Triethoxyoctylsilane

Base Information

• Chemical Name: Triethoxyoctylsilane
• CAS No.: 2943-75-1
• Deprecated CAS: 1247019-87-9
• Molecular Formula: C14H32O3Si
• Molecular Weight: 276.492
• Hs Code.: 29310095
• European Community (EC) Number: 220-941-2
• NSC Number: 42964
• UNII: LDC331P08E
• DSSTox Substance ID: DTXSID2029246
• Nikkaji Number: J183.124K
• Wikidata: Q27282931
• NCI Thesaurus Code: C84028
• RXCUI: 1310586
• Metabolomics Workbench ID: 152531
• ChEMBL ID: CHEMBL3185786
• Mol file: 2943-75-1.mol

Synonyms:octyltriethoxysilane

Chemical Property of Triethoxyoctylsilane

Chemical Property:

• Appearance/Colour: colorless transparent liquid
• Vapor Pressure: 0.137mmHg at 25°C
• Melting Point: -40oC
• Refractive Index: n20/D 1.417(lit.)
• Boiling Point: 224.4 °C at 760 mmHg
• Flash Point: 101.3 °C
• PSA: 27.69000
• Density: 0.88 g/cm³
• LogP: 4.39530
• Storage Temp.: Store below +30°C.
• Sensitive.: Moisture Sensitive
• Solubility.: Acetonitrile (Slightly), Chloroform (Slightly)
• Water Solubility.: reacts
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 13
• Exact Mass: 276.21207141
• Heavy Atom Count: 18
• Complexity: 159

Purity/Quality:

98% ^*data from raw suppliers

Triethoxy(octyl)silane ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36-37/39

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Metals -> Metalloid Compounds (Silicon)
• Canonical SMILES: CCCCCCCC[Si](OCC)(OCC)OCC
• Description: Triethoxyoctylsilane is a monomeric medium-chain alkylfunctional silane. It is a clear colourless liquid and soluble in common non-polar organic solvent. Triethoxyoctylsilane can be used as a surface modifier to generate hydrophobicity (e.g. on concrete, glass, inorganic pigments, or mineral fillers). When diluted with an appropriate solvent, it can be used in the formulation of water repellent products. Upon proper application, the formulated product will penetrate and provide water repellency by chemically reacting with the cementitious substrate. Treated substrates are hydrophobic and retain their original appearance.
• Uses: Triethoxy(octyl)silane is a hydrophobization agent used to limit coalescence in solid-stabilized emulsions.

Technology Process of Triethoxyoctylsilane

There total 17 articles about Triethoxyoctylsilane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

oct-1-ene (111-66-0,25068-25-1) + Triethoxysilane (998-30-1) → triethoxy(octyl)silane (2943-75-1)

Guidance literature:

at 90 ℃; for 5h; Inert atmosphere;

Reference yield: 95.0%

Triethylsilanol (597-52-4) + oct-1-ene (111-66-0,25068-25-1) → triethoxy(octyl)silane (2943-75-1)

Guidance literature:

With (^iPrPNN^Et)FeBr₂; sodium triethylborohydride; In toluene; at -34 - 20 ℃; for 3h; Inert atmosphere;

DOI:10.1021/ja404963f

Reference yield: 88.0%

→ triethoxy(octyl)silane (2943-75-1)

Guidance literature:

upstream raw materials:

tetraethoxy orthosilicate

n-octylmagnesium chloride

ethanol

octyltrichlorosilane

Downstream raw materials:

ethyl (2-benzyloxycarbonyl-ethyl)phosphinate

phosphonic acid diethyl ester

N'-methyl-N'-phenyloctane-1-sulfonohydrazide

N'-benzyl-N'-phenyloctane-1-sulfonohydrazide

Refernces

• 1、 -. "THE PROCESS FOR THE PREPARATION AND USE OF HAIR TREATMENT COMPOSITIONS CONTAINING ORGANIC C1-C6 ALKOXY SILANES". . . Retrieved 2022/01/12.
• 2、 Huo, Yingpeng,Hu, Jiwen,Tu, Yuanyuan,Huang, Zhenzhu,Lin, Shudong,Luo, Xiaojiong,Feng, Chao. "Efficient magnetically separable heterogeneous platinum catalyst bearing imidazolyl schiff base ligands for hydrosilylation". . . Retrieved 2021/02/06.