Coenzyme Q0 - ≥97% , CAS No.605-94-7

CAS: 605-94-7 Cat. No.: C106269 Molecular Weight: 182.17 Beilstein Registry Number: 1640422 EC Number: 210-100-8

GRADE & PURITY ≥97%

Synonyms

2,3-Dimethoxy 5-methyl-1,4-benzoquinone | EINECS 210-100-8 | Q0 | FT-0609676 | Ubiquinone 0 | Ubiquinone Qo | ubiquinone-Q0 | 2,3 dimethoxy 5-methyl 1,4 benzoquinone | 2,3-Dimethoxy-5-methyl-p-benzoquinone | 2,3-Dimethoxy-5-methylbenzo-1,4-quinone | InChI

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Specifications

Synonyms

2, 3-Dimethoxy 5-methyl-1, 4-benzoquinone | EINECS 210-100-8 | Q0 | FT-0609676 | Ubiquinone 0 | Ubiquinone Qo | ubiquinone-Q0 | 2, 3 dimethoxy 5-methyl 1, 4 benzoquinone | 2, 3-Dimethoxy-5-methyl-p-benzoquinone | 2, 3-Dimethoxy-5-methylbenzo-1, 4-quinone | InChI

Specifications & Purity

≥97%

Storage

Store at 2-8°C, Protected from light

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Action Type

MODULATOR

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 504754328
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754328
• Canonical Smiles: CC1=CC(=O)C(=C(C1=O)OC)OC
• IUPAC Name: 2,3-dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione
• InChIKey: UIXPTCZPFCVOQF-UHFFFAOYSA-N
• INCHI: 1S/C9H10O4/c1-5-4-6(10)8(12-2)9(13-3)7(5)11/h4H,1-3H3
• Isomeric SMILES: CC1=CC(=O)C(=C(C1=O)OC)OC
• WGK Germany: 2
• Molecular Weight: 182.17
• Beilstein: 1640422
• Reaxy-Rn: 1640422
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1640422&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Prenol lipids
      • Subclass Quinone and hydroquinone lipids
        • Level5 Prenylquinones
          • Level6 Ubiquinones

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Prenol lipids
• Subclass: Quinone and hydroquinone lipids
• Intermediate Tree Nodes: Prenylquinones
• Direct Parent: Ubiquinones
• Alternative Parents: P-benzoquinones Vinylogous esters Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Ubiquinone skeleton - Quinone - P-benzoquinone - Vinylogous ester - Cyclic ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as ubiquinones. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methyl(1,4-benzoquinone) moiety to which an isoprenyl group is attached at ring position 2(or 6).
• External Descriptors: a ubiquinone

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Trichoplusia ni (986 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Sensitivity: Light sensitive.
• Melt Point(°C): 58-60°C
• Molecular Weight: 182.170 g/mol
• XLogP3: 0.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 182.058 Da
• Monoisotopic Mass: 182.058 Da
• Topological Polar Surface Area: 52.600 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 323.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Ruipeng Shen, Min Li, Shuo Wang, Yu-Mo Zhang, Sean Xiao-An Zhang.  (2025)  An electrochromic device based on dynamic coordination and the dissociation of Fe2+/Fe3+ and a leuco dye with an improved cycle life.  Journal of Materials Chemistry C,      [PMID:] [10.1039/D4TC04582C]

2. Xiao Tu, Jiaxin Hu, Jinghao Peng, Qihan Chen, Yangle Zhao, Zemao Gu.  (2025)  Discovery of thymoquinone analogues with high anthelmintic activity against monogenean infections in goldfish (Carassius auratus).  VETERINARY PARASITOLOGY,      [PMID:39837239] [10.1016/j.vetpar.2025.110401]