E1505
Ethyl 2-cyanoacrylate
liquid
Synonyme(s) :
ethyl 2-cyanoprop-2-enoate
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A propos de cet article
Formule empirique (notation de Hill) :
C6H7NO2
Numéro CAS:
Poids moléculaire :
125.13
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
230-391-5
MDL number:
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Laissez-nous vous aiderInChI key
FGBJXOREULPLGL-UHFFFAOYSA-N
InChI
1S/C6H7NO2/c1-3-9-6(8)5(2)4-7/h2-3H2,1H3
SMILES string
CCOC(=O)C(=C)C#N
form
liquid
storage temp.
2-8°C
Quality Level
Catégories apparentées
General description
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.
Application
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.
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Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Classe de stockage
10 - Combustible liquids
wgk
WGK 1
flash_point_f
185.0 °F - closed cup
flash_point_c
85 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
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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)
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
Xiaofeng Li et al.
Journal of colloid and interface science, 340(1), 93-97 (2009-09-12)
Hollow microspheres of poly(ethyl alpha-cyanoacrylate) were prepared via vapor phase polymerization using micro-waterdroplets as template and initiator. Depending on the ratio of the shell thickness to the radius, the hollow microspheres would crimple to form either microballoons or microcups during
Histopathological effects of ethyl 2-cyanoacrylate tissue adhesive following surgical application: an experimental study
Kaplan M, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association For Cardio-Thoracic Surgery, 25(2), 167-172 (2004)
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