Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Editor

Personal info

View

About

Terms

Javascript disabled

Please enable Javascript support in your browser to use this application.

Instructions on how to enable JavaScript on different browsers can be found here: http://www.google.com/support/bin/answer.py?answer=23852.

[edit this page]

Chemical Compound Review:

AGN-PC-00G76H 2,6-diethylaniline

Synonyms: SureCN262868, ACMC-1AZ3X, CCRIS 2688, AG-G-04995, ANW-32844, ...

Osano, O. et al., Newsome, W.H. et al., Osano, O. et al., El-Gogary, T.M. et al., Taningher, M. et al., et al.

El-Gogary, Diab, El-Tantawy,

Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.

Disease relevance of CCRIS 2688

The most common teratogenic effects observed were edema for alachlor as opposed to axial flexures and eye abnormalities for 2,6-diethylaniline and 2-ethyl-6-methylaniline [1].

High impact information on CCRIS 2688

Alachlor, metolachlor and their respective environmentally stable aniline degradation products, 2,6-diethylaniline and 2-ethyl-6-methylaniline were analyzed in water and sediment samples from 9 sites along River Nzoia, Kenya using gas chromatography [2].
Alachlor and 2,6 diethylaniline content in blood serum was quantified [3].
Rat liver was also studied for DNA damage after administration of 2,6-diethylaniline, one of alachlor's major metabolites [4].
Spectroscopic studies of molecular interactions involving 2,6-diethylaniline and N-ethylaniline donors and iodine as an electron acceptor in different solvents [5].
Alachlor [2-chloro-2',6'-diethyl-N-(methoxymethyl)acetanilide] was determined by hydrolysis to 2,6-diethylaniline with 6N HCl and quantitation of the heptafluorobutyryl derivative by gas chromatography with electron capture detection [6].

References

Developmental disorders in embryos of the frog Xenopus laevis induced by chloroacetanilide herbicides and their degradation products. Osano, O., Admiraal, W., Otieno, D. Environ. Toxicol. Chem. (2002) [Pubmed]
The fate of chloroacetanilide herbicides and their degradation products in the Nzoia Basin, Kenya. Osano, O., Nzyuko, D., Tole, M., Admiraal, W. Ambio. (2003) [Pubmed]
Determination of serum levels of 2,6 diethylaniline in laboratory animal treated with Alachlor. Galati, R., Federico, A., Cortese, G., Zito, R. Anticancer Res. (1998) [Pubmed]
Lack of alachlor induced DNA damage as assayed in rodent liver by the alkaline elution test. Taningher, M., Terranova, M.P., Airoldi, L., Chiappetta, L., Parodi, S. Toxicology (1993) [Pubmed]
Spectroscopic studies of molecular interactions involving 2,6-diethylaniline and N-ethylaniline donors and iodine as an electron acceptor in different solvents. El-Gogary, T.M., Diab, M.A., El-Tantawy, S.F. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy (2007) [Pubmed]
Determination of residues of alachlor and its metabolite in corn, soybeans, and potatoes as heptafluorobutyryl-2,6-diethylaniline. Newsome, W.H., Collins, P., Lewis, D. Journal - Association of Official Analytical Chemists. (1986) [Pubmed]

Contributions to this collaborative article are from individual authors of WikiGenes or mined by the WikiGenes Data Mining Engine from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.About WikiGenes Open Access Licence Privacy Policy Terms of Use apsburg

The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

Editor

Share