Tetrachloroethylene supplier

Name
1,1,2,2-Tetrach loroethylene
EINECS 204-825-9
CAS No. 127-18-4
Article Data322
CAS DataBase
Density 1.653 g/cm³
Solubility 0.015 g/100 mL (20 °C) in water
Melting Point -22 °C
Formula C₂Cl₄
Boiling Point 119.1 °C at 760 mmHg
Molecular Weight 165.834
Flash Point 27.4 °C
Transport Information UN 1897 6.1/PG 3
Appearance colourless liquid with ether-like odour
Safety 23-36/37-61-45-24-16-7
Risk Codes 40-51/53-23/25-11-39/23/24/25-23/24/25
Molecular Structure
Hazard Symbols Xn,N,T,F
Synonyms Ethene,tetrachloro- (9CI);Ethylene, tetrachloro- (8CI);1,1,2,2-Tetrachloroethene;Ankilostin;Antisal 1;Asahi Perchlor;Didakene;Dilatin PT;Ethylene tetrachloride;F 1110;F 1110 (halocarbon);Fedal-Un;Freon 1110;NSC 9777;Nema;PCE;PCE (chlorohydrocarbon);PerSec;Perchlorethylene;Perchloroethylene;Perclene;Perklone;PersaP 3;R 1110;Tetlen;Tetracap;Tetraguer;Tetraleno;Tetropil;
PSA 0.00000
LogP 3.06820

Synthetic route

: 55596-11-7
N-(2,2,2-trichloroethylidene)benzenesulfonamide

: 21326-49-8
complex of sulfur dioxide with dimethylamine

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 67-66-3
chloroform

C: 13707-43-2
N,N-dimethyl-N′-(phenylsulfonyl)formimidamide

Conditions

Conditions	Yield
In dichloromethane at 20℃; for 24h;	A n/a B n/a C 98%

...Expand

: 55596-11-7
N-(2,2,2-trichloroethylidene)benzenesulfonamide

: 109-89-7
diethylamine

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 67-66-3
chloroform

C: 29665-24-5
N1,N1-diethyl-N2-phenylsulfonylformamidine

Conditions

Conditions	Yield
In dichloromethane at 0℃; for 24h;	A n/a B n/a C 98%

...Expand

: 67-72-1
hexachloroethane

: 127-18-4
1,1,2,2-tetrachloroethylene

Conditions

Conditions	Yield
In tetrachloromethane at 300℃; for 0.000555556h; Temperature; Flow reactor; Pyrolysis;	97%
at 600℃;
With pyrographite at 700℃;

: 87-68-3
Hexachlorobutadiene

: 127-18-4
1,1,2,2-tetrachloroethylene

Conditions

Conditions	Yield
With aluminum (III) chloride; chlorine at 280 - 750℃; Temperature;	95%

: 55596-11-7
N-(2,2,2-trichloroethylidene)benzenesulfonamide

: 124-40-3
dimethyl amine

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 67-66-3
chloroform

C: 13707-43-2
N,N-dimethyl-N′-(phenylsulfonyl)formimidamide

Conditions

Conditions	Yield
In dichloromethane at 20℃; for 24h;	A n/a B n/a C 92%

...Expand

: 55596-11-7
N-(2,2,2-trichloroethylidene)benzenesulfonamide

: 21326-49-8
complex of sulfur dioxide with dimethylamine

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 67-66-3
chloroform

C: N-Phenylsulfonyl-N,N'-dimethylformamidine hydrochloride

Conditions

Conditions	Yield
In Trichloroethylene at 20℃; for 24h;	A n/a B n/a C 89%

...Expand

: 7294-43-1
octachloro-cyclobutane

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 87-68-3
Hexachlorobutadiene

