2,2-Bis((acryloyloxy)methyl)propane-1,3-diyl diacrylate,80%(stabilized with MEHQ)

Name: 2,2-Bis((acryloyloxy)methyl)propane-1,3-diyl diacrylate,80%(stabilized with MEHQ)
Brand: ChemScene
Availability: InStock
Rating: 5 (1 reviews)

CAS No. 4986-89-4
Cat. No. CS-0143144
Molecule weight352.34
Purity80%(stabilized with MEHQ)
MDL No.MFCD00015334

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Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
Inaccessible (Haz class 6.1 or 9), Domestic	$68.00+
Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
Accessible (Haz class 3, 4, 5 or 8), International	$238.00+

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2,2-Bis((acryloyloxy)methyl)propane-1,3-diyl diacrylate,80%(stabilized with MEHQ)|CS-0143144

Structure of 4986-89-4

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General Information

CAS No. 4986-89-4
Cat. No. CS-0143144
Purity 80%(stabilized with MEHQ)
MDL No. MFCD00015334
Storage 4°C, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₇H₂₀O₈
Molecular Weight 352.34
Synonym(s) Pentaerythritol tetraacrylate
SMILES C=CC(OCC(COC(C=C)=O)(COC(C=C)=O)COC(C=C)=O)=O

Description

Pentaerythritol tetraacrylate (PETA) is a hydrophobic tetrafunctional monomer that is majorly used as a crosslinking agent that facilitates an improvement in the surface morphology of the polymeric material. It can be synthesized by the suspension of pentaerythritol in the solution of triethylamine and dichloromethane. PETA can be used in coatings, adhesives, sealants, surface coating, and composites. Its reactivity and ability to form densely crosslinked networks make it an essential component in the formulation of UV-curable materials. PETA is also used as a key component in the preparation of biocompatible polypeptide-based interpenetrating network (IPN) hydrogels, which find applications in tissue engineering, drug delivery systems, or biomedical devices.Pentaerythritol tetraacrylate can be used as a monomer:To synthesize polymer electrolytes for the fabrication of lithium-sulfur batteries.In the formulation of UV-curable epoxy acrylate coatings, to improve their mechanical properties and performance.To prepare multifunctional silicone acrylate prepolymers for use in UV-curable coatings, to improve their mechanical and anti-oxygen inhibition properties.In the UV-curable ink formulations.

Synthesis

Route1
- 115-77-5
- 814-68-6
- ~99%
- In-stock
  
  4986-89-4
References
- Ma, Xinpeng; Zhou, Zhuxian; Jin, Erlei; Sun, Qihang; Zhang, Bo; Tang, Jianbin; Shen, Youqing Macromolecules, 2013 , vol. 46, # 1 p. 37 - 42
Route2
- 504-61-0
- 115-77-5
- In-stock
  
  150-76-5
- 79-10-7
- ~%
- In-stock
  
  4986-89-4
References
- Bayer Aktiengesellschaft Patent: US4059721 A1, 1977 ;

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H315-H317-H319
Precautionary Statements : P261-P264-P272-P280-P302+P352-P362-P501

Quality Control

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Computational Chemistry Data

TPSA 105.2
LogP 0.8896
H_Acceptors 8
H_Donors 0
Rotatable_Bonds 12

Other Classifications

Building Blocks Functional Group Ester

Building Blocks Skeleton Fatty chain compounds

Material Science Polymer Materials Macromolecular Monomer

Material Science Polymer/Macromolecule Reagents Monomers Acrylic Monomers

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2,2-Bis((acryloyloxy)methyl)propane-1,3-diyl diacrylate,80%(stabilized with MEHQ)

CAS No. 4986-89-4

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