Trifluoromethane

Base Information Edit

Chemical Name:Trifluoromethane
CAS No.:75-46-7
Deprecated CAS:185009-29-4
Molecular Formula:CHF3
Molecular Weight:70.0141
Hs Code.:2903399090
European Community (EC) Number:200-872-4
ICSC Number:0577
UN Number:1984,3136
UNII:ZJ51L9A260
DSSTox Substance ID:DTXSID0026410
Nikkaji Number:J2.392B
Wikipedia:Fluoroform
Wikidata:Q410612,Q83047504
Metabolomics Workbench ID:52288
Mol file:75-46-7.mol

Synonyms:CHF3;FC-23;fluorocarbon-11;fluoroform;Freon 23;trifluoromethane

Suppliers and Price of Trifluoromethane

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 72 raw suppliers

Chemical Property of Trifluoromethane Edit

Chemical Property:

Appearance/Colour:colourless gas
Vapor Pressure:25200mmHg at 25°C
Melting Point:-160 °C(lit.)
Refractive Index:1.179
Boiling Point:−84°C(lit.)
PSA：0.00000
Density:1.133 g/cm³
LogP:1.17850
Water Solubility.:slightly
XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:70.00303452
Heavy Atom Count:4
Complexity:8
Transport DOT Label:Non-Flammable Gas

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s): F
Hazard Codes:F
Safety Statements: S38:;

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Chemical Classes:Solvents -> Chlorofluorocarbons
Canonical SMILES:C(F)(F)F
Inhalation Risk:On loss of containment this substance can cause suffocation by lowering the oxygen content of the air in confined areas.
Effects of Short Term Exposure:Inhalation of the vapour may cause depression of the central nervous system. The liquid may cause frostbite. Exposure could cause cardiac arrythmia and asphyxiation.

Technology Process of Trifluoromethane

There total 640 articles about Trifluoromethane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 74.0%

: 359-64-8
iodo-bis-trifluoromethyl-phosphine

: 75-46-7
trifluoromethan

: 374-09-4
(trifluoromethyl)phosphonic acid

Guidance literature:: With H₂O; H₂O₂; In water; byproducts: iodine; 30 min shaking with H2O at 20°C excluding air; dropwise addn. of H2O2; filtration; washing (H2O); 5-6 d freeze-drying; sublimation;
DOI:10.1039/JR9540003598

Reference yield: 60.0%

: 650-52-2
bis(trifluoromethyl)chlorophosphine

: 75-46-7
trifluoromethan

: 374-09-4
(trifluoromethyl)phosphonic acid

Guidance literature:: With H₂O; H₂O₂; In water; 30 min shaking with H2O at 20°C excluding air; dropwise addn. of H2O2; washing (H2O); 5-6 d freeze-drying; sublimation;
DOI:10.1039/JR9540003598