C: 6130-82-1
hexachlorocyclobutene

Conditions

Conditions	Yield
at 506℃; Product distribution;	A 0.3% B 86% C 1.2%

...Expand

: 56-23-5
tetrachloromethane

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 34557-54-5
methane

C: 67-66-3
chloroform

D: 201230-82-2
carbon monoxide

Conditions

Conditions	Yield
With iron(II,III) oxide; sodium chloride at 25℃; pH=8.9; Kinetics;	A 0.01% B 1% C 5.2% D 82%
With hydroxysulfate green rust In water at 20℃; for 575h; pH=7.6; Product distribution;

...Expand

: 76-01-7
pentachloroethane

: 127-18-4
1,1,2,2-tetrachloroethylene

Conditions

Conditions	Yield
With methyl diethylphosphinate at 150℃; for 10h;	75%
With chlorine at 379.84℃; Gas phase; chemoselective reaction;	33.8%
With nickel dichloride at 330℃;

: 79-34-5
1,1,2,2-tetrachloroethane

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 79-01-6
Trichloroethylene

Conditions

Conditions	Yield
With hydrogenchloride; oxygen at 379.84℃; for 18h;	A 20.8% B 64.3%
With CuCl2/KCl/attapulgite; chlorine at 379.84℃; Gas phase; chemoselective reaction;	A 16.6% B 45%

: 79-34-5
1,1,2,2-tetrachloroethane

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 79-01-6
Trichloroethylene

C: 76-01-7
pentachloroethane

Conditions

Conditions	Yield
With hydrogenchloride; oxygen at 379.84℃;	A 20.8% B 64.3% C 6.1%

...Expand

: 473-29-0
N,N-Dichlorobenzenesulfonamide

: 540-59-0
1,2-Dichloroethylene

A: 98-10-2
benzenesulfonamide

B: 127-18-4
1,1,2,2-tetrachloroethylene

C: 79-01-6
Trichloroethylene

D: 55596-11-7
N-(2,2,2-trichloroethylidene)benzenesulfonamide

E: 113791-97-2
N-(2,2-dichloroethylidene)benzenesulfonamide

F: 79054-58-3
N-{2,2-dichloro-1-[(phenylsulfonyl)amino]ethyl}benzenesulfonamide

Conditions

Conditions	Yield
at 55℃; for 22h; Product distribution; other time, other temperature, other initiator;	A n/a B n/a C n/a D n/a E n/a F 54.1%

...Expand

: 473-29-0
N,N-Dichlorobenzenesulfonamide

: 540-59-0
1,2-Dichloroethylene

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 79-01-6
Trichloroethylene

C: 55596-11-7
N-(2,2,2-trichloroethylidene)benzenesulfonamide

D: 113791-97-2
N-(2,2-dichloroethylidene)benzenesulfonamide

E: 79054-58-3
N-{2,2-dichloro-1-[(phenylsulfonyl)amino]ethyl}benzenesulfonamide

F: 79-34-5
1,1,2,2-tetrachloroethane

Conditions

Conditions	Yield
at 55℃; for 22h; Product distribution; other time, other temperature, other initiator;	A n/a B n/a C n/a D n/a E 54.1% F n/a

...Expand

: 67-72-1
hexachloroethane

: Ce(3+)*3C4H14NSi2(1-)*2C4H8O

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: tetramethyldisilazane

Conditions

Conditions	Yield
In toluene for 18h; Reagent/catalyst; Solvent; Time; Inert atmosphere;	A n/a B 45%

...Expand

: 540-59-0
1,2-Dichloroethylene

: 17260-65-0
N,N-dichloro-4-chlorobenzenesulfonamide

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 98-64-6
4-Chlorobenzenesulfonamide

C: 81924-15-4
N-(2,2,2-trichloroethylidene)-4-chlorobenzenesulfonamide

D: 113791-98-3
N-(2,2-dichloroethylidene)-p-chlorobenzenesulfonamide

E: 113792-01-1
N-<2,2-dichloro-1-(N-p-chlorobenzenesulfonamido)ethyl>-p-chlorobenzenesulfonamide

