2-Iodo-1,1,1-trifluoroethane supplier

Name
2-Iodo-1,1,1-trifluoroethane
EINECS 206-541-0
CAS No. 353-83-3
Article Data14
CAS DataBase
Density 2.169 g/cm³
Solubility insoluble in water
Melting Point
Formula C₂H₂F₃I
Boiling Point 53.7 °C at 760 mmHg
Molecular Weight 209.938
Flash Point 7.4 °C
Transport Information
Appearance clear colorless to pink liquid
Safety 26-36-37/39
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms 1,1,1-Trifluoro-2-iodoethane;1-Iodo-2,2,2-trifluoroethane;2,2,2-Trifluoro-1-iodoethane;2,2,2-Trifluoroethyl iodide;
PSA 0.00000
LogP 1.98370

Synthetic route

: 13735-81-4
1-styrenyloxytrimethylsilane

: 166903-46-4
1-[hydroxy(tosyloxy)iodo]-1H,1H-perfluoroethane

A: 353-83-3
1,1,1-trifluoro-2-iodoethane

B: 7257-94-5
1-phenyl-2-(p-tolylsulfonyloxy)ethanone

Conditions

Conditions	Yield
In dichloromethane for 1h; Ambient temperature;	A n/a B 58%

...Expand

: 6651-36-1
1-(Trimethylsilyloxy)cyclohexene

: 166903-46-4
1-[hydroxy(tosyloxy)iodo]-1H,1H-perfluoroethane

A: 353-83-3
1,1,1-trifluoro-2-iodoethane

B: 81447-34-9
2-(tosyloxy)cyclohexanone

Conditions

Conditions	Yield
In dichloromethane at 0℃; for 3h;	A n/a B 56%

...Expand

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

: 353-83-3
1,1,1-trifluoro-2-iodoethane

Conditions

Conditions	Yield
With potassium bromide at 300℃; for 0.333333h;	36%

: 358-63-4
tris(2,2,2-trifluoroethyl) phosphate

: 353-83-3
1,1,1-trifluoro-2-iodoethane

Conditions

Conditions	Yield
With Pentaethylene glycol; sodium iodide

: 420-93-9
1-bromo-1,1-difluoro-2-iodoethane

A: 353-83-3
1,1,1-trifluoro-2-iodoethane

B: 75-38-7
Vinylidene fluoride

Conditions

Conditions	Yield
With mercury(I) fluoride at 140℃;

: 371-67-5
2,2,2-trifluorodiazoethane

: 353-83-3
1,1,1-trifluoro-2-iodoethane

Conditions

Conditions	Yield
With hydrogen iodide; toluene at -75℃;

: 433-06-7
2,2,2-Trifluoroethyl p-toluenesulfonate

: 353-83-3
1,1,1-trifluoro-2-iodoethane

Conditions

Conditions	Yield
With sodium iodide; diethylene glycol

: 64-69-7
Iodoacetic acid

A: 353-83-3
1,1,1-trifluoro-2-iodoethane

B: 51100-31-3
bis-(1,1-difluoro-2-iodo-ethyl) ether

Conditions

Conditions	Yield
With sulfur tetrafluoride at 60℃; for 3h;
With sulfur tetrafluoride at 26℃; for 21h;

: 75-11-6
diiodomethane

: 1514-87-0
metyhyl chlorodifluoroacetate

: 353-83-3
1,1,1-trifluoro-2-iodoethane

Conditions

Conditions	Yield
With potassium fluoride; copper(l) iodide; cadmium(II) iodide In N,N,N,N,N,N-hexamethylphosphoric triamide at 120℃; for 8h;	78 % Turnov.

