1,1,1,3-Tetrachloro-propane supplier

Name
1,1,1,3-Tetrachloro-propane
EINECS 213-981-7
CAS No. 1070-78-6
Article Data69
CAS DataBase
Density 1.471 g/cm³
Solubility
Melting Point -35 °C
Formula C₃H₄Cl₄
Boiling Point 161.259 °C at 760 mmHg
Molecular Weight 181.877
Flash Point 51.41 °C
Transport Information
Appearance Colorless
Safety
Risk Codes
Molecular Structure
Hazard Symbols Xi
Synonyms 1,1,1,3-Tetrachloropropane;HCC 250fb;
PSA 0.00000
LogP 2.98550

Synthetic route

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

: 1070-78-6
1,1,1,3-tetrachloropropane

Conditions

Conditions	Yield
With iron; trimethyl orthoformate at 100℃; under 1500.15 Torr; for 1h;	98.1%
With iron(III) chloride; phosphoric acid tributyl ester; iron at 110℃; under 5931.67 Torr; Reagent/catalyst; Pressure; Flow reactor; Large scale;	96%
iron(III) chloride; triethyl phosphate; iron at 110 - 134℃; under 1875.19 - 6000.6 Torr; Autoclave; Inert atmosphere;	91%

: 2547-61-7
Trichloromethanesulfonyl chloride

: 74-85-1
ethene

: 1070-78-6
1,1,1,3-tetrachloropropane

Conditions

Conditions	Yield
With benzene; dibenzoyl peroxide at 70℃; under 20594.2 Torr;

: 7789-89-1
1,1,1-trichloropropane

: 1070-78-6
1,1,1,3-tetrachloropropane

Conditions

Conditions	Yield
beim Chlorieren; zunaechst im Sonnenlicht in der Dampfphase, dann in fluessiger Phase unter Kuehlung;

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

A: 2467-10-9
1,1,1,5-tetrachloropentane

B: 2677-33-0
1,1,5-trichloro-pent-1-ene

C: 1070-78-6
1,1,1,3-tetrachloropropane

D: 13275-19-9
1,1,1,3-tetrachlorobutane

Conditions

Conditions	Yield
With diethyl amine hydrochloride; 2-hydroxy-2-phenylacetophenone; iron(III) chloride In isopropyl alcohol Further byproducts given;

...Expand

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

A: 2467-10-9
1,1,1,5-tetrachloropentane

B: 2677-33-0
1,1,5-trichloro-pent-1-ene

C: 1070-78-6
1,1,1,3-tetrachloropropane

D: 34909-84-7
1,3,5-trichloro-2-pentene

Conditions

Conditions	Yield
With diethyl amine hydrochloride; 2-hydroxy-2-phenylacetophenone In isopropyl alcohol Further byproducts given;

...Expand

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

A: 2467-10-9
1,1,1,5-tetrachloropentane

B: 1070-78-6
1,1,1,3-tetrachloropropane

C: 13275-19-9
1,1,1,3-tetrachlorobutane

D: 24616-07-7
1,3,3,5-tetrachloropentane

Conditions

Conditions	Yield
With 2-hydroxy-2-phenylacetophenone; diethylamine; iron(III) chloride In isopropyl alcohol Further byproducts given;

...Expand

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

A: 2467-10-9
1,1,1,5-tetrachloropentane

B: 1070-78-6
1,1,1,3-tetrachloropropane

C: 24616-07-7
1,3,3,5-tetrachloropentane

D: 34909-84-7
1,3,5-trichloro-2-pentene

Conditions

Conditions	Yield
With diethyl amine hydrochloride; 2-hydroxy-2-phenylacetophenone; iron(III) chloride Further byproducts given;

...Expand

: 56-23-5
tetrachloromethane

: 187737-37-7
propene

: 74-85-1
ethene

A: 2467-10-9
1,1,1,5-tetrachloropentane

B: 13275-22-4
1,1,1,5-tetrachloro-3-methylhexane

C: 1070-78-6
1,1,1,3-tetrachloropropane

D: 13275-19-9
1,1,1,3-tetrachlorobutane

E: 3922-36-9
1,1,1,7-tetrachloroheptane

F: 17977-23-0, 29293-15-0, 29293-20-7, 29293-21-8, 29293-22-9, 31031-26-2
1,1,1,7-tetrachloro-3,5-dimethyl-octane

