Difference between revisions of "Substance:Ethyl acetate"

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{| class="wikitable" border="0" style="float: right;"
 
{| class="wikitable" border="0" style="float: right;"
 
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  |<!--column1-->[[File:Ethyl acetate.png|150px|Structure of ethyl acetate]]
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  |<!--column1-->[[File:EthylAcetate.png|100px|Structure of ethyl acetate]]
 
  |<!--column2-->[[File:EthylAcetateFullStructure.png‎|200px|Structure of ethyl acetate with all atoms shown]]
 
  |<!--column2-->[[File:EthylAcetateFullStructure.png‎|200px|Structure of ethyl acetate with all atoms shown]]
 
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*Molar mass: 88.1051
 
*Molar mass: 88.1051
 
*CAS Registry Number: 141-78-6
 
*CAS Registry Number: 141-78-6
*IUPAC name: 1,2-diphenylethane-1,2-dione
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*IUPAC name: Ethyl acetate
 
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*Appearance: Colorless liquid with an ether-like, fruity odor.
REMAINDER NEED FIXING
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*Boiling point: 77 °C
*Appearance: Yellow crystals or powder
 
*Melting point: 94-95 °C
 
 
*Solubility properties: Not available
 
*Solubility properties: Not available
*Safety sheet: [http://msds.chem.ox.ac.uk/BE/benzil.html From Oxford University]
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*Safety sheet: [http://www.chemadvisor.com/SymyxMSDS/ohsdoc.pl?OHSNUMBER=OHS08750&DOCTYPE=SUMMARY From ChemAdvisor]
*Spectra: [http://webbook.nist.gov/cgi/cbook.cgi?ID=C134816&Units=SI&Type=IR-SPEC&Index=1#IR-SPEC IR], <sup>1</sup>H NMR, [http://www.ebi.ac.uk/nmrshiftdb/portal/js_pane/P-Results/nmrshiftdbaction/showDetailsFromHome/molNumber/10005895 <sup>13</sup>C NMR], MS ([http://www.massbank.jp/jsp/FwdRecord.jsp?type=disp&id=JP001411 1], [http://www.massbank.jp/jsp/FwdRecord.jsp?type=disp&id=JP009582 2], [http://www.massbank.jp/jsp/FwdRecord.jsp?type=disp&id=JP010530 3], [http://www.massbank.jp/jsp/FwdRecord.jsp?type=disp&id=JP009582 4]).  Also check on [http://riodb01.ibase.aist.go.jp/sdbs/cgi-bin/cre_index.cgi?lang=eng SDBS].
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*Spectra: [http://webbook.nist.gov/cgi/cbook.cgi?ID=C141786&Units=SI&Type=IR-SPEC&Index=1#IR-SPEC IR], [http://www.ebi.ac.uk/nmrshiftdb/portal/js_pane/P-Results/nmrshiftdbaction/showDetailsFromHome/molNumber/10008694 <sup>1</sup>H NMR], [http://www.ebi.ac.uk/nmrshiftdb/portal/js_pane/P-Results/nmrshiftdbaction/showDetailsFromHome/molNumber/10008694 <sup>13</sup>C NMR], [http://www.massbank.jp/jsp/FwdRecord.jsp?type=disp&id=JP001797 MS].  Also check on [http://riodb01.ibase.aist.go.jp/sdbs/cgi-bin/cre_index.cgi?lang=eng SDBS].
  
 
==From Wikipedia==
 
==From Wikipedia==
'''Benzil''' (systematically known as 1,2-diphenyl-1,2-ethanedione) is the organic compound with the formula (C<sub>6</sub>H<sub>5</sub>CO)<sub>2</sub>, generally abbreviated (PhCO)<sub>2</sub>. This yellow solid is one of the most common diketones.  Its main use is as a photoinitiator in polymer chemistry.<ref name=Ullmann>Hardo Siegel, Manfred Eggersdorfer "Ketones" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, 2002 by Wiley-VCH, Wienheim. {{DOI|10.1002/14356007.a15_077}}</ref>  [http://en.wikipedia.org/wiki/Benzil Read more...] or [http://en.wikipedia.org/w/index.php?title=Benzil&action=edit edit at Wikipedia].
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Ethyl acetate (systematically, ethyl ethanoate, commonly abbreviated EtOAc or EA) is the organic compound with the formula CH<sub>3</sub>COOCH<sub>2</sub>CH<sub>3</sub>. This colorless liquid has a characteristic sweet smell (similar to pear drops) like certain glues or nail polish removers, in which it is used. Ethyl acetate is the ester of ethanol and acetic acid; it is manufactured on a large scale for use as a solvent. In 1985, about 400,000 tons were produced yearly in Japan, North America, and Europe combined. In 2004, an estimated 1.3M tons were produced worldwide. [http://en.wikipedia.org/wiki/Ethyl_acetate Read more...] or [http://en.wikipedia.org/w/index.php?title=Ethyl_acetate&action=edit edit at Wikipedia].
  
 
==References==
 
==References==

Latest revision as of 00:21, 10 September 2010

Structure of ethyl acetate Structure of ethyl acetate with all atoms shown
  • Main ChemSpider page
  • Molecular formula: C4H8O2
  • Molar mass: 88.1051
  • CAS Registry Number: 141-78-6
  • IUPAC name: Ethyl acetate
  • Appearance: Colorless liquid with an ether-like, fruity odor.
  • Boiling point: 77 °C
  • Solubility properties: Not available
  • Safety sheet: From ChemAdvisor
  • Spectra: IR, 1H NMR, 13C NMR, MS. Also check on SDBS.

From Wikipedia

Ethyl acetate (systematically, ethyl ethanoate, commonly abbreviated EtOAc or EA) is the organic compound with the formula CH3COOCH2CH3. This colorless liquid has a characteristic sweet smell (similar to pear drops) like certain glues or nail polish removers, in which it is used. Ethyl acetate is the ester of ethanol and acetic acid; it is manufactured on a large scale for use as a solvent. In 1985, about 400,000 tons were produced yearly in Japan, North America, and Europe combined. In 2004, an estimated 1.3M tons were produced worldwide. Read more... or edit at Wikipedia.

References