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| SKU | Size | Availability |
Price | Qty |
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P478262-250g
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250g |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$331.90
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| Synonyms | Butyl 2-methylprop-2-enoate--methyl 2-methylprop-2-enoate (1/1) | Dianal BR-113 | Methyl Methacrylate n-Butyl Methacrylate | butyl 2-methylprop-2-enoate;methyl 2-methylprop-2-enoate | DTXSID30909118 | Methyl methacrylate butyl methacrylate | Entellan | WH |
|---|---|
| Specifications & Purity | average Mw ~150,000 |
| Product Description |
Description Poly(butyl methacrylate-co-methyl methacrylate) (P(BMA-co-MMA) ) may be used to synthesize porous interpenetrating polymer network (IPN) with low-density polymers. These IPN structures are applicable as membranes for separation of liquid mixtures due to their high mechanical strength and selectivity. P(BMA-co-MMA) particles may be used to encapsulate single non-aggregated semiconducting quantum dots (QDs) for size enlargement.These hybrid organic/inorganic nanostructures may be used as single photon sources.Binding agent for printing inks and foil, hardboard and ceramic lacquers. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Carboxylic acid derivatives |
| Intermediate Tree Nodes | Carboxylic acid esters - Alpha,beta-unsaturated carboxylic esters |
| Direct Parent | Enoate esters |
| Alternative Parents | Methyl esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Not available |
| Substituents | Enoate ester - Methyl ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as enoate esters. These are an alpha,beta-unsaturated carboxylic ester of general formula R1C(R2)=C(R3)C(=O)OR4 (R4= organyl compound) in which the ester C=O function is conjugated to a C=C double bond at the alpha,beta position. |
| External Descriptors | Not available |
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| IUPAC Name | butyl 2-methylprop-2-enoate;methyl 2-methylprop-2-enoate |
|---|---|
| INCHI | InChI=1S/C8H14O2.C5H8O2/c1-4-5-6-10-8(9)7(2)3;1-4(2)5(6)7-3/h2,4-6H2,1,3H3;1H2,2-3H3 |
| InChIKey | WHLPIOPUASGRQN-UHFFFAOYSA-N |
| Smiles | CCCCOC(=O)C(=C)C.CC(=C)C(=O)OC |
| Isomeric SMILES | CCCCOC(=O)C(=C)C.CC(=C)C(=O)OC |
| PubChem CID | 62798 |
| Solubility | esters, ketones, glycol ethers and aromatics: soluble; ethanol and ; water: insoluble |
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| Flash Point(°F) | Not applicable |
| Flash Point(°C) | Not applicable |
| Melt Point(°C) | Tg(DSC) 52℃ (onset) |
| 1. Gao Die, Zhu Qingqing, Liu Peng, Zhou Qing, Cheng Xiujie, Liu Li, Xu Junli, Lu Xingmei. (2023) Efficient Pretreatment of Corn Straw with Ionic Liquid Composite System. Journal of Inorganic and Organometallic Polymers and Materials, 33 (7): (2000-2012). |