F: 79-34-5
1,1,2,2-tetrachloroethane

Conditions

Conditions	Yield
at 55℃; for 22h; Product distribution; other time, other temperature, other initiator;	A n/a B n/a C n/a D n/a E 40.4% F n/a

...Expand

: 18163-67-2
(2,2-dichloro-vinyl)-trimethyl-silane

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 79-01-6
Trichloroethylene

C: Trimethyl-(1,2,2,2-tetrachloro-ethyl)-silane

D: Chloromethyl-dimethyl-(1,2,2,2-tetrachloro-ethyl)-silane

Conditions

Conditions	Yield
With chlorine for 3h; Further byproducts given;	A 1% B 5% C 30% D 33%
With chlorine for 3h; Further byproducts given;	A 1% B 7% C 30% D 33%

...Expand

: 79-01-6
Trichloroethylene

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 76-01-7
pentachloroethane

Conditions

Conditions	Yield
With chlorine at 379.84℃; Reagent/catalyst; Temperature;	A 8.1% B 11.2%

: 56-23-5
tetrachloromethane

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 67-72-1
hexachloroethane

Conditions

Conditions	Yield
at 580℃; for 0.00433333h; Rate constant; Mechanism; several condition investigated;	A 10.18% B 2.51%
at 394.5 - 445.3℃; under 83.3 - 161.6 Torr; Kinetics; Equilibrium constant; Thermodynamic data; eq. const. at 696.6 K; ΔH at 298 K;
at 600 - 1500℃;

: 37823-96-4
pentacarbonyl(methoxyphenylmethylene)tungsten(0)

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 74-87-3
methylene chloride

C: 75-09-2
dichloromethane

D: 67-66-3
chloroform

Conditions

Conditions	Yield
In tetrachloromethane byproducts: HCl, Cl2; further products; N2; stirred; gas-chromy., MAS; elem. anal.;	A 6.8% B 2% C 0.2% D 3.6%

...Expand

: 110-89-4
piperidine

: 56-23-5
tetrachloromethane

: 76-01-7
pentachloroethane

: 127-18-4
1,1,2,2-tetrachloroethylene

Conditions

Conditions	Yield
at 20℃;

...Expand

: 56-23-5
tetrachloromethane

: 75-28-5
Isobutane

: 67-72-1
hexachloroethane

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 507-20-0
tertiary butyl chloride

Conditions

Conditions	Yield
at 140℃;

...Expand

: 56-23-5
tetrachloromethane

: 127-18-4
1,1,2,2-tetrachloroethylene

Conditions

Conditions	Yield
Beim Durchleiten durch ein rotgluehendes Rohr;
at 1300 - 1400℃;
With hydrogen

: 56-23-5
tetrachloromethane

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 118-74-1
hexachlorobenzene

Conditions

Conditions	Yield
at 700℃;

: 187737-37-7
propene

: 127-18-4
1,1,2,2-tetrachloroethylene

Conditions

Conditions	Yield
With tetrachloromethane; chlorine at 800℃;

: 60-29-7
diethyl ether

: 67-72-1
hexachloroethane

: 925-90-6
ethylmagnesium bromide

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 630-20-6
1,1,1,2-tetrachoroethane

C: 76-01-7
pentachloroethane

D: 79-34-5
1,1,2,2-tetrachloroethane

...Expand

: 60-29-7
diethyl ether

: 67-72-1
hexachloroethane

: 141-52-6
sodium ethanolate

: 127-18-4
1,1,2,2-tetrachloroethylene

Conditions

Conditions	Yield
at 140℃;

...Expand

: 60-29-7
diethyl ether

: 67-72-1
hexachloroethane

: phenylmagnesium bromide

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 630-20-6
1,1,1,2-tetrachoroethane

