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Merck
CN

07-4260

Sigma-Aldrich

N,N-Dimethylaniline

SAJ first grade, ≥99.0%

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About This Item

Linear Formula:
C6H5N(CH3)2
CAS Number:
121-69-7
Molecular Weight:
121.18
Beilstein:
507140
MDL number:
MFCD00008304
UNSPSC Code:
12352100
PubChem Substance ID:
329748438

Key Documents

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grade

SAJ first grade

Assay

≥99.0%

form

liquid

availability

available only in Japan

refractive index

n20/D 1.557 (lit.)

pH

7.4 (20 °C, 1.2 g/L)

bp

193-194 °C (lit.)

mp

1.5-2.5 °C (lit.)

density

0.956 g/mL at 25 °C (lit.)

SMILES string

CN(C)c1ccccc1

InChI

1S/C8H11N/c1-9(2)8-6-4-3-5-7-8/h3-7H,1-2H3

InChI key

JLTDJTHDQAWBAV-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - Carc. 2

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

143.6 °F

Flash Point(C)

62 °C

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
A3022
A3736
A1443
A1190
A9143

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Sergei I Snovida et al.
Journal of the American Society for Mass Spectrometry, 19(8), 1138-1146 (2008-05-31)
This study demonstrates the application of 2,5-dihydrohybenzoic acid/aniline (DHB/An) and 2,5-dihydroxybenzoic acid/N,N-dimethylaniline (DHB/DMA) matrices for automated identification and quantitative analysis of native oligosaccharides by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS). Both matrices are shown to be superior to pure DHB
R J Berckmans et al.
Clinical chemistry, 34(7), 1451-1455 (1988-07-01)
In this simple, sensitive, and rapid enzymatic method for the determination of oxalate in urine or plasma, oxalate oxidase (EC 1.2.3.4) prepared from barley seedlings is used to convert oxalate to carbon dioxide and hydrogen peroxide, which is determined photometrically
Sergei I Snovida et al.
Rapid communications in mass spectrometry : RCM, 21(22), 3711-3715 (2007-10-24)
The use of a novel 2,5-dihydroxybenzoic acid/N,N-dimethylaniline (DHB/DMA) matrix-assisted laser desorption/ionization (MALDI) matrix for detection and quantitative analysis of native N-linked oligosaccharides was investigated in this study. Substantial improvements in sensitivity were observed relative to the signals obtained with a
Chunsen Li et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(34), 8492-8503 (2009-03-27)
Two types of tertiary amine oxidation processes, namely, N-dealkylation and N-oxygenation, by compound I (Cpd I) of cytochrome P450 are studied theoretically using hybrid DFT calculations. All the calculations show that both N-dealkylation and N-oxygenation of trimethylamine (TMA) proceed preferentially
Subashani Maniam et al.
Organic letters, 10(10), 1885-1888 (2008-04-16)
Cyclodextrin [2]rotaxanes have been prepared by coupling dimethylanilines with dicarboxylic acids using DMT-MM, in aqueous solutions of alpha-cyclodextrin, and the example illustrated shows unusual fluorescence emission and other spectroscopic behavior characteristic of the formation of molecular wires in solution, similar
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