4-Methylcyclohexanemethanol
Names
IUPAC name
(4-Methylcyclohexyl)methanol
Other names
  • 1-(hydroxymethyl)-4-methylcyclohexane
  • 4-methylcyclohexyl-1-carbinol
  • MCHM
  • hexahydro-p-tolyl-carbinol (archaic)
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.131.091
EC Number
  • 609-038-8
UNII
  • InChI=1S/C8H16O/c1-7-2-4-8(6-9)5-3-7/h7-9H,2-6H2,1H3
    Key: OSINZLLLLCUKJH-UHFFFAOYSA-N
  • CC1CCC(CC1)CO
Properties
C8H16O
Molar mass 128.215 g·mol−1
Appearance Colourless liquid
Odor mint-like, licorice-like (trans)
Density 0.9074 g/cm3
Boiling point 202 °C (396 °F; 475 K)[1]
low
1.4617[2]
Hazards
GHS labelling:[3]
GHS07: Exclamation mark
Warning
H315, H319, H335
Flash point 80 °C (176 °F; 353 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

4-Methylcyclohexanemethanol (MCHM, systematic name 4-methylcyclohexylmethanol) is an organic compound with the formula CH3C6H10CH2OH. Classified as a saturated higher alicyclic primary alcohol. Both cis and trans isomers exist, depending on the relative positions of the methyl (CH3) and hydroxymethyl (CH2OH) groups on the cyclohexane ring. Commercial samples of MCHM consists of a mixture of these isomers as well as other components that vary with the supplier.

The cis and trans isomers of MCHM.

It is a colourless oil with a faint mint-like alcohol odor.[4] The trans isomer has a particularly low odor threshold (~7 ppb in water) and a more licorice-like quality which is not associated with the less detectable cis isomer.[5][6] Like other 8-carbon alcohols, such as 1-octanol, this compound is only slightly soluble in water but highly soluble in many organic solvents. The solubility of 1-octanol in water is 2.3 grams per liter.

Synthesis and production

It was first prepared in 1908 by Bouveault–Blanc reduction of a methylcyclohexanecarboxylate ester.[4]

It is also produced as a byproduct (ca. 1%) in the production of cyclohexanedimethanol, a commodity chemical, during hydrogenation of dimethyl terephthalate.[7]

C6H4(CO2CH3)2 + 8 H2 → CH3C6H10CH2OH + 2 CH3OH + H2O

Uses

It has been patented for use in air fresheners.[8]

U.S. Patent 4915825 describes a froth flotation process for cleaning coal where a mixture of 95% MCHM, 4% water, and 0.1% 4-methylcyclohexanemethanol monoether (such as 4-(methoxymethyl)cyclohexanemethanol) is used as a frothing agent, and finely divided coal particles adhere to air bubbles induced into the agent which rise to the surface. Other cyclohexane-based alcohols can also be used. MCHM has the advantage of being less toxic than previous frothing agents containing 2-ethylhexanol.[9] The original patent owners let the patent expire after eight years for failure to pay maintenance fees.[10]

Health and safety

Reliable information on health and safety of this compound is limited. The ChemSpider entry for MCHM indicates that it has been evaluated for ligand activity via SimBioSys's LASSO analysis, which predicted low to no activity on 40 biologically significant receptors, indicating a low likelihood for significant biological activity on them.[11] Eastman Chemical Company's MSDS for "crude" (unpurified) MCHM, as supplied by NPR, reports an oral LD-50 of 825 mg/kg and a dermal LD-50 greater than 2,000 mg/kg, both in rats.[12] Further data from Eastman's internal studies was released after the Elk River, West Virginia (2014) spill, including the studies upon which the LD-50 estimate was based and one 28-day study of oral toxicity of pure MCHM which concluded that 400 mg/kg doses were associated with erythropoietic, liver, and kidney effects, though these were not considered more than "minor toxicity" and the "no observed effect" level was considered to be 100 mg/kg/day.[13]

A World Health Organization study of the toxicity of alicyclic primary alcohols and related alicyclic carbohydrates (of which MCHM is one type) found that LD-50 values for substances in this class generally "ranged from 890 to 5700 mg/kg bw for rats and > 1000 to 4000 mg/kg bw for mice, demonstrating that the oral acute toxicity of alicyclic primary alcohols, aldehydes, acids and related esters is low".[14] The same study indicated that these alcohols are metabolized primarily to corresponding carboxylic acids, which in the case of MCHM is 4-methylcyclohexanecarboxylic acid (CAS 13064-83-0), a naphthenic acid. The toxicity and environmental properties of these naphthenic acids have been well studied recently due to their occurrence as a major contaminant in water used for extraction of oil from tar sands.[15] Naphthenic acids have both acute and chronic toxicity to fish and other organisms.[15] The methyl ester of this acid is also listed as one of the major impurities in the "crude MCHM" as supplied by Eastman.[12]

