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7460-74-4

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7460-74-4 Usage

Description

VALERIC ACID PHENYLETHYL ESTER, also known as Phenethyl valerate or 2-phenylethanol valerate, is a fatty acid ester that is obtained through the formal condensation of 2-phenylethanol with valeric acid. It is an organic compound with a distinctive aromatic odor and is commonly found in various essential oils, particularly in rose oil.

Uses

Used in Fragrance Industry:
VALERIC ACID PHENYLETHYL ESTER is used as a fragrance ingredient for its pleasant and floral scent. It is commonly employed in the formulation of perfumes, colognes, and other scented products to provide a unique and appealing aroma.
Used in Flavor Industry:
In the flavor industry, VALERIC ACID PHENYLETHYL ESTER is used as a flavoring agent to impart a sweet, floral, and slightly fruity taste to various food and beverage products. It is particularly useful in the creation of flavors for confectionery, baked goods, and soft drinks.
Used in Pharmaceutical Industry:
VALERIC ACID PHENYLETHYL ESTER is used as a pharmaceutical agent due to its potential therapeutic properties. It has been studied for its potential anti-inflammatory, analgesic, and antipyretic effects, making it a candidate for the development of new drugs to treat various conditions.
Used in Cosmetic Industry:
In the cosmetic industry, VALERIC ACID PHENYLETHYL ESTER is used as an active ingredient in skincare and hair care products. Its aromatic properties make it suitable for use in aromatherapy, while its potential anti-inflammatory and soothing effects can benefit skin and hair health.
Used in Aromatherapy:
VALERIC ACID PHENYLETHYL ESTER is used in aromatherapy as an essential oil component for its calming and uplifting effects on the mind and body. It can be used in massage oils, diffusers, or inhaled directly to promote relaxation, reduce stress, and improve mood.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 7460-74-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7460-74:
(6*7)+(5*4)+(4*6)+(3*0)+(2*7)+(1*4)=104
104 % 10 = 4
So 7460-74-4 is a valid CAS Registry Number.

7460-74-4SDS

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 2-phenylethyl pentanoate

1.2 Other means of identification

Product number -
Other names phenethyl pentanoate

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:7460-74-4 SDS

7460-74-4Downstream Products

7460-74-4Relevant articles and documents

The scope and mechanism of palladium-catalysed Markovnikov alkoxycarbonylation of alkenes

Li, Haoquan,Dong, Kaiwu,Jiao, Haijun,Neumann, Helfried,Jackstell, Ralf,Beller, Matthias

, p. 1159 - 1166 (2016/11/28)

Hydroesterification reactions represent a fundamental type of carbonylation reaction and constitute one of the most important industrial applications of homogeneous catalysis. Over the past 70 years, numerous catalyst systems have been developed that allow for highly linear-selective (anti-Markovnikov) reactions and are used in industry to produce linear carboxylates starting from olefins. In contrast, a general catalyst system for Markovnikov-selective alkoxycarbonylation of aliphatic olefins remains unknown. In this paper, we show that a specific palladium catalyst system consisting of PdX2/N-phenylpyrrole phosphine (X, halide) catalyses the alkoxycarbonylation of various alkenes to give the branched esters in high selectivity (branched selectivity up to 91%). The observed (and unexpected) selectivity has been rationalized by density functional theory computation that includes a dispersion correction.

Solubilizing agents for active or functional organic compounds

-

Page/Page column 3, (2008/06/13)

An active or functional organic compound is solubilized by an ester of an aryl alcohol, e.g., phenethyl, benzyl or substituted benzyl alcohol, and an alkyl or cycloalkyl carboxylic acid, or by a carbonate of said aryl alcohol and an alkyl or cycloalkyl carbonic acid.

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