydrogenhalosilane to a hydrosilylation reaction in the presence of a hydrosilylation catalyst and an ether compound having no aliphatic triple bond.A method of conducting a hydrosilylation reaction between a diene-type compound that has vinyl groups on both terminals and a hydrogenhalosilane in the presence of a hydrosilylation catalyst and an ether compound having no aliphatic triple bond.