TRIFLUOROETHYL ALCOHOL D3 - Names and Identifiers
TRIFLUOROETHYL ALCOHOL D3 - Physico-chemical Properties
| Molecular Formula | C2H3F3O
|
| Molar Mass | 100.04 |
| Density | 1.415 g/mL at 25 °C(lit.) |
| Melting Point | -44 °C(lit.) |
| Boling Point | 77-80 °C(lit.) |
| Flash Point | 85 °F |
| Appearance | Morphological Liquid |
| Storage Condition | Flammables area |
| Stability | Hygroscopic |
| Refractive Index | n20/D 1.3(lit.) |
| Use | Uses Trifluoroethanol is an organic compound, abbreviated as TFE. It is a colorless, water-soluble liquid with an odor similar to ethanol. Due to the strong electron-withdrawing effect of trifluoromethyl, trifluoroethanol is much more acidic than ethanol, and can form a stable complex with hydrogen bonds with heterocyclic compounds. Trifluoroethanol is used as a solvent in organic chemistry. The oxidation reaction of sulfur compounds with hydrogen peroxide often uses TFE as a solvent. |
TRIFLUOROETHYL ALCOHOL D3 - Risk and Safety
| Risk Codes | R10 - Flammable
R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
R38 - Irritating to the skin
R41 - Risk of serious damage to eyes
R48/20 -
|
| Safety Description | S16 - Keep away from sources of ignition.
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
|
| UN IDs | UN 1987 3/PG 3 |
| WGK Germany | 3 |
| HS Code | 28459010 |
| Hazard Class | 3 |
| Packing Group | III |
TRIFLUOROETHYL ALCOHOL D3 - Introduction
2,2,2-TRIFLUOROETHANOL-D3 is a special organic compound, also known as 2,2,2-TRIFLUOROETHANOL-D3. Its molecular formula is CD3CFOD, where hydrogen atoms are replaced by deuterium atoms (D).
Nature:
1. 2,2,2-TRIFLUOROETHANOL-D3 is a colorless liquid with a pungent odor.
2. It is soluble in many organic solvents, such as ethanol and ether.
3. 2,2,2-TRIFLUOROETHANOL-D3 is a stable compound and is not easy to decompose.
Use:
1. 2,2,2-TRIFLUOROETHANOL-D3 is often used as a solvent in NMR (nuclear magnetic resonance) spectra. It can provide deuterium signal and does not react with most compounds, so it has important applications in chemical detection and structural analysis.
2. 2,2,2-TRIFLUOROETHANOL-D3 can also be used for synthetic purposes. Due to its special structure, it can be used as a solvent or starting material for organic synthesis reactions.
Method:
2,2,2-TRIFLUOROETHANOL-D3 is usually prepared by deuteration reaction. One method is to react trifluoroethanol with deuterium gas, replacing hydrogen atoms with deuterium atoms in the reaction. This reaction is carried out in the presence of a catalyst. Alkali catalysts such as sodium or potassium are generally used.
Safety Information:
1. 2,2,2-TRIFLUOROETHANOL-D3 is generally considered to be a low toxic compound and has no obvious acute toxicity.
2. When using 2,2,2-TRIFLUOROETHANOL-D3, you should follow the laboratory safety procedures and avoid direct contact with skin and eyes. Wear personal protective equipment such as gloves and goggles if necessary.
3. For people exposed to 2,2,2-TRIFLUOROETHANOL-D3 for a long time, there may be a certain chronic risk, but the relevant data are lacking.
4. When handling and storing 2,2,2-TRIFLUOROETHANOL-D3, avoid contact with oxygen and high temperature to prevent fire or explosion.
Last Update：2024-04-10 22:29:15