Conditions

Conditions	Yield
With dibenzoyl peroxide at 90℃; for 3h; Product distribution; variation of the reactant ratio;

...Expand

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

A: 2467-10-9
1,1,1,5-tetrachloropentane

B: 1070-78-6
1,1,1,3-tetrachloropropane

Conditions

Conditions	Yield
FeIIFe2IIICl8(CH3CN)6 In N,N-dimethyl acetamide; acetonitrile at 130℃; under 15200 Torr; for 4h; Product distribution; Mechanism; other concentrations of CH3CN, DMA; other catalyst;	A 1.6 % Turnov. B 98.4 % Turnov.
FeIIFe2IIICl8(CH3CN)6 In N,N-dimethyl acetamide; acetonitrile at 130℃; under 15200 Torr; for 4h;	A 1.6 % Turnov. B 98.4 % Turnov.

...Expand

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

A: 2467-10-9
1,1,1,5-tetrachloropentane

B: 1070-78-6
1,1,1,3-tetrachloropropane

C: 3922-36-9
1,1,1,7-tetrachloroheptane

D: 1561-48-4
1,1,1,9-tetrachloro-nonane

E: 3922-34-7
1,1,1,11-tetrachloro-undecane

Conditions

Conditions	Yield
With chromium(0) hexacarbonyl at 120℃; Product distribution; relative rate of telomerization initiated by Cr(CO)6 and further initiator; partial chain-transfer constants;

...Expand

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

A: 2467-10-9
1,1,1,5-tetrachloropentane

B: 1070-78-6
1,1,1,3-tetrachloropropane

C: 3922-36-9
1,1,1,7-tetrachloroheptane

D: 24616-07-7
1,3,3,5-tetrachloropentane

Conditions

Conditions	Yield
With dimanganese decacarbonyl; isopropyl alcohol at 120℃; for 2h; Product distribution; other reagents, reagents ratios;

...Expand

: 56-23-5
tetrachloromethane

: 6565-20-4
3,3,3-trichloro-propyl

A: 3170-80-7
trichloromethyl radical

B: 1070-78-6
1,1,1,3-tetrachloropropane

Conditions

Conditions	Yield
at 39.9℃; Rate constant;

...Expand

: 67-66-3
chloroform

: 53220-05-6
1,3,3,3-tetrachloro-propyl

A: 3170-80-7
trichloromethyl radical

B: 1070-78-6
1,1,1,3-tetrachloropropane

Conditions

Conditions	Yield
at 21.9℃; Rate constant;

...Expand

: 6565-20-4
3,3,3-trichloro-propyl

: 1070-78-6
1,1,1,3-tetrachloropropane

Conditions

Conditions	Yield
With tetrachloromethane at 40℃; Rate constant;

: 56-23-5
tetrachloromethane

: 13043-82-8
acetyl propionyl peroxide

A: 74-87-3
methylene chloride

B: 34557-54-5
methane

C: 75-00-3
chloroethane

D: 1070-78-6
1,1,1,3-tetrachloropropane

E: 64-19-7
acetic acid

F: 141-78-6
ethyl acetate

Conditions

Conditions	Yield
at 59.9 - 99.9℃; for 150h; Product distribution; Kinetics; Rate constant;

...Expand

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

: 7732-18-5
water

: 94-36-0
dibenzoyl peroxide

A: 2467-10-9
1,1,1,5-tetrachloropentane

B: 1070-78-6
1,1,1,3-tetrachloropropane

C: 3922-36-9
1,1,1,7-tetrachloroheptane

D: 1561-48-4
1,1,1,9-tetrachloro-nonane

Conditions

Conditions	Yield
at 95℃; under 73550.8 Torr;
at 95℃; under 73550.8 Torr; bei der Reaktion koennen Explosionen auftreten;
at 95℃; under 73550.8 Torr; analoge Reaktionen mit Propen, Octen-(1) und Hexadien-(2.5) bezw. mit Vinylacetat;
at 95℃; under 73550.8 Torr;
at 95℃; under 73550.8 Torr; analoge Reaktionen mit Propen, Octen-(1) und Hexadien-(2.5) bezw. mit Vinylacetat;

