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2,2-Bis(3-amino-4-hydroxyphenyl)hexafluoropropane (also known as BAPHF, BAPHFP, and BAPHFPP) is an organofluorine compound with a variety of applications in scientific research and laboratory experiments. It is a colorless, water-soluble liquid that is highly stable and non-toxic. BAPHF has been used in a range of bioc...
2,2-Bis(3-amino-4-hydroxyphenyl)hexafluoropropane (also known as BAPHF, BAPHFP, and BAPHFPP) is an organofluorine compound with a variety of applications in scientific research and laboratory experiments. It is a colorless, water-soluble liquid that is highly stable and non-toxic. BAPHF has been used in a range of biochemical and physiological experiments, as well as in the synthesis of various compounds.
2,2-Bis(3-amino-4-hydroxyphenyl)hexafluoropropane (BAHPFP) plays a crucial role in the synthesis and development of various advanced materials. Fu Ju-sun (2007) reported its use in creating fluorine-containing polybenzoxazole monomers, emphasizing its potential in the development of high-performance polymers (Fu Ju-sun, 2007). Similarly, a study by W. Xiao-xia (2014) detailed the synthesis of BAHPFP from 2,2-bis(4-hydroxyphenyl)hexafluoropropane, highlighting its applicability in large-scale production and industrial applications (W. Xiao-xia, 2014).
BAHPFP's applications extend significantly into polymer science. S. K. Kim et al. (2004) synthesized a series of polyimides from BAHPFP, which exhibited better solubility in organic solvents, making them useful in microelectronics due to their low dielectric constant and high thermal stability (S. K. Kim et al., 2004). Blanca Díez et al. (2018) utilized BAHPFP in the preparation of aromatic poly(ortho-hydroxyamide)s for gas separation membranes, demonstrating its versatility in creating materials with superior gas separation properties (Blanca Díez et al., 2018) .
BAHPFP has been used in developing sensors, as illustrated by Pinaki S. Bhadury et al. (2005) in their study of coating materials for nerve agent sensors. They synthesized a monomer related to BAHPFP for use in toxic chemical warfare agent detection (Pinaki S. Bhadury et al., 2005).
Yu Xin-hai (2009) explored the use of BAHPFP in creating novel epoxy adhesives, demonstrating its effectiveness in enhancing the properties of these adhesives (Yu Xin-hai, 2009).
G. Milczarek and A. Ciszewski (2004) highlighted BAHPFP's use in modifying glassy carbon electrodes, making it a valuable component in developing selective and sensitive voltammetric sensors for biochemical analysis (G. Milczarek & A. Ciszewski, 2004) .
Research by E. Hamciuc et al. (2007) underscored the potential of BAHPFP in producing aromatic polyimides with pendant hydroxylic groups, which are applicable in advanced optical and electronic devices due to their high thermal stability and solubility in organic solvents (E. Hamciuc et al., 2007).
Product Name : | 4,4'-(Perfluoropropane-2,2-diyl)bis(2-aminophenol) | ||
CAS No. : | 83558-87-6 | Molecular Weight : | 366.26 |
MDL No. : | MFCD00039147 | Purity/ Specification : | |
Molecular Formula : | C15H12F6N2O2 | Storage : | Keep in dark place,Inert atmosphere,Room temperature |
Boiling Point : | - |
GHS Pictogram : | |||
Signal Word : | Warning | Precautionary Statements : | P261-P305+P351+P338 |
UN# : | N/A | Class : | N/A |
Hazard Statements : | H315-H319-H335 | Packing Group : | N/A |