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93804-29-6 Usage


DIMETHYLMETHOXY-N-OCTYLSILANE, also known as Methoxy(dimethyl)octylsilane, is an organosilane compound characterized by its dimethylmethoxy group and an octylsilane chain. It is known for its ability to form stable covalent bonds with various substrates, particularly in the context of surface modification and functionalization.


Used in Surface Modification Industry:
DIMETHYLMETHOXY-N-OCTYLSILANE is used as a functionalizing agent for partially oxidized porous silicon. It serves to enhance the surface properties of porous silicon by introducing silane groups, which can improve the material's stability, biocompatibility, and other functional characteristics. This application is particularly relevant in the development of advanced materials for various industries, such as electronics, pharmaceuticals, and biomedical engineering, where the modification of surfaces can lead to improved performance and novel functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 93804-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,8,0 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93804-29:
146 % 10 = 6
So 93804-29-6 is a valid CAS Registry Number.

93804-29-6 Well-known Company Product Price

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  • Aldrich

  • (375977)  Methoxy(dimethyl)octylsilane  98%

  • 93804-29-6

  • 375977-5G

  • 724.23CNY

  • Detail



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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017


1.1 GHS Product identifier

Product name methoxy-dimethyl-octylsilane

1.2 Other means of identification

Product number -
Other names Dimethyloctylmethoxysilane

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:93804-29-6 SDS

93804-29-6Relevant articles and documents

Utilization of a Trimethylsilyl Group as a Synthetic Equivalent of a Hydroxyl Group via Chemoselective C(sp3)-H Borylation at the Methyl Group on Silicon

Torigoe, Takeru,Ohmura, Toshimichi,Suginome, Michinori

, p. 2943 - 2956 (2017/03/23)

A conversion of trimethylsilylalkanes into the corresponding alcohols is established based on an iridium-catalyzed, chemoselective C(sp3)-H borylation of the methyl group on silicon. The (borylmethyl)silyl group formed by C(sp3)-H borylation is treated with H2O2/NaOH, and the resulting (hydroxymethyl)silyl group is converted into a hydroxyl group by Brook rearrangement, followed by oxidation of the resulting methoxysilyl group under Tamao conditions. An alternative route proceeding through the formylsilyl group formed from a (hydroxymethyl)silyl group by Swern oxidation is also established. The method is applicable to substituted trimethylsilylcycloalkanes and 1,1-dimethyl-1-silacyclopentane for conversion into the corresponding stereodefined cycloalkyl alcohols and 1,4-butanediol.

Oxidation of 2-Pyridyldimethylsilyl Group to Hydroxyl Group by H2O2/KF. Implication of Fluoride Ion Accelerated 2-Pyridyl-Silyl Bond Cleavage

Itami, Kenichiro,Mitsudo, Koichi,Yoshida, Jun-Ichi

, p. 8709 - 8714 (2007/10/03)


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