C: 76-01-7
pentachloroethane

D: 79-34-5
1,1,2,2-tetrachloroethane

...Expand

: 75-34-3
1,1-dichloroethane

: 127-18-4
1,1,2,2-tetrachloroethylene

Conditions

Conditions	Yield
With chlorine; pyrographite at 450℃;

: 812-25-9
pentachloropropionyl chloride

A: 127-18-4
1,1,2,2-tetrachloroethylene

B: 67-72-1
hexachloroethane

Conditions

Conditions	Yield
With aluminium trichloride at 60℃;

: 127-18-4
1,1,2,2-tetrachloroethylene

: 373-91-1
hypofluorous acid trifluoromethyl ester

: 136649-69-9
1,1,2,2-tetrachloro-1-fluoro-2-trifluoromethoxyethane

Conditions

Conditions	Yield
at 40.6℃;	99.5%
at 160 - 195℃; under 750.075 Torr; for 31h;	84.3%

: 127-18-4
1,1,2,2-tetrachloroethylene

: 681141-90-2
5-methyl-1H-2-benzothiopyran-1-one

: 2aα,8bα-1,1,2,2-tetrachloro-2,2a-dihydro-8-methyl-1H-cyclobuta[c][2]benzothiopyran-4-one

Conditions

Conditions	Yield
In acetonitrile for 12h; Irradiation;	97%

: 127-18-4
1,1,2,2-tetrachloroethylene

: 1182649-23-5
Pd(CN(2,6-(2,6-(i-Pr)2C6H3)2C6H3))2

: Pd(η2-C2Cl4)(CN(2,6-(2,6-(i-Pr)2C6H3)2C6H3))2

Conditions

Conditions	Yield
In toluene; pentane for 0.25h; Inert atmosphere; Schlenk technique; Glovebox;	97%

: 127-18-4
1,1,2,2-tetrachloroethylene

A: 306-83-2
1,1,1-trifluoro-2,2-dichloroethane

B: 354-21-2
1,1,2-trichloro-2,2-difluoroethane

C: 354-14-3
freon-121

D: 2837-89-0
1,1,1,2-tetrafluoro-2-chloroethane

Conditions

Conditions	Yield
With hydrogen fluoride; antimony(III) fluoride; antimony pentafluoride at 125 - 139℃; under 16351.6 - 18376.8 Torr; for 3.7h;	A 92.4% B 0.9% C 0.01% D 0.4%
With hydrogen fluoride; antimony(III) fluoride; antimony pentafluoride at 122 - 140℃; under 17926.8 - 20252 Torr; for 3.6h;	A 89.8% B 0.3% C 0.08% D 3.1%
With hydrogen fluoride; antimony(III) fluoride; antimony pentafluoride at 124 - 140℃; under 18001.8 - 19201.9 Torr; for 3.1h;	A 87.2% B 1.1% C 0.01% D 0.5%

...Expand

: 127-18-4
1,1,2,2-tetrachloroethylene

: 20427-59-2
copper hydroxide

: 109-76-2
Trimethylenediamine

: Cu2(C10H16N4Cl4)(H2O)4(4+)*4Cl(1-)*8H2O = [Cu2(C10H16N4Cl4)(H2O)4]Cl4*8H2O

Conditions

Conditions	Yield
In water; butan-1-ol refluxing in butanol (10 h), extraction (water); pptn. from aq. phase (concn., cooling); elem. anal.;	92%

...Expand

: 127-18-4
1,1,2,2-tetrachloroethylene

: 90838-72-5, 110410-38-3, 134435-95-3, 86633-16-1, 81925-28-2, 86646-19-7
(E)-tert-butyldimethyl[3-(tributylstannyl)prop-2-enyloxy]silane

: 1638292-74-6
(6E,10E)-8,9-Bis((E)-3-((tert-butyldimethylsilyl)oxy)prop-1-en-1-yl)-2,2,3,3,14,14,15,15-octamethyl-4,13-dioxa-3,14-disilahexadeca-6,8,10-triene

