Welcome to LookChem.com Sign In|Join Free
  • or
Pentaerythritol tetramethylacrylate (PETA) is a colorless, transparent, and viscous liquid chemical compound with the molecular formula C13H18O8. It is derived from pentaerythritol, a tetrafunctional alcohol, and methacrylic acid, an unsaturated carboxylic acid. PETA is widely used as a reactive diluent in the production of various types of acrylic resins, such as pressure-sensitive adhesives, UV-curable coatings, and optical lenses. It serves to reduce the viscosity of the resin mixture, improve the processability, and enhance the final product's performance. PETA is also known for its excellent compatibility with other monomers and its ability to improve the mechanical properties and weather resistance of the resulting polymers.

3253-41-6

Post Buying Request

3253-41-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

3253-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3253-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,5 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3253-41:
(6*3)+(5*2)+(4*5)+(3*3)+(2*4)+(1*1)=66
66 % 10 = 6
So 3253-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H28O8/c1-12(2)16(22)26-11-20(9,10)21(27-17(23)13(3)4,28-18(24)14(5)6)29-19(25)15(7)8/h1,3,5,7,11H2,2,4,6,8-10H3

3253-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name PENTAERYTHRITOL TETRAMETHACRYLATE

1.2 Other means of identification

Product number -
Other names 2,2-bis[[(2-methyl-1-oxoallyl)oxy]methyl]-1,3-propanediyl bismethacrylate

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:3253-41-6 SDS

3253-41-6Relevant academic research and scientific papers

A containing 2, 6 - di-tert-butyl phenol anti-oxidant and its preparation method

-

Paragraph 0020; 0055; 0056, (2017/09/26)

The invention reveals a 2,6-di-tert-butylphenol-containing anti-oxidant and a novel preparation method thereof. The method takes titanium, zirconium, hafnium, bismuth, antimony metal complexes as green catalysts, a two-step system is substituted by a series reaction one step method technology, and a high efficiency metal complex catalyst capable of simultaneously catalyzing a direct esterification reaction and a Michael addition reaction is employed to prepare the novel anti-oxidant. The method takes acrylic acid (or acrylic acid ester), pentaerythritol and 2,6-di-tert-butylphenol as main raw materials, under organic solvent or solvent-free condition, the titanium, zirconium, hafnium, bismuth, antimony metal complex green catalysts are reacted to obtain the novel anti-oxidant with high yield. The method has the advantages of low cost, high yield, simple operation and no pollution, and has certain feasibility for realizing industrial production. The preparation method is the green approach with low cost.

Photo-initiated thiol-ene "click" hydrogels from RAFT-synthesized poly(N-isopropylacrylamide)

Ooi, Huey Wen,Jack, Kevin S.,Whittaker, Andrew K.,Peng, Hui

, p. 4626 - 4636 (2013/10/21)

Despite the efficiency and robustness of the widely used copper-catalyzed 1,3-dipolar cycloaddition reaction, the use of copper as a catalyst is often not attractive, particularly for materials intended for biological systems. The use of photo-initiated thiol-ene as an alternative "click" reaction to synthesize "model networks" is investigated here. Poly(N- isopropylacrylamide) precursors were synthesized by reversible addition fragmentation chain transfer (RAFT) polymerization and were designed to have trithiocarbonate moieties as end groups. This structure design provides opportunity for subsequent end-group modifications in preparation for thiol-ene "click." Two reaction routes have been proposed and studied to yield thiol and ene moieties. The advantages and disadvantages of each reaction path were investigated to propose a simple but efficient route to prepare copper-free "click" hydrogels.

Process for the Preparation of (Meth)Acrylates of Tetra-Or Polyhydric Alcohols

-

Page/Page column 3, (2008/12/07)

Process for the preparation of acrylic and methacrylic acid esters by transesterification of (meth)acrylic acid esters of the formula I: where R1 is H or CH3 and R2 is an alkyl radical having 1 to 40 carbon atoms, with alkanols which have four or more esterifiable hydroxyl groups, characterized in that 0.01 to 10% by weight, based on the total reaction mixture, of lithium amide catalysts are used as transesterification catalyst.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 3253-41-6