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Merck
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409928

Sigma-Aldrich

N,N-Dimethyl-o-toluidine

99%

Sinónimos:

2,N,N-Trimethylaniline, 2-Methyl-N,N-dimethylaniline, N,N,2-Trimethylaniline, N,N,2-Trimethylbenzenamine, N,N-Dimethyl-2-methylaniline, N,N-Dimethyl-o-methylaniline, o-Methyl-N,N-dimethylaniline, o-Methyldimethylaniline

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About This Item

Fórmula lineal:
CH3C6H4N(CH3)2
Número de CAS:
609-72-3
Peso molecular:
135.21
EC Number:
210-199-8
MDL number:
MFCD00035789
UNSPSC Code:
12352100
PubChem Substance ID:
24865677
NACRES:
NA.22

Quality Level

200

assay

99%

form

liquid

refractive index

n20/D 1.525 (lit.)

bp

76 °C/18 mmHg (lit.)

density

0.929 g/mL at 25 °C (lit.)

SMILES string

CN(C)c1ccccc1C

InChI

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

InChI key

JDEJGVSZUIJWBM-UHFFFAOYSA-N

General description

Complexing ability of N,N-dimethyl-o-toluidine with iodine has been evaluated. Influence of tetramethylethylenediamine on the lithiation of o- and p-N,N-dimethyl-o-toluidine has been studied.

Application

N,N-Dimethyl-o-toluidine may be employed as starting reagent for the synthesis of roseoflavin.

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - STOT RE 2

Storage Class

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

wgk_germany

WGK 1

flash_point_f

145.4 °F - closed cup

flash_point_c

63 °C - closed cup

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Photo-dynamics of roseoflavin and riboflavin in aqueous and organic solvents.
Zirak P, et al.
Chemical Physics, 358(1), 111-122 (2009)
Effect of tetramethylethylenediamine on the metalation of o- and p-N,N-dimethyltoluidines with n-butyllithium. Deuteration and electrophilic condensation of intermediate lithioamines.
Ludt RE, et al.
The Journal of Organic Chemistry, 35(5), 1288-1296 (1970)
Molecular Complexes and Their Spectra. X. Molecular Complexes between Iodine and N, N-Dimethylaniline Derivatives.
Tsubomura H.
Journal of the American Chemical Society, 82(1), 40-45 (1960)
Ségolène Villotte et al.
Molecules (Basel, Switzerland), 25(1) (2020-01-08)
Iodonium salts are well established photoacid generators, cationic photoinitiators, as well as additives commonly used in photoredox catalytic cycles. However, as a strong limitation, iodonium salts are characterized by low light absorption properties for λ > 300 nm so that

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