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26553-46-8

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26553-46-8 Usage

General Description

Ethyl 3-hexenoate, also known as ethyl trans-3-hexenoate, is a colorless liquid with a fruity, sweet, and floral aroma. It is commonly used as a flavoring agent and fragrance ingredient in the food and cosmetic industries. This chemical is naturally found in fruits such as bananas, apples, and oranges, and is responsible for their characteristic scent. Ethyl 3-hexenoate is also used in the production of perfumes, soaps, and other scented products. In addition, it is utilized as a solvent in various chemical processes. The compound is considered safe for use in foods and is generally recognized as safe (GRAS) by the FDA.

Check Digit Verification of cas no

The CAS Registry Mumber 26553-46-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,5 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26553-46:
(7*2)+(6*6)+(5*5)+(4*5)+(3*3)+(2*4)+(1*6)=118
118 % 10 = 8
So 26553-46-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c1-3-5-6-7-8(9)10-4-2/h5-6H,3-4,7H2,1-2H3/b6-5+

26553-46-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ETHYL 3-HEXENOATE

1.2 Other means of identification

Product number -
Other names Ethyl trans-hex-3-enoate

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:26553-46-8 SDS

26553-46-8Relevant articles and documents

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Brown,H.C.,Nambu,H.

, p. 1761 - 1763 (1970)

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Epoxidation of Fatty Acid Esters with Aqueous Hydrogen Peroxide in the Presence of Molybdenum Oxide-Tributyltin Chloride on Charcoal Catalyst

Itoi, Yasushi,Inoue, Masami,Enomoto, Saburo

, p. 3941 - 3944 (1986)

The epoxidation of fatty acid esters was carried out with a 30percent aqueous hydrogen peroxide in the presence of a molybdenum oxide-tributyltin chloride on a charcoal catalyst in 2-propanol at 50 degC.Such inner olefins as ethyl erucate and ethyl oleate gave good yields of 77 and 76percent, respectively.Ethyl elaidate, a trans-form of ethyl oleate, was less reactive (40percent yield).Several vegetable oils such as rapeseed oil, olive oil, soybean oil, cottonseed oil, corn oil, and linseed oil were oxidized with the oxirane oxygen contents of 5.3 to 3.5percent.

Method for regio- and stereoselective synthesis of (E)-Β,γ- unsaturated acids from aldehydes under solvent-free conditions

Zhang, Shi-Jie,Hu, Wei-Xiao

experimental part, p. 3093 - 3100 (2010/12/19)

Synthesis of (E)-β,-γunsaturated acids from aldehydes with malonic acid has been explored under solvent-free conditions. The modified Knoevenagel condensation reaction with N-methyl morpholine (NMM) as catalyst exhibits highly β,-γ regioselectivity and exclusively E-stereoselectivity. A mechanism accounting for both regio- and stereoselectivity has been proposed and preliminarily studied. Copyright Taylor & Francis Group, LLC.

Silica-supported dendrimer-palladium complex-catalyzed selective hydrogenation of dienes to monoolefins

Zweni, Pumza P.,Alper, Howard

, p. 725 - 731 (2007/10/03)

The selective hydrogenation of cyclic and acyclic dienes to monoolefins occurs under very mild conditions, in the presence of silica-supported PAMAM-Pd complexes. The activity and selectivity of this reaction is sensitive to the dendrimer structure. These dendritic complexes display excellent recycle properties, retaining activity for up to eight recycles.

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