Skip to Content
Merck
All Photos(1)

Key Documents

187933

Sigma-Aldrich

3-Methoxyphenethyl alcohol

97%

Synonym(s):

2-(3-Methoxyphenyl)ethanol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3OC6H4CH2CH2OH
CAS Number:
Molecular Weight:
152.19
Beilstein:
1863114
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.538 (lit.)

bp

141-143 °C/12 mmHg (lit.)

density

1.075 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

COc1cccc(CCO)c1

InChI

1S/C9H12O2/c1-11-9-4-2-3-8(7-9)5-6-10/h2-4,7,10H,5-6H2,1H3

InChI key

UPPGEJSCUZMCMW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

3-Methoxyphenethyl alcohol was used as starting reagent during the synthesis of 3-methoxy-2,6-dimethyl- phenethyl alcohol.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

An interesting synthesis of 3-methoxy-2, 6-dimethylphenethyl alcohol.
Meyer AL and Turner RB.
Tetrahedron, 27(13), 2609-2615 (1971)
Min Kyung Song et al.
Journal of agricultural and food chemistry, 67(7), 2028-2035 (2019-01-31)
Caffeic acid phenethyl ester (CAPE) is an ester of a hydroxycinnamic acid (phenylpropanoid) and a phenylethanoid (2-phenylethanol; 2-PE), which has long been used in traditional medicine. Here, we synthesized 54 hydroxycinnamic acid-phenylethanoid esters by feeding 64 combinations of hydroxycinnamic acids
Kuo-Ching Wen et al.
International journal of molecular sciences, 14(12), 23420-23440 (2013-11-30)
Melanin is responsible for skin color and plays a major role in defending against harmful external factors such as ultraviolet (UV) irradiation. Tyrosinase is responsible for the critical steps of melanogenesis, including the rate-limiting step of tyrosine hydroxylation. The mechanisms

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service