2,6-二乙基苯胺结构式
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常用名 | 2,6-二乙基苯胺 | 英文名 | 2,6-Diethylaniline |
|---|---|---|---|---|
| CAS号 | 579-66-8 | 分子量 | 149.233 | |
| 密度 | 0.9±0.1 g/cm3 | 沸点 | 244.3±9.0 °C at 760 mmHg | |
| 分子式 | C10H15N | 熔点 | 3-4 °C | |
| MSDS | 中文版 美版 | 闪点 | 123.3±0.0 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
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Ferrocene-based guanidine derivatives: in vitro antimicrobial, DNA binding and docking supported urease inhibition studies.
Eur. J. Med. Chem. 85 , 438-49, (2014) Some novel ferrocenyl guanidines 1-8 were synthesized and characterized by different spectroscopic methods, elemental analysis and single crystal X-rays diffraction techniques. The crystallographic studies revealed that the existence of the strong non-bonding... |
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Further evidence of an inverted region in proton transfer within the benzophenone/substituted aniline contact radical ion pairs; importance of vibrational reorganization energy.
J. Phys. Chem. A 110(20) , 6408-14, (2006) The dynamics of proton transfer within the triplet contact radical ion pair of a variety of substituted benzophenones with N,N-diethylaniline, N,N-dimethyl-p-toluinide, and N,N-diallylaniline are examined in solvents of varying polarity. The correlation of th... |
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Spectroscopic studies of molecular interactions involving 2,6-diethylaniline and N-ethylaniline donors and iodine as an electron acceptor in different solvents.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 66(1) , 94-101, (2007) The charge-transfer complexes of 2,6-diethylaniline (DEA) and N-ethylaniline (NEA) with iodine, as a typical sigma-acceptor were studied spectrophotometrically in chloroform, dichloromethane and carbontetrachloride solutions. Spectral data, formation constant... |
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Biodegradation of alachlor by soil streptomycetes.
Appl. Microbiol. Biotechnol. 64(5) , 712-7, (2004) Streptomycetes resistant to the herbicide alachlor [2-chloro-2',6'-diethyl- N-(methoxymethyl) acetanilide] were used in degradation assays to characterize the products of alachlor biodegradation. Of six strains tested, Streptomyces sp. LS166, LS177, and LS182... |
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Determination of alachlor and its metabolite 2,6-diethylaniline in microbial culture medium using online microdialysis enriched-sampling coupled to high-performance liquid chromatography.
J. Agric. Food Chem. 59(15) , 8078-85, (2011) In this study, a simple and novel microdialysis sampling technique incorporating hollow fiber liquid phase microextraction (HF-LPME) coupled online to high-performance liquid chromatography (HPLC) for the one-step sample pretreatment and direct determination ... |
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Urinary biomonitoring for alachlor exposure in commercial pesticide applicators by immunoassay.
Bull. Environ. Contam. Toxicol. 54(2) , 245-50, (1995)
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Enzymatic synthesis of 4-amino-3,5-diethylphenyl sulfate, a rodent metabolite of alachlor.
J. Agric. Food Chem. 47(5) , 2125-9, (1999) Rat liver tissue homogenates were utilized for in vitro enzymatic conversion of 2,6-diethylaniline (DEA) to the important alachlor metabolite 4-amino-3,5-diethylphenyl sulfate (ADEPS), which was also generated as a radiolabeled standard for use in metabolism ... |
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Lack of alachlor induced DNA damage as assayed in rodent liver by the alkaline elution test.
Toxicology 85(2-3) , 117-22, (1993) Alachlor was studied in vivo for its capability to induce DNA damage, as evaluated by the alkaline elution test. The experiments were performed in mouse and rat liver after acute or subacute intraperitoneal or per os administrations of the chemical at subleth... |
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An evaluation of the feasibility of using cytogenetic damage as a biomarker for alachlor exposure.
Mutat. Res. 441(1) , 95-101, (1999) Alachlor is a widely used herbicide for which there is significant human exposure, principally through groundwater contamination and inhalation. Because alachlor is purported to be carcinogenic and mutagenic, we initiated studies to determine if induced cytog... |
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Metal-enhanced fluorescence exciplex emission
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 85(1) , 134-8, (2012) Graphical abstract Metal-enhanced exciplex formation studied using Silver island films to enhance both monomer and complex (exciplex) formation in the near-field. |