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About This Item
Linear Formula:
CH3OC6H4CH2OH
CAS Number:
Molecular Weight:
138.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-273-6
Beilstein/REAXYS Number:
636654
MDL number:
Assay:
98%
Form:
solid
Quality Level
assay
98%
form
solid
refractive index
n20/D 1.544 (lit.)
bp
259 °C (lit.)
mp
22-25 °C (lit.)
solubility
alcohol: freely soluble, diethyl ether: freely soluble, water: insoluble
density
1.113 g/mL at 25 °C (lit.)
functional group
hydroxyl
SMILES string
COc1ccc(CO)cc1
InChI
1S/C8H10O2/c1-10-8-4-2-7(6-9)3-5-8/h2-5,9H,6H2,1H3
InChI key
MSHFRERJPWKJFX-UHFFFAOYSA-N
General description
4-Methoxybenzyl alcohol is commonly used as a reagent to protect hydroxyl groups on alcohols, and phenols. 4-Methoxybenzyl alcohol on condensation with the silanol groups of fumed silica nanoparticles yields modified silica nanoparticles. It undergoes catalytic photooxidation by flavin-zinc(II)-cyclen complex to yield the corresponding benzaldehyde.
Application
4-Methoxybenzyl alcohol was used to study the photocatalytic oxidation of 4-methoxybenzyl alcohol to p-anisaldehyde.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1B
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Valeria B Arce et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 11(6), 1032-1040 (2012-03-17)
The knowledge of photochemical kinetics in colloidal systems is important in understanding environmental photochemistry on dispersed solid surfaces. As model materials for the chemically sorbed organic compounds present in natural environments, modified silica nanoparticles (NPs) were obtained here by condensation
Selective photocatalytic oxidation of 4-methoxybenzyl alcohol to p-anisaldehyde in organic-free water in a continuous annular fixed bed reactor.
Loddo V, et al.
International Journal of Chemical Reactor Engineering, 5(1) (2007)
Radek Cibulka et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 10(24), 6224-6231 (2004-10-16)
Flavin-zinc(II)-cyclen 10 contains a covalently linked substrate binding site (zinc(II)-cyclen) and a chromophore unit (flavin). Upon irradiation, compound 10 effectively oxidizes 4-methoxybenzyl alcohol (11-OCH3) to the corresponding benzaldehyde both in water and in acetonitrile. In the presence of air, the
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 136905-100G | 04061838731524 |
| 136905-500G | 04061838731531 |
| 136905-5G | 04061838731548 |
