Conditions | Yield |
---|---|
With 4-Cl-3,5-(NO2)2-C6H2COCF3 In water; toluene at 19.84℃; Equilibrium constant; Further Variations:; Reagents; |
N,N-dimethyl-formamide
sodium trichloroacetate
Conditions | Yield |
---|---|
With trichloroacetic acid |
sodium trichloroacetate
Conditions | Yield |
---|---|
In acetonitrile for 1h; Heating; | 99% |
Conditions | Yield |
---|---|
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; |
Conditions | Yield |
---|---|
In acetonitrile at 0 - 5℃; for 2h; Irradiation; | 98% |
sodium trichloroacetate
2-nitro-benzaldehyde
2-nitro-α-(trichloromethyl)benzyl alcohol
Conditions | Yield |
---|---|
With malonic acid In dimethyl sulfoxide at 20℃; for 0.666667h; | 98% |
Conditions | Yield |
---|---|
In acetonitrile for 1h; Heating; | 97% |
Conditions | Yield |
---|---|
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃; | 97% |
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃; | 93% |
sodium trichloroacetate
4-fluorobenzaldehyde
(+/-)-2,2,2-trichloro-1-(4-fluorophenyl)ethanol
Conditions | Yield |
---|---|
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃; | 97% |
sodium trichloroacetate
(4-isopropylbenzaldehyde)
1-(4-isopropylphenyl)-2,2,2-trichloroethanol
Conditions | Yield |
---|---|
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃; | 97% |
Conditions | Yield |
---|---|
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃; | 97% |
sodium trichloroacetate
4-methoxy-benzaldehyde
2,2,2-trichloro-1-(4-methoxyphenyl)ethan-1-ol
Conditions | Yield |
---|---|
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
sodium trichloroacetate
tert-butyldimethylsilyl chloride
tert-butyldimethyl[2,2,2-trichloro-1-(3-iodophenyl)ethoxy]silane
Conditions | Yield |
---|---|
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
4-methoxy-benzaldehyde
tert-butyldimethylsilyl chloride
tert-butyldimethyl[2,2,2-trichloro-1-(4-methoxyphenyl)ethoxy]silane
Conditions | Yield |
---|---|
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
sodium trichloroacetate
1,1,1-trichloro-5-phenyl-5-hexen-2-ol
Conditions | Yield |
---|---|
With trichloroacetic acid | 96% |
4-Trifluoromethylbenzaldehyde
sodium trichloroacetate
tert-butyldimethylsilyl chloride
tert-butyldimethyl[2,2,2-trichloro-1-(4-trifluoromethylphenyl)ethoxy]silane
Conditions | Yield |
---|---|
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
benzaldehyde
tert-butyldimethylsilyl chloride
tert-butyldimethyl(2,2,2-trichloro-1-phenylethoxy)silane
Conditions | Yield |
---|---|
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
4-nitrobenzaldehdye
4-nitro-α-(trichloromethyl)benzyl alcohol
Conditions | Yield |
---|---|
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
tert-butyldimethylsilyl chloride
β-naphthaldehyde
tert-butyldimethyl(2,2,2-trichloro-1-naphthylen-2-ylethoxy)silane
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃; | 95% |
nonan-1-al
sodium trichloroacetate
1,1,1-trichloro-2-decanol
Conditions | Yield |
---|---|
With trichloroacetic acid In N,N-dimethyl-formamide at 5 - 20℃; for 17.5h; | 95% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; Inert atmosphere; | 95% |
furan-3-carboxaldehyde
sodium trichloroacetate
trichloroacetic acid
2,2,2-trichloro-1-furan-2-yl-ethanol
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; Inert atmosphere; | 95% |
N-methylpyrrole aldehyde
sodium trichloroacetate
tert-butyldimethylsilyl chloride
2-[1-(tert-butyldimethylsilanyloxy)-2,2,2-trichloroethyl]-1-methyl-1H-pyrrole
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
With trichloroacetic acid In N,N-dimethyl-formamide at 5 - 20℃; for 17.5h; | 94% |
3-allylsalicylaldehyde
sodium trichloroacetate
tert-butyldimethylsilyl chloride
1-allyl-2-(tert-butyldimethylsilanyloxy)-3-[1-(tert-butyldimethylsilanyloxy)-2,2,2-trichloroethyl]benzene
Conditions | Yield |
---|---|
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]
sodium trichloroacetate
A
triphenylbismuth bis(trichloroacetate)
B
triphenylbismuthane
Conditions | Yield |
---|---|
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
sodium trichloroacetate
2,2,2-trichloro-1-(thien-2-yl)-ethanol
Conditions | Yield |
---|---|
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
4-(tert-butyldimethylsilanyloxy)butanal
Conditions | Yield |
---|---|
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃; | 93% |
sodium trichloroacetate
β-naphthaldehyde
2,2,2-trichloro-1-(naphthalen-2-yl)ethan-1-ol
Conditions | Yield |
---|---|
With trichloroacetic acid In N,N-dimethyl-formamide at 20℃; | 93% |
Conditions | Yield |
---|---|
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
sodium trichloroacetate
trichloroacetic acid
C12H22Cl3NO3S
Conditions | Yield |
---|---|
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% |
IUPAC Name:Sodium 2,2,2-trichloroacetate (650-51-1)
Synonyms: Erbitox t95g ; Sodium trichloroacetate ; Tca sodium ; Tca sodium salt;trichloroacetic acid sodium salt ; Aceticacid,trichloro-,sodiumsalt;acpgrasskiller ; Alliedarcadiansodiumtca
CAS: 650-51-1
MF: C2Cl3NaO2
MW: 185.37
MS:
EINECS: 211-479-2
Mol File: 650-51-1.mol
Flash Point: 66.3 °C
Enthalpy of Vaporization: 47.69 kJ/mol
Boiling Point: 196.5 °C at 760 mmHg
Vapour Pressure: 0.17 mmHg at 25°C
Melting point:300 °C
Storage temp: 0-6°C
Sensitive: Hygroscopic
Merck: 14,9627
BRN: 3572664
Appearance: White to almost white powder
1.Trichloroacetic acid sodium salt (650-51-1) is used for antacid for Vinyl sulfone reactive printing process.
