Chemistry:Bicine
From HandWiki
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| Names | |
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| IUPAC name
N,N-Bis(2-hydroxyethyl)glycine
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| Systematic IUPAC name
[Bis(2-hydroxyethyl)amino]acetic acid | |
| Other names
Diethylolglycine; Diethanol glycine; Dihydroxyethylglycine; BHG
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| Identifiers | |
3D model (JSmol)
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| Abbreviations | DHEG |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
PubChem CID
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| UNII | |
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| Properties | |
| C6H13NO4 | |
| Molar mass | 163.17 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Tracking categories (test):
Bicine is an organic compound used as a buffering agent. It is one of Good's buffers and has a pKa of 8.35 at 20 °C.[1] It is prepared by the reaction of glycine with ethylene oxide, followed by hydrolysis of the resultant lactone.[2]
Bicine is a contaminant in amine systems used for gas sweetening. It is formed by amine degradation in the presence of O2, SO2, H2S or Thiosulfate.[3]
See also
References
- ↑ N,N-Bis(2-hydroxyethyl)glycine at ChEBI
- ↑ The Merck Index (10th ed.). Rahway, NJ: Merck & Co.. 1983. p. 453. ISBN 0-911910-27-1. https://archive.org/details/merckindexencycl00wind.
- ↑ Lawson, Gary (2003). "Amine Plant Corrosion Reduced by Removal of Bicine". Gas Processors Association Annual Convention. http://www.mprservices.com/pdfs/reducing.pdf.
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