Difference between revisions of "Acetanilide"
Physchim62 (talk | contribs) (Imported from http://en.wikipedia.org/w/index.php?title=Acetanilide&oldid=310239223) |
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| ImageSize1 = 200px | | ImageSize1 = 200px | ||
| ImageName = Acetanilide | | ImageName = Acetanilide | ||
| − | | IUPACName = ''N''- | + | | IUPACName = ''N''-phenylacetamide |
| Section1 = {{Chembox Identifiers | | Section1 = {{Chembox Identifiers | ||
| InChI = 1/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10) | | InChI = 1/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10) | ||
| + | | StdInChI = InChI=1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10) | ||
| + | | InChIKey = FZERHIULMFGESH-UHFFFAOYAA | ||
| + | | StdInChIKey = FZERHIULMFGESH-UHFFFAOYSA-N | ||
| CASNo = 103-84-4 | | CASNo = 103-84-4 | ||
| CASNo_Ref = {{cascite}} | | CASNo_Ref = {{cascite}} | ||
| Line 18: | Line 21: | ||
| Reference = <ref>{{RubberBible62nd|page=C-67}}.</ref><ref name="SIDS">{{SIDS-ref | title = Acetanilide | id = Acetanilide | date = September 2003}}.</ref> | | Reference = <ref>{{RubberBible62nd|page=C-67}}.</ref><ref name="SIDS">{{SIDS-ref | title = Acetanilide | id = Acetanilide | date = September 2003}}.</ref> | ||
| Formula = C<sub>6</sub>H<sub>5</sub>NH(COCH<sub>3</sub>) | | Formula = C<sub>6</sub>H<sub>5</sub>NH(COCH<sub>3</sub>) | ||
| − | | MolarMass = 135. | + | | MolarMass = 135.16 g/mol |
| Density = 1.219 g/cm<sup>3</sup> | | Density = 1.219 g/cm<sup>3</sup> | ||
| − | | | + | | MeltingPtC = 113.7 |
| − | | | + | | BoilingPtC = 304 |
| Solubility = 0.4 g/100 mL at 20 °C | | Solubility = 0.4 g/100 mL at 20 °C | ||
| SolubleOther = soluble in [[ethanol]], [[diethyl ether]], [[acetone]], [[benzene]] | | SolubleOther = soluble in [[ethanol]], [[diethyl ether]], [[acetone]], [[benzene]] | ||
| Line 28: | Line 31: | ||
}} | }} | ||
| Section7 = {{Chembox Hazards | | Section7 = {{Chembox Hazards | ||
| − | | Reference = <ref>{{ | + | | Reference = <ref>{{GHS class NZ|id=12901|accessdate=2009-08-26}}.</ref><ref name="MSDS">{{citation | url = http://ptcl.chem.ox.ac.uk/MSDS/AC/acetanilide.html | webpage = Safety data for acetanilide | publisher = Physical Chemistry Laboratory, University of Oxford}}.</ref> |
| ExternalMSDS = [http://physchem.ox.ac.uk/MSDS/AC/acetanilide.html External MSDS] | | ExternalMSDS = [http://physchem.ox.ac.uk/MSDS/AC/acetanilide.html External MSDS] | ||
| EUIndex = not listed | | EUIndex = not listed | ||
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Acetanilide can be produced by reacting [[acetic anhydride]] with [[aniline]]: | Acetanilide can be produced by reacting [[acetic anhydride]] with [[aniline]]: | ||
:C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> + (CH<sub>3</sub>CO)<sub>2</sub> → C<sub>6</sub>H<sub>5</sub>NHCOCH<sub>3</sub> + CH<sub>3</sub>COOH | :C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub> + (CH<sub>3</sub>CO)<sub>2</sub> → C<sub>6</sub>H<sub>5</sub>NHCOCH<sub>3</sub> + CH<sub>3</sub>COOH | ||
