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Merck
CN

36765

2,6-Diethylaniline

PESTANAL®, analytical standard

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
EC Number:
209-445-7
UNSPSC Code:
41116107
PubChem Substance ID:
329755501
Beilstein/REAXYS Number:
1423626
MDL number:
MFCD00007753

Key Documents

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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

grade

analytical standard

vapor pressure

0.02 mmHg ( 20 °C)

product line

PESTANAL®

assay

98-100% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

refractive index

n20/D 1.545 (lit.)

bp

243 °C (lit.)

density

0.906 g/mL at 25 °C (lit.)

application(s)

agriculture
environmental

format

neat

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

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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Certificates of Analysis (COA)

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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
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
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
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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