549797
Acryloyl chloride
97.0%, contains <210 ppm MEHQ as stabilizer
Sinónimos:
2-Propenoyl chloride
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About This Item
Fórmula lineal:
CH2=CHCOCl
Número de CAS:
Peso molecular:
90.51
Beilstein:
635744
Número CE:
Número MDL:
Código UNSPSC:
12162002
ID de la sustancia en PubChem:
NACRES:
NA.23
Productos recomendados
densidad de vapor
>1 (vs air)
Nivel de calidad
presión de vapor
1.93 psi ( 20 °C)
Análisis
97.0%
contiene
<210 ppm MEHQ as stabilizer
índice de refracción
n20/D 1.435 (lit.)
bp
72-76 °C (lit.)
densidad
1.114 g/mL at 25 °C (lit.)
temp. de almacenamiento
2-8°C
cadena SMILES
ClC(=O)C=C
InChI
1S/C3H3ClO/c1-2-3(4)5/h2H,1H2
Clave InChI
HFBMWMNUJJDEQZ-UHFFFAOYSA-N
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Descripción general
Acryloyl chloride is a derivative of acrylic acid and is widely used as a reactive monomer in the synthesis of various polymers with desired properties such as good transparency, flexibility, excellent mechanical and thermal properties, and resistance to moisture and chemicals. Acryloyl chloride contains both an acryloyl group (-CH2=CHC(O)Cl) and a chloride functional group (-Cl) in its structure. This combination of functional groups enables acryloyl chloride to undergo polymerization reactions and participate in copolymerization processes. In the field of polymers, acryloyl chloride is commonly used in the production of acrylic polymers, such as polyacrylates and polymethacrylates. These polymers have a wide range of applications, including coatings, adhesives, sealants, textiles, and biomedical materials.
Aplicación
Acryloyl chloride can used as a monomer in the synthesis of:
- Acrylic polymers via radical polymerization or copolymerization. These acrylic polymers can be tailored to possess the desired properties for biomedical coatings, including biocompatibility, adhesion to the device surface, and durability.
- Poly(styrene-co-acryloyl chloride) copolymer by crosslinked networks with styrene. The resulting crosslinked polymer can then be functionalized or modified by various chemical reactions to introduce specific properties or functionalities desired for the application as a polymer support or an electrophilic scavenger resin.
- Acrylamide-modified chitosan.
- Ulvan acrylate macromer via esterification of hydroxyl groups of polysaccharides. This macromer can be used to prepare ulvan-based thermosensitive hydrogels.
- Degradable peptide cross-linker by the acrylation of the amine groups of lysine residues and glutamine within peptide sequences.
Palabra de señalización
Danger
Frases de peligro
Clasificaciones de peligro
Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Met. Corr. 1 - Skin Corr. 1A
Riesgos supl.
Código de clase de almacenamiento
3 - Flammable liquids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
30.2 °F
Punto de inflamabilidad (°C)
-1 °C
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