Conditions

Conditions	Yield
With palladium diacetate; XPhos at 60℃; Stille Cross Coupling; Inert atmosphere;	90%
With palladium diacetate; XPhos at 60℃; Stille Cross Coupling; Inert atmosphere;	90%

: 127-18-4
1,1,2,2-tetrachloroethylene

: 58207-97-9
tributyl[(E)-2-trimethylsilylethenyl]stannane

: 1638178-58-1
((1E,5E)-3,4-bis((E)-2-(trimethylsilyl)vinyl)hexa-1,3,5-triene-1,6-diyl)bis(trimethylsilane)

Conditions

Conditions	Yield
With palladium diacetate; XPhos at 60℃; Stille Cross Coupling; Inert atmosphere;	89%
With palladium diacetate; XPhos at 60℃; Stille Cross Coupling; Inert atmosphere;	89%

: 127-18-4
1,1,2,2-tetrachloroethylene

: 20607-43-6
sodium isopropanethiolate

: 39137-72-9
tetrakis-isopropylsulfanyl-ethene

Conditions

Conditions	Yield
In N,N,N,N,N,N-hexamethylphosphoric triamide for 1h; Ambient temperature;	85%

: 127-18-4
1,1,2,2-tetrachloroethylene

: 373-91-1
hypofluorous acid trifluoromethyl ester

A: 76-12-0
CFC-112a

B: 354-17-6
dichloro-fluoro-acetyl chloride

C: 136649-69-9
1,1,2,2-tetrachloro-1-fluoro-2-trifluoromethoxyethane

D: 76-02-8
Trichloroacetyl chloride

E: Dichloro-trifluoromethoxy-acetyl chloride

F COCl2: COCl2

Conditions

Conditions	Yield
With oxygen at 40.9℃; under 420.8 Torr; for 1.97833h; Product distribution; Mechanism; Rate constant; var. of partial pressure, temp.;	A n/a B n/a C n/a D 85% E n/a F n/a

...Expand

: 127-18-4
1,1,2,2-tetrachloroethylene

: 118050-71-8, 118050-81-0
fac-tricarbonyl(bis(diphenylphosphino)ethane)(η1-methyldithiobenzoate)tungsten

: mer-tricarbonyl(bis(diphenylphosphino)ethane)(η2-methyldithiobenzoate)tungsten * tetrachloroethene

Conditions

Conditions	Yield
In tetrahydrofuran isomerization in THF within about 48 h;; concn.; pptn. with tetrachloroethene; elem. anal.;;	85%

: 127-18-4
1,1,2,2-tetrachloroethylene

: 1112-67-0
tetrabutyl-ammonium chloride

: C2Cl12Si4(2-)*2C16H36N(1+)

Conditions

Conditions	Yield
With hexachlorodisilane In dichloromethane at -10 - 20℃; for 12h; Inert atmosphere;	85%

: 127-18-4
1,1,2,2-tetrachloroethylene

: 111-88-6
Octanethiol

A: 36061-42-4
Octyl-<1.2.2-trichlor-vinyl>-sulfid

B: 130920-00-2
1-((E)-1,2-Dichloro-2-octylsulfanyl-vinylsulfanyl)-octane

Conditions

Conditions	Yield
With potassium hydroxide In ethanol; N,N-dimethyl-formamide at 60 - 70℃;	A n/a B 83%

...Expand

: 127-18-4
1,1,2,2-tetrachloroethylene

: 105522-49-4
diamantane-3-spiro-3'-diazirine

: 30651-01-5
3-chlorodiamantane

Conditions

Conditions	Yield
Irradiation;	83%

: 127-18-4
1,1,2,2-tetrachloroethylene

A: 306-83-2
1,1,1-trifluoro-2,2-dichloroethane

B: 354-21-2
1,1,2-trichloro-2,2-difluoroethane

C: 2837-89-0
1,1,1,2-tetrafluoro-2-chloroethane

Conditions

Conditions	Yield
With hydrogen fluoride; antimony(III) fluoride; antimony pentafluoride at 129 - 143℃; under 17626.8 - 19502 Torr; for 4.1h;	A 80.5% B 0.3% C 5.1%
With hydrogen fluoride; antimony pentafluoride at 135 - 143℃; under 18751.9 Torr; for 2.7h;	A 26% B 0.6% C 25.8%

