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ETHYLTRIMETHYLAMMONIUM HYDROXIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30382-83-3

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30382-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30382-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,8 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30382-83:
(7*3)+(6*0)+(5*3)+(4*8)+(3*2)+(2*8)+(1*3)=93
93 % 10 = 3
So 30382-83-3 is a valid CAS Registry Number.

30382-83-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethylethylammonium hydroxide

1.2 Other means of identification

Product number -
Other names ethyl-trimethyl-ammonium, hydroxide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30382-83-3 SDS

30382-83-3Relevant academic research and scientific papers

Eco-friendly acetylcholine-carboxylate bio-ionic liquids for controllable: N-methylation and N-formylation using ambient CO2 at low temperatures

Zhao, Wenfeng,Chi, Xiaoping,Li, Hu,He, Jian,Long, Jingxuan,Xu, Yufei,Yang, Song

, p. 567 - 577 (2019/02/14)

Catalytic fixation of CO2 to produce valuable fine chemicals is of great significance to develop a green and sustainable circulation of excessive carbon in the environment. Herein, a series of non-toxic, biodegradable and recyclable acetylcholine-carboxylate bio-ionic liquids with different cations and anions were simply synthesized for producing formamides and methylamines using atmospheric CO2 as a carbon source, and phenylsilane as a hydrogen donor. The selectivity toward products was tuned by altering the reaction temperature under solvent or solvent-free conditions. N-Methylamines (ca. 96% yield) were obtained in acetonitrile at 50 °C, while N-formamides (ca. 99% yield) were attained without a solvent at 30 °C. The established bio-ionic liquid catalytic system found a wide range of applicability in substrates and possessed a high potentiality in scale-up to gram-grade production. The developed catalytic system was fairly stable, which could be easily reused without an apparent loss of reactivity, possibly due to the strong electrostatic interactions between the cation and anion. The combination of experimental and computational results explicitly elucidated the reaction mechanism: PhSiH3 activated by a bio-IL was favorable for the formation of silyl formate from hydrosilylation of CO2, followed by a reaction with an amine to give an N-formamide, while an N-methylamine was formed by further hydrosilylation of the N-formamide.

Ionic motions and phase transitions in solid trimethylethylammonium tetrafluroberate studied by by1H, 19F, and14N NMR, powder X-ray diffraction and differential scanning calorimetry

Ono, Hiroshi,Ikeda, Ryuichi,Ishida, Hiroyukl

, p. 1833 - 1838 (2007/10/03)

1H, 19F, and 14N NMR, powder X-ray diffraction, and differential scanning calorimetry (DSC) were studied for trimethylethylammonium tetrafluoroborate, (CH3)3NC2H5BF4. Five solid phases, named I, II, III, IV, and V in the order of decreasing temperature, were obtained in the temperature range 77-630 K. The transition temperatures and the corresponding enthalpy changes determined by DSC were 222K (0.16kj moi-1), 239K (1.8 kJ mol-1), 293 K (2.1 kJ mol-1), and 362 K (4.5 kJ mol-1). X-ray powder patterns showed that Phase I and II form an NaCl-type cubic lattice (a = 10.14 A, Z = 4) and a tetragonal lattice (a = 8.59, c = 6,24 A, Z = 2), respectively. The NMR study revealed that the canonic orientation in Phase I and II is dynamically disordered. Moreover, since the self-diffusion of anions and the Isotropie rotation of cations were observed in Phase I, this phase can be considered as a mesophase very close to the plastic phase. In Phases II, III, IV, and V we have detected the isotropic reorientation of anions, the anisotropic tumbling of cations, the C′3 reorientation of the whoie (CH3)3N group about C-N bond axis, and the C3 reorientation of the CH3 groups. The motional parameters were evaluated for these cationic and anionic motions. VCH Verlagsgesellschaft mbH, 1996.

Process for producing a high purity quaternary ammonium hydroxide

-

, (2008/06/13)

A process for production of high purity quaternary ammonium hydroxides, comprising electrolyzing quaternary ammonium hydrogencarbonates represented by the general formula: (wherein the symbols are as defined in the appended claims) in an electrolytic cell comprising an anode compartment and a cathode compartment defined by a cation exchange membrane. In accordance with this process, high purity quaternary ammonium hydroxides can be produced with high electrolytic efficiency and further without causing corrosion of equip-ment. Since the quaternary ammonium hydroxides produced by the present invention are of high purity, they can be effectively used as, for example, cleaners, etchants or developers for wafers in the production of IC and LSI in the field of electronics and semiconductors.

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