Английская Википедия:Ethylene thiourea

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Версия от 21:48, 4 марта 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Chembox | ImageFile = Ethylenethiourea.png | ImageSize = 134 | PIN = Imidazolidine-2-thione | OtherNames = 1,3-Ethylene-2-thiourea, ''N'',''N''-Ethylenethiourea |Section1={{Chembox Identifiers | CASNo = 96-45-7 | CASNo_Ref = {{cascite|correct|CAS}} | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 24FOJ4N18S | PubChem = 2723650 | ChemSpiderID = 2005851 | SMILES = C1CNC(=S)N1 | InChI = 1...»)
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Шаблон:Chembox Ethylene thiourea (ETU) is an organosulfur compound with the formula Шаблон:Chem2. It is an example of an N,N-disubstituted thiourea. It is a white solid. It is synthesized by treating ethylenediamine with carbon disulfide.[1]

Ethylene thioureas are an excellent accelerant of vulcanization of neoprene rubbers. In commercial use is the N,N'-diphenylethylenethiourea. Due to reproductive toxicity, carcinogenicity, and mutagenicity, alternatives are being sought to the ethylenethioureas. One candidate replacement is N-methyl-2-thiazolidinethione.[2]

Ethylene thiourea can be used as a biomarker of exposure to ethylenebisdithiocarbamates (EBDTCs), which are frequently employed as fungicides in agriculture, mainly on fruits, vegetables and ornamental plants.[3]

EPA classification

EPA (United States Environmental Protection Agency) has classified ethylene thiourea as a Group B2, probable human carcinogen.[4] Ethylene thiourea has been shown to be a potent teratogen (causes birth defects) in rats orally or dermally exposed.

See also

References

Шаблон:Reflist