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132179

Sigma-Aldrich

2,4,6-Trimethylaniline

98%

Synonyme(s) :

Mesidine

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About This Item

Formule linéaire :
(CH3)3C6H2NH2
Numéro CAS:
88-05-1
Poids moléculaire :
135.21
Numéro Beilstein :
636559
Numéro CE :
201-794-3
Numéro MDL:
MFCD00007740
Code UNSPSC :
12352100
ID de substance PubChem :
24847550
Nomenclature NACRES :
NA.22

Niveau de qualité

200

Pureté

98%

Forme

liquid

Indice de réfraction

n20/D 1.551 (lit.)

Point d'ébullition

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

Densité

0.963 g/mL at 25 °C (lit.)

Chaîne SMILES 

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

Clé InChI

KWVPRPSXBZNOHS-UHFFFAOYSA-N

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Catégories apparentées

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).

Pictogrammes

Skull and crossbones
GHS06

Mention d'avertissement

Danger

Mentions de danger

H302 + H312,H315,H319,H330

Classification des risques

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

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

204.8 °F - closed cup

Point d'éclair (°C)

96 °C - closed cup

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCL6514
BCCK5353
BCCD5454
BCCJ7640
BCCD1218

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Salma Shirin et al.
Environmental science & technology, 45(24), 10369-10377 (2011-11-05)
Sulfonated anthracenedione dyes are medium priority organic compounds targeted for environmental assessment under the Government of Canada's Chemical Management Plan (CMP). Since organic compounds undergo transformations in environmental matrices, understanding these transformations is critical for a proper assessment of their
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
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)
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
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
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