Ethyl carbamate

Names
Preferred IUPAC name

Ethyl carbamate

Other names

Carbamic acid ethyl ester, Urethane, Ethylurethane

Identifiers

CAS Number

* 51-79-6 Y

3D model (JSmol)

* Interactive image
* Interactive image

3DMet  |

* B00312

ChEBI |

* CHEBI:17967 Y

ChEMBL |

* ChEMBL462547 Y

ChemSpider |

* 5439 Y

DrugBank |

* DB04827 Y

EC Number |

* 200-123-1

KEGG |

* C01537 Y

MeSH | Urethane

PubChem CID

* 5641

RTECS number |

* FA8400000

UNII |

* 3IN71E75Z5 Y

UN number | 2811

InChI

* InChI=1S/C3H7NO2/c1-2-6-3(4)5/h2H2,1H3,(H2,4,5) Y

Key: JOYRKODLDBILNP-UHFFFAOYSA-N Y

* InChI=1/C3H7NO2/c1-2-6-3(4)5/h2H2,1H3,(H2,4,5)

Key: JOYRKODLDBILNP-UHFFFAOYAY

SMILES

* CCOC(N)=O

* O=C(OCC)N

Properties

Chemical formula

| 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)

Solubility in water

| 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

Dipole moment

| 2.59 D[1][2]
Hazards
Main hazards | Harmful if swallowed
May cause cancer
GHS pictograms |
GHS Signal word | Danger

GHS hazard statements

| H302, H350

GHS precautionary statements

| PP201Script error: No such module "Preview warning".Category:GHS errors, PP301+P312+P330Script error: No such module "Preview warning".Category:GHS errors, PP308+P313Script error: No such module "Preview warning".Category:GHS errors
NFPA 704 (fire diamond)  |

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).

Y verify (what is YN ?)
Infobox references

Tracking categories (test):

* SizeSet

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.

## Contents

* 1 Synthesis
* 2 Uses
* 2.1 Biomedical applications
* 2.2 Other uses
* 3 Occurrence in beverages and food
* 4 Hazards
* 5 Detection in alcoholic beverages
* 6 Related compounds
* 7 See also
* 8 References
* 9 External links

## Synthesis

It is produced industrially by heating urea and ethyl alcohol.[4] It also arises by the action of ammonia on ethyl chloroformate.[5] File:Synthesis of ethyl carbamate.tif

## Uses

### Biomedical applications

Ethyl carbamate was originally used as an antineoplastic agent, hypnotic, sclerosing agent, adjunct to sulfonamide therapy, and topical bactericide.[6] It was discovered to be carcinogenic in 1943[7] and largely ineffective at treating multiple myeloma, according to a study published in 1966.[8] It was removed from the market in the US, UK and Canada in 1963[9] and was classified as a 2B carcinogen by the IARC in 1974.[10]

However, its use in Japan as a co-solvent in water for dissolving water-insoluble analgesics used for post-operation pain, at doses estimated to be at levels that are carcinogenic in mice, continued until 1975.[11] Miller has suggested that this may have been the "largest number (millions) of humans exposed to the largest doses of a pure carcinogen that is on record" and called for studies to determine the effects on Japanese cancer rates to be performed.[12]

Ethyl carbamate continues to be used as an anaesthetic in animal experiments, with more than 100 animal studies using ethyl carbamate published each year.[13][14] 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.[15] It also does not depress neuronal activity in the cortex to the same extent as isoflurane.[16]

### Other uses

Ethyl carbamate was primarily ual 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 intermediates in the manufacture of pesticides, cosmetics and pharmaceuticals.[17]

## Occurrence in beverages and food

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).[18] Other foods and beverages prepared by means of fermentation also contain ethyl carbamate. For example, bread has been found to contain 2 ppb;[19] as much as 20 ppb has been found in some samples of soy sauce.[20] 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:

File:Ethanol urea reaction.tif

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.[18]

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[21] and other actions.[22] Furthermore, some strains of yeast have been developed to help reduce ethyl carbamate during commercial production of alcoholic beverages.[23]

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.[24]

## Hazards

Template:Text-source

No direct studies have found ethyl carbamate to be acutely toxic to or carcinogenic in humans.[25] However, studies with rats, mice, and hamsters have shown that ethyl carbamate causes cancer when administered orally, injected, or applied to the skin,[17] and the lowest fatal dose in rats, mice, and rabbits was calculated to be 1.2 g/kg at the least. When ethyl carbamate was used medicinally, about 50% of the patients exhibited nausea and vomiting, and long-time use led to gastroenteric hemorrhages.[26] The compound has almost no odor and a cooling, saline, bitter taste.Cite error: Closing `</ref>` missing for `<ref>` tag

Studies in Hong Kong (2009)[27] and Korea (2015)[28] 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 concluded that the margin of exposure to 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.[29] Ethyl carbamate exposure through alcoholic beverages has been discussed by multiple health authorities,[30] while the cumulative daily exposure in the typical diet is also an issue of rising concern that merits closer observation.[30] The Korean study concluded that "it would be desirable to closely monitor ethyl carbamate levels in Korean foods and find ways to reduce the daily intake."[28]

The following US regulators have mentioned urethane:

* NESHAP: Listed as a Hazardous Air Pollutant (HAP)[31]
* Comprehensive Environmental Response, Compensation, and Liability Act: Reportable Quantity (RQ) = 100 lb[32]
* Emergency Planning and Community Right-To-Know Act, EPA's Toxics Release Inventory: A listed substance subject to RCRA reporting requirements[33]
* RCRA Listed Hazardous Waste: substance - U238[34]

## Detection in alcoholic beverages

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.[35][36]

Miniaturized liquid-liquid extraction (mLLE) followed by LC-MS/MS can be used to determine EC in wine, without using derivatizing agents.[37]

## Related compounds

Other carbamates include methyl carbamate,[38] butyl carbamate,[39] and phenyl carbamate (m. p. 149–152 °C),[40] 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.[41][38][39] These other carbamates (methyl, butyl, and phenyl) are only used in small quantities for research purposes.

