모든 사진(3)
About This Item
Linear Formula:
CH3C6H4NH2
CAS Number:
Molecular Weight:
107.15
Beilstein:
471281
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
bp:
200 °C (lit.)
vapor pressure:
1 hPa ( 42 °C)
7 hPa ( 68 °C)
7 hPa ( 68 °C)
추천 제품
vapor density
3.9 (vs air)
vapor pressure
1 hPa ( 42 °C)
7 hPa ( 68 °C)
분석
99%
양식
powder, crystals or chunks
autoignition temp.
899 °F
expl. lim.
6.6 %
bp
200 °C (lit.)
mp
41-46 °C (lit.)
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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관련 카테고리
일반 설명
p-Toluidine is an aromatic amine. It can be detected in the water samples by homogeneous liquid-liquid extraction followed by ion mobility spectrometry (HLLE-IMS).
애플리케이션
p-Toluidine may be used for the determination of hemoglobin adducts of aromatic amines in nonsmokers and smokers of blond- or black-tobacco cigarettes. It may be used for the preparation of bidentate Schiff base ligand, via condensation with salicylaldehyde.
신호어
Danger
유해 및 위험 성명서
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
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
이미 열람한 고객
Amin Ashori et al.
Bulletin of environmental contamination and toxicology, 94(4), 474-478 (2014-11-28)
In this research, homogeneous liquid-liquid extraction followed by ion mobility spectrometry (HLLE-IMS) with corona discharge ionization source has been developed for the determination of p-toluidine. The analyte was extracted by single-phase extraction in a ternary solvent system and then the
M S Bryant et al.
Proceedings of the National Academy of Sciences of the United States of America, 85(24), 9788-9791 (1988-12-01)
Hemoglobin adducts of 15 aromatic amines were determined in nonsmokers and smokers of blond- or black-tobacco cigarettes living in Turin, Italy. The subjects were all males age 55 or less and were representative of the population previously examined in a
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)
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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