cas 19781-29-4|| where to buy 4-Octanone, 3-ethyl-

Product Name:4-Octanone, 3-ethyl-

IUPAC Name:3-ethyloctan-4-one

: CAS：19781-29-4; Molecular Formula：C10H20O; Purity：95%+

: Catalog Number：CM696160; Molecular Weight：156.27

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Product Details

: CAS NO:19781-29-4; Molecular Formula:C10H20O; Melting Point:-; Smiles Code:CCCCC(=O)C(CC)CC; Density:

: Catalog Number:CM696160; Molecular Weight:156.27; Boiling Point:; MDL No:MFCD00048806; Storage:

Category Infos

: Aliphatic Chain Compounds; Aliphatic chain compounds include aliphatic compounds and chain compounds containing other elements or groups. Aliphatic hydrocarbons are hydrocarbons with the basic properties of aliphatic compounds. In aliphatic compounds, carbon atoms are arranged in straight chain, branched chain or cyclic, which are respectively called straight chain aliphatic hydrocarbons, branched chain aliphatic hydrocarbons and alicyclic hydrocarbons. Some cyclic hydrocarbons are different in nature from aromatic hydrocarbons, and are very similar to aliphatic hydrocarbons. Such cyclic hydrocarbons are called alicyclic hydrocarbons. In this way, aliphatic hydrocarbons become a general term for all hydrocarbons except aromatic hydrocarbons. Aliphatic hydrocarbons and their derivatives (including halogenated hydrocarbons) and alicyclic hydrocarbons and their derivatives are collectively referred to as aliphatic compounds.

Product Other Information

Product Overview	3-Ethyl-4-octanone is a chemical compound that is commonly used in scientific research. It is a ketone that is often used in the synthesis of other compounds, and it has a range of biochemical and physiological effects.
Synthesis Method	The synthesis of 3-ethyl-4-octanone can be achieved through a number of different methods. One common method is through the reaction of 3-pentanone with 1-bromooctane in the presence of a base such as potassium carbonate. Another method involves the reaction of 3-pentanone with 1-octene in the presence of a catalyst such as palladium on carbon.
Chemical Properties	3-ethyl-4-octanone has the advantage of using in lab experiments is its availability and ease of synthesis. It is also relatively stable and easy to handle. However, one limitation is its potential toxicity, which may limit its use in certain applications.
Synthesis and Application	It is commonly used in the synthesis of other compounds, such as pheromones and natural products. It has also been used in the development of new drugs and as a flavoring agent in the food industry. In addition, 3-ethyl-4-octanone has been used in studies of insect behavior and as a marker for identifying certain plant species.
Future Directions	One area of interest is its potential use as a natural insecticide or repellent. It may also have applications in the development of new drugs or as a flavoring agent in the food industry. In addition, further research is needed to fully understand its mechanism of action and potential impact on human health and the environment.