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36766

2,6-Dimethylaniline

PESTANAL®, analytical standard

Synonym(s):

2,6-Xylidine, 2-Amino-1,3-dimethylbenzene, 2-Amino-m-xylene

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About This Item

Linear Formula:
(CH3)2C6H3NH2
CAS Number:
Molecular Weight:
121.18
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
201-758-7
Beilstein/REAXYS Number:
636332
MDL number:
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grade

analytical standard

Quality Level

vapor pressure

<0.01 mmHg ( 20 °C)

product line

PESTANAL®

assay

~99%

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

refractive index

n20/D 1.560 (lit.)

bp

214 °C/739 mmHg (lit.)

mp

10-12 °C (lit.)

density

0.984 g/mL at 25 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

Cc1cccc(C)c1N

InChI

1S/C8H11N/c1-6-4-3-5-7(2)8(6)9/h3-5H,9H2,1-2H3

InChI key

UFFBMTHBGFGIHF-UHFFFAOYSA-N

Legal Information

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

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This Item
D146005D145807137863
format

neat

format

-

format

-

format

-

assay

~99%

assay

99%

assay

99%

assay

98%

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

technique(s)

-

technique(s)

-

grade

analytical standard

grade

-

grade

-

grade

-

product line

PESTANAL®

product line

-

product line

-

product line

-

mp

10-12 °C (lit.)

mp

10-12 °C (lit.)

mp

2.5 °C (lit.)

mp

7-9 °C


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Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

195.8 °F - closed cup

flash_point_c

91 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter



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Bozena Kaczmarczyk et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(2), 369-376 (2007-03-03)
The reaction of aniline with p-dibenzoylobenzene (K1) can lead to Z/Z, Z/E and E/E isomers however the only Z/Z and E/E were formed. At room temperature these isomers may be separated, thus the corresponding FTIR spectra could be recorded. The
Nalinrut Masomboon et al.
Journal of hazardous materials, 192(1), 347-353 (2011-06-08)
The kinetics of 2,6-dimethylaniline degradation by Fenton process, electro-Fenton process and photoelectro-Fenton process was investigated. This study attempted to eliminate the potential interferences from intermediates by making a kinetics comparison of Fenton, electro-Fenton and photoelectro-Fenton methods through use initial rate
Ming-Wei Chao et al.
Toxicological sciences : an official journal of the Society of Toxicology, 130(1), 48-59 (2012-07-27)
Several alkylanilines with structures more complex than toluidines have been associated epidemiologically with human cancer. Their mechanism of action remains largely undetermined, and there is no reported evidence that it replicates that of multicyclic aromatic amines even though the principal



Global Trade Item Number

SKUGTIN
36766-1G-R04061831827446
36766-250MG-R04061841423133
36766-250MGR04061841390763

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