Methacrylic anhydride
94%, containing 0.2% topanol stabilizer
- Product Code: 204788
Alias:
Methacrylic anhydride
CAS:
760-93-0
Properties:
To avoid polymerization, it is recommended that the room temperature should not exceed 20℃.
| Molecular Weight: | 154.16 g./mol | Molecular Formula: | C₈H₁₀O₃ |
|---|---|---|---|
| EC Number: | 212-084-8 | MDL Number: | MFCD00008586 |
| Melting Point: | -20°C | Boiling Point: | 87 °C13 mm Hg(lit.) |
| Density: | 1.04 g/mL at 20 °C | Storage Condition: | 2-8℃ |
Product Description:
Used primarily as a reactive intermediate in organic synthesis, especially in modifying biomolecules such as proteins and peptides. It selectively reacts with primary amines and sulfhydryl groups, making it valuable for crosslinking or functionalizing amino acids and nucleic acids. Commonly employed in the preparation of hydrogels and polymer-based drug delivery systems due to its ability to introduce methacrylate functionalities that can undergo radical polymerization. Also utilized in surface modification of materials to introduce polymerizable groups for coatings or immobilization of bioactive molecules. Its reactivity allows for controlled conjugation in bioconjugate chemistry, useful in diagnostics and biosensor development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5ml | 10-20 days | ฿290.00 |
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| 25ml | 10-20 days | ฿730.00 |
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| 100ml | 10-20 days | ฿1,700.00 |
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| 500ml | 10-20 days | ฿3,940.00 |
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| 2.5L | 10-20 days | ฿14,110.00 |
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Methacrylic anhydride
Used primarily as a reactive intermediate in organic synthesis, especially in modifying biomolecules such as proteins and peptides. It selectively reacts with primary amines and sulfhydryl groups, making it valuable for crosslinking or functionalizing amino acids and nucleic acids. Commonly employed in the preparation of hydrogels and polymer-based drug delivery systems due to its ability to introduce methacrylate functionalities that can undergo radical polymerization. Also utilized in surface modification of materials to introduce polymerizable groups for coatings or immobilization of bioactive molecules. Its reactivity allows for controlled conjugation in bioconjugate chemistry, useful in diagnostics and biosensor development.
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| Stable in pH range | - |
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