Category: 2495-37-6

Ester is a chemical compound derived from an oxoacid (organic or inorganic) in which at least one –OH hydroxyl group is replaced by an –O– alkyl (alkoxy) group, 2495-37-6, formula is C11H12O2, Name is Benzyl methacrylate. as in the substitution reaction of a carboxylic acid and an alcohol. Recommanded Product: Benzyl methacrylate.

Zhu, Yifan;Jin, Tao;Lian, Tianquan;Egap, Eilaf research published 《 Enhancing the efficiency of semiconducting quantum dot photocatalyzed atom transfer radical polymerization by ligand shell engineering》, the research content is summarized as follows. Manipulating the ligand shell of semiconducting quantum dots (QDs) has proven to be a promising strategy to enhance their photocatalytic performance for small mol. transformations, such as H₂ evolution and CO₂ reduction However, ligand-controlled catalysis for macromols., which differ from small mols. in penetrability and charge transfer behavior due to their bulky sizes, still remains undiscovered. Here, we systematically investigate the role of surface ligands in the photocatalytic performance of cadmium selenide (CdSe) QDs in light-induced atom transfer radical polymerization (ATRP) by using thiol-based ligands with various polarities and chain lengths. A highly enhanced polymerization efficiency was observed when 3-mercapto propionic acid (MPA), a short-chain and polar ligand, was used to modify the CdSe QDs’ surface, achieving high chain-end fidelity, good temporal control, and a dispersity of 1.18, while also tolerating a wide-range of functional monomers ranging from acrylates to methacrylates and fluorinated monomers. Transient absorption spectroscopy and time-resolved photoluminescence studies reveal interesting mechanistic details of electron and hole transfers from the excited QDs to the initiators and 3-MPA capping ligands, resp., providing key mechanistic insight of these ligand controlled and QD photocatalyzed ATRP processes. The thiolate ligands were found to serve as an efficient hole acceptor for QDs, which facilitates the formation of a charge-separated state, followed by electron transfer from the conduction band edge to initiators and ultimately suppressing charge recombination within the QD. (c) 2021 American Institute of Physics.

2495-37-6, Benzyl methacrylate, also known as Benzyl methacrylate, is a useful research compound. Its molecular formula is C11H12O2 and its molecular weight is 176.21 g/mol. The purity is usually 95%.
Benzyl methacrylate is a chemical compound that belongs to the group of benzyl compounds. It has a copolymer structure with methyl ethyl methacrylate (MEMA) and hydroxyl groups. Benzyl methacrylate is produced by polymerization of benzyl chloride with allyl carbonate in the presence of radiation, forming a polymeric matrix. The morphology of this copolymer depends on the length of the benzyl chains and the concentration of MEMA., Recommanded Product: Benzyl methacrylate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Ester is a chemical compound derived from an oxoacid (organic or inorganic) in which at least one –OH hydroxyl group is replaced by an –O– alkyl (alkoxy) group, 2495-37-6, formula is C11H12O2, Name is Benzyl methacrylate. as in the substitution reaction of a carboxylic acid and an alcohol. HPLC of Formula: 2495-37-6.

Zhu, Ren-Man;Yang, Cheng-Lin;Chang, Zi-Xuan;Pan, Cai-Yuan;Zhang, Wen-Jian;Hong, Chun-Yan research published 《 Synchronous Synthesis of Polymeric Vesicles with Controllable Size and Low-Polydispersity by Polymerization-Induced Self-Assembly》, the research content is summarized as follows. The size and size distribution of polymeric nanoparticles have great impact on their physicochem. and biol. properties. Polymerization-induced self-assembly (PISA) has been demonstrated to be an efficient method to fabricate various polymeric nanoparticles, among which polymeric vesicles have attracted great interest due to their unique hollow structure. However, polymeric vesicles with relatively broad size distributions and random size are normally formed, which is problematic for many potential applications. Herein, we report the synthesis of polymeric vesicles with low-polydispersity and controllable size by polymerization-induced self-assembly. A mixed macro RAFT agent of three different poly(ethylene glycol) (PEG_m-CPADB) was used to mediate the RAFT dispersion copolymerization of 7-(2-methacryloyloxyethoxy)-4-methylcoumarin (CMA) and benzyl methacrylate (BzMA), which generated vesicles with low-polydispersity (< 0.1) and controllable size in the scope of sub-100 nm. In comparison, RAFT dispersion copolymerization of CMA and BzMA using a single PEG-CPADB as the macro RAFT agent generated vesicles with adjustable but obviously larger size and broader size distributions (> 0.1). The results demonstrate that the ternary stabilizers play a crucial role in the formation of small and low-polydispersity vesicles.

HPLC of Formula: 2495-37-6, Benzyl methacrylate, also known as Benzyl methacrylate, is a useful research compound. Its molecular formula is C11H12O2 and its molecular weight is 176.21 g/mol. The purity is usually 95%.
Benzyl methacrylate is a chemical compound that belongs to the group of benzyl compounds. It has a copolymer structure with methyl ethyl methacrylate (MEMA) and hydroxyl groups. Benzyl methacrylate is produced by polymerization of benzyl chloride with allyl carbonate in the presence of radiation, forming a polymeric matrix. The morphology of this copolymer depends on the length of the benzyl chains and the concentration of MEMA., 2495-37-6.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. 2495-37-6, formula is C11H12O2, Name is Benzyl methacrylate. They perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Recommanded Product: Benzyl methacrylate.

Zheng, Mingxin;Ye, Qiquan;Chen, Xi;Zeng, Min;Song, Guangjie;Zhang, Jun;Yuan, Jinying research published 《 In situ generation and evolution of polymer toroids by liquid crystallization-assisted seeded dispersion polymerization》, the research content is summarized as follows. An effective method is presented for preparing high solid content azobenzene-containing triblock copolymer toroidal assemblies by liquid crystallization-assisted seeded dispersion polymerization Vesicles are prepared via polymerization-induced self-assembly (PISA), and used as seeds for further chain extension. By introducing smectic liquid crystalline (LC) ordering into the core-forming block, toroids are formed in situ during the polymerization The morphol. transformation from toroids to barrels is observed under UV irradiation due to the photo-isomerization of the azobenzene mesogens. This strategy expands the scope of tunable anisotropic morphologies for potential functional nanomaterials based on a LC copolymer by seeded dispersion polymerization

Recommanded Product: Benzyl methacrylate, Benzyl methacrylate, also known as Benzyl methacrylate, is a useful research compound. Its molecular formula is C11H12O2 and its molecular weight is 176.21 g/mol. The purity is usually 95%.
Benzyl methacrylate is a chemical compound that belongs to the group of benzyl compounds. It has a copolymer structure with methyl ethyl methacrylate (MEMA) and hydroxyl groups. Benzyl methacrylate is produced by polymerization of benzyl chloride with allyl carbonate in the presence of radiation, forming a polymeric matrix. The morphology of this copolymer depends on the length of the benzyl chains and the concentration of MEMA., 2495-37-6.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Polyesters are important plastics, with monomers linked by ester moieties. Phosphoesters form the backbone of DNA molecules. 2495-37-6, formula is C11H12O2, Name is Benzyl methacrylate.Nitrate esters, such as nitroglycerin, are known for their explosive properties. Product Details of C11H12O2.

Zhao, Maoji;Zhu, Shuaishuai;Yang, Xue;Wang, Yong;Zhou, Xingping;Xie, Xiaolin research published 《 A Porphyrinic Donor-Acceptor Conjugated Porous Polymer as Highly Efficient Photocatalyst for PET-RAFT Polymerization》, the research content is summarized as follows. Heterogeneous catalysts offer a highly desirable platform for exploring environmental-benign transformation systems, yet, they typically suffer from significant loss of catalytic efficiency compared with their homogeneous counterparts. Here, the facile synthesis of a porphyrinic conjugated porous polymer incorporated with imidazolium bromide moieties by taking advantage of the Debus-Radziszewski reaction is reported. Owing to the unique donor-acceptor structure, this heterogeneous and metal-free photocatalyst exhibits much improved catalytic activity compared with its small mol. analogs in photoinduced electron transfer reversible addition-fragmentation chain transfer (PET-RAFT) polymerization, producing polymers with narrow distribution (D = 1.06-1.18) and high degree of chain-end fidelity. Moreover, the heterogeneous catalyst can be easily separated at the end of polymerization by centrifugation and recycled for five independent PET-RAFT polymerizations without obvious decreases in catalytic efficiency.

2495-37-6, Benzyl methacrylate, also known as Benzyl methacrylate, is a useful research compound. Its molecular formula is C11H12O2 and its molecular weight is 176.21 g/mol. The purity is usually 95%.
Benzyl methacrylate is a chemical compound that belongs to the group of benzyl compounds. It has a copolymer structure with methyl ethyl methacrylate (MEMA) and hydroxyl groups. Benzyl methacrylate is produced by polymerization of benzyl chloride with allyl carbonate in the presence of radiation, forming a polymeric matrix. The morphology of this copolymer depends on the length of the benzyl chains and the concentration of MEMA., Product Details of C11H12O2

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. 2495-37-6, formula is C11H12O2, Name is Benzyl methacrylate. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Safety of Benzyl methacrylate.

