ETHYL ACETOACETATE (3-13C)
- Product Name
- ETHYL ACETOACETATE (3-13C)
- CAS No.
- 61973-42-0
- Chemical Name
- ETHYL ACETOACETATE (3-13C)
- Synonyms
- ETHYL ACETOACETATE (3-13C);Ethyl acetoacetate (3,4-13C?, 99%);Ethyl acetoacetate-3-13C;ETHYL ACETOACETATE-3-13C, 99 ATOM % 13C
- CBNumber
- CB6304254
- Molecular Formula
- C6H10O3
- Formula Weight
- 131.15
- MOL File
- 61973-42-0.mol
ETHYL ACETOACETATE (3-13C) Property
- 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
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38-41
- Safety Statements
- 26-36
- RIDADR
- UN 1993 / PGIII
- WGK Germany
- 1
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 489271
- Product name
- Ethyl acetoacetate-3-13C
- Purity
- 99 atom %
- Packaging
- 500mg
- Price
- $437
- Updated
- 2025/07/31
ETHYL ACETOACETATE (3-13C) Chemical Properties,Usage,Production
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
ETHYL ACETOACETATE (3-13C) Preparation Products And Raw materials
Raw materials
Preparation Products
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