61214-14-0

Basic information

• Product Name: (3-chloropropyl)tris(1-methylethoxy)silane
• Synonyms: (3-chloropropyl)tris(1-methylethoxy)silane;(3-Chloropropyl)triisopropoxysilane
• CAS NO: 61214-14-0
• Molecular Formula: C₁₂H₂₇ClO₃Si
• Molecular Weight: 282.87948
• EINECS: 262-665-5
• Mol File: 61214-14-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 274.4 °C at 760 mmHg
• Flash Point: 100.3 °C
• Appearance: /
• Density: 0.962 g/cm³
• Vapor Pressure: 0.0091mmHg at 25°C
• Refractive Index: 1.432
• CAS DataBase Reference: (3-chloropropyl)tris(1-methylethoxy)silane(CAS DataBase Reference)
• NIST Chemistry Reference: (3-chloropropyl)tris(1-methylethoxy)silane(61214-14-0)
• EPA Substance Registry System: (3-chloropropyl)tris(1-methylethoxy)silane(61214-14-0)

Safety Data

• Hazardous Substances Data: 61214-14-0(Hazardous Substances Data)

Usage

General Description

(3-chloropropyl)tris(1-methylethoxy)silane is a chemical compound that belongs to the organosilicon group. It is commonly used as an adhesion promoter and coupling agent in organic-inorganic hybrid materials, coatings, and adhesives. The molecule consists of three 1-methylethoxy groups attached to a central silicon atom, with a 3-chloropropyl group serving as the functional reactive site. (3-chloropropyl)tris(1-methylethoxy)silane is highly reactive and is often used in the production of silane-modified polymers for construction, automotive, and electronics applications. It is important to handle and store this chemical with caution, as it can be hazardous if not used properly.

InChI:InChI=1/C12H27ClO3Si/c1-10(2)14-17(9-7-8-13,15-11(3)4)16-12(5)6/h10-12H,7-9H2,1-6H3

Upstream product

• 2550-06-3 3-chloropropyltrichlorosilane 
• 67-63-0 isopropyl alcohol 

Downstream Products

• 1632260-26-4 3-(tri(iso-propoxy)silyl)propyl 2-(2-bromophenyl)-2-diazoacetate 
• 1632260-34-4 3-(tri(iso-propoxy)silyl)propyl 2-(2-bromophenyl)acetate 

Relevant articles and documents

Photoresponsive ordered hybrid materials containing a bridged azobenzene group

This paper describes the synthesis of 4,4′-[(triisopropoxysilyl) propyloxy]azobenzene and the preparation of the ordered hybrid material containing the bridged azobenzene moieties within the framework by using the direct liquid crystal templating approach. We show that a sizable fraction of the azobenzene groups is reversibly photoisomerized though the chromophore is covalently linked to the silica matrix at both ends. In contrast, the photoisomerization did not occur in the corresponding material prepared in the absence of template. This is explained by a regular dilution of the chromophores into silica thanks to the template used for the preparation of the material. The Royal Society of Chemistry 2005.

Cyclic diol-derived blocked mercaptofunctional silane compositions

Diol derived blocked mercaptofunctional silane compositions in which the silanes comprise cyclic and bridged alkoxy groups derived from hydrocarbon-based diols and processes for their preparation are provided. Also provided are rubber compositions comprising the cyclic diol-derived blocked mercaptofunctional silanes, processes for their preparation and articles of manufacture comprising the rubber compositions, in particular, automotive tires and components thereof.