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123226

Sigma-Aldrich

Anisole

ReagentPlus®, 99%

Synonym(s):

Methoxybenzene, Methyl phenyl ether

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100 ML
$91.70
1 L
$178.00
4 L
$415.00
18 L
$1,450.00

$91.70


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100 ML
$91.70
1 L
$178.00
4 L
$415.00
18 L
$1,450.00

About This Item

Linear Formula:
CH3OC6H5
CAS Number:
Molecular Weight:
108.14
Beilstein/REAXYS Number:
506892
EC Number:
MDL number:
UNSPSC Code:
12352112
eCl@ss:
39023603
PubChem Substance ID:
NACRES:
NA.21
assay:
99%
bp:
154 °C (lit.)
vapor pressure:
10 mmHg ( 42.2 °C)

$91.70


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vapor density

3.7 (vs air)

Quality Level

vapor pressure

10 mmHg ( 42.2 °C)

product line

ReagentPlus®

assay

99%

form

liquid

autoignition temp.

887 °F

expl. lim.

0.34-6.3 %

refractive index

n20/D 1.516 (lit.)

bp

154 °C (lit.)

mp

−37 °C (lit.)

density

0.995 g/mL at 25 °C (lit.)

SMILES string

COc1ccccc1

InChI

1S/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3

Inchi Key

RDOXTESZEPMUJZ-UHFFFAOYSA-N

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General description

Anisole can be obtained from the reaction between methyl formate and sodium phenolate or potassium phenolate at high temperature and pressure.[1]

Application

Anisole has been used as a dopant to improve the sensitivity of photoionization at atmospheric pressure, which can be used as a source in the detection of nonpolar compounds using liquid chromatography coupled with mass spectrometry.[2] It has also been used to improve the molecular fragmentation which further increases the background signal intensity in hyperthermal surface ionization source, when coupled with time-of-flight mass spectrometer.[3]

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3 - STOT SE 3

target_organs

Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

109.4 °F - closed cup

flash_point_c

43 °C - closed cup


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Adolfsson H, et al.
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 37 (2014)
"Hyperthermal surface ionization in a time-of-flight mass spectrometer"
Weickhardt C and Draack L
Eur. J. Mass Spectrom., 6(4), 319- 323 (2000)
"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)
Adam F Lee et al.
Dalton transactions (Cambridge, England : 2003), 39(43), 10473-10482 (2010-10-05)
Size-controlled, catalytically active PVP-stabilised Pd nanoparticles have been studied by operando liquid phase XAS during the Suzuki cross-coupling of iodonanisole and phenylboronic acid in MeOH-toluene using KOMe base. XAS reveals nanoparticles are stable to metal leaching throughout the reaction, with
Shouhui Zhang et al.
The Journal of organic chemistry, 75(19), 6732-6735 (2010-09-09)
A CuI-catalyzed direct access to sulfides from disulfides via C-H bond cleavage of di- or trimethoxybenzene is described. The procedure utilizes O(2) as a clean and cheap oxidant. Direct selenation of the C-H bond also took place under this procedure.

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