Acryloyl chloride, 96%, stab. with 400ppm phenothiazine
Acryloyl chloride, 96%, stab. with 400ppm phenothiazine
Acryloyl chloride, 96%, stab. with 400ppm phenothiazine
Acryloyl chloride, 96%, stab. with 400ppm phenothiazine
Thermo Scientific Chemicals

Acryloyl chloride, 96%, stab. with 400ppm phenothiazine

CAS: 814-68-6 | C3H3ClO | 90.51 g/mol
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50 g
10 g
Catalog number ALFL10363.18
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Quantity:
50 g
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Specifications
Chemical Name or MaterialAcryloyl chloride
Name Notestabilized with 400ppm phenothiazine
CAS814-68-6
Health Hazard 1H225-H302-H314-H330-H335
Health Hazard 2GHS H Statement
H225-H330-H314-H318-H302
Highly flammable liquid and vapor.
Fatal if inhaled.
Causes severe skin burns and eye damage.
Causes serious eye damage.
Harmful if swallowed.
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Acryloyl chloride is used in the production of plastics. It plays an important role in the preparation of acrylate monomers and polymers. It also acts as a substrate for cross-metathesis. Further, it is utilized in organic synthesis for the introduction of acrylic groups into other compounds.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Acryloyl chloride is used in the production of plastics. It plays an important role in the preparation of acrylate monomers and polymers. It also acts as a substrate for cross-metathesis. Further, it is utilized in organic synthesis for the introduction of acrylic groups into other compounds.

Solubility
Miscible with water.

Notes
Moisture and light sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with alcohols, oxidizing agents, strong bases and polymerizing initiators.
RUO – Research Use Only

General References:

  1. Warneke, J.; Plaumann, M.; Wang, Z.; Böhler, E.; Kemken, D.; Kelm, S.; Leibfritz, D.; Azov, V. A. New insights into the old reaction between acryloyl chlorides and pyridine. Tetrahedron Lett. 2015, 56 (9), 1124-1127.
  2. Lee, P. W.; Scrape, P. G.; Butler, L. G.; Lee, Y. P. Two HCl-Elimination Channels and Two CO-Formation Channels Detected with Time-Resolved Infrared Emission upon Photolysis of Acryloyl Chloride [CH2CHC(O)Cl] at 193 nm. J. Phys. Chem. A 2015, 119 (28), 7293-7304.