Phenazine - ≥98% , CAS No.92-82-0

CAS: 92-82-0 Cat. No.: P104715 Molecular Weight: 180.21 Beilstein Registry Number: 126500 EC Number: 202-193-9

GRADE & PURITY ≥98%

Synonyms

5-23-08-00389 (Beilstein Handbook Reference) | NCGC00245795-01 | CU-01000131491-2 | Dibenzo[b,e]pyrazine | InChI=1/C12H8N2/c1-2-6-10-9(5-1)13-11-7-3-4-8-12(11)14-10/h1-8 | UNII-2JHR6K463W | Z104474738 | AMY25819 | CHEBI:36674 | PHENAZINE [MI] | Phenazine,

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

5-23-08-00389 (Beilstein Handbook Reference) | NCGC00245795-01 | CU-01000131491-2 | Dibenzo[b, e]pyrazine | InChI=1/C12H8N2/c1-2-6-10-9(5-1)13-11-7-3-4-8-12(11)14-10/h1-8 | UNII-2JHR6K463W | Z104474738 | AMY25819 | CHEBI:36674 | PHENAZINE [MI] | Phenazine,

Specifications & Purity

≥98%

Storage

Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488179852
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488179852
• Canonical Smiles: C1=CC=C2C(=C1)N=C3C=CC=CC3=N2
• IUPAC Name: phenazine
• InChIKey: PCNDJXKNXGMECE-UHFFFAOYSA-N
• INCHI: 1S/C12H8N2/c1-2-6-10-9(5-1)13-11-7-3-4-8-12(11)14-10/h1-8H
• Isomeric SMILES: C1=CC=C2C(=C1)N=C3C=CC=CC3=N2
• WGK Germany: 3
• RTECS: SG1360000
• Molecular Weight: 180.21
• Beilstein: 126500
• Reaxy-Rn: 126500
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=126500&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Diazanaphthalenes
      • Subclass Benzodiazines
        • Level5 Quinoxalines
          • Level6 Phenazines and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Diazanaphthalenes
• Subclass: Benzodiazines
• Intermediate Tree Nodes: Quinoxalines
• Direct Parent: Phenazines and derivatives
• Alternative Parents: Pyrazines Benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Phenazine - Benzenoid - Pyrazine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as phenazines and derivatives. These are polycyclic aromatic compounds containing a phenazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a pyrazine ring.
• External Descriptors: a small molecule

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(Human)

PRNP Tchem Prion protein (409 Activities)

Discover Target: PRNP

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HepG2 (196354 Activities)

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POLI Tchem DNA polymerase iota (116820 Activities)

Discover Target: POLI

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APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)

Discover Target: APEX1

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

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GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

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MBNL1 Tbio Muscleblind-like protein 1 (34431 Activities)

Discover Target: MBNL1

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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

Discover Target: CBX1

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Associated Targets(non-human)

ampC Beta-lactamase AmpC (62480 Activities)

Discover Target: ampC

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Staphylococcus aureus (210822 Activities)

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Staphylococcus epidermidis (22802 Activities)

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Mapt Microtubule-associated protein tau (6 Activities)

Discover Target: Mapt

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

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FTL Ferritin light chain (43324 Activities)

Discover Target: FTL

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Mechanisms of Action

Chemical and Physical Properties

• Solubility: Insoluble in water；Soluble in ether, alcohol, benzene
• Sensitivity: Moisture sensitive.
• Melt Point(°C): 175℃
• Molecular Weight: 180.200 g/mol
• XLogP3: 2.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 180.069 Da
• Monoisotopic Mass: 180.069 Da
• Topological Polar Surface Area: 25.800 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 162.000
• 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. Mingli Xu, Fengxue Zhang, Yanhui Zhang, Chen Wu, Xue Zhou, Xinping Ai, Jiangfeng Qian.  (2023)  Controllable synthesis of a Na-enriched Na4V2(PO4)3 cathode for high-energy sodium-ion batteries: a redox-potential-matched chemical sodiation approach.  Chemical Science,  14  (44): (12570-12581).  [PMID:38020371] [10.1039/D3SC03498D]

2. Jing-Hong Liu, Yu-Yun Zheng, Jian-Ming Ouyang.  (2023)  Antioxidant Activities and Cytotoxicity of the Regulated Calcium Oxalate Crystals on HK-2 Cells of Polysaccharides from Gracilaria lemaneiformis with Different Molecular Weights.  Foods,  12  (5): (1031).  [PMID:36900548] [10.3390/foods12051031]

3. Qianqian Luo, Chunli Jiang, Hechun Lin, Chunhua Luo, Ruijuan Qi, Hui Peng.  (2019)  Elastic flexibility of ferroelectric supramolecular co-crystals.  SOFT MATERIALS,      [PMID:] [10.1080/1539445X.2019.1653911]

4. Yanjiao Xu, Mengbo Zhang, Hengyu Zhong, Shuying Xie, Xuxin Zhu, Haomiao Zhang, Jingdai Wang, Yongrong Yang.  (2024)  Advanced stackable membrane microreactor for gas–liquid-solid reactions: Design, operation, and scale-up.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.158798]

5. Xiangjun Ding, Mengdan Xu, Haili Li, Xueling Li, Meiqing Li.  (2024)  Improvement of in vivo iron bioavailability using mung bean peptide-ferrous chelate.  FOOD RESEARCH INTERNATIONAL,      [PMID:38945571] [10.1016/j.foodres.2024.114602]

6. Lihuan Xu, Qiang Fei, Lin Yao, Chang Su.  (2024)  Triphenylamine-containing dihydrophenazine copolymers with adjustable multi-electron redox characteristics and their application as cathodes in lithium-organic batteries.  Journal of Materials Chemistry A,  12  (22): (13320-13327).  [PMID:] [10.1039/D4TA00778F]

7. Hao-Tian Zhu, Mi Chen, Ai-Jun Wang, Pei-Xin Yuan, Jiu-Ju Feng.  (2025)  Charge-Regulated Reduction Potential of Phenazine Enabling Electrochemiluminescence for Monitoring Riboflavin in Beans Germination.  ANALYTICA CHIMICA ACTA,      [PMID:41167879] [10.1016/j.aca.2025.344700]

8. Zhongyao Zhang, Hengyu Zhong, Yanjiao Xu, Mengbo Zhang, Haomiao Zhang, Jingdai Wang, Yongrong Yang.  (2025)  Impacts of Heat Treatment and Long-Term Storage on Methylaluminoxane Composition, Catalytic Activity, and Polyethylene Properties.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.5c01770]

9. Gulraiz Tanvir, Kamran Amin, Zhixiang Wei.  (2026)  Bridging Energy and Power Density Gap: Multi-Redox CMP/CNT Composite as High Loading Organic Cathode for Lithium-Ion Battery.  Small Methods,      [PMID:41691393] [10.1002/smtd.202502090]

10. Furan Pang, Xiaolu Li, Fu Yu, Wentao Wang, Hanxue Hou, Luping Zhao, Cheng Li.  (2026)  Optimization of Thermal-Alkaline Treatment Combined with Solid-State Fermentation for Enhanced Production of Bioactive Protein Hydrolysates from Corn Germ Meal.  Foods,  15  (5): (933).  [PMID:41829205] [10.3390/foods15050933]

11. Ya Zou, Zhouhong Tan, Jiaqian Li, Anzhong Peng, Jieli He.  (2026)  Rapid and sensitive fluorescence detection of clozapine via g-C3N4 nanosheet-based quenching.  Analytical Methods,      [PMID:] [10.1039/D5AY02159F]