868-77-9
868-77-9
Chemical Structure
2-Hydroxyethyl methacrylate
- CAS No.: 868-77-9
- Formula:C6H10O3
- Molecular Weight:130.14
IUPAC Name: 2-hydroxyethyl methacrylate
InChIKey: WOBHKFSMXKNTIM-UHFFFAOYSA-N
SMILES: CC(C(OCCO)=O)=C
Biological Activity: 2-Hydroxyethyl methacrylate (HEMA) is a monomer used in the synthesis of various polymers, and the polymer PHEMA of 2-Hydroxyethyl methacrylate is widely used in the synthesis of dental composite materials[1][2][3].
| Cat. No. | 상품명 | Purity | 제품 설명 | Pricing | |||||||||||||||||||
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2-Hydroxyethyl methacrylate | 99.24% | 2-Hydroxyethyl methacrylate (HEMA) is a monomer used in the synthesis of various polymers, and the polymer PHEMA of 2-Hydroxyethyl methacrylate is widely used in the synthesis of dental composite materials. | ||||||||||||||||||||
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2-Hydroxyethyl methacrylate-13C | 2-Hydroxyethyl methacrylate-13C is the 13C--labeled 2-Hydroxyethyl methacrylate (HY-W012723). 2-Hydroxyethyl methacrylate (HEMA) is a monomer used in the synthesis of various polymers, and the polymer PHEMA of 2-Hydroxyethyl methacrylate is widely used in the synthesis of dental composite materials. | |||||||||||||||||||||
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Propargyl methacrylate | Propargyl methacrylate is an effective electrolyte additive used to stabilize the formation of the solid electrolyte interface (SEI) layer on meso-porous carbon microbeads (MCMB) in lithium-ion batteries. | |||||||||||||||||||||
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Enbucrilate | 98.0% | Enbucrilate (Butyl cyanoacrylate) is a cyanoacrylate ester that has been used as surgical tissue adhesive. | ||||||||||||||||||||
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Glycidyl methacrylate | 99.36% | Glycidyl methacrylate is a bifunctional monomer containing both a polymerizable methacrylate double bond and a reactive epoxy group. Glycidyl methacrylate can be introduced into polymer backbones via free radical polymerization, and its epoxy group undergoes ring-opening reactions with nucleophilic groups such as amines, carboxylic acids and thiols, thus being used for the preparation of functional polymers, surface-grafted materials and crosslinkable biomaterials. Glycidyl methacrylate is applicable to research related to polymer chemistry, biomaterials, surface modification and drug delivery materials. | ||||||||||||||||||||
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2-(Ethyl(propyl)amino)ethyl methacrylate | 2-(Ethyl (propyl) amino) ethyl methacrylate (EPEMA) is an acid-responsive reagent and chemical intermediate. 2-(Ethyl (propyl) amino) ethyl methacrylate can be used for the synthesis of pDMA-pEPEMA. The protonation of 2-(Ethyl (propyl) amino) ethyl methacrylate in pDMA-pEPEMA under acidic conditions triggers the responsive release of Cortistatin. 2-(Ethyl (propyl) amino) ethyl methacrylate can be used in the research of diabetic ulcers. | |||||||||||||||||||||
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Methyl 3-hydroxypropanoate | 99.82% | Methyl 3-hydroxypropanoate is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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[2-(Methacryloyloxy)ethyl]trimethylammonium chloride | [2-(Methacryloyloxy)ethyl]trimethylammonium chloride is a biochemical assay reagent. | |||||||||||||||||||||
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Ethylene glycol dimethacrylate | 98.91% | Ethylene glycol dimethacrylate is a diester formed by the condensation of Ethylene glycol (HY-Y0338) and Methacrylic acid. Ethylene glycol dimethacrylate is a cross-linking agent for polymers. Ethylene glycol dimethacrylate increases Apoptosis, GPx4, SOD2, ROS. Ethylene glycol dimethacrylate is cytotoxic and genotoxic. Ethylene glycol dimethacrylate exhibits cross-linking activity, enhancing the mechanical properties and stability of materials. | ||||||||||||||||||||
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Ethyl acetate-PEG1 | Ethyl acetate-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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Hydroxy-PEG3-2-methylacrylate | Hydroxy-PEG3-2-methylacrylate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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Ethyl hydroxyacetate | 99.99% | Ethyl hydroxyacetate is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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References
- [1]. André Jochums, et al. Influence of 2-hydroxyethyl methacrylate (HEMA) exposure on angiogenic differentiation of dental pulp stem cells (DPSCs). Dent Mater. 2021 Mar;37(3):534-546. [Content Brief]
- [2]. Montheard J P, et al. 2-hydroxyethyl methacrylate (HEMA): chemical properties and applications in biomedical fields[J]. Journal of Macromolecular Science, Part C: Polymer Reviews, 1992, 32(1): 1-34.