...Expand

: 56-23-5
tetrachloromethane

: 78-67-1
2,2'-azobis(isobutyronitrile)

: 74-85-1
ethene

A: 1070-78-6
1,1,1,3-tetrachloropropane

B Cl-n-CCl3: Cl-n-CCl3

Conditions

Conditions	Yield
at 90 - 110℃; under 73550.8 - 110326 Torr;

...Expand

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

: 94-36-0
dibenzoyl peroxide

air: air

A: 1070-78-6
1,1,1,3-tetrachloropropane

B Cl-n-CCl3: Cl-n-CCl3

Conditions

Conditions	Yield
at 90 - 95℃; unter Druck;

...Expand

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

pentacarbonyl iron: pentacarbonyl iron

A: 1070-78-6
1,1,1,3-tetrachloropropane

B Cl-n-CCl3: Cl-n-CCl3

Conditions

Conditions	Yield
at 95 - 100℃; under 58840.6 Torr;

...Expand

: 56-23-5
tetrachloromethane

: 13043-82-8
acetyl propionyl peroxide

A: 74-87-3
methylene chloride

B: 75-00-3
chloroethane

C: 1070-78-6
1,1,1,3-tetrachloropropane

D: 5912-58-3
1-chloroethyl acetate

E: 64-19-7
acetic acid

F: 141-78-6
ethyl acetate

G CH2ClCH2Cl, CH3OC(O)CH2CH3, CH3CH2CH2Cl, CH3CCl3, (CH3)2CHCl, CH3CH2CH3, CH3CH3, CH4: CH2ClCH2Cl, CH3OC(O)CH2CH3, CH3CH2CH2Cl, CH3CCl3, (CH3)2CHCl, CH3CH2CH3, CH3CH3, CH4

Conditions

Conditions	Yield
at 69.9℃; Product distribution; other temperature; thermolysis and photolysis in CCl4 and or in MeOH+CCl4 at different temperatures; lifetime of acyloxy radicals produces by decomposition of APP; decarboxylation rate constants of acyloxy radicals;

...Expand

: 56-23-5
tetrachloromethane

: 74-85-1
ethene

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

B: 1070-78-6
1,1,1,3-tetrachloropropane

C: 2233-00-3
3,3,3-trichloro-1-propene

D: 67-72-1
hexachloroethane

Conditions

Conditions	Yield
In tetrachloromethane other Radiation; γ-radiation of C2H4 in CCl4;; yields given;;

...Expand

: 597-64-8
tetraethyltin

A: 75-00-3
chloroethane

B: 1070-78-6
1,1,1,3-tetrachloropropane

C: 67-72-1
hexachloroethane

D: 866-55-7
dichlorodiethylstannane

Conditions

Conditions	Yield
With tetrachloromethane byproducts: C4H10, C2H6, C2H4; Irradiation (UV/VIS); for 120 h; further byproduct: CHCl3;

...Expand

: 1070-78-6
1,1,1,3-tetrachloropropane

: 754-12-1
2,3,3,3-tetrafluoro-propene

Conditions

Conditions	Yield
Stage #1: 1,1,1,3-tetrachloropropane With iron at 115℃; for 3h; Stage #2: With tetradecafluorohexane; fluorine at -60℃; Inert atmosphere; Stage #3: With hydrogen fluoride at 300℃; under 3000.3 Torr; Pressure; Temperature; Concentration; Reagent/catalyst;	99.7%
Stage #1: 1,1,1,3-tetrachloropropane With tetrabutylammomium bromide; sodium hydroxide In water at 32 - 35℃; under 760.051 Torr; for 17h; Stage #2: With fluorine In hydrogen fluoride at -60℃; under 760.051 Torr; Inert atmosphere; liquid HF; Stage #3: With hydrogen fluoride at 220 - 250℃; under 760.051 Torr;

: 1070-78-6
1,1,1,3-tetrachloropropane

: 21700-31-2
1,1,1,2,3-pentachloro-propane

Conditions

Conditions	Yield
Stage #1: 1,1,1,3-tetrachloropropane With iron(III) chloride at 85℃; under 1005.1 Torr; Industrial scale; Stage #2: With chlorine at 30℃; Temperature; Industrial scale;	96%
Stage #1: 1,1,1,3-tetrachloropropane With aluminum (III) chloride In N,N-dimethyl acetamide at 25℃; for 0.166667h; Stage #2: With chlorine In N,N-dimethyl acetamide at 25℃; for 1.5h;	95%
Stage #1: 1,1,1,3-tetrachloropropane With potassium hydroxide; Aliquat 336 In water at 80℃; for 3h; Stage #2: With chlorine at 0℃; for 3h; UV-irradiation;

