CHEBI:19030 - 1-aminopropan-2-ol

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ChEBI Name 1-aminopropan-2-ol ChEBI ID CHEBI:19030 Definition Any amino alcohol that is propan-2-ol substituted by an amino group at position 1. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:610 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 C3H9NO Net Charge 0 Average Mass 75.10970 Monoisotopic Mass 75.06841 InChI InChI=1S/C3H9NO/c1-3(5)2-4/h3,5H,2,4H2,1H3 InChIKey HXKKHQJGJAFBHI-UHFFFAOYSA-N SMILES CC(O)CN Metabolite of Species Details Escherichia coli (NCBI:txid562) See: PubMed Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) Biological Role(s): Escherichia coli metabolite Any bacterial metabolite produced during a metabolic reaction in Escherichia coli. View more via ChEBI Ontology ChEBI Ontology Outgoing 1-aminopropan-2-ol (CHEBI:19030) has role Escherichia coli metabolite (CHEBI:76971) 1-aminopropan-2-ol (CHEBI:19030) is a amino alcohol (CHEBI:22478) 1-aminopropan-2-ol (CHEBI:19030) is a secondary alcohol (CHEBI:35681) Incoming 1-aminopropan-2-yl phosphate (CHEBI:19029) has functional parent 1-aminopropan-2-ol (CHEBI:19030) diisopropanolamine (CHEBI:143266) has functional parent 1-aminopropan-2-ol (CHEBI:19030) (2R)-1-aminopropan-2-ol (CHEBI:15675) is a 1-aminopropan-2-ol (CHEBI:19030) IUPAC Name 1-aminopropan-2-ol Synonyms Sources 1-methyl-2-aminoethanol NIST Chemistry WebBook 2-hydroxypropylamine NIST Chemistry WebBook α-aminoisopropyl alcohol NIST Chemistry WebBook isopropanolamine NIST Chemistry WebBook monoisopropanolamine NIST Chemistry WebBook Manual Xrefs Databases 1-Amino-2-propanol Wikipedia C05771 KEGG COMPOUND ECMDB04013 ECMDB HMDB0012136 HMDB View more database links Registry Numbers Types Sources 605275 Reaxys Registry Number Reaxys 78-96-6 CAS Registry Number ChemIDplus 78-96-6 CAS Registry Number NIST Chemistry WebBook Citations Types Sources 4362743 PubMed citation Europe PMC 5329339 PubMed citation Europe PMC Last Modified 10 June 2019