Sodium trifluoroacetate
Sodium trifluoroacetate Basic information
- Product Name:
- Sodium trifluoroacetate
- Synonyms:
-
- SodiuM trifluoroacetate, 98%, 98%
- Sodium 2,2,2-trifluoroethanoate, Trifluoroacetic acid, sodium salt
- Trifluoroacetic acid, sodiuM salt, 97% 100GR
- Trifluoroacetic acid, sodiuM salt, 97% 25GR
- sodiumperfluoroacetate
- trifluoro-aceticacisodiumsalt
- TRIFLUOROACETIC ACID SODIUM SALT
- SODIUM TRIFLUOROACETATE
- CAS:
- 2923-18-4
- MF:
- C2F3NaO2
- MW:
- 136.01
- EINECS:
- 220-879-6
- Product Categories:
-
- metal acetate salt
- top
- Mol File:
- 2923-18-4.mol
Sodium trifluoroacetate Chemical Properties
- Melting point:
- 205-207 °C (dec.) (lit.)
- Density
- 1.49 g/mL (lit.)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- solubility
- H2O: 1 M at 20 °C, clear, colorless
- form
- Crystalline Powder
- color
- White
- Specific Gravity
- 1.49
- PH
- 7 (H2O, 20℃)
- Water Solubility
- 625 g/L (25 ºC)
- Sensitive
- Hygroscopic
- Hydrolytic Sensitivity
- 6: forms irreversible hydrate
- BRN
- 3597949
- Stability:
- Hygroscopic
- InChIKey
- UYCAUPASBSROMS-UHFFFAOYSA-M
- LogP
- 1.238 (est)
- CAS DataBase Reference
- 2923-18-4(CAS DataBase Reference)
- EPA Substance Registry System
- Acetic acid, trifluoro-, sodium salt (2923-18-4)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36-37/39
- RIDADR
- 2811
- WGK Germany
- 1
- RTECS
- AK0250000
- F
- 3-10
- Hazard Note
- Irritant/Hygroscopic
- TSCA
- T
- HazardClass
- 6.1
- PackingGroup
- II
- HS Code
- 29159080
MSDS
- Language:English Provider:Sodium trifluoroacetate
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
Sodium trifluoroacetate Usage And Synthesis
Chemical Properties
Sodium trifluoroacetate is an organic metal compound with the chemical formula CF3COONa. It is a white crystalline powderr that easily absorbs moisture. This compound has the ability to add a trifluoromethyl group to halogenated aromatic hydrocarbons.
Uses
Sodium trifluoroacetate is used in acid catalyzed reactions. It is also used as an intermediate for active pharmaceutical ingredients (API). Further, it acts as a precursor for the trifluoromethylation of aldehydes using copper(I) halide as a catalyst.
Preparation
It can be obtained by reacting trifluoroacetic acid with sodium carbonate or sodium hydroxide.
Purification Methods
A possible contaminant is NaCl. The solid is treated with CF3CO2H and evaporated twice. Its solubility in CF3CO2H is 13.1% at 29.8o. The residue is crystallised from dilute EtOH, and the solid is dried in vacuum at 100o. [Hara & Cady J Am Chem Soc 76 4285 1954.] It can be precipitated from EtOH by adding dioxane, then recrystallising several times from hot absolute EtOH. Dry it at 120-130o/1mm. [Beilstein 2 IV 461.]
Sodium trifluoroacetate Preparation Products And Raw materials
Preparation Products
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Sodium trifluoroacetate(2923-18-4)Related Product Information
- Diclofenac sodium
- Sodium benzoate
- Sodium chloride
- Trifluoroacetic acid
- Sodium hydroxide
- Sodium formate
- Sodium bicarbonate
- Sodium acetate
- Sodium carbonate
- Sodium gluconate
- Silver trifluoroacetate
- Trifluoroacetic anhydride
- Potassium trifluoroacetate
- Sodium thiophosphate
- Sodium thioglycolate
- 8-CHLOROADENOSINE-3',5'-CYCLIC MONOPHOSPHOROTHIOATE, RP-ISOMER SODIUM SALT
- PALLADIUM(II) TRIFLUOROACETATE
- 2-Bromoethyl trifluoromethanesulphonate