## See also

* Carbamate
* Methyl carbamate

## References

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". http://www.stenutz.eu/chem/solv6.php?name=ethyl carbamate.
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. "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a05_051.
5. ↑ The Merck Index, 11th Edition, 9789
6. ↑ IARC (1974) (in en). Some Anti-Thyroid and Related Substances, Nitrofurans and Industrial Chemicals. pp. 112. ISBN 978-92-832-1207-2. https://publications.iarc.who.int/Book-And-Report-Series/Iarc-Monographs-On-The-Identification-Of-Carcinogenic-Hazards-To-Humans/Some-Anti-Thyroid-And-Related-Substances-Nitrofurans-And-Industrial-Chemicals-1974.
7. ↑ Nettleship, A; Henshaw, PS; Meyer, HL (1943). "Induction of Pulmonary Tumors in Mice With Ethyl Carbamate (Urethane)" (in en). JNCI: Journal of the National Cancer Institute 4 (3): 309. doi:10.1093/jnci/4.3.309. ISSN 1460-2105. https://academic.oup.com/jnci/article/4/3/309/940587/Induction-of-Pulmonary-Tumors-in-Mice-With-Ethyl.
8. ↑ Holland, JR; Hosley, H; Scharlau, C; Carbone, PP; Frei, E, 3rd; Brindley, CO; Hall, TC; Shnider, BI et al. (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.
9. ↑ "Urethane" (in en). https://go.drugbank.com/drugs/DB04827.
10. ↑ "Urethane (IARC Summary & Evaluation, Volume 7, 1974)". https://www.inchem.org/documents/iarc/vol07/urethane.html.
11. ↑ Nomura, T. (October 1975). "Urethan (Ethyl Carbamate) as a Cosolvent of Drugs Commonly Used Parenterally in Humans". Nomura Cancer Research 35 (10): 2895–2899. PMID 1157055. https://cancerres.aacrjournals.org/content/canres/35/10/2895.full.pdf.
12. ↑ 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 (Wiley) 82 (12): 1323–1324. doi:10.1111/j.1349-7006.1991.tb01799.x. ISSN 0910-5050. PMID 1778753.
13. ↑ Virginia Commonwealth University, The Chemical/Biological Safety Section (CBSS) of the Office of Environmental Health and Safety, Working with Urethane , 2006. Accessed May 13, 2006
14. ↑ 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.
15. ↑ 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.
16. ↑ 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.
17. ↑ 17.0 17.1 "Fourteenth Report on Carcinogens, Urethane". NTP National Toxicology Program, NIEHS, National Institutes of Health. 2016. https://ntp.niehs.nih.gov/sites/default/files/ntp/roc/content/profiles/urethane.pdf.
18. ↑ 18.0 18.1 Segal, Marian (20 June 2006). "FDA/CFSAN FDA Consumer: Too Many Drinks Spiked with Urethane (April, 1988)". http://www.cfsan.fda.gov/~frf/fc0488ur.html.
19. ↑ 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.
20. ↑ 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.
21. ↑ "Metabolic Engineering of Saccharomyces cerevisiae to Minimize the Production of Ethyl Carbamate in Wine". American Journal of Enology and Viticulture 57 (2): 113–124. 2006. doi:10.5344/ajev.2006.57.2.113.
22. ↑ Butzke, C E & L F Bisson, Ethyl Carbamate Preventative Action Manual , Department of Viticulture & Enology, U. of CA, Davis, CA, for US FDA, 1997 accessed May 13, 2006
23. ↑ Canada, Environment and Climate Change (2010-02-15). "New substances: risk assessment summary EAU-288 - Canada.ca". http://www.ec.gc.ca/subsnouvelles-newsubs/default.asp?lang=En&n=AECC21AD-1.
24. ↑ "Cancer risk assessment of ethyl carbamate in alcoholic beverages". BMC Cancer 10: 266. 2010. doi:10.1186/1471-2407-10-266. PMID 20529350.
25. ↑ Humans, IARC Working Group on the Evaluation of Carcinogenic Risks to (2010), "Evaluation and Rationale" (in en), Alcohol Consumption and Ethyl Carbamate (International Agency for Research on Cancer), https://www.ncbi.nlm.nih.gov/books/NBK326563/, retrieved 2026-05-01
26. ↑ 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.
27. ↑ "RA39_EC_in_food_e.pdf". https://docs.google.com/viewer?url=https://www.cfs.gov.hk/english/programme/programme_rafs/files/RA39_EC_in_food_e.pdf.
28. ↑ 28.0 28.1 Ryu, Dayeon; Choi, Bogyoung; Kim, Eunjoo; Park, Seri; Paeng, Hwijin; Kim, Cho-il; Lee, Jee-yeon; Yoon, Hae Jung et al. (2015-09-30). "Determination of Ethyl Carbamate in Alcoholic Beverages and Fermented Foods Sold in Korea". Toxicological Research (The Korean Society of Toxicology) 31 (3): 289–297. doi:10.5487/tr.2015.31.3.289. ISSN 1976-8257. PMID 26483888.
29. ↑ "www.fao.org". http://www.fao.org/3/a-at877e.pdf.
30. ↑ 30.0 30.1 "WHO | JECFA". https://apps.who.int/food-additives-contaminants-jecfa-database/chemical.aspx?chemID=5199.
31. ↑ US EPA, OAR (2015-12-16). "Initial List of Hazardous Air Pollutants with Modifications" (in en). https://www.epa.gov/haps/initial-list-hazardous-air-pollutants-modifications.
32. ↑ "40 CFR 302.4 -- Hazardous substances and reportable quantities." (in en). https://www.ecfr.gov/current/title-40/part-302/section-302.4.
33. ↑ "40 CFR Part 372 -- Toxic Chemical Release Reporting: Community Right-to-Know" (in en). https://www.ecfr.gov/current/title-40/part-372.
34. ↑ "EPA Hazardous Waste Codes | Environmental Safety, Sustainability and Risk" (in en). https://essr.umd.edu/about/environmental-affairs/regulated-waste/epa-hazardous-waste-codes.
35. ↑ 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". Analytica Chimica Acta 811: 29–35. doi:10.1016/j.aca.2013.12.018. PMID 24456591. Bibcode: 2014AcAC..811...29L. https://estudogeral.sib.uc.pt/bitstream/10316/27137/1/Rapid and sensitive methodology for determination of ethyl carbamate in fortified wines.pdf.
36. ↑ Weber, J. V.; Sharypov, V. I. (2009). "Ethyl carbamate in foods and beverages: a review". Environmental Chemistry Letters 7 (3): 233–247. doi:10.1007/s10311-008-0168-8. Bibcode: 2009EnvCL...7..233W.
37. ↑ 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" (in en). Food Analytical Methods 11 (2): 327–333. doi:10.1007/s12161-017-1002-3. ISSN 1936-9751.
38. ↑ 38.0 38.1 National Library of Medicine, Hazardous Data Bank, Methyl Carbamate 2006b, accessed May 13, 2006 at http://toxnet.nlm.nih.gov
39. ↑ 39.0 39.1 National Library of Medicine, Hazardous Data Bank, Butyl Carbamate 2006c, accessed May 13, 2006 at http://toxnet.nlm.nih.gov
40. ↑ Dean, J. A. (editor), Lange's Handbook of Chemistry, 13th Ed., 1985, p. 7-586, #p191.
41. ↑ Cite error: Invalid `<ref>` tag; no text was provided for refs named `HSDB 2006a`

## External links

* NLM Hazardous Substances Databank - Ethyl carbamate

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*[CID]: Compound ID
*[H302]: Harmful if swallowed
*[H350]: May cause cancer