Jump to content

2,4,6-Trichloroanisole

From Wikipedia, the free encyclopedia
2,4,6-Trichloroanisole
Chemical structure of 2,4,6-trichloroanisole
Ball-and-stick model of the 2,4,6-trichloroanisole molecule
Names
Preferred IUPAC name
1,3,5-Trichloro-2-methoxybenzene
Other names
2,4,6-Trichloroanisole
TCA
2,4,6-Trichloromethoxybenzene
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.001.585 Edit this at Wikidata
EC Number
  • 201-743-5
KEGG
RTECS number
  • MFCD00000588
UNII
  • InChI=1S/C7H5Cl3O/c1-11-7-5(9)2-4(8)3-6(7)10/h2-3H,1H3 checkY
    Key: WCVOGSZTONGSQY-UHFFFAOYSA-N checkY
  • InChI=1/C7H5Cl3O/c1-11-7-5(9)2-4(8)3-6(7)10/h2-3H,1H3
    Key: WCVOGSZTONGSQY-UHFFFAOYAT
  • COc1c(Cl)cc(Cl)cc1Cl
  • Clc1cc(Cl)cc(Cl)c1OC
Properties
C7H5Cl3O
Molar mass 211.47 g·mol−1
Melting point 60 to 62 °C (140 to 144 °F; 333 to 335 K)
Boiling point 140 °C (284 °F; 413 K) at 28 Torr
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H302, H319, H413
P264, P270, P273, P280, P301+P312, P305+P351+P338, P330, P337+P313, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

2,4,6-Trichloroanisole (TCA) is an organic compound with the formula CH3OC6H2Cl3. It is the symmetric isomer of trichloroanisole. It is a colorless solid.

Occurrence

[edit]

2,4,6-Trichloroanisole represents one of the strongest of off-flavors, substances "generated naturally in foods/beverages [that considerably] deteriorate the quality" of such products.[1][2] It is also a component of some drinking waters.[3] It has also been detected in blood samples.[4]

Wine

[edit]

As of 2000, TCA was considered the primary chemical compound responsible for the phenomenon of cork taint in wines,[5][1] and it has an unpleasant earthy, musty and moldy smell.[2]

Coffee

[edit]

TCA has also been suggested as cause of the "Rio defect" in coffees from Brazil and other parts of the world,[6] which refers to a taste described as "medicinal, phenolic, or iodine-like".[7] In investigation of the mechanism of its role in producing off-flavor effects, it was found to "attenuate olfactory transduction by suppressing cyclic nucleotide-gated channels, without evoking odorant responses."[1]

Formation

[edit]

TCA is formed by the methylation of 2,4,6-trichlorophenol.[8][7] More generally, it may be produced when naturally occurring airborne fungi and bacteria are presented with chlorinated phenolic compounds, which they then convert into chlorinated anisole derivatives.[9] Species implicated include those of the genera Aspergillus, Penicillium, Actinomycetes, Botrytis (e.g. Botrytis cinerea), Rhizobium, or Streptomyces.[10][11][9]

The chlorophenol precursor, 2,4,6-trichlorophenol, is used as a fungicide; more generally, related compounds can originate as contaminants found in some pesticides and wood preservatives, or as by-products of the chlorine bleaching process used to sterilize or bleach wood, paper, and other materials.[12]

Further reading

[edit]
  • Marsili, R. (2000). "Solid-Phase Microextraction: Food Technology Applications". In Wilson, Ian D. (ed.). Encyclopedia of Separation Science. New Yor, NY: Academic Press. pp. 4178–4190. doi:10.1016/B0-12-226770-2/06791-0. ISBN 9780122267703. Over the last two decades, the incidence of mouldy and musty off-flavours in cork-sealed wines has increased significantly. 2,4,6-Trichloroanisole (TCA) has been identified as the primary chemical responsible for cork taint. The human olfactometry threshold for TCA is 4–10 ng L−1 in white wine and 50 ng L−1 in red wine. In the case of wine, a worldwide loss of roughly US$1 billion per year is attributed to cork taint.
  • Science Direct Staff (June 2023). "2-4-6-Trichloroanisole" (Science Direct citation sample/listing). Retrieved June 26, 2023.
  • Buser, H.R.; Zanier, C. & Tanner, H. (1982). "Identification of 2,4,6-Trichloroanisole as a Potent Compound Causing Cork Taint in Wine". Journal of Agricultural and Food Chemistry. 30 (2): 359–362. doi:10.1021/jf00110a037.{{cite journal}}: CS1 maint: multiple names: authors list (link) An early primary research report on the role of TCA in cork taint.

