549797
Chlorure d'acryloyle
97.0%, contains <210 ppm MEHQ as stabilizer
Synonyme(s) :
Chlorure de 2-propénoyle
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About This Item
Formule linéaire :
CH2=CHCOCl
Numéro CAS:
Poids moléculaire :
90.51
Numéro Beilstein :
635744
Numéro CE :
Numéro MDL:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23
Produits recommandés
Densité de vapeur
>1 (vs air)
Niveau de qualité
Pression de vapeur
1.93 psi ( 20 °C)
Pureté
97.0%
Contient
<210 ppm MEHQ as stabilizer
Indice de réfraction
n20/D 1.435 (lit.)
Point d'ébullition
72-76 °C (lit.)
Densité
1.114 g/mL at 25 °C (lit.)
Température de stockage
2-8°C
Chaîne SMILES
ClC(=O)C=C
InChI
1S/C3H3ClO/c1-2-3(4)5/h2H,1H2
Clé InChI
HFBMWMNUJJDEQZ-UHFFFAOYSA-N
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Catégories apparentées
Description générale
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.
Application
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.
Mention d'avertissement
Danger
Mentions de danger
Classification des risques
Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Met. Corr. 1 - Skin Corr. 1A
Risques supp
Code de la classe de stockage
3 - Flammable liquids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
30.2 °F
Point d'éclair (°C)
-1 °C
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The present study is focused on the exploitation and conversion of sulphated polysaccharides obtained from waste algal biomass into high value added material for biomedical applications. ulvan, a sulphated polysaccharide extracted from green seaweeds belonging to Ulva sp. was selected
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Hydrogels composed of N-isopropylacrylamide (NIPAAm) and acrylic acid (AAc) were prepared by redox polymerization with peptide cross-linkers to create an artificial extracellular matrix (ECM) amenable for testing hypotheses regarding cell proliferation and migration in three dimensions. Peptide degradable cross-linkers were
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An automated procedure for the radiosynthesis of the labeling synthon [11C]acryloyl chloride was developed and applied for labeling several N-acryl amides with carbon-11. [11C]-6-acrylamido-4-(3,4-dichloro-6-fluoroanilino)quinazoline (ML03), a novel PET biomarker targeting the epidermal growth factor receptor tyrosine kinase (EGFr-TK) in cancer
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