Re: Formal- or formol- ?
<< Previous Message | Next Message >>
From: | "J. A. Kiernan" <jkiernan@julian.uwo.ca> |
To: | John Difford <adford@compuserve.com> |
Reply-To: | |
Date: | Thu, 14 Oct 1999 01:16:51 -0400 (EDT) |
Content-Type: | TEXT/PLAIN; charset=US-ASCII |
On Wed, 13 Oct 1999, John Difford (Royal Free) wrote:
> John Kiernan has stated in a recent communication to Histonet that when
> naming a formaldehyde-containing fixative the correct usage is formal-
> (as in formal-saline) and he cites J. R. Baker as the authority for this
> view.
>
> 1. Baker did not approve of the use of formol-, that is true, but then
> he did not approve of formal- either. Read his book for the reasons.
Thanks for the correction. Baker's book was but a foot from my right
hand when I typed my little ditty, but being left-handed I didn't
actually bother to check what I incorrectly thought I remembered.
> 2. The first person to describe the effect of formaldehyde solution as a
> fixative for tissues was Ferdinand Blum (in 1893)...
This was a discovery like anaesthesia that wasted no time
getting around the world. In 1895 Pierre Fish (an American
pathologist) published a zinc-formalin mixture for fixing
brains, and his paper had 3 or 4 references to 1894 papers
on formaldehyde fixation. The wheel, once invented, gets
reinvented again and again and again.
> ... He [Blum] was using
> a commercially produced solution called ' Formol' ...
> Hence, since Blum was the first to describe Formol- as a fixative,
> we should give him priority in the manner of naming.
Walker's "Formaldehyde," 3rd ed., (1964) says Formalin and Formol
were European trade-names for the concentrated solution (Chap 4).
Formals are compounds with -CH2-O-CH2- (ether-like) linkages, and
the term embraces the many compounds, including the product of
reaction with 2 methanol molecules (= methylal; also called formal
or dimethoxymethane). Larger (polymeric) formals are more rapidly
hydrolysed than smaller ones, but even methylal is in equilibrium
with methanol, water and methylene glycol (Chap 10). This is
why polymer formation is inhibited by putting some methanol in
a strong aqueous formaldehyde solution such as formalin. (For this
I did check in the book.)
It really doesn't matter much, but formal- may be more appropriate
chemically, if not historically, than formol-. This is all a bit
silly really, because form?l-saline has long been superceded by
better solutions such as the many NBFs and form?l-calciums.
An -al ending seems better for an aldehyde than -ol, which
seems to signify an alcohol or a phenol. I rest my case.
John A. Kiernan,
Department of Anatomy & Cell Biology,
The University of Western Ontario,
LONDON, Canada N6A 5C1
Phone: (519) 661-2111 <-- NEW NUMBER
FAX (Department): (519) 661-3936
E-mail: kiernan@uwo.ca
<< Previous Message | Next Message >>