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Ethyl 3-methylvalerate, also known as Ethyl 3-methylpentanoate, is an organic compound with a fruity, sweet, green, berry, and melon aroma. It is characterized by its blueberry note and has a low aroma threshold value, making it easily detectable even at very low concentrations.

5870-68-8

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5870-68-8 Usage

Uses

Used in Flavor and Fragrance Industry:
Ethyl 3-methylvalerate is used as a flavoring agent for its fruity, sweet, and green aroma, particularly resembling the scent of blueberries. Its low aroma threshold value allows it to be used effectively in small quantities to enhance the flavor and aroma of various food products.
Used in Perfumery:
In the perfumery industry, Ethyl 3-methylvalerate is used as a fragrance ingredient to add a fresh, fruity, and slightly sweet note to perfume compositions. Its green and berry undertones can contribute to creating a more complex and natural scent profile.
Used in the Food Industry:
Ethyl 3-methylvalerate is used as an additive in the food industry to impart a fruity and sweet flavor to products, such as beverages, candies, and desserts. Its natural occurrence in various fruits and its ability to mimic the taste of blueberries make it a desirable ingredient for enhancing the flavor of food products.
Used in the Cosmetic Industry:
In the cosmetic industry, Ethyl 3-methylvalerate can be used as a fragrance component in personal care products, such as lotions, creams, and shampoos. Its pleasant and natural aroma can provide a sensory experience that enhances the overall appeal of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 5870-68-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5870-68:
(6*5)+(5*8)+(4*7)+(3*0)+(2*6)+(1*8)=118
118 % 10 = 8
So 5870-68-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2/c1-4-7(3)6-8(9)10-5-2/h7H,4-6H2,1-3H3

5870-68-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (A18868)  Ethyl 3-methylvalerate, 98%   

  • 5870-68-8

  • 5g

  • 288.0CNY

  • Detail
  • Alfa Aesar

  • (A18868)  Ethyl 3-methylvalerate, 98%   

  • 5870-68-8

  • 25g

  • 1149.0CNY

  • Detail

5870-68-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-Methylvalerate

1.2 Other means of identification

Product number -
Other names ethyl 3-methylpentanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5870-68-8 SDS

5870-68-8Relevant academic research and scientific papers

Catalytic functionalization of methane and light alkanes in supercritical carbon dioxide

Fuentes, M. Angeles,Olmos, Andrea,Caballero, Ana,Perez, Pedro J.,Munoz, Bianca K.,Jacob, Kane,Etienne, Michel,Gonzalez-Nunez, M. Elena,Mello, Rossella,Asensio, Gregorio

supporting information, p. 11013 - 11018,6 (2015/01/07)

The development of catalytic methods for the effective functionalization of methane yet remains a challenge. The best system known to date is the so-called Catalytica Process based on the use of platinum catalysts to convert methane into methyl bisulfate with a TOF rate of 10-3 s. In this contribution, we report a series of silver complexes containing perfluorinated tris(indazolyl)borate ligands that catalyze the functionalization of methane into ethyl propionate upon reaction with ethyl diazoacetate (EDA) by using supercritical carbon dioxide (scCO2) as the reaction medium. The employment of this reaction medium has also allowed the functionalization of ethane, propane, butane, and isobutane.

Copper-catalyzed enantioselective conjugate addition of Grignard reagents to α,β-unsaturated esters

Lopez, Fernando,Harutyunyan, Syuzanna R.,Meetsma, Auke,Minnaard, Adriaan J.,Feringa, Ben L.

, p. 2752 - 2756 (2007/10/03)

(Chemical Equation Presented) Stable dinuclear Cu complexes have been used to catalyze the conjugate addition of inexpensive and readily available Grignard reagents to acyclic α,β-unsaturated esters. The method provides the correspending β-substituted optically active esters in high yields and with excellent enantioselectivities (see scheme). R3 = cyclohexyl, R 4 = Ph or R3 = Ph, R4 = cyclohexyl.

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