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线性分子式:
CH3OC6H5
化学文摘社编号:
分子量:
108.14
NACRES:
NA.21
PubChem Substance ID:
eCl@ss:
39023603
UNSPSC Code:
12352112
EC Number:
202-876-1
MDL number:
Beilstein/REAXYS Number:
506892
Assay:
99%
Bp:
154 °C (lit.)
Vapor pressure:
10 mmHg ( 42.2 °C)
InChI key
RDOXTESZEPMUJZ-UHFFFAOYSA-N
InChI
1S/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3
SMILES string
COc1ccccc1
vapor density
3.7 (vs air)
vapor pressure
10 mmHg ( 42.2 °C)
product line
ReagentPlus®
assay
99%
form
liquid
autoignition temp.
887 °F
expl. lim.
0.34-6.3 %
dilution
(for general lab use)
refractive index
n20/D 1.516 (lit.)
bp
154 °C (lit.)
mp
−37 °C (lit.)
density
0.995 g/mL at 25 °C (lit.)
Quality Level
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General description
甲酸甲酯与酚酸钠或酚酸钾在高温高压下反应可得到苯甲醚。
Application
苯甲醚已被用作掺杂剂来提高大气压下光电离的灵敏度,在使用液相色谱耦合质谱法检测非极性化合物时可作为来源。在高温表面电离源中,当与飞行时间质谱仪联用时,它还被用于改善分子碎片,从而进一步提高背景信号强度。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3 - STOT SE 3
target_organs
Central nervous system
存储类别
3 - Flammable liquids
flash_point_f
109.4 °F - closed cup
flash_point_c
43 °C - closed cup
法规信息
危险化学品
此项目有
"A silica-based monolithic column in capillary HPLC and CEC coupled with ESI-MS or electrospray-atmospheric-pressure laser ionization-MS"
Droste S, et al.
Electrophoresis, 26(21), 4098-4103 (2005)
"Hyperthermal surface ionization in a time-of-flight mass spectrometer"
Weickhardt C and Draack L
Eur. J. Mass Spectrom., 6(4), 319- 323 (2000)
Adolfsson H, et al.
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 37 (2014)
Fiona Wong et al.
Environmental science & technology, 45(3), 876-881 (2011-01-05)
Shipboard measurements of organohalogen compounds in air and surface seawater were conducted in the Canadian Arctic in 2007-2008. Study areas included the Labrador Sea, Hudson Bay, and the southern Beaufort Sea. High volume air samples were collected at deck level
Zhiyun Du et al.
Organic & biomolecular chemistry, 10(21), 4164-4171 (2012-03-30)
Described in this study is the ability of tetrabutylammonium salts (TBAX) to mediate an efficient mono- or di-demethylation removing one or two out of five aromatic methoxy methyl groups situated in similar chemical microenvironments in a H-bonded macrocyclic aromatic pentamer.
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