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Sigma-Aldrich

2,4,6-Trimethylaniline

98%

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Synonym(s):
Mesidine
Linear Formula:
(CH3)3C6H2NH2
CAS Number:
Molecular Weight:
135.21
Beilstein:
636559
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.551 (lit.)

bp

108-110 °C/11 mmHg (lit.)
233 °C (lit.)

density

0.963 g/mL at 25 °C (lit.)

SMILES string

Cc1cc(C)c(N)c(C)c1

InChI

1S/C9H13N/c1-6-4-7(2)9(10)8(3)5-6/h4-5H,10H2,1-3H3

InChI key

KWVPRPSXBZNOHS-UHFFFAOYSA-N

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1 of 4

This Item
M15001192376458880
form

liquid

form

liquid

form

solid

form

(Powder or Solid or Crystals or Semi-Solid or Liquid)

refractive index

n20/D 1.551 (lit.)

refractive index

n20/D 1.565 (lit.)

refractive index

-

refractive index

n20/D 1.575 (lit.)

bp

108-110 °C/11 mmHg (lit.), 233 °C (lit.)

bp

248-249 °C (lit.)

bp

-

bp

172-173 °C/24 mmHg (lit.)

density

0.963 g/mL at 25 °C (lit.)

density

1.065 g/mL at 25 °C (lit.)

density

-

density

1.313 g/mL at 25 °C (lit.)

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

204.8 °F - closed cup

Flash Point(C)

96 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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The synthetic, spectroscopic, structural, and biological studies of a bis(arylimino)pyridine Ru(III) chloride compound containing the ligand, 2,6-bis(2,4,6-trimethylphenyliminomethyl)pyridine are reported. The bis(arylimino)pyridine ligand, with three donor nitrogen atoms, was synthesized by condensation of 2,6-pyridinedicarboxaldehyde with 2,4,6-trimethylaniline. The Ru(III) complex, with formula
S K Clark et al.
Molecular immunology, 20(12), 1379-1384 (1983-12-01)
Inhibition of the catalytic activity of horseradish peroxidase by rabbit antisera was measured using alternate enzyme substrates. The same general inhibition curve patterns were obtained regardless of the electron donor or hydroperoxide used. In all cases typical biphasic inhibition patterns
2,4,5- and 2,4,6-Trimethylaniline and their hydrochlorides.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 27, 177-188 (1982-04-01)
Inder Pal Singh Kapoor et al.
Journal of hazardous materials, 173(1-3), 173-180 (2009-09-08)
Nitrate and perchlorate salts of 2,4,6-trimethylaniline have been prepared and characterized by X-ray crystallography and gravimetric analyses. Their thermal decomposition has been studied by TG, TG-DSC and ignition/explosion delays. It has been observed that proton transfer from substituted anilinium ion

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