149381
2,6-Diethylaniline
98%
Synonym(s):
2-Amino-1,3-diethylbenzene
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About This Item
Linear Formula:
(C2H5)2C6H3NH2
CAS Number:
Molecular Weight:
149.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-445-7
Beilstein/REAXYS Number:
1423626
MDL number:
Assay:
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
Related Categories
General description
The 2,6-diethylaniline complexes with iodine, as a sigma-acceptor, were studied spectrophotometrically in chloroform, dichloromethane and carbontetrachloride solutions.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
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
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Urinary biomonitoring for alachlor exposure in commercial pesticide applicators by immunoassay.
R E Biagini et al.
Bulletin of environmental contamination and toxicology, 54(2), 245-250 (1995-02-01)
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
Q Li et al.
Mutation research, 395(2-3), 151-157 (1998-02-18)
N,N-Diethylaniline is a reagent used in organic synthesis and is an important intermediate in the manufacturing of dyes. To evaluate its genotoxicity, we examined whether it can induce sister chromatid exchanges (SCEs) in human lymphocytes. We found that N,N-diethylaniline significantly
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
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