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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
Beilstein:
637903
EC Number:
207-716-4
MDL number:
MFCD00002343
UNSPSC Code:
12352100
PubChem Substance ID:
24893344
NACRES:
NA.22

Key Documents

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Quality Level

100

Assay

97%

form

crystals

mp

204-206 °C (lit.)

SMILES string

CC(=O)c1cc(O)ccc1O

InChI

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

InChI key

WLDWSGZHNBANIO-UHFFFAOYSA-N

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

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)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

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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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
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
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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