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2198-61-0

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2198-61-0 Usage

Description

Isoamyl hexanoate has a fruity odor. May be prepared by esterification of caproic acid with the isomeric amyl alcohols obtained from fusel oil and other sources.

Chemical Properties

Different sources of media describe the Chemical Properties of 2198-61-0 differently. You can refer to the following data:
1. Isoamyl hexanoate has an apple, pineapple, fruity, green, sweet odor.
2. Colorless liquid

Occurrence

Reported found in rind of California orange, apple, apricot, banana, grapefruit peel, grapes, pineapple, strawberry, cheeses, beer, cognac, rum, whiskies, sherry, grape wines, passion fruit, plum, brandy (plum, pear and apple), strawberry and bilberry wine, cherimoya, and mastic gum leaf and fruit oil.

Uses

Isoamyl Hexanoate is a synthetic flavoring agent that is a stable, colorless liquid of fruity odor. It is soluble in alcohol, fixed oils, and mineral oil. Storage should be in glass, tin, or resin-lined containers. It is used in fruit flavors such as banana and pineapple for applications in desserts, candy, and ice cream at 4–22 ppm.

Preparation

By esterification of caproic acid with the isomeric amyl alcohols obtained from fusel oil and other sources.

Definition

ChEBI: A fatty acid ester obtained by the formal condensation of the carboxy group of hexanoic acid (caproic acid) with the alcoholic hydroxy group of 3-methylbutan-1-ol (isoamylol).

Taste threshold values

Taste characteristics at 25 ppm: fruity, green, pineapple with a waxy nuance

Check Digit Verification of cas no

The CAS Registry Mumber 2198-61-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,9 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2198-61:
(6*2)+(5*1)+(4*9)+(3*8)+(2*6)+(1*1)=90
90 % 10 = 0
So 2198-61-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H22O2/c1-4-5-6-7-11(12)13-9-8-10(2)3/h10H,4-9H2,1-3H3

2198-61-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylbutyl hexanoate

1.2 Other means of identification

Product number -
Other names ISOAMYL HEXANOATE

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:2198-61-0 SDS

2198-61-0Synthetic route

i-Amyl alcohol
123-51-3

i-Amyl alcohol

hexanoic acid
142-62-1

hexanoic acid

3-methylbutyl hexanoate
2198-61-0

3-methylbutyl hexanoate

Conditions
ConditionsYield
With sulfuric acid In benzene
With rapeseed lipase acetone powder In hexane at 40℃; for 48h; Enzymatic reaction;93 %Chromat.
With 2,2,4-trimethylpentane; Candida rugosa lipase (Type VII); water at 39.84℃; for 4h; Enzymatic reaction;

2198-61-0Downstream Products

2198-61-0Relevant articles and documents

Lipase-catalyzed synthesis of ethyl hexanoate in microemulsion system

Tan, Zhongqin,Han, Xiaoxiang,Hu, Xiaoli,Du, Huan,Bao, Xiuxiu

, p. 9675 - 9678 (2014/01/06)

This paper studied lipase-catalyzed synthesis of ethyl hexanoate in dodecylbenzenesulfonic acid/isooctane/water microemulsion system. The effect of several parameters, such as w0 ([H2O]/[surfactant]) value, reaction time, reaction temperature, oil phase solvent, buffer solution pH value of microemulsion system on the esterification have been investigated. The results showed that the best experimental conditions for catalytic synthesis ethyl hexanoate were as follows: w0 = 4, reaction time 4 h, reaction temperature 40 °C, buffer solution pH 7. Under these conditions, the conversion of ethyl hexanoate can reach 98.5 %. Lipase-catalyzed synthesis of ethyl hexanoate in dodecylbenzenesulfonic acid inverse microemulsion system has triple mechanism, namely acid catalyzes, microemulsion catalyzes and enzyme catalyzes.

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