Difference between revisions of "Isopropanol"
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===Relevant Sciencemadness threads=== | ===Relevant Sciencemadness threads=== | ||
| + | *[http://www.sciencemadness.org/talk/viewthread.php?tid=24835 High Purity Isopropanol] | ||
| + | *[http://www.sciencemadness.org/talk/viewthread.php?tid=18628 drying isopropanol] | ||
| + | *[http://www.sciencemadness.org/talk/viewthread.php?tid=21495 Isopropyl Alcohol (2-propanol) Peroxides] | ||
[[Category:Chemical compounds]] | [[Category:Chemical compounds]] | ||
Revision as of 18:52, 23 September 2015
Isopropanol, or isopropyl alcohol, is a secondary alcohol. It provides the familiar smell of rubbing alcohol, where it is frequently used although this may be ethanol. Isopropanol is the largest carbon chain alcohol to be miscible with water and is a common OTC solvent.
Contents
Properties
Chemical
Isopropanol is a generally nonreactive (inorganically speaking) alcohol. It can be dehydrated, and is a common reagent in organic chemistry.
Anhydrous isopropanol is used to neutralise small quantities of sodium or potassium metal, as the reaction with the alcohol is mild compared to with water and removes any reactive metal that may pose a danger if left in the lab. This property allows for the production of metal isopropoxides.
A violent runaway reaction happens when isopropanol comes into contact with a nitration bath. Toxic nitrogen dioxide is produced in a rapid reaction as the isopropanol is not nitrated but oxidised by the acids.
Isopropanol can be reacted with nitrous acid to for isopropyl nitrite and with mixed acids to form isopropyl nitrate.
Physical
Isopropanol is clear, has an alcohol-like smell, burns on contact with cuts, is an antiseptic, and is miscible in water. It is a good, cheap solvent.
Availability
Isopropanol is available in concentrations anywhere from 60% to 99% (the rest being water) for a variety of applications, often cleaning electronics or sold as 'rubbing alcohol'. The most common concentrations are 70% and 91%. These store-bought solutions can be salted out up to a concentration of about 91% using sodium chloride, and nearly all water can be separated by salting out with sodium hydroxide, though this may inadvertently contaminate the isopropanol and produce sodium isopropoxide. Dry isopropanol has the potential to form explosive peroxides when distilled, so it is highly recommended that these distillations are carefully monitored if done at all.
Preparation
Isopropanol is produced by hydrogenation of acetone over a nickel catalyst. It can also be obtained by hydrolysing esters containing an isopropyl group.
Projects
- Chloroform synthesis
- Isopropyl chloride
- Isopropyl nitrite
- Isopropanol peroxide (EXTREMELY DANGEROUS!!!)
Handling
Safety
Isopropanol is flammable. It has low toxicity and it's much less toxic than methanol or ethylene glycol. Vapours of dry isopropanol can potentially be explosive.
Storage
Isopropanol should be stored in closed bottles. As it is prone to forming peroxides over long periods of time, a small amount of antioxidant should be added, unless it already has.
Disposal
Isopropanol can be safely burned. Old bottles that have been exposed to air should be checked for any peroxides and if there are any, they should be neutralized if safely possible.
