Skip to Content
Merck
All Photos(2)

Documents

149381

Sigma-Aldrich

2,6-Diethylaniline

98%

Synonym(s):

2-Amino-1,3-diethylbenzene

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
(C2H5)2C6H3NH2
CAS Number:
579-66-8
Molecular Weight:
149.23
Beilstein:
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

Looking for similar products? Visit Product Comparison Guide

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

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

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

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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)
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
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service