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1185-59-7

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1185-59-7 Usage

Description

Tetraethylammonium acetate is a quaternary ammonium salt that serves as a catalyst in various chemical reactions. It is characterized by its ability to facilitate the formation of copolymers and is known for its effectiveness in the synthesis of specific polymers.

Uses

Used in Polymer Synthesis Industry:
Tetraethylammonium acetate is used as a catalyst for the preparation of carbon dioxide-cyclohexene epoxide alternating copolymer. It is employed in conjunction with an aluminum complex-ammonium salt system to enhance the efficiency and effectiveness of the copolymerization process. This application is particularly relevant in the production of biodegradable and environmentally friendly materials, as well as in the development of new materials with unique properties for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1185-59-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1185-59:
(6*1)+(5*1)+(4*8)+(3*5)+(2*5)+(1*9)=77
77 % 10 = 7
So 1185-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H20N.C2H4O2.4H2O/c1-5-9(6-2,7-3)8-4;1-2(3)4;;;;/h5-8H2,1-4H3;1H3,(H,3,4);4*1H2/q+1;;;;;/p-1

1185-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetraethyl Ammonium Acetate

1.2 Other means of identification

Product number -
Other names Tetraethylammonium acetate

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:1185-59-7 SDS

1185-59-7Relevant articles and documents

Synthesis of isosorbide-based polycarbonates via melt polycondensation catalyzed by quaternary ammonium ionic liquids

Sun, Wei,Xu, Fei,Cheng, Weiguo,Sun, Jian,Ning, Guoqing,Zhang, Suojiang

, p. 908 - 917 (2017)

A series of quaternary ammonium ionic liquids (ILs) were synthesized and employed as catalysts for the production of poly(isosorbide carbonate) (PIC) from diphenyl carbonate and isosorbide via a melt polycondensation process. The relationship between the anions of the ILs and the catalytic activities was investigated, and the readily-prepared IL tetraethylammonium imidazolate (TEAI) was found to exhibit the highest catalytic activity. After optimizing the reaction conditions, a PIC with a weight-average molecular weight (Mw) of 25600 g/mol was obtained, in conjunction with an isosorbide conversion of 92%. As a means of modifying the molecular flexibility and thermal properties of the PIC, poly(aliphatic diol-co-isosorbide carbonate)s (PAIC)s were successfully synthesized, again using TEAI, and polymers with Mw values ranging from 29000 to 112000 g/mol were obtained. 13C NMR analyses determined that the PAIC specimens had random microstructures, while differential scanning calorimetry demonstrated that each of the PAICs were amorphous and had glass transition temperatures ranging from 50 to 115 °C. Thermogravimetric analyses found Td-5% values ranging from 316 to 332 °C for these polymers. Based on these data, it is evident that the incorporation of linear or cyclohexane-based diol repeating units changed the thermal properties of the PIC.

CATHODIC ESTERIFICATION OF CARBOXYLIC ACIDS

Awata, Takeshi,Baizer, Manuel M.,Nonaka, Tsutomu,Fuchigami, Toshio

, p. 371 - 374 (2007/10/02)

A cathodic method for the esterification of carboxylic acids under mild conditions was found.The esterification proceeded smoothly at room temperature by the reaction of alkylating with quaternary ammonium carboxylates formed in a cathode chamber.

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