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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C6H5C2H5
CAS 번호:
Molecular Weight:
106.17
NACRES:
NA.06
PubChem Substance ID:
eCl@ss:
39011201
UNSPSC Code:
12352002
EC Number:
202-849-4
MDL number:
Beilstein/REAXYS Number:
1901871
Assay:
99.8%
Grade:
anhydrous
Bp:
136 °C (lit.)
Vapor pressure:
10 mmHg ( 20 °C), 19 mmHg ( 37.7 °C)
grade
anhydrous
Quality Level
vapor density
3.7 (vs air)
vapor pressure
10 mmHg ( 20 °C), 19 mmHg ( 37.7 °C)
assay
99.8%
form
liquid
autoignition temp.
810 °F
expl. lim.
6.7 %
impurities
<0.002% water, <0.005% water (100 mL pkg)
evapn. residue
<0.0005%
refractive index
n20/D 1.495 (lit.)
bp
136 °C (lit.)
mp
−95 °C (lit.)
density
0.867 g/mL at 25 °C (lit.)
SMILES string
CCc1ccccc1
InChI
1S/C8H10/c1-2-8-6-4-3-5-7-8/h3-7H,2H2,1H3
InChI key
YNQLUTRBYVCPMQ-UHFFFAOYSA-N
Application
Ethylbenzene may be used as a starting material to synthesize:
- Acetophenone via selection oxidation in the presence of potassium dichromate supported on neutral alumina and using air as the oxidizing agent.
- Styrene via dehydrogenation over nanodiamonds in an oxygen-lean environment.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 2 - STOT RE 2
target_organs
hearing organs
저장 등급
3 - Flammable liquids
wgk
WGK 1
flash_point_f
71.6 °F - closed cup
flash_point_c
22.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Selective and Stable Ethylbenzene Dehydrogenation to Styrene over Nanodiamonds under Oxygen?lean Conditions
Diao J, et al.
ChemSusChem, 9(7), 662-666 (2016)
Catalytic oxidation of ethylbenzene to acetophenone using alumina-supported dichromate: Process optimisation and development of a continuous process.
Chisem IC, et al.
Organic Process Research & Development, 1(5), 365-369 (1997)
Preparation and Characterization of MCM-41@ PEI? Mn as a New Organic-Inorganic Hybrid Nanomaterial and Study of its Catalytic Role in the Oxidation of Cyclohexene, Ethyl Benzene, and Toluene in the Presence of H2O2 as an Oxidant.
Tarasi R, et al.
Bull. Korean Chem. Soc., 37(4), 529-537 (2016)


