Anthraquinone - Melting point standard , CAS No.84-65-1

CAS: 84-65-1 Cat. No.: A119546 Molecular Weight: 208.21 Beilstein Registry Number: 390030 EC Number: 201-549-0
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GRADE & PURITY Melting point standard ? Melting-point standard — certified material with a known, sharp melting point. Use to calibrate and verify melting-point apparatus.
Synonyms
Anthracene,10-dihydro-9,10-dioxo- | Anthraquinone, 97% | Spectrum3_001501 | Morkit | 9,10-dihydroanthracene-9,10-dione | A-8000 | KBio2_007143 | 030MS0JBDO | Anthraquinone 100 microg/mL in Acetonitrile | InChI=1/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-
Storage
Room temperature
Shipped In
Normal
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1g
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Why this grade

Melting point standard Melting point standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 38 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
Anthracene, 10-dihydro-9, 10-dioxo- | Anthraquinone, 97% | Spectrum3_001501 | Morkit | 9, 10-dihydroanthracene-9, 10-dione | A-8000 | KBio2_007143 | 030MS0JBDO | Anthraquinone 100 microg/mL in Acetonitrile | InChI=1/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-
Specifications & Purity
Melting point standard
Storage
Room temperature
Shipped In
Normal
Grade
Melting point standard
Names and Identifiers
Canonical SmilesC1=CC=C2C(=C1)C(=O)C3=CC=CC=C3C2=O
IUPAC Nameanthracene-9,10-dione
InChIKeyRZVHIXYEVGDQDX-UHFFFAOYSA-N
INCHI1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H
Isomeric SMILES C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3C2=O
WGK Germany 1
RTECS CB4725000
Molecular Weight 208.21
Beilstein 390030
Reaxy-Rn 390030
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=390030&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassAnthracenes
SubclassAnthraquinones
Intermediate Tree Nodes Not available
Direct ParentAnthraquinones
Alternative Parents Aryl ketones  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Anthraquinone - 9,10-anthraquinone - Aryl ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone.
External Descriptors an anthraquinone
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDK4 Tchem Pyruvate dehydrogenase kinase isoform 4 (177 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AGS (1999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
J82 (505 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MRC5 (9203 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MES-1 (413 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A2780 (11979 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT1 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 5 (407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A1 Tchem UDP-glucuronosyltransferase 1-1 (448 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PMP22 Tbio Peripheral myelin protein 22 (699 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A8 Tbio UDP-glucuronosyltransferase 1-8 (233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Cdc25b Dual specificity phosphatase Cdc25B (32 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zea mays (820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Columba livia (47 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Botrytis cinerea (4183 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lactuca sativa (1092 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Dusp6 Dual specificity protein phosphatase 6 (459 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Dusp1 Dual specificity protein phosphatase 1 (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cucumis sativus (803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Erwinia amylovora (182 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sclerotinia sclerotiorum (877 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Solanum lycopersicum (493 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FTL Ferritin light chain (43324 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor (6467 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Estrogen receptor (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Verticillium dahliae (119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Capsicum annuum (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sclerotinia minor (10 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Solanum melongena (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Brassica oleracea var. italica (9 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Brassica oleracea (32 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cucumis melo (2 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot NumberCertificate TypeDateItem
A2629740Certificate of AnalysisJan 08, 2026 A119546
F2327331Certificate of AnalysisApr 07, 2025 A119546
Chemical and Physical Properties
Flash Point(°F)365 °F
Flash Point(°C) 185℃
Boil Point(°C)377°C
Melt Point(°C)286°C
Molecular Weight208.210 g/mol
XLogP33.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass208.052 Da
Monoisotopic Mass208.052 Da
Topological Polar Surface Area34.100 Ų
Heavy Atom Count16
Formal Charge0
Complexity261.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
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17. Jufeng Huang, Wei Xing, Fazle Subhan, Xiuli Gao, Peng Bai, Zhen Liu, Youhe Wang, Qingzhong Xue, Zifeng Yan.  (2017)  Functionalization of petroleum coke-based mesoporous carbon for synergistically enhanced capacitive performance.  JOURNAL OF MATERIALS RESEARCH,  32  (7): (1248-1257).  [PMID:] [10.1557/jmr.2017.36]
18. Qiming Zhao, Kexian Chen, Wensong Zhang, Jia Yao, Haoran Li.  (2015)  Efficient metal-free oxidation of ethylbenzene with molecular oxygen utilizing the synergistic combination of NHPI analogues.  JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL,      [PMID:] [10.1016/j.molcata.2015.03.017]
19. Xingqiang Wu, Shuxuan Liang, Xusheng Ge, Yunkai Lv, Hanwen Sun.  (2015)  Synthesis and evaluation of dummy molecularly imprinted microspheres for the specific solid-phase extraction of six anthraquinones from slimming tea.  JOURNAL OF SEPARATION SCIENCE,  38  (8): (1263-1270).  [PMID:25677958] [10.1002/jssc.201401341]
20. Gong Hao, He Zihao, Peng Anlin, Zhang Xin, Cheng Biao, Sun Yue, Zheng Ling, Huang Kun.  (2014)  Effects of several quinones on insulin aggregation.  Scientific Reports,  (1): (1-8).  [PMID:25008537] [10.1038/srep05648]
21. Zhen Chen, Yan Wang, Zebing Ning, Qi Huang, Jia Zhou, Faquan Yu.  (2024)  Conjugated Microporous Polymer/TiS2 Composite Cathode for High-Performance Lithium-Rechargeable Batteries.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.4c02203]
22. Zhengkai Li, Heng Wang, Hanwen Yan, Hao Wang, Zhencai Zhang, Yiwen Zhang, Junyu Chu, Feng Huo, Fei Xu.  (2024)  Design and Synthesis of Optical Biobased Polycarbonates with High Refractive Index and Low Birefringence.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.3c04461]
23. Liang Zhou, Jie Zhou, Yicen Dong, Yangjie Wu, Zhangying Xi, Zixuan Lu, Juying Lei, Jinlong Zhang, Yongdi Liu.  (2024)  Insight on photocatalytic synchronous oxidation and reduction for pollutant removal: Chemical energy conversion between macromolecular organic pollutants and heavy metal.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:39038377] [10.1016/j.jhazmat.2024.135236]
24. Ning Xia, Fengli Gao, Gang Liu, Yong Chang, Lin Liu.  (2024)  Pyrroloquinoline quinone exhibiting peroxidase-mimicking property for colorimetric assays.  ANALYTICA CHIMICA ACTA,      [PMID:39643317] [10.1016/j.aca.2024.343468]
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33. Renzhi Xiong, Yiting Sun, Jiahao Huang, Fangde Liu, Yanhe Xiao, Baochang Cheng, Shuijin Lei.  (2025)  Defect-engineered WO3−x@Zn3In2S6−x S-scheme heterojunction with atomic interfacial bonds for efficient photothermal-assisted photocatalytic H2O2 production.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.164909]
34. Ya Chu, Weiqiang Zhang, Baoye Hu, Jinghong Wen, Mengmei Qin, Guangjiu Zhao.  (2025)  Unveiling the Surface Exciton Dynamics in K-Doped Perovskite Quantum Dots Using Chiral Ligands Enables Efficient White LEDs.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.5c04871]
35. Renzhi Xiong, Xiao Xiao, Yanjie Song, Keqin Chen, Yanhe Xiao, Baochang Cheng, Shuijin Lei.  (2025)  1D/2D Sb2S3@SnIn4S8 core-shell S-scheme heterojunction: A bifunctional photocatalyst for concurrent H2 production and antibiotic degradation in wastewater.  INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,      [PMID:] [10.1016/j.ijhydene.2025.152248]
36. Rong Fang, Jiao Ma, Meiling Wang, Kunpeng Guo.  (2025)  Humic acid mediated self-signal molecularly imprinted electrochemical sensor for cortisol detection.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.116374]
37. Renzhi Xiong, Dongchen Duan, Xiaoxue Ke, Keqin Chen, Yanhe Xiao, Baochang Cheng, Shuijin Lei.  (2026)  Wurtzite/Kesterite Cu2ZnSnS4 S-Scheme Heterophase Junction: A Robust Catalyst for Photothermal-Assisted Photocatalytic CO2 Reduction and Environmental Remediation.  CHEMISTRY OF MATERIALS,      [PMID:] [10.1021/acs.chemmater.5c02359]
38. Tianlong Huang, Zhen Mu, Yuanxiang Zhang, Maosheng Cui, Xiaoxiao Wang, Yang Zhang, Lingxiu Chen, Xiaolan Xue.  (2026)  A ZIF-8/carbon-modified commercial PEP separator enabling stable magnesium deposition and effective quinone shuttle suppression in magnesium–organic batteries.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2026.187437]
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