324574-95-0

Basic information

• Product Name: EMMPNTF2
• Synonyms: EMMPNTF2
• CAS NO: 324574-95-0
• Molecular Formula: C11H20F6N2O5S2
• Molecular Weight: 438.4
• EINECS: -0
• Mol File: 324574-95-0.mol

Chemical Properties

• Melting Point: 28.7 °C
• Appearance: /
• Density: 1.4405 g/cm3(Temp: 25 °C)
• CAS DataBase Reference: EMMPNTF2(CAS DataBase Reference)
• NIST Chemistry Reference: EMMPNTF2(324574-95-0)
• EPA Substance Registry System: EMMPNTF2(324574-95-0)

Safety Data

• Hazardous Substances Data: 324574-95-0(Hazardous Substances Data)

Usage

Uses

Used in Mechanical Systems:
EMMPNTF2 is used as a lubricant for its ability to reduce friction and wear in various mechanical systems, ensuring smooth operation and extending the life of equipment.
Used in Electronics and Semiconductor Industries:
In the electronics and semiconductor industries, EMMPNTF2 serves as a solvent, taking advantage of its high boiling point and low surface tension to effectively dissolve and process materials in manufacturing processes.
Used in Heat Resistance Applications:
Due to its high boiling point, EMMPNTF2 is utilized in applications that require heat resistance, such as in high-temperature manufacturing processes or as a component in heat-resistant materials.
Used in Wetting Applications:
The low surface tension of EMMPNTF2 makes it suitable for use in wetting applications, where it can help to spread and coat surfaces evenly, improving the performance of coatings and other surface treatments.
Used in Industrial and Manufacturing Processes:
EMMPNTF2's non-flammable and non-reactive nature makes it a safe and versatile chemical for a wide range of industrial and manufacturing processes, reducing the risk of accidents and ensuring consistent performance.

Upstream product

• 82113-65-3 bis(trifluoromethanesulfonyl)amide 
• 5414-19-7 1,1'-oxybis(2-bromo-ethane) 
• 110-68-9 N-n-butyl-N-methylamine 
• 90076-65-6 bis(trifluoromethane)sulfonimide lithium 
• 109-02-4 4-methyl-morpholine 

Relevant articles and documents

Apparent molar volumes and expansivities of ionic liquids based on N -Alkyl- N -methylmorpholinium cations in acetonitrile

Densities of some acetonitrile solutions of ionic liquids based on N-alkyl-N-methyl-morpholinium cations, N-ethyl-N-methylmorpholinium bis(trifluoromethanesulfonyl)imide, N-butyl-N-methylmorpholinium bis(trifluoromethanesulfonyl)imide, N-methyl-N-octylmorpholinium bis(trifluoromethanesulfonyl)imide and N-decyl-N-methylmorpholinium bis(trifluoromethanesulfonyl)imide were measured at T = (298.15-318.15) K and at atmospheric pressure. From density data the apparent molar volumes and partial molar volumes of the ILs at infinite dilution as well as the limiting apparent molar expansibilities and the Hepler's constant values have been evaluated. The results have been discussed in terms of the effect that alkyl chain length of the ILs and experimental temperature have on the ionic liquid-acetonitrile interactions occurring in the studied solutions.

Ionic liquids based on N-alkyl-N-methylmorpholinium salts as potential electrolytes

Ionic liquids based on N-alkyl-N-methylmorpholinium salts have been synthesized and the physical and electrochemical characteristics of this family of ionic liquids have been investigated for use as electrolytes.

Rational selection of the cation of an ionic liquid to control the reaction outcome of a substitution reaction

A range of ionic liquids was examined as solvents for a substitution reaction. They were chosen through rationally varying the ionic liquid cation in order to enhance the rate constant. Access to charge and electron-withdrawing substituents benefitted rat

Facile, high-yielding preparation of pyrrolidinium, piperidinium, morpholinium and 2,3-dihydro-1H-isoindolinium salts and ionic liquids from secondary amines

High yield and purity heterocyclic ionic liquids can be obtained via the microwave irradiation of equimolar amounts of a secondary amine and of an α,ω-dibromoalkane (i.e., 1,4-dibromobutane, 1,5-dibromopentane, bis(2-bromoethyl)ether, or α,α′-dibromo-o-xylene) in water, in the presence of potassium carbonate, followed by anion exchange with lithium bis(trifluoromethanesulfonyl)imide, affording pyrrolidinum, piperidinium and morpholinium ionic liquids, respectively. Using this methodology, a large number of homologous ionic liquids can be prepared from a small number of readily available and relatively cheap starting materials, including a new class of ionic liquids based on the 2,3-dihydro-1H-isoindolinium ring system. Analysis (using SWOT and the GSK greenness assessments) of this synthetic method and comparison with current literature preparations reveals that this new method delivers significant benefits across a range of relevant parameters.

Cyclic quaternary ammonium ionic liquids with perfluoroalkyltrifluoroborates: Synthesis, characterization, and properties

New cyclic quaternary ammonium salts, composed of N-alkyl(alkyl ether)-N-methylpyrrolidinium, -oxazolidinium, -piperidinium, or -morpholinium cations (alkyl = nC4H9, alkyl ether = CH 3,OCH2, CH3,OCH2CH2) and a perfluoroalkyltrifluoroborate anion ([RFBF3] -, RF = CF3, C2F5, nC3,F7, nC4F9), were synthesized and characterized. Most of these salts are liquids at room temperature. The key properties of these salts - phase transitions, thermal stability, density, viscosity, conductivity, and electrochemical windowswere measured and compared to those of their corresponding [BF4] and [(CF3SO 2)2N]- salts. The structural effect on all the above properties was intensively studied in terms of the identity of the cation and anion, variation of the side chain in the cation (i.e., alkyl versus alkyl ether), and change in the length of the pertluoroalkyl group (RF) in the [RFBF3,]- ion. The reduction of Li + ions and reoxidation of Li metal took place in pure N-butyl-N-methyl pyrrolidinium pentafluoroethyltrifluoroborate as the supporting electrolyte. Such comprehensive studies enhance the knowledge necessary to design and optimize ionic liquids for many applications, including electrolytes. Some of these new salts show desirable properties, including low melting points, high thermal stabilities, low viscosities, high conductivities, and wide electrochemical windows, and may thus be potential candidates for use as electrolytes in high-energy storage devices. In addition, many salts are ionic plastic crystals.