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137863

Sigma-Aldrich

3,5-Dimethylaniline

98%

Sinónimos:

1-Amino-3,5-dimethylbenzene, 3,5-Xylidine, 5-Amino-m-xylene

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About This Item

Fórmula lineal:
(CH3)2C6H3NH2
Número de CAS:
108-69-0
Peso molecular:
121.18
Beilstein/REAXYS Number:
507051
EC Number:
203-607-0
MDL number:
MFCD00007813
UNSPSC Code:
12352100
PubChem Substance ID:
24848222
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.557 (lit.)

bp

104-105 °C/14 mmHg (lit.)

mp

7-9 °C

density

0.972 g/mL at 25 °C (lit.)

SMILES string

Cc1cc(C)cc(N)c1

InChI

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

InChI key

MKARNSWMMBGSHX-UHFFFAOYSA-N

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General description

3,5-Dimethylaniline is the reagent commonly useful in the manufacture of dyes. It undergoes polymerization in the presence of cerium(IV) sulfate as an oxidant.

Application

3,5-Dimethylaniline was used in the synthesis of chiral packing materials for high performance liquid chromatography.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - STOT RE 2

Storage Class

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

wgk_germany

WGK 3

flash_point_f

215.1 °F - closed cup

flash_point_c

101.7 °C - closed cup

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Chemical preparation of polyaniline and its derivatives by using cerium (IV) sulfate.
Yan H and Toshima N.
Synt. Metals, 69(1), 151-152 (1995)
The enantiomeric recognition of dihydropyrimidonic compounds by chiral selectors derived from 4-or 2-chloro-3, 5-dinitrobenzoic acid.
Gazic I, et al.
Tetrahedron Asymmetry, 16(6), 1175-1182 (2005)
Soumya Mukherjee et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 24(45), 11771-11778 (2018-05-29)
Fluorous organic building blocks were utilized to develop two self-assembled, hydrophobic, fluorinated porous organic polymers (FPOPs), namely, FPOP-100 and FPOP-101. Comprehensive mechanical analyses of these functionalised triazine network polymers marked the introduction of mechanical stiffness among all porous organic network
Robert J Strife et al.
Journal of chromatography. A, 1216(41), 6970-6973 (2009-09-08)
The assessment of human exposure to specific isomers of dimethylanilines (DMA's) is of interest for the evaluation of potential exposure-health outcome relationships. Improved analytical methods will help in identifying the environmental sources of such exposures. The separation of all six
Ming-Wei Chao et al.
Toxicological sciences : an official journal of the Society of Toxicology, 141(1), 300-313 (2014-06-29)
Epidemiological studies have demonstrated extensive human exposure to the monocyclic aromatic amines, particularly to 3,5-dimethylaniline, and found an association between exposure to these compounds and risk for bladder cancer. Little is known about molecular mechanisms that might lead to the
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