Difference between revisions of "Methyl iodide"

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==Projects==
 
==Projects==
 
*Make esters
 
*Make esters
 +
*Make toluene
  
 
==Handling==
 
==Handling==

Revision as of 16:23, 7 July 2016

Methyl iodide
Names
IUPAC name
Iodomethane
Other names
Methyl iodine
Monoiodomethane
Identifiers
Jmol-3D images Image
Properties
CH3I
Molar mass 141.94 g/mol
Appearance Colorless liquid
Brownish liquid (old sample)
Odor Pungent, ether-like
Density 2.28 g/cm3 (At 20 °C)
Melting point −66.5 °C (−87.7 °F; 206.7 K)
Boiling point 42.5 °C (108.5 °F; 315.6 K)
14 g/L (at 20 °C)
Solubility Miscible with alcohol, diethyl ether
Vapor pressure 54.4 kPa (at 20 °C)
Hazards
Safety data sheet ScienceLab
Related compounds
Related compounds
Ethyl iodide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Methyl iodide or iodomethane is an organic chemical compound, which appears as a dense liquid, insoluble in water, mainly used as a methylating agent. It has the chemical formula CH3I, sometimes written as MeI.

Properties

Chemical

Methyl iodide will hydrolyze in the presence of an alkali to methanol and iodide:

CH3I + MOH → CH3OH + MI

Physical

Methyl iodide is a dense, colorless (though old samples have a brownish color) liquid, immiscible in water, but miscible with many solvents such as diethyl ether, ethanol, methanol and soluble in acetone and carbon tetrachloride. Methyl iodide has a strong and pungent ether-like odor.

Availability

Methyl iodide is sold by various chemical suppliers, though it's difficult to acquire. It can sometimes be found on eBay.

Methyl iodide used to be available as a pesticide up until 2012, when it was removed due to its carcinogenic effects.

Preparation

Methyl iodide can be prepared by reacting methanol with hydroiodic acid or hydrogen iodide. The methanol does not need to be anydrous.[1]

Projects

  • Make esters
  • Make toluene

Handling

Safety

Iodomethane is toxic and carcinogenic.

Methyl iodide MUST be kept away from heavy metals, such as mercury, lead, cadmium, arsenic or thallium, as this will generate extremely toxic heavy methyl iodides, which are more toxic than their corresponding metals. It's ABSOLUTELY CRUCIAL to avoid contact with mercury amalgam, as this will yield the volatile compound dimethylmercury, one of the most deadly contact poisons known, second only to nerve agents, which readily penetrates butyl, latex, neoprene and PVC protective equipment.

Storage

Methyl iodide must be stored in amber bottles, in dark well ventilated places, away from light. Copper or silver wire can be added as a stabilizer.

Disposal

Methyl iodide can be hydrolyzed to methanol with sodium hydroxide.

References

  1. http://www.orgsyn.org/demo.aspx?prep=CV2P0399

Relevant Sciencemadness threads