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650-51-1 Usage

Description

Sodium trichloroacetate is a chemical compound with the formula C2HCl3O2Na. It is a white crystalline solid that is soluble in water and has a variety of applications in different industries.

Uses

Used in Microscopy:
Sodium trichloroacetate is used as a decalcifier and fixative in microscopy, helping to preserve and prepare samples for examination.
Used in Protein Precipitation:
It is also used as a precipitant of protein, aiding in the separation and purification of proteins in various applications.
Used in Herbicide Formulations:
Sodium trichloroacetate is used in herbicide formulations to control the growth of unwanted plants.
Used in Textile Industry:
In the textile industry, sodium trichloroacetate is used as an acid binding reagent in the dyeing process, helping to improve the colorfastness and quality of dyed fabrics.
Used in Protein Denaturation:
Sodium trichloroacetate has been reported to be an effective denaturation reagent for proteins. It has been applied to poly(l-lysine) and poly(l-glutamic acid) to study its effects on a coil-to-helix transition and on the chemical reactivities of the ε-amino group of poly(l-lysine). The addition of sodium trichloroacetate to poly-(l-lysine) induces a helical conformation even at neutral pH where the ε-amino group of the polymer is protonated.
Used in Organic Synthesis:
Sodium trichloroacetate, in combination 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, which can be used in various organic synthesis reactions.

Hazard

Toxic by ingestion, irritant to skin and eyes.

Flammability and Explosibility

Nonflammable

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

Check Digit Verification of cas no

The CAS Registry Mumber 650-51-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 650-51:
(5*6)+(4*5)+(3*0)+(2*5)+(1*1)=61
61 % 10 = 1
So 650-51-1 is a valid CAS Registry Number.
InChI:InChI=1/C2HCl3O2/c3-2(4,5)1(6)7/h(H,6,7)

650-51-1 Well-known Company Product Price

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  • Alfa Aesar

  • (A17004)  Sodium trichloroacetate, 97%   

  • 650-51-1

  • 10g

  • 193.0CNY

  • Detail
  • Alfa Aesar

  • (A17004)  Sodium trichloroacetate, 97%   

  • 650-51-1

  • 250g

  • 245.0CNY

  • Detail
  • Alfa Aesar

  • (A17004)  Sodium trichloroacetate, 97%   

  • 650-51-1

  • 1000g

  • 788.0CNY

  • Detail
  • Alfa Aesar

  • (A17004)  Sodium trichloroacetate, 97%   

  • 650-51-1

  • 5000g

  • 3210.0CNY

  • Detail
  • Sigma-Aldrich

  • (31525)  TCA  PESTANAL®, analytical standard

  • 650-51-1

  • 31525-250MG

  • 312.39CNY

  • Detail
  • Aldrich

  • (190780)  Sodiumtrichloroacetate  97%

  • 650-51-1

  • 190780-5G

  • 285.48CNY

  • Detail
  • Aldrich

  • (190780)  Sodiumtrichloroacetate  97%

  • 650-51-1

  • 190780-100G

  • 355.68CNY

  • Detail

650-51-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name TCA-sodium

1.2 Other means of identification

Product number -
Other names sodium trichloroacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:650-51-1 SDS

650-51-1Synthetic route

C45H94N(1+)*C2Cl3O2(1-)

C45H94N(1+)*C2Cl3O2(1-)

sodium picrate
3324-58-1

sodium picrate

A

sodium trichloroacetate
650-51-1

sodium trichloroacetate

B

tri(nonyl)octadecylammonium picrate

tri(nonyl)octadecylammonium picrate

Conditions
ConditionsYield
With 4-Cl-3,5-(NO2)2-C6H2COCF3 In water; toluene at 19.84℃; Equilibrium constant; Further Variations:; Reagents;
N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

sodium trichloroacetate
650-51-1

sodium trichloroacetate

Conditions
ConditionsYield
With trichloroacetic acid
sodium trichloroacetate
650-51-1

sodium trichloroacetate

N-Ethylphenanthridinium iodide

N-Ethylphenanthridinium iodide

5-Ethyl-6-trichloromethyl-5,6-dihydro-phenanthridine

5-Ethyl-6-trichloromethyl-5,6-dihydro-phenanthridine

Conditions
ConditionsYield
In acetonitrile for 1h; Heating;99%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

benzaldehyde
100-52-7

benzaldehyde

2,2,2-trichloro-1-phenylethanol
2000-43-3

2,2,2-trichloro-1-phenylethanol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 5 - 20℃; for 17.5h;98%
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;96%
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;89%
In 1,2-dimethoxyethane
With tetrabutylammomium bromide In chloroform; water for 0.133333h; microwave irradiation;
sodium trichloroacetate
650-51-1

sodium trichloroacetate

2-methylisoquinolinium iodide
3947-77-1

2-methylisoquinolinium iodide

2-Methyl-1-trichloromethyl-1,2-dihydro-isoquinoline

2-Methyl-1-trichloromethyl-1,2-dihydro-isoquinoline

Conditions
ConditionsYield
In acetonitrile at 0 - 5℃; for 2h; Irradiation;98%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

