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2-tert-butyl-5-ethylphenol is an organic compound with the molecular formula C12H18O. It is a derivative of phenol, characterized by the presence of a tert-butyl group (a methyl group attached to a tertiary carbon) at the 2-position and an ethyl group at the 5-position on the phenol ring. 2-tert-butyl-5-ethylphenol is known for its antioxidant properties and is commonly used as a stabilizer in the polymer industry to prevent degradation caused by heat, light, and oxygen exposure. It is also used as a preservative in various applications due to its ability to inhibit the growth of microorganisms. The compound is a colorless to pale yellow liquid with a distinctive odor and is insoluble in water but soluble in organic solvents.

4237-25-6

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4237-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4237-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,3 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4237-25:
(6*4)+(5*2)+(4*3)+(3*7)+(2*2)+(1*5)=76
76 % 10 = 6
So 4237-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O/c1-5-9-6-7-10(11(13)8-9)12(2,3)4/h6-8,13H,5H2,1-4H3

4237-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butyl-5-ethylphenol

1.2 Other means of identification

Product number -
Other names CTK8D5662

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:4237-25-6 SDS

4237-25-6Downstream Products

4237-25-6Relevant academic research and scientific papers

Selective process for preparting 2,4- or 3,6-di-substituted phenol compounds

-

, (2008/06/13)

A selective process for preparing a 2,4- or 3,6-di-substituted phenol compound which comprises reacting an olefin compound of the formula: STR1 wherein R1 is hydrogen, halogen, alkyl, halogen substituted alkyl, aryl, halogen substituted-aryl or alkyl substituted-aryl; and R2, R3 and R4 are the same or different and each is hydrogen, halogen, alkyl, halogen substituted-alkyl or aralkyl; with a phenol compound of the formula: STR2 wherein R5 is hydrogen, hydroxy, halogen, alkyl, halogen substituted-alkyl, alkoxy or --C(R6)(R7)CH(R8)(R9) (wherein R6 is hydrogen, halogen, alkyl, halogen substituted-alkyl, aryl, halogen substituted-aryl or alkyl substituted-aryl; and R7, R8 and R9 are the same or different and each is hydrogen, halogen, alkyl, halogen substituted-alkyl or aralkyl), in the presence of a phosphorus compound and a carboxylic acid compound as catalysts. The methods of the present invention, which is used a phosphorus compound and a carboxylic acid compound as catalysts, are enable to make the separation procedures easy, make the reaction process and time short, not to produce any colored resultant product, and reduce that cost in manufacturing procedures.

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