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1,6-Bis(triethoxysilyl)hexane is an organosilicon compound that functions as a silane coupling agent. It is characterized by a six-carbon chain with two triethoxysilyl groups attached at the first and sixth carbon, which makes it an effective cross-linking agent for polymers and other materials. 1,6-Bis(triethoxysilyl)hexane enhances the bonding between organic polymers and inorganic surfaces, thereby improving the overall adhesion and mechanical properties of the materials it is applied to. Moreover, it serves as a water scavenger, contributing to the improved moisture resistance of the materials.

52034-16-9

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52034-16-9 Usage

Uses

Used in Coatings Industry:
1,6-Bis(triethoxysilyl)hexane is used as a surface modifier and adhesion promoter in the coatings industry to enhance the bonding between the coating and the substrate, leading to improved durability and performance of the coated surfaces.
Used in Adhesives Industry:
In the adhesives industry, 1,6-Bis(triethoxysilyl)hexane is utilized as a cross-linking agent to improve the adhesion strength between different materials, ensuring a stronger and more reliable bond.
Used in Sealants Industry:
1,6-Bis(triethoxysilyl)hexane is employed as a component in sealants to increase their moisture resistance and mechanical properties, making them more effective in sealing applications and protecting against environmental factors.

Check Digit Verification of cas no

The CAS Registry Mumber 52034-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,3 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52034-16:
(7*5)+(6*2)+(5*0)+(4*3)+(3*4)+(2*1)+(1*6)=79
79 % 10 = 9
So 52034-16-9 is a valid CAS Registry Number.

52034-16-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name triethoxy(6-triethoxysilylhexyl)silane

1.2 Other means of identification

Product number -
Other names 3,12-Dioxa-4,11-disilatetradecane,4,4,11,11-tetraethoxy

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:52034-16-9 SDS

52034-16-9Downstream Products

52034-16-9Relevant academic research and scientific papers

Bridged polysesquioxane host matrices containing lanthanides chelated by organic guest ligands, and methods of making such matrices

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Page 12-13, (2008/06/13)

Bridged polysesquioxane compositions comprising: a bridged polysesquioxane host matrix comprising sesquioxane moieties and organic moieties, the sesquioxane moieties comprising a metallic element, the organic moieties interposed between sesquioxane moieties; and a guest molecule comprising a lanthanide atom; at least some of the organic moieties comprising a substituent selected from the group consisting of electron withdrawing functional groups and electron donating functional groups. Processes for making such bridged polysesquioxane compositions. Gain media and active materials for upconversion lasers comprising such bridged polysesquioxane compositions. Light can be amplified by fluorescence emissions from the bridged polysesquioxane compositions.

SILICIUMORGANISCHE VERBINDUNGEN LXXXVIII. DISILATRANYLALKANE

Birkofer, Leonhard,Grafen, Klaus

, p. 143 - 148 (2007/10/02)

By hydrosilation of triethoxyvinylsilane (1), 1,5-hexadiene (10) and 3,3-dimethyl-3-sila-1,4-pentadiene (14) with triethoxysilane (2) we obtained 1,2-bis(triethoxysilyl)ethane (3), 1,6-bis(triethoxysilyl)hexane (11) and 1,5-bis(triethoxysilyl)-3,3-dimethyl-3-silapentane (15).The reaction of 3 with triethanolamine (4), triisopropanolamine (6) and tris(1-t-butyl-ethanol)amine (8) leads to the 1,2-disilatranylethanes 5, 7 and 9.The 1,6-disilatranylhexanes 12 and 13 are formed from 11, 4 and 6 respectively, and 15 with 4 gives 3,3-dimethyl-1,5-disilatranyl-3-silapentane (16).

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