Item | parameter |
Name | Methacryloyl chloride |
Synonyms | methacrylchloride |
CAS | 920-46-7 |
Molecular Formula | C4H5ClO |
Formula Weight | 104.53 |
Appearance | ---- |
Melting Point | -60°C |
Boiling point | 95-96 °C(lit.) |
Assay | 99% |
Water | <0.5% |
Residue on ignition | <0.5% |
Stability | Stable |
Storage Temp | Store below +30°C. |
Product Name: | Methacryloyl chloride |
Synonyms: | 2-METHYLPROPENOYL CHLORIDE;methacrylchloride;Methacrylic chloride;methacrylicacidchloride;methacrylicchloride;methacrylolchloride;Methylacryloyl chloride |
CAS: | 920-46-7 |
MF: | C4H5ClO |
MW: | 104.53 |
EINECS: | 213-058-9 |
Product Categories: | ACID CHLORIDES;Polymer Science;Acid Halides;Acrylic Monomers;Building Blocks;Carbonyl Compounds;Acrylic Monomers;Methacrylate;Acid Halides;Carbonyl Compounds;Organic Building Blocks;Chemical Synthesis;Materials Science;Organic Building Blocks;Monomers |
Mol File: | 920-46-7.mol |
Methacryloyl chloride is used in the manufacture of polymers:
Monomer 2-methacrylamido-caprolactam was prepared by reacting methacryloyl chloride with racemic a-amino-e-caprolactam.
Functional monomer was prepared by reacting methacryloyl chloride and L-histidine.
A series of amide monomers were synthesized by amidation of methacryloyl chloride with amines and grafted onto commercial poly(ether sulfone) (PES) membranes using irradiation from atmospheric pressure plasma (APP).
Reaction of methacryloyl chloride with the hydroxyl groups on the surfaces of HEMA/NVP microspheres was performed, leading to the introduction of polymerisable double bonds onto the surfaces of microspheres.
Star-shaped poly(d,l-lactide) oligomers with 2, 3 and 6 arms were synthesised, end-functionalised with methacryloyl chloride and photo-crosslinked in the presence of ethyl lactat e as a non-reactive diluent.
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