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2,6-DIISOPROPYL-4-METHYLPHENOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20766-99-8

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20766-99-8 Usage

Appearance

White, waxy solid

Odor

Slight phenolic odor

Use

Antioxidant and preservative in food, cosmetics, and pharmaceuticals

Solubility

Soluble in organic solvents, insoluble in water

Function

Prevents oxidation and prolongs shelf life in fatty foods and oils

Additional Properties

Exhibits antimicrobial properties

Applications

Used in personal care products to prevent rancidity and spoilage

Regulatory Approval

Approved for use in food and cosmetics by regulatory agencies

Controversy

Some studies suggest potential links to cancer and other adverse health outcomes

Check Digit Verification of cas no

The CAS Registry Mumber 20766-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,6 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20766-99:
(7*2)+(6*0)+(5*7)+(4*6)+(3*6)+(2*9)+(1*9)=118
118 % 10 = 8
So 20766-99-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O/c1-8(2)11-6-10(5)7-12(9(3)4)13(11)14/h6-9,14H,1-5H3

20766-99-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2,6-di(propan-2-yl)phenol

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-1-methyl-3.5-diisopropyl-benzol

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:20766-99-8 SDS

20766-99-8Relevant academic research and scientific papers

LiAIH4 promoted reductive deoxygenation of hydroxybenzyl alcohols via benzoquinone methide intermediates

Baik, Woonphil,Lee, Hyun Joo,Koo, Sangho,Kim, Byeong Hyo

, p. 8125 - 8128 (2007/10/03)

Primary and secondary hydroxybenzyl alcohols react with LiAIH4 in chlorobenzene to give the corresponding alkylphenols. The reaction proceeds through the formation of benzoquinone methide as an intermediate. An example of [4+2] cycloaddition of benzoquinone methide is also reported.

Phenol transalkylation process

-

, (2008/06/13)

Phenols having an unsubstituted ortho position are transalkylated in the ortho position by mixing them with an ortho-alpha-branched alkylphenol (e.g., 2,6-di-sec-butylphenol) and an aluminum phenoxide catalyst and heating the mixture to 100°-350°C., preferably in a closed system and in the presence of olefin corresponding in structure to the ortho-alpha-branched alkyl group.

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