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

A: 75-01-4
chloroethylene

B: 353-83-3
1,1,1-trifluoro-2-iodoethane

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

D: 76-16-4
Hexafluoroethane

E: 359-11-5
1,1,2-trifluoroethylene

F: 107-06-2
1,2-dichloro-ethane

Conditions

Conditions	Yield
Rate constant; Thermodynamic data; Ambient temperature; Irradiation; Eo;

...Expand

: C20H17F3OP(1+)*I(1-)

: 353-83-3
1,1,1-trifluoro-2-iodoethane

Conditions

Conditions	Yield
In solid at 160 - 190℃; Yield given;

: 371-67-5
2,2,2-trifluorodiazoethane

: 10034-85-2
hydrogen iodide

: 108-88-3
toluene

: 353-83-3
1,1,1-trifluoro-2-iodoethane

Conditions

Conditions	Yield
at -75℃;

...Expand

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

: 7553-56-2
iodine

red phosphorus: red phosphorus

: 353-83-3
1,1,1-trifluoro-2-iodoethane

...Expand

: 420-93-9
1-bromo-1,1-difluoro-2-iodoethane

mercury (I)-fluoride: mercury (I)-fluoride

A: 353-83-3
1,1,1-trifluoro-2-iodoethane

B: 75-38-7
Vinylidene fluoride

Conditions

Conditions	Yield
at 140℃;

...Expand

: trans-bis(dimethylglyoximato)(CH2CF3)(4-cyanopyridine)cobalt(III)

: 7553-56-2
iodine

: {CoI(NC5H4(CN))(NOC(CH3)C(CH3)NOH)2}

B: 353-83-3
1,1,1-trifluoro-2-iodoethane

Conditions

Conditions	Yield
In benzene Kinetics; iodinolysis with I2 in benzene soln. at 305 K;

...Expand

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 407-25-0
trifluoroacetic anhydride

: 100422-04-6
(2,2,2-trifluoroethyl)-λ3-iodanediyl bis(2,2,2-trifluoroacetate)

Conditions

Conditions	Yield
Stage #1: trifluoroacetic anhydride With dihydrogen peroxide; trifluoroacetic acid In water at 0℃; for 0.0833333h; Stage #2: 1,1,1-trifluoro-2-iodoethane at 0 - 20℃;	100%
Stage #1: trifluoroacetic anhydride With dihydrogen peroxide at 0℃; for 0.166667h; Inert atmosphere; Stage #2: 1,1,1-trifluoro-2-iodoethane at 0 - 22℃; for 24h; Inert atmosphere;	90%
Stage #1: trifluoroacetic anhydride With dihydrogen peroxide; trifluoroacetic acid In water at 0℃; for 0.0833333h; Inert atmosphere; Stage #2: 1,1,1-trifluoro-2-iodoethane In water at 0 - 20℃; for 20h; Inert atmosphere;

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 76-05-1
trifluoroacetic acid

: 407-25-0
trifluoroacetic anhydride

: 100422-04-6
(2,2,2-trifluoroethyl)-λ3-iodanediyl bis(2,2,2-trifluoroacetate)

Conditions

Conditions	Yield
Stage #1: trifluoroacetic acid; trifluoroacetic anhydride With dihydrogen peroxide In water at 0℃; for 0.0833333h; Stage #2: 1,1,1-trifluoro-2-iodoethane In water at 0 - 20℃; for 20h;	100%
In water; dihydrogen peroxide at 0 - 20℃;	40%

...Expand

: 885028-69-3
5-amino-4-fluoro-2-methylbenzene-1-thiol

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulfanyl]phenylamine

Conditions

Conditions	Yield
With rongalite; potassium hydroxide In N,N-dimethyl-formamide at 20℃; for 2h;	99%
With rongalite; potassium hydroxide In N,N-dimethyl-formamide at 20℃; for 2h;	99%
With rongalite; potassium hydroxide In N,N-dimethyl-formamide at 20℃; for 2h;	99%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 219832-01-6
(2,6-bis[(di-tert-butylphosphino)methyl]phenyl)rhodium dinitrogen

: 230636-00-7
Rh(I)(CH2CF3)(2,6-(CH2P(t)Bu2)2C6H3)

Conditions

Conditions	Yield
In benzene-d6 inert atmosphere; 1-4 equiv. of CF3CH2I, room temp.; evapn.; NMR-spectroscopy;	99%

: dimethyl(N,N,N',N',-tetramethylethanediamine)platinum

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 660390-90-9, 660417-21-0
trans-Pt(N,N,N',N'-tetramethylethylenediamine)(CH2CF3)(CH3)2I

Conditions

Conditions	Yield
In toluene (N2); CF3CH2I added to a suspn. of Pt complex at -78°C, stirred for ca. 10 min; evapd. (vac., below 0°C);	99%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 663152-74-7
trifluoroprop-1-yn-1-ylxenonium(II) tetrafluoroborate

