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Butanoic acid, 3-iodo-, ethyl ester, also known as ethyl 3-iodobutyrate, is an organic compound with the chemical formula C6H11IO2. It is a colorless liquid with a fruity odor and is used as a flavoring agent in the food and beverage industry. This ester is derived from butanoic acid, which has an iodine atom attached to the third carbon, and is esterified with ethanol. Ethyl 3-iodobutyrate is characterized by its unique combination of fruity and earthy notes, making it a valuable component in the creation of various flavor profiles. It is synthesized through the reaction of 3-iodobutanoic acid with ethanol in the presence of a catalyst, such as sulfuric acid. The compound is typically used in small quantities to enhance the aroma of food products, and its safety and regulatory status are well-established, with it being generally recognized as safe (GRAS) by the US Food and Drug Administration.

7425-50-5

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7425-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7425-50-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,2 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7425-50:
(6*7)+(5*4)+(4*2)+(3*5)+(2*5)+(1*0)=95
95 % 10 = 5
So 7425-50-5 is a valid CAS Registry Number.

7425-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl β-iodobutyrate

1.2 Other means of identification

Product number -
Other names β-Jod-buttersaeure-ethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:7425-50-5 SDS

7425-50-5Relevant academic research and scientific papers

Mild and phosphine-free iron-catalyzed cross-coupling of nonactivated secondary alkyl halides with alkynyl grignard reagents

Cheung, Chi Wai,Ren, Peng,Hu, Xile

supporting information, p. 2566 - 2569 (2014/05/20)

A simple protocol for iron-catalyzed cross-coupling of nonactivated secondary alkyl bromides and iodides with alkynyl Grignard reagents at room temperature has been developed. A wide range of secondary alkyl halides and terminal alkynes are tolerated to a

Stereoselective synthesis of cyclopropanone ketals via silyl chloride promoted cyclization of β-zinciopropionates

Yasui, Keigo,Tanaka, Shuji,Tamaru, Yoshinao

, p. 6881 - 6900 (2007/10/02)

Alkyl, allyl, and propargyl β-iodopropionates undergo a cyclopropanation by the reaction with zinc-copper couple and TBDMSCI in THF to give 1-alkoxy-, 1-allyloxy- and 1-propargyloxy-1-tert-butyldimethylsiloxycyclopropanes in moderate or good yields. β-Iodo-α-methylpropionates 2 and 6 provide trans-5 and trans-8 selectively, which β-iodobutyrates 3 and 7 furnish cis-5 and cis-8 selectively.

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