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132179

Sigma-Aldrich

2,4,6-Trimethyl-anilin

98%

Synonym(e):

Mesidin

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About This Item

Lineare Formel:
(CH3)3C6H2NH2
CAS-Nummer:
88-05-1
Molekulargewicht:
135.21
Beilstein:
636559
EG-Nummer:
201-794-3
MDL-Nummer:
MFCD00007740
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24847550
NACRES:
NA.22

Qualitätsniveau

200

Assay

98%

Form

liquid

Brechungsindex

n20/D 1.551 (lit.)

bp

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

Dichte

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

InChIKey

KWVPRPSXBZNOHS-UHFFFAOYSA-N

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Verwandte Kategorien

Anwendung

  • 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).

Piktogramme

Skull and crossbones
GHS06

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

204.8 °F - closed cup

Flammpunkt (°C)

96 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCL6514
BCCK5353
BCCD5454
BCCJ7640
BCCD1218

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2,4,6-Trimethyl-m-phenylendiamin 96%

Sigma-Aldrich

263885

2,4,6-Trimethyl-m-phenylendiamin

4-Brom-2,6-dimethylanilin 98%

Sigma-Aldrich

192376

4-Brom-2,6-dimethylanilin

2,6-Dimethylanilin 99%

Sigma-Aldrich

D146005

2,6-Dimethylanilin

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
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)
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
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