ETHYL ACETOACETATE (3-13C)
ETHYL ACETOACETATE (3-13C) Basic information
- Product Name:
- ETHYL ACETOACETATE (3-13C)
- Synonyms:
-
- ETHYL ACETOACETATE (3-13C)
- ETHYL ACETOACETATE-3-13C, 99 ATOM % 13C
- Ethyl acetoacetate-3-13C
- Ethyl acetoacetate (3,4-13C?, 99%)
- CAS:
- 61973-42-0
- MF:
- C6H10O3
- MW:
- 131.15
- Product Categories:
-
- Alphabetical Listings
- E-FStable Isotopes
- Metabolic Research
- Other
- Stable Isotopes
- Mol File:
- 61973-42-0.mol
ETHYL ACETOACETATE (3-13C) Chemical Properties
- 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.)
- Flash point:
- 84 °C
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38-41
- Safety Statements
- 26-36
- RIDADR
- UN 1993 / PGIII
- WGK Germany
- 1
ETHYL ACETOACETATE (3-13C) Usage And Synthesis
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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