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Ethyl 2-Cyanoacrylate

Ethyl 2-Cyanoacrylate

  • CAT Number: R009840
  • CAS Number: 7085-85-0
  • Molecular Formula: C6H7NO2
  • Molecular Weight: 125.127
  • Purity: ≥95%
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Ethyl 2-cyanoacrylate(CAT: R009840) is a chemical compound known for its adhesive properties. It is commonly used in the manufacturing of instant or “super” glues. Ethyl 2-cyanoacrylate polymerizes rapidly upon contact with moisture, forming strong bonds between various surfaces, including metals, plastics, and rubber. Its fast-curing and high-strength characteristics make it a popular choice for a wide range of bonding applications in industries such as construction, automotive, and manufacturing.

Catalog Number R009840
CAS Number 7085-85-0
Molecular Formula

C6H7NO2

Purity 95%
Storage -20°C
IUPAC Name ethyl 2-cyanoprop-2-enoate
InChI InChI=1S/C6H7NO2/c1-3-9-6(8)5(2)4-7/h2-3H2,1H3
InChIKey FGBJXOREULPLGL-UHFFFAOYSA-N
SMILES CCOC(=O)C(=C)C#N
Reference

<p>
<span style=”color:#000000;”><span style=”font-size:12px;”><span style=”font-family:arial,helvetica,sans-serif;”>1.Tseng, Yin-Chao, Suong-Hyu Hyon, and Yoshito Ikada. &quot;Modification of synthesis and investigation of properties for 2-cyanoacrylates.&quot;&nbsp;<i style=”font-family: Arial, sans-serif; font-size: 13px;”>Biomaterials</i>&nbsp;11.1 (1990): 73-79.<br />
2.Tomlinson, S. K., et al. &quot;The use of near-infrared spectroscopy for the cure monitoring of an ethyl cyanoacrylate adhesive.&quot;&nbsp;<i style=”font-family: Arial, sans-serif; font-size: 13px;”>Vibrational spectroscopy</i>&nbsp;40.1 (2006): 133-141.<br />
3.Kaplan, Mehmet, et al. &quot;Histopathological effects of ethyl 2-cyanoacrylate tissue adhesive following surgical application: an experimental study.&quot;&nbsp;<i style=”font-family: Arial, sans-serif; font-size: 13px;”>European journal of cardio-thoracic surgery</i>&nbsp;25.2 (2004): 167-172.</span></span></span></p>

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