Skip to Content
Merck
CN

137863

3,5-Dimethylaniline

98%

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
(CH3)2C6H3NH2
CAS Number:
108-69-0
Molecular Weight:
121.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848222
EC Number:
203-607-0
Beilstein/REAXYS Number:
507051
MDL number:
MFCD00007813
Assay:
98%
Form:
liquid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

MKARNSWMMBGSHX-UHFFFAOYSA-N

InChI

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

SMILES string

Cc1cc(C)cc(N)c1

assay

98%

form

liquid

Quality Level

200

bp

104-105 °C/14 mmHg (lit.)

mp

7-9 °C

density

0.972 g/mL at 25 °C (lit.)

Related Categories

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

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

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SDBB6690
SDBB5739
SDBB3724
BCCH1870
BCCJ5765

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

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)
Chemical preparation of polyaniline and its derivatives by using cerium (IV) sulfate.
Yan H and Toshima N.
Synt. Metals, 69(1), 151-152 (1995)
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
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
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
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