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796883

Sigma-Aldrich

3,4-dihydroxyphenylacetone

95%

Synonym(s):

1-(3,4-Dihydroxyphenyl)-2-propanone, 1-(3′,4′-Dihydroxyphenyl)-2-propanone

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About This Item

Empirical Formula (Hill Notation):
C9H10O3
CAS Number:
2503-44-8
Molecular Weight:
166.17
MDL number:
MFCD03093024
UNSPSC Code:
12352100
PubChem Substance ID:
329768555
NACRES:
NA.22

Assay

95%

form

powder

functional group

ketone

SMILES string

CC(CC1=CC(O)=C(O)C=C1)=O

InChI

1S/C9H10O3/c1-6(10)4-7-2-3-8(11)9(12)5-7/h2-3,5,11-12H,4H2,1H3

InChI key

JQXBETDGCMQLMK-UHFFFAOYSA-N

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General description

3,4-dihydroxyphenylacetoneis an alkylbenzene. 3,4-dihydroxyphenylacetone is the product of oxidative deamination of α-methylDopa. The product is intended for forensic and research purposes.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW5748
MKCV1433
MKCS6367
MKCS2309
MKCS2279

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Mammalian Dopa decarboxylase: structure, catalytic activity and inhibition
Bertoldi M.
Archives of Biochemistry and Biophysics, 546, 1-7 (2014)
Mohammadreza Shariatgorji et al.
Nature methods, 16(10), 1021-1028 (2019-09-25)
We present a mass spectrometry imaging (MSI) approach for the comprehensive mapping of neurotransmitter networks in specific brain regions. Our fluoromethylpyridinium-based reactive matrices facilitate the covalent charge-tagging of molecules containing phenolic hydroxyl and/or primary or secondary amine groups, including dopaminergic

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