Welcome to LookChem.com Sign In|Join Free

CAS

  • or

3069-40-7

Post Buying Request

3069-40-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3069-40-7 Usage

Description

Trimethoxy(octyl)silane, an organosilane compound, is a colorless transparent liquid with unique chemical properties that make it a versatile surface modifier. It is known for its ability to interact with various materials, enhancing their performance and functionality.

Uses

Used in Polymer Encapsulation:
Trimethoxy(octyl)silane is used as an additive for polymer encapsulation, where it improves the overall properties of the encapsulated material. It enhances the durability, stability, and resistance to environmental factors, making the encapsulated product more reliable and long-lasting.
Used in Controlled Drug Delivery:
Trimethoxy(octyl)silane is also utilized in the development of controlled drug delivery systems. Its unique interaction with biopolymers and macromolecules allows for the precise and sustained release of therapeutic agents, ensuring optimal therapeutic effects and minimizing side effects.
Used in Surface Modification:
Trimethoxy(octyl)silane is employed as a surface modifier to alter the properties of various materials, such as improving their hydrophobicity, adhesion, or reducing friction. This modification can be applied across different industries, including automotive, aerospace, and electronics, to enhance the performance and longevity of products.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 3069-40-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3069-40:
(6*3)+(5*0)+(4*6)+(3*9)+(2*4)+(1*0)=77
77 % 10 = 7
So 3069-40-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H26O3Si/c1-5-6-7-8-9-10-11-15(12-2,13-3)14-4/h5-11H2,1-4H3

3069-40-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (42698)  n-Octyltrimethoxysilane, 97+%   

  • 3069-40-7

  • 5g

  • 124.0CNY

  • Detail
  • Alfa Aesar

  • (42698)  n-Octyltrimethoxysilane, 97+%   

  • 3069-40-7

  • 25g

  • 619.0CNY

  • Detail
  • Alfa Aesar

  • (42698)  n-Octyltrimethoxysilane, 97+%   

  • 3069-40-7

  • 100g

  • 2192.0CNY

  • Detail
  • Aldrich

  • (376221)  Trimethoxy(octyl)silane  96%

  • 3069-40-7

  • 376221-25ML

  • 1,302.21CNY

  • Detail

3069-40-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Trimethoxyoctylsilane

1.2 Other means of identification

Product number -
Other names 1-TRIMETHOXYSILYL OCTANE

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:3069-40-7 SDS

3069-40-7Synthetic route

trimethoxysilane
2487-90-3

trimethoxysilane

trans-2-Octene
13389-42-9

trans-2-Octene

n-octyltrimethoxysilane
3069-40-7

n-octyltrimethoxysilane

Conditions
ConditionsYield
With 2C4H9O(1-)*Ni(2+)*(x)KCl In tetrahydrofuran at 20℃; for 4h; Inert atmosphere; Sealed tube;95%
trimethoxysilane
2487-90-3

trimethoxysilane

oct-1-ene
111-66-0

oct-1-ene

n-octyltrimethoxysilane
3069-40-7

n-octyltrimethoxysilane

Conditions
ConditionsYield
With 2C4H9O(1-)*Ni(2+)*(x)KCl In tetrahydrofuran at 20℃; for 12h; Glovebox; Inert atmosphere;89%
Stage #1: oct-1-ene With Wilkinson's catalyst for 0.0833333h;
Stage #2: trimethoxysilane at 90℃; for 5h;
75.9%
With cobalt pivalate; [1,3-bis(2,4,6-trimethylphenyl)imidazol]-2-ylidene In neat (no solvent) at 80℃; for 24h; Inert atmosphere;40%
methanol
67-56-1

methanol

octyltrichlorosilane
5283-66-9

octyltrichlorosilane

n-octyltrimethoxysilane
3069-40-7

n-octyltrimethoxysilane

Conditions
ConditionsYield
With pyridine
methanol
67-56-1

methanol

oct-1-ene
111-66-0

oct-1-ene

n-octyltrimethoxysilane
3069-40-7

n-octyltrimethoxysilane

Conditions
ConditionsYield
Stage #1: oct-1-ene With trichlorosilane; dihydrogen hexachloroplatinate In isopropyl alcohol; toluene at 50℃;
Stage #2: methanol With urea In isopropyl alcohol; toluene at 50℃;
n-octyltrimethoxysilane
3069-40-7

n-octyltrimethoxysilane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: HSiCl3, H2PtCl6*6H2O / benzene; tetrahydrofuran / 110 °C / 73550.8 Torr
2: pyridine
View Scheme
trimethoxysilane
2487-90-3

trimethoxysilane

oct-1-ene
111-66-0

oct-1-ene

A

n-octyltrimethoxysilane
3069-40-7

n-octyltrimethoxysilane

B

C11H26O3Si

C11H26O3Si

Conditions
ConditionsYield
With 4'-phenyl-2,2':6',2-terpyridine; cobalt(II) 2-ethylhexanoate at 60℃; for 3h; Sealed tube;
18-crown-6 ether
17455-13-9

