Difference between revisions of "2,4,6-tri-tert-butylphenol"

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{{Definition|title=2,4,6-tri-''tert''-butylphenol
 
{{Definition|title=2,4,6-tri-''tert''-butylphenol
  
|definition=2,4,6-tri-''tert''-butylphenol is a chemical which has been confused with an other chemical called dodecylphenol which has the same molecular formula but a different structure.
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|definition=2,4,6-tri-''tert''-butylphenol is a chemical which has been confused with an other chemical called dodecylphenol which has the same molecular formula but a different structure<ref name=O>[https://www.ospar.org/documents?v=6977 OSPAR background document on 2,4,6-tri-''tert''-butylphenol]</ref>. }}
<ref name = OECD>[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf  OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]</ref>
 
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== Notes ==
 
== Notes ==
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Less than 50 tonnes of 2,4,6-tri-''tert''-butylphenol is used in the EU each year. It can be used as an intermediate in the production of antioxidants, which are used in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by discharges. <ref name = OECD>[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf  OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]</ref>
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Less than 50 tonnes of 2,4,6-tri-''tert''-butylphenol are used in the EU each year. It can be used as an intermediate in the production of antioxidants, in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by discharges<ref name=O/>.  
  
It is a chemical with a low volatility, making it unlike to enter the atmosphere, where it would be rapidly degraded.  
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It is a chemical with a low [[volatile|volatility]], making it unlikely that it enters the atmosphere, where it would be degraded rapidly. It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments. Both in water and sediments, it isn't readily (bio)degraded and considered [[persistent]].   
It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments, in both mediums it isn't readily (bio)degraded and considered persistent.   
 
 
It has a high tendency to [[bioaccumulation|bioaccumulate]] and is likely to [[biomagnification|biomagnify]] through [[food chain|food chains]].
 
It has a high tendency to [[bioaccumulation|bioaccumulate]] and is likely to [[biomagnification|biomagnify]] through [[food chain|food chains]].
In fresh water is has been shown to be acutely toxic for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively.  
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There is currently no information available the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It is however estimated (by modelling the emissions) that concentrations might be as high as 0,32 µg/l.<ref name = OECD>[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf  OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]</ref>
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In fresh water is has been shown to be acutely [[toxic]] for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively.  
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There is currently little information available on the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It has been estimated (by modelling the emissions) that concentrations might reach 0,32 µg/l<ref name=O/>.
 
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== See also ==
 
== See also ==
  
[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf OSPAR background document on 2,4,6-tri-''tert''-butylphenol]  
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[https://pubchem.ncbi.nlm.nih.gov/compound/2_4_6-Tri-tert-butylphenol pubchem 2,4,6-tri-''tert''-butylphenol]  
 
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{{author
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|AuthorFullName=Daphnis De Pooter
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|AuthorName=Daphnisd}}
  
 
==References==
 
==References==
 
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<references/>
  
[[Category:Coastal and marine pollution]]
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[[Category:Toxicity chemicals]]

Latest revision as of 12:58, 9 August 2020

Definition of 2,4,6-tri-tert-butylphenol:
2,4,6-tri-tert-butylphenol is a chemical which has been confused with an other chemical called dodecylphenol which has the same molecular formula but a different structure[1].
This is the common definition for 2,4,6-tri-tert-butylphenol, other definitions can be discussed in the article

Notes

2,4,6-tri-tert-butylphenol
6PPD
Formula
C18H300

Less than 50 tonnes of 2,4,6-tri-tert-butylphenol are used in the EU each year. It can be used as an intermediate in the production of antioxidants, in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by discharges[1].

It is a chemical with a low volatility, making it unlikely that it enters the atmosphere, where it would be degraded rapidly. It has a low water solubility (0,521 mg/l) and a strong tendency to adsorb to soils and sediments. Both in water and sediments, it isn't readily (bio)degraded and considered persistent. It has a high tendency to bioaccumulate and is likely to biomagnify through food chains.

In fresh water is has been shown to be acutely toxic for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. There is currently little information available on the levels of 2,4,6-tri-tert-butylphenol in the marine environment. It has been estimated (by modelling the emissions) that concentrations might reach 0,32 µg/l[1].


Environmental standards and legislation

Included in the OSPAR list of substances of priority action


See also

pubchem 2,4,6-tri-tert-butylphenol


The main author of this article is Daphnis De Pooter
Please note that others may also have edited the contents of this article.

Citation: Daphnis De Pooter (2020): 2,4,6-tri-tert-butylphenol. Available from http://www.coastalwiki.org/wiki/2,4,6-tri-tert-butylphenol [accessed on 25-11-2024]


References