Zhao, Jing;Han, Muyue;Li, Lin research published 《 Modeling and characterization of shape memory properties and decays for 4D printed parts using stereolithography》, the research content is summarized as follows. The integration of shape memory materials into additive manufacturing has added a new dimension of time to conventional 3D printing and enabled innovative product designs with high tailorability and adaptability. To date, most studies on shape memory effects mainly adopt exptl. approaches to characterize the material responsiveness to various stimulation conditions considering a single thermomech. loading cycle. The information regarding the cyclic shape memory behaviors as well as the potential additive manufacturing-induced impacts on the achieved shape memory performance is limited. In this paper, the shape memory behaviors of the stereolithog. printed thermo-responsive structures are theor. modeled by jointly considering the influences from both the printing process and the shape memory process. The cyclic shape memory effects are anal. characterized and exptl. validated using methacrylate copolymers under iterative thermomech. loadings. Meanwhile, case studies are presented to provide insights into shape memory behaviors upon the impacts of various levels of critical process parameters. The results indicate an exceptional prediction accuracy of 96.24% and 95.73% for the established shape fixity and recovery models, resp. It is also observed that the printing process parameters, including layer thickness and scan speed, have considerable impacts on the shape memory performance of the printed parts.

Safety of Benzyl methacrylate, Benzyl methacrylate, also known as Benzyl methacrylate, is a useful research compound. Its molecular formula is C11H12O2 and its molecular weight is 176.21 g/mol. The purity is usually 95%.
Benzyl methacrylate is a chemical compound that belongs to the group of benzyl compounds. It has a copolymer structure with methyl ethyl methacrylate (MEMA) and hydroxyl groups. Benzyl methacrylate is produced by polymerization of benzyl chloride with allyl carbonate in the presence of radiation, forming a polymeric matrix. The morphology of this copolymer depends on the length of the benzyl chains and the concentration of MEMA., 2495-37-6.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Polyesters are important plastics, with monomers linked by ester moieties. Phosphoesters form the backbone of DNA molecules. 2495-37-6, formula is C11H12O2, Name is Benzyl methacrylate.Nitrate esters, such as nitroglycerin, are known for their explosive properties. Safety of Benzyl methacrylate.

Zhao, Haitao;Li, Haihui;Tian, Chun;Zhang, Lifen;Cheng, Zhenping research published 《 Facile Synthesis of Unimodal Polymethacrylates with Narrow Dispersity via NIR LED Light-Controlled Bromine-Iodine Transformation Reversible-Deactivation Radical Polymerization》, the research content is summarized as follows. A facile and clean strategy for synthesizing unimodal polymethacrylates with narrow dispersity (D < 1.10) is successfully developed by a near-IR (NIR) light-emitting diode (LED) light (λ_max = 740 nm)-controlled in situ bromine-iodine transformation reversible-deactivation radical polymerization system without the use of NIR dyes and expensive catalysts. In this system, alkyl iodide Et α-iodophenylacetate (EIPA) initiator is generated in situ by the nucleophilic substitution reaction between an alkyl bromide compound Et α-bromophenylacetate and sodium iodide (NaI). At the same time, excessive NaI is also acted as a highly active catalyst by forming halogen bonds with terminal iodine of the polymer chains in this system to make it capable of precisely synthesizing polymethacrylates with narrow dispersities (D = 1.03-1.10). In addition, the strong penetration ability of NIR LED light is illustrated by the successful polymerization even through 11 pieces of A4 paper.

2495-37-6, Benzyl methacrylate, also known as Benzyl methacrylate, is a useful research compound. Its molecular formula is C11H12O2 and its molecular weight is 176.21 g/mol. The purity is usually 95%.
Benzyl methacrylate is a chemical compound that belongs to the group of benzyl compounds. It has a copolymer structure with methyl ethyl methacrylate (MEMA) and hydroxyl groups. Benzyl methacrylate is produced by polymerization of benzyl chloride with allyl carbonate in the presence of radiation, forming a polymeric matrix. The morphology of this copolymer depends on the length of the benzyl chains and the concentration of MEMA., Safety of Benzyl methacrylate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. 2495-37-6, formula is C11H12O2, Name is Benzyl methacrylate. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. COA of Formula: C11H12O2.