18-crown-6 ether

n-octyltrimethoxysilane
3069-40-7

n-octyltrimethoxysilane

benzene-1,2-diol
120-80-9

benzene-1,2-diol

C12H24KO6(1+)*C20H25O4Si(1-)

C12H24KO6(1+)*C20H25O4Si(1-)

Conditions
ConditionsYield
With potassium methanolate In methanol at 20℃; for 3h; Schlenk technique; Inert atmosphere;85%
n-octyltrimethoxysilane
3069-40-7

n-octyltrimethoxysilane

C8H17O3Si(3-)*3Na(1+)

C8H17O3Si(3-)*3Na(1+)

Conditions
ConditionsYield
With sodium hydroxide In water for 4h; Reflux;
n-octyltrimethoxysilane
3069-40-7

n-octyltrimethoxysilane

diisopropyl (1-nonylcyclopropyl)phosphonate

diisopropyl (1-nonylcyclopropyl)phosphonate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: potassium methanolate / methanol / 3 h / 20 °C / Schlenk technique; Inert atmosphere
2: [4,4′-bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis{3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC}iridium(III) hexafluorophosphate / dimethyl sulfoxide / 24 h / 20 °C / Schlenk technique; Inert atmosphere; Irradiation
View Scheme

3069-40-7Downstream Products

3069-40-7Relevant articles and documents

THE PROCESS FOR THE PREPARATION AND USE OF HAIR TREATMENT COMPOSITIONS CONTAINING ORGANIC C1-C6 ALKOXY SILANES

-

, (2022/01/12)

The subject of the present application is a method for the preparation and use of an agent for the treatment of keratinous material, in particular human hair, comprising the following steps: (1) Mixing one or more organic C1-C6 alkoxy silanes with water,(2) optionally, partial, or complete removal from the reaction mixture of the C1-C6 alcohols liberated by the reaction in step (1),(3) if necessary, addition of one or more cosmetic ingredients,(4) Filling of the preparation into a packaging unit,(5) Storage of the preparation in the packaging unit for a period of at least about 5 days; and(6) Application of the preparation on the keratinous material.

METHOD FOR TREATING HAIR, COMPRISING THE APPLICATION OF AN ORGANIC SILICON COMPOUND, AN ALKALISING AGENT AND A FILM-FORMING POLYMER

-

, (2022/01/08)

It is an object of the present disclosure to provide a method for treating keratinous material, in particular human hair, comprising the following steps: Application of a water-containing agent (a) to the keratinous material, wherein the agent (a) has and contains a pH of at least 9.6:(a1) at least one organic silicon compound selected from the group including silanes having one, two or three silicon atoms, and(a2) at least one alkalizing agent selected from the group including ammonia, alkanolamines and basic amino acids, andApplication of an agent (b) to the keratinous material, wherein the agent (b) includes:(b1) at least one film-forming polymer.

Platinum(II) complexes bearing bulky Schiff base ligands anchored onto mesoporous SBA-15 supports as efficient catalysts for hydrosilylation

Huo, Yingpeng,Hu, Jiwen,Lin, Shudong,Ju, Xingming,Wei, Yanlong,Huang, Zhenzhu,Hu, Yangfei,Tu, Yuanyuan

, (2019/04/26)

Reported herein is an easy-to-prepare novel heterogeneous catalyst of platinum complexes bearing binary ligands of bidentate naphthalenolimine and cyclo-1,5-octadiene that are anchored onto mesoporous silica SBA-15. The presence of the binary ligands not only stabilized the platinum, but also enabled the platinum atoms to form nanoclusters with diameters of ca 1?nm, and led to high platinum loading (8.69?wt%). Moreover, the platinum catalyst exhibited high catalytic activity towards hydrosilylation of terminal alkenes and styrene with silanes under mild and solvent-free conditions, with excellent regioselectivity.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 3069-40-7