Diethyl lutidinate
Clinical data
Trade namesStemoxydine; Mexoryl SBU
Other namesDiethyl 2,4-pyridinedicarboxylic acid
2,4-Pyridinedicarboxylic acid diethyl ester
Routes of
administration		topical
Identifiers
  • Diethyl pyridine-2,4-dicarboxylate
CAS Number
PubChem CID
UNII
CompTox Dashboard (EPA)
ECHA InfoCard100.114.112
Chemical and physical data
FormulaC11H13NO4
Molar mass223.228 g·mol−1
3D model (JSmol)
  • CCOC(=O)C1=CC(=NC=C1)C(=O)OCC
  • InChI=1S/C11H13NO4/c1-3-15-10(13)8-5-6-12-9(7-8)11(14)16-4-2/h5-7H,3-4H2,1-2H3[1]
  • Key:MUUDQLHCIAOWPR-UHFFFAOYSA-N[1]

Diethyl lutidinate is a chemical compound. It has been studied for its potential use in hair care.[2]

It can be synthesized by reacting lutidinic acid with ethanol at elevated temperature in presence of sulfuric acid.[3]

References

  1. 1 2 3 "Diethyl lutidinate". pubchem.
  2. ↑ Jitsukawa S, Rathman-Josserand M, Bernard BA (2014). "Human hair follicle stem/progenitor cells and hypoxia: a new hair care approach with diethyl pyridine-2,4-dicarboxylate". Fragrance Journal (in Japanese). 42 (6): 12–19.
  3. ↑ Shin, Hyunseo; Moon, Bongjin; Kwon, Hoejun. Transition metal complex containing tetradentate nitrogen donor ligand and electrochemical biosensor comprising same. 2022. WO 2022145982 A1.
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