25266-13-1

Basic information

• Product Name: 2-OCTYL ACRYLATE POLYMER
• Synonyms: Poly(n-octyl acrylate) (in Toluene;PolynoctylacrylateintolueneUnitweightdoesnotincludewto;2-OCTYL ACRYLATE POLYMER;POLY(2-OCTYL ACRYLATE);POLY(N-OCTYL ACRYLATE);N-OCTYL ACRYLATE POLYMER;2-propenoicacid,octylester,homopolymer;Poly(2-octyl acrylate) (in toluene
• CAS NO: 25266-13-1
• Molecular Formula: C11 H20 O2
• Molecular Weight: 184.28
• Mol File: 25266-13-1.mol
• Article Data: 22

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-OCTYL ACRYLATE POLYMER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-OCTYL ACRYLATE POLYMER(25266-13-1)
• EPA Substance Registry System: 2-OCTYL ACRYLATE POLYMER(25266-13-1)

Safety Data

• Hazardous Substances Data: 25266-13-1(Hazardous Substances Data)

Usage

Description

2-Octyl acrylate polymer, also known as poly(2-octyl acrylate), is a synthetic polymer that is commonly used in the production of adhesives, sealants, coatings, and various other industrial and consumer products. It is a viscous liquid at room temperature and is known for its flexibility, high elongation, and good adhesion properties. The polymer is often used as a base material for pressure-sensitive adhesives, particularly in applications that require a strong bond with flexible substrates. Additionally, it can be modified with various additives to enhance its performance and tailor it to specific applications. Overall, 2-octyl acrylate polymer is a versatile and valuable material in the field of polymer chemistry and industrial manufacturing.

Uses

Used in Adhesives and Sealants Industry:
2-Octyl acrylate polymer is used as a base material for pressure-sensitive adhesives for its strong bond with flexible substrates and good adhesion properties.
Used in Coatings Industry:
2-Octyl acrylate polymer is used in the production of coatings due to its flexibility and high elongation, making it suitable for various applications.
Used in Consumer Products:
2-Octyl acrylate polymer is used in the manufacturing of various consumer products, such as tapes and labels, due to its strong adhesion and flexibility.
Used in Industrial Manufacturing:
2-Octyl acrylate polymer is used in industrial manufacturing for its versatility and ability to be modified with various additives to enhance its performance and tailor it to specific applications.

Upstream product

• 111-87-5 octanol 
• 74-86-2 acetylene 
• 79-10-7 acrylic acid 
• 814-68-6 acryloyl chloride 
• 140-88-5 ethyl acrylate 
• 1663-39-4 tert-Butyl acrylate 
• 292638-85-8 acrylic acid methyl ester 
• 123563-83-7 8-bromooctyl acrylate 
• 629-41-4 1,8-Octanediol 
• 79918-35-7 8-iodo-1-octanol 
• 50816-19-8 8-bromooctanol 
• 109182-97-0 Acrylic acid 8-iodo-octyl ester 
• 2177-18-6 vinyl acrylate 
• 3840-67-3 sulfuric acid mono-(2-carbamoyl-ethyl) ester 

Relevant articles and documents

Hydrophobic Nanoparticles Reduce the β-Sheet Content of SEVI Amyloid Fibrils and Inhibit SEVI-Enhanced HIV Infectivity

Semen-derived enhancer of virus infection (SEVI) fibrils are naturally abundant amyloid aggregates found in semen that facilitate viral attachment and internalization of human immunodeficiency virus (HIV) in cells, thereby increasing the probability of infection. Mature SEVI fibrils are composed of aggregated peptides exhibiting high β-sheet secondary structural characteristics. Herein, we show that polymers containing hydrophobic side chains can interact with SEVI and reduce its β-sheet content by ～45% compared with the β-sheet content of SEVI in the presence of polymers with hydrophilic side chains, as estimated by polarization modulation-infrared reflectance absorption spectroscopy measurements. A nanoparticle (NP) formulation of this hydrophobic polymer reduced SEVI-mediated HIV infection in TMZ-bl cells by 60% compared with the control treatment. Although these NPs lacked specific amyloid-targeting groups, thus requiring high concentrations to observe biological activity, the use of hydrophobic interactions to alter the secondary structure of amyloids represents a useful approach to neutralizing the SEVI function. These results could, therefore, have general implications in the design of novel materials that can modify the activity of amyloids associated with a variety of other neurological and systemic diseases.

METHODS OF MAKING (ALK)ACRYLIC ESTERS IN FLOW REACTORS

A method of making an (alk)acrylic ester in a microflow reactor.

PROCESS FOR PREPARING 4-HYDROXYBUTYL ACRYLATE

A process for preparing 4-hydroxybutyl acrylate by transesterifying an alkyl acrylate with 1,4-butanediol in the presence of a dialkyltin oxide such that each of the alkyl groups has 4 to 8 carbon atoms, characterized in that the amount of the dialkyltin oxide is adjusted to 0.00001 to 0.01 moles per one mole of the alkyl acrylate.