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Subject:
Phenol. Origin - and how to avoid ?
Category: Science Asked by: alsinger-ga List Price: $17.77 |
Posted:
19 Apr 2006 05:56 PDT
Expires: 19 May 2006 05:56 PDT Question ID: 720541 |
I know that phenol is something to avoid. What is the origin (how does it develop) ? How can it be avoided or kept at a minimum (maybe there are some regulations indicating maximum permitted) ? It is in particular phenol related to coffee which has my interest, but phenol in other products can also be mentioned. |
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There is no answer at this time. |
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Subject:
Re: Phenol. Origin - and how to avoid ?
From: myoarin-ga on 19 Apr 2006 14:01 PDT |
The above is apparently from this or a related website: http://www.atsdr.cdc.gov/tfacts115.html |
Subject:
Re: Phenol. Origin - and how to avoid ?
From: zeroentropy-ga on 21 Apr 2006 12:22 PDT |
http://en.wikipedia.org/wiki/Phenol |
Subject:
Re: Phenol. Origin - and how to avoid ?
From: seavun-ga on 21 May 2006 01:38 PDT |
1.Metabolic activation of phenol by human myeloperoxidase and horseradish peroxidase http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=3023815&dopt=Abstract The oxidation of phenol catalyzed by human myeloperoxidase and horseradish peroxidase resulted in extensive binding of phenol-derived metabolites to boiled rat liver protein. This binding paralleled closely the removal of phenol from the incubations and was inhibited from 83 to 99% by the addition of the antioxidants, ascorbate and glutathione, suggesting that metabolism and binding were occurring via a one-electron oxidation pathway. Metabolic studies employing both human myeloperoxidase and horseradish peroxidase resulted in the identification of 4,4'-biphenol and diphenoquinone as the principal identifiable metabolites. The addition of reduced glutathione to incubations containing horseradish peroxidase resulted in the formation of two conjugate species. These conjugate species were identified by fast atom bombardment mass spectrometry to be glutathione conjugates of diphenoquinone. The major gluthathione conjugate was identified as 3-(glutathion-S-yl)-4,4'-biphenol by NMR spectroscopy. These results suggest that the formation of highly reactive species through the peroxidase-mediated metabolism of phenol and other phenolic compounds could play an important role in the hematopoietic toxicity observed during chronic benzene exposure. 2.Scientists Warns 'No-Phenol' Digestive Enzymes 'Dangerous' Autism Treatment Enzymes, amino acids and phenol in autism http://www.autismtoday.com/articles/nophenoldangerous.html 3.Metabolic pathways of the diseased potato http://www.scri.sari.ac.uk/TiPP/pps/Chart.pdf |
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