Caprolactam
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| Names | |||
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IUPAC name
Azepan-2-one
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| Other names
ε-Caprolactam, 1-Aza-2-cycloheptanone, 2-Azacycloheptanone, Capron PK4, Cyclohexanone iso-oxime, Extrom 6N, Hexahydro-2-azepinone, Hexahydro-2H-azepin-2-one (9CI), Hexanolactame, aminocaproic lactam
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| Identifiers | |||
105-60-2 
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| 3D model (Jmol) | Interactive image | ||
| ChEBI |
CHEBI:28579
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| ChEMBL |
ChEMBL276218
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| ChemSpider |
7480
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| ECHA InfoCard | 100.003.013 | ||
| EC Number | 203-313-2 | ||
| KEGG |
C06593
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| PubChem | 7768 | ||
| UNII |
6879X594Z8
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| Properties | |||
| C6H11NO | |||
| Molar mass | 113.16 g·mol−1 | ||
| Appearance | White solid | ||
| Density | 1.01 g/cm3 | ||
| Melting point | 69.2 °C (156.6 °F; 342.3 K) | ||
| Boiling point | 270.8 °C (519.4 °F; 544.0 K) at 1013.25 hPa | ||
| 866.89 g/L (22 °C) | |||
| Vapor pressure | 0.00000008 mmHg (20° C) | ||
| Hazards | |||
| R-phrases | R20, R22, R36/37/38 | ||
| Flash point | 125 °C (257 °F; 398 K) | ||
| Explosive limits | 1.4%-8.0% | ||
| US health exposure limits (NIOSH): | |||
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PEL (Permissible)
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none | ||
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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 (what is  ?) |
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| Infobox references | |||
Caprolactam (CPL) is an organic compound with the formula (CH2)5C(O)NH. This colourless solid is a lactam (a cyclic amide) of caproic acid. Approximately 4.5 billion kilograms are produced annually. Caprolactam is the precursor to Nylon 6, a widely used synthetic polymer.
Caprolactam was first described in the late 1800s when it was prepared by the cyclization of ε-aminocaproic acid, the product of the hydrolysis of caprolactam. Given the commercial significance of Nylon-6, many methods have been developed for the production of caprolactam. Most of the caprolactam is synthesised from cyclohexanone (1), which is first converted to its oxime (2). Treatment of this oxime with acid induces the Beckmann rearrangement to give caprolactam (3):
The immediate product of the acid-induced rearrangement is the bisulfate salt of caprolactam. This salt is neutralized with ammonia to release the free lactam and cogenerate ammonium sulfate. In optimizing the industrial practices, much attention is directed toward minimizing the production of ammonium salts.
The other major industrial route involves formation of the oxime from cyclohexane using nitrosyl chloride. The advantage of this method is that cyclohexane is less expensive than cyclohexanone. In earlier times, caprolactam was prepared by treatment of caprolactone with ammonia.
Cyclohexanone with hydrazoic acid (and H2SO4 or Lewis acid cat.) has also been reported. This is known as a Schmidt ring expansion.
Almost all caprolactam produced goes into the manufacture of Nylon-6. The conversion entails a ring-opening polymerization:
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Wikipedia