Skip to Content
MilliporeSigma
All Photos(1)

Documents

796883

Sigma-Aldrich

3,4-dihydroxyphenylacetone

95%

Synonym(s):

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

Sign Into View Organizational & Contract Pricing


About This Item

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

Quality Level

Assay

95%

form

powder

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

Looking for similar products? Visit Product Comparison Guide

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

Levodopa Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1271

Levodopa

Dopamine hydrochloride

Sigma-Aldrich

H8502

Dopamine hydrochloride

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service