Names | |
---|---|
Preferred IUPAC name
Hexane-1,6-diyl di(prop-2-enoate) | |
Other names
HDDA, HDODA
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.032.641 |
EC Number |
|
PubChem
CID
|
|
UNII | |
UN number | 3082 |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C12H18O4 | |
Molar mass | 226.272 g·mol−1 |
Appearance | Colorless oil |
Hazards | |
GHS labelling: | |
Warning | |
H315, H317, H319 | |
P261, P264, P272, P280, P302+P352, P305+P351+P338, P321, P332+P313, P333+P313, P337+P313, P362, P363, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
1,6-Hexanediol diacrylate (HDDA or HDODA) is a difunctional acrylate ester monomer used in the manufacture of polymers. [1] [2] It is particularly useful for use in ultraviolet light cure applications. [3] Furthermore, it is also used in adhesives, sealants, alkyd coatings, elastomers, photopolymers, and inks for improved adhesion, hardness, abrasion and heat resistance. [4] Like other acrylate monomers it is usually supplied with a radical inhibitor such as hydroquinone added. [5]
The material is prepared by acid-catalyzed esterification of 1,6-hexanediol with acrylic acid. [6]
As the molecule has acrylic functionality, it is capable of undergoing the Michael reaction with an amine. This allows it use in epoxy chemistry where its use speeds up the cure time considerably. [7]
Names | |
---|---|
Preferred IUPAC name
Hexane-1,6-diyl di(prop-2-enoate) | |
Other names
HDDA, HDODA
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.032.641 |
EC Number |
|
PubChem
CID
|
|
UNII | |
UN number | 3082 |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C12H18O4 | |
Molar mass | 226.272 g·mol−1 |
Appearance | Colorless oil |
Hazards | |
GHS labelling: | |
Warning | |
H315, H317, H319 | |
P261, P264, P272, P280, P302+P352, P305+P351+P338, P321, P332+P313, P333+P313, P337+P313, P362, P363, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
1,6-Hexanediol diacrylate (HDDA or HDODA) is a difunctional acrylate ester monomer used in the manufacture of polymers. [1] [2] It is particularly useful for use in ultraviolet light cure applications. [3] Furthermore, it is also used in adhesives, sealants, alkyd coatings, elastomers, photopolymers, and inks for improved adhesion, hardness, abrasion and heat resistance. [4] Like other acrylate monomers it is usually supplied with a radical inhibitor such as hydroquinone added. [5]
The material is prepared by acid-catalyzed esterification of 1,6-hexanediol with acrylic acid. [6]
As the molecule has acrylic functionality, it is capable of undergoing the Michael reaction with an amine. This allows it use in epoxy chemistry where its use speeds up the cure time considerably. [7]