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Tetraethylammonium formate is a chemical compound composed of a positively charged tetraethylammonium ion and a negatively charged formate ion. It is a crystalline solid known for its use as a phase transfer catalyst in organic synthesis, a reagent in chemical research, a precursor for the synthesis of other organic compounds, and for enhancing the solubility of various substances in organic solvents. It also finds applications in the electrochemical industry and as a buffer solution in biochemical studies. With its low toxicity, it is considered relatively safe for laboratory and industrial use when handled properly.

38410-12-7

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38410-12-7 Usage

Uses

Used in Organic Synthesis:
Tetraethylammonium formate is used as a phase transfer catalyst for facilitating reactions between organic and inorganic compounds, improving the efficiency and selectivity of various organic synthesis processes.
Used in Chemical Research:
It serves as a reagent in chemical research, aiding in the investigation of reaction mechanisms, the synthesis of new compounds, and the study of chemical properties.
Used as a Precursor in Organic Compound Synthesis:
Tetraethylammonium formate is utilized as a precursor in the synthesis of other organic compounds, contributing to the development of new chemical entities and materials.
Used for Enhancing Solubility:
It is employed to improve the solubility of various substances in organic solvents, which is crucial for the dissolution of poorly soluble compounds and can impact reaction rates and yields.
Used in the Electrochemical Industry:
Tetraethylammonium formate finds applications in the electrochemical industry, where it may be used in processes such as electroplating or the development of electrochemical devices.
Used as a Buffer Solution in Biochemical Studies:
It is used as a buffer solution in biochemical research to maintain stable pH conditions, which is essential for the proper functioning of enzymes and other biological processes in vitro.

Check Digit Verification of cas no

The CAS Registry Mumber 38410-12-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,1 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38410-12:
(7*3)+(6*8)+(5*4)+(4*1)+(3*0)+(2*1)+(1*2)=97
97 % 10 = 7
So 38410-12-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H20N.CH2O2/c1-5-9(6-2,7-3)8-4;2-1-3/h5-8H2,1-4H3;1H,(H,2,3)/q+1;/p-1

38410-12-7SDS

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 tetraethylazanium,formate

1.2 Other means of identification

Product number -
Other names Tetraethylammonium formate

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:38410-12-7 SDS

38410-12-7Upstream product

38410-12-7Relevant academic research and scientific papers

Reactivity of a biomimetic W(iv) bis-dithiolene complex with CO2 leading to formate production and structural rearrangement

Seo, Junhyeok,Shearer, Jason,Williard, Paul G.,Kim, Eunsuk

supporting information, p. 17441 - 17444 (2019/12/23)

A mononuclear W(iv) bis-dithiolene complex stabilized by an oxo ligand shows a reductive reactivity toward CO2, from which formate and a dinuclear W(v) complex are generated. An unusual structural rearrangement was observed during the reaction. Structural and spectroscopic characterization for a novel triply bridged dinuclear W(v) complex is reported.

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