Iodomethane

Iodomethane
Names
Preferred IUPAC name
Iodomethane
Other names
  • Methyl iodide
  • Methyl iodine
  • Monoiodomethane
Identifiers
3D model (JSmol)
Abbreviations
  • Halon 10001
  • MeI
969135
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.745
EC Number
  • 200-819-5
1233
KEGG
MeSH methyl+iodide
PubChem CID
RTECS number
  • PA9450000
UNII
UN number 2644
  • InChI=1S/CH3I/c1-2/h1H3 Y
    Key: INQOMBQAUSQDDS-UHFFFAOYSA-N Y
SMILES
  • CI
Properties
CH3I
Molar mass 141.939 g·mol−1
Appearance Colorless liquid
Odor Pungent, ether-like
Density 2.28 g·mL−1
Melting point −66.5 °C; −87.6 °F; 206.7 K
Boiling point 42.4 to 42.8 °C; 108.2 to 108.9 °F; 315.5 to 315.9 K
14 g·L−1 (at 20 °C, 68 °F)
log P 1.609
Vapor pressure 54.4 kPa (at 20 °C, 68 °F)
1.4 μmol·Pa−1·kg−1
Magnetic susceptibility (χ)
−57.2·10−6 cm3·mol−1
Refractive index (nD)
1.530–1.531
Structure
Molecular shape
Tetrahedron
Thermochemistry
82.75 J·K−1·mol−1
Std enthalpy of
formation fH298)
−14.1 – −13.1 kJ·mol−1
−808.9 – −808.3 kJ·mol−1
Hazards
GHS labelling:
Danger
H301, H312, H315, H331, H335, H351
P261, P280, P301+P310, P311
NFPA 704 (fire diamond)
3
0
0
Lethal dose or concentration (LD, LC):
LD50 (median dose)
  • 76 mg·kg−1 (oral, rat)
  • 800 mg·kg−1 (dermal, guinea pig)
LC50 (median concentration)
  • 1550 ppm (rat, 30 min)
  • 860 ppm (mouse, 57 min)
  • 220 ppm (rat, 4 hr)
LCLo (lowest published)
3800 ppm (rat, 15 min)
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 5 ppm (28 mg/m3) [skin]
REL (Recommended)
Ca TWA 2 ppm (10 mg/m3) [skin]
IDLH (Immediate danger)
Ca [100 ppm]
Related compounds
Related iodomethanes
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Iodomethane, also called methyl iodide, and commonly abbreviated "MeI", is the chemical compound with the formula CH3I. It is a dense, colorless, volatile liquid. In terms of chemical structure, it is related to methane by replacement of one hydrogen atom by an atom of iodine. It is naturally emitted by rice plantations in small amounts. It is also produced in vast quantities estimated to be greater than 214,000 tons annually by algae and kelp in the world's temperate oceans, and in lesser amounts on land by terrestrial fungi and bacteria. It is used in organic synthesis as a source of methyl groups.

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