Ethyl carbamate

From Wikipedia, the free encyclopedia
Ethyl carbamate
Structural formula of ethyl carbamate
Names
Preferred IUPAC name
Ethyl carbamate
Other names
Carbamic acid ethyl ester, Urethane, Ethylurethane
Identifiers
3D model (JSmol)
3DMet
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.000.113 Edit this at Wikidata
EC Number
  • 200-123-1
KEGG
MeSH Urethane
RTECS number
  • FA8400000
UNII
UN number 2811
  • InChI=1S/C3H7NO2/c1-2-6-3(4)5/h2H2,1H3,(H2,4,5) checkY
    Key: JOYRKODLDBILNP-UHFFFAOYSA-N checkY
  • InChI=1/C3H7NO2/c1-2-6-3(4)5/h2H2,1H3,(H2,4,5)
    Key: JOYRKODLDBILNP-UHFFFAOYAY
  • CCOC(N)=O
  • O=C(OCC)N
Properties
C3H7NO2
Molar mass 89.094 g·mol−1
Appearance White crystals
Density 1.056 g cm−3
Melting point 46 to 50 °C (115 to 122 °F; 319 to 323 K)
Boiling point 182 to 185 °C (360 to 365 °F; 455 to 458 K)
0.480 g cm−3 at 15 °C
log P -0.190(4)
Vapor pressure 1.3 kPa at 78 °C
Acidity (pKa) 13.58
2.59 D[1][2]
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Harmful if swallowed
May cause cancer
GHS labelling:[3]
GHS07: Exclamation markGHS08: Health hazard
Danger
H302, H350
P201, P301+P312+P330, P308+P313
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
2
0
Flash point 92 °C (198 °F; 365 K)
Related compounds
Related compounds
 Methyl carbamate
Propyl carbamate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Ethyl carbamate (also called urethane) is an organic compound with the formula CH3CH2OC(O)NH2. It is an ester of carbamic acid and a white solid. Despite its name, it is not a component of polyurethanes. Because it is a carcinogen, it is rarely used, but naturally forms in low quantities in many types of fermented foods and drinks.

Synthesis[edit]

It is produced industrially by heating urea and ethyl alcohol.[4] It arise also by the action of ammonia on ethyl chloroformate.[5]

Synthesis of ethyl carbamate
Synthesis of ethyl carbamate

Uses[edit]

Biomedical applications[edit]

Ethyl carbamate has been used as an antineoplastic agent and for other medicinal purposes, but this application ended after it was discovered to be carcinogenic in 1943. However, Japanese usage in medical injections continued and from 1950 to 1975 an estimated 100 million 2 ml ampules of 7-to-15% solutions of ethyl carbamate were injected into patients as a co-solvent in water for dissolving water-insoluble analgesics used for post-operation pain. These doses were estimated to be at levels that are carcinogenic in mice.[6] This practice was stopped in 1975. "This regrettable medical situation appears to have involved the largest number (millions) of humans exposed to the largest doses of a pure carcinogen that is on record".[7] The author, U.S. cancer researcher James A. Miller, called for studies to determine the effects on Japanese cancer rates to be performed but apparently none were ever done.[citation needed]

Prior to World War II, ethyl carbamate saw relatively heavy use in the treatment of multiple myeloma before it was found to be toxic, carcinogenic, and largely ineffective.[8] By US FDA regulations, ethyl carbamate has been withdrawn from pharmaceutical use. However, small quantities of ethyl carbamate are also used in laboratories as an anesthetic for animals.[9]

Ethyl carbamate was reclassified as a Group 2A carcinogen by IARC in 2007.

