SODIUM TRICHLOROACETATE

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
Product Categories:
Mol File:650-51-1.mol
SODIUM TRICHLOROACETATE Structure
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
pka0.6[at 20 ℃]
color White to off-white
Water Solubility Soluble in water, ethanol, methanol, acetone.
Sensitive Hygroscopic
Merck 14,9627
BRN 3572664
InChIKeySAQSTQBVENFSKT-UHFFFAOYSA-M
LogP-2.67 at 25℃
CAS DataBase Reference650-51-1(CAS DataBase Reference)
EPA Substance Registry SystemSodium trichloroacetate (650-51-1)
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 Data650-51-1(Hazardous Substances Data)
ToxicityLD50 orl-rat: 3320 mg/kg KSKZAN 18(3),46,80
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
SODIUM TRICHLOROACETATE Usage And Synthesis
Chemical PropertiesWhite to almost white powder
UsesAs a decalcifier and fixative in microscopy; also as a precipitant of protein. As herbicide.
UsesSodium 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.
UsesSodium 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.
DefinitionChEBI: TCA-sodium is an organic molecular entity.
HazardToxic by ingestion, irritant to skin and eyes.
Flammability and ExplosibilityNonflammable
Safety ProfileModerately 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 materialsNitric acid-->Chloral-->Trichloroacetic acid-->Sodium 2,4,6-trinitrophenate
Preparation ProductsTETRACHLOROCYCLOPROPENE-->1,1,1-TRICHLOROACETONE
Hexane Hydrazine sulfate Sodium acetate trihydrate Phenol Trichloroisocyanuric acid Trichloroacetonitrile Ethyl trichloroacetate Triclosan Sodium chlorate Trichloroacetic acid Sodium dichloroacetate SODIUM TRICHLOROACETATE Chloroacetic acid Dichloroacetic acid SODIUM TRICHLOROACETATE (TRICHLOROACETIC ACID SODIUM SALT) Dichloroacetate Sodium chloroacetate

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