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 Structure
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
Specific Gravity1.49
color White
PH7 (H2O, 20℃)
Water Solubility 625 g/L (25 ºC)
Sensitive Hygroscopic
Hydrolytic Sensitivity6: forms irreversible hydrate
BRN 3597949
Stability:Hygroscopic
InChIKeyUYCAUPASBSROMS-UHFFFAOYSA-M
LogP1.238 (est)
CAS DataBase Reference2923-18-4(CAS DataBase Reference)
EPA Substance Registry SystemAcetic 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
3-10
Hazard Note Irritant/Hygroscopic
TSCA T
HazardClass 6.1
PackingGroup II
HS Code 29159080
MSDS Information
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Sodium trifluoroacetate English
SigmaAldrich English
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Sodium trifluoroacetate Usage And Synthesis
Chemical PropertiesWhite crystalline powder
UsesSodium 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.
Purification MethodsA 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 Products2-(TRIFLUOROMETHYL)-4-ISOCYANATOPYRIDINE-->(Trifluoromethyl)trimethylsilane-->3-Trifluoromethylpyridine-->2-Trifluoromethyl-6-pyridinecarboxylic acid-->2-(TRIFLUOROMETHYL)-PYRIDINE-4-CARBOXALDEHYDE-->1,4-Bis(trifluoromethyl)-benzene-->PHENYL TRIFLUOROACETATE-->3,4,5-TRIFLUOROBENZOTRIFLUORIDE-->Bis(triphenylphosphine)iminium trifluoroacetate-->TRIMETHYLSILYL TRIFLUOROACETATE-->Pentamethylbenzene-->3-METHYLBENZOTRIFLUORIDE-->N-Butyltrifluoroacetamide
Sodium benzoate Sodium acetate SODIUM FLUOROACETATE Difluoroacetic acid sodium Sodium chloride Trifluoroacetic acid Diclofenac sodium SODIUM DIFLUOROACETATE Sodium trifluoroacetate Silver trifluoroacetate Sodium formate Sodium bicarbonate SODIUM TRIFLUOROACETATE-1-13C, 99 ATOM % 13C,SODIUM TRIFLUOROACETATE-1-13C Sodium hydroxide Sodium gluconate 8-CHLOROADENOSINE-3',5'-CYCLIC MONOPHOSPHOROTHIOATE, RP-ISOMER SODIUM SALT Sodium carbonate

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