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Merck

236314

p-Toluidine

99.6%

동의어(들):

4-Aminotoluene, 4-Methylaniline

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제품정보 (DICE 배송 시 비용 별도)

Linear Formula:
CH3C6H4NH2
CAS 번호:
106-49-0
Molecular Weight:
107.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854162
EC Number:
203-403-1
Beilstein/REAXYS Number:
471281
MDL number:
MFCD00007906
Assay:
99.6%
Bp:
200 °C (lit.)
Vapor pressure:
0.26 mmHg ( 25 °C), 0.66 mmHg ( 38 °C)

주요 문서

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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

0.26 mmHg ( 25 °C), 0.66 mmHg ( 38 °C)

assay

99.6%

form

crystalline

autoignition temp.

899 °F

expl. lim.

6.6 %

pH

7.8 (7 g/L)

bp

200 °C (lit.)

mp

41-46 °C (lit.)

solubility

water: soluble 135 part(lit.), acetone: freely soluble(lit.), alcohol: freely soluble(lit.), carbon disulfide: freely soluble(lit.), diethyl ether: freely soluble(lit.), methanol: freely soluble(lit.), oil: freely soluble(lit.)

density

0.973 g/mL at 25 °C (lit.)

Quality Level

200

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관련 카테고리

General description

p-Toluidine undergoes oxidative coupling reaction with catecholamine to form an orange water-soluble dye during flow injection-spectrophotometric determination of catecholamine drugs.

Application

p-Toluidine has been used in preparation of:
  • aromatic azo compounds
  • bidentate Schiff base ligands via condensation with salicylaldehyde

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

저장 등급

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

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시험 성적서(COA)

Lot/Batch Number
BCCP2073
BCCN1334
BCCM8077
BCCM0715
BCCM2400

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문서 라이브러리 방문

Flow injection-spectrophotometeric determination of some catecholamine drugs in pharmaceutical preparations via oxidative coupling reaction with< i> p</i>-toluidine and sodium periodate.
Abdulrahman LK, et al.
Analytica Chimica Acta, 538(1), 331-335 (2005)
Ruthenium (II) complexes containing bidentate Schiff bases and their antifungal activity.
Dharmaraj N, et al.
Transition Met. Chem. (London), 26(1-2), 105-109 (2001)
Abdessamad Grirrane et al.
Nature protocols, 5(3), 429-438 (2010-03-06)
This protocol describes the aerobic oxidation of aromatic anilines to aromatic azo compounds using gold (Au) nanoparticles supported on TiO(2) as a catalyst. Yields above 98% are achieved under a few bars of oxygen pressure. It should be noted that
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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