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D149705

Sigma-Aldrich

2,6-Dimethylbenzoquinone

99%

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About This Item

Linear Formula:
(CH3)2C6H2-1,4-(=O)2
CAS Number:
Molecular Weight:
136.15
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

solid

mp

71-73 °C (lit.)

SMILES string

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

InChI

1S/C8H8O2/c1-5-3-7(9)4-6(2)8(5)10/h3-4H,1-2H3

InChI key

SENUUPBBLQWHMF-UHFFFAOYSA-N

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

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’.

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A C Stewart
The Biochemical journal, 204(3), 705-712 (1982-06-15)
1. Photosynthetic electron transport from water to lipophilic Photosystem II acceptors was stimulated 3--5-fold by high concentrations (greater than or equal to 1 M) of salts containing anions such as citrate, succinate and phosphate that are high in the Hofmeister
D Kim et al.
Chemistry & biology, 5(2), 103-117 (1998-03-13)
The temporal and spatial control of the transition from vegetative to parasitic growth is critical to any parasite, but is essential to the sessile parasitic plants. It has been proposed that this transition in Striga spp. is controlled simply by
Sam Hay et al.
The journal of physical chemistry. B, 111(13), 3488-3495 (2007-03-29)
The electrochemistry of 2,6-dimethylbenzoquinone (DMBQ) has been characterized for three different systems: DMBQ freely solvated in aqueous buffer; DMBQ bound to a neutral, blocked cysteine (N-acetyl-L-cysteine methyl ester) and the resulting DMBQ-bCys compound solvated in aqueous buffer; and DMBQ bound
Mustafa Odabaşoğlu et al.
Acta crystallographica. Section C, Crystal structure communications, 61(Pt 4), o240-o242 (2005-04-05)
Molecules of the title compound, C8H9NO2, are linked into sheets by a combination of C-H...N, O-H...N and O-H...O hydrogen bonds and C-H...pi interactions. The hydrogen bonds are arranged as described by the graph-set ring notations R(2)(2)(7) and R(3)(3)(5), and a
Argyrides Argyrou et al.
Biochemistry, 42(7), 2218-2228 (2003-02-20)
Lipoamide dehydrogenase catalyzes the reversible NAD(+)-dependent oxidation of the dihydrolipoyl cofactors that are covalently attached to the acyltransferase components of the pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, and glycine reductase multienzyme complexes. It contains two redox centers: a tightly, but noncovalently, bound

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