| | Identification | Back Directory |  | [Name] 
 ETHYL ACETOACETATE (3-13C)
 |  | [CAS] 
 61973-42-0
 |  | [Synonyms] 
 ETHYL ACETOACETATE (3-13C)
 ETHYL ACETOACETATE-3-13C, 99 ATOM % 13C
 |  | [Molecular Formula] 
 C6H10O3
 |  | [MDL Number] 
 MFCD00083953
 |  | [MOL File] 
 61973-42-0.mol
 |  | [Molecular Weight] 
 131.15
 | 
 | Chemical Properties | Back Directory |  | [Melting point ] 
 -43 °C (lit.)
 |  | [Boiling point ] 
 181 °C (lit.)
 |  | [density ] 
 1.037 g/mL at 25 °C
 |  | [refractive index ] 
 n20/D 1.419(lit.)
 |  | [Fp ] 
 84 °C
 | 
 | Hazard Information | Back Directory |  | [Uses] 
 Ethyl acetoacetate-13C is the 13C labeled Ethyl acetoacetate[1]. Ethyl acetoacetate (Ethyl acetylacetate) is an ester widely used as an intermediate in the synthesis of many varieties of compounds[2][3][4]. Ethyl acetoacetate is an inhibitor of bacterial biofilm[5].
 |  | [References] 
 [1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. DOI:10.1177/1060028018797110
 [2] Rao M.Uppu, et al. Enantioselective catalytic asymmetric hydrogenation of ethyl acetoacetate in room temperature ionic liquids. Biochemical and Biophysical Research Communications. 1996 Dec; 229(3):764-769.
 [3] Leo F. Salter, et al. A dual‐frequency Belousov Zhabotinskii oscillating reaction with ethyl acetoacetate as organic substrate. substrate. International Journal of Chemical Kinetics. 1982. 14(8), 815–821.
 [4] Iqbal S, et al. 2-Oxo-1,2,3,4-tetrahydropyrimidines Ethyl Esters as Potent β- Glucuronidase Inhibitors: One-pot Synthesis, In vitro and In silico Studies. Med Chem. 201814(8):818-830. DOI:10.2174/1573406414666180525105325
 [5] Horne SM, et al. Acetoacetate and ethyl acetoacetate as novel inhibitors of bacterial biofilm. Lett Appl Microbiol. 2018 Apr66(4):329-339. DOI:10.1111/lam.12852
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