38775
2,3-Dimethoxy-5-methyl-p-benzoquinone
≥98.0% (HPLC)
Synonym(s):
Coenzyme Q0
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About This Item
Empirical Formula (Hill Notation):
C9H10O4
CAS Number:
Molecular Weight:
182.17
EC Number:
210-100-8
UNSPSC Code:
41106305
MDL number:
Beilstein/REAXYS Number:
1640422
InChI
1S/C9H10O4/c1-5-4-6(10)8(12-2)9(13-3)7(5)11/h4H,1-3H3
InChI key
UIXPTCZPFCVOQF-UHFFFAOYSA-N
SMILES string
COC1=C(OC)C(=O)C(C)=CC1=O
assay
≥98.0% (HPLC)
Other Notes
Coenzyme Q
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Biochemistry, Bioenergetics and Clinical Applications of Ubiquinone,G.Lenaz ed, 517-517 (1985)
Wei Yuan et al.
Journal of chromatography. A, 1218(18), 2561-2568 (2011-03-23)
Thiol and disulfide levels are critical to maintaining the redox potential of a cell. Perturbations of these levels are important in disease pathogenesis. To improve endogenous mammalian metabolome quantitation, thiol specific tagging, extraction and relative quantitation were undertaken. Reduced and
B K Rao et al.
Biochemistry, 39(12), 3285-3296 (2000-03-22)
The isolated cytochrome (cyt) b(6)f complex from spinach is inhibited by Cu(2+) with a K(D) of about 1 microM at pH 7.6 in the presence of 1.6 microM decyl-plastoquinol (C(10)-PQH(2)) as a substrate. Inhibition was competitive with respect to C(10)-PQH(2)
Wen-Wu Li et al.
Journal of the American Chemical Society, 127(17), 6140-6141 (2005-04-28)
Ubiquinone-0, menaquinone-0, and 2,3,5-trimethyl-1,4-benzoquinone were site-specifically bound to free cysteine of proteins (yeast iso-1 cytochrome c as a model protein) through thioether bond formation. Model thioether quinone conjugates showed unexpected reactivity to cysteine of proteins as their parent quinones by
Qiong Guo et al.
The Journal of biological chemistry, 277(8), 6104-6110 (2001-12-19)
The redox properties and thiol reactivity of quinones play critical roles in their therapeutic and toxicological properties. The present study was undertaken to investigate the binding activity of ubiquinone 0 (UQ(0)) to human oxyhemoglobin (HbO(2)) using electron spin resonance (ESR).
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