...Expand

Tetrachloroethylene Specification

The IUPAC name of Perchlorethylene is 1,1,2,2-tetrachloroethene. With the CAS registry number 127-18-4, it is also named as Tetrachloroethylene. The product's categories are Organics; Analytical Chemistry; Standard Solution of Volatile Organic Compounds for Water & Soil Analysis; Standard Solutions (VOC). Besides, it is colourless liquid with ether-like odour, which should be stored in a cool, dry, ventilated warehouse at 0-6 °C. It is stable, but incompatible with strong oxidizing agents, alkali metals, aluminium, strong bases. In addition, its molecular formula is C₂Cl₄ and molecular weight is 165.83.

The other characteristics of this product can be summarized as: (1)EINECS: 204-825-9; (2)ACD/LogP: 2.95; (3)# of Rule of 5 Violations: 0; (4)ACD/LogD (pH 5.5): 2.95; (5)ACD/LogD (pH 7.4): 2.95; (6)ACD/BCF (pH 5.5): 102.96; (7)ACD/BCF (pH 7.4): 102.96; (8)ACD/KOC (pH 5.5): 960.03; (9)ACD/KOC (pH 7.4): 960.03; (10)#H bond acceptors: 0; (11)#H bond donors: 0; (12)#Freely Rotating Bonds: 0; (13)Index of Refraction: 1.519; (14)Molar Refractivity: 30.45 cm³; (15)Molar Volume: 100.3 cm³; (16)Surface Tension: 35.6 dyne/cm; (17)Density: 1.653 g/cm³; (18)Flash Point: 27.4 °C; (19)Melting Point: -22 °C; (20)FreezingPoint: -22.0 °C; (21)Solubility in water: 0.015 g/100 mL (20 °C); (22)Enthalpy of Vaporization: 34.68 kJ/mol; (23)Boiling Point: 119.1 °C at 760 mmHg; (24)Vapour Pressure: 19.3 mmHg at 25 °C.

Preparation of Perchlorethylene: this chemical can be prepared by the reaction of 1,2-Dichloroethane with Chlorine. This reaction can be catalyzed by a mixture of potassium chloride and aluminium chloride at temperature of 400 °C.
ClCH₂CH₂Cl + 3 Cl₂ → Cl₂C=CCl₂ + 4 HCl

Uses of Perchlorethylene: thos chemical is an excellent solvent for organic materials. It is often used in dry cleaning. And it is also used as a mixture with other chlorocarbons to degrease metal parts in the automotive and other metalworking industries. Additionally, it can be used as paint stripper and spot remover. It has been used for the treatment for hookworm infestation. Furthermore, it can be used as an intermediate in the manufacture of HFC-134a and related refrigerants.

When you are using this chemical, please be cautious about it as the following: it may cause damage to health which is reflected in some aspects. It is toxic by inhalation and if swallowed or in contact with skin, and may even have very serious irreversible effect. Then it has limited evidence of a carcinogenic effect to our health. It is not only harmful to our health but also to our environment. This is dangerous for the environment for it may present an immediate or delayed danger to one or more components of the environment; Then it is toxic to aquatic organisms and may cause long-term adverse effects in the aquatic environment. What's more, it is highly flammable because it may catch fire in contact with air, only needing brief contact with an ignition source, and it has a very low flash point or evolve highly flammable gases in contact with water.

