Diethyl lutidinate

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
ChemSpider
UNII
CompTox Dashboard (EPA)
ECHA InfoCard100.114.112 Edit this at Wikidata
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
  • Key:MUUDQLHCIAOWPR-UHFFFAOYSA-N

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

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

References

  1. 1 2 3 "Diethyl lutidinate". pubchem. Archived from the original on February 16, 2018.
  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.