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Merck
CN

89630

p-Toluidine

for spectrophotometric det. of Au, Tl(III), W, ≥99.0%

Synonym(s):

4-Aminotoluene, 4-Methylaniline

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About This Item

Linear Formula:
CH3C6H4NH2
CAS Number:
106-49-0
Molecular Weight:
107.15
UNSPSC Code:
12352200
NACRES:
NA.21
PubChem Substance ID:
329769756
EC Number:
203-403-1
Beilstein/REAXYS Number:
471281
MDL number:
MFCD00007906
Assay:
≥99.0% (GC)
≥99.0%
Technique(s):
UV/Vis spectroscopy: suitable
Bp:
200 °C (lit.)
Vapor pressure:
1 hPa ( 42 °C)
7 hPa ( 68 °C)

Key Documents

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Product Name

p-Toluidine, for spectrophotometric det. of Au, Tl(III), W, ≥99.0%

InChI key

RZXMPPFPUUCRFN-UHFFFAOYSA-N

InChI

1S/C7H9N/c1-6-2-4-7(8)5-3-6/h2-5H,8H2,1H3

SMILES string

Cc1ccc(N)cc1

vapor density

3.9 (vs air)

vapor pressure

1 hPa ( 42 °C)
7 hPa ( 68 °C)

assay

≥99.0% (GC)
≥99.0%

form

crystals

autoignition temp.

899 °F

quality

for spectrophotometric det. of Au, Tl(III), W

expl. lim.

6.6 %

technique(s)

UV/Vis spectroscopy: suitable

bp

200 °C (lit.)

mp

41-46 °C (lit.)
42-45 °C

solubility

ethanol: 1 g/10 mL (Hot)

density

0.973 g/mL at 25 °C (lit.)

Quality Level

100

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Other Notes

Reagent for the spectrophotometric det. of Tl(III), Au and W

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Skin Sens. 1A

Storage Class

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

wgk

WGK 3

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCN1334
BCCM8077
BCCM0715
BCCM2400
BCCK4226

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N. Mishra et al.
Analyst, 112, 1131-1131 (1987)
K.S. Patel et al.
Analytical Chemistry, 58, 1547-1547 (1986)
G. Pfrepper
Fresenius Journal of Analytical Chemistry, 193, 179-179 (1963)
D R Doerge et al.
Chemical research in toxicology, 4(5), 556-560 (1991-09-01)
The metabolism of three arylamine substrates by H2O2 in the presence of each of the peroxidative enzymes chloroperoxidase (CPX) and pea seed peroxygenase (PSM) was conducted with normal H2O2 and with 18O-labeled H2O2. The resulting C-nitroso aromatic metabolites were examined
J C Kennelly et al.
Mutation research, 137(1), 39-45 (1984-07-01)
The conventional Ames assay metabolising system was confirmed to be deficient in its ability to N-acetylate. This may render the test less sensitive to compounds which normally have an acetylation step during their in vivo activation to carcinogens. The addition
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