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36766

2,6-Dimethylaniline

PESTANAL®, analytical standard

Sinónimos:

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

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Fórmula lineal:
(CH3)2C6H3NH2
Número CAS:
87-62-7
Peso molecular:
121.18
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755502
EC Number:
201-758-7
Beilstein/REAXYS Number:
636332
MDL number:
MFCD00007747

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InChI key

UFFBMTHBGFGIHF-UHFFFAOYSA-N

InChI

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

SMILES string

Cc1cccc(C)c1N

grade

analytical standard

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

Quality Level

100

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

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1 of 4

Este artículo
D146005442327240915
2,6-Dimethylaniline PESTANAL&#174;, analytical standard

Supelco

36766

2,6-Dimethylaniline

2,6-Dimethylaniline 99%

Sigma-Aldrich

D146005

2,6-Dimethylaniline

2,6-Dimethylaniline analytical standard

Supelco

442327

2,6-Dimethylaniline

2,4-Dimethylaniline &#8805;99%

Sigma-Aldrich

240915

2,4-Dimethylaniline

format

neat

format

-

format

neat

format

-

assay

~99%

assay

99%

assay

>99% (GC)

assay

≥99%

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

grade

analytical standard

grade

-

grade

analytical standard

grade

-

product line

PESTANAL®

product line

-

product line

-

product line

-

vapor pressure

<0.01 mmHg ( 20 °C)

vapor pressure

<0.01 mmHg ( 20 °C)

vapor pressure

<0.01 mmHg ( 20 °C)

vapor pressure

0.16 mmHg ( 25 °C)

Legal Information

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

signalword

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

Clase de almacenamiento

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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Certificados de análisis (COA)

Lot/Batch Number
BCCJ6526
BCCH5486
BCBW2126
BCBS3628V

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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
Paul L Skipper et al.
Chemical research in toxicology, 19(8), 1086-1090 (2006-08-22)
Aromatic amines such as 2-naphthylamine and 4-aminobiphenyl are established human bladder carcinogens. Experimental evidence for carcinogenicity of monocylic aromatic amines is limited mostly to other organs, but a recent epidemiologic study of bladder cancer found that 2,6-dimethyl- (2,6-DMA), 3,5-dimethyl- (3,5-DMA)
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
Ana P Ferreira Gregorio et al.
Mycological research, 110(Pt 2), 161-168 (2006-02-21)
During the interaction of two tropical agaric fungi, Marasmius pallescens and Marasmiellus troyanus, on agar media, initial deadlock between the two mycelia was ultimately followed by take-over by M. troyanus. When shaken liquid cultures of these two fungi were mixed
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