Molecular Formula | C10H19NO2 |
Molar Mass | 185.26 |
Density | 0.922g/mLat 25°C(lit.) |
Melting Point | -60°C |
Boling Point | 80°C10mm Hg(lit.) |
Flash Point | 170°F |
Vapor Presure | 11Pa at 20℃ |
Appearance | clear liquid |
Color | Colorless to Almost colorless |
pKa | 9.18±0.25(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | n20/D 1.444(lit.) |
Physical and Chemical Properties | Colorless transparent liquid. Freezing Point |
Hazard Symbols | Xn - Harmful |
Risk Codes | R20 - Harmful by inhalation R36/38 - Irritating to eyes and skin. R43 - May cause sensitization by skin contact |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37 - Wear suitable protective clothing and gloves. |
UN IDs | NA 1993 / PGIII |
WGK Germany | 1 |
RTECS | OZ4150000 |
HS Code | 29224999 |
Decomposition | 176-178 ºC |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Use | This product has reactive amino group and polymerizable vinyl group, which can increase adhesion and thermosetting, it can improve the crosslinking and the coloring properties of dyes and pigments, and can be used for the preparation of thermosetting coatings, antistatic agents, dyeing aids, lubricating oil additives, adhesives, leather processing agents, combustion aids and the like. diethylaminoethyl Methacrylate with reactive amino group and polymerizable vinyl group, can increase the adhesion, thermosetting, due to the role of ionic bonds, can improve the crosslinking and coloring properties of dyes and pigments, it can be used to prepare thermosetting coatings, antistatic agents, dyeing aids, lubricating oil additives, adhesives, leather processing agents, combustion improvers and the like. |
production method | results from the interaction of methacrylic acid with diethylaminoethanol ([100-37-8]). |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |