D223204

Duroquinone

97%

Manufacturer: Sigma Aldrich

CAS Number: 527-17-3

Synonym(S): 2,3,5,6-Tetramethyl-1,4-benzoquinone, Tetramethyl-p-benzoquinone

Select a Size

Pack Size SKU Availability Price
1 G D223204-1-G In Stock ₹ 4,650.00
5 G D223204-5-G In Stock ₹ 9,820.00

D223204 - 1 G

₹ 4,650.00

In Stock

Quantity

1

Base Price: ₹ 4,650.00

GST (18%): ₹ 837.00

Total Price: ₹ 5,487.00

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

Other Options

Image Product Name Manufacturer Price Range
50-185-8423
Sigma Aldrich Fine Chemicals Biosciences Duroquinone 97% | 527-17-3 | MFCD00001604 | 5G
Sigma Aldrich Fine Chemicals Biosciences ₹ 16,665.38
50-212-7658
eMolecules​ Duroquinone | 527-17-3 | MFCD00001604 | 5g
eMolecules​ ₹ 10,831.04
50-241-9762
eMolecules​ Ambeed / 2356-Tetramethylcyclohexa-25-diene-14-dione / 250mg / 575774784 / A275277 / / 527-17-3 / MFCD00001604 / 164.204 / C10H12O2
eMolecules​ ₹ 2,153.55
CS-0153601
Duroquinone
ChemScene ₹ 1,711.20 - ₹ 48,598.08
AB73336
527-17-3 | Duroquinone
A2B Chem ₹ 1,197.84 - ₹ 34,052.88

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Description

  • General description: Duroquinone is an organic oxidant that belongs to the class of 1,4-benzoquinones, is used in redox flow Li–O2 batteries.[1]
  • 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).

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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powder

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110-112 °C (lit.)

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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

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PWGJDPKCLMLPJW-UHFFFAOYSA-N

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