Jump to content

Caprolactam

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by 144.29.1.20 (talk) at 20:34, 27 March 2013 (→‎Synthesis and production). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Caprolactam
Names
IUPAC name
Azepan-2-one
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
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.013 Edit this at Wikidata
EC Number
  • 203-313-2
KEGG
UNII
  • InChI=1S/C6H11NO/c8-6-4-2-1-3-5-7-6/h1-5H2,(H,7,8) checkY
    Key: JBKVHLHDHHXQEQ-UHFFFAOYSA-N checkY
  • InChI=1/C6H11NO/c8-6-4-2-1-3-5-7-6/h1-5H2,(H,7,8)
    Key: JBKVHLHDHHXQEQ-UHFFFAOYAF
  • O=C1NCCCCC1
Properties
C6H11NO
Molar mass 113.16 g/mol
Appearance white solid
Density 1,01 g/cm3
Melting point 69,2 °C
Boiling point 270,8°C at 1013.25 hPa
4560 g/L (20 °C)
Hazards
Flash point 125 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Caprolactam is an organic compound with the formula (CH2)5C(O)NH. This colourless solid is a lactam or a cyclic amide of caproic acid. Approximately 2 billion kilograms are produced annually. Caprolactam is the precursor to Nylon 6, a widely used synthetic polymer.[1]

Synthesis and production

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 Beckmann Rearrangement

The immediate product of the acid-induced rearrangement is the sulfate 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.[1]

Uses

Almost all caprolactam produced goes into the production of Nylon-6. The conversion entails a ring-opening polymerization:

n (CH2)5C(O)NH → [(CH2)5C(O)NH]n

Nylon-6 is widely used in fibers and plastics.

Safety

Caprolactam is an irritant and is mildly toxic, with an LD50 of 1.1 g/kg (rat, oral). In 1991, it was included on the list of hazardous air pollutants by the U.S. Clean Air Act of 1990. It was subsequently removed from the list in 1993.[2] In water, caprolactam hydrolyzes to aminocaproic acid, which is used medicinally.

As of 2011 caprolactam had the unusual status of being the only chemical in the International Agency for Research on Cancer's lowest hazard category, Group 4 "probably not carcinogenic to humans".[3]

References

  1. ^ a b Josef Ritz, Hugo Fuchs, Heinz Kieczka, William C. Moran "Caprolactam" Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2002. doi:10.1002/14356007.a05_031
  2. ^ EPA - Modifications To The 112(b)1 Hazardous Air Pollutants
  3. ^ Agents Classified by the IARC Monographs, Volumes 1–102 (PDF), WHO, retrieved July 15, 2011
Retrieved from "https://en.wikipedia.org/w/index.php?title=Caprolactam&oldid=547326653"