Ethyl 2-methyl-4-pentenoate

  • CasNo：53399-81-8
  • purity：99%
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What is the Ethyl 2-methyl-4-pentenoate ?

Ethyl 2-methyl-4-pentenoate is , while it's Molecular Formula is C8H14 O2. Used in Flavor and Fragrance Industry:
Ethyl 2-methyl-4-pentenoate is used as a flavoring agent for its fruity, estry, apple, and pineapple taste characteristics with tropical and cooling nuances. It is particularly suitable for enhancing the flavor of various food products and beverages.
Used in Perfumery:
Ethyl 2-methyl-4-pentenoate is used as a fragrance ingredient for its fruity, green, banana-pineapple odor. It is an essential component in the creation of various perfumes and colognes, contributing to their unique and appealing scents.
Used in Cosmetics:
In the cosmetics industry, Ethyl 2-methyl-4-pentenoate is used as a scent additive to provide a pleasant and refreshing aroma to various cosmetic products such as lotions, creams, and body washes.
Used in the Pharmaceutical Industry:
Ethyl 2-methyl-4-pentenoate can also be used in the pharmaceutical industry as a component in the development of drugs that require a specific taste or aroma profile for improved patient compliance and acceptance.

What is the CAS number for Ethyl 2-methyl-4-pentenoate ?

The CAS number of Ethyl 2-methyl-4-pentenoate is 53399-81-8.

More information of Ethyl 2-methyl-4-pentenoate 53399-81-8 are:

Synonyms

2-Methyl-4-pentenoicacid ethyl ester; Ethyl 2-methyl-4-pentenoate

CAS?Number

53399-81-8

Molecular Formula

C8H14 O2

Molecular Weight

142.198

Density

0.873

Melting Point

-65.52°C (estimate)

Boiling Point

153-155 ºC(lit.)

Flash Point

41 ºC

HS CODE

2916190090

PSA

26.30000

LogP

1.76170

What is Ethyl 2-methyl-4-pentenoate (53399-81-8) used for?

Ethyl 2-methyl-4-pentenoate is an organic compound with a fruity, green, banana-pineapple odor. It is characterized by its ester functional group and is known for its distinct taste and aroma profile.

InChI:InChI=1/C8H14O2/c1-4-6-7(3)8(9)10-5-2/h4,7H,1,5-6H2,2-3H3/t7-/m1/s1

Articles related to Ethyl 2-methyl-4-pentenoate:

Article

Source

Structure-activity studies of fluoroalkyl-substituted γ-butyrolactone and γ-thiobutyrolactone modulators of GABA(A) receptor function

Canney, Daniel J.,Lu, Hwang-Fun,McKeon, Ann C.,Yoon, Kong-Woo,Xu, Kun,Holland, Katherine D.,Rothman, Steven M.,Ferrendelli, James A.,Covey, Douglas F.

, p. 43 - 55 (1998)

Remote control of regio- and diastereoselectivity in the hydroformylation of bishomoallylic alcohols with catalytic amounts of a reversibly bound directing group

Gruenanger, Christian U.,Breit, Bernhard

supporting information; experimental part, p. 967 - 970 (2010/05/02)

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