Catalog Number |
ACM245679189 |
CAS |
245679-18-9 |
Structure |
![{[CurrentData.Name]}](https://resource.alfa-chemistry.com/structure/245679-18-9.gif) |
Description |
1,3-Bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazolium tetrafluoroborate (1,3-BTDHI-TFB) is an organic ionic liquid (IL) that has recently been studied for its potential applications in scientific research. The unique properties of 1,3-BTDHI-TFB make it an attractive choice for use in various scientific experiments. This paper will discuss the synthesis method, scientific research applications, mechanism of action, biochemical and physiological effects, advantages and limitations for lab experiments, and future directions of 1,3-BTDHI-TFB. |
Synonyms |
1,3-Dimesityl-4,5-Dihydro-1H-Imidazol-3-Ium Tetrafluoroborate |
IUPAC Name |
1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-1-ium;tetrafluoroborate |
Molecular Weight |
394.3 g/mol |
Molecular Formula |
C21H27BF4N2 |
Canonical SMILES |
[B-](F)(F)(F)F.CC1=CC(=C(C(=C1)C)N2CC[N+](=C2)C3=C(C=C(C=C3C)C)C)C |
InChI |
InChI=1S/C21H27N2.BF4/c1-14-9-16(3)20(17(4)10-14)22-7-8-23(13-22)21-18(5)11-15(2)12-19(21)6;2-1(3,4)5/h9-13H,7-8H2,1-6H3;/q+1;-1 |
InChI Key |
VNRDQIOMNLIVQJ-UHFFFAOYSA-N |
Melting Point |
290-296 °C |
Purity |
98% |
Appearance |
Off-white powder |
Application |
1,3-BTDHI-TFB has been studied for its potential applications in scientific research. It has been used as a solvent for various reactions, including the synthesis of organic compounds, the extraction of proteins and nucleic acids, and the dissolution of inorganic salts. Additionally, 1,3-BTDHI-TFB has been used as an electrolyte in electrochemical cells, as a medium for enzymatic reactions, and as a catalyst for the synthesis of polymers. |
Complexity |
398 |
Covalently-Bonded Unit Count |
2 |
Exact Mass |
394.22g/mol |
GHS Pictogram |
Corrosive; Irritant |
Heavy Atom Count |
28 |
Isomeric SMILES |
[B-](F)(F)(F)F.CC1=CC(=C(C(=C1)C)N2CC[N+](=C2)C3=C(C=C(C=C3C)C)C)C |
Monoisotopic Mass |
394.22g/mol |
Properties |
1,3-BTDHI-TFB has been studied for its potential biochemical and physiological effects. It has been found to be non-toxic and non-mutagenic, making it safe for use in laboratory experiments. Additionally, 1,3-BTDHI-TFB has been found to have antioxidant and anti-inflammatory properties, as well as the ability to inhibit the growth of certain bacteria and fungi. |
Rotatable Bond Count |
2 |
Topological Polar Surface Area |
6.2A^2 |