: trifluoroprop-1-yn-1-yl(2,2,2-trifluoroethyl)iodonium tetrafluoroborate

Conditions

Conditions	Yield
With hydrogen fluoride at -20 - 15℃; for 1h; Inert atmosphere;	99%
In hydrogen fluoride byproducts: Xe; HF (liquid); soln. of CF3CCXe(BF4) (-20°C) in anhyd. HF added to stirred neat CF3CH2I (-20°C), stirred at 15°C for 1 h; volatiles evapd., residue washed (CH2Cl2, 5°C), dried (vac.); (1)H, (13)C, (19)F NMR;	99%

: 500011-95-0
2-(3-chloro-pyridin-2-yl)-5-oxo-2,5-dihydro-1H-pyrazole-3-carboxylic acid ethyl ester

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: ethyl 1-(3-chloro-2-pyridinyl)-3-(2,2,2-trifluoroethoxy)-1H-pyrazole-5-carboxylate

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 100℃;	99%
With potassium carbonate In N,N-dimethyl-formamide at 100℃;

: 500011-88-1
2-(3-chloro-pyridin-2-yl)-5-oxo-pyrazolidine-3-carboxylic acid ethyl ester

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: ethyl 1-(3-chloro-2-pyridinyl)-3-(2,2,2-trifluoroethoxy)-1H-pyrazole-5-carboxylate

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 100℃; for 3h;	99%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 696-62-8
para-iodoanisole

: 130612-75-8
(2,2,2-trifluoroethyl) (4-methoxyphenyl) sulfide

Conditions

Conditions	Yield
With sulfur; sodium tetrahydroborate; 1,10-Phenanthroline; [(1,10-phenanthroline)Cu(μ-SCH2CF3)]2 In N,N-dimethyl-formamide at 90℃; for 12h; Kinetics; Reagent/catalyst; Temperature; Solvent; Inert atmosphere; Sealed tube;	99%
With sodium tetrahydroborate; 1,10-Phenanthroline; iodine; sulfur In N,N-dimethyl-formamide at 80℃; for 16h; Inert atmosphere;	84%

: 636-98-6
p-nitrobenzene iodide

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: (4-nitrophenyl)(2,2,2-trifluoroethyl)sulfane

Conditions

Conditions	Yield
With sodium tetrahydroborate; 1,10-Phenanthroline; iodine; sulfur In N,N-dimethyl-formamide at 80℃; for 16h; Inert atmosphere;	99%
With sulfur; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 85℃; for 12h; Inert atmosphere; Sealed tube;	99%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 586-78-7
para-nitrophenyl bromide

: (4-nitrophenyl)(2,2,2-trifluoroethyl)sulfane

Conditions

Conditions	Yield
With sodium tetrahydroborate; 1,10-Phenanthroline; iodine; sulfur In N,N-dimethyl-formamide at 95℃; for 1h; Inert atmosphere;	99%
With sulfur; sodium tetrahydroborate; copper(l) iodide; dimedone In N,N-dimethyl-formamide at 95℃; for 12h; Inert atmosphere; Sealed tube;	96%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 5326-38-5
2-iodo-5-nitrotoluene

: (2-methyl-4-nitrophenyl)(2,2,2-trifluoroethyl)sulfane

Conditions

Conditions	Yield
With sulfur; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 85℃; for 12h; Inert atmosphere; Sealed tube;	99%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 51934-41-9
4-iodobenzoic acid ethyl ester

: ethyl 4-((2,2,2-trifluoroethyl)thio)benzoate

Conditions

Conditions	Yield
With sulfur; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 85℃; for 12h; Inert atmosphere; Sealed tube;	99%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 1121-86-4
1-Fluoro-3-iodobenzene

: 62158-90-1
(2,2,2-trifluoroethyl) (3-fluorophenyl) sulfide

Conditions

Conditions	Yield
With sulfur; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 85℃; for 12h; Inert atmosphere; Sealed tube;	99%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 2523-42-4
2-iodo-9H-fluorene

: (9H-fluoren-2-yl)(2,2,2-trifluoroethyl)selane

Conditions

Conditions	Yield
With potassium hexafluorophosphate; selenium; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 95℃; for 16h; Sealed tube;	99%

