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Bis(2-hydroxyethyl)ammonium 4-nitrobenzoate, also known as 4-nitrobenzoic acid bis(2-hydroxyethyl)ammonium salt, is a chemical compound with the molecular formula C10H14N2O5. It is a derivative of 4-nitrobenzoic acid, where the carboxylic acid group is neutralized by bis(2-hydroxyethyl)amine, resulting in the formation of an ammonium salt. Bis(2-hydroxyethyl)ammonium 4-nitrobenzoate is characterized by its yellow crystalline appearance and is soluble in water. It is used in various applications, including as a chemical intermediate in the synthesis of pharmaceuticals and other organic compounds. The compound's properties, such as its solubility and reactivity, make it a valuable component in the preparation of certain drugs and other chemical products.

7394-43-6

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7394-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7394-43-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7394-43:
(6*7)+(5*3)+(4*9)+(3*4)+(2*4)+(1*3)=116
116 % 10 = 6
So 7394-43-6 is a valid CAS Registry Number.

7394-43-6Downstream Products

7394-43-6Relevant academic research and scientific papers

Thermal and kinetics studies of primary, secondary and tertiary alkanolammonium salts of 4-nitrobenzoic acid

Crisan, Manuela,Vlase, Gabriela,Szerb, Elisabeta I.,Vlase, Titus

, p. 1409 - 1418 (2018)

Nitrobenzoic derivatives are chemically and biologically significant molecules, recently listed as active ingredients in the medical-pharmaceutic field. A series of p-nitrobenzoic acid salts were synthesized with different substituted alkanolamine (ethanolamine, diethanolamine and triethanolamine) via proton exchange reactions and characterized. Fourier transform infrared spectroscopy—FTIR-UATR, and a combination of thermal techniques (differential scanning calorimetry—DSC, and thermogravimetric analysis—TGA) with hot-stage microscopy were used in order to demonstrate the formation of salts and to analyse thermal stability and phase transitions. The aim of this study is to investigate thermal behaviour and kinetics of this class of compounds, previously poorly examined, which offers interesting phase transformations in the solid state. DSC indicated that the synthesized salts had very distinct melting points. Diethanolamine and triethanolamine used as cation in the formation of multicomponent systems with 4-nitrobenzoic acid lead to melting points near 100?°C, compared to compound based on ethanolamine. Calorimetric and thermogravimetric data indicate the absence of solvate forms in all studied compounds. TGA and kinetic experiments allowed the calculation of the activation energy, revealing that triethanolammonium salt has the highest stability in this studied series of compounds.

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