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2,3-Dimethylhydrochinon

Name: 2,3-Dimethylhydrochinon
Brand: ALDRICH

97%

Synonym(e):

1,4-Dihydroxy-2,3-dimethylbenzene, 2,3-Dimethyl-1,4-benzenediol

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About This Item

Lineare Formel:

(CH₃)₂C₆H₂-1,4-(OH)₂

CAS-Nummer:

608-43-5

Molekulargewicht:

138.16

Beilstein:

636976

MDL-Nummer:

MFCD00009997

UNSPSC-Code:

12162002

PubChem Substanz-ID:

24857938

NACRES:

NA.23

Assay

97%

Form

powder

mp (Schmelzpunkt)

223-225 °C (lit.)

SMILES String

Cc1c(C)c(O)ccc1O

InChI

1S/C8H10O2/c1-5-6(2)8(10)4-3-7(5)9/h3-4,9-10H,1-2H3

InChIKey

BXJGUBZTZWCMEX-UHFFFAOYSA-N

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Allgemeine Beschreibung

2,3-Dimethylhydroquinone is an alkyl p-hydroquinone that can be used as a chain breaking antioxidant and an electron donor for redox intermediates. It acts as an antioxidant due to its characteristic to terminate kinetic chains on reaction with peroxy radicals.

Anwendung

2,3-Dimethylhydroquinone can be used as an antioxidant for lipid peroxidation. It is also used in the synthesis of benzofuran-5-ols which can further be utilized as antifungal agents in biological applications.

Piktogramme

GHS07

Signalwort

Warning

H-Sätze

H315,H319,H335

P-Sätze

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

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Electrochemical oxidation of 2, 3-dimethylhydroquinone in the presence of 1, 3-dicarbonyl compounds

Hosseiny D, et al.

The Journal of Organic Chemistry, 71(5), 2139-2142 (2006)

The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism.

Marco Persico et al.

Scientific reports, 7, 45485-45485 (2017-04-07)

In the present work we performed a combined experimental and computational study on the interaction of the natural antimalarial endoperoxide plakortin and its synthetic analogue 4a with heme. Obtained results indicate that the studied compounds produce reactive carbon radical species

Substituted p-hydroquinones as inhibitors of lipid peroxidation

Roginsky V, et al.

Chemistry and Physics of Lipids, 125(1), 49-58 (2003)

C-H activation and metalation at electrode surfaces: 2,3-dimethyl-1,4-dihydroxybenzene on Pd(pc) and Pd(111) studied by TLE, HREELS and DFT.

Alnald Javier et al.

Dalton transactions (Cambridge, England : 2003), 43(39), 14798-14805 (2014-08-28)

Previous studies, based on thin-layer electrochemistry (TLE), in situ scanning tunneling microscopy (EC-STM), high-resolution electron energy loss spectroscopy (HREELS) and density functional theory (DFT) computations, on the chemical adsorption of hydroquinone from aqueous solutions onto atomically smooth Pd (and Pt)

Synthesis and antifungal activity of benzofuran-5-ols

Ryu C, et al.

Bioorganic & Medicinal Chemistry Letters, 20(22), 6777-6780 (2010)

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