Chlorinated paraffins

Chlorinated paraffins (CPs) are complex mixtures of polychlorinated n-alkanes. The chlorination degree of CPs can vary between 30 and 70 wt%. CPs are subdivided according to their carbon chain length into short-chain CPs (SCCPs, C10–13), medium-chain CPs (MCCPs, C14–17) and long-chain CPs (LCCPs, C>17). Depending on chain length and chlorine content, CPs are colorless or yellowish liquids or solids.[1]

Structure of 2,3,4,5,6,8-hexachlorodecane, an example of a short-chained chlorinated paraffin (61% Cl by weight)
Structure of 2,5,6,7,8,11,15-heptachloroheptadecane, an example of a medium-chain chlorinated paraffin (52% Cl by weight)


Chlorinated paraffins are synthesized by reaction of chlorine gas with unbranched paraffin fractions (<2 % isoparaffins, <100 ppm aromatics) at a temperature of 80–100 °C.[2] The radical substitution may be promoted by UV-light.[3][1]

CxH(2x+2) + y Cl2 → CxH(2xy+2)Cly + y HCl

When the desired degree of chlorination is achieved, residues of hydrochloric acid and chlorine are blown off with nitrogen. Epoxidized vegetable oil, glycidyl ether or organophosphorous compounds may be added to the final product for improved stability at high temperatures.[4][5]

Commercial products have been classified as substances of unknown or variable composition. CPs are complex mixtures of chlorinated n-alkanes containing thousands of homologues and isomers[6] which are not completely separated by standard analytical methods.[7]

CPs are produced in Europe, North America, Australia, Brazil, South Africa and Asia.[8] In China, where most of the world production capacity is located, 600,000 tons of chlorinated paraffins were produced in 2007.[9] Production and use volumes of CPs exceeded 1,000,000 tons in 2013.[10]

Industrial applicationsEdit

Production of CPs for industrial use started in the 1930s,[11] with global production in 2000 being about 2 million tonnes.[12] Currently, over 200 CP formulations are in use for a wide range of industrial applications, such as flame retardants and plasticisers, as additives in metal working fluids, in sealants, paints, adhesives, textiles, leather fat and coatings.[13][1]


Short-chain CPs are classified as persistent and their physical properties (octanol-water partition coefficient (logKOW) 4.4–8, depending on the chlorination degree) imply a high potential for bioaccumulation. SCCPs are classified as toxic to aquatic organisms, and carcinogenic to rats and mice. Therefore, it was concluded that SCCPs have PBT and vPvB properties and they were added to the Candidate List of substances of very high concern for Authorisation under REACH Regulation.[14] SCCPs (average chain length of C12, chlorination degree 60 wt%) were categorised in group 2B as possibly carcinogenic to humans from the International Agency for Research on Cancer (IARC).[15] In 2017, it was agreed to globally ban SCCPs under the Stockholm Convention on Persistent Organic Pollutants, effective December 2018. However, also MCCPs are toxic to the aquatic environment and persistent; MCCPs in soil, biota, and most of the sediment cores show increasing time trends over the last years to decades; MCCP concentrations in sediment close to local sources exceed toxicity thresholds such as the PNEC.[10]

Chlorinated paraffins have been detected in marine life such as cetaceans (whales) and bivalves (molluscs). Of particular concern is fetal accumulation in whales, with the chemicals beginning to build-up in the offspring before they are even born.[16]


  1. ^ a b c Rossberg, M.; Lendle, W.; Pfleiderer, G.; Tögel, A.; Dreher, E. L.; Langer, E.; Rassaerts, H.; Kleinschmidt, P.; Strack (2006). "Chlorinated Hydrocarbons". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a06_233.pub2.
  2. ^ Brooke 2009, pp. 4, 23.
  3. ^ Lassen 2014, p. 50.
  4. ^ Kellersohn 1998.
  5. ^ Brooke 2009, p. 5.
  6. ^ Tomy 1997, pp. 2764–2765.
  7. ^ Lassen 2014, p. 30.
  8. ^ Lassen 2014, pp. 50–51.
  9. ^ De Boer 2010, p. 8.
  10. ^ a b Juliane Glüge, Lena Schinkel, Konrad Hungerbühler, Ronan Cariou, Christian Bogdal (2018). "Environmental Risks of Medium-Chain Chlorinated Paraffins (MCCPs): A Review" (PDF). Environmental Science & Technology. 52 (12): 6743–6760. doi:10.1021/acs.est.7b06459.CS1 maint: multiple names: authors list (link)
  11. ^ Kenne 1996.
  12. ^ "SETAC SciCon Session Summaries – SETAC Globe". Chlorinated Paraffins – State of Science, Insights, Challenges and the Way Forward. Retrieved 10 August 2021.
  13. ^ De Boer 2010, p. 9.
  14. ^ "Candidate List of substances of very high concern for Authorisation: Alkanes, C10–13, chloro (Short Chain Chlorinated Paraffins)". ECHA. Retrieved 2 January 2020.
  15. ^ IARC 1990, p. 70.
  16. ^ Yuan, Bo; McLachlan, Michael S.; Roos, Anna M.; Simon, Malene; Strid, Anna; de Wit, Cynthia A. (9 August 2021). "Long-Chain Chlorinated Paraffins Have Reached the Arctic". Environmental Science & Technology Letters: acs.estlett.1c00470. doi:10.1021/acs.estlett.1c00470.


  • De Boer J., El-Sayed Ali T., Fiedler H., Legler J., Muir D. C., Nikiforov V. A., Tomy G. T., Tsunemi, K. (2010). The handbook of environmental chemistry 10: Chlorinated paraffins. Berlin: Springer-Verlag. ISBN 978-3-642-10760-3.
  • Brooke, DM; Crookes, MJ; Merckel, MD (2009). Environmental risk assessment: long-chain chlorinated paraffins, Bristol, UK: Environment Agency.
  • "Chlorinated paraffins" (PDF). IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. 48: 55–72. 1990. ISBN 978-92-832-1248-5. PMID 2197463.
  • Kellersohn, Thomas (1998). Chlorinated paraffins, in Ullmann’s encyclopedia of industrial chemistry, electronic release, 6th ed. Weinheim: Wiley-VCH.
  • Kenne, Kerstin; Ahlborg, Ulf G (1996). Chlorinated paraffins, IPCS, Environmental Health Criteria 181; Geneva: World Health Organization. ISBN 9241571810.
  • Lassen, Carsten et al. (2014). Survey of short-chain and medium-chain paraffins, Copenhagen: Danish Ministry of Environment, Environmental Protection Agency.
  • Tomy, Gregg T. et al. (1997). Quantifying C10-C13 polychloroalkanes in environmental samples by high-resolution gas chromatography/electron capture negative ion high-resolution mass spectrometry, Analytical Chemistry 69, 2764–2765.

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