| − | The preparation used to be a traditional experiment in introductory organic chemistry lab classes,<ref>See, e.g., {{citation | | + | The preparation used to be a traditional experiment in introductory organic chemistry lab classes,<ref>See, e.g., {{citation | webpage = The preparation of acetanilide from aniline | url = http://wwwchem.uwimona.edu.jm/lab_manuals/c10expt23.html | publisher = Department of Chemistry, University of the West Indies at Mona, Jamaica | accessdate = 2009-08-26}}; {{citation | last 1 = Reeve | first1 = Wilkins | last2 = Lowe | first2 = Valerie C. | title = Preparation of Acetanilide from Nitrobenzene | journal = J. Chem. Educ. | volume = 56 | issue = 7 | pages = 488 | year = 1979}}: the latter preparation includes the reduction of nitrobenzene to aniline.</ref> but it has now been widely replaced by the prpearation of either [[paracetamol]] or [[aspirin]], both of which teach the same practical techniques (especially [[recrystallization]] of the product) but which avoid the use of aniline, a suspected [[carcinogen]]. |
Acetanilide is slightly soluble in water, and stable under most conditions.<ref name="MSDS"/> Pure crystals are plate shaped and colorless to white. | Acetanilide is slightly soluble in water, and stable under most conditions.<ref name="MSDS"/> Pure crystals are plate shaped and colorless to white. | ||
Latest revision as of 17:41, 26 August 2009
| Acetanilide | |
|---|---|
| |
| |
| IUPAC name | N-phenylacetamide |
| Identifiers | |
| InChI | InChI=1/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10) |
| InChIKey | FZERHIULMFGESH-UHFFFAOYAA |
| Standard InChI | InChI=InChI=1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10) |
| Standard InChIKey | FZERHIULMFGESH-UHFFFAOYSA-N |
| CAS number | [] |
| EC number | |
| ChemSpider | |
| SMILES | |
| Properties[1][2] | |
| Chemical formula | C6H5NH(COCH3) |
| Molar mass | 135.16 g/mol |
| Density | 1.219 g/cm3 |
| Melting point |
113.7 °C, 387 K, 237 °F |
| Boiling point |
304 °C, 577 K, 579 °F |
| Solubility in water | 0.4 g/100 mL at 20 °C |
| Solubility | soluble in ethanol, diethyl ether, acetone, benzene |
| log P | 1.16 (23 ºC) |
| Vapor pressure | 2 Pa (20 ºC) |
| Hazards[3][4] | |
| Material safety data sheet (MSDS) | External MSDS |
| EU index number | not listed |
| GHS pictograms | 
|
| GHS signal word | WARNING |
| GHS hazard statements | H302 |
| GHS precautionary statements | P264, P270, P301+312, P330, P501 |
| Autoignition temp. | 545 ºC (1013 ºF) |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
Acetanilide[5] is an odourless solid chemical of leaf or flake-like appearance. It is also known as N-phenylacetamide, acetanil, or acetanilid, and was formerly known by the trade name Antifebrin.
Preparation and properties
Acetanilide can be produced by reacting acetic anhydride with aniline:
- C6H5NH2 + (CH3CO)2 → C6H5NHCOCH3 + CH3COOH
The preparation used to be a traditional experiment in introductory organic chemistry lab classes,[6] but it has now been widely replaced by the prpearation of either paracetamol or aspirin, both of which teach the same practical techniques (especially recrystallization of the product) but which avoid the use of aniline, a suspected carcinogen.
Acetanilide is slightly soluble in water, and stable under most conditions.[4] Pure crystals are plate shaped and colorless to white.
Applications
Acetanilide is used as an inhibitor in hydrogen peroxide and is used to stabilize cellulose ester varnishes. It has also found uses in the intermediation in rubber accelerator synthesis, dyes and dye intermediate synthesis, and camphor synthesis. Acetanilide is used as a precursor in the synthesis of penicillin and other pharmaceuticals.[2]
In the 19th century acetanilide was one of a large number of compounds used as experimental photographic developers.
