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Merck
CN

H35803

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:
Molecular Weight:
166.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
209-012-2
MDL number:
Assay:
99%
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Quality Level

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



pictograms

Exclamation mark

signalword

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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves



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In vitro and in vivo evaluation of ibuprofen-paeonol conjugate.
Dan Wu et al.
Journal of controlled release : official journal of the Controlled Release Society, 152 Suppl 1, e98-100 (2011-12-27)
Chien-Shan Cheng et al.
Cancer management and research, 12, 641-651 (2020-02-27)
Paeonol, a natural product derived from the root of Cynanchum paniculatum (Bunge) K. Schum and the root of Paeonia suffruticosa Andr. (Ranunculaceae) has attracted extensive attention for its anti-cancer proliferation effect in recent years. The present study examined the role
Shu-zhi Zhong et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 37(17), 2603-2606 (2012-12-15)
To investigate the protective effect of paeonol on amyloid beta1-42 (Abeta1-42)-induced neurotoxicity and its mechanism. Hippocampal neurons of well-grown newborn SD rats and differentiated SH-SY5Y cell lines were cultured with various concentrations of paeonol (1, 5, 10 micromol x L(-1)



Global Trade Item Number

SKUGTIN
H35803-1G04061833793503
H35803-10G04061833793480