Trifluoromethyl iodide
[CAS# 2314-97-8]

Identification

• Classification: Chemical reagent >> Organic reagent >> Halogenated aliphatic hydrocarbon
• Name: Trifluoromethyl iodide
• Synonyms: Trifluoroiodomethane; Iodotrifluoromethane
• Molecular Formula: CF₃I
• Molecular Weight: 195.91
• CAS Registry Number: 2314-97-8
• EC Number: 219-014-5
• SMILES: C(F)(F)(F)I

Properties

• Density: 2.4±0.1 g/cm³ Calc.^*, 2.361 g/mL (Expl.)
• Melting point: -110 ºC (Expl.)
• Boiling point: -21.1±8.0 ºC 760 mmHg (Calc.)^*, -22.5 ºC (Expl.)
• Flash point: -26.9±5.6 ºC (Calc.)^*
• Index of refraction: 1.415 (Calc.)^*, 1.379 (Expl.)

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS04;GHS08 Warning
• Hazard Statements: H280-H341
• Precautionary Statements: P203-P280-P318-P405-P410+P403-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Germ cell mutagenicity	Muta.	2	H341
Gases under pressure (compressed)	Press. Gas (Comp.)		H280
Gases under pressure (liquid)	Press. Gas (Liq.)		H280
Chronic hazardous to the aquatic environment	Aquatic Chronic	3	H412

• Transport Information: UN 1956

Discovory and Applicatios

Trifluoromethyl iodide, also known by its chemical formula CF₃I, is a halogenated organic compound that has been known and studied since the early 20th century. It belongs to the class of trifluoromethyl halides, with a structure consisting of a trifluoromethyl group (−CF₃) bonded to an iodine atom. It is a colorless gas at room temperature and pressure, with a boiling point of approximately −22 °C, and is commonly stored in pressurized cylinders or under refrigeration.

The synthesis of trifluoromethyl iodide was first achieved through halogen exchange reactions, particularly involving the reaction of trifluoromethyl halides with iodine-containing reagents. Early methods included the reaction of trifluoromethyl mercury derivatives with iodine, which yielded CF₃I as a volatile byproduct. Later developments introduced more practical and safer methods using non-metallic reagents. For example, CF₃I can be prepared by the iodination of trifluoromethyl precursors using elemental iodine or iodine monochloride under controlled conditions.

One of the major scientific interests in trifluoromethyl iodide stems from its utility as a trifluoromethylating agent. The introduction of the trifluoromethyl group (−CF₃) into organic molecules significantly alters their chemical and biological properties, including increased lipophilicity, metabolic stability, and bioavailability. These features are especially important in the development of agrochemicals and pharmaceuticals. CF₃I has been widely used in trifluoromethylation reactions, particularly in radical-mediated and photochemical processes. Under UV or visible light, the C–I bond in CF₃I undergoes homolytic cleavage to generate the CF₃ radical, which can add to unsaturated compounds such as alkenes, alkynes, and aromatics.

In addition to radical-based chemistry, CF₃I has also been used in metal-catalyzed trifluoromethylation, involving palladium, copper, and nickel complexes. These reactions enable the formation of carbon–carbon and carbon–heteroatom bonds bearing trifluoromethyl substituents. The development of such methodologies has been of great interest in modern synthetic organic chemistry, enabling the late-stage functionalization of complex molecules.

Trifluoromethyl iodide has also been examined for its potential environmental and industrial applications. One notable area of interest is its proposed use as a fire suppression agent. Due to its high density, thermal stability, and relatively low ozone-depleting potential compared to chlorofluorocarbons, CF₃I has been considered as a possible replacement for halons in fire extinguishing systems. In this context, it can function by absorbing heat and generating iodine radicals that interrupt flame-propagating radical chain reactions. However, due to toxicity concerns and the release of reactive iodine species, its application in occupied spaces is limited and regulated.

In atmospheric chemistry, CF₃I has been studied as a trace compound with implications for ozone chemistry. Although it is less persistent in the atmosphere compared to long-lived halocarbons, its photodissociation can contribute to the release of iodine atoms, which catalyze the breakdown of ozone. This environmental effect, while less severe than traditional chlorofluorocarbons, still limits widespread industrial use.

From a safety perspective, trifluoromethyl iodide is a compound that requires careful handling. It is toxic by inhalation, and exposure can result in respiratory and central nervous system effects. Its reactivity and volatility necessitate proper ventilation, containment, and storage. Despite these concerns, it remains an important reagent in laboratory and industrial contexts where its unique reactivity can be harnessed under controlled conditions.

In summary, trifluoromethyl iodide is a valuable compound in synthetic and applied chemistry, with established roles in radical trifluoromethylation, catalysis, and specialty fire suppression systems. Its discovery and continued study have contributed to advances in organofluorine chemistry, environmental science, and materials development.

References

1962 International Union of Crystallography Commission on Crystal Structure Data List of 1958 publications containing new data on crystal structures. Journal of Structural Chemistry, 3(3).
DOI: 10.1007/bf01151496

2024 Recent progress in carbene-catalyzed fluoroalkylation. Science China Chemistry, 67(6).
DOI: 10.1007/s11426-024-1981-1

2024 Nucleophilic trifluoromethylation with CF3H/LiHMDS: probing the nucleophilic reactivity of LiCF3 species. Science China Chemistry, 67(9).
DOI: 10.1007/s11426-024-2289-7