2-nitro-benzaldehyde
552-89-6

2-nitro-benzaldehyde

2-nitro-α-(trichloromethyl)benzyl alcohol
62798-94-1

2-nitro-α-(trichloromethyl)benzyl alcohol

Conditions
ConditionsYield
With malonic acid In dimethyl sulfoxide at 20℃; for 0.666667h;98%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

N-methylquinaldinium iodide
876-87-9

N-methylquinaldinium iodide

1,2-Dimethyl-4-trichloromethyl-1,4-dihydro-quinoline

1,2-Dimethyl-4-trichloromethyl-1,4-dihydro-quinoline

Conditions
ConditionsYield
In acetonitrile for 1h; Heating;97%
Octanal
124-13-0

Octanal

sodium trichloroacetate
650-51-1

sodium trichloroacetate

1,1,1-trichlorononan-2-ol
4776-43-6

1,1,1-trichlorononan-2-ol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;97%
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;93%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

4-fluorobenzaldehyde
459-57-4

4-fluorobenzaldehyde

(+/-)-2,2,2-trichloro-1-(4-fluorophenyl)ethanol
394-56-9

(+/-)-2,2,2-trichloro-1-(4-fluorophenyl)ethanol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;97%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

(4-isopropylbenzaldehyde)
122-03-2

(4-isopropylbenzaldehyde)

1-(4-isopropylphenyl)-2,2,2-trichloroethanol
55011-04-6

1-(4-isopropylphenyl)-2,2,2-trichloroethanol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;97%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

3-Fluorobenzaldehyde
456-48-4

3-Fluorobenzaldehyde

2,2,2-trichloro-1-(3-fluoro-phenyl)-ethanol

2,2,2-trichloro-1-(3-fluoro-phenyl)-ethanol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;97%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

2,2,2-trichloro-1-(4-methoxyphenyl)ethan-1-ol
14337-31-6

2,2,2-trichloro-1-(4-methoxyphenyl)ethan-1-ol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;97%
In dimethyl sulfoxide at 20℃; Reagent/catalyst; Solvent; Time;93%
With tetrabutylammomium bromide In chloroform; water for 0.133333h; microwave irradiation;
m-iodobenzaldehyde
696-41-3

m-iodobenzaldehyde

sodium trichloroacetate
650-51-1

sodium trichloroacetate

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

tert-butyldimethyl[2,2,2-trichloro-1-(3-iodophenyl)ethoxy]silane
1027382-22-4

tert-butyldimethyl[2,2,2-trichloro-1-(3-iodophenyl)ethoxy]silane

Conditions
ConditionsYield
Stage #1: m-iodobenzaldehyde; sodium trichloroacetate In N,N-dimethyl-formamide at 20℃; for 0.666667h;
Stage #2: tert-butyldimethylsilyl chloride With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 8h; Further stages.;
97%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

tert-butyldimethyl[2,2,2-trichloro-1-(4-methoxyphenyl)ethoxy]silane
1027382-19-9

tert-butyldimethyl[2,2,2-trichloro-1-(4-methoxyphenyl)ethoxy]silane

Conditions
ConditionsYield
Stage #1: sodium trichloroacetate; 4-methoxy-benzaldehyde In N,N-dimethyl-formamide at 20℃; for 0.666667h;
Stage #2: tert-butyldimethylsilyl chloride With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 8h; Further stages.;
97%
4-phenyl-4-penten-1-al
51758-24-8

4-phenyl-4-penten-1-al

sodium trichloroacetate
650-51-1

sodium trichloroacetate

1,1,1-trichloro-5-phenyl-5-hexen-2-ol
402942-45-4

1,1,1-trichloro-5-phenyl-5-hexen-2-ol

Conditions
ConditionsYield
With trichloroacetic acid96%
4-Trifluoromethylbenzaldehyde
455-19-6

