1,2,3-Trimethyl-1-(2-propen-1-yl)-1H-benz[e]indolium bromide
1,2,3-Trimethyl-1-(2-propen-1-yl)-1H-benz[e]indolium bromide
CAS: 891503-79-0
Molecular Formula: C18H20BrN
1,2,3-Trimethyl-1-(2-propen-1-yl)-1H-benz[e]indolium bromide - Names and Identifiers
| Name | 1,2,3-Trimethyl-1-(2-propen-1-yl)-1H-benz[e]indolium bromide |
| Synonyms | 1H-Benz[e]indoliuM 1,2,3-Trimethyl-1-(2-propen-1-yl)-1H-benz[e]indolium bromide 1,2,3-Trimethyl-1-(2-propen-1-yl)-1H-benzo[e]indolium bromide |
| CAS | 891503-79-0 |
| InChI | InChI=1/C18H20N.BrH/c1-5-12-18(3)13(2)19(4)16-11-10-14-8-6-7-9-15(14)17(16)18;/h5-11H,1,12H2,2-4H3;1H/q+1;/p-1 |
1,2,3-Trimethyl-1-(2-propen-1-yl)-1H-benz[e]indolium bromide - Physico-chemical Properties
| Molecular Formula | C18H20BrN |
| Molar Mass | 330.26 |
1,2,3-Trimethyl-1-(2-propen-1-yl)-1H-benz[e]indolium bromide - Introduction
The 1,2,3-Trimethyl-1-(2-propen-1-yl)-1H-benz[e]indolium bromide is an organic compound, which is usually represented by the abbreviation of TMPIB. The following is a description of its nature, use, formulation and safety information:
Nature:
-Appearance: Usually a colorless crystalline solid.
-Solubility: Soluble in some organic solvents, such as methanol, ethanol and dichloromethane.
-Melting point: about 150°C-160°C.
Use:
- TMPIB is a compound widely used in fluorescent probes, which can be used in the fields of biological fluorescence imaging, cell imaging and protein detection.
-It is usually used as a labeling reagent that binds to nucleic acids or proteins, and plays the role of labeling and detection in research.
Preparation Method:
-Generally, the preparation of TMPIB is completed by the reaction of 1,2, 3-trimethylindole and propenyl bromide (2-bromopropane).
-This reaction is usually carried out in an organic solvent (such as dichloromethane) and carried out under basic conditions. TMPIB is produced during the reaction.
Safety Information:
- TMPIB has limited toxicity data, but as a laboratory compound, it should be handled in accordance with general safe practices.
-It may cause irritation to the skin, eyes and respiratory tract, so avoid contact with skin, eyes and inhalation of its particles during operation.
-When performing experimental use, operate in well-ventilated conditions and wear appropriate personal protective equipment, such as gloves, goggles and laboratory coats. Before use, it is best to consult the safety data and substance data sheets and follow the relevant safety guidelines.
Nature:
-Appearance: Usually a colorless crystalline solid.
-Solubility: Soluble in some organic solvents, such as methanol, ethanol and dichloromethane.
-Melting point: about 150°C-160°C.
Use:
- TMPIB is a compound widely used in fluorescent probes, which can be used in the fields of biological fluorescence imaging, cell imaging and protein detection.
-It is usually used as a labeling reagent that binds to nucleic acids or proteins, and plays the role of labeling and detection in research.
Preparation Method:
-Generally, the preparation of TMPIB is completed by the reaction of 1,2, 3-trimethylindole and propenyl bromide (2-bromopropane).
-This reaction is usually carried out in an organic solvent (such as dichloromethane) and carried out under basic conditions. TMPIB is produced during the reaction.
Safety Information:
- TMPIB has limited toxicity data, but as a laboratory compound, it should be handled in accordance with general safe practices.
-It may cause irritation to the skin, eyes and respiratory tract, so avoid contact with skin, eyes and inhalation of its particles during operation.
-When performing experimental use, operate in well-ventilated conditions and wear appropriate personal protective equipment, such as gloves, goggles and laboratory coats. Before use, it is best to consult the safety data and substance data sheets and follow the relevant safety guidelines.
Last Update：2024-04-09 20:49:11
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