People can use the following data to convert to the molecule structure.
(1)Canonical SMILES: C(=C(Cl)Cl)(Cl)Cl
(2)InChI: InChI=1S/C2Cl4/c3-1(4)2(5)6
(3)InChIKey: CYTYCFOTNPOANT-UHFFFAOYSA-N

The toxicity data is as follows:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
cat	LDLo	oral	4gm/kg (4000mg/kg)	BEHAVIORAL: SLEEP BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)	American Journal of Hygiene. Vol. 9, Pg. 430, 1929.
child	TDLo	oral	545mg/kg (545mg/kg)	BEHAVIORAL: COMA	Journal of Toxicology, Clinical Toxicology. Vol. 23, Pg. 103, 1985.
dog	LD50	intraperitoneal	2100mg/kg (2100mg/kg)	LIVER: LIVER FUNCTION TESTS IMPAIRED	Toxicology and Applied Pharmacology. Vol. 10, Pg. 119, 1967.
dog	LDLo	intravenous	85mg/kg (85mg/kg)		Quarterly Journal of Pharmacy & Pharmacology. Vol. 7, Pg. 205, 1934.
dog	LDLo	oral	4gm/kg (4000mg/kg)	BEHAVIORAL: SLEEP BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)	American Journal of Hygiene. Vol. 9, Pg. 430, 1929.
human	TCLo	inhalation	96ppm/7H (96ppm)	PERIPHERAL NERVE AND SENSATION: LOCAL ANESTHETIC SENSE ORGANS AND SPECIAL SENSES: CONJUNCTIVE IRRITATION: EYE BEHAVIORAL: "HALLUCINATIONS, DISTORTED PERCEPTIONS"	National Technical Information Service. Vol. PB257-185,
man	TCLo	inhalation	600ppm/10M (600ppm)	SENSE ORGANS AND SPECIAL SENSES: CONJUNCTIVE IRRITATION: EYE BEHAVIORAL: GENERAL ANESTHETIC	AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 5, Pg. 566, 1952.
mouse	LC50	inhalation	5200ppm/4H (5200ppm)		Acta Pharmacologica et Toxicologica. Vol. 9, Pg. 303, 1953.
mouse	LD	intraperitoneal	> 500mg/kg (500mg/kg)		"Summary Tables of Biological Tests," National Research Council Chemical-Biological Coordination Center. Vol. 4, Pg. 378, 1952.
mouse	LD50	oral	8100mg/kg (8100mg/kg)	BEHAVIORAL: GENERAL ANESTHETIC	National Technical Information Service. Vol. PB257-185,
mouse	LD50	subcutaneous	65gm/kg (65000mg/kg)	BEHAVIORAL: SLEEP BEHAVIORAL: ATAXIA	Journal of Pharmacology and Experimental Therapeutics. Vol. 123, Pg. 224, 1958.
rabbit	LD	skin	> 3228mg/kg (3228mg/kg)		National Technical Information Service. Vol. AD-A180-198,
rabbit	LDLo	oral	5gm/kg (5000mg/kg)	BEHAVIORAL: SLEEP BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)	American Journal of Hygiene. Vol. 9, Pg. 430, 1929.
rabbit	LDLo	subcutaneous	2200mg/kg (2200mg/kg)		Quarterly Journal of Pharmacy & Pharmacology. Vol. 7, Pg. 205, 1934.
rat	LC50	inhalation	34200mg/m³/8H (34200mg/m³)		American Industrial Hygiene Association Journal. Vol. 20, Pg. 364, 1959.
rat	LD50	intraperitoneal	4678mg/kg (4678mg/kg)		Environmental Research. Vol. 40, Pg. 411, 1986.
rat	LD50	oral	2629mg/kg (2629mg/kg)		American Industrial Hygiene Association Journal. Vol. 20, Pg. 364, 1959.
rat	LDLo	intratracheal	450mg/kg (450mg/kg)		National Technical Information Service. Vol. OTS0520615,

Product Name

1,1,2,2-Tetrach loroethylene

Synthetic route

Tetrachloroethylene Specification

Related Products

Hot Products