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Sodium trifluoroacetate

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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
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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)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
RIDADR 
2811
WGK Germany 
1
RTECS 
AK0250000
3-10
Hazard Note 
Irritant/Hygroscopic
TSCA 
T
HazardClass 
6.1
PackingGroup 
II
HS Code 
29159080

MSDS

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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.]

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