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线性分子式:
C6H5CH3
化学文摘社编号:
分子量:
92.14
UNSPSC Code:
12352002
NACRES:
NA.21
PubChem Substance ID:
EC Number:
203-625-9
Beilstein/REAXYS Number:
635760
MDL number:
Assay:
≥99.5%
Grade:
ACS reagent
Technique(s):
toxicology assay: suitable
Bp:
110-111 °C (lit.)
Vapor pressure:
22 mmHg ( 20 °C), 26 mmHg ( 25 °C)
assay
≥99.5%
form
liquid
InChI key
YXFVVABEGXRONW-UHFFFAOYSA-N
InChI
1S/C7H8/c1-7-5-3-2-4-6-7/h2-6H,1H3
SMILES string
Cc1ccccc1
grade
ACS reagent
vapor density
3.2 (vs air)
vapor pressure
22 mmHg ( 20 °C), 26 mmHg ( 25 °C)
autoignition temp.
997 °F
expl. lim.
7 %
technique(s)
toxicology assay: suitable
impurities
H2SO4, passes test (darkened), ≤0.003% S compounds, ≤0.03% Water
evapn. residue
≤0.001%
refractive index
n/D 1.496 (lit.)
bp
110-111 °C (lit.)
mp
-93 °C (lit.)
solubility
acetone: miscible(lit.), alcohol: miscible(lit.), carbon disulfide: miscible(lit.), chloroform: miscible(lit.), glacial acetic acid: miscible(lit.)
density
0.865 g/mL at 25 °C (lit.)
Quality Level
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General description
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.
Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.
Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.
Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.
Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.
Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.
Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.
Toluene, also known as methylbenzene, is a flammable liquid with a pungent odor. It is a constituent of crude oil. Toluene is widely used as a precursor for synthesizing benzene, a gasoline additive, and as a solvent in the paint industry. Its toxicological effects have been investigated. Alkylation of toluene to form p-xylene with high selectivity using modified ZSM (Zeolite Socony Mobil)-5-class zeolite catalysts has been reported. Electrical properties of graphene can be altered by doping it with toluene, which serves as an electron donor. Temperature programmed hydrogenation (TPH) of toluene in the gas phase in the presence of supported metal catalysts has been studied.
signalword
Danger
Hazard Classifications
Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 2 Inhalation - STOT SE 3
target_organs
Central nervous system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
39.9 °F - closed cup
flash_point_c
4.4 °C - closed cup
法规信息
新产品
此项目有
Temperature programmed hydrogenation of toluene.
Slioor RI, et al.
Catalysis Letters, 121(1-2), 24-32 (2008)
Toluene.
von Burg R.
Journal of Applied Toxicology, 13(6), 441-446 (1993)
Selective alkylation of toluene with methanol to produce para-xylene.
Kaeding WW, et al.
J. Catal., 67(1), 159-174 (1981)
Electrochemical doping of graphene with toluene.
Kaverzin AA, et al.
Carbon, 49(12), 3829-3834 (2011)
Liang Guo et al.
Journal of chromatography. A, 1286, 9-15 (2013-03-19)
For the first time, a novel one-step sample preparation method that combines microwave assisted extraction and solvent bar microextraction (MAE-SBME) with analysis by gas chromatography-mass spectrometry (GC-MS), was developed for the fast and efficient determination of polycyclic aromatic hydrocarbons (PAHs)
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