10052-47-8 Usage
Uses
Used in Chemical Industry:
Triethylmethylammonium chloride is used as a phase transfer catalyst for facilitating reactions between organic and inorganic compounds, enhancing the efficiency and selectivity of various chemical processes.
Used in Catalyst Synthesis:
Triethylmethylammonium chloride is used as an organic template in the synthesis of zeolites, which are porous materials with a high surface area and tunable pore structure. These zeolites can act as catalysts in various industrial applications, such as petroleum refining,精细化工, and environmental remediation, due to their unique properties and ability to selectively adsorb and activate reactant molecules.
Used in Environmental Remediation:
Triethylmethylammonium chloride can be employed in the synthesis of zeolites for environmental applications, such as the removal of heavy metals and organic pollutants from water and soil. The zeolites' high adsorption capacity and ion exchange properties make them suitable for treating contaminated environments and purifying resources.
Used in Fine Chemicals:
Triethylmethylammonium chloride can be utilized in the synthesis of zeolites for use in fine chemicals production, where precise control over reaction conditions and selectivity is crucial. The zeolites can act as catalysts or catalyst supports, enabling the production of high-quality specialty chemicals and pharmaceuticals with improved yields and purity.
Check Digit Verification of cas no
The CAS Registry Mumber 10052-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,5 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10052-47:
(7*1)+(6*0)+(5*0)+(4*5)+(3*2)+(2*4)+(1*7)=48
48 % 10 = 8
So 10052-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H18N/c1-5-8(4,6-2)7-3/h5-7H2,1-4H3
10052-47-8Relevant articles and documents
Alkylation of ammonium salts catalyzed by imidazolium-based ionic liquid catalysts
Zheng, Zhuo Qun,Wang, Jie,Wu, Ting Hua,Zhou, Xiao Ping
, p. 1095 - 1101 (2008/03/27)
Quaternary ammonium salts were synthesized from ammonium salts and dialkyl carbonates over imidazolium ionic liquid catalysts. The reaction gave almost stoichiometric amounts of the quaternary ammonium salts for halides and nitrates. It was found that the electron-donating property of the alkyl moieties of ammonium cations, the electrophilic nature of the alkyl group of the carbonate, the acidity of the acid that the anion of the ammonium salt corresponds to, and the steric hindrance of the ammonium salts and the dialkyl carbonates are the key factors that influence the yields of quaternary ammonium salts. Strong electron-donating alkyl groups on the nitrogen atom of the ammonium salt, electron-withdrawing groups on the methylene carbon of dialkyl carbonate, and weaker steric hindrance of the starting ammonium salts and dialkyl carbonates favor the alkylation reaction of ammonium salts.
The synthesis of quaternary ammonium salts from ammonium salts and dialkyl carbonate
Zheng, Zhuoqun,Wu, Tinghua,Zhou, Xiaoping
, p. 1864 - 1865 (2008/03/14)
Quaternary ammonium salts were synthesized from ammonium salts and dialkyl carbonates over an ionic liquid catalyst 1-ethyl-3-methylimidazolium bromide. The Royal Society of Chemistry 2006.