See also

[edit]

References

[edit]
  1. ^ a b c Takeuchi, Hiroko; Kato, Hiroyuki & Kurahashi, Takashi (2013-09-16). "2,4,6-Trichloroanisole is a Potent Suppressor of Olfactory Signal Transduction". Proceedings of the National Academy of Sciences. 110 (40): 16235–16240. Bibcode:2013PNAS..11016235T. doi:10.1073/pnas.1300764110. ISSN 1091-6490. PMC 3791788. PMID 24043819.{{cite journal}}: CS1 maint: multiple names: authors list (link)[non-primary source needed]
  2. ^ a b Jackson, Ron S. (2009). "Chapter 3: Olfactory Sensations". Wine tasting: a professional handbook. Food science and technology international series (2nd ed.). Academic Press. ISBN 978-0-12-374181-3.
  3. ^ Young, W.F.; Horth, H.; Crane, R.; Ogden, T.; Arnott, M. (1996). "Taste and odour threshold concentrations of potential potable water contaminants". Water Research. 30 (2): 331–340. Bibcode:1996WatRe..30..331Y. doi:10.1016/0043-1354(95)00173-5.
  4. ^ Hovander, t. Malmberg, m. Athanasia, L.; Malmberg, T.; Athanasiadou, M.; Athanassiadis, I.; Rahm, S.; Bergman, A.; Wehler, E. K. (2002). "Identification of Hydroxylated PCB Metabolites and Other Phenolic Halogenated Pollutants in Human Blood Plasma". Archives of Environmental Contamination and Toxicology. 42 (1): 105–117. Bibcode:2002ArECT..42..105H. doi:10.1007/s002440010298. PMID 11706375.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ^ Marsili, R. (2000). "Solid-Phase Microextraction: Food Technology Applications". In Wilson, Ian D. (ed.). Encyclopedia of Separation Science. New Yor, NY: Academic Press. pp. 4178–4190. doi:10.1016/B0-12-226770-2/06791-0. ISBN 9780122267703. Over the last two decades, the incidence of mouldy and musty off-flavours in cork-sealed wines has increased significantly. 2,4,6-Trichloroanisole (TCA) has been identified as the primary chemical responsible for cork taint. The human olfactometry threshold for TCA is 4–10 ng L−1 in white wine and 50 ng L−1 in red wine. In the case of wine, a worldwide loss of roughly US$1 billion per year is attributed to cork taint.
  6. ^ These include Central and South America.[citation needed]
  7. ^ a b Spadone, Jean Claude; Takeoka, Gary & Liardon, Remy (1990). "Analytical Investigation of Rio Off-Flavor in Green Coffee". Journal of Agricultural and Food Chemistry. 38: 226–233. doi:10.1021/jf00091a050.{{cite journal}}: CS1 maint: multiple names: authors list (link) Note, at best, this source states that 2,4,6-trichlorophenol is "the probable precursor of TCA".
  8. ^ Pereira, Helena (2007-01-01), Pereira, Helena (ed.), "Chapter 14 - Wine and cork", Cork, Amsterdam: Elsevier Science B.V., pp. 305–327, ISBN 978-0-444-52967-1, retrieved 2024-01-14
  9. ^ a b Cravero, Maria Carla; Bonello, Federica; Pazo Alvarez, Maria del Carmen; Tsolakis, Christos; Borsa, Daniela (24 June 2015). "The sensory evaluation of 2,4,6-trichloroanisole in wines: The sensory evaluation of 2,4,6-trichloroanisole in wines". Journal of the Institute of Brewing. 121 (3): 411–417. doi:10.1002/jib.230.
  10. ^ Crane, Louise (22 March 2019). "Trichloroanisole: Cork taint". Chemistry World. Retrieved 2024-01-14.
  11. ^ With regard to circumstantial evidence, Spodone, et al., op. cit., note that Rio off-flavor is associated with "beans heavily infested with various fungi (Aspergilli, Fusaria, Penicillia, Rhizopus, etc.) and bacteria (Lactobacilli, Streptrococci)".
  12. ^ NTP (National Toxicology Program). 2021. "2,4,6-Trichlorophenol", Report on Carcinogens, Fifteenth Edition. Research Triangle Park, NC: U.S. Department of Health and Human Services, Public Health Service. https://ntp.niehs.nih.gov/go/roc15 DOI: https://doi.org/10.22427/NTP-OTHER-1003
Retrieved from "https://en.wikipedia.org/w/index.php?title=2,4,6-Trichloroanisole&oldid=1241178986"