Difference between revisions of "Diphenylamine"
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[[Arylation]] with [[iodobenzene]] gives [[triphenylamine]].<ref>http://www.orgsyn.org/demo.aspx?prep=CV1P0544</ref> | [[Arylation]] with [[iodobenzene]] gives [[triphenylamine]].<ref>http://www.orgsyn.org/demo.aspx?prep=CV1P0544</ref> | ||
| + | |||
| + | Oxidation of diphenylamine with [[potassium permanganate]] yields tetraphenylhydrazine. | ||
Diphenylamine slowly oxidizes in air, turning gray, yellow, orange or brown. | Diphenylamine slowly oxidizes in air, turning gray, yellow, orange or brown. | ||
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==Projects== | ==Projects== | ||
*Make triphenylamine | *Make triphenylamine | ||
| − | *Stabilizer for energetic materials, such as [[smokeless powder]] | + | *Stabilizer for reagents and energetic materials, such as [[smokeless powder]] |
*Redox indicator in alkaline redox titrations | *Redox indicator in alkaline redox titrations | ||
*Diphenylamine test for nitrates | *Diphenylamine test for nitrates | ||
*Synthesis of azo dyes (Metanil Yellow, Disperse Orange 1, Acid orange 5, etc.) | *Synthesis of azo dyes (Metanil Yellow, Disperse Orange 1, Acid orange 5, etc.) | ||
| + | *Synthesis of tetraphenylhydrazine | ||
*Apple scald inhibitor | *Apple scald inhibitor | ||
| Line 194: | Line 197: | ||
[[Category:Aromatic compounds]] | [[Category:Aromatic compounds]] | ||
[[Category:Amines]] | [[Category:Amines]] | ||
| + | [[Category:Secondary amines]] | ||
[[Category:Bases]] | [[Category:Bases]] | ||
[[Category:Organic bases]] | [[Category:Organic bases]] | ||
Latest revision as of 22:46, 24 August 2023
| Names | |
|---|---|
| IUPAC name
N-Phenylaniline
| |
| Other names
Anilinobenzene
C.I. 10355 Diphenylazane N-Phenylbenzenamine N,N-Diphenylamine Phenylaminobenzene Phenylbenzenamine | |
| Properties | |
| C12H11N (C6H5)2NH | |
| Molar mass | 169.23 g/mol |
| Appearance | White colorless solid |
| Odor | Dry plant-like |
| Density | 1.16 g/cm3 |
| Melting point | 53 °C (127 °F; 326 K) |
| Boiling point | 302 °C (576 °F; 575 K) |
| 0.003 g/100 ml (0 °C) 0.00316 g/100 ml (15 °C) 0.007 g/100 ml (28 °C) 0.012 g/100 ml (50 °C) 0.032 g/100 ml (85 °C)[1] | |
| Solubility | Reacts with acids Soluble in acetone, benzene, carbon disulfide, carbon tetrachloride, diethyl ether, ethanol, ethyl acetate, methanol, pyridine, xylene |
| Solubility in acetone | 239.83 g/100 ml (0 °C) 298.59 g/100 ml (28 °C) |
| Solubility in benzene | 110.674 g/100 ml (0 °C) 277.99 g/100 ml (28 °C) |
| Solubility in carbon disulfide | 112.452 g/100 ml (0 °C) 314.12 g/100 ml (28 °C) |
| Solubility in carbon tetrachloride | 27.734 g/100 ml (0 °C) 122.63 g/100 ml (28 °C) |
| Solubility in chloroform | 86.545 g/100 ml (0 °C) 206.26 g/100 ml (28 °C) |
| Vapor pressure | 6.7·10-4 mmHg (25 °C) |
| Thermochemistry | |
| Std enthalpy of
formation (ΔfH |
142.5 kJ/mol |
| Hazards | |
| Safety data sheet | Sigma-Aldrich |
| Flash point | 152 °C (306 °F; 425 K) |
| Lethal dose or concentration (LD, LC): | |
| LD50 (Median dose)
|
2,900 mg/kg (mouse, oral) |
| Related compounds | |
| Related compounds
|
Aniline Triphenylamine |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Diphenylamine is an organic compound with the formula (C6H5)2NH. The compound is a derivative of aniline, consisting of an amine bound to two phenyl groups.
Contents
Properties
Chemical
Diphenylamine is a weak base, with a Kb of 10−14. It reacts with acids to form salts.
Diphenylamine undergoes various cyclisation reactions. With sulfur, it gives phenothiazine, a precursor to pharmaceuticals.[2]
- (C6H5)2NH + 2 S → S(C6H4)2NH + H2S
With iodine, it undergoes dehydrogenation to give carbazole, with release of hydrogen iodide:
- (C6H5)2NH + I2 → (C6H4)2NH + 2 HI
Arylation with iodobenzene gives triphenylamine.[3]
Oxidation of diphenylamine with potassium permanganate yields tetraphenylhydrazine.
Diphenylamine slowly oxidizes in air, turning gray, yellow, orange or brown.
Physical
Diphenylamine is a colorless solid, insoluble in water but very soluble in organic solvents. Impure product tends to be gray or brown.
Availability
Diphenylamine is sold by chemical suppliers.
Preparation
Diphenylamine is manufactured by the thermal deamination of aniline over oxide catalysts:
- 2 C6H5NH2 → (C6H5)2NH + NH3
Can also be prepared by reacting acetanilidie with bromobenzene. The reaction yields N,N-diphenylacetamide, which is hydrolyzed with HCl to crude diphenylamine hydrochloride, which is then purified to diphenylamine.[4]
Projects
- Make triphenylamine
- Stabilizer for reagents and energetic materials, such as smokeless powder
- Redox indicator in alkaline redox titrations
- Diphenylamine test for nitrates
- Synthesis of azo dyes (Metanil Yellow, Disperse Orange 1, Acid orange 5, etc.)
- Synthesis of tetraphenylhydrazine
- Apple scald inhibitor
Handling
Safety
Diphenylamine appears to be moderate toxic. It can cause severe irritation to the eyes, though it is not a skin irritant. Diphenylamine targets the red blood cell system and can cause abnormal erythropoiesis in the spleen, and thus congestion of the spleen, and haemosiderosis. Changes in liver and kidneys were found upon longer exposure.
Diphenylamine has low acute and short-term toxicity to birds, but is very toxic to aquatic organisms. Risk to biological methods of sewage treatment was assessed as low.
Storage
In closed airtight bottles, away from acids and air.
Disposal
Can be neutralized by burning it in an incinerator.
References
- ↑ Seidell A. Solubilities of organic compounds. - 3ed., vol.2. - New York: D. Van Nostrand Company, 1941
- ↑ https://onlinelibrary.wiley.com/doi/10.1002/14356007.a02_303 T. Kahl, K.-W. Schröder, F. R. Lawrence, W. J. Marshall, Hartmut Höke, Rudolf Jäckh, "Aniline" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH: Weinheim
- ↑ http://www.orgsyn.org/demo.aspx?prep=CV1P0544
- ↑ https://www.prepchem.com/synthesis-of-diphenylamine/
