|
|
| | 2-(Trifluoromethyl)acrylic acid Basic information |
| | 2-(Trifluoromethyl)acrylic acid Chemical Properties |
| Melting point | 51-52 °C (lit.) | | Boiling point | 86 °C | | density | 1.3949 (estimate) | | Fp | 179 °F | | storage temp. | 2-8°C | | pka | 2.07±0.11(Predicted) | | form | Chunks | | color | Light yellow | | Water Solubility | Soluble in water. | | InChI | InChI=1S/C4H3F3O2/c1-2(3(8)9)4(5,6)7/h1H2,(H,8,9) | | InChIKey | VLSRKCIBHNJFHA-UHFFFAOYSA-N | | SMILES | C(O)(=O)C(C(F)(F)F)=C | | CAS DataBase Reference | 381-98-6(CAS DataBase Reference) |
| Hazard Codes | C,Xi | | Risk Statements | 34-36/37/38 | | Safety Statements | 26-36/37/39-45-37/39 | | RIDADR | UN 3261 8/PG 2 | | WGK Germany | 3 | | Hazard Note | Corrosive | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29161900 | | Storage Class | 8A - Combustible corrosive hazardous materials | | Hazard Classifications | Skin Corr. 1B |
| | 2-(Trifluoromethyl)acrylic acid Usage And Synthesis |
| Chemical Properties | LIGHT YELLOW TRANSPARENT CHUNKS | | Uses | 2-(Trifluoromethyl)acrylic acid is used as an acidic functional monomer for molecular imprinting of nicotine. And also used in the conventional functional monomer methacrylic acid. | | Uses | 2-(Trifluoromethyl)acrylic acid (TFMAA) is a strong acid functional monomer, which shows a good performance in the solid-phase extraction of domoic acid. It can also be used in the preparation of molecularly imprinted polymers that show diastereoselectivity for cinchona alkaloids. |
| | 2-(Trifluoromethyl)acrylic acid Preparation Products And Raw materials |
|