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![]() | Menthol was one of the Natural sciences good articles, but it has been removed from the list. There are suggestions below for improving the article to meet the good article criteria. Once these issues have been addressed, the article can be renominated. Editors may also seek a reassessment of the decision if they believe there was a mistake. | ||||||||||||
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Current status: Delisted good article |
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Is menthol a covalent or ionic compound?
The previous version of this page stated that menthol is "actually extremely toxic", and proceeded to talk about amounts "as small as a teaspoon", taken every day. That can hardly be called "extremely" toxic. Many substances can be toxic when taken in large quantities (and a teaspoon is quite alot).
Thus, I've changed the wordage to "quite toxic". (15/03/2005)
Is the information on homeopathy really necessary? Some radical theories suggest that skepticism similarly interferes with the potency of homeopathic remedies.
--Thanks to whoever amended this - in hindsight, disclaimerising the pseudoscientific status of homeopathy was the right thing to do.
is menthol also used in peppermint schnapps? rthrust@gmail.com
I'm incerted LD50 (becouse "low" or "high" toxic is very indefinite). In drinks most use flavoring agents which consist of natural essential oils, synth. substances etc. Alexandrov 08:24, 29 September 2005 (UTC)
Would we want a picture of menthol in its crystalline form on the main page? I have the means to get a picture of it up here.... Killerrobotdude 06:08, 25 April 2006 (UTC)
Under "Properties", only solubility in water is listed. Shouldn't it also list solubility in alcohol? Troother ( talk) 15:22, 22 September 2022 (UTC)
The discussion of the diagram says, "Natural menthol exists as one pure stereoisomer, nearly always the (1R,2S,5R) form (bottom left of diagram below)." However, while the verbal description (1R,2S,5R) matches up with other reference sources, e.g. [ [1]] indicates that l-menthol occurs in the upper left-hand corner of the diagram. I cross-checked this against the Merck Index, 14th edition, and it agreed with PubChem. Unfortunately, the diagram itself seems to be mislabeled or using a different convention from the other sources for diagramming the positions, thus resulting in a discrepancy. As I'm not a chemist, I would appreciate if someone would check the diagram and deal with the inconsistency. Iainuki ( talk) 20:18, 7 April 2010 (UTC)
You're right, and your edit has fixed it. -- Rifleman 82 ( talk) 23:24, 7 April 2010 (UTC)
I've just come across this and I believe that the diagram is actually correct. You may have made a mistake when considering rotation of the compound to view the structure on Pubchem from the same angle as the diagram shown, but the structure on pubchem is the same as the one in the bottom left corner (as will be the one in the Merck Index). I've checked the Beilstein database just to make sure that the stereochemistry is correct and that the (1R,2S,5R) isomer corresponds to the laevorotatory optical isomer. Taking this into account I will revert the change to correct the paragraph. Sam Eyley ( talk) 18:17, 15 April 2010 (UTC)
I noticed that the references are cited, but they have manual superscripts. It should use the automatically numbered references so that the article can be edited without having to renumber all the superscripts. -- R'nway [ T C ] 02:57, 16 June 2006 (UTC)
If you look up Calcium Channel Blocker it lists Menthol in the "other" section.
Does it actually have that ability? Where can I get more information?
Interesting.
Thanks,
Ben
Article claims that 400 000 tons of menthol are manufactured each year, but primary external link: http://www.leffingwell.com/menthol1/menthol1.htm says 'in excess of 6,300' (which sounds a lot less). Which is right? quota 12:06, 13 August 2007 (UTC)
This article was promoted to WP:GA on December 7, 2005, so it is clearly time for a re-review. Unfortunately, as the Good Article criteria have changed considerably since then, the article no longer meets the criteria. I find numerous issues with several criteria:
Due to the many issues with this article, I think the best thing to do is to delist. It can be renominated at WP:GAN once the issues are addressed and it meets the Good Article criteria. Cheers! Dr. Cash ( talk) 17:19, 10 December 2007 (UTC)
A hydrogen atom is shown alongside the hydroxide, and two hydrogens together. Should the extra hydrogens appear in the vacant places on the other side?
This article talk page was automatically added with {{ WikiProject Food and drink}} banner as it falls under Category:Food or one of its subcategories. If you find this addition an error, Kindly undo the changes and update the inappropriate categories if needed. The bot was instructed to tagg these articles upon consenus from WikiProject Food and drink. You can find the related request for tagging here . Maximum and careful attention was done to avoid any wrongly tagging any categories , but mistakes may happen... If you have concerns , please inform on the project talk page -- TinucherianBot ( talk) 01:08, 4 July 2008 (UTC)
L-Menthol has been added based on the following http://www.sigmaaldrich.com/catalog/ProductDetail.do?lang=en&N4=W266590%7CALDRICH&N5=SEARCH_CONCAT_PNO%7CBRAND_KEY&F=SPEC -- 58.38.45.229 ( talk) 12:57, 29 June 2009 (UTC)
Any information about plant adaptation and the reasons plants produce menthol would be a welcome addition to this article. . . -- 71.111.194.50 ( talk) 10:40, 28 October 2009 (UTC)
Does menthol destroy spermatozoa on contact?
If someone wants to do the work of paraphrasing/extracting the important information, The toxicology data on Menthol can be found here, http://www.inchem.org/documents/jecfa/jecmono/v042je04.htm research and meta-analysis courtesy of the World Health Origination.
ref: Safety evaluation of certain food additives. WHO Food Additives Series, No. 42, 1999, no 930 on INCHEM. 219.90.192.25 ( talk) 03:31, 9 February 2011 (UTC)
Infobox - Melting point - What is "35-33-31"? What is the difference between "(-)-form" & "(-)-isomer"? Note that the biosynthesis also includes an oxidation (along with "several reduction and isomerization steps"). Applications - typo - diastereomERic (last sentence) 69.72.92.88 ( talk) 06:53, 3 October 2014 (UTC)
The article tells nothing about the differences betwean the stereoisomers. For some reason menthol is always used in "levomenthol" form, wich is probably the same isomer as the natural one. Are the rest of the isomers ineffective? Or just inconvinient to produce? 84.236.68.24 ( talk) 08:26, 14 October 2016 (UTC)
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This article doesn't mention the diarrhedic properties of menthol. As someone who has taken dextromethorphan on a regular basis, menthol is the ingredient in cough syrup that causes severe diarrhea for abusers. Floydian τ ¢ 15:38, 3 August 2022 (UTC)
Could someone put the molecule diagram on the main article Treonsverdery ( talk) 10:14, 14 April 2023 (UTC)
Under knee cap vain is damage can be healed with the right product I’m looking at molecule for healing 2600:1003:B017:D0F3:A9B6:D7B5:1AE5:6D5D ( talk) 20:08, 23 November 2023 (UTC)