Talk:Amyl alcohol

Page move suggestion

 * The following discussion is an archived debate of the . Please do not modify it. Subsequent comments should be made in a new section on the talk page. No further edits should be made to this section. 

No move Duja ► 09:25, 17 January 2007 (UTC)

At present, Pentanol redirects to 1-Pentanol. It would be better to have this article there, and have amyl alcohol (an obsolete trivial name), redirect to Pentanol, which could then link to the various isomers. --Slashme 07:18, 8 January 2007 (UTC)
 * I don't think that Amyl alcohol is an obsolete name - it gives more than twice as many hits (1.2m) in Google than does pentanol (0.5m, even though the latter is a common fragment in more complex names). Despite this, I think I could go along with the name change myself - many chemical catalogues use pentanol as the main name, and they are often slow to change.  Also, many students are unfamiliar with the term amyl but they all learn pentyl.  Post a comment at WP:Chem to get more opinions. Walkerma 08:01, 8 January 2007 (UTC)
 * Though I know the name amyl alcohol for pentanol, I think in this case the more commonly used name in the lab is pentanol, Hence, I support the move. --Dirk Beetstra T  C 08:12, 8 January 2007 (UTC)

Oppose move (and create the proper discussion page per instructions at WP:RM and get the "discuss" link there). Amyl alcohol remains the more common name. Make the obvious fix and redirect pentanol to the more general amyl alcohol rather than to one particular isomer out of eight of them. Why such convoluted reasoning? Gene Nygaard 01:30, 9 January 2007 (UTC)
 * More general, I'll try it on some UK PhD-students today, but I believe they will not know amyl alcohol, but know pentanol, whereas they do know acetic acid, formaldehyde .. I don't think the google test discussed above gives reliable answers here (if ever). --Dirk Beetstra T  C 09:09, 9 January 2007 (UTC)
 * So, how will you know that the results of your original research are not a Manual of Style issue?


 * Note also that most of the Google hits for "amyl alcohol" will be for the subjects of this article, but many of the hits for pentanol will not be for them but rather things such as (2,3,4,5)tetrahydroxy-pentanol (xylitol), 4-methyl-2-pentanol and 2,4-Dimethyl-3-pentanol and 2,3-Dimethyl-1-pentanol and the like. In addition, the terms amylalcohol and pentyl alcohol and n-pentyl alcohol (in addition to the n in generic references, 1-pentyl alcohol, etc.) and amylol are also used for the subject of this article, yet for some strange reason they are redlinks here. Why is that?


 * OTOH, Walkerma overstatated the case for his Google results, searching for just the two words for the 1.2 million hits (this would include anything with "amyl nitrate" and any alcohol, for example) and not the phrase "amyl alcohol", which still gives over a quarter of a million hits, and something with over a quarter of a million hits is not unknown and obsolete. Gene Nygaard 04:22, 10 January 2007 (UTC)
 * The above discussion is preserved as an archive of the debate. Please do not modify it. Subsequent comments should be made in a new section on this talk page. No further edits should be made to this section.

What's the boiling point of 2-methyl-2-butanol? 102 C or 112 C? Both numbers are given. —Preceding unsigned comment added by 83.188.218.228 (talk) 23:11, 8 November 2009 (UTC)

Incorrect IUPAC Names Currently Listed
Currently, the IUPAC name column does not correspond to the IUPAC official guidelines for naming alcohols. For example, the secondary alcohol 2-pentanol is listed as pentan-2-ol. While this designation is sometimes used colloquially, it is not compliant with current IUPAC guidelines, and is thus incorrect. — Preceding unsigned comment added by Amlong.897 (talk • contribs) 18:12, 27 July 2014 (UTC)

"Carbinol" obsolete?
Are the "carbinol" names obsolete? (They seem to have been taken from the 1911 Britannica).--Jorge Stolfi (talk) 07:35, 30 August 2020 (UTC)

Conflicting data?
The last paragraph referring to the tertiary isomer gives different melting and boiling points to the main article on that isomer - and conflicts with the boiling point in the table above. Barti Ddu (talk) 09:21, 16 May 2021 (UTC)