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132179

Sigma-Aldrich

2,4,6-Trimethylaniline

98%

Synonym(s):

Mesidine

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About This Item

Linear Formula:
(CH3)3C6H2NH2
CAS Number:
Molecular Weight:
135.21
Beilstein:
636559
EC Number:
MDL number:
UNSPSC Code:
12352100
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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Related Categories

Application

  • Synthesis and crystal structures of N,2,4,6-tetra-methyl-anilinium tri-fluoro-methane-sulfonate and N-iso-propyl-idene-N,2,4,6-tetra-methyl-anilinium tri-fluoro-methane-sulfonate.: This study presents the synthesis and structural analysis of two compounds derived from 2,4,6-Trimethylaniline, contributing to understanding its role in organic synthesis and crystal engineering (Stewart et al., 2024).
  • Analysis of aromatic amines in human urine using comprehensive multi-dimensional gas chromatography-mass spectrometry (GCxGC-MS).: This paper explores advanced analytical techniques for detecting aromatic amines, including 2,4,6-Trimethylaniline, demonstrating its relevance in environmental and biological studies (Lorenzo-Parodi et al., 2024).
  • Efficient Rhodium-Catalyzed Multicomponent Reaction for the Synthesis of Novel Propargylamines.: This research highlights the use of 2,4,6-Trimethylaniline in developing new catalytic methods, showcasing its importance in pharmaceutical intermediate synthesis (Rubio-Pérez et al., 2015).

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Mario Thevis et al.
Journal of the American Society for Mass Spectrometry, 14(6), 658-670 (2003-06-05)
The diuretic agents bumetanide, xipamide, indapamide, and related compounds were investigated in order to determine the effect of different ionization sites on their collisionally activated dissociation and the corresponding fragmentation pathways. Therefore, analytes were selectively alkylated, and structural analogues as
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
L Alvarez-Rodriguez et al.
Journal of AOAC International, 82(4), 937-947 (1999-08-13)
A flow-injection (FI) spectrophotometric system is proposed for the determination of phenols and carbamates. In the FI manifolds, the solutions of phenols or carbamates (the latter after hydrolysis with NaOH) were injected into a diazonium ion carrier stream at pH
L Alvarez-Rodríguez et al.
The Analyst, 122(5), 459-463 (1997-05-01)
The spectrophotometric determination of the carbamate pesticides carbaryl, bendiocarb, carbofuran, methiocarb, promecarb and propoxur is proposed. The pesticides are hydrolyzed in alkaline medium to 1-naphthol or phenolates, which are coupled with diazotized trimethylaniline (TMA) in a sodium dodecyl sulfate micellar
Ariadna Garza-Ortiz et al.
Inorganic chemistry, 47(15), 6964-6973 (2008-07-03)
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

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