4-Trifluoromethylbenzaldehyde

sodium trichloroacetate
650-51-1

sodium trichloroacetate

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

tert-butyldimethyl[2,2,2-trichloro-1-(4-trifluoromethylphenyl)ethoxy]silane
1027382-23-5

tert-butyldimethyl[2,2,2-trichloro-1-(4-trifluoromethylphenyl)ethoxy]silane

Conditions
ConditionsYield
Stage #1: 4-Trifluoromethylbenzaldehyde; sodium trichloroacetate In N,N-dimethyl-formamide at 20℃; for 0.666667h;
Stage #2: tert-butyldimethylsilyl chloride With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 8h; Further stages.;
96%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

benzaldehyde
100-52-7

benzaldehyde

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

tert-butyldimethyl(2,2,2-trichloro-1-phenylethoxy)silane
1027382-16-6

tert-butyldimethyl(2,2,2-trichloro-1-phenylethoxy)silane

Conditions
ConditionsYield
Stage #1: sodium trichloroacetate; benzaldehyde In N,N-dimethyl-formamide at 20℃; for 0.666667h;
Stage #2: tert-butyldimethylsilyl chloride With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 8h; Further stages.;
96%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

4-nitrobenzaldehdye
555-16-8

4-nitrobenzaldehdye

4-nitro-α-(trichloromethyl)benzyl alcohol
54075-25-1

4-nitro-α-(trichloromethyl)benzyl alcohol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;95%
With malonic acid In dimethyl sulfoxide at 20℃; for 0.666667h;90%
With tetrabutylammomium bromide In chloroform; water for 0.0833333h; microwave irradiation;
sodium trichloroacetate
650-51-1

sodium trichloroacetate

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

β-naphthaldehyde
66-99-9

β-naphthaldehyde

tert-butyldimethyl(2,2,2-trichloro-1-naphthylen-2-ylethoxy)silane
1027382-25-7

tert-butyldimethyl(2,2,2-trichloro-1-naphthylen-2-ylethoxy)silane

Conditions
ConditionsYield
Stage #1: sodium trichloroacetate; β-naphthaldehyde In N,N-dimethyl-formamide at 20℃; for 0.666667h;
Stage #2: tert-butyldimethylsilyl chloride With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 8h; Further stages.;
95%
furfural
98-01-1

furfural

sodium trichloroacetate
650-51-1

sodium trichloroacetate

2,2,2-trichloro-1-furan-2-yl-ethanol
70033-16-8

2,2,2-trichloro-1-furan-2-yl-ethanol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;95%
nonan-1-al
124-19-6

nonan-1-al

sodium trichloroacetate
650-51-1

sodium trichloroacetate

1,1,1-trichloro-2-decanol
263904-14-9, 133950-30-8

1,1,1-trichloro-2-decanol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 5 - 20℃; for 17.5h;95%
undecylaldehyde
112-44-7

undecylaldehyde

sodium trichloroacetate
650-51-1

sodium trichloroacetate

trichloroacetic acid
76-03-9

trichloroacetic acid

1,1,1-trichlorododec-11-en-2-ol

1,1,1-trichlorododec-11-en-2-ol

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; Inert atmosphere;95%
furan-3-carboxaldehyde
498-60-2

furan-3-carboxaldehyde

sodium trichloroacetate
650-51-1

sodium trichloroacetate

trichloroacetic acid
76-03-9

trichloroacetic acid

2,2,2-trichloro-1-furan-2-yl-ethanol
70033-16-8

2,2,2-trichloro-1-furan-2-yl-ethanol

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; Inert atmosphere;95%
N-methylpyrrole aldehyde
1192-58-1

N-methylpyrrole aldehyde

sodium trichloroacetate
650-51-1

sodium trichloroacetate

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

2-[1-(tert-butyldimethylsilanyloxy)-2,2,2-trichloroethyl]-1-methyl-1H-pyrrole
1027382-30-4

2-[1-(tert-butyldimethylsilanyloxy)-2,2,2-trichloroethyl]-1-methyl-1H-pyrrole

Conditions
ConditionsYield
Stage #1: N-methylpyrrole aldehyde; sodium trichloroacetate In N,N-dimethyl-formamide at 20℃; for 0.666667h;
Stage #2: tert-butyldimethylsilyl chloride With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 8h; Further stages.;
94%
undecylaldehyde
112-44-7

undecylaldehyde

sodium trichloroacetate
650-51-1

sodium trichloroacetate

1,1,1-trichlorododecan-2-ol
96502-92-0

1,1,1-trichlorododecan-2-ol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 5 - 20℃; for 17.5h;94%
3-allylsalicylaldehyde
24019-66-7

