5575-48-4

Basic information

• Product Name: N-DECYLTRIMETHOXYSILANE
• Synonyms: N-DECYLTRIMETHOXYSILANE;N-Decyltrimethoxysilan;AY-43-210MC;KBM-3103C;KBM-310C
• CAS NO: 5575-48-4
• Molecular Formula: C13H30O3Si
• Molecular Weight: 262.46
• Mol File: 5575-48-4.mol
• Article Data: 4

Chemical Properties

• Melting Point: -37°C
• Boiling Point: 115 °C
• Flash Point: 117°C
• Appearance: /
• Density: 0.9
• Vapor Pressure: 0.237mmHg at 25°C
• Refractive Index: 1.4220
• Water Solubility: Soluble in organic solvents. Insoluble in water.
• Sensitive: Moisture Sensitive
• BRN: 8625082
• CAS DataBase Reference: N-DECYLTRIMETHOXYSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: N-DECYLTRIMETHOXYSILANE(5575-48-4)
• EPA Substance Registry System: N-DECYLTRIMETHOXYSILANE(5575-48-4)

Safety Data

• Statements: 36/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 5575-48-4(Hazardous Substances Data)

Usage

Uses

n-Decyltrimethoxysilane is used as a coupling agent and as a pharmaceutical intermediate.

InChI:InChI=1/C13H30O3Si/c1-5-6-7-8-9-10-11-12-13-17(14-2,15-3)16-4/h5-13H2,1-4H3

Upstream product

• 67-56-1 methanol 
• 13829-21-5 n-decyltrichlorosilane 
• 2487-90-3 trimethoxysilane 
• 7433-56-9 (E)-5-decene 
• 872-05-9 1-Decene 

Relevant articles and documents

METHOD FOR PRODUCING ORGANOXYSILANE

PROBLEM TO BE SOLVED: To provide a method for easily producing high quality alkoxysilane without sublimating contaminant urea and urea hydroxide in the distillation of an alkoxysilane layer after separating an alcohol solution layer with urea and urea hydroxide dissolved therein when chlorosilane is reacted with alcohol in a presence of urea. SOLUTION: The method for producing organoxysilane represented by formula (3) comprises: reacting chlorosilane represented by formula (1) with alcohol represented by formula (2) in a presence of urea; removing hydrogen chloride generated by the above reaction, urea hydroxide produced by reaction of urea, and urea in a reaction system as an alcohol solution dissolved in alcohol in the reaction system from the system; and thereafter distilling an obtained organoxysilane layer with metal alkoxide added to the layer, where R1 and R2 are monovalent hydrocarbon groups, a is an integer of 1-3, b is an integer of 0-2, a+b is an integer of 1-3, and R3 is a monovalent hydrocarbon group. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

An Easily Accessed Nickel Nanoparticle Catalyst for Alkene Hydrosilylation with Tertiary Silanes

The first efficient and non-precious nanoparticle catalyst for alkene hydrosilylation with commercially relevant tertiary silanes has been developed. The nickel nanoparticle catalyst was prepared in situ from a simple nickel alkoxide precatalyst Ni(OtBu)2?x KCl. The catalyst exhibits high activity for anti-Markovnikov hydrosilylation of unactivated terminal alkenes and isomerizing hydrosilylation of internal alkenes. The catalyst can be applied to synthesize a single terminal alkyl silane from a mixture of internal and terminal alkene isomers, and to remotely functionalize an internal alkene derived from a fatty acid.