CAS 51-79-6
:Carbamic acid, ethyl ester
Description:
Carbamic acid, ethyl ester, also known as ethyl carbamate, is an organic compound with the molecular formula C3H7NO2. It is characterized by its colorless, viscous liquid form and has a faint, sweet odor. Ethyl carbamate is soluble in water, alcohol, and ether, which makes it versatile in various chemical applications. The compound is primarily used in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of certain polymers. It is important to note that ethyl carbamate can be formed as a byproduct in the fermentation process of alcoholic beverages and is considered a potential carcinogen. Its structure features a carbamate functional group, which consists of a carbonyl group (C=O) bonded to a nitrogen atom (N) that is also connected to an ethyl group (C2H5). Due to its biological activity and potential health implications, the handling and use of ethyl carbamate are subject to regulatory scrutiny in many regions.
Formula:C3H7NO2
InChI:InChI=1S/C3H7NO2/c1-2-6-3(4)5/h2H2,1H3,(H2,4,5)
InChI key:InChIKey=JOYRKODLDBILNP-UHFFFAOYSA-N
SMILES:O(C(N)=O)CC
Synonyms:- Carbaminsaeure-Aethylester
- Ethyl aminoformate
- Ethyl carbamate
- Ethyl urethane
- Ethylurethane
- Leucethane
- Nsc 746
- O-Ethylurethane
- Pracarbamine
- Uretano
- Urethan
- Urethane
- Urethane (ethyl carbamate)
- Poly(carbonate urethane)
- Ethyluretan
- Aethylurethan
- Carbamicacidethylester
- See more synonyms
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Found 13 products.
Ethyl Carbamate
CAS:Formula:C3H7NO2Purity:>98.0%(GC)(N)Color and Shape:White to Almost white powder to crystalineMolecular weight:89.09Ethyl carbamate, 98%
CAS:<p>Ethyl carbamate in its molten state is good solvent for various organic materials, preparation modification of amino resins, as solubilizer.This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to t</p>Formula:C3H7NO2Purity:98%Color and Shape:Crystalline powder, WhiteMolecular weight:89.09Urethane
CAS:<p>Urethane (Ethylurethane) was an antineoplastic agent .Now is used for other medicinal purposes.</p>Formula:C3H7NO2Purity:99.01%Color and Shape:SoildMolecular weight:89.09Urethane
CAS:Formula:C3H7NO2Purity:≥ 98.0%Color and Shape:White to almost white crystalline powder or crystalsMolecular weight:89.09Ethyl carbamate
CAS:Ethyl carbamateFormula:C3H7NO2Purity:99%Color and Shape: colourless/white crystalsMolecular weight:89.09g/molUrethane-13C,15N
CAS:Controlled Product<p>Applications Urethane-13C, 15N is an intermediate for the synthesis of Diclazuril-13C3,15N2 (D436202), which is the labelled analogue of Diclazuril (D436200). Diclazuril is a nucleotide analogue with broad-spectrum anticoccidial activity and a coccidiostat.<br>References Maes, L., et al.: J. Parasitol., 74, 931 (1988)<br></p>Formula:CC2H715NO2Color and Shape:NeatMolecular weight:91.079Urethane
CAS:Controlled Product<p>Applications Urethane is a naturally occurring contaminant in fermented foods, particularly wine, stone-fruit brandies, and bread. This substance is reasonably anticipated to be a human carcinogen (1) despite being an additive in some alcoholic beverages and foods (2). It binds covalently with DNA however due to its low unavoidable daily intake, it is considered of negligible concern (3).Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA). Environmental contaminants; Food contaminants.<br>References 1. Mirvish, S. et al.: Adv. Cancer Res. 1968;11:1-42.2. Battaglia R. et al.: Food Addit Contam. 1990 Jul-Aug;7(4):477-96. 3. Zimmerli B. et al.: Mutat Res. 1991 Mar-Apr;259(3-4):325-50.<br></p>Formula:C3H7NO2Color and Shape:White To Off-WhiteMolecular weight:89.09Urethane
CAS:Controlled Product<p>Urethane is a carbamate that inhibits the polymerase chain reaction. It has been used as a model system for carcinogenesis because it induces squamous cell carcinomas in rats and mice. Urethane is metabolized by hydrolysis to urethane, which is an inhibitor of phosphodiesterases. This inhibition can lead to decreased levels of dinucleotide phosphate, which may be responsible for the effects on energy metabolism seen in animals given urethane. The mechanism of action of urethane on growth factor-β1 is unknown, but it causes toxic effects on polymorphonuclear leucocytes and other cells in vitro. Urethane also has been shown to inhibit the activity of enzymes involved in DNA synthesis and protein synthesis, leading to cytotoxicity.</p>Formula:C3H7NO2Purity:Min. 95%Molecular weight:89.09 g/mol










