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3-Phenylpropyl butyrate, a chemical compound with the molecular formula C13H16O2, is a clear colorless liquid known for its pleasant fruity and floral aroma. It is derived from the esterification of butyric acid and 3-phenylpropanol, resulting in a sweet, fruity odor reminiscent of apple or pear. 3-PHENYLPROPYL BUTYRATE is considered safe for consumption in small amounts and is approved as a food additive by regulatory agencies.

7402-29-1

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7402-29-1 Usage

Uses

Used in Food and Beverage Industry:
3-Phenylpropyl butyrate is used as a flavoring agent for its distinctive sweet, fruity aroma that resembles the scent of apple or pear. It enhances the taste and aroma of various food and beverage products, contributing to a more enjoyable consumer experience.
Used in Perfume and Fragrance Industry:
3-Phenylpropyl butyrate is utilized in the production of perfumes and fragrances due to its appealing fruity and floral scent. It adds depth and complexity to fragrance compositions, creating a more sophisticated and attractive scent profile for various personal care and household products.

Check Digit Verification of cas no

The CAS Registry Mumber 7402-29-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7402-29:
(6*7)+(5*4)+(4*0)+(3*2)+(2*2)+(1*9)=81
81 % 10 = 1
So 7402-29-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O2/c1-2-7-13(14)15-11-6-10-12-8-4-3-5-9-12/h3-5,8-9H,2,6-7,10-11H2,1H3

7402-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylpropyl butanoate

1.2 Other means of identification

Product number -
Other names Phenylpropyl butyrate

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:7402-29-1 SDS

7402-29-1Downstream Products

7402-29-1Relevant academic research and scientific papers

Visible-light-promoted conversion of alkyl benzyl ether to alkyl ester or alcohol via O-α-sp3 C-H cleavage

Lu, Ping,Hou, Tianyuan,Gu, Xiangyong,Li, Pixu

, p. 1954 - 1957 (2015/04/27)

A mild and high-yielding visible-light-promoted conversion of alkyl benzyl ethers to the alkyl esters or alkyl alcohols was developed. Mechanistic studies provided evidence for a radical chain reaction involving the homolytic cleavage of O-α-sp3 C-H bonds in the substrate as one of the propagation steps. We propose that α-bromoethers are key intermediates in the transformation.

An efficient N-heterocyclic carbene based ruthenium-catalyst: Application towards the synthesis of esters and amides

Malineni, Jagadeesh,Merkens, Carina,Keul, Helmut,M?ller, Martin

, p. 80 - 83 (2013/07/26)

A highly stable benzimidazolylidene based N-heterocyclic carbene (NHC) ruthenium catalyst was prepared starting with readily accessible starting materials. Under inert gas atmosphere and in air the catalyst showed high activity for the direct synthesis of esters from primary alcohols and of amides from primary alcohols and amines. Di-, tri-, and oligo-amides were obtained by using specific starting materials.

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