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Sigma-Aldrich

Poly(ethylene glycol) diacrylate

average MN 575, cross-linking reagent polymerization reactions, acrylate, 400-600 ppm MEHQ as inhibitor

Synonym(s):

Polyethylene glycol, PEG diacrylate

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

product name

Poly(ethylene glycol) diacrylate, average Mn 575

form

liquid

mol wt

average Mn 575

contains

400-600 ppm MEHQ as inhibitor

reaction suitability

reagent type: cross-linking reagent
reaction type: Polymerization Reactions

refractive index

n20/D 1.467

viscosity

57 cP(25 °C)(lit.)

solubility

H2O: soluble

density

1.12 g/mL at 25 °C

Ω-end

acrylate

α-end

acrylate

polymer architecture

shape: linear
functionality: homobifunctional

storage temp.

2-8°C

SMILES string

OCCO.OC(=O)C=C

InChI

1S/C8H10O4/c1-3-7(9)11-5-6-12-8(10)4-2/h3-4H,1-2,5-6H2

InChI key

KUDUQBURMYMBIJ-UHFFFAOYSA-N

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Application

Dental compounds, offset inks, varnishes and flexible coatings.

Features and Benefits

Contributes to chemical resistance, flexibility, adhesion, low shrinkage, abrasion resistance and impact strength.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

219.2 °F

Flash Point(C)

104 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Chueh-Yu Wu et al.
Advanced materials (Deerfield Beach, Fla.), 27(48), 7970-7978 (2015-10-29)
Microparticles with complex 3D shape and composition are produced using a novel fabrication method, optical transient liquid molding, in which a 2D light pattern exposes a photopolymer precursor stream shaped along the flow axis by software-aided inertial flow engineering.
Ruohong Shi et al.
Small (Weinheim an der Bergstrasse, Germany), 16(37), e2002946-e2002946 (2020-08-11)
Hydrogels with the ability to change shape in response to biochemical stimuli are important for biosensing, smart medicine, drug delivery, and soft robotics. Here, a family of multicomponent DNA polymerization motor gels with different polymer backbones is created, including acrylamide-co-bis-acrylamide

Articles

Scientists at Sigma-Aldrich® routinely determine number-average molecular weight (Mn) by 1H NMR end-group analysis for polymers having Mn values under 3,000.

In this article, we will discuss the benefits and limitations of several 2D and 3D scaffold patterning techniques that can be applied in the presence of cells. Although these methods will be discussed in the context of poly(ethylene glycol) (PEG)-based hydrogels, they can technically be applied to any optically transparent, photoactive substrate.

Protocols

We presents an article regarding Polymer Analysis by NMR.

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