Diethyl lutidinate

Diethyl lutidinate
Clinical data
Trade names	Stemoxydine; Mexoryl SBU
Other names	Diethyl 2,4-pyridinedicarboxylic acid; 2,4-Pyridinedicarboxylic acid diethyl ester
Routes of; administration	topical
Identifiers
	IUPAC name Diethyl pyridine-2,4-dicarboxylate;
CAS Number	41438-38-4;
PubChem CID	170509;
UNII	4SN4572M5S;
CompTox Dashboard (EPA)	DTXSID00961682 ;
ECHA InfoCard	100.114.112
Chemical and physical data
Formula	C11H13NO4
Molar mass	223.228 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CCOC(=O)C1=CC(=NC=C1)C(=O)OCC;
	InChI 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.^[2]

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

References

^ ^a ^b ^c ^d "Diethyl lutidinate". pubchem.
^ 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.
^ 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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