E1505
Ethyl 2-cyanoacrylate
liquid
Sinónimos:
ethyl 2-cyanoprop-2-enoate
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About This Item
Fórmula empírica (notación de Hill):
C6H7NO2
Número de CAS:
Peso molecular:
125.13
Número CE:
Número MDL:
Código UNSPSC:
12162002
ID de la sustancia en PubChem:
NACRES:
NA.23
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Formulario
liquid
temp. de almacenamiento
2-8°C
cadena SMILES
CCOC(=O)C(=C)C#N
InChI
1S/C6H7NO2/c1-3-9-6(8)5(2)4-7/h2-3H2,1H3
Clave InChI
FGBJXOREULPLGL-UHFFFAOYSA-N
Descripción general
Ethyl 2-cyanoacrylate belongs to the class of monomers known as cyanoacrylates. Ethyl 2-cyanoacrylate polymers are primarily used as adhesives due to their fast-setting and strong bonding properties. They are widely utilized for bonding a variety of materials, including metals, plastics, rubber, ceramics, and wood. These adhesives are used in industries such as automotive, electronics, crafts, and general repairs. Ethyl 2-cyanoacrylate adhesives find applications in industrial and manufacturing processes. They are used for sealing products, encapsulating electronics, and securing parts during assembly.
Aplicación
Ethyl 2-cyanoacrylate, commonly known as super glue, has several uses in the field of bioadhesives:
- Wound Closure: Ethyl 2-cyanoacrylate is often used in medical settings to close small cuts and wounds. It forms a strong bond when it comes into contact with moisture, effectively sealing the wound.
- Tissue Adhesives: In surgical and medical applications, ethyl 2-cyanoacrylate is used to adhere tissues together. It can be used as an alternative to traditional sutures or staples in certain procedures.
- Drug Delivery Systems: In some cases, ethyl 2-cyanoacrylate has been investigated as a component in drug delivery systems and tissue engineering due to its biocompatibility and ability to form strong bonds with biological materials.
- It can also be mixed with hydrophobic silica nanoparticles for the designing of cotton fabrics for medical applications.
Palabra de señalización
Warning
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órganos de actuación
Respiratory system
Código de clase de almacenamiento
10 - Combustible liquids
Clase de riesgo para el agua (WGK)
WGK 1
Punto de inflamabilidad (°F)
185.0 °F - closed cup
Punto de inflamabilidad (°C)
85 °C - closed cup
Equipo de protección personal
Eyeshields, Faceshields, Gloves
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Anja Graf et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 37(1), 53-61 (2009-01-27)
The purpose of this study was to optimise entrapment of insulin in poly(alkylcyanoacrylate) nanoparticles prepared from microemulsions with different microstructure containing isopropyl myristate, caprylocaproyl macrogolglycerides, polyglyceryl oleate and insulin solution and to investigate the in vitro release and bioactivity of
T Landegren et al.
International journal of oral and maxillofacial surgery, 39(7), 705-712 (2010-05-04)
Cyanoacrylate adhesive has been suggested as an alternative to suturing when repairing severed peripheral nerves. The authors examined the cytotoxic effect of ethyl-cyanoacrylate on the human neuroblastoma cell line SH-SY5Y and compared it with the effects of butyl-cyanoacrylate (Histoacryl), an
Asymmetric superhydrophobic/superhydrophilic cotton fabrics designed by spraying polymer and nanoparticles
Sasaki K, et al.
ACS Applied Materials & Interfaces, 8(1), 651-659 (2015)
Qiwen Chen et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(44), 12458-12464 (2011-09-20)
A carbon nanotube/poly(ethyl 2-cyanoacrylate) (CNT/PECA) composite electrode was developed for enhanced amperometric detection. The composite electrode was fabricated on the basis of water-vapor-initiated polymerization of a mixture of CNTs and ethyl 2-cyanoacrylate in the bore of a piece of fused
Ana Isabel Quilez-Molina et al.
Polymers, 12(9) (2020-09-10)
Applications of cyanoacrylate monomers are generally limited to adhesives/glues (instant or superglues) and forensic sciences. They tend to polymerize rapidly into rigid structures when exposed to trace amounts of moisture. Transforming cyanoacrylate monomers into transparent polymeric films or coatings can
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