D223204
Duroquinone
97%
Synonym(s):
2,3,5,6-Tetramethyl-1,4-benzoquinone, Tetramethyl-p-benzoquinone
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 g | Available to ship TODAYfromMILWAUKEE | $93.00 | |
| 5 g | Available to ship TODAYfromMILWAUKEE | $169.00 |
About This Item
Empirical Formula (Hill Notation):
C10H12O2
CAS Number:
Molecular Weight:
164.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-409-8
Beilstein/REAXYS Number:
1909128
MDL number:
Assay:
97%
Form:
powder
$93.00
Available to ship TODAYDetails
Subscriptions are currently unavailable.
Ships Every 4 weeks
assay
97%
form
powder
mp
110-112 °C (lit.)
SMILES string
CC1=C(C)C(=O)C(C)=C(C)C1=O
InChI
1S/C10H12O2/c1-5-6(2)10(12)8(4)7(3)9(5)11/h1-4H3
InChI key
WAMKWBHYPYBEJY-UHFFFAOYSA-N
General description
Duroquinone is an organic oxidant that belongs to the class of 1,4-benzoquinones, is used in redox flow Li–O2 batteries.
Application
- Role of Duroquinone in Photosynthetic Research: A study on purple bacterial photosynthetic reaction centers highlighted Duroquinone′s role when incorporated into the QA binding site, impacting the isotope edited FTIR difference spectra, crucial for understanding energy conversion processes in photosynthesis (Zhao et al., 2013).
- Duroquinone as a Molecular Ion Source: Research demonstrated the generation of molecular negative ions by Duroquinone, showcasing its potential in mass spectrometry applications for studying molecular ionization and longevity (Khvostenko et al., 2012).
- Duroquinone in Biochemical Sensors: Investigation into the optimization of gold electrode surfaces with photosystem II monolayers revealed Duroquinone′s critical role in enhancing sensor responses, applicable in biochemical sensor technology (Maly et al., 2005).
- Cytotoxicity of Duroquinone Congeners: A comparative study of 14 p-benzoquinone congeners, including Duroquinone, used quantitative structure-toxicity relationships to evaluate cytotoxicity in rat hepatocytes and PC12 cells, relevant for safety assessments in chemical manufacturing (Siraki et al., 2004).
1 of 1
This Item | |||
|---|---|---|---|
| assay 97% | assay 99% | assay - | assay ≥97% (HPLC) |
| Quality Level 200 | Quality Level 100 | Quality Level 200 | Quality Level 100 |
| mp 110-112 °C (lit.) | mp >300 °C (lit.) | mp 110-113 °C | mp - |
| form powder | form - | form solid | form liquid |
Still not finding the right product?
Explore all of our products under Duroquinone
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Revealing the catalytic pathway of a quinone-mediated oxygen reduction reaction in aprotic Li--O 2 batteries
Wu S, et al.
Journal of the Chemical Society. Chemical Communications, 58, 1025-1028 (2022)
Bingsheng Zhou et al.
Aquatic toxicology (Amsterdam, Netherlands), 77(2), 136-142 (2006-01-18)
Toxicity of many waterborne organic contaminants to aquatic organisms is mediated through oxidative damages resulting from the production of reactive oxygen species (ROS). Using duroquinone as a model ROS inducer, we carried out in vitro and in vivo experiments to
J Maly et al.
Analytical and bioanalytical chemistry, 381(8), 1558-1567 (2005-04-12)
Mass transport of the bulk of the analyte to the electrode and through the bioactive layer can be significantly improved by use of the nanoelectrode array and defined arrangement of protein film. This phenomenon has been studied by (i) atomic-force
Global Trade Item Number
| SKU | GTIN |
|---|---|
| D223204-5G | 04061831826548 |
| D223204-1G | 04061825597713 |