2.Trichloroacetic acid sodium salt (650-51-1) is the main raw material for production of certain pesticides
Add the chloral and concentrated nitric acid into reactor, heated and dissolved, then got trichloroacetic acid , add sodium hydroxide aqueous solution, concentration, crystallization, filtration, drying ,derive Trichloroacetic acid sodium salt (650-51-1).
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
cat | LD50 | oral | 4gm/kg (4000mg/kg) | PERIPHERAL NERVE AND SENSATION: FLACCID PARALYSIS WITHOUT ANESTHESIA (USUALLY NEUROMUSCULAR BLOCKAGE) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: MUSCLE WEAKNESS | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 32(1), Pg. 48, 1967. |
chicken | LD50 | oral | 4280mg/kg (4280mg/kg) | Down to Earth. Vol. 35, Pg. 25, 1979. | |
guinea pig | LD50 | oral | 6gm/kg (6000mg/kg) | PERIPHERAL NERVE AND SENSATION: FLACCID PARALYSIS WITHOUT ANESTHESIA (USUALLY NEUROMUSCULAR BLOCKAGE) BEHAVIORAL: MUSCLE WEAKNESS BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 32(1), Pg. 48, 1967. |
mammal (species unspecified) | LD50 | unreported | 3300mg/kg (3300mg/kg) | "Chemistry of Pesticides," Melnikov, N.N., New York, Springer-Verlag New York, Inc., 1971Vol. -, Pg. 121, 1971. | |
mouse | LD50 | oral | 3600mg/kg (3600mg/kg) | Pesticide Chemicals Official Compendium, Association of the American Pesticide Control Officials, Inc., 1966. Vol. -, Pg. 1061, 1966. | |
rabbit | LD | skin | > 10100mg/kg (10100mg/kg) | BEHAVIORAL: FOOD INTAKE (ANIMAL) | National Technical Information Service. Vol. OTS0545852, |
rabbit | LD50 | oral | 6gm/kg (6000mg/kg) | PERIPHERAL NERVE AND SENSATION: FLACCID PARALYSIS WITHOUT ANESTHESIA (USUALLY NEUROMUSCULAR BLOCKAGE) BEHAVIORAL: MUSCLE WEAKNESS BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 32(1), Pg. 48, 1967. |
rat | LC50 | inhalation | > 365gm/m3/4H (365000mg/m3) | "Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A377, Pg. 1983, | |
rat | LD50 | oral | 3320mg/kg (3320mg/kg) | Khimiya v Sel'skom Khozyaistve. Chemistry in Agriculture. Vol. 18(3), Pg. 46, 1980. | |
rat | LD50 | skin | > 2gm/kg (2000mg/kg) | "Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A377, Pg. 1983, |
Reported in EPA TSCA Inventory.
Hazard Codes Xi,N
Risk Statements 37-50/53
37: Irritating to the respiratory system
50/53: Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment
Safety Statements 46-60-61
46: If swallowed, seek medical advice immediately and show this container or label
60: This material and/or its container must be disposed of as hazardous waste
61: Avoid release to the environment. Refer to special instructions safety data sheet
RIDADR UN 3077 9/PG 3
WGK Germany 2
RTECS AJ9100000
PackingGroup III
Chemical properties: Trichloroacetic acid sodium salt (650-51-1) is a white flaky crystal, melting point> 300 ℃, soluble in water, solubility of 50 g/100 ml, pH value of 7.5. break down easily at high temperatures or in steam. Easy to deliquescence, there are stimulating flavor.
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