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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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G. Pfrepper
Fresenius Journal of Analytical Chemistry, 193, 179-179 (1963)
K.S. Patel et al.
Analytical Chemistry, 58, 1547-1547 (1986)
N. Mishra et al.
Analyst, 112, 1131-1131 (1987)
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
Shunji Ito et al.
The Journal of organic chemistry, 70(6), 2285-2293 (2005-03-12)
[reaction: see text] N,N-Di(6-azulenyl)-p-toluidine (1a) and N,N,N',N'-tetra(6-azulenyl)-p-phenylenediamine (2a) and their derivatives with 1,3-bis(ethoxycarbonyl) substituents on each 6-azulenyl group (1b and 2b) were prepared by Pd-catalyzed amine azulenylation and characterized as a study into new aromatic amines for multistage amphoteric redox

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