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Merck

65760

N-Methylaniline

purum, ≥98.0% (GC)

Synonym(s):

Monomethylaniline

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About This Item

Linear Formula:
C6H5NHCH3
CAS Number:
100-61-8
Molecular Weight:
107.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329760102
EC Number:
202-870-9
Beilstein/REAXYS Number:
741982
MDL number:
MFCD00008283

Key Documents

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Product Name

N-Methylaniline, purum, ≥98.0% (GC)

InChI key

AFBPFSWMIHJQDM-UHFFFAOYSA-N

InChI

1S/C7H9N/c1-8-7-5-3-2-4-6-7/h2-6,8H,1H3

SMILES string

CNc1ccccc1

grade

purum

assay

≥98.0% (GC)

refractive index

n20/D 1.571 (lit.)
n20/D 1.571

bp

196 °C (lit.)

mp

−57 °C (lit.)

density

0.989 g/mL at 25 °C (lit.)

functional group

amine

Quality Level

200

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signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - STOT RE 2 Oral

target_organs

Liver,spleen,Bone marrow

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

185.0 °F - closed cup

flash_point_c

85 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK5898
BCCH2263
BCCD0298
BCCB9686
BCBS7450V

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Y Itoh et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 40(5), 1013-1019 (2005-05-13)
Photolysis of 1,3,5-trichlorobenzene (TCB) in moderate concentration (0.5 mM) in the presence of several additives was examined in 10 mM of cationic and nonionic surfactant solutions. Additions of small amounts of hydrophobic additives, n-dodecanethiol (1 mM), n-dodecyldimethylamine (<2.5 mM), and
Cai Jianguo et al.
Chemosphere, 61(4), 502-509 (2005-10-06)
In the present study, a hydrophilic bifunctional polymeric resin (LS-2) with sulfonic groups was synthesized, and the adsorption performance of three aniline compounds, aniline, 4-methylaniline, and 4-nitroaniline onto LS-2 was compared with that on the commercial Amberlite XAD-4. The uptake
Yang-fang Ye et al.
Journal of environmental sciences (China), 16(2), 343-347 (2004-05-13)
A bacterium (designated strain Y1) degrading acetanilide herbicide mefenacet was isolated from aerobic sludge. Based on the analyses of partial 16S rRNA gene, cellular fatty acid and BIOLOG-GN, and general physiological and biochemical characteristics, strain Y1 was identified as Sphingobacterium
Jonathan L Sessler et al.
Chemical communications (Cambridge, England), (14)(14), 1892-1894 (2005-03-30)
A novel porphyrin-fullerene dyad assembled through Watson-Crick hydrogen bonds is described; this system undergoes photoinduced electron transfer upon irradiation with visible light to produce a charge separated state that is substantially longer lived than that of previous dyads of this
Israel González et al.
Organic letters, 11(8), 1677-1680 (2009-04-10)
N-Methylanilines are readily synthesized in high yields through the copper(II)-promoted coupling of anilines and methylboronic acid. This method represents a new approach for the selective monomethylation of anilines, and it is the first reported example of a Chan-Lam coupling involving
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