Cyclohexanedimethanol

The closely related compound cyclohexanedimethanol (CAS 105-08-8) exhibits low toxicity (3.5 g/kg) when fed orally to rats.[16]

Cyclohexanemethanol

Cyclohexanemethanol (or cyclohexylmethanol, CHM, CAS 100-49-2), another closely related compound, which differs only in lacking a methyl substituent, has been found as a naturally occurring fusel alcohol in mango wine at concentrations of 1.45 mg/L, in which it is considered an aroma constituent.[17] LASSO analysis predicts low to no activity on 40 receptors, similarly to MCHM.[18]

p-menthan-7-ol

CHM with a methylethyl (or isopropyl) substituent group at the same position as the methyl group in 4-methylcyclohexanemethanol (cis-4-(1-methylethyl) cyclohexane methanol, CAS 13828-37-0) is regarded as a flavoring and fragrance agent, sometimes listed under the synonym p-menthan-7-ol, and was the subject of a review article on its toxicological and dermatological properties in 2008.[19] Among other findings, Bhatia et al. reported a 14-day oral toxicity study in rats with doses of 10.0 g/kg by gavage with no deaths or toxic effects observed, nor any abnormalities on necropsy. Dermal application of "neat" (pure, undiluted) cis-p-menthan-7-ol at 2 g/kg bodyweight produced toxic effects in rats and rabbits.

Various patch tests of cis-p-menthan-7-ol on human volunteers with concentrations of 10%, 15%, and 20% produced irritation in one instance, and a "questionable" reaction in another. These both occurred out of a group of 102 volunteers with a 15% concentration in diethyl phthalate and ethanol. However, a longer-term (six-week) repetition of that test as a sensitization study failed to produce any reactions.[19]

A WHO study concluded that p-menthan-7-ol was of "no safety concern" for human consumption at high levels of 2.5 μg/kg of bodyweight and for typical levels in Japan of 0.03 μg/day.[20]

2,4-dimethylcyclohexanemethanol

Another CHM derivative, 2,4-dimethylcyclohexanemethanol (CAS 68480-15-9, also dihydrofloralol or floral methanol), which has two methyl substituents instead of one, is frequently marketed as a fragrance or flavor additive. One web site, Fantastic Flavours provides a list of recognized flavor additives for Japan, which includes 2,4-dimethylcyclohexanemethanol by virtue of being in the group of aliphatic higher alcohols.[21]

Incidents

On 9 January 2014, approximately 10,000 US gal (38,000 L) of impure MCHM leaked from a storage tank near the banks of the Elk River near Charleston, West Virginia (U.S.), from where an undetermined amount entered the river and was taken into the local water system (1,272 gallons were reported recovered).[22][23][24] State and federal agencies declared a state of emergency and ordered over 300,000 residents in nine counties—one sixth of West Virginia's population—not to drink or use tap water for any purpose other than flushing toilets.[25] The external affairs manager of West Virginia American Water said that the spill originated with Freedom Industries, a Charleston company.[26]

