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THPA, also known as Trimethylolpropane triacrylate, is a multifunctional monomer used in the polymer and coatings industry. It is a colorless to pale yellow liquid with a slight odor and is known for its excellent compatibility with various monomers and resins. THPA enhances the performance properties of the final product, such as adhesion, flexibility, and durability.

52858-57-8

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52858-57-8 Usage

Uses

Used in Photoresist Applications:
THPA is used as a monomer in the formation of photoresists, which are essential in the semiconductor industry for the production of microelectronic components. Its use in photoresists allows for the creation of high-resolution patterns on silicon wafers during the manufacturing process.
Used in Coatings Industry:
THPA is used as a comonomer in the coatings industry to improve the adhesion, flexibility, and durability of the final product. Its compatibility with various monomers and resins makes it a valuable addition to the formulation of coatings, inks, and adhesives.
Used as a Protected Acrylic Acid:
THPA can also be used as a protected acrylic acid, which is beneficial in various chemical reactions and processes. The protection of the acrylic acid group allows for controlled reactions and can improve the overall efficiency of the process.

Check Digit Verification of cas no

The CAS Registry Mumber 52858-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,5 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52858-57:
(7*5)+(6*2)+(5*8)+(4*5)+(3*8)+(2*5)+(1*7)=148
148 % 10 = 8
So 52858-57-8 is a valid CAS Registry Number.

52858-57-8 Well-known Company Product Price

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  • Aldrich

  • (790567)  2-Tetrahydropyranyl acrylate  contains <500 ppm inhibitor, ≥97%

  • 52858-57-8

  • 790567-5G

  • 2,713.23CNY

  • Detail

52858-57-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name oxan-2-yl prop-2-enoate

1.2 Other means of identification

Product number -
Other names tetrahydropyranyl acrylate

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:52858-57-8 SDS

52858-57-8Downstream Products

52858-57-8Relevant academic research and scientific papers

Microfluidically fabricated pH-responsive anionic amphiphilic microgels for drug release

Lu,Tarn,Pamme,Georgiou

, p. 3086 - 3093 (2016)

Amphiphilic microgels of different composition based on the hydrophilic, pH-responsive acrylic acid (AA) and the hydrophobic, non-ionic n-butyl acrylate (BuA) were synthesised using a lab-on-a-chip device. Hydrophobic droplets were generated via a microfluidic platform that contained a protected form of AA, BuA, the hydrophobic crosslinker, ethylene glycol dimethacrylate (EGDMA), and a free radical initiator in an organic solvent. These hydrophobic droplets were photopolymerised within the microfluidic channels and subsequently hydrolysed, enabling an integrated platform for the rapid, automated, and in situ production of anionic amphiphilic microgels. The amphiphilic microgels did not feature the conventional core-shell structure but were instead based on random amphiphilic copolymers of AA and BuA and hydrophobic crosslinks. Due to their amphiphilic nature they were able to encapsulate and deliver both hydrophobic and hydrophilic moieties. The model drug delivery and the swelling ability of the microgels were influenced by the pH of the surrounding aqueous solution and the hydrophobic content of the microgels.

Tailoring pH-responsive acrylic acid microgels with hydrophobic crosslinks for drug release

Lu,Tarn,Pamme,Georgiou

, p. 4524 - 4529 (2015)

Amphiphilic microgels based on the hydrophilic acrylic acid (AA) and hydrophobic crosslinks of different compositions were synthesised using a lab-on-a-chip device. The microgels were formed by polymerising hydrophobic droplets. The droplets were generated via a microfluidic platform and contained a protected form of AA, a hydrophobic crosslinker (ethylene glycol dimethacrylate, EGDMA) and a free radical initiator in an organic solvent. Following photopolymerisation and subsequent hydrolysis, AA based microgels of amphiphilic nature were produced and it was demonstrated that they can successfully deliver both hydrophilic as well as hydrophobic moieties. The model drug delivery and the swelling ability of the microgels were influenced by the pH of the aqueous solution as well as the crosslinking density and hydrophobic content of the microgels.

Catalyzed process for reacting carboxylic acids with vinyl ethers

-

, (2008/06/13)

The present invention relates to a process for the reaction of carboxylic acids with vinyl ethers using a non-polymeric pyridine hydrochloride and/or polymeric vinylpyridine hydrochloride as a catalyst.

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