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28084-48-2

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28084-48-2 Usage

General Description

4-Hydroxyphenyl 4-hydroxybenzoate, also known as p-hydroxyphenyl p-hydroxybenzoate, is a chemical compound belonging to the class of phenylbenzoates. It is commonly used as a UV filter in sunscreen and cosmetic products due to its ability to absorb and block harmful UV radiation. 4-Hydroxyphenyl 4-hydroxybenzoate exhibits strong antioxidant properties, which makes it effective in protecting the skin from the damaging effects of free radicals and UV-induced oxidative stress. Additionally, 4-Hydroxyphenyl 4-hydroxybenzoate has been studied for its potential as an anticancer agent and for its ability to modulate inflammatory responses in the skin. Overall, this chemical serves an important role in the formulation of sunscreens and skincare products for its photoprotective and skin-soothing properties.

Check Digit Verification of cas no

The CAS Registry Mumber 28084-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,8 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28084-48:
(7*2)+(6*8)+(5*0)+(4*8)+(3*4)+(2*4)+(1*8)=122
122 % 10 = 2
So 28084-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O4/c14-10-3-1-9(2-4-10)13(16)17-12-7-5-11(15)6-8-12/h1-8,14-15H

28084-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-hydroxyphenyl) 4-hydroxybenzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid,4-hydroxy-,4-hydroxyphenyl ester

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:28084-48-2 SDS

28084-48-2Relevant articles and documents

Liquid crystal elastomer actuator with serpentine locomotion

Wang, Meng,Hu, Xin-Bao,Zuo, Bo,Huang, Shuai,Chen, Xu-Man,Yang, Hong

, p. 7597 - 7600 (2020)

A snake-mimic soft actuator composed of a bilayered liquid crystal elastomer ribbon and two serrated feet is reported in this work. Under repeated on/off near-infrared light irradiation, this actuator can move forward relying on a reversible shape morphin

Epoxy compound, composition, material for semiconductor package, molded product, electrical and electronic device, and semiconductor package

-

Paragraph 0221-0226, (2021/05/15)

Epoxy compounds, compositions, materials for semiconductor packages, molded products, electrical and electronic devices, and semiconductor packages are provided. The epoxy compound is represented by the following Chemical Formula 1 and has at least one mesogenic naphthalene unit. In Chemical Formula 1, at least one of M1, M2, or M3, which is a mesogenic unit, is a naphthalene unit. M1, M2, M3, L1, L2, and E1 and E2 are as defined in the detailed description. The chemical formula (1) is E1-M1-L1-M2-L2-M3-E2.

SuFEx-based synthesis of polysulfates

Dong, Jiajia,Sharpless, K. Barry,Kwisnek, Luke,Oakdale, James S.,Fokin, Valery V.

supporting information, p. 9466 - 9470 (2014/11/07)

High-molecular-weight polysulfates are readily formed from aromatic bis(silyl ethers) and bis(fluorosulfates) in the presence of a base catalyst. The reaction is fast and proceeds well under neat conditions or in solvents, such as dimethyl formamide or N-methylpyrrolidone, to provide the desired polymers in nearly quantitative yield. These polymers are more resistant to chemical degradation than their polycarbonate analogues and exhibit excellent mechanical, optical, and oxygen-barrier properties. High-molecular-weight polysulfates are readily formed from aromatic bis(silyl ethers) and bis(fluorosulfates) in the presence of a base catalyst. The polymers were obtained in nearly quantitative yield under neat conditions, they are more resistant to chemical degradation than their polycarbonate analogues and exhibit excellent mechanical, optical, and oxygen-barrier properties. BPA=bisphenol A.

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