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SODIUM TRICHLOROACETATE

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SODIUM TRICHLOROACETATE Basic information

Product Name:
SODIUM TRICHLOROACETATE
Synonyms:
  • ERBITOX T95G
  • SODIUM TRICHLOROACETATE
  • TCA-SODIUM
  • TCA SODIUM SALT
  • TRICHLOROACETIC ACID SODIUM SALT
  • Aceticacid,trichloro-,sodiumsalt
  • sodio(tricloroacetatodi)
  • sodium(trichloracetatede)
CAS:
650-51-1
MF:
C2Cl3NaO2
MW:
185.37
EINECS:
211-479-2
Mol File:
650-51-1.mol
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SODIUM TRICHLOROACETATE Chemical Properties

Melting point:
300 °C
Density 
0.9 g/cm3
storage temp. 
Sealed in dry,Room Temperature
form 
Powder or Granular Powder
pka
0.6[at 20 ℃]
color 
White to off-white
Water Solubility 
Soluble in water, ethanol, methanol, acetone.
Sensitive 
Hygroscopic
Merck 
14,9627
BRN 
3572664
InChIKey
SAQSTQBVENFSKT-UHFFFAOYSA-M
LogP
-2.67 at 25℃
CAS DataBase Reference
650-51-1(CAS DataBase Reference)
EPA Substance Registry System
Sodium trichloroacetate (650-51-1)
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Safety Information

Hazard Codes 
Xi,N
Risk Statements 
37-50/53
Safety Statements 
46-60-61
RIDADR 
UN 3077 9/PG 3
WGK Germany 
2
RTECS 
AJ9100000
TSCA 
Yes
HazardClass 
9
PackingGroup 
III
HS Code 
29154000
Hazardous Substances Data
650-51-1(Hazardous Substances Data)
Toxicity
LD50 orl-rat: 3320 mg/kg KSKZAN 18(3),46,80

MSDS

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SODIUM TRICHLOROACETATE Usage And Synthesis

Chemical Properties

White to almost white powder

Uses

As a decalcifier and fixative in microscopy; also as a precipitant of protein. As herbicide.

Uses

Sodium trichloroacetate, is used in acid binding reagent in the textile industry in the dying process. Sodium trichloroacetate has been reported previously to be an effective denaturation reagent for proteins was applied to poly(l-lysine) and poly(l-glutamic acid) to see its effects on a coil-to-helix transition and on the chemical reactivities of the ε-amino group of poly(l-lysine). Addition of sodium trichloroacetate to poly-(l-lysine) induced a helical conformation even at neutral pH where the ε-amino group of the polymer was protonated.

Uses

Sodium trichloroacetate with trichloroacetic acid (TCA) undergoes rapid decarboxylation in dimethylformamide (DMF) in the presence of aldehydes to form nucleophilic trichloromethyl anion, which then adds to the aldehydes to form trichloromethyl carbinols. It can also undergo thermal decarboxylation in aprotonic solvents in the presence of olefins to generate dichlorocarbene as an intermediate.

Definition

ChEBI: TCA-sodium is an organic molecular entity.

Hazard

Toxic by ingestion, irritant to skin and eyes.

Flammability and Explosibility

Non flammable

Safety Profile

Moderately toxic by ingestion andintravenous routes. Human mutation data reported. Largedoses cause central nervous system depression. Used as anherbicide. Bags of the salt can ignite spontaneously instorage. When heated to decomposition it emits very

SODIUM TRICHLOROACETATE Preparation Products And Raw materials

Raw materials

Preparation Products

SODIUM TRICHLOROACETATESupplier

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