Zhang, Tongtong;Zhan, Chengdong;Huang, Xiangyue;Huang, Yinghui;Zong, Lina;Hong, Liangzhi;Ngai, To research published 《 Adaptive Morphology of Surface-Segregated Micelles Synthesized from Polymerization-Induced Self-Assembly Co-Mediated by a Binary Mixture of Macro-RAFT Agents》, the research content is summarized as follows. Surface-segregated micelles (SSMs) have shown potential applications in drug delivery, bioimaging, and Pickering emulsions due to their adaptive characteristics. A diverse set of SSMs are prepared by reversible addition-fragmentation transfer (RAFT)-mediated polymerization-induced self-assembly (PISA). However, the obtained self-assembled structures are mostly limited to spherical forms, and SSMs with a hierarchical structure are not yet prepared In this study, SSMs with various hierarchical structures are generated by the dispersion polymerization of benzyl methacrylate (BzMA) co-mediated by a binary mixture of poly(2-(dimethylamino)ethyl methacrylate) and polydimethylsiloxane as macromol. chain-transfer agents (macro-CTAs). The obtained structures include cylinders, vesicles, large compound micelles, and bundles of hoops. The morphol. evolution of these structures and vesicle size can be readily tuned by varying the composition of the binary mixture of macro-CTAs. This study expands the scope of RAFT-mediated PISA for synthesizing well-defined polymer nano-objects with higher-order morphologies for various applications.

COA of Formula: C11H12O2, Benzyl methacrylate, also known as Benzyl methacrylate, is a useful research compound. Its molecular formula is C11H12O2 and its molecular weight is 176.21 g/mol. The purity is usually 95%.
Benzyl methacrylate is a chemical compound that belongs to the group of benzyl compounds. It has a copolymer structure with methyl ethyl methacrylate (MEMA) and hydroxyl groups. Benzyl methacrylate is produced by polymerization of benzyl chloride with allyl carbonate in the presence of radiation, forming a polymeric matrix. The morphology of this copolymer depends on the length of the benzyl chains and the concentration of MEMA., 2495-37-6.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. 2495-37-6, formula is C11H12O2, Name is Benzyl methacrylate. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. HPLC of Formula: 2495-37-6.

Zhang, Jianxiong;Duan, Junjin;Chen, Dong;Ma, Yuhong;Yang, Wantai research published 《 Direct Photolysis RAFT Polymerization of (Metha)acrylate with 2-Cyano-2-propyldodecyl Trithiocarbonate as Mediator》, the research content is summarized as follows. A direct photolysis reversible addition-fragmentation chain transfer (RAFT) polymerization of (meth)acrylates is developed with 2-cyano-2-propyldodecyl trithiocarbonate (TTP), which plays the dual role as photoinitiator and chain transfer agent. The polymerizations can be efficiently activated by blue light while maintaining a linear increase in M_n vs. conversion. With poly(Me methacrylate)-TTP (PMMA-TTP, M_n = 6700 g mol^-1, ETH = 1.29) as precursor, a higher mol. weight PMMA (M_n = 14 600 g mol^-1, ETH = 1.67) by chain extension, and a series of block copolymers, including poly(Me methacrylate)-b-poly(glycidyl methacrylate), poly(Me methacrylate)-b-poly(tert-Bu methacrylate), and poly(Me methacrylate)-b-poly(benzyl methacrylate)(PMMA-b-PBnMA), are prepared The M_n, NMR = 14,900 g mol^-1 of PMMA-b-PBnMA measured by NMR is very close to M_n, GPC = 14,200 g mol^-1 determined by gel permeation chromatog. Furthermore, the polymerization of acrylates exhibits higher controllability in regarding to dispersity (ETH < 1.20) compared to those of polymethacrylates (ETH = 1.10-1.80). With poly(Me acrylate) (PMA-TTP, M_n = 11,900 g mol^-1, ETH = 1.09) as macro-RAFT agent, a higher mol. weight PMA (M_n = 23,500 g mol^-1, ETH = 1.28) by chain extension, and PMA-b-PBnA (M_n = 26,500 g mol^-1, ETH = 1.19) are also prepared A pos. synergic effect is demonstrated by enhanced apparent polymerization rates at elevated temperature For example, the apparent polymerization rates of MA increases from 0.0860 to 0.115 h^-1 with temperature rising from 32 to 50°.

2495-37-6, Benzyl methacrylate, also known as Benzyl methacrylate, is a useful research compound. Its molecular formula is C11H12O2 and its molecular weight is 176.21 g/mol. The purity is usually 95%.
Benzyl methacrylate is a chemical compound that belongs to the group of benzyl compounds. It has a copolymer structure with methyl ethyl methacrylate (MEMA) and hydroxyl groups. Benzyl methacrylate is produced by polymerization of benzyl chloride with allyl carbonate in the presence of radiation, forming a polymeric matrix. The morphology of this copolymer depends on the length of the benzyl chains and the concentration of MEMA., HPLC of Formula: 2495-37-6

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. 2495-37-6, formula is C11H12O2, Name is Benzyl methacrylate. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Reference of 2495-37-6.

