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Trimethoxyoctylsilane

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Trimethoxyoctylsilane Basic information

Product Name:
Trimethoxyoctylsilane
Synonyms:
  • covasils
  • Silane, trimethoxyoctyl-
  • N-OCTYLTRIMETHOXYSILANE
  • n-Octyltrimethoxysilane(1-Trimethoxysilyl octane)
  • OCTYLTRIMETHOXYSILANE
  • TRIMETHOXY-OCTYLSILANE
  • TRIMETHOXYCAPRYLYLSILANE
  • TriMethoxy-n-octylsilane
CAS:
3069-40-7
MF:
C11H26O3Si
MW:
234.41
EINECS:
221-338-7
Product Categories:
  • silane
  • Alkyl
  • Alkoxy Silanes
  • Hydrophobing Agents
Mol File:
3069-40-7.mol
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Trimethoxyoctylsilane Chemical Properties

Boiling point:
75 °C
Density 
0.907 g/mL at 25 °C(lit.)
vapor pressure 
0-12790Pa at 20-25℃
refractive index 
n20/D 1.416(lit.)
Flash point:
216 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Soluble in common non-polar organic solvent.
form 
Liquid
Specific Gravity
0.907
color 
Colorless to yellow
Water Solubility 
59-1000g/L at 20℃
Sensitive 
Moisture Sensitive
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
BRN 
1926957
InChIKey
NMEPHPOFYLLFTK-UHFFFAOYSA-N
LogP
-0.82-3.9 at 20-24℃
CAS DataBase Reference
3069-40-7(CAS DataBase Reference)
NIST Chemistry Reference
N-Octyltrimethoxysilane(3069-40-7)
EPA Substance Registry System
Silane, trimethoxyoctyl- (3069-40-7)
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Safety Information

Risk Statements 
36/38-36/37/38
Safety Statements 
23-24/25-26/37
RIDADR 
UN2924
WGK Germany 
1
21
TSCA 
No
HazardClass 
3
PackingGroup 
III
HS Code 
29319090

MSDS

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Trimethoxyoctylsilane Usage And Synthesis

Chemical Properties

Colorless transparent liquid

Uses

Trimethoxy(octyl)silane is a surface modifier used as additive for polymer encapsulation and for controlled drug delivery.

General Description

Trimethoxy(octyl)silane is an organosilane. The effect of hydrolyzed silane on the penetration of water into a lamellar liquid crystal was studied.

Flammability and Explosibility

Not classified

Synthesis

2487-90-3

111-66-0

3069-40-7

GENERAL STEPS: All catalytic reactions were carried out in 10 mL flat-bottomed tubes without inert gas protection. 1-Octene (4.0 mmol) was added to the dry reaction tube with an appropriate amount of catalyst and stirred for 5 minutes. Subsequently, trimethoxysilane (4.4 mmol) was added and the reaction mixture was heated to a set temperature and stirred for the indicated time. After completion of the reaction, it was cooled to room temperature. The product phase was separated by decantation, and the conversion of 1-octene and the selectivity of octyltrimethoxysilane were analyzed using an Agilent 26890N/59731 GC-MS system equipped with a DB-5 column (30 m × 2.5 mm × 0.25 μm). The 1H NMR (400 MHz) and 13C NMR (100.6 MHz) spectra of the products were recorded on a Bruker Advance spectrometer using tetramethylsilane (TMS) as an internal standard and the solvents were methanol-d4 or DMSO-d6.

References

[1] Angewandte Chemie - International Edition, 2016, vol. 55, # 40, p. 12295 - 12299
[2] Angew. Chem., 2016, vol. 128, p. 12483 - 12487,5
[3] Journal of Organometallic Chemistry, 2014, vol. 765, p. 59 - 63
[4] Patent: US2017/260215, 2017, A1. Location in patent: Paragraph 0239; 0243
[5] Angewandte Chemie - International Edition, 2015, vol. 54, # 48, p. 14523 - 14526

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