References

  1. ↑ Allen, C. F. H.; Ball, W. L.; Young, D. M. (1933). "Dihydro-p-tolualdehyde". Canadian Journal of Research. 9 (2): 169–174. Bibcode:1933CJRes...9..169A. doi:10.1139/cjr33-078.
  2. ↑ Cooke, R. G.; Macbeth, A. Killen (1939). "262. Epimeric alcohols of the cyclohexane series. Part II. 4-Methyl- and 4-isopropyl-cyclohexyl-1-carbinols". Journal of the Chemical Society (Resumed): 1245. doi:10.1039/jr9390001245.
  3. ↑ "C&L Inventory". echa.europa.eu. Retrieved 13 December 2021.
  4. 1 2 Perkin, William Henry; Pope, William Jackson (1908). "CIX.—Experiments on the synthesis of 1-methylcyclo-hexylidene-4-acetic acid. Part I". Journal of the Chemical Society, Transactions. 93: 1075–85. doi:10.1039/CT9089301075.
  5. ↑ "Tests elucidate the odor properties of the contaminants affecting West Virginia residents". Technology.org. Virginia Tech. 28 March 2014. Retrieved 12 June 2014.
  6. ↑ A similar distinction has been reported in the closely related compound p-menthan-7-ol, where the cis isomer has a "fresh" lily-of-the-valley scent while the trans isomer has a "powerful cumin-like" odor. US Patent Application No. 20110269846 Formulations with high percentage cis-p-menthan-7-ol and preparation thereof
  7. ↑ Werle, Peter; Morawietz, Marcus; Lundmark, Stefan; Sörensen, Kent; Karvinen, Esko; Lehtonen, Juha (2008). "Alcohols, Polyhydric". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a01_305.pub2. ISBN 978-3-527-30673-2.
  8. ↑ Nagamura, Yusei; Satoh, Yuuichi; Tatsumi, Jun; Yamamura, Kunihiro. "Method for producing alcohols such as cyclohexanedimethanol" (European Patent Application EP1090902).
  9. ↑ US patent 4915825, Richard D. Christie, Randall J. Fortin, Anthony E. Gross, "Process for coal flotation using 4-methyl cyclohexane methanol frothers", published 1990-04-10, assigned to Nalco Chemical Company
  10. ↑ Google Patents, US 4915825, Legal Events
  11. ↑ 4-Methylcyclohexanemethanol. ChemSpider.
  12. 1 2 Eastman Chemical Company. "Material Safety Data Sheet" (PDF). Retrieved 18 January 2014.
  13. ↑ Eastman Crude MCHM Studies
  14. ↑ Speijers, G.J.A.; A. Renwick. "Alicyclic Primary Alcohols, Aldehydes, Acids, and Related Esters". WHO FOOD ADDITIVES SERIES: 50. INCHEM: International Programme on Chemical Safety. Retrieved 19 January 2014.
  15. 1 2 Allen, E. W. (2008). "Process water treatment in Canada's oil sands industry: I. Target pollutants and treatment objectives" (PDF). Journal of Environmental Engineering and Science. 7 (2): 123–138. doi:10.1139/S07-038. Archived from the original (PDF) on 1 February 2014. Retrieved 22 January 2014.
  16. ↑ "MSDS for 1,4-Cyclohexanedimethanol". Sigma-Aldrich.
  17. ↑ Reddy, LV; KY Sudheer; OV Reddy (June 2010). "Analysis of volatile aroma constituents of wine produced from Indian mango (Mangifera indica L.) by GC-MS". Indian Journal of Microbiology. 50 (2): 183–91. doi:10.1007/s12088-010-0028-7. PMC 3450322. PMID 23100826.
  18. ↑ Cyclohexylmethanol
  19. 1 2 Bhatia, S.P.; McGinty, D.; Letizia, C.S.; Api, A.M. (November 2008). "Fragrance Material Review on cis-p-menthan-7-ol". Food and Chemical Toxicology. 46 (11): S201–S203. doi:10.1016/j.fct.2008.06.035. PMID 18640213.
  20. ↑ Seventy-third meeting of the Joint FAO/ WHO Expert Committee on Food Additives (JECFA) (2011). Safety evaluation of certain food additives and contaminants (PDF). Geneva: Safety evaluation of certain food additives and contaminants Prepared by the Seventy-third meeting of the Joint FAO/ WHO Expert Committee on Food Additives (JECFA) WHO FOOD ADDITIVES SERIES: 64 World Health Organization. p. 52. ISBN 978-924-166064-8.
  21. ↑ Minister of Health, Labour and Welfare. "Flavor Agents as Food Additives" (PDF). Retrieved 19 January 2014.
  22. ↑ "300,000 warned not to drink water after W. Va. spill". USA Today. 11 January 2014.
  23. ↑ "DEP Estimates 7,500 Gallons of Chemical Leaked". WSAZ. 12 January 2014.
  24. ↑ West Virginia Department of Environmental Protection. "Freedom Industries revises estimate for spill" (PDF). Retrieved 29 January 2014.
  25. ↑ "Chemical Leak Causes Water Emergency in West Virginia; Plant Shut Down". NPR. The Two Way (blog). 10 January 2014.
  26. ↑ Bratu, Becky; Austin, Henry (10 January 2014). "West Virginia chemical spill cuts water to up to 300,000, state of emergency declared". NBC News.
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