<?xml version="1.0" encoding="UTF-8"?>
<compound>
  <id type="integer">4824</id>
  <title>T3D4769</title>
  <common-name>Ethanolamine</common-name>
  <description>Ethanolamine is a viscous, hygroscopic amino alcohol with an ammoniacal odor. It is widely distributed in biological tissue and is a component of lecithin. It is used as a surfactant, fluorometric reagent, and to remove CO2 and H2S from natural gas and other gases.</description>
  <cas>141-43-5</cas>
  <pubchem-id>700</pubchem-id>
  <chemical-formula>C2H7NO</chemical-formula>
  <weight>61.08</weight>
  <appearance></appearance>
  <melting-point>10.5°C</melting-point>
  <boiling-point>171°C</boiling-point>
  <density nil="true"/>
  <solubility>1000.0 mg/mL</solubility>
  <specific-gravity nil="true"/>
  <flash-point nil="true"/>
  <vapour-pressure nil="true"/>
  <route-of-exposure nil="true"/>
  <target nil="true"/>
  <mechanism-of-toxicity nil="true"/>
  <metabolism nil="true"/>
  <toxicity nil="true"/>
  <lethaldose nil="true"/>
  <carcinogenicity>No indication of carcinogenicity to humans (not listed by IARC).</carcinogenicity>
  <use-source>This is an endogenously produced metabolite found in the human body. It is used in metabolic reactions, catabolic reactions or waste generation.</use-source>
  <min-risk-level nil="true"/>
  <health-effects nil="true"/>
  <symptoms nil="true"/>
  <treatment nil="true"/>
  <created-at type="dateTime">2014-09-11T05:15:49Z</created-at>
  <updated-at type="dateTime">2026-05-14T17:59:54Z</updated-at>
  <interacting-proteins nil="true"/>
  <wikipedia>http://en.wikipedia.org/wiki/Ethanolamine</wikipedia>
  <uniprot-id nil="true"/>
  <kegg-compound-id>C00189</kegg-compound-id>
  <omim-id nil="true"/>
  <chebi-id>16000</chebi-id>
  <biocyc-id>ETHANOL-AMINE</biocyc-id>
  <ctd-id nil="true"/>
  <stitch-id nil="true"/>
  <drugbank-id>DB03994</drugbank-id>
  <pdb-id>ETA</pdb-id>
  <actor-id nil="true"/>
  <organism nil="true"/>
  <export type="boolean">true</export>
  <metabolizing-proteins nil="true"/>
  <transporting-proteins nil="true"/>
  <moldb-smiles>NCCO</moldb-smiles>
  <moldb-formula>C2H7NO</moldb-formula>
  <moldb-inchi>InChI=1S/C2H7NO/c3-1-2-4/h4H,1-3H2</moldb-inchi>
  <moldb-inchikey>HZAXFHJVJLSVMW-UHFFFAOYSA-N</moldb-inchikey>
  <moldb-average-mass type="decimal">61.0831</moldb-average-mass>
  <moldb-mono-mass type="decimal">61.052763851</moldb-mono-mass>
  <origin>Endogenous</origin>
  <state>Liquid</state>
  <logp>-1.31</logp>
  <hmdb-id>HMDB00149</hmdb-id>
  <chembl-id>CHEMBL104943</chembl-id>
  <chemspider-id>13835336</chemspider-id>
  <structure-image-file-name nil="true"/>
  <structure-image-content-type nil="true"/>
  <structure-image-file-size type="integer" nil="true"/>
  <structure-image-updated-at type="dateTime" nil="true"/>
  <biodb-id nil="true"/>
  <synthesis-reference>&lt;p&gt;John W. Varwig, &amp;#8220;Method of making the ethanolamine salt of N-nitrosophenylhydroxylamine.&amp;#8221; U.S. Patent US4898976, issued February, 1969.&lt;/p&gt;</synthesis-reference>
  <structure-image-caption nil="true"/>
  <chemdb-id>CHEM003726</chemdb-id>
  <dsstox-id>DTXSID6022000</dsstox-id>
  <toxcast-id nil="true"/>
  <stoff-ident-origin nil="true"/>
  <stoff-ident-id nil="true"/>
  <susdat-id>NS00001908</susdat-id>
  <iupac>2-aminoethan-1-ol</iupac>
  <moldb-polar-surface-area>46.25</moldb-polar-surface-area>
  <moldb-refractivity>16.2111</moldb-refractivity>
  <moldb-polarizability>6.63098407374692</moldb-polarizability>
  <moldb-rotatable-bond-count>1</moldb-rotatable-bond-count>
  <moldb-acceptor-count>2</moldb-acceptor-count>
  <moldb-donor-count>2</moldb-donor-count>
  <moldb-pka-strongest-acidic>15.61009842450122</moldb-pka-strongest-acidic>
  <moldb-pka-strongest-basic>9.554610607853252</moldb-pka-strongest-basic>
  <moldb-physiological-charge>1</moldb-physiological-charge>
  <moldb-number-of-rings>0</moldb-number-of-rings>
  <moldb-alogps-logp>-1.53</moldb-alogps-logp>
  <moldb-alogps-logs>1.14</moldb-alogps-logs>
  <moldb-alogps-solubility>8.49e+02 g/l</moldb-alogps-solubility>
</compound>