Ethyl carbamate is frequently used as an anaesthetic in animal experiments, with more than 100 animal studies using ethyl carbamate published each year.[10] One advantage of using ethyl carbamate is that it has a very long duration of action, with some adult rats remaining anaesthetised 24 hours after administration of the drug.[11] It also does not depress neuronal activity in the cortex to the same extent as isoflurane.[12]

Other uses[edit]

Formerly, ethyl carbamate was used as a chemical intermediate in the preparation of amino resins, that were in turn used as crosslinking agents for permanent-press textile treatments to create "wash-and-wear" fabrics. Other uses included as solvent or intermediary in the manufacture of pesticides, cosmetics and pharmaceuticals.[13]

Occurrence in beverages and food[edit]

The widespread presence of ethyl carbamate in alcoholic beverages was discovered during the mid-1980s. To raise public awareness of this issue, the U.S. Center for Science in the Public Interest published, in 1987, Tainted Booze: The Consumer's Guide to Urethane in Alcoholic Beverages. Studies have shown that most, if not all, yeast-fermented alcoholic beverages contain traces of ethyl carbamate (15 ppb to 12 ppm).[14] Other foods and beverages prepared by means of fermentation also contain ethyl carbamate. For example, bread has been found to contain 2 ppb;[15] as much as 20 ppb has been found in some samples of soy sauce.[16] Amounts of both ethyl carbamate and methyl carbamate have also been found in wines, sake, beer, brandy, whiskey and other fermented alcoholic beverages.

It has been shown that ethyl carbamate forms from the reaction of ethanol with urea:

This reaction occurs much faster at higher temperatures, and therefore higher concentrations of ethyl carbamate are found in beverages that are heated during processing, such as brandy, whiskey, and other distilled beverages. Additionally, heating after bottling either during shipping or in preparation will cause ethyl carbamate levels to rise further.

The urea in wines results from the metabolism of arginine or citrulline by yeast or other organisms. The urea waste product is initially metabolised inside the yeast cell until it builds up to a certain level. At that point, it is excreted externally where it is able to react with the alcohol to create ethyl carbamate.

In 1988, wine and other alcoholic beverage manufacturers in the United States agreed to control the level of ethyl carbamate in wine to less than 15 ppb (parts per billion), and in stronger alcoholic drinks to less than 125 ppb.[14]

Although the urea cannot be eliminated, it can be minimized by controlling the fertilization of grape vines, minimizing their heat exposure, using self-cloning yeast[17] and other actions.[18] Furthermore, some strains of yeast have been developed to help reduce ethyl carbamate during commercial production of alcoholic beverages.[19]

Another important mechanism for ethyl carbamate formation in alcoholic beverages is the reaction from cyanide as precursor, which causes comparably high levels in spirits derived from cyanogenic plants, such as rhum agricole.[20]

Hazards[edit]

Ethyl carbamate is not acutely toxic to humans, as reflected by its use as a medicine. Acute toxicity studies show that the lowest fatal dose in rats, mice, and rabbits equals 1.2 g/kg or more. When ethyl carbamate was used medicinally, about 50% of the patients exhibited nausea and vomiting, and long-time use led to gastroenteric hemorrhages.[21] The compound has almost no odor and a cooling, saline, bitter taste.[22]

Studies with rats, mice, and hamsters have shown that ethyl carbamate causes cancer when administered orally, injected, or applied to the skin, but no adequate studies of cancer in humans caused by ethyl carbamate has been reported due to the ethical considerations of such studies.[23] However, in 2007, the International Agency for Research on Cancer raised ethyl carbamate to a Group 2A carcinogen that is "probably carcinogenic to humans", one level below fully carcinogenic to humans. IARC has stated that ethyl carbamate can be "reasonably anticipated to be a human carcinogen based on sufficient evidence of carcinogenicity in experimental animals".[24] In 2006, the Liquor Control Board of Ontario in Canada rejected imported cases of sherry due to excessive levels of ethyl carbamate.

Studies in Hong Kong (2009)[25] and Korea (2015)[26] outline the extent of the accumulative exposure to ethyl carbamate in daily life. Fermented foods such as soy sauce, kimchi, soybean paste, breads, rolls, buns, crackers and bean curd, along with wine, sake and plum wine, were found to be the foods with the highest ethyl carbamate levels in traditional Asian diets.

