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Postion:Product Catalog >Organic Chemistry>Carboxylic acids and derivatives>Carboxylic acid esters and derivatives> Ethyl acetoacetate
	Ethyl acetoacetate
  • 	Ethyl acetoacetate

Ethyl acetoacetate

Price $1
Package 1kg
Min. Order: 1kg
Supply Ability: 100KG
Update Time: 2019-07-06

Product Details

Product Name: Ethyl acetoacetate CAS No.: 141-97-9
Min. Order: 1kg Purity: 99%
Supply Ability: 100KG Release date: 2019/07/06

AD68

 
Ethyl acetoacetate Basic information
Product Name: Ethyl acetoacetate
Synonyms: FEMA 2415;LABOTEST-BB LT01690211;EAA;ETHYL 3-OXOBUTANATE;ETHYL 3-OXOBUTANOATE;ETHYL 3-OXOBUTANOIC ACID;ETHYL 3-OXOBUTYRATE;ETHYL 3-KETOBUTANOATE
CAS: 141-97-9
MF: C6H10O3
MW: 130.14
EINECS: 205-516-1
Product Categories: Pharmaceutical Intermediates;Organics;API intermediates;Miscellaneous;ester Flavor;Analytical Reagents;Analytical Reagents for General Use;Analytical/Chromatography;Building Blocks;C6 to C7;Carbonyl Compounds;Chemical Synthesis;E-H;Esters;Organic Building Blocks;Puriss p.a.;Organic synthesis;Solvent
Mol File: 141-97-9.mol
Article illustration
 
Ethyl acetoacetate Chemical Properties
Melting point  −43 °C(lit.)
Boiling point  181 °C(lit.)
density  1.029 g/mL at 20 °C(lit.)
vapor density  4.48 (vs air)
vapor pressure  1 mm Hg ( 28.5 °C)
refractive index  n20/D 1.419
FEMA  2415 | ETHYL ACETOACETATE
Fp  185 °F
storage temp.  Store below +30°C.
solubility  116 g/L (20°C)
pka 11(at 25℃)
form  Liquid
color  APHA: ≤15
PH 4.0 (110g/l, H2O, 20℃)
Relative polarity 0.577
explosive limit 1.0-54%(V)
Water Solubility  116 g/L (20 ºC)
Merck  14,3758
BRN  385838
Stability: Stable. Incompatible with acids, bases, oxidizing agents, reducing agents, alkali metals. Combustible.
InChIKey XYIBRDXRRQCHLP-UHFFFAOYSA-N
CAS DataBase Reference 141-97-9(CAS DataBase Reference)
NIST Chemistry Reference Butanoic acid, 3-oxo-, ethyl ester(141-97-9)
EPA Substance Registry System Butanoic acid, 3-oxo-, ethyl ester(141-97-9)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36
Safety Statements  26-24/25
RIDADR  UN 1993
WGK Germany  1
RTECS  AK5250000
TSCA  Yes
HazardClass  3.2
PackingGroup  III
HS Code  29183000
Hazardous Substances Data 141-97-9(Hazardous Substances Data)
Toxicity LD50 orally in rats: 3.98 g/kg (Smyth)
MSDS Information
Provider Language
Acetoacetic ester English
SigmaAldrich English
ACROS English
ALFA English
 
Ethyl acetoacetate Usage And Synthesis
Chemical Properties Colourless, clear liquid
Uses Ethyl acetoacetate (EAA) is used as starting material for the syntheses of alpha-substituted acetoacetic esters and cyclic compounds, e.g. pyrazole, pyrimidine and coumarin derivatives as well as intermediate for vitamins and pharmaceuticals. Product Data Sheet
Definition This compound is a tautomer at room temperature consisting of about 93% keto form and 7% enol form.
General Description A colorless liquid with a fruity odor. Flash point 185°F. Boiling point 365°F. May cause adverse health effects if ingested or inhaled. May irritate to skin, eyes and mucous membranes. Used in organic synthesis and in lacquers and paints.
Air & Water Reactions Flammable.
Reactivity Profile Ethyl acetoacetate, a beta-keto ester, is more reactive than many esters. Undergoes an exothermic cleavage reaction in the presence of concentrated base. Reacts with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Mixing with 2,2,2-tris(bromomethyl)ethanol and zinc led to an explosion [US Patent 3 578 619, Crotonaldehyde may rapidly polymerize with Ethyl acetoacetate (Soriano, D.S. et al. 1988. Journal of Chemical Education 65:637.).1971].
Hazard Toxic by ingestion and inhalation; irritant to skin and eyes.
Health Hazard Liquid may cause mild irritation of eyes.
Safety Profile eye irritant. Combustible liquid when exposed to heat or flame; can react with oxidzing materials. Explosive reaction when heated with Zn + tribromoneopentyl alcohol or 2,2,2- tris(bromomethy1)ethanol. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS.
Purification Methods Shake the ester with small amounts of saturated aqueous NaHCO3 (until no further effervescence), then with water. Dry it with MgSO4 or CaCl2 and distil it under reduced pressure. [Beilstein 3 IV 1528.]
 

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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