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Hexafluoropropene Trimer, also known as HFP Trimer, is an organofluorine compound that has been gaining attention in the scientific community due to its unique properties. It is composed of three hexafluoropropene molecules and has a molecular formula of C6F12. HFP Trimer is a colorless gas that has a boiling point of ...
Hexafluoropropene Trimer, also known as HFP Trimer, is an organofluorine compound that has been gaining attention in the scientific community due to its unique properties. It is composed of three hexafluoropropene molecules and has a molecular formula of C6F12. HFP Trimer is a colorless gas that has a boiling point of -30°C, making it useful for a wide range of applications. It is also non-toxic, non-flammable, and non-corrosive, making it a safe and efficient compound to work with. HFP Trimer has been used in many scientific research applications, such as the synthesis of novel materials, and its mechanism of action and biochemical and physiological effects have been studied extensively.
Hexafluoropropene trimers (HFPT) react with primary amines to form corresponding enamines and enimines, indicating potential applications in chemical synthesis. The interaction with ammonia leads to the formation of adducts and enables the study of intramolecular cyclization, contributing to the understanding of fluorine chemistry and its applications (D. P. Del'tsova, L. Gervits, & A. Kadyrov, 1996).
HFPT is involved in the synthesis of functional derivatives, reacting with nucleophilic agents like alcohols and phenols. This process leads to the formation of products by substituting fluorine atoms in the HFPT molecule, which is crucial in understanding the reactivity and potential applications of HFPT in material science and organic chemistry (K. N. Makarov et al.).
The photoinduced fluorination of HFPT leads to the synthesis of branched perfluoroalkanes. This process involves a mechanism of elimination–readdition of CF3 groups, which is significant for the development of new materials and the study of reaction mechanisms in fluorine chemistry (C. Tonelli & V. Tortelli, 1990).
The oligomerization of hexafluoropropene can yield a mixture of dimers and trimers. These oligomers have potential applications in creating fluorine-carbon surfactants, which are important in various industrial and pharmaceutical applications (Zhou Hai-an, 2005).
The preparation and isomerization of HFPT oligomers in the presence of fluoride ions have been studied, which is significant for understanding the reaction mechanisms and potential applications in synthesizing new fluorinated compounds (N. Ishikawa & A. Sekiya, 1972).
The direct gas-phase fluorination of HFPT has been explored, leading to the formation of stable perfluororadicals. This study is important for applications in fluoropolymer manufacturing and the development of new materials (M. Novikova, V. Zakharov, & A. Denisov, 1992).
The study of non-bond FF nuclear spin couplings in HFPT provides insights into the molecular structure and behavior of these compounds, which is crucial for applications in NMR spectroscopy and material science (F. Cavagna & C. Schumann, 1975).
Product Name : | Hexafluoropropene trimer | ||
CAS No. : | 6792-31-0 | Molecular Weight : | 450.07 |
MDL No. : | MFCD00043821 | Purity/ Specification : | |
Molecular Formula : | C9F18 | Storage : | Sealed in dry,2-8°C |
Boiling Point : | - |
GHS Pictogram : | |||
Signal Word : | Danger | Precautionary Statements : | P261-P280-P305+P351+P338 |
UN# : | 1993 | Class : | 3 |
Hazard Statements : | H225-H302-H312-H315-H319-H332-H335 | Packing Group : | Ⅲ |