3-allylsalicylaldehyde

sodium trichloroacetate
650-51-1

sodium trichloroacetate

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

1-allyl-2-(tert-butyldimethylsilanyloxy)-3-[1-(tert-butyldimethylsilanyloxy)-2,2,2-trichloroethyl]benzene
1027381-97-0

1-allyl-2-(tert-butyldimethylsilanyloxy)-3-[1-(tert-butyldimethylsilanyloxy)-2,2,2-trichloroethyl]benzene

Conditions
ConditionsYield
Stage #1: 3-allylsalicylaldehyde; sodium trichloroacetate In N,N-dimethyl-formamide at 20℃; for 0.666667h;
Stage #2: tert-butyldimethylsilyl chloride With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 16h; Further stages.;
93%
μ-oxobis[(4-methylbenzenesulfonato)triphenylbismuth]
119987-71-2

μ-oxobis[(4-methylbenzenesulfonato)triphenylbismuth]

sodium trichloroacetate
650-51-1

sodium trichloroacetate

A

triphenylbismuth bis(trichloroacetate)
28719-49-5

triphenylbismuth bis(trichloroacetate)

B

triphenylbismuthane
603-33-8

triphenylbismuthane

Conditions
ConditionsYield
In toluene byproducts: sodium 4-methylbenzenesulfonate; heated for 2 h at 80-90°C; cooled, filtered, solvent-removed, extd. (petroleum ether);A 93%
B 92%
thiophene-2-carbaldehyde
98-03-3

thiophene-2-carbaldehyde

sodium trichloroacetate
650-51-1

sodium trichloroacetate

2,2,2-trichloro-1-(thien-2-yl)-ethanol
35320-27-5

2,2,2-trichloro-1-(thien-2-yl)-ethanol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;93%
With malonic acid In dimethyl sulfoxide at 20℃; for 0.666667h;60%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

4-(tert-butyldimethylsilanyloxy)butanal
87184-81-4

4-(tert-butyldimethylsilanyloxy)butanal

5-(tert-butyldimethylsilyloxy)-1,1,1-trichloropentan-2-ol

5-(tert-butyldimethylsilyloxy)-1,1,1-trichloropentan-2-ol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;93%
sodium trichloroacetate
650-51-1

sodium trichloroacetate

β-naphthaldehyde
66-99-9

β-naphthaldehyde

2,2,2-trichloro-1-(naphthalen-2-yl)ethan-1-ol
77495-23-9, 19126-08-0

2,2,2-trichloro-1-(naphthalen-2-yl)ethan-1-ol

Conditions
ConditionsYield
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃;93%
C11H21NO3S
956352-18-4

C11H21NO3S

sodium trichloroacetate
650-51-1

sodium trichloroacetate

C12H22Cl3NO3S
1192423-81-6

C12H22Cl3NO3S

Conditions
ConditionsYield
Stage #1: C11H21NO3S; sodium trichloroacetate With trichloroacetic acid In N,N-dimethyl-formamide at 23 - 26℃; for 1h;
Stage #2: With sodium hydrogencarbonate In water; N,N-dimethyl-formamide
93%
C11H21NO3S
956352-18-4

C11H21NO3S

sodium trichloroacetate
650-51-1

sodium trichloroacetate

trichloroacetic acid
76-03-9

trichloroacetic acid

C12H22Cl3NO3S
1192423-81-6

C12H22Cl3NO3S

Conditions
ConditionsYield
Stage #1: C11H21NO3S; sodium trichloroacetate; trichloroacetic acid In N,N-dimethyl-formamide at 18 - 26℃; for 1h;
Stage #2: With sodium hydrogencarbonate In N,N-dimethyl-formamide
93%

650-51-1Relevant articles and documents

Effect of solvating additives on anion-exchange extraction of trichloroacetate anions from aqueous solutions with trinonyloctadecylammonium picrate in toluene

Rakhma'ko,Gulevich,Kiiko,Kovalevich

, p. 69 - 73 (2008/02/04)

The solvation effect of trifluoroacetophenone derivatives on anion-exchange extraction of trichloroacetate anions from aqueous phase with trinonyloctadecylammonium picrate in toluene was studied. Pleiades Publishing, Inc., 2006.

Trihalocyclopropyl carbonates

-

, (2008/06/13)

When the reaction of aldehydes with alkali metal trihaloacetates is carried out in the presence of a highly polar aprotic solvent (DMF, DMSO), novel organic alkali metal carbonates, which are precursors of pyrethroid insecticides, are formed in high yields and at a high rate. Novel sulfonates and dihalophosphites, derived from these carbonates have also been claimed.

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