Description

Ocrilate (Octyl 2-cyanoprop-2-enoate) is a high-purity cyanoacrylate ester with the molecular formula C₁₂H₁₉NO₂ and CAS number 6701-17-3. This specialized monomer is widely recognized for its superior adhesive properties, particularly in medical and industrial applications. Its IUPAC name, octyl 2-cyanoprop-2-enoate, reflects its structural composition featuring an octyl ester group attached to a cyanoacrylate backbone. Ocrilate exhibits rapid polymerization upon exposure to moisture, forming strong, flexible bonds with excellent resistance to biodegradation. Available in rigorously controlled batches, this product is ideal for researchers developing surgical adhesives, wound closure systems, or advanced polymer formulations. Each shipment includes comprehensive analytical documentation (GC, NMR) to ensure consistency and performance.

Properties

• CAS Number: 6701-17-3
• Complexity: 250
• IUPAC Name: octyl 2-cyanoprop-2-enoate
• InChI: InChI=1S/C12H19NO2/c1-3-4-5-6-7-8-9-15-12(14)11(2)10-13/h2-9H2,1H3
• InChI Key: RPQUGMLCZLGZTG-UHFFFAOYSA-N
• Exact Mass: 209.141578849
• Molecular Formula: C12H19NO2
• Molecular Weight: 209.28
• SMILES: CCCCCCCCOC(=O)C(=C)C#N
• Topological: 50.1
• Monoisotopic Mass: 209.141578849
• Synonyms: Ocrilate, OCRYLATE, 6701-17-3, Octyl 2-cyanoacrylate, Octyl cyanoacrylate, Ocrilato, Octyl-2-cyanoacrylate, Ocrylate [USAN], octyl 2-cyanoprop-2-enoate, 2-Propenoic acid, 2-cyano-, octyl ester, Ocrilate [INN], 2-octyl cyanocrylate, 6C655P1XVG, Ocrilat, Ocrilatum, Octyl (2-cyanacylat), Ocrilatum [INN-Latin], Ocrilato [INN-Spanish], UNII-6C655P1XVG, EINECS 229-748-8, Ocrylate (USAN/INN), OCRILATE [MART.], OCRILATE [WHO-DD], SCHEMBL29891, CHEMBL2105181, OCTYL CYANOACRYLATE [MI], DTXSID10217208, MFCD00868122, 2-OCTYL CYANOCRYLATE [VANDF], DB15086, HY-29347, SY318615, NS00036086, D05219, H43065, Q7077122

Application

Ocrilate is primarily utilized as a medical-grade adhesive for wound closure and surgical applications due to its rapid polymerization and biocompatibility. It serves as a key component in liquid bandages and tissue adhesives, offering superior flexibility compared to shorter-chain cyanoacrylates. Researchers also employ ocrilate in developing controlled-release drug delivery systems where its polymerization kinetics can be tailored. Industrial applications include specialty adhesives for electronics assembly requiring moisture-resistant bonds.

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.