Home > Publications database > Estrogen-active nonylphenols from an isomer-specific viewpoint: a systematic numbering system and future trends > print

001     49810
005     20190625111110.0
024 7 _ |2 pmid
|a pmid:16341851
024 7 _ |2 DOI
|a 10.1007/s00216-005-0181-8
024 7 _ |2 WOS
|a WOS:000234299600027
024 7 _ |a altmetric:13594665
|2 altmetric
037 _ _ |a PreJuSER-49810
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Biochemical Research Methods
084 _ _ |2 WoS
|a Chemistry, Analytical
100 1 _ |a Günther, K.
|b 0
|u FZJ
|0 P:(DE-Juel1)129325
245 _ _ |a Estrogen-active nonylphenols from an isomer-specific viewpoint: a systematic numbering system and future trends
260 _ _ |a Berlin
|b Springer
|c 2006
300 _ _ |a 542 - 546
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Analytical and Bioanalytical Chemistry
|x 1618-2642
|0 8664
|y 2
|v 384
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a 4-Nonylphenols (NPs) are very important environmentally relevant substances. They are persistent, toxic, endocrine-disrupting chemicals that are priority hazardous substances of the EU Water Framework Directive. NPs are degradation products of 4-nonylphenol ethoxylates (NPEs), a widely used group of nonionic surfactants. The technical synthesis of NP leads to a complex mixture of NPs consisting of isomeric compounds that have different branched nonyl side chains. It has recently become clear that an isomer-specific view is absolutely necessary when it comes to correctly evaluating the biological effects of NPs and their behavior in the environment, including degradation processes. To rationalize the identification of individual NP isomers in scientific studies, we have developed a numbering system for all possible NP isomers that follows the IUPAC rules of substituent characterization in alkylphenols. The 211 possible constitutional isomers of NP are numbered according to a hierarchical and logical system. In the future, multidimensional coupling systems--for example GCxGC-TOF-MS--will be needed to study these highly complex class of substances.
536 _ _ |a Terrestrische Umwelt
|c P24
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK407
|x 0
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Chemistry, Organic: methods
650 _ 2 |2 MeSH
|a Chemistry, Organic: trends
650 _ 2 |2 MeSH
|a Estrogens: chemistry
650 _ 2 |2 MeSH
|a Isomerism
650 _ 2 |2 MeSH
|a Molecular Structure
650 _ 2 |2 MeSH
|a Phenols: chemistry
650 _ 2 |2 MeSH
|a Terminology as Topic
650 _ 7 |0 0
|2 NLM Chemicals
|a Estrogens
650 _ 7 |0 0
|2 NLM Chemicals
|a Phenols
650 _ 7 |a J
|2 WoSType
700 1 _ |a Kleist, E.
|b 1
|u FZJ
|0 P:(DE-Juel1)129345
700 1 _ |a Thiele, B.
|b 2
|u FZJ
|0 P:(DE-Juel1)129410
773 _ _ |a 10.1007/s00216-005-0181-8
|g Vol. 384, p. 542 - 546
|p 542 - 546
|q 384<542 - 546
|0 PERI:(DE-600)1459122-4
|t Analytical and bioanalytical chemistry
|v 384
|y 2006
|x 1618-2642
856 7 _ |u http://dx.doi.org/10.1007/s00216-005-0181-8
909 C O |o oai:juser.fz-juelich.de:49810
|p VDB
913 1 _ |k P24
|v Terrestrische Umwelt
|l Terrestrische Umwelt
|b Erde und Umwelt
|0 G:(DE-Juel1)FUEK407
|x 0
914 1 _ |y 2006
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |k ICG-III
|l Phytosphäre
|d 31.12.2006
|g ICG
|0 I:(DE-Juel1)VDB49
|x 0
970 _ _ |a VDB:(DE-Juel1)77906
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)IBG-2-20101118
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IBG-2-20101118
981 _ _ |a I:(DE-Juel1)ICG-3-20090406

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