In 2005, the JECFA (Joint FAO/WHO Expert Committee On Food Additives) risk-assessment evaluation of ethyl carbamate[27] concluded that the MOE intake of ethyl carbamate from daily food and alcoholic beverages combined is of concern, and mitigation measures to reduce ethyl carbamate in some alcoholic beverages should continue. There is little doubt[28] that ethyl carbamate in alcoholic beverages is very important to health authorities, while the cumulative daily exposure in the typical diet is also an issue of rising concern that merits closer observation. The Korean study concluded: "It would be desirable to closely monitor ethyl carbamate levels in Korean foods and find ways to reduce the daily intake."

The IARC evaluation has led to the following US regulatory actions:[citation needed]

  • NESHAP: Listed as a Hazardous Air Pollutant (HAP)
  • Comprehensive Environmental Response, Compensation, and Liability Act: Reportable Quantity (RQ) = 100 lb
  • Emergency Planning and Community Right-To-Know Act, EPA's Toxics Release Inventory: A listed substance subject to RCRA reporting requirements
  • RCRA Listed Hazardous Waste: substance - U238

Detection in alcoholic beverages[edit]

The concerns raised by the toxicological aspects of EC together with the low concentration levels (µg/L) found in wines, as well as the occurrence of interferences on detection, has motivated several researchers to develop new methods to determine it in wines. Several extraction and chromatographic techniques have been used, including continuous liquid–liquid extraction (LLE) with Soxhlet apparatus, derivatization with 9-xanthydrol followed by high-performance liquid chromatography (HPLC) with fluorescence detection and even LLE after derivatization, followed by gas chromatography coupled with mass spectrometry detection (GC–MS). On the other hand, the reference method set by the International Organization of Vine and Wine (OIV) uses solid phase extraction (SPE) preceding GC–MS quantification. Other methods also make use of SPE, but use gas chromatography with mass spectrometry (MDGC/MS) and liquid chromatography with tandem mass spectrometry (LC–MS/MS) for detection. Most of the methodologies found in the literature to quantify EC use gas chromatography, using LLE and SPE as extraction techniques. Nevertheless, several efforts have also been done to develop new methodologies to determine EC without using long procedures and hard-working analyses, combining precision to high sensitivity. In this regard, headspace solid phase microextraction (HS-SPME) has been gaining great highlighting and alternative methodologies has been proposed using the most recent identification and quantification technology, such as gas chromatography with tandem mass spectrometry detection (GC–MS/MS) and two-dimensional gas chromatography with time-of-flight mass spectrometry (GC × GC–ToFMS).

Microextraction by packed sorbent (MEPS) is also feasible. MEPS/GC–MS methodology has been applied to quantify EC in wines.[29][30]

Miniaturized liquid-liquid extraction (mLLE) followed by LC-MS/MS can be used to determine EC in wine, without using derivatizing agents.[31]

Related compounds[edit]

Other carbamates include methyl carbamate,[32] butyl carbamate,[33] and phenyl carbamate (m. p. 149–152 °C),[34] which can also be prepared from the corresponding chloroformate and ammonia. These esters are white, crystalline solids at room temperature. Except for the phenyl carbamate, they sublime at moderate temperatures; methyl carbamate sublimes at room temperatures. The first two and ethyl carbamate are very soluble in water, benzene, and ether.[22][32][33] These other carbamates (methyl, butyl, and phenyl) are only used in small quantities for research purposes.

See also[edit]

References[edit]

