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Merck
CN

D107603

2′,5′-Dihydroxyacetophenone

97%

Synonym(s):

2,5-Dihydroxyphenyl methyl ketone, 2-Acetyl-1,4-dihydroxybenzene, 2-Acetylhydroquinone, Acetylquinol, Quinacetophenone

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About This Item

Linear Formula:
(HO)2C6H3COCH3
CAS Number:
490-78-8
Molecular Weight:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893344
EC Number:
207-716-4
Beilstein/REAXYS Number:
637903
MDL number:
MFCD00002343

Key Documents

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Product Name

2′,5′-Dihydroxyacetophenone, 97%

InChI key

WLDWSGZHNBANIO-UHFFFAOYSA-N

InChI

1S/C8H8O3/c1-5(9)7-4-6(10)2-3-8(7)11/h2-4,10-11H,1H3

SMILES string

CC(=O)c1cc(O)ccc1O

assay

97%

form

crystals

mp

204-206 °C (lit.)

Quality Level

100

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Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
01905HJ
13906LH
01517JH
U15550
S25857

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Christiane Östreicher et al.
Journal of proteomics, 166, 27-38 (2017-07-10)
Cytoprotective effects by upregulating cellular expression levels of antioxidant proteins are attributed to a significant number of food ingredients. Evaluation of those cytoprotective effects and identification of the most active components requires reliable and comprehensive proteomic strategies. Thus, promising potential
Junhai Yang et al.
Journal of mass spectrometry : JMS, 53(10), 1005-1012 (2018-08-04)
We describe the use of aromatic ketones and cinnamyl ketones that have high vacuum stability for analyzing tissue sections using matrix-assisted laser desorption/ionization imaging mass spectrometry. Specifically, the matrix, (E)-4-(2,5-dihydroxyphenyl)but-3-en-2-one (2,5-cDHA) provides high sensitivity and high vacuum stability while producing
Wojciech Michno et al.
Journal of neurochemistry, 152(5), 602-616 (2019-10-13)
One of the major hallmarks of Alzheimer's disease (AD) pathology is the formation of extracellular amyloid β (Aβ) plaques. While Aβ has been suggested to be critical in inducing and, potentially, driving the disease, the molecular basis of AD pathogenesis

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