>From the Encyclopedia Britannica, 11th Edition (1910):

METHYL ALCOHOL (CH3OH),the simplest aliphatic alcohol; an impure form is
known in commerce as wood-spirit, being produced in the destructive
distillation of wood. The name methyl, from [EMAIL PROTECTED], wine, I%?J, wood,
explains its origin. Discovered by Boyle in 1661, it was first carefully
studied by Dumas and PŽligot in 1831; its synthesis from its elements
(through methane and methyl chloride)was effected by Berthelot in 1858.
It is manufactured by distilling wood in iron retorts at about 500¡C.,
when an aqueous distillate, containing methyl alcohol, acetone, acetic
acid and methyl acetic ester, is obtained. This is neutralized with lime
and redistilled in order to remove acetic acid. The distillate is
treated with anhydrous calcium chloride, the crystalline compound formed
with the alcohol being separated and decomposed by redistilling with
water. The aqueous product is then dehydrated with potash or lime. To
obtain it perfectly pure the crude alcohol is combined with benzoic or
acetic acid, and the resulting ester separated, purified, and finally
decomposed with potash. Methyl alcohol is also obtained in the dry
distillation of molasses. The amount of methyl alcohol present in wood
spirit is determined by converting it into methyl iodide by acting with
phosphorus iodide; and the acetone by converting it into iodoform by
boiling with an alkaline solution of iodine in potassium iodide; ethyl
alcohol is detected by giving acetylene on heating with concentrated
sulphuric acid, methyl alcohol, under the same circumstances, giving
methyl ether. 

Pure methyl alcohol is a colourless mobile liquid, boiling at
66¡-67¡,and having a specific gravity of 0.8142 at 0¡C. If has a burning
taste, and generally a spirituous odour but when absolutely pure it is
said to be odourless. It mixes in all proportions with water, alcohol
and ether. Its compound with calcium chloride has the formula
CaCl2.4CH3.OH, and with barium oxide BaO.2CH3OH. Oxidation gives
formaldehyde, formic acid and carbonic acid; chlorine and bromine react,
but less readily than with ethyl alcohol. The chief industrial
applications are for making denatured alcohol (q.v.), and as a solvent,
e.g. in varnish manufacture; it is also used for a fuel; a purer product
is extensively used in the colour and fine chemical industries.


-- 
Remember September 11, 2001 but don't forget July 4, 1776

Rather than make war on the American people and their
liberties, ...Congress should be looking for ways
to empower them to protect themselves when
warranted.

They that can give up essential liberty to obtain a little temporary
safety deserve neither liberty nor safety. - Benjamin Franklin


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