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82654-98-6

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82654-98-6 Usage

Description

Vanillyl butyl ether is an ether of monohydroxybenzoic acid. It is added to food products as a flavoring agent. It is also present in cosmetics and personal care products. It has a characteristic trigeminal, burning, hot pepper nature and can be used in spice flavors like pepper, cinnamon and ginger, as well as blends for some baked applications, including cookies. It has some other applications include flavoring for alcoholic and non-alcoholic beverages with herbal, berry, vanilla, cola, ginger ale, root beer, hot chocolate, chai, ice tea and mints. It can also be used as a warming agent.

Chemical Properties

Vanillyl butyl ether has a weak, vanillic, acidic odor.

Uses

Vanillyl butyl ether is a compound hypothesized to have warming and vasodilation mechanisms when applied on the skin as a cream.

General Description

Vanillyl butyl ether is an alkoxy-substituted benzyl derivative mainly used as a flavoring agent.

Biochem/physiol Actions

Taste at 10-15%

Check Digit Verification of cas no

The CAS Registry Mumber 82654-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,5 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82654-98:
(7*8)+(6*2)+(5*6)+(4*5)+(3*4)+(2*9)+(1*8)=156
156 % 10 = 6
So 82654-98-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O3/c1-3-4-7-15-9-10-5-6-11(13)12(8-10)14-2/h5-6,8,13H,3-4,7,9H2,1-2H3

82654-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Butoxymethyl)-2-methoxyphenol

1.2 Other means of identification

Product number -
Other names 4-(butoxymethyl)-2-methoxyphenol

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:82654-98-6 SDS

82654-98-6Downstream Products

82654-98-6Relevant articles and documents

Synthetic method of vanillyl alcohol ether

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Paragraph 0021-0025, (2019/07/08)

The invention discloses a synthetic method of vanillyl alcohol ether, and belongs to the technical field of the industry of fine chemicals. The synthetic method comprises the following steps that vanillin is dissolved in a solvent, uniform stirring is carried out, then metal complex hydride and an alkylating reagent are added into the mixed solvent, a reaction is carried out for 3-4 hours at 30-40DEG C, a vanillyl alcohol ether solution is obtained, and the vanillyl alcohol ether solution is separated and purified to obtain the vanillyl alcohol ether. The synthetic method of the vanillyl alcohol ether has the advantages that the vanillyl alcohol ether is prepared by adopting a one-pot method, the operation is simple, the reaction conditions are mild, the reaction process is easy to control, the production cost is low, three wastes are few, and the vanillyl alcohol ether prepared through the synthetic method is high in yield and purity, and easily achieves industrial production.

Sulfated tungstate as hydroxyl group activator for preparation of benzyl, including p-methoxybenzyl ethers of alcohols and phenols

Katkar, Kamlesh V.,Veer, Sachin D.,Akamanchi, Krishnacharya G.

supporting information, p. 1893 - 1901 (2016/11/25)

Sulfated tungstate was found to be an effective heterogeneous and reusable catalyst for hydroxy group activation–mediated preparation of benzylic ethers including p-methoxybenzylic ethers of a wide range of alcohols and phenols under mild reaction conditions.

A general method for the preparation of ethers using water-resistant solid lewis acids

Corma, Avelino,Renz, Michael

, p. 298 - 300 (2008/02/08)

(Chemical Equation Presented) This most ethereal of cascades: Water-resistant single isolated Lewis acids within the framework of molecular sieves act as excellent general catalysts for the synthesis of ethers (see scheme). On this basis, an environmentally friendly process has been developed for the preparation of fine chemicals that involves a one-pot Meerwein-Ponndorf-Verley reduction/etherification cascade.

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