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2-Butanone
[CAS# 78-93-3]

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CAS: 78-93-3
Product: 2-Butanone
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Identification
Classification Organic raw materials >> Ketone compound
Name 2-Butanone
Synonyms Ethyl methyl ketone; Methyl ethyl ketone; MEK
Molecular Structure CAS # 78-93-3, 2-Butanone, Ethyl methyl ketone, Methyl ethyl ketone, MEK
Molecular Formula C4H8O
Molecular Weight 72.11
CAS Registry Number 78-93-3
EC Number 201-159-0
FEMA 2170
SMILES CCC(=O)C
Properties
Density 0.806
Melting point -87 ºC
Boiling point 80 ºC
Refractive index 1.378-1.38
Flash point -7 ºC
Water solubility 290 g/L (20 ºC)
Safety Data
Hazard Symbols symbol symbol   GHS02;GHS07 Danger    Details
Hazard Statements H225-H336-H319    Details
Precautionary Statements P210-P233-P240-P241-P242-P243-P261-P264+P265-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P319-P337+P317-P370+P378-P403+P233-P403+P235-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Flammable liquidsFlam. Liq.2H225
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H336
Specific target organ toxicity - single exposureSTOT SE3H335
Specific target organ toxicity - single exposureSTOT SE3H371
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2AH319
Transport Information UN 1193;UN 1232
SDS Available
up Discovory and Applicatios
2-Butanone, also known as methyl ethyl ketone (MEK), is a colorless, flammable liquid with a sweet odor and the chemical formula C4H8O. Its discovery dates back to the early 20th century, with its first synthesis being reported in 1906 by the German chemist Hans Fischer. Initially, 2-butanone was produced through the dry distillation of calcium acetate, but later methods developed more efficient routes for its synthesis, including the hydrogenation of acetone and the dehydrogenation of 2-butanol.

The primary application of 2-butanone is as a solvent in various industrial processes. Its ability to dissolve a wide range of substances makes it an ideal choice in the manufacturing of plastics, coatings, and adhesives. It is commonly used in the formulation of lacquers and paints due to its rapid evaporation rate and excellent solvent properties, which help achieve a smooth finish. Additionally, 2-butanone serves as a cleaning agent for metals and machinery, facilitating the removal of oils and greases.

In the field of pharmaceuticals, 2-butanone is utilized as a solvent and reagent in the synthesis of various chemical compounds. Its role in organic synthesis includes serving as an intermediate in the production of other chemicals, such as methyl isobutyl ketone and 2,3-butanedione, which are important in the manufacture of flavorings and fragrances.

Moreover, 2-butanone has applications in the food industry as a flavoring agent. It contributes to the flavor profile of certain food products, enhancing their appeal. The compound is also studied for its potential use in the production of biofuels, as it can be derived from renewable resources through fermentation processes.

Despite its widespread utility, exposure to 2-butanone can pose health risks, including irritation of the eyes, skin, and respiratory tract. Prolonged exposure can lead to more severe health effects, emphasizing the need for proper handling and safety measures in industrial settings.

In conclusion, 2-butanone is a versatile chemical with significant applications in various industries, including solvents for paints and coatings, cleaning agents, and intermediates in pharmaceutical synthesis. Its discovery and subsequent development have made it a valuable compound in both industrial and laboratory settings.

References

2005. Synthesis of acetals and ketals catalyzed by tungstosilicic acid supported on active carbon. Journal of Zhejiang University. Science, 6(5).
DOI: 10.1631/jzus.2005.b0373

2024. Data-Driven Chemistry for Developing Organic Synthesis Routes for Functional Chemicals. Drug Development Supported by Informatics, Not applicable.
DOI: 10.1007/978-981-97-4828-0_12

2024. Contemporary Breakthroughs and Diverse Chemistry Innovations in Waterborne Polyurethane. Journal of Polymers and the Environment, 32(8).
DOI: 10.1007/s10924-024-03437-9
Market Analysis Reports
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