Log In Sign up
The largest database of trusted experimental protocols

Isobornyl acrylate iba

Manufactured by Merck Group
Visit Supplier

Isobornyl acrylate (IBA) is a chemical compound used in the production of various polymers and acrylic resins. It serves as a monomer, contributing to the formation of larger molecular structures. The core function of IBA is to provide specific physical and chemical properties to the end products.

Automatically generated - may contain errors

Lab products found in correlation

Sodium bicarbonate, by Thermo Fisher Scientific (1 mentions) Sodium chloride (nacl), by Carl Roth (1 mentions) Sodium sulfate, by Merck Group (1 mentions) Acetic anhydride, by Merck Group (1 mentions) Azobisisobutyronitrile, by Merck Group (1 mentions) Methyl acrylate ma, by Merck Group (1 mentions) Trioxane, by Merck Group (1 mentions) Acetic acid, by Cambridge Isotopes (1 mentions) Biphenyl, by Merck Group (1 mentions) Acryloyl chloride, by Thermo Fisher Scientific (1 mentions) Cyanomethyl dodecyl trithiocarbonate, by Merck Group (1 mentions) Cdcl3, by Cambridge Isotopes (1 mentions) 2 5 bis 5 tert butyl benzoxazol 2 yl thiophene bbot, by Merck Group (1 mentions)

Close spelling variants of this product

Isobornyl acrylate (13 citations)

2 protocols using isobornyl acrylate iba

1

Synthesis and Purification of Polymeric Reagents

Check if the same lab product or an alternative is used in the 5 most similar protocols
Azobisisobutyronitrile
(AIBN, Sigma-Aldrich) was recrystallized from methanol prior to use.
Isobornyl acrylate (IBA; technical, Sigma-Aldrich) and lauryl acrylate
(LA; >98%, TCI) were passed over a basic alumina column prior to
use
to remove the stabilizer. Methyl acrylate (MA; 99%, Sigma-Aldrich)
was distilled prior to use. Pyridine, dichloromethane (DCM), and triethylamine
were distilled over calcium hydride (CaH2) prior to use.
Cyanomethyl dodecyl trithiocarbonate (CDT) was synthesized according
to a procedure mentioned in the literature.44 (link) 2-(Dodecylthiocarbonothioylthio)-2-methylpropionic acid (DDMAT;
98%, Sigma-Aldrich), trioxane (≥99%, Sigma-Aldrich), biphenyl
(>99%, Sigma-Aldrich), acetophenone (AP; 99%, Sigma-Aldrich), sodium
sulfate (≥99%, Sigma-Aldrich), acetic anhydride (≥99%,
Sigma-Aldrich), trans-2-[3-(4-tert-butylphenyl)-2-methyl-2-propenylidene]-malononitrile (DCTB; Sigma-Aldrich,
>98%), potassium trifluoroacetate (KTFA; Sigma-Aldrich, 98%), acryloyl
chloride (96%, Alfa Aesar), furfuryl alcohol (≥98%, Fischer
Scientific), hydrogen chloride (HCl; 37% solution in H2O, Acros Organics), sodium bicarbonate (>99%, Acros organics),
sodium
chloride (≥99.8%, Roth), tert-butyl methylether
(TBME; 99.9%), acetic acid (AcOH; 99.7%), and CDCl3 (99.8%,
Cambridge Isotope Laboratories) were used as received. All other solvents
were obtained from Biosolve and were used as received.
Stouten J., Vanpoucke D.E., Van Assche G, & Bernaerts K.V. (2020). UV-Curable Biobased Polyacrylates Based on a Multifunctional Monomer Derived from Furfural. Macromolecules, 53(4), 1388-1404.
+ Open protocol
+ Expand
2

Functionalized Borosilicate Glass Surfaces

Check if the same lab product or an alternative is used in the 5 most similar protocols
Borosilicate glass surfaces, in either slide form (Fisher Scientific) or large plate form (McMaster-Carr), were used as the substrates for surface functionalization. Silane coupling agents with different organofunctional groups (Gelest) were all used as received for fabrication of model functionalized surfaces (Table 1). Ethanol (EtOH, Fisher Scientific) was used as received for hydrolysis and condensation of silane coupling agents onto the substrates. Ebecryl 230 (Allnex), isobornyl acrylate (IBA, Sigma-Aldrich), diphenyl (2,4,6-trimethylbenzoyl) phophine oxide (TPO, Sigma-Aldrich), and 2,5-bis(5-tert-butyl-benzoxazol-2-yl) thiophene (BBOT, Sigma-Aldrich) were used as received for the urethane acrylate resin system. Molded polytetrafluoroethylene (PTFE) bars were acquired from McMaster-Carr. All other chemicals in this work were used as received from Sigma-Aldrich.
Wang Y., Hansen C.J., Wu C.C., Robinette E.J, & Peterson A.M. (2021). Effect of surface wettability on the interfacial adhesion of a thermosetting elastomer on glass. RSC Advances, 11(49), 31142-31151.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!