  1. ^ Exner, Otto (1977). "Dipole moments, configurations and conformations of molecules containing X...Y groups". Double-Bonded Functional Groups: Vol. 1 (1977). Chichester, UK: John Wiley & Sons, Ltd. pp. 1–92. doi:10.1002/9780470771501.ch1. ISBN 978-0-470-77150-1.
  2. ^ "ethyl carbamate". stenutz.eu. Retrieved 6 April 2021.
  3. ^ Record of Ethyl carbamate in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 13 December 2021.
  4. ^ Jäger, Peter; Rentzea, Costin N.; Kieczka, Heinz. "Carbamates and Carbamoyl Chlorides". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a05_051. ISBN 978-3527306732.
  5. ^ The Merck Index, 11th Edition, 9789
  6. ^ Nomura, T. (October 1975). "Urethan (Ethyl Carbamate) as a Cosolvent of Drugs Commonly Used Parenterally in Humans" (PDF). Nomura Cancer Research. 35 (10): 2895–2899. PMID 1157055.
  7. ^ Miller, James A. (1991). "The Need for Epidemiological Studies of the Medical Exposures of Japanese Patients to the Carcinogen Ethyl Carhamate (Urethane) from 1950 to 1975". Japanese Journal of Cancer Research. 82 (12). Wiley: 1323–1324. doi:10.1111/j.1349-7006.1991.tb01799.x. ISSN 0910-5050. PMC 5918349. PMID 1778753.
  8. ^ Holland, JR; Hosley, H; Scharlau, C; Carbone, PP; Frei, E, 3rd; Brindley, CO; Hall, TC; Shnider, BI; Gold, GL; Lasagna, L; Owens, AH Jr; Miller, SP (1966). "A controlled trial of urethane treatment in multiple myeloma". Blood. 27 (3): 328–42. doi:10.1182/blood.V27.3.328.328. PMID 5933438.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link)
  9. ^ Virginia Commonwealth University, The Chemical/Biological Safety Section (CBSS) of the Office of Environmental Health and Safety, Working with Urethane Archived 2013-05-11 at the Wayback Machine, 2006. Accessed May 13, 2006
  10. ^ Hara, K.; Harris, R.A. (2002). "The anesthetic mechanism of urethane: the effects on neurotransmitter-gated ion channels". Anesthesia & Analgesia. 94 (2): 313–8. doi:10.1213/00000539-200202000-00015. PMID 11812690. S2CID 13806836.
  11. ^ Field, K.J.; White, W.J.; Lang, C.M. (1993). "Anaesthetic effects of chloral hydrate, pentobarbitone and urethane in adult male rats". Laboratory Animals. 27 (3): 258–69. doi:10.1258/002367793780745471. PMID 8366672.
  12. ^ Rojas, M.J.; Navas, J.A.; Rector, D.M. (2006). "Evoked response potential markers for anesthetic and behavioral states". American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 291 (1): R189–96. doi:10.1152/ajpregu.00409.2005. PMID 16455771. S2CID 18569834.
  13. ^ "Fourteenth Report on Carcinogens, Urethane" (PDF). NTP National Toxicology Program, NIEHS, National Institutes of Health. 2016. Retrieved 6 April 2021.
  14. ^ a b Segal, Marian (20 June 2006). "FDA/CFSAN FDA Consumer: Too Many Drinks Spiked with Urethane (April, 1988)". cfsan.fda.gov. Archived from the original on 20 June 2006. Retrieved 6 April 2021.
  15. ^ Haddon W F; M I Mancini; M Mclaren; A Effio; L A Harden; R I Egre; J L Bradford (1994). "Occurrence of ethyl carbamate (urethane) in US and Canadian breads:measurements by gas chromatography-mass spectrometry". Cereal Chemistry. 71 (2): 207–215.
  16. ^ Matsudo T; T Aoki; K Abe; N Fukuta; T Higuchi; M Sasaki; K Uchida (1993). "Determination of ethyl carbamate in soy sauce and its possible precursor". J Agric Food Chem. 41 (3): 352–356. doi:10.1021/jf00027a003.
