Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

42914

Sigma-Aldrich

Pinosylvin monomethyl ether

≥97.0% (HPLC)

Synonym(s):

(E)-3-Hydroxy-5-methoxystilbene, (E)-3-Methoxy-5-(2-phenylethenyl)phenol, 5-Methoxy-3-stilbenol, Pinosylvin 3-methyl ether

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C15H14O2
CAS Number:
35302-70-6
Molecular Weight:
226.27
Beilstein:
1875807
MDL number:
MFCD00210546
UNSPSC Code:
12352200
PubChem Substance ID:
329756282

Assay

≥97.0% (HPLC)

form

solid

mp

118-122 °C

SMILES string

COc1cc(O)cc(\C=C\c2ccccc2)c1

InChI

1S/C15H14O2/c1-17-15-10-13(9-14(16)11-15)8-7-12-5-3-2-4-6-12/h2-11,16H,1H3/b8-7+

InChI key

JVIXPWIEOVZVJC-BQYQJAHWSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Pinosylvin, a pre-infectious stilbenoid toxin, is used to study its properties as a fungitoxin and potential therapeutic agent. Pinosylvin monomethyl ether, a methylated derivative of pinosylvin, may be used as a reference material in the analysis of stibenoid toxins. Pinosylvin monomethyl ether may also be used as a representative stilbene to study its biological actions and therapeutic value in processes such as cell survival, apoptosis and cell mobility.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

新产品

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

Caterina Villari et al.
Tree physiology, 32(7), 867-879 (2012-06-22)
Conifer bark beetles are often associated with fungal complexes whose components have different ecological roles. Some associated species are nutritionally obligate fungi, serving as nourishment to the larvae, whereas others are pathogenic blue-stain fungi known to be involved in the
Dag Ekeberg et al.
Journal of chromatography. A, 1109(2), 267-272 (2006-02-14)
A method for quantitative determination of extractives from heartwood of Scots pine (Pinus sylvestris L.) using gas chromatography (GC) with flame ionization detection (FID) was developed. The limit of detection (LOD) was 0.03 mg/g wood and the linear range (r
C C Celimene et al.
Phytochemistry, 56(2), 161-165 (2001-02-24)
The effects of pinosylvin, pinosylvin monomethyl ether, pinosylvin dimethyl ether, and resveratrol on the fungal shoot blight and canker pathogen of conifers Sphaeropsis sapinea were examined in vitro. Effects of compounds, isolates, and concentrations on both conidial germination and mycelial
François Simard et al.
Phytotherapy research : PTR, 22(7), 919-922 (2008-04-05)
Methanol extracts of wood from Pinus resinosa were found to be selectively cytotoxic against human lung carcinoma cells, A549 (IC50 41 +/- 6 microg/mL), human colorectal adenocarcinoma cells, DLD-1 (IC50 47 +/- 4 microg/mL) in comparison with healthy cells, WS1
Julien Gabaston et al.
Journal of separation science, 43(6), 1080-1088 (2020-01-24)
Pine knots are a rich source of lignans, flavonoids, and stilbenes. These bioactive compounds are widely known for their roles to combat human disorders but also to protect plants against pathogens. In order to gain knowledge inside their potential activities
View All Related Papers

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