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Phenol 85, also known as 85% phenol solution, is a widely used chemical compound with the chemical formula C6H5OH. It is a colorless crystalline solid that is soluble in water and has a distinctive smell. Phenol 85 is primarily used as a disinfectant and preservative in various applications, such as medical and industrial settings, due to its ability to denature proteins and disrupt the cell membranes of microorganisms. It is also used in the production of resins, plastics, and pharmaceuticals. However, it is important to note that phenol is toxic and can cause skin irritation, burns, and respiratory issues if not handled properly.

6029-54-5

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6029-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6029-54-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6029-54:
(6*6)+(5*0)+(4*2)+(3*9)+(2*5)+(1*4)=85
85 % 10 = 5
So 6029-54-5 is a valid CAS Registry Number.

6029-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-[[4-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]piperazin-1-yl]methyl]phenol

1.2 Other means of identification

Product number -
Other names N,N-bis(3,5-di-tert-butyl-4-hydroxybenzyl)piperazine

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:6029-54-5 SDS

6029-54-5Downstream Products

6029-54-5Relevant academic research and scientific papers

Reaction of 3,5-Di-tert-butyl-4-hydroxybenzyl Acetate with Amines

Bukharov,Nugumanova,Mukmeneva

, p. 1605 - 1608 (2007/10/03)

3,5-Di-tert-butyl-4-hydroxybenzyl acetate reacts with primary and secondary amines to give mainly the corresponding benzylamines. Base-catalyzed transformation of 3,5-di-tert-butyl-4-hydroxybenzyl acetate into 2,6-di-tert-butyl-4-methylene-2,5-cyclohexadienone occurs to a small extent. The major product of the reaction of 3,5-di-tert-butyl-4-hydroxybenzyl acetate with aqueous ammonia is bis(3,5-di-tert-butyl-4-hydroxybenzyl) ether which is formed by the action of ammonium acetate liberated during the process.

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