  17. ^ Coulon J, Husnik JI, Inglis DL, van der Merwe GK, Lonvaud A, Erasmus DJ, van Vuuren HJ (2006). "Metabolic Engineering of Saccharomyces cerevisiae to Minimize the Production of Ethyl Carbamate in Wine". American Journal of Enology and Viticulture. 57 (2): 113–124. doi:10.5344/ajev.2006.57.2.113. S2CID 44808594.
  18. ^ Butzke, C E & L F Bisson, Ethyl Carbamate Preventative Action Manual Archived 2006-06-19 at the Wayback Machine, Depart. of Viticulture & Enology, U. of CA, Davis, CA, for US FDA, 1997 accessed May 13, 2006
  19. ^ Canada, Environment and Climate Change (2010-02-15). "New substances: risk assessment summary EAU-288 - Canada.ca". www.ec.gc.ca.
  20. ^ Lachenmeier DW, Lima MC, Nóbrega IC, Pereira JA, Kerr-Corrêa F, Kanteres F, Rehm J (2010). "Cancer risk assessment of ethyl carbamate in alcoholic beverages". BMC Cancer. 10: 266. doi:10.1186/1471-2407-10-266. PMC 2892455. PMID 20529350.
  21. ^ Office of Toxic Substances, Chemical Hazard Information Profile Urethane, CAS No. 51-79-6, U.S. EPA, Washington, D.C., 12 pages, 26 references, 1979, accessed May 13, 2006 at http://toxnet.nlm.nih.gov.[full citation needed]
  22. ^ a b National Library of Medicine, Hazardous Data Bank, Ethyl Carbamate 2006a, accessed May 13, 2006 at http://toxnet.nlm.nih.gov/.[full citation needed]
  23. ^ IARC, 1974[clarification needed]
  24. ^ NTP 2005[clarification needed]
  25. ^ "RA39_EC_in_food_e.pdf" (PDF). Retrieved 2020-04-12.
  26. ^ Ryu, Dayeon; Choi, Bogyoung; Kim, Eunjoo; Park, Seri; Paeng, Hwijin; Kim, Cho-il; Lee, Jee-yeon; Yoon, Hae Jung; Koh, Eunmi (2015-09-30). "Determination of Ethyl Carbamate in Alcoholic Beverages and Fermented Foods Sold in Korea". Toxicological Research. 31 (3). The Korean Society of Toxicology: 289–297. doi:10.5487/tr.2015.31.3.289. ISSN 1976-8257. PMC 4609976. PMID 26483888.
  27. ^ "www.fao.org" (PDF). Retrieved 2020-04-12.
  28. ^ "WHO | JECFA". Retrieved 2020-04-12.
  29. ^ Leça, J. M.; Pereira, V.; Pereira, A. C.; Marques, J. C. (2014). "Rapid and sensitive methodology for determination of ethyl carbamate in fortified wines using microextraction by packed sorbent and gas chromatography with mass spectrometric detection" (PDF). Analytica Chimica Acta. 811: 29–35. Bibcode:2014AcAC..811...29L. doi:10.1016/j.aca.2013.12.018. hdl:10316/27137. PMID 24456591.
  30. ^ Weber, J. V.; Sharypov, V. I. (2009). "Ethyl carbamate in foods and beverages: a review". Environmental Chemistry Letters. 7 (3): 233–247. Bibcode:2009EnvCL...7..233W. doi:10.1007/s10311-008-0168-8. S2CID 95933716.
  31. ^ Leça, João M.; Pereira, Vanda; Pereira, Ana C.; Marques, José C. (2017-08-15). "A Sensitive Method for the Rapid Determination of Underivatized Ethyl Carbamate in Fortified Wine by Liquid Chromatography-Electrospray Tandem Mass Spectrometry". Food Analytical Methods. 11 (2): 327–333. doi:10.1007/s12161-017-1002-3. hdl:10400.13/3725. ISSN 1936-9751. S2CID 102508529.
  32. ^ a b National Library of Medicine, Hazardous Data Bank, Methyl Carbamate 2006b, accessed May 13, 2006 at http://toxnet.nlm.nih.gov
  33. ^ a b National Library of Medicine, Hazardous Data Bank, Butyl Carbamate 2006c, accessed May 13, 2006 at http://toxnet.nlm.nih.gov
  34. ^ Dean, J. A. (editor), Lange's Handbook of Chemistry, 13th Ed., 1985, p. 7-586, #p191.

External links[edit]

Retrieved from "https://en.wikipedia.org/w/index.php?title=Ethyl_carbamate&oldid=1206466890"