: 1070-78-6
1,1,1,3-tetrachloropropane

: 2567-14-8
3,3-dichloroallyl chloride

Conditions

Conditions	Yield
With iron(II) chloride tetrahydrate at 90 - 100℃;	95%
With iron(II) chloride at 95℃; for 8h;	95%
at 450℃;

: 1070-78-6
1,1,1,3-tetrachloropropane

: 127-09-3
sodium acetate

: 3039-54-1
γ,γ-Dichloroallyl acetate

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 130 - 150℃; for 6h;	95%

: 1070-78-6
1,1,1,3-tetrachloropropane

: 677-21-4
1,1,1-trifluoropropylene

Conditions

Conditions	Yield
With hydrogen fluoride at 225 - 250℃;	90%
With hydrogen fluoride; activated by HF amorphous Zn/chromia catalyst at 200℃; under 760.051 Torr; for 15h; Inert atmosphere;	100 %Chromat.
With hydrogen fluoride; activated by HF amorphous Zn/chromia catalyst at 200℃; under 760.051 Torr; for 15h; Inert atmosphere;	100 %Chromat.

: 1070-78-6
1,1,1,3-tetrachloropropane

: 754-05-2
ethenyltrimethylsilane

A: 114066-69-2, 114066-71-6
Trimethyl-((Z)-1,3,5-trichloro-pent-3-enyl)-silane

B: 114066-70-5
Trimethyl-((Z)-1,3,5-trichloro-pent-2-enyl)-silane

C: 114066-68-1
Trimethyl-(1,3,3,5-tetrachloro-pentyl)-silane

Conditions

Conditions	Yield
With iron pentacarbonyl; triphenylphosphine at 130℃; for 3h; further reagents DMFA, HMPTA, 2-propanol; Yield given. Yields of byproduct given. Title compound not separated from byproducts;	A n/a B n/a C 88%
With iron pentacarbonyl; triphenylphosphine at 130℃; for 3h; further reagents DMFA, HMPTA, 2-propanol; Yields of byproduct given;	A n/a B n/a C 88%

...Expand

: 592-41-6
1-hexene

: 1070-78-6
1,1,1,3-tetrachloropropane

: 58468-01-2
1,3,3,5-tetrachlorononane

Conditions

Conditions	Yield
With iron pentacarbonyl In N,N-dimethyl-formamide at 105℃; for 3h;	85%
With iron pentacarbonyl; N,N-dichloro-4-chlorobenzenesulfonamide In N,N,N,N,N,N-hexamethylphosphoric triamide at 105℃;

: 1070-78-6
1,1,1,3-tetrachloropropane

: 327-62-8
potassium propionate

: 133455-75-1
3,3-Dichloroallylpropionate

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 130 - 150℃; for 6h;	85%

: 1070-78-6
1,1,1,3-tetrachloropropane

A: 21700-31-2
1,1,1,2,3-pentachloro-propane

B: 2567-14-8
3,3-dichloroallyl chloride

C: 10436-39-2
1,1,2,3-Tetrachloropropene

Conditions

Conditions	Yield
With iron(III) chloride; chlorine at 82℃; under 1277.21 Torr; for 15.33h; Product distribution / selectivity;	A 82.9% B 3.4% C 8.1%

...Expand

: 1070-78-6
1,1,1,3-tetrachloropropane

: 20395-25-9
1,1,3-trichloropropane

Conditions

Conditions	Yield
With trans-Mo2(μ-N,N′-bis(4-methoxyphenyl)formamidinato-κ2N:N′)2(OOCCH3)2; 1-methyl-3,6-bis(trimethylsilyl)-1,4-cyclohexadiene; tetrabutyl-ammonium chloride In [D3]acetonitrile at 80℃; for 3h; Catalytic behavior; Reagent/catalyst; Solvent;	73%
With iron pentacarbonyl; cyclohexanol at 130 - 140℃; for 3.5h; Product distribution; further reagents, percent of conversion;	60%
With lithium aluminium tetrahydride; Trichlorbutylstannan In diethyl ether
With bis(cyclopentadienyl)dihydrozirconium In toluene at 20℃; further reagents; Yield given;
With trans-Mo2(μ-N,N′-bis(4-methoxyphenyl)formamidinato-κ2N:N′)2(OOCCH3)2; 1-methyl-3,6-bis(trimethylsilyl)-1,4-cyclohexadiene In [D3]acetonitrile at 80℃; for 3h; Kinetics; Catalytic behavior; Concentration; Reagent/catalyst;	85 %Spectr.

: 5464-28-8
1,3-dioxolane-4-methanol

: 1070-78-6
1,1,1,3-tetrachloropropane

: 127719-52-2
4-(3,3,3-Trichloro-propoxymethyl)-[1,3]dioxolane

Conditions

Conditions	Yield
With potassium hydroxide; 18-crown-6 ether for 4h; Ambient temperature;	60%

: 557-98-2
2-chloropropene

: 1070-78-6
1,1,1,3-tetrachloropropane

: 85413-77-0
1,3,3,5,5-pentachlorohexane

Conditions

Conditions	Yield
N,N,N,N,N,N-hexamethylphosphoric triamide; iron pentacarbonyl at 130 - 135℃; for 2h;	60%
With trans-bisdinitrogenbis(1,2-diphenylphosphinoethane)molybdenum(0) In acetonitrile at 140℃; for 3h; further reagents Mo(CO)6, Mo(CO)5PPh3, cis-Mo(CO)4(PPh3)2, cis-Mo(CO)4(dppe), cis-Mo(CO)2(dppe)2, MoH4(dppe)2;	75 % Chromat.

: 1070-78-6
1,1,1,3-tetrachloropropane

: 460-35-5
3-chloro-1,1,1-trifluoropropane

Conditions

Conditions	Yield
With antimonypentachloride; antimony(III) fluoride In 1,2-dichloro-ethane Ambient temperature;	57%
With antimony dichloride trifluoride; antimony(III) fluoride; 1,2-dichloro-ethane
With antimony dichloride trifluoride; dichloromethane; antimony(III) fluoride

: 592-76-7
1-Heptene

: 1070-78-6
1,1,1,3-tetrachloropropane

: 1,3,3,5-tetrachlorodecane

Conditions

Conditions	Yield
iron pentacarbonyl; N,N-dimethyl-formamide at 105℃; for 3h;	52%

: 1070-78-6
1,1,1,3-tetrachloropropane

A: 819-00-1
1,1-difluoro-1,3-dichloropropane

B: 818-99-5
1-fluoro-1,1,3-trichloropropane

C: 121612-64-4
1,1-Dichloro-1,3-difluoro-propane

Conditions

Conditions	Yield
With bromine trifluoride; tin(IV) chloride In 1,1,2-Trichloro-1,2,2-trifluoroethane at 20 - 25℃;	A 11% B 51% C 10%

...Expand

: 1070-78-6
1,1,1,3-tetrachloropropane

: 107-94-8
chloropropionic acid

Conditions

Conditions	Yield
With sulfuric acid

: 1070-78-6
1,1,1,3-tetrachloropropane

: 58468-00-1
1,3,3,4,4,6-hexachloro-hexane

Conditions

Conditions	Yield
With water; iron

: 1070-78-6
1,1,1,3-tetrachloropropane

A: 58468-00-1
1,3,3,4,4,6-hexachloro-hexane

B: 62021-38-9
1,3,4,6-tetrachloro-hex-3-ene

Conditions

Conditions	Yield
With ammonia; platinum Hydrogenation;

: 1070-78-6
1,1,1,3-tetrachloropropane

: 62021-38-9
1,3,4,6-tetrachloro-hex-3t-ene

Conditions

Conditions	Yield
With ammonia; platinum Hydrogenation;

: 1070-78-6
1,1,1,3-tetrachloropropane

A: 460-35-5
3-chloro-1,1,1-trifluoropropane

B: 819-00-1
1,1-difluoro-1,3-dichloropropane

Conditions

Conditions	Yield
With antimony dichloride trifluoride; α,α,α-trifluorotoluene; antimony(III) fluoride

