Chemical structure of the alkylphenol nonylphenol

Alkylphenols are a family of organic compounds obtained by the alkylation of phenols. The term is usually reserved for commercially important propylphenol, butylphenol, amylphenol, heptylphenol, octylphenol, nonylphenol, dodecylphenol and related "long chain alkylphenols" (LCAPs). Methylphenols and ethylphenols are also alkylphenols, but they are more commonly referred to by their specific names, cresols and xylenols.[1]

Production

The long-chain alkylphenols are prepared by alkylation of phenol with alkenes:

C6H5OH + RR'C=CHR" → RR'CH−CHR"−C6H4OH

In this way, about 500M kg/y are produced.[1]

Environmental controversy over nonylphenols

Alkylphenols are xenoestrogens.[2] Long chain Alkylphenols have the most potent estrogenic activity.[2] The European Union has implemented sales and use restrictions on certain applications in which nonylphenols are used because of their alleged "toxicity, persistence, and the liability to bioaccumulate" but the United States EPA has taken a slower approach to make sure that action is based on sound science.[3]

Uses of long-chain alkylphenols

Alkylphenols is a raw non-polar material when paired with their percussor alkylphenols ethoxylate a water-soluble material where the long-chain alkylphenols are used extensively as precursors to the detergents, as additives for fuels and lubricants, polymers, and as components in phenolic resins. [4] These compounds are also used as building block chemicals that are also used in making fragrances, thermoplastic elastomers, antioxidants, oil field chemicals and fire retardant materials. Through the downstream use in making alkylphenolic resins, alkylphenols are also found in tires, adhesives, coatings, carbonless copy paper and high performance rubber products. They have been used in industry for over 40 years.

References

  1. 1 2 Helmut Fiege; Heinz-Werner Voges; Toshikazu Hamamoto; Sumio Umemura; Tadao Iwata; Hisaya Miki; Yasuhiro Fujita; Hans-Josef Buysch; Dorothea Garbe; Wilfried Paulus (2002). "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_313. ISBN 978-3527306732.
  2. 1 2 Kochukov, Y.; Jeng, J.; Watson, S. (May 2009). "Alkylphenol xenoestrogens with varying carbon chain lengths differentially and potently activate signaling and functional responses in GH3/B6/F10 somatomammotropes". Environmental Health Perspectives. 117 (5): 723–730. doi:10.1289/ehp.0800182. ISSN 0091-6765. PMC 2685833. PMID 19479013.
  3. ↑ European Bans on Surfactant Trigger Transatlantic Debate
  4. ↑ J. Kovarova, J. Blahova, L. Divisova, Z.Svobodova. "Alkylphenol ethoxylates and alkylphenols– update information on occurrence,fate and toxicity in aquatic environment". PMID 24597317.{{cite web}}: CS1 maint: multiple names: authors list (link)
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