Production Method 1

78560-44-8

83048-65-1

Reaction Conditions

1.1 Solvents: Methanol

Reference

Preparation of (fluoroalkyl)alkoxysilanes from (fluoroalkyl)chlorosilanes and alcohols

, Japan, , ,

1H,1H,2H,2H-Perfluorodecyltrimethoxysilane Raw materials

• 1h,1h,2h,2h-Perfluorodecyltrichlorosilane

1H,1H,2H,2H-Perfluorodecyltrimethoxysilane Preparation Products

• 1H,1H,2H,2H-Perfluorodecyltrimethoxysilane (83048-65-1)

• 1. An aptasensor for detection of potassium ions based on RecJf exonuclease mediated signal amplification
  Bidou Wang,Xifeng Chen Analyst, 2014,139, 5695-5699
• 2. Aggregated-fluorescent detection of PFAS with a simple chip
  Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170
• 3. An alumina stabilized graphene oxide wrapped SnO2 hollow sphere LIB anode with improved lithium storage?
  Xiang Liu,Qian Sun,A. B. Djuri?i?,Maohai Xie,Baohu Dai,Jinyao Tang,Charles Surya,Changzhong Liao,Kaimin Shih RSC Adv., 2015,5, 100783-100789
• 4. An anti-ultrasonic-stripping effect in confined micro/nanoscale cavities and its applications for efficient multiscale metallic patterning?
  Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
• 5. An aqueous ammonia sensor based on an inkjet-printed polyaniline nanoparticle-modified electrode
  Karl Crowley,Eimer O'Malley,Aoife Morrin,Malcolm R. Smyth,Anthony J. Killard Analyst, 2008,133, 391-399

• Solvents and Organic Chemicals Organic Compounds Aldehyde/Ketone
• Material Chemicals High Polymer Materials

Introduction to 1H,1H,2H,2H-Perfluorodecyltrimethoxysilane (CAS No. 83048-65-1)

1H,1H,2H,2H-Perfluorodecyltrimethoxysilane, a compound with the chemical formula C12F25Si(OCH3)3, is a specialized organosilicon compound that has garnered significant attention in the field of materials science and chemical engineering. This compound is characterized by its unique structure, which combines a long perfluorodecyl group with three methoxy silane groups. The perfluorodecyl group imparts exceptional hydrophobicity and thermal stability, while the methoxy groups provide reactive sites for further functionalization. These properties make it an invaluable material in various applications, including surface modification, polymerization, and the development of advanced coatings.

The CAS No. 83048-65-1 of this compound is a critical identifier in chemical databases and literature, ensuring precise classification and retrieval of information related to its synthesis, applications, and safety considerations. This number is universally recognized by chemists and researchers as a unique identifier for chemical substances, facilitating accurate communication and collaboration across international scientific communities.

One of the most compelling aspects of 1H,1H,2H,2H-Perfluorodecyltrimethoxysilane is its ability to enhance the performance of materials through surface modification. The perfluorodecyl group is known for its low surface energy and excellent chemical inertness, making it an ideal candidate for creating superhydrophobic surfaces. These surfaces have applications in self-cleaning technologies, anti-fogging coatings, and corrosion-resistant materials. Recent research has demonstrated the effectiveness of this compound in creating durable hydrophobic coatings on various substrates, including metals and plastics.

Moreover, the trimethoxysilane groups in the molecule allow for further chemical modifications through hydrolysis and condensation reactions. This reactivity enables the integration of additional functional groups into the material's surface or bulk structure. For instance, researchers have explored the use of this compound in producing silane-functionalized polymers that exhibit enhanced thermal stability and mechanical strength. These polymers are particularly useful in high-performance applications such as aerospace components and electronic devices.

In recent years, there has been growing interest in the application of fluorinated silicones in biomedical technologies. The unique properties of 1H,1H,2H,2H-Perfluorodecyltrimethoxysilane make it a promising candidate for developing biocompatible coatings for medical implants. Studies have shown that fluorinated silicones can significantly reduce biofilm formation on implant surfaces by creating a barrier that inhibits microbial adhesion. This property is crucial for preventing infections associated with long-term implant use.

The compound's thermal stability is another key factor contributing to its versatility. With a high decomposition temperature range (typically above 200°C), it can withstand extreme conditions without degradation. This makes it suitable for use in high-temperature environments such as automotive components and industrial machinery. Additionally, its resistance to UV radiation enhances its applicability in outdoor coatings that require long-term durability.

Environmental considerations are also an important aspect when evaluating the use of 1H,1H,2H,2H-Perfluorodecyltrimethoxysilane. While fluorinated compounds are known for their persistence in the environment due to their chemical stability, research efforts are ongoing to develop more sustainable alternatives or methods for their degradation. Current studies are exploring biodegradable fluorinated silicones that retain the desirable properties of traditional fluorinated compounds while reducing environmental impact.

The synthesis of 1H,1H,2H,2H-Perfluorodecyltrimethoxysilane involves multi-step organic reactions that require precise control over reaction conditions to ensure high yield and purity. The process typically begins with the preparation of perfluorodecanol followed by its conversion into perfluorodecylchlorosilane through chlorination reactions. Subsequently, methanolysis is performed to introduce the methoxy groups onto the silicon atom. Advanced catalytic systems have been developed to optimize these steps while minimizing side reactions.

In conclusion,1H,H?,H?-Hperfluorodecytrimethoxysilane (CAS No. 83048-65-1) represents a significant advancement in functional material development due to its unique combination of hydrophobicity,thermal stability,and reactivity. Its applications span across various industries including aerospace,biomedical technologies,and environmental engineering demonstrating its broad utility as well as potential future growth areas within material science research

• 246234-80-0((3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluorodecyl)triisopropoxysilane)
• 109134-39-6(Silane, (3,3,4,4,5,5,5-heptafluoropentyl)trimethoxy-)
• 51851-37-7(1H,1H,2H,2H-Perfluorooctyltriethoxysilane)
• 101947-16-4(1H,1H,2H,2H-Perfluorodecyltriethoxysilane)
• 521084-64-0(Silane,(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)tripropoxy-)
• 146090-84-8(1H,1H,2H,2H-Perfluorododecyltriethoxysilane)
• 102390-98-7(Triethoxy(1H,1H,2H,2H-nonafluorohexyl)silane)
• 221453-23-2(Silane,(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl)trimethoxy-)
• 85857-16-5(1H,1H,2H,2H-Perfluorooctyltrimethoxysilane)
• 85877-79-8(Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane)