Skip to Content
Merck
All Photos(3)

Documents

H35803

Sigma-Aldrich

2′-Hydroxy-4′-methoxyacetophenone

99%

Synonym(s):

Paeonol, Resacetophenone 4-O-methyl ether

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
HOC6H3(OCH3)COCH3
CAS Number:
552-41-0
Molecular Weight:
166.17
EC Number:
209-012-2
MDL number:
MFCD00008730
UNSPSC Code:
12352100
PubChem Substance ID:
24895579
NACRES:
NA.22

Assay

99%

mp

48-50 °C (lit.)

SMILES string

O=C(C)C1=CC=C(OC)C=C1O

InChI

1S/C9H10O3/c1-6(10)8-4-3-7(12-2)5-9(8)11/h3-5,11H,1-2H3

InChI key

UILPJVPSNHJFIK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

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

Rui-guang Wu et al.
International journal of pharmaceutics, 438(1-2), 91-97 (2012-09-18)
Thermotropic phase behavior of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) liposomes containing 5 mol% cholesterol, or 5 mol% stigmasterol, or 5 mol% paeonol have been investigated by differential scanning calorimetry (DSC) and synchrotron X-ray diffraction (XRD) techniques, to investigate the competitive molecular interaction among
Yue-Qin Wang et al.
Biological & pharmaceutical bulletin, 35(5), 767-772 (2012-06-13)
Atherosclerosis is a chronic inflammatory disease characterized by increased expression of adhesion molecules, which contribute to monocytes adhesion to vascular endothelial cells (VECs). Paeonol, an active compound isolated from cortex Moutan, has been shown to have therapeutic effects on atherosclerotic
Ji-Yong Liu et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 47(2), 244-249 (2012-04-19)
Investigation of the pharmacokinetics of paeonol microemulsion, microemulsion-based gels and marketed paeonol ointments by the skin-blood synchronous microdialysis coupled with LC/MS is reported in this study. The microdialysis systems were established by linear probes and concentric circles probes. In vivo
Qiuling Wang et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 37(7), 920-924 (2012-07-17)
To study on the effect of different processing methods on the contents of seven major constituents in wild and cultivated Paeonia lactiflora, gallic acid, catechin, albiflorin, paeoniflorin, pentagalloylglucose, benzoic acid and paeonol, in order to provide reference basis for different
Feng Qin et al.
Journal of AOAC International, 94(6), 1778-1784 (2012-02-11)
A simple, sensitive, and reliable ultra-performance liquid chromatography (UPLC) method has been developed for simultaneous determination of 22 major constituents in modified xiaoyao san (MXS), a multiherbal formula. The chromatographic separation was performed on an ACQUITY UPLC BEH C18 column
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