: 132034-89-0
4-iododibenzo[b,d]thiophene

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 1360594-83-7
4-(2,2,2-trifluoroethyl)dibenzo[b,d]thiophene

Conditions

Conditions	Yield
With nickel(II) iodide; 1,1'-bis-(diphenylphosphino)ferrocene; manganese; 4,4'-di-tert-butyl-2,2'-bipyridine In N,N-dimethyl acetamide at 80℃; for 24h; Inert atmosphere; Sealed tube;	99%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 407-25-0
trifluoroacetic anhydride

A: 100422-04-6
(2,2,2-trifluoroethyl)-λ3-iodanediyl bis(2,2,2-trifluoroacetate)

B: 76-05-1
trifluoroacetic acid

Conditions

Conditions	Yield
With dihydrogen peroxide at -15 - 20℃; for 72h;	A 98% B n/a

...Expand

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 4387-36-4
2-iodobenzonitrile

: 2-((2,2,2-trifluoroethyl)selanyl)benzonitrile

Conditions

Conditions	Yield
With potassium hexafluorophosphate; selenium; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 95℃; for 16h; Sealed tube;	98%
With selenium; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 95℃; for 16h; Inert atmosphere;	98%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 8-bromo-2-phenyl-4H-pyrazolo[1,5-a]quinazolin-5-one

: 8-bromo-2-phenyl-4-(2,2,2-trifluoro-ethyl)-4H-pyrazolo[1,5-a]quinazolin-5-one

Conditions

Conditions	Yield
With sodium hydride In N,N-dimethyl-formamide; mineral oil at 150℃; for 0.166667h; Cooling with ice; Microwave irradiation;	97%
Stage #1: 8-bromo-2-phenyl-4H-pyrazolo[1,5-a]quinazolin-5-one With sodium hydride In N,N-dimethyl-formamide; mineral oil for 0.25h; Cooling with ice; Stage #2: 1,1,1-trifluoro-2-iodoethane In N,N-dimethyl-formamide; mineral oil at 150℃; for 0.0833333h; Cooling with ice; Microwave irradiation;	97%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 491-30-5
1-isoquinolone

: 2-(2,2,2-trifluoroethyl)isoquinolin-1(2H)-one

Conditions

Conditions	Yield
With caesium carbonate In N,N-dimethyl-formamide at 50℃; for 3h;	97%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 2113-51-1
2-iodobiphenyl

: [1,1′-biphenyl]-2-yl(2,2,2-trifluoroethyl)sulfane

Conditions

Conditions	Yield
With sulfur; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 85℃; for 12h; Inert atmosphere; Sealed tube;	97%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 14452-30-3
3'-iodoacetophenone

: 1-(3-((2,2,2-trifluoroethyl)thio)phenyl)ethanone

Conditions

Conditions	Yield
With sulfur; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 85℃; for 12h; Inert atmosphere; Sealed tube;	97%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 766-85-8
3-methoxy-1-iodobenzene

: (3-methoxyphenyl)(2,2,2-trifluoroethyl)selane

Conditions

Conditions	Yield
With potassium hexafluorophosphate; selenium; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 95℃; for 16h; Catalytic behavior; Reagent/catalyst; Temperature; Sealed tube;	97%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 15164-44-0
p-(iodophenyl)carboxaldehyde

: 4-(2,2,2-trifluoroethyl)benzaldehyde

Conditions

Conditions	Yield
With nickel(II) iodide; 1,1'-bis-(diphenylphosphino)ferrocene; manganese; 4,4'-di-tert-butyl-2,2'-bipyridine In N,N-dimethyl acetamide at 80℃; for 24h; Inert atmosphere; Sealed tube;	96%
With copper In dimethyl sulfoxide at 120℃; for 55h; Schlenk technique; Inert atmosphere; Sealed tube;	63%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 1133-80-8
2-bromo-9H-fluorene

: (9H-fluoren-2-yl)(2,2,2-trifluoroethyl)selane

Conditions

Conditions	Yield
With potassium hexafluorophosphate; selenium; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 95℃; for 16h; Sealed tube;	96%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 159143-75-6
2-hydroxy-3,17β-bis(benzyloxy)estra-1,3,5(10)-triene

