Salt synthesis of monoethanolamine with oxyethylenendiphosphonic acid

Views: 111 / PDF downloads: 62

Authors

S Belykh
K Zhumanov
A Bakibaev
S Panshina
V Malkov
O Kotelnikov
L Tsoy
V Massalimova
Е Baibazarova

DOI:

https://doi.org/10.32523/2616-6771-2018-125-4-14-18

Abstract

The interaction of monoethanolamine with 1-hydroxyethylidene diphosphonic acid was studied tor the Cirst time
It was shown that in reaction ratios of 1:2 and 1:3 the reaction product is a salt, which has biologically active properties and
can be used as a special homogenizing additive and an amplifier of moisturizing components as well. The compound obtained
was characterized by NMR spectroscopy.

Downloads

Download data is not yet available.

Downloads

PDF (Русский)

Published

2022-11-23

Issue

Vol. 125 No. 4 (2018)

Section

Статьи

Most read articles by the same author(s)

О Ponomarenko, С Panshina 2, A Bakibaev, A Tashenov, Synthesis and identification of bicyclic bisurea esters , BULLETIN of the L.N. Gumilyov Eurasian National University. Chemistry. Geography. Ecology Series: Vol. 128 No. 3 (2019)
A Bakibaev, M Sadvakassova, R Erkasov, A Atagulova, Identification and analysis of N-arylalkyl-N’-acylureas by magnetic nuclear resonance , BULLETIN of the L.N. Gumilyov Eurasian National University. Chemistry. Geography. Ecology Series: Vol. 129 No. 4 (2019)
A Bakibaev, M Sadvakassova, R Erkasov, A Atagulova, Identification and analysis of N-alkyl-N’-arylalkylureas by nuclear magnetic resonance , BULLETIN of the L.N. Gumilyov Eurasian National University. Chemistry. Geography. Ecology Series: Vol. 130 No. 1 (2020)
A Bakibaev , M Sadvakassova, R Erkasov, A Sorvanov, A Аtagulova, Study of the effect of substituents on the displacement of chemical shifts of N, N’-diarylureas in the nuclear magnetic resonance spectra , BULLETIN of the L.N. Gumilyov Eurasian National University. Chemistry. Geography. Ecology Series: Vol. 131 No. 2 (2020)