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2,6-di-tert-butyl-4-(1-phenylethyl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17540-76-0

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17540-76-0 Usage

General Description

2,6-di-tert-butyl-4-(1-phenylethyl)phenol, also known as propylparaben or E216, is a chemical compound commonly used as a preservative in various products, including pharmaceuticals, personal care products, and food. It is known for its antimicrobial properties, which help to prevent the growth of bacteria, mold, and yeast in these products. Despite its widespread use, there has been some concern about potential health risks associated with propylparaben, particularly in relation to its estrogenic activity and potential endocrine-disrupting effects. As a result, some regulatory agencies have imposed restrictions on its use, and there is ongoing research into its safety and potential alternatives.

Check Digit Verification of cas no

The CAS Registry Mumber 17540-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,4 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17540-76:
(7*1)+(6*7)+(5*5)+(4*4)+(3*0)+(2*7)+(1*6)=110
110 % 10 = 0
So 17540-76-0 is a valid CAS Registry Number.

17540-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-(1-phenylethyl)phenol

1.2 Other means of identification

Product number -
Other names 4-(1-phenylethyl)-2,6-ditert-butyl-phenol

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:17540-76-0 SDS

17540-76-0Relevant academic research and scientific papers

B(C6F5)3 catalyzed direct nucleophilic substitution of benzylic alcohols: an effective method of constructing C-O, C-S and C-C bonds from benzylic alcohols

Meng, Shan-Shui,Wang, Qian,Huang, Gong-Bin,Lin, Li-Rong,Zhao, Jun-Ling,Chan, Albert S. C.

, p. 30946 - 30949 (2018/09/13)

An efficient and general method of nucleophilic substitution of benzylic alcohols catalyzed by non-metallic Lewis acid B(C6F5)3 was developed. The reaction could be carried out under mild conditions and more than 35 exampl

A [...] alcohol compound arylation method

-

Paragraph 0033-0035, (2019/01/08)

The invention belongs to the field of organic synthesis, discloses a [...] alcohol compound arylation of the method, the animal pen alcohol type compounds with aryl compound mixed, added to the solvent with the catalyst 35 fluorine phenyl borane, 60 - 120

Polybutylbenzylphenols and benzyl-3,4-methylenedioxybenzenes in insect population control

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, (2008/06/13)

Certain polybutylbenzylphenols and benzyl-3,4-methylenedioxybenzenes are useful for insect control especially as insect chemosterilants and oviposition inhibitors. The benzyl-3,4-methylenedioxybenzenes also find utility as growth inhibitors for mosquito larvae.

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