Molecular Formula | C6H10O3 |
Molar Mass | 130.14 |
Density | 1.044g/mLat 25°C(lit.) |
Melting Point | -92°C |
Boling Point | 77°C5mm Hg(lit.) |
Flash Point | 193°F |
Water Solubility | The water solubility of hydroxypropyl acrylate is estimated to be 307g/L(25°C) |
Vapor Presure | 1Pa at 20℃ |
Vapor Density | 4.5 (vs air) |
Appearance | clear liquid |
Color | Colorless to Almost colorless |
Refractive Index | n20/D 1.445(lit.) |
Physical and Chemical Properties | Density 1.044 boiling point 77°C (5 mmHg) refractive index 1.445 flash point 193 °F |
Use | Can be used for the production of adhesives, thermosetting coatings, fiber treatment agents and synthetic resin copolymer modifier, can also be used for the preparation of lubricating oil additives |
Hazard Symbols | T - Toxic |
Risk Codes | R23/24/25 - Toxic by inhalation, in contact with skin and if swallowed. R34 - Causes burns 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. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
UN IDs | UN 1760 8/PG 3 |
WGK Germany | 1 |
RTECS | UD3610000 |
HS Code | 29161290 |
Hazard Class | 8 |
Packing Group | II |
Raw Materials | Acrylic acid Acrylic acid Hydroquinone Propylene oxide Propylene oxide |
Downstream Products | AA|HPA |
LogP | 0.2 at 25℃ |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
introduction | hydroxypropyl acrylate is a colorless and transparent liquid, which can be miscible with water in any proportion and also dissolves most organic solvents. It can be used to produce adhesives, thermosetting coatings, fiber treatment agents and modifiers for synthetic resin copolymers, and can also be used to prepare lubricating oil additives. Used as a functional monomer as a crosslinking monomer of an acrylic resin, it is possible to improve the adhesion, weather resistance, drug resistance, impact resistance and gloss of the product. |
application | hydroxypropyl acrylate can be used to produce adhesives, thermosetting coatings, fiber treatment agents and modifiers for synthetic resin copolymers, and can also be used to prepare lubricating oil additives. Used as a functional monomer as a crosslinking monomer of an acrylic resin, it is possible to improve the adhesion, weather resistance, drug resistance, impact resistance and gloss of the product. Used in the manufacture of synthetic resins, adhesives, thermosetting coatings, etc. It is also used in the manufacture of fiber treatment agents, latex, printing inks, medical materials, etc. |
use | can be used to produce adhesives, thermosetting coatings, fiber treatment agents and modifiers for synthetic resin copolymers, and can also be used to prepare lubricating oil additives, etc. can be used to produce thermosetting coatings, adhesives, fiber treatment agents and modifiers for synthetic resin copolymers. It can also be used as one of the main crosslinking functional group monomers used in acrylic resins. It is mainly used to manufacture thermosetting acrylic coatings, photocurable coatings, photosensitive coatings, textile treatment agents, adhesives, paper processing, water quality stabilizers and polymer materials. It has the characteristics of low usage, but can significantly improve the performance of the product |
production method | 1. acrylic acid is prepared by oxidation of propylene or hydrolysis of acrylonitrile. Then the acrylic acid and propylene oxide in the catalyst and iron, aluminum, chromium and other polymerization inhibitors under the action of the addition reaction, the formation of acrylic acid-2-hydroxypropyl ester crude product, after degassing, distillation to obtain the finished product. The main reaction is as follows: |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |