1,1,1-Trifluoro-2-chloroethane supplier

Name
2-Chloro-1,1,1-trifluoroethane
EINECS
CAS No. 75-88-7
Article Data68
CAS DataBase
Density 1.389
Solubility
Melting Point -105°C
Formula C2H2 Cl F3
Boiling Point 7°C
Molecular Weight 118.486
Flash Point
Transport Information
Appearance
Safety A poison by inhalation. Experimental reproductive effects. Questionable carcinogen with experimental carcinogenic data. When heated to decomposition it emits toxic fumes of F⁻.
Risk Codes R59
Molecular Structure
Hazard Symbols Xi
Synonyms (Chloromethyl)trifluoromethane;1,1,1-Trifluoro-2-chloroethane; 1,1,1-Trifluorochloroethane;1,1,1-Trifluoroethyl chloride; 1-Chloro-2,2,2-trifluoroethane;2,2,2-Trifluoro-1-chloroethane; 2,2,2-Trifluorochloroethane;2,2,2-Trifluoroethyl chloride; 2-Chloro-1,1,1-trifluoroethane; F 133a; FC 133a;Forane 133a; Freon 133a; Genetron 133a; HCFC 133a; R 133a
PSA 0.00000
LogP 1.78750

Synthetic route

: 79-01-6
Trichloroethylene

: 75-88-7
1,1,1-trifluoro-2-chloroethane

Conditions

Conditions	Yield
With hydrogen fluoride; antimony pentafluoride at 100℃; for 1h; Temperature; Autoclave;	97%
With hydrogen fluoride; tantalum pentafluoride at 0 - 140℃; under 25858.1 Torr; for 10.5h; Product distribution / selectivity; Neat (no solvent);	90%
With hydrogen fluoride; tantalum pentafluoride at 100 - 140℃; under 25858.1 Torr; for 6h;	80%

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

: 75-88-7
1,1,1-trifluoro-2-chloroethane

Conditions

Conditions	Yield
With hydrogen fluoride; antimonypentachloride at 80 - 90℃; Autoclave;	92.3%
With hydrogen fluoride; antimonypentachloride; chlorine at 120℃;

: 1649-08-7
1,2-dichloro-1,1-difluoroethane

: 75-88-7
1,1,1-trifluoro-2-chloroethane

Conditions

Conditions	Yield
With 1,1,2-trichloro-1-fluoroethane; hydrogen fluoride; tantalum pentachloride at 0 - 140℃; for 2h; Product distribution / selectivity; Neat (no solvent);	87.5%
With hydrogen fluoride; tantalum pentachloride at 0 - 140℃; for 2.5h; Product distribution / selectivity; Neat (no solvent);	22%
With antimony dichloride trifluoride; hydrogen fluoride at 144℃; under 33097.9 Torr;

: 75-89-8
2,2,2-trifluoroethanol

: 421-83-0
trifluoromethane sulfonyl chloride

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 333-36-8
1,1,1-trifluoro-2-(2,2,2-trifluoroethoxy)ethane

C: 6226-25-1
2,2,2-trifluoroethyl trifluoromethanesulphonate

Conditions

Conditions	Yield
With potassium carbonate; tetra-n-propylammonium bromide In water at 10.2 - 23.3℃; for 4 - 7h; Product distribution / selectivity;	A 0.2 %Chromat. B 0.13 - 0.28 %Chromat. C 82%

...Expand

: 354-58-5
1,1,1-Trichloro-2,2,2-trifluoroethane

: 75-88-7
1,1,1-trifluoro-2-chloroethane

Conditions

Conditions	Yield
With ammonium persulfate; ammonium formate In N,N-dimethyl-formamide at 30 - 40℃;	77%

: 811-95-0
1,1,2-trichloro-1-fluoroethane

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 1649-08-7
1,2-dichloro-1,1-difluoroethane

Conditions

Conditions	Yield
With hydrogen fluoride; tantalum pentachloride at 110℃; for 1.5h;	A 22% B 74%

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

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 359-10-4
1-Chloro-2,2-difluoroethene

Conditions

Conditions	Yield
With water; zinc unter Zusatz eines Netzmittels;

: 359-10-4
1-Chloro-2,2-difluoroethene

: 75-88-7
1,1,1-trifluoro-2-chloroethane

Conditions

Conditions	Yield
With aluminum(III) fluoride; hydrogen fluoride at 300℃;
With hydrogen fluoride; boron trifluoride at 25℃;

: 79-01-6
Trichloroethylene

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 354-15-4
1,2,2-trichloro-1,2-difluoroethane

C: 76-13-1
1,1,2-Trichloro-1,2,2-trifluoroethane

D: 76-12-0
CFC-112a

Conditions

Conditions	Yield
With cobalt (III) fluoride at 120℃; Further byproducts given;

...Expand

: 79-11-8
chloroacetic acid

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 38217-12-8
bis-(2-chloro-1,1-difluoro-ethyl) ether

Conditions

Conditions	Yield
With sulfur tetrafluoride at 65℃; for 3h;

: 593-71-5
Chloroiodomethane

: 2314-97-8
iodotrifluoromethane

: 75-88-7
1,1,1-trifluoro-2-chloroethane

Conditions

Conditions	Yield
Ambient temperature; Irradiation; Hg2I2, Hg;

: 75-38-7
Vinylidene fluoride

: 22082-78-6
trifluoromethyl hypochlorite

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 25957-33-9
Trifluormethyl-1,1-difluor-2-chloraethylaether

Conditions

Conditions	Yield
In trichlorofluoromethane at -111 - 22℃; for 20h; Product distribution; various temperatures, olefins, solvents and times;	A 50 % Spectr. B 50 % Spectr.
In trichlorofluoromethane at -111 - 22℃; for 20h; Yield given. Title compound not separated from byproducts;

...Expand

: 75-38-7
Vinylidene fluoride

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 25957-33-9
Trifluormethyl-1,1-difluor-2-chloraethylaether

Conditions

Conditions	Yield
With trifluoromethyl hypochlorite In trichlorofluoromethane at -111 - 22℃; for 20h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;

: 79-01-6
Trichloroethylene

A: 811-97-2
1,1,1,2-tetrafluoroethane

B: 75-88-7
1,1,1-trifluoro-2-chloroethane

Conditions

Conditions	Yield
With hydrogen fluoride; chromium(III) oxide at 250℃; Mechanism; Product distribution; hydrofluorination, chlorine/fluorine exchange mechanism; effect of DF substitution for HF;	A 10 % Chromat. B 90 % Chromat.
With chromium(III) oxide; hydrogen fluoride at 653℃; for 18h; Product distribution; Further Variations:; Temperatures; Fluorination; Addition; Substitution;
With chromium fluoride; magnesium fluoride; hydrogen fluoride at 200℃; under 7600 Torr; Product distribution; Further Variations:; Pressures;

: 151-67-7
1,1,1-trifluoro-2-bromo-2-chloroethane

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 359-10-4
1-Chloro-2,2-difluoroethene

Conditions

Conditions	Yield
With perchloric acid; CoW7-; sodium perchlorate In water; acetonitrile at 20℃; Rate constant; Product distribution; pH 7; reaction with Co(II)sepuchrate2- at 50 deg C; electron transfer reactions of polyhaloalkanes with Co(II)W12O407- and Co(II)sepulchrate2+, order of reactivity toward Co(II)W12O407-, trapping experiments with N-t-butyl-α-phenylnitrone;
With liver microsomes Enzyme kinetics; Enzymatic reaction;

: 28760-99-8
1,1,1-trifluoro-2-chloroethyl radical

: 75-88-7
1,1,1-trifluoro-2-chloroethane

Conditions

Conditions	Yield
With isopropyl alcohol

: 58911-30-1
3-chloro-3-(trifluoromethyl)diazirine

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 79-38-9
Chlorotrifluoroethylene

Conditions

Conditions	Yield
Irradiation;
Irradiation; radiation > 300 nm;

: 354-58-5
1,1,1-Trichloro-2,2,2-trifluoroethane

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

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

Conditions

Conditions	Yield
With hydrogen; RhCl(PPh3)3 In tetrahydrofuran at 100℃; under 6080 Torr; for 5h; Product distribution; further catalysts and times; effect of bases;	A 3.5 % Chromat. B 94.6 % Chromat.
With hydrogen; RhCl(PPh3)3 In tetrahydrofuran at 100℃; under 6080 Torr; for 5h;	A 3.5 % Chromat. B 94.6 % Chromat.

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

: 100-52-7
benzaldehyde

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 359-10-4
1-Chloro-2,2-difluoroethene

C: 67230-92-6
2-chloro-3,3-difluoro-1-phenyl-2-propenol

D: 103654-96-2, 121591-61-5, 121591-67-1
1-(α,α-dichloro-β,β,β-trifluoroethyl)benzylalcohol

E: 138950-21-7
2-chloro-1,1,1-trifluoro-3-phenylpropan-3-ol

Conditions

Conditions	Yield
With zinc; copper(l) chloride In N,N-dimethyl-formamide Product distribution; Mechanism; Ambient temperature; various concentrations; without catalyst; further aldehydes;	A 24 % Spectr. B 20 % Spectr. C 37 % Spectr. D 3 % Spectr. E 12 % Spectr.

...Expand

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

: 100-52-7
benzaldehyde

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: 67230-92-6
2-chloro-3,3-difluoro-1-phenyl-2-propenol

C: 103654-96-2, 121591-61-5, 121591-67-1
1-(α,α-dichloro-β,β,β-trifluoroethyl)benzylalcohol

D: 138950-21-7
2-chloro-1,1,1-trifluoro-3-phenylpropan-3-ol

Conditions

Conditions	Yield
With zinc; copper(l) chloride 1.) DMF, 24 h; 2.) DMF; Yield given. Multistep reaction. Yields of byproduct given;

...Expand

: 370-69-4
tris(2,2,2-trifluoroethyl)phosphite

: 75-87-6
chloral

A: 75-88-7
1,1,1-trifluoro-2-chloroethane

B: Phosphoric acid 2,2-dichloro-vinyl ester bis-(2,2,2-trifluoro-ethyl) ester

Conditions

Conditions	Yield
Heating;

...Expand

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 75-89-8
2,2,2-trifluoroethanol

: 333-36-8
1,1,1-trifluoro-2-(2,2,2-trifluoroethoxy)ethane

Conditions

Conditions	Yield
With potassium hydroxide In 1,2-dimethoxyethane at 70℃; for 4h; Temperature;	97.4%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 75-89-8
2,2,2-trifluoroethanol

Conditions

Conditions	Yield
With potassium γ-hydroxybutyrate In 4-butanolide at 200℃; under 11251.1 Torr; for 6h;	96%
With 4-butanolide; potassium hydroxide at 200℃; under 11251.1 Torr; for 6h;	68%
With potassium acetate; ethylene glycol; acetic acid

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 753-90-2
trifluoroethylamine

Conditions

Conditions	Yield
With dmap; ammonia at 110℃; Temperature;	94%
With ammonia; water at 190℃;
With ammonia; water at 185℃;

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 68716-49-4
p-bromophenylboronic acid pinacol ester

: 1310949-87-1
4,4,5,5-tetramethyl-2-(4-(2,2,2-trifluoroethyl)phenyl)-1,3,2-dioxaborolane

Conditions

Conditions	Yield
With 4,4'-di-tert-butyl-2,2'-bipyridine; magnesium chloride; nickel dibromide; zinc In N,N-dimethyl acetamide at 80℃; for 12h; Inert atmosphere; Schlenk technique;	94%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 17878-47-6
(3-bromophenyl)trimethylsilane

: trimethyl(3-(2,2,2-trifluoroethyl)phenyl)silane

Conditions

Conditions	Yield
With 4,4'-di-tert-butyl-2,2'-bipyridine; magnesium chloride; nickel dibromide; zinc In N,N-dimethyl acetamide at 80℃; for 12h; Inert atmosphere; Schlenk technique;	93%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: mercury dichloride

: chloro(chlorodifluorovinyl)mercury

Conditions

Conditions	Yield
With BuLi In tetrahydrofuran; diethyl ether (N2); BuLi slowly added to stirred soln. of ligand (1 equiv.) in Et2O at-80°C; react. temp. was maintained between -55°C and -80. degree.C for 2 h; HgCl2 (1 equiv.) in THF added at -110°C; warmedto -35°C for few h; warmed to room temp.; solvent vol. reduced in vac. to half; hexane added; mixt. was allowed to settle; filtered under N2; solvent removed in vac.; washed (hexane); elem. anal.;	87%

Yield

With BuLi In tetrahydrofuran; diethyl ether (N2); BuLi slowly added to stirred soln. of ligand (1 equiv.) in Et2O at-80°C; react. temp. was maintained between -55°C and -80. degree.C for 2 h; HgCl2 (1 equiv.) in THF added at -110°C; warmedto -35°C for few h; warmed to room temp.; solvent vol. reduced in vac. to half; hexane added; mixt. was allowed to settle; filtered under N2; solvent removed in vac.; washed (hexane); elem. anal.;

87%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 32316-92-0
naphthalene-2-boronic acid

: 1204295-99-7
2-(2,2,2-trifluoroethyl)naphthalene

Conditions

Conditions	Yield
With [2,2]bipyridinyl; nickel(II) bromide dimethoxyethane; potassium phosphate In dimethyl sulfoxide at 80℃; for 30h; Inert atmosphere; Sealed tube;	87%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 127-08-2
potassium acetate

: 406-93-9
4,4,4-trifluorobutyric acid

Conditions

Conditions	Yield
Stage #1: 1,1,1-trifluoro-2-chloroethane; potassium acetate In 1-methyl-pyrrolidin-2-one at 180℃; for 23h; Autoclave; Sealed tube; Stage #2: With acetic anhydride In 1-methyl-pyrrolidin-2-one at 35 - 40℃; for 3h; Reagent/catalyst; Solvent;	86.5%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 591-18-4
1-Bromo-3-iodobenzene

: 1-bromo-2-(1-chloro-2,2-difluoro-vinyl)-benzene

Conditions

Conditions	Yield
Stage #1: 1,1,1-trifluoro-2-chloroethane With n-butyllithium; diisopropylamine; zinc(II) chloride In tetrahydrofuran at 15 - 20℃; for 2h; Stage #2: 1-Bromo-3-iodobenzene With tetrakis(triphenylphosphine) palladium(0) at 20℃; for 18h;	85%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 591-18-4
1-Bromo-3-iodobenzene

A: m-bromo-α-chloro-β,β-styrene

B: 1,4-bis-(1-chloro-2,2-difluoro-vinyl)-benzene

Conditions

Conditions	Yield
Stage #1: 1,1,1-trifluoro-2-chloroethane With zinc(II) chloride; lithium diisopropyl amide In tetrahydrofuran at 20℃; for 2h; Stage #2: 1-Bromo-3-iodobenzene; tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 20℃; for 18h;	A 85% B 1%

...Expand

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 5720-07-0
4-methoxyphenylboronic acid

: 157928-44-4
1-methoxy-4-(2,2,2-trifluoroethyl)benzene

Conditions

Conditions	Yield
With [2,2]bipyridinyl; nickel(II) bromide dimethoxyethane; potassium phosphate In dimethyl sulfoxide at 80℃; for 30h; Inert atmosphere; Sealed tube;	85%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 49562-28-9
fenofibrate

: isopropyl 2-methyl-2-(4-(4-(2,2,2-trifluoroethyl)benzoyl)phenoxy)propanoate

Conditions

Conditions	Yield
With 4,4'-di-tert-butyl-2,2'-bipyridine; magnesium chloride; nickel dibromide; zinc In N,N-dimethyl acetamide at 80℃; for 12h; Inert atmosphere; Schlenk technique;	85%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 1461-22-9
tributyltin chloride

: 214422-68-1
tributyl(chlorodifluorovinyl)tin

Conditions

Conditions	Yield
With BuLi In diethyl ether BuLi added to soln. of ligand in Et2O at -80°C; after 2 h soln. of Bu3SnCl in Et2O (dissolved at -80°C) added slowly at -110°C; warmed to room temp. overnight; hexane added; filtered; solvent removed on rotary evaporator; distd. in vac. (242°C, 0.2 mmHg); elem. anal.;	84%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 2767-54-6
triethyltin bromide

: 329911-50-4
triethyl(chlorodifluorovinyl)tin

Conditions

Conditions	Yield
With BuLi In diethyl ether (N2); BuLi added to soln. of ligand in Et2O at -80°C; after 2 h soln. of Et3SnBr in Et2O (dissolved at -80°C) added slowly at -110°C; warmed to room temp. overnight; hexane added; filtered; solvent removed on rotary evaporator; distd. in vac. (182°C, 0.2 mmHg); elem. anal.;	84%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 624-31-7
4-tolyl iodide

: 4-methyl-α-chloro-β,β-difluorostyrene

Conditions

Conditions	Yield
Stage #1: 1,1,1-trifluoro-2-chloroethane With n-butyllithium; diisopropylamine; zinc(II) chloride In tetrahydrofuran at 15 - 20℃; for 2h; Stage #2: 4-tolyl iodide With tetrakis(triphenylphosphine) palladium(0) at 20℃; for 12h;	83%
Stage #1: 1,1,1-trifluoro-2-chloroethane With zinc(II) chloride; lithium diisopropyl amide In tetrahydrofuran at 20℃; for 2h; Stage #2: 4-tolyl iodide; tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 20℃; for 12h;	83%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 86-74-8
9H-carbazole

: 9-(2,2,2-trifluoroethyl)-9H-carbazole

Conditions

Conditions	Yield
With caesium carbonate In N,N-dimethyl-formamide for 16h; Inert atmosphere;	83%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 3972-65-4
1-bromo-4-tert-butylbenzene

: 1099597-89-3
1-(tert-butyl)-4-(2,2,2-trifluoroethyl)benzene

Conditions

Conditions	Yield
With 4,4'-di-tert-butyl-2,2'-bipyridine; magnesium chloride; nickel dibromide; zinc In N,N-dimethyl acetamide at 80℃; for 12h; Inert atmosphere; Schlenk technique;	83%

: 193694-04-1
N-TBS-4-bromoindole

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 1-(tert-butyldimethylsilyl)-4-(2,2,2-trifluoroethyl)-1H-indole

Conditions

Conditions	Yield
With 4,4'-di-tert-butyl-2,2'-bipyridine; magnesium chloride; nickel dibromide; zinc In N,N-dimethyl acetamide at 80℃; for 20h; Inert atmosphere; Schlenk technique;	83%

: 75-88-7
1,1,1-trifluoro-2-chloroethane

: 17282-40-5
N-(ethoxycarbonylmethyl)pyridinium bromide

: 2-fluoro-indolizine-3-carboxylic acid ethyl ester

Conditions

Conditions	Yield
With potassium carbonate; triethylamine In N,N-dimethyl-formamide at 80℃; for 24h;	82%

1,1,1-Trifluoro-2-chloroethane Chemical Properties

Molecular Structure of 1,1,1-Trifluoro-2-chloroethane (CAS NO.75-88-7):

EINECS: 200-912-0
IUPAC Name: 2-Chloro-1,1,1-trifluoroethane
Molecular Formula: C₂H₂ClF₃
Molecular Weight: 118.485490 g/mol
XLogP3-AA: 1.9
H-Bond Donor: 0
H-Bond Acceptor: 3
Canonical SMILES: C(C(F)(F)F)Cl
InChI: InChI=1S/C2H2ClF3/c3-1-2(4,5)6/h1H2
InChIKey: CYXIKYKBLDZZNW-UHFFFAOYSA-N
Index of Refraction: 1.298
Molar Refractivity: 16.62 cm³
Molar Volume: 89.3 cm³
Surface Tension: 14.3 dyne/cm
Density: 1.326 g/cm³
Enthalpy of Vaporization: 24.48 kJ/mol
Boiling Point: 6.9 °C at 760 mmHg
Vapour Pressure: 1430 mmHg at 25 °C
Melting Point: -105 °C
Water Solubility: 365.4 mg/L at 25 °C
BRN: 1733200

1,1,1-Trifluoro-2-chloroethane Toxicity Data With Reference

1.		orl-rat TDLo:78 g/kg/1Y-I:CAR,REP		TXAPA9 Toxicology and Applied Pharmacology. 72 (1984),15.
2.		ihl-mus LC50:15 pph/1H		BJANAD British Journal of Anesthesia. 37 (1965),716.

1,1,1-Trifluoro-2-chloroethane Consensus Reports

IARC Cancer Review: Group 3 IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 7 ,1987,p. 56.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; Animal Limited Evidence IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 41 ,1986,p. 253.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) . Reported in EPA TSCA Inventory.

1,1,1-Trifluoro-2-chloroethane Safety Profile

Safety Information of 1,1,1-Trifluoro-2-chloroethane (CAS NO.75-88-7):
Hazard Codes: Xi
Hazard Note: Irritant
Risk Statements: 59
R59:Dangerous to the ozone layer
Safety Statements: 9-23-59
S9:Keep container in a well-ventilated place
S23:Do not breathe vapour
S59:Refer to manufacturer / supplier for information on recovery / recycling
RIDADR: 1983
TSCA: T
HazardClass: 2.2
A poison by inhalation. Experimental reproductive effects. Questionable carcinogen with experimental carcinogenic data. When heated to decomposition it emits toxic fumes of F⁻.

1,1,1-Trifluoro-2-chloroethane Specification

1,1,1-Trifluoro-2-chloroethane with CAS Registry Number of 75-88-7 is a colorless, odorless gas. It is also known as 1,1,1-Trifluoroethyl chloride ; 1-Chloro-2,2,2-trifluoroethane ; 2,2,2-Trifluorochloroethane ; 2-Chloro-1,1,1-trifluoroethane ; 4-01-00-00128 (Beilstein Handbook Reference) ; CCRIS 154 ; CFC 133a ; FC 133a ; Forane 133a ; Freon 133a ; Genetron 133a ; HCFC 133a ; HCFC-133a ; HSDB 6949 ; R 133a ; Chloro-1,1,1-trifluoroethane ; Ethane, 2-chloro-1,1,1-trifluoro- ; 1-Chloro-2,2,2-trifluoroethane or Refrigerant gas R 133a [UN1983] [Non-flammable gas] ; Chlorotrifluoroethane ; HCFC-133a ; UN1983 . It can react violently with strong reducing agents and undergo oxidation with strong oxidizing agents and under extremes of temperature.

Product Name

2-Chloro-1,1,1-trifluoroethane

Synthetic route

1,1,1-Trifluoro-2-chloroethane Chemical Properties

1,1,1-Trifluoro-2-chloroethane Toxicity Data With Reference

1,1,1-Trifluoro-2-chloroethane Consensus Reports

1,1,1-Trifluoro-2-chloroethane Safety Profile

1,1,1-Trifluoro-2-chloroethane Specification

Related Products

Hot Products