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线性分子式:
(C2H5)2C6H3NH2
化学文摘社编号:
分子量:
149.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-445-7
Beilstein/REAXYS Number:
1423626
MDL number:
产品名称
2,6-二乙基苯胺, 98%
InChI key
FOYHNROGBXVLLX-UHFFFAOYSA-N
InChI
1S/C10H15N/c1-3-8-6-5-7-9(4-2)10(8)11/h5-7H,3-4,11H2,1-2H3
SMILES string
CCc1cccc(CC)c1N
vapor pressure
0.02 mmHg ( 20 °C)
assay
98%
refractive index
n20/D 1.545 (lit.)
bp
243 °C (lit.)
density
0.906 g/mL at 25 °C (lit.)
Quality Level
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General description
在氯仿、二氯甲烷和四氯化碳溶液中,2,6-二乙基苯胺与碘的复合物(作为σ受体)已通过分光光度法进行了研究。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
239.0 °F - closed cup
flash_point_c
115 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
R Galati et al.
Anticancer research, 18(2A), 979-982 (1998-06-06)
In order to estimate the environmental risk of the use of Alachlor, experiments on laboratory animals were conducted. Alachlor and 2,6 diethylaniline content in blood serum was quantified. Three groups of male ACI/T rats and C3H/FEJ mice were treated with
L Durães Sette et al.
Applied microbiology and biotechnology, 64(5), 712-717 (2004-01-17)
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 were able to grow at an alachlor concentration of
Yongxia Zhang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 85(1), 134-138 (2011-11-01)
In this letter, we report the first observation of metal-enhanced exciplex fluorescence, observed from anthracene in the presence of diethylaniline. Anthracene in the presence of diethylaniline in close proximity to Silver Island Films (SIFs) shows enhanced monomer and exciplex emission
S J Logusch et al.
Journal of agricultural and food chemistry, 47(5), 2125-2129 (1999-12-20)
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 studies. ADEPS formation in rodents is
A D Kligerman et al.
Mutation research, 441(1), 95-101 (1999-05-04)
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 cytogenetic damage could be used
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