CHEBI:63921 - 2-butoxyethanol

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ChEBI Name 2-butoxyethanol ChEBI ID CHEBI:63921 Definition A primary alcohol that is ethanol in which one of the methyl hydrogens is replaced by a butoxy group. A high-boiling (171°C) colourless liquid, it is used as a solvent for paints and inks, as well as in some dry cleaning solutions. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License Read full article at Wikipedia Formula C6H14O2 Net Charge 0 Average Mass 118.17420 Monoisotopic Mass 118.09938 InChI InChI=1S/C6H14O2/c1-2-3-5-8-6-4-7/h7H,2-6H2,1H3 InChIKey POAOYUHQDCAZBD-UHFFFAOYSA-N SMILES CCCCOCCO Roles Classification Chemical Role(s): protic solvent A polar solvent that is capable of acting as a hydron (proton) donor. (via glycol ether ) Application(s): protic solvent A polar solvent that is capable of acting as a hydron (proton) donor. (via glycol ether ) View more via ChEBI Ontology ChEBI Ontology Outgoing 2-butoxyethanol (CHEBI:63921) has role protic solvent (CHEBI:48356) 2-butoxyethanol (CHEBI:63921) is a glycol ether (CHEBI:172390) 2-butoxyethanol (CHEBI:63921) is a primary alcohol (CHEBI:15734) Incoming bis(2-butoxyethyl)phthalate (CHEBI:79937) has functional parent 2-butoxyethanol (CHEBI:63921) IUPAC Name 2-butoxyethanol Synonyms Sources 2-hydroxyethyl n-butyl ether NIST Chemistry WebBook 3-oxa-1-heptanol ChemIDplus BuOCH2CH2OH ChEBI butoxyethanol ChemIDplus butyl cellosolve ChemIDplus butyl glycol NIST Chemistry WebBook butyl oxitol ChemIDplus ethylene glycol butyl ether NIST Chemistry WebBook ethylene glycol mono-n-butyl ether ChemIDplus ethylene glycol monobutyl ether ChEBI glycol butyl ether ChemIDplus n-butoxyethanol ChemIDplus O-butyl ethylene glycol ChemIDplus Manual Xrefs Databases 1364 PPDB 2-Butoxyethanol Wikipedia C19355 KEGG COMPOUND HMDB0031327 HMDB US2448767 Patent View more database links Registry Numbers Types Sources 111-76-2 CAS Registry Number ChemIDplus 111-76-2 CAS Registry Number NIST Chemistry WebBook 1732511 Reaxys Registry Number Reaxys Citations Types Sources 15371241 PubMed citation Europe PMC 15705494 PubMed citation Europe PMC 22330932 PubMed citation Europe PMC 9372852 PubMed citation Europe PMC Last Modified 06 May 2021