SKL1510 - Names and Identifiers
Name | 1-Methyl-3-octyl-1H-imidazolium salt with 2,2,2-trifluoro-N-(trifluoroacetyl)acetamide
|
Synonyms | SKL1510 OMIMNTF2 1-Methyl-3-octylimidazol-1-ium 2,2,2-trifluoro-N-(2,2,2-trifluoroacetyl)ethanimidate 1-Octyl-3-methylimidazolium bis(2,2,2-trifluoroacetyl)imide 3-Methyl-1-octyl-1H-imidazol-3-ium bis(trifluoroacetyl)azanide 1-Methyl-3-octyl-3-imidazolium Bis(2,2,2-trifluoroacetyl)amide 1-Methyl-3-octyl-1H-imidazolium salt with 2,2,2-trifluoro-N-(trifluoroacetyl)acetamide
|
CAS | 862731-66-6
|
EINECS | 200-145-6 |
SKL1510 - Physico-chemical Properties
Molecular Formula | C13H24F6N3O4S2
|
Molar Mass | 464.32 |
Storage Condition | Inert atmosphere,Room Temperature |
SKL1510 - Reference
Reference Show more | 1. [IF=4.411] Xiaodong Huang et al."Magnetic Solid-Phase Extraction of Dichlorodiphenyltrichloroethane and Its Metabolites from Environmental Water Samples Using Ionic Liquid Modified Magnetic Multiwalled Carbon Nanotube/Zeolitic Imidazolate Framework-8 as Sorbent."Mol 2. [IF=3.361] Xiaodong Huang et al."Magnetic solid-phase extraction of pyrethroid insecticides from tea infusions using ionic liquid-modified magnetic zeolitic imidazolate framework-8 as an adsorbent."Rsc Adv. 2019 Nov;9(67):39272-39281 |
SKL1510 - Introduction
salt with 2,2,2-trifluoro-N-(trifluoroacetyl)acetamide is an imidazolium ionic liquid compound with the chemical formula [C8C1IM][TF2N]. It has the following properties and uses:
Nature:
-Appearance: colorless liquid
-Melting Point: About -35 ℃
-Boiling point: About 200-210 ℃
-Density: approx. 1.24g/cm³
-Solubility: Soluble in polar solvents such as water, alcohols and ethers, insoluble in non-polar solvents such as alkanes
-Stability: stable at room temperature, but will decompose at high temperature
-Non-flammable
Use:
-As a solvent: Due to its good solubility and ionic liquid properties, it can be used in catalytic reactions and catalyst synthesis, as well as research and development of electrochemical, chemical sensors and biochemical sensors and other fields.
-As a liquid-liquid extractant: It can be used to separate and purify compounds, such as sulfates, chlorides and organic compounds, with good selectivity and efficiency.
Method:
The preparation of salt with 2,2, 2-trifluororo-N-(trifluoroacetyl)acetamide is usually carried out by the following steps:
1. Reaction of 2,2, 2-trifluoroacetoyl chloride (TF2CCl) with 1-octyl imidazole ([C8H1IM]) yields 3-methyl -1-octyl -1H-imidazole.
2. The generated 3-methyl -1-octyl-1H-imidazole is reacted with amino chloro trifluoroacetic acid amide salt (NH2Cl[TF2N]) at 25-30 ℃, the final product was formed as salt with 2,2,2-trifluoro-N-(trifluoroacetyl)acetamide.
Safety Information:
-(trifluoroacetyl)acetamide has low toxicity, but it still needs to be used carefully and avoid contact with skin and eyes.
-Wear appropriate protective measures such as gloves, goggles, etc. during handling and preparation.
-Keep away from open flames and high temperature items to prevent fire and explosion.
Last Update:2024-04-10 22:29:15