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Names | |||
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IUPAC name
Diiodomethane
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Identifiers | |||
3D model (Jmol)
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1696892 | |||
ChemSpider | |||
ECHA InfoCard | 100.000.765 | ||
EC Number | 200-841-5 | ||
MeSH | methylene+iodide | ||
PubChem CID
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RTECS number | PA8575000 | ||
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Properties | |||
CH2I2 | |||
Molar mass | 267.84 g·mol−1 | ||
Appearance | Colorless liquid | ||
Density | 3.325 g mL−1 | ||
Melting point | 5.4 to 6.2 °C; 41.6 to 43.1 °F; 278.5 to 279.3 K | ||
Boiling point | 182.1 °C; 359.7 °F; 455.2 K | ||
1.24 g L−1 (at 20 °C) | |||
Henry's law
constant (kH) |
23 μmol Pa−1 kg−1 | ||
-93.10·10−6 cm3/mol | |||
Structure | |||
Tetragonal | |||
Tetrahedron | |||
Thermochemistry | |||
133.81 J K−1 mol−1 | |||
Std enthalpy of
formation (ΔfH |
67.7–69.3 kJ mol−1 | ||
Std enthalpy of
combustion (ΔcH |
−748.4–−747.2 kJ mol−1 | ||
Hazards | |||
Safety data sheet | hazard.com | ||
GHS pictograms | |||
GHS signal word | DANGER | ||
H302, H315, H318, H335 | |||
P261, P280, P305+351+338 | |||
EU classification (DSD)
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Xn | ||
R-phrases | R22, R36/37/38 | ||
S-phrases | S26 | ||
NFPA 704 | |||
Flash point | 110 °C (230 °F; 383 K) | ||
Related compounds | |||
Related alkanes
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Related compounds
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|||
Infobox references | |||
Diiodomethane or methylene iodide, commonly abbreviated "MI", is an organoiodine compound. Diiodomethane is a colorless liquid; however, it decomposes upon exposure to light liberating iodine, which colours samples brownish. It is slightly soluble in water, but soluble in organic solvents. It has a relatively high refractive index of 1.741, and a surface tension of 0.0508 N·m−1.
Because of its high density, diiodomethane is used in the determination of the density of mineral and other solid samples. It can also be used as an optical contact liquid, in conjunction with the gemmological refractometer, for determining the refractive index of certain gemstones. Diiodomethane is a reagent in the Simmons–Smith reaction, serving as a source of the free radical methylene (carbene), :CH
2.
Although commercially available, it can be prepared by reducing iodoform with elemental phosphorus or sodium arsenite:
Diiodomethane can also be prepared from dichloromethane by the action of sodium iodide in acetone in the Finkelstein reaction:
Alkyl iodides are alkylating agents and contact should be avoided.