Pharmaceutical use
Acetanilide was the first aniline derivative serendipitously found to possess analgesic as well as antipyretic properties, and was quickly introduced into medical practice under the name of Antifebrin by A. Cahn and P. Hepp in 1886.[7] But its (apparent) unacceptable toxic effects, the most alarming being cyanosis due to methemoglobinemia, prompted the search for supposedly less toxic aniline derivatives such as phenacetin.[8] After several conflicting results over the ensuing fifty years, it was established in 1948 that acetanilide was mostly metabolized to paracetamol (USAN: acetaminophen) in the human body, and that it was the paracetamol that was responsible for the analgesic and antipyretic properties.[9][10][11][12] The observed methemoglobinemia after acetanilide administration was ascribed to the small proportion of acetanilide that is hydrolyzed to aniline in the body.[note 1] Acetanilide is no longer used as a drug in its own right, although the success of its metabolite – paracetamol (acetaminophen) – is well known.
Notes
- ↑ The presence of aniline as an impurity in 19th century batches of acetanilide drugs cannot be ruled out. In this sense as well, paracetamol (acetaminophen) is safer than acetanilide, as (1) the corresponding impurity would be 4-aminophenol, which is less toxic than aniline; and (2) in vivo hydrolysis of the amide group in paracetamol appears to be negligeable.
References
- ↑ CRC Handbook of Chemistry and Physics, 62nd ed.; Weast, Robert C., Ed.; CRC Press: Boca Raton, FL, 1981; p C-67. ISBN 0-8493-0462-8.
- ↑ 2.0 2.1 Acetanilide; SIDS Initial Assessment Report; Organisation for Economic Co-operation and Development, September 2003, <http://www.inchem.org/documents/sids/sids/Acetanilide.pdf>.
- ↑ HSNO Chemical Classification Information Database, <http://www.ermanz.govt.nz/Chemicals/ChemicalDisplay.aspx?SubstanceID=12901> (accessed 26 August 2009), New Zealand Environmental Risk Management Authority.
- ↑ 4.0 4.1 Safety data for acetanilide, <http://ptcl.chem.ox.ac.uk/MSDS/AC/acetanilide.html>, Physical Chemistry Laboratory, University of Oxford.
- ↑ Acetanilide, <http://chemicalland21.com/lifescience/phar/ACETANILIDE.htm>.
- ↑ See, e.g., The preparation of acetanilide from aniline, <http://wwwchem.uwimona.edu.jm/lab_manuals/c10expt23.html> (accessed 26 August 2009), Department of Chemistry, University of the West Indies at Mona, Jamaica; Preparation of Acetanilide from Nitrobenzene. J. Chem. Educ. 1979, 56 (7), 488: the latter preparation includes the reduction of nitrobenzene to aniline.
- ↑ Cahn, A.; Hepp, P. Das Antifebrin, ein neues Fiebermittel. Centralbl. Klin. Med. 1886, 7, 561–64.
- ↑ Bertolini, A.; Ferrari, A.; Ottani, A.; Guerzoni, S.; Tacchi, R.; Leone, S. Paracetamol: new vistas of an old drug. CNS drug reviews 2006, 12 (3–4), 250–75. PMID 17227290. DOI: 10.1111/j.1527-3458.2006.00250.x.
- ↑ Lester, D.; Greenberg, L. A. Metabolic fate of acetanilide and other aniline derivatives. II. Major metabolites of acetanilide in the blood. J. Pharmacol. Exp. Ther. 1947, 90, 68.
- ↑ Brodie, B. B.; Axelrod, J. The estimation of acetanilide and its metabolic products, aniline, N-acetyl p-aminophenol and p-aminophenol (free and total conjugated) in biological fluids and tissues. J. Pharmacol. Exp. Ther. 1948, 94 (1), 22–28. PMID 18885610.
- ↑ Brodie, B. B.; Axelrod, J. The fate of acetanilide in man. J. Pharmacol. Exp. Ther. 1948, 94 (1), 29–38. PMID 18885611, <http://profiles.nlm.nih.gov/HH/A/A/A/D/_/hhaaad.pdf>
- ↑ Flinn, Frederick B.; Brodie, Bernard B. The effect on the pain threshold of N-acetyl p-aminophenol, a product derived in the body from acetanilide. J. Pharmacol. Exp. Ther. 1948, 94 (1), 76–77. PMID 18885618.
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