: 1070-78-6
1,1,1,3-tetrachloropropane

A: 21700-31-2
1,1,1,2,3-pentachloro-propane

B: 23153-23-3
1,1,1,3,3-pentachloropropane

Conditions

Conditions	Yield
With chlorine at 100℃; Irradiation.mit UV-Licht;
With chlorine; triphenylbismuthane at 140 - 150℃; under 2585.81 Torr; for 2h; Sealed tube; Inert atmosphere;
With chlorine at 130 - 150℃; under 2585.81 Torr; for 2h; Sealed tube; Inert atmosphere;
With iron(III) chloride at 41.2℃; Temperature; Reagent/catalyst;

: 1070-78-6
1,1,1,3-tetrachloropropane

A: 2567-14-8
3,3-dichloroallyl chloride

B: 2233-00-3
3,3,3-trichloro-1-propene

Conditions

Conditions	Yield
With 2-ethoxy-ethanol; potassium hydroxide at 80℃;
With potassium hydroxide at 0 - 5℃;
With potassium hydroxide; Aliquat 336 In water at 80℃; for 3h;

: 1070-78-6
1,1,1,3-tetrachloropropane

: 62-53-3
aniline

: N-(3,3,3-trichloro-propyl)-aniline

: 1070-78-6
1,1,1,3-tetrachloropropane

: 100-61-8
N-methylaniline

: 99360-52-8
N-methyl-N-(3,3,3-trichloro-propyl)-aniline

: 1070-78-6
1,1,1,3-tetrachloropropane

: 71-43-2
benzene

: 38862-78-1
1,1-dichloro-3-phenylpropene

Conditions

Conditions	Yield
With antimonypentachloride

1,1,1,3-Tetrachloro-propane Chemical Properties

IUPAC Name: 1,1,1,3-Tetrachloro-propane
The MF of 1,1,1,3-Tetrachloro-propane (CAS NO.1070-78-6) is C₃H₄Cl₄.

The MW of 1,1,1,3-Tetrachloro-propane (CAS NO.1070-78-6) is 181.88.
Synonyms of 1,1,1,3-Tetrachloro-propane (CAS NO.1070-78-6): 1,1,1,3-Tetrachloro-propan ; Propane,1,1,1,3-tetrachloro- ; Tetrachloropropane
Index of Refraction: 1.482
EINECS: 213-981-7
Density: 1.471 g/ml
Flash Point: 51.4 °C
Boiling Point: 161.3 °C
Melting Point: -35 °C

1,1,1,3-Tetrachloro-propane Uses

1,1,1,3-Tetrachloro-propane (CAS NO.1070-78-6) is used for the preparation of three allyl chloride, trifluoro-propylene, also as solvent.

1,1,1,3-Tetrachloro-propane Toxicity Data With Reference

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
mouse	LDLo	oral	1mL/kg (1mL/kg)		National Technical Information Service. Vol. OTS0520626,
rabbit	LD50	skin	> 2mL/kg (2mL/kg)		National Technical Information Service. Vol. OTS0520626,
rat	LCLo	inhalation	4700ppm/6H (4700ppm)	BEHAVIORAL: ATAXIA	National Technical Information Service. Vol. OTS0520625,
rat	LD50	oral	490mg/kg (490mg/kg)		Office of Toxic Substances Report. Vol. OTS0515505,

1,1,1,3-Tetrachloro-propane Consensus Reports

Reported in EPA TSCA Inventory.

1,1,1,3-Tetrachloro-propane Safety Profile

Moderately toxic by ingestion. When heated to decomposition it emits toxic fumes of Cl⁻. See also CHLORINATED HYDROCARBONS, ALIPHATIC.Safety information of 1,1,1,3-Tetrachloro-propane (CAS NO.1070-78-6):
Hazard Codes Irritant Xi
RTECS TZ7000000

Product Name

1,1,1,3-Tetrachloro-propane

Synthetic route

1,1,1,3-Tetrachloro-propane Chemical Properties

1,1,1,3-Tetrachloro-propane Uses

1,1,1,3-Tetrachloro-propane Toxicity Data With Reference

1,1,1,3-Tetrachloro-propane Consensus Reports

1,1,1,3-Tetrachloro-propane Safety Profile

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