Names | |
---|---|
Preferred IUPAC name
2-Methylpropyl 2-cyanoprop-2-enoate | |
Other names
2-Methylpropyl 2-cyanopropenoate
Isobutyl 2-cyanoacrylate Bucrylate | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.012.690 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C8H11NO2 | |
Molar mass | 153.181 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Isobutyl cyanoacrylate is an isomer of butyl cyanoacrylate. It is used in medical procedures either to close incisions and lacerations without the use of sutures, or as an adjunct to strengthen the suturing. [1] This use is possible because it is a bactericidal liquid monomer which, in the presence of small amounts of moisture, rapidly polymerizes to form a strong adhesive. [2]
Names | |
---|---|
Preferred IUPAC name
2-Methylpropyl 2-cyanoprop-2-enoate | |
Other names
2-Methylpropyl 2-cyanopropenoate
Isobutyl 2-cyanoacrylate Bucrylate | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.012.690 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C8H11NO2 | |
Molar mass | 153.181 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Isobutyl cyanoacrylate is an isomer of butyl cyanoacrylate. It is used in medical procedures either to close incisions and lacerations without the use of sutures, or as an adjunct to strengthen the suturing. [1] This use is possible because it is a bactericidal liquid monomer which, in the presence of small amounts of moisture, rapidly polymerizes to form a strong adhesive. [2]