: 192062-06-9
2-(2',2',2'-Trifluoroethoxy)-3,17β-Dibenzyloxyestra-1,3,5(10)-Triene

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide a) 110 deg C, 3 h, b) 130 deg C, 2 h;	95%

: 4282-77-3
9-(prop-2-yn-1-yl)-9H-carbazole

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 9-(5,5,5-trifluoropent-2-ynyl)-9,9a-dihydro-4aH-carbazole

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane; tris-(dibenzylideneacetone)dipalladium(0); bis[2-(diphenylphosphino)phenyl] ether In toluene at 80℃; for 24h; Inert atmosphere; Schlenk technique;	95%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 618-91-7
methyl 3-iodo-benzoate

: 647856-12-0
methyl 3-((2,2,2-trifluoroethyl)thio)benzoate

Conditions

Conditions	Yield
With sulfur; sodium tetrahydroborate; copper(l) iodide; 1,10-Phenanthroline In N,N-dimethyl-formamide at 85℃; for 12h; Inert atmosphere; Sealed tube;	95%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 28131-17-1
2-(4-bromophenyl)acrylic acid

: 1180670-65-8
1-(4'-bromophenyl)-4,4,4-trifluoro-1-butanone

Conditions

Conditions	Yield
With tert.-butylhydroperoxide; copper acetylacetonate; silver sulfate; triethylamine In water; acetonitrile at 80℃; for 0.5h; Sealed tube; Microwave irradiation;	95%

: 353-83-3
1,1,1-trifluoro-2-iodoethane

: 1383569-21-8
2-[4-(4-iodobenzoyl)phenoxy]-2-methylpropanoic acid isopropyl ester

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

Conditions

Conditions	Yield
With nickel(II) iodide; 1,1'-bis-(diphenylphosphino)ferrocene; manganese; 4,4'-di-tert-butyl-2,2'-bipyridine In N,N-dimethyl acetamide at 80℃; for 24h; Inert atmosphere; Sealed tube;	95%

2-Iodo-1,1,1-trifluoroethane Specification

The Ethane,1,1,1-trifluoro-2-iodo-, with CAS registry number 353-83-3, has the systematic name of 1,1,1-trifluoro-2-iodoethane. And its IUPAC name is the same one. This chemical is a kind of clear colorless to pink liquid. What's more, its EINECS is 206-541-0.

Physical properties of Ethane,1,1,1-trifluoro-2-iodo-: (1)ACD/LogP: 1.97; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.97; (4)ACD/LogD (pH 7.4): 1.97; (5)ACD/BCF (pH 5.5): 18.61; (6)ACD/BCF (pH 7.4): 18.61; (7)ACD/KOC (pH 5.5): 282.19; (8)ACD/KOC (pH 7.4): 282.19; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 0 Å²; (13)Index of Refraction: 1.424; (14)Molar Refractivity: 24.74 cm³; (15)Molar Volume: 96.7 cm³; (16)Polarizability: 9.8×10^-24cm³; (17)Surface Tension: 21.8 dyne/cm; (18)Enthalpy of Vaporization: 28.45 kJ/mol; (19)Vapour Pressure: 266 mmHg at 25°C.

Uses of Ethane,1,1,1-trifluoro-2-iodo-: it can be used to produce 1,1,1-trifluoro-octane. This reaction will need reagent AIBN (2,2'-azobisisobutyronitrile).

When you are using this chemical, please be cautious about it as the following:
The Ethane,1,1,1-trifluoro-2-iodo- irritates to eyes, respiratory system and skin. When use it, wear suitable protective clothing, gloves and eye/face protection. If contact with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1)SMILES: FC(F)(F)CI
(2)InChI: InChI=1/C2H2F3I/c3-2(4,5)1-6/h1H2
(3)InChIKey: RKOUFQLNMRAACI-UHFFFAOYAI
(4)Std. InChI: InChI=1S/C2H2F3I/c3-2(4,5)1-6/h1H2
(5)Std. InChIKey: RKOUFQLNMRAACI-UHFFFAOYSA-N

Product Name

2-Iodo-1,1,1-trifluoroethane

Synthetic route

2-Iodo-1,1,1-trifluoroethane Specification

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