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ETHYL CROTONATE

ETHYL CROTONATE Structure
ETHYL CROTONATE
  • CAS No.10544-63-5
  • Chemical Name:ETHYL CROTONATE
  • CBNumber:CB2241197
  • Molecular Formula:C6H10O2
  • Formula Weight:114.14
  • MOL File:10544-63-5.mol
ETHYL CROTONATE Property
  • Melting point 37.22°C (estimate)
  • Boiling point 142-143 °C(lit.)
  • Density 0.918 g/mL at 25 °C(lit.)
  • vapor density 3.9 (vs air)
  • refractive index n20/D 1.424(lit.)
  • FEMA 3486 | ETHYL TRANS-2-BUTENOATE
  • Flash point 36 °F
  • storage temp. Flammables area
  • form Liquid
  • color Clear colorless
  • Odor at 10.00 % in dipropylene glycol. pungent fruity acrid ester
  • Odor Type fermented
  • JECFA Number 1806
  • LogP 1.806 (est)
  • EPA Substance Registry System 2-Butenoic acid, ethyl ester (10544-63-5)
Safety
  • Hazard Codes  :F,C
  • Risk Statements  :11-34
  • Safety Statements  :16-26-36/37/39-45
  • RIDADR  :UN 1862 3/PG 2
  • WGK Germany  :2
  • RTECS  :GQ3500000
  • HS Code  :29161900
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordWarning
  • Hazard statements H226-H319
  • Precautionary statements P264-P280-P305+P351+P338-P337+P313P

ETHYL CROTONATE Chemical Properties,Usage,Production

  • Chemical Properties clear colorless liquid
  • Chemical Properties Ethyl crotonate has a powerful, sour, caramellic-fruity odor.
  • Occurrence Reported found in Fragaria vesca. Also reported found in guava fruit, guava peel, pineapple, white wine, yellow passion fruit, fresh mango, naranjilla fruit, mussel, loganberry, apple, papaya, concord grape, strawberry, rum, cocoa, plum, kiwifruit and other natural sources.
  • Uses Crotonic Acid Ethyl Ester, is an intermediate for the preparation of various pharmaceutical compounds. It can be used for the synthesis of (+)-trans-Trikentrin A.
  • Definition ChEBI: Ethyl crotonate is a fatty acid ester.
  • Preparation By esterification of crotonic acid with ethyl alcohol in the presence of concentrated H2SO4.
  • Taste threshold values Taste characteristics at 10 ppm: rum, cognac and pungent with caramellic and fruity nuances.
  • Synthesis Reference(s) Journal of the American Chemical Society, 112, p. 2716, 1990 DOI: 10.1021/ja00163a038
    Synthetic Communications, 14, p. 701, 1984 DOI: 10.1080/00397918408059583
  • General Description A clear colorless liquid with a pungent odor. Flash point 36°F. Less dense than water and insoluble in water. Vapors heavier than air.
  • Air & Water Reactions Highly flammable. Insoluble in water.
  • Reactivity Profile ETHYL CROTONATE is an ester. Esters react 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. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides.
  • Health Hazard May cause toxic effects if inhaled or absorbed through skin. Inhalation or contact with material may irritate or burn skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.
  • Fire Hazard HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.
  • Safety Profile Slightly toxic by ingestion. Corrosive. An eye irritant and lachrymator. A flammable liquid. When heated to decomposition it emits acrid smoke and irritating fumes.
ETHYL CROTONATE Preparation Products And Raw materials
Raw materials
Preparation Products
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ETHYL CROTONATE Spectrum
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