Ethanolamine Oleate

CAS 2272-11-9 0 current recordsSmall Molecule

Who holds supplier records for Ethanolamine Oleate? No organisation holds a current US Type II DMF or EU CEP for Ethanolamine Oleate in the registers PharmaTek covers.

Sources: FDA Drug Master File list, EDQM certification database, FDA Orange Book. Record updated 2 Nov 2026. How we read these records

Reading the evidence

  • No current DMF or CEP on record

    The covered registers hold no supplier record for this substance. This is not evidence that no one makes it: suppliers may file under another name, sell outside the US and EU, or use an ASMF.

Current records (0)

Organisations holding an active US FDA Type II Drug Master File or a CEP for Ethanolamine Oleate. Country is the organisation's recorded country, not necessarily the manufacturing site.

Not found in the covered registers (FDA DMF list, EDQM). This is not evidence that no supplier exists.

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Overview

Ethanolamine Oleate is a small molecule active pharmaceutical ingredient (ChEMBL CHEMBL3989529).

Chemical identity

IUPAC name
2-aminoethanol;(Z)-octadec-9-enoic acid
Canonical SMILES
CCCCCCCC/C=C\CCCCCCCC(=O)O.C(CO)N
InChIKey
KGWDUNBJIMUFAP-KVVVOXFISA-N
Synonyms
Ethamolin, Ethanolamine oleate, NSC-760382, Oldamin, Monoethanolamine oleate, Monolate, Moramin, Neosclerol, Varicetin, Varex, Esclerosina, Antivariz

Record history

PharmaTek records which organisations hold a current DMF or CEP for Ethanolamine Oleate every week, starting 23 Oct 2026. Additions and lapses will appear here from the next weekly release.

Monitoring pilot: get an email when these records change. Places are confirmed by a person; nothing is sent until then. All changes this week

What these records establish

  • An active DMF means a confidential file is held by the FDA and can be referenced; the FDA does not approve or disapprove DMFs.
  • A CEP confirms monograph suitability for the EU market; it is not a GMP certificate, and the holder may not be the manufacturer.
  • Historical records show a past filing, not current supply.
  • Company GMP certificates are matched to the organisation, not to the site making this substance.
  • A substance missing from these registers is not evidence that no supplier exists.
For suppliers

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