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149381

Sigma-Aldrich

2,6-Diethylaniline

98%

Synonym(s):

2-Amino-1,3-diethylbenzene

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About This Item

Linear Formula:
(C2H5)2C6H3NH2
CAS Number:
579-66-8
Molecular Weight:
149.23
Beilstein/REAXYS Number:
1423626
EC Number:
209-445-7
MDL number:
MFCD00007753
UNSPSC Code:
12352100
PubChem Substance ID:
24848950
NACRES:
NA.22

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.)

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
M Taningher et al.
Toxicology, 85(2-3), 117-122 (1993-12-31)
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
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