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
Beilstein:
1423626
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
vapor pressure
0.02 mmHg ( 20 °C)
Quality Level
Assay
98%
refractive index
n20/D 1.545 (lit.)
bp
243 °C (lit.)
density
0.906 g/mL at 25 °C (lit.)
SMILES string
CCc1cccc(CC)c1N
InChI
1S/C10H15N/c1-3-8-6-5-7-9(4-2)10(8)11/h5-7H,3-4,11H2,1-2H3
InChI key
FOYHNROGBXVLLX-UHFFFAOYSA-N
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General description
The 2,6-diethylaniline complexes with iodine, as a sigma-acceptor, were studied spectrophotometrically in chloroform, dichloromethane and carbontetrachloride solutions.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
239.0 °F - closed cup
Flash Point(C)
115 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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
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
Tarek M El-Gogary et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 66(1), 94-101 (2006-07-04)
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 constants and effect of solvent have been determined. Spectral characteristics and formation constants
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)
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