Zeng, Min;Zhou, Shuo;Sui, Xiaofeng;Yuan, Jinying research published 《 Effect of Solvophilic Chain Length in PISA Particles on Pickering Emulsion》, the research content is summarized as follows. The morphol. of polymeric nanoparticles prepared by polymerization-induced self-assembly (PISA) is depended on the d.p. of the solvophilic and solvophobic blocks. Herein, a series of poly(N,N-dimethylaminoethyl methacrylate)-b-poly(benzyl methacrylate) (PDMA-b-PBzMA) diblock copolymer spherical nanoparticles were synthesized via reversible addition-fragmentation chain transfer (RAFT) mediated PISA. These diblock copolymer nanoparticles are with nearly the same hydrodynamic size and solvophobic chain length, but with different solvophilic chain length. We used these nanoparticles to stabilize the oil-in-water pickering emulsion. We find that the stability of pickering emulsion increases with the length of solvophilic chain of the nanoparticles. Moreover, the droplet size of the pickering emulsion can be tailored by varying the oil/water ratio and concentration of nanoparticles.

2495-37-6, Benzyl methacrylate, also known as Benzyl methacrylate, is a useful research compound. Its molecular formula is C11H12O2 and its molecular weight is 176.21 g/mol. The purity is usually 95%.
Benzyl methacrylate is a chemical compound that belongs to the group of benzyl compounds. It has a copolymer structure with methyl ethyl methacrylate (MEMA) and hydroxyl groups. Benzyl methacrylate is produced by polymerization of benzyl chloride with allyl carbonate in the presence of radiation, forming a polymeric matrix. The morphology of this copolymer depends on the length of the benzyl chains and the concentration of MEMA., Reference of 2495-37-6

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. 2495-37-6, formula is C11H12O2, Name is Benzyl methacrylate. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Application of C11H12O2.

Yue, Qi;Wen, Shang-Pin;Fielding, Lee A. research published 《 Preparation and characterisation of graphene oxide containing block copolymer worm gels》, the research content is summarized as follows. This paper reports a generic method for preparing reinforced nanocomposite worm-gels. Aqueous poly(glycerol monomethacrylate)-b-poly(2-hydroxypropyl methacrylate) (PGMA-PHPMA) and methanolic poly(glycerol monomethacrylate)-b-poly(benzyl methacrylate) (PGMA-PBzMA) worm gels were prepared by RAFT-mediated polymerization-induced self-assembly (PISA). The former system undergoes a reversible worm-to-sphere degelation transition upon cooling to 5°C while the latter system undergoes the same transition on heating to 56°C. This transition allows these copolymer dispersions to be readily mixed with graphene oxide (GO) while in a low viscosity state and form nanocomposite gels on returning to room temperature via a sphere-to-worm transition. Various quantities of GO were added to the studied copolymer dispersions at a fixed copolymer content of 15% weight/weight A general trend was observed whereby relatively small quantities of GO caused the gel strength of the nanocomposite gel to be higher than that of the pristine worm-gel, as determined by oscillatory rheol. Addnl. quantities of GO resulted in gel weakening or prevented gel-reformation altogether. For instance, 15% weight/weight PGMA52-PHPMA130 worm gels had a storage modulus (G’) of approx. 1.5 kPa. The addition of 1.5% weight/weight GO based on the copolymer caused G’ to increase to approx. 4.0 kPa but >1.5% weight/weight GO resulted in gel strengths <1.0 kPa. A combination of aqueous electrophoresis and transmission electron microscopy measurements were used to investigate the mechanism of nanocomposite gel formation. It was observed that the PGMA-based copolymers readily absorb onto the surface of GO. Thus, the role of GO is both to strengthen the worm-gels when an optimal concentration of GO is used, but also prevent worm-reformation if too much copolymer becomes absorbed on the surface of the sheets.

Application of C11H12O2, Benzyl methacrylate, also known as Benzyl methacrylate, is a useful research compound. Its molecular formula is C11H12O2 and its molecular weight is 176.21 g/mol. The purity is usually 95%.
Benzyl methacrylate is a chemical compound that belongs to the group of benzyl compounds. It has a copolymer structure with methyl ethyl methacrylate (MEMA) and hydroxyl groups. Benzyl methacrylate is produced by polymerization of benzyl chloride with allyl carbonate in the presence of radiation, forming a polymeric matrix. The morphology of this copolymer depends on the length of the benzyl chains and the concentration of MEMA., 2495-37-6.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics