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H35803

Sigma-Aldrich

2′-Hydroxy-4′-methoxyacetophenone

99%

Synonym(s):

Paeonol, Resacetophenone 4-O-methyl ether

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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

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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)

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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
Mei-Hua Bao et al.
Journal of ethnopharmacology, 146(2), 543-551 (2013-01-30)
Paeonol is an active compound isolated from traditional Chinese medicine, and has been shown to have anti-atherosclerosis, anti-inflammatory, antioxidant effects. The present investigation was undertaken to determine the suppression effects of paeonol on oxidized low-density lipoprotein (ox-LDL) induced endothelial cell
Liqin Ding et al.
Xenobiotica; the fate of foreign compounds in biological systems, 42(12), 1206-1212 (2012-06-12)
Paeonol, a major component of Paeonia suffruticosa Andrews, is used in clinical situations in China as a natural anti-inflammatory agent. The aim of the present study is to investigate the metabolism of paeonol in humans. Six metabolites were isolated from
Bendong Chen et al.
Molecules (Basel, Switzerland), 17(4), 4672-4683 (2012-04-24)
The study investigated the immunity and antioxidant potential of paeonol by employing a hepatocellular carcinoma (HCC) rat model. Three doses of paeonol (20, 40, 60 mg/kg b.w. orally) were administrated to diethylnitrosamine (DEN)-induced HCC rats. Results showed that paeonol significantly
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
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