56318-71-9

Usage

Uses

Used in Surface Modification Industry:
N-Decyldimethylsilane is used as a surface modification agent to provide water repellency and enhance adhesion properties on various substrates. Its ability to alter the surface characteristics of materials makes it valuable in improving the performance and durability of products.
Used in Synthesis of Organosilicon Compounds:
As a building block, N-Decyldimethylsilane is utilized in the synthesis of other organosilicon compounds. Its role in creating complex and functionalized silane-based materials contributes to the advancement of material science and chemical research.
Used in Production of Silicone-based Materials:
N-Decyldimethylsilane plays a crucial role in the production of silicone-based materials, which are known for their thermal stability, flexibility, and resistance to environmental degradation. Its contribution to the formulation of these materials is significant in various applications, including sealants, adhesives, and coatings.
Used in Drug Delivery Systems:
N-Decyldimethylsilane has potential applications in the field of drug delivery systems. Its unique properties may be harnessed to improve the efficiency and targeting of drug delivery, offering new possibilities for pharmaceutical development.
Used as a Reactive Intermediate in Organic Synthesis:
Due to its reactivity and compatibility with various organic compounds, N-Decyldimethylsilane serves as a reactive intermediate in organic synthesis. This allows for the creation of new chemical entities and the modification of existing ones, expanding the scope of organic chemistry.

InChI:InChI=1/C12H27Si/c1-4-5-6-7-8-9-10-11-12-13(2)3/h4-12H2,1-3H3

Upstream product

• 1066-35-9 dimethylmonochlorosilane 
• 112-29-8 1-bromo dodecane 
• 872-05-9 1-Decene 
• 18033-75-5 dimethylmethoxysilane 
• 17049-50-2 n-decyl magnesium bromide 
• 38051-57-9 N-decyldimethylchlorosilane 

Downstream Products

• 112-30-1 1-Decanol 
• 38051-57-9 N-decyldimethylchlorosilane 
• 56318-63-9 Decyl-dimethyl-pentafluorophenyloxy-silane 

Relevant academic research and scientific papers

Alkoxy Hydrosilanes As Surrogates of Gaseous Silanes for Hydrosilylation of Alkenes

Me2SiH2, MeSiH3, and SiH4 are gaseous and flammable silanes that are inconvenient to use in chemical reactions. Catalytic amounts of a nickel pincer complex and NaOtBu are reported to allow the synthesis of alkyl hydrosilanes from alkenes and alkoxy hydrosilanes, leading to the replacement of Me2SiH2, MeSiH3, and SiH4 by Me2(MeO)SiH, Me(EtO)2SiH, and (MeO)3SiH in hydrosilylation reactions of alkenes. The scope and mechanism of the reactions are also described.

Trialkylsilylethynyl-substituted triphenylenes and hexabenzocoronenes: Highly soluble liquid crystalline materials and their hole transport abilities

Four triphenylene (TP) and four hexa-peri-hexabenzocoronene (HBC) derivatives with trialkylsilylethynyl groups were prepared and characterized by differential scanning calorimetry, polarizing optical microscopy, and X-ray diffraction measurements. All compounds were highly soluble in less-polar organic solvents and exhibited a columnar phase, Colh or Colr for the TPs, and Colh for the HBCs. The hole transport ability in the HBCs' columnar phase, 0.4-1.5×10-3 cm2 V-1 s-1 at 40-180°C, and its temperature dependence were determined by the time-of-flight method using a solution technique.

Predictability of thermal and electrical properties of end-capped oligothiophenes by a simple bulkiness parameter

The branching topology of end groups attached to several series of oligothiophenes has a systematic effect on thermal and electrical properties of the oligomers. The series were synthesized in a modular approach and show a distinct drop of the melting point Tm on increasing bulkiness of the substituents. The same trend can be found for the dissociation temperatures Tdis of aggregates in solution. Similarly, monolayer OFET mobilities μFET are significantly decreasing with increasing bulkiness of the substituents. A simple geometric model is presented quantitatively correlating the transition temperatures and mobilities with the substituents' structure based on a bulkiness parameter P, which allows predicting Tm, T dis, and μFET of corresponding not yet synthesized oligomers with branched substituents. This model might be generally applicable for end-capped rod-like conjugated oligomers.