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89630

Supelco

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:
Molecular Weight:
107.15
Beilstein:
471281
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
NACRES:
NA.21

vapor density

3.9 (vs air)

Quality Level

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.)

SMILES string

Cc1ccc(N)cc1

InChI

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

InChI key

RZXMPPFPUUCRFN-UHFFFAOYSA-N

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Other Notes

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

Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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N. Mishra et al.
Analyst, 112, 1131-1131 (1987)
G. Pfrepper
Fresenius Journal of Analytical Chemistry, 193, 179-179 (1963)
K.S. Patel et al.
Analytical Chemistry, 58, 1547-1547 (1986)
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
Paul G Stevenson et al.
Journal of chromatography. A, 1218(45), 8255-8263 (2011-10-11)
Several simple techniques are presented for the identification of the boundaries of chromatographic peaks. These methods provide a significant reduction in the time needed to perform the rapid, automatic calculation of the central peak moments and to evaluate the quality

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