1,4-Dihydroxyanthraquinone - ≥96% , CAS No.81-64-1

CAS: 81-64-1 Cat. No.: D104680 Peso molecular: 240.21 Beilstein Registry Number: 1914036 Número EC: 201-368-7
Disponible para pedir
GRADE & PURITY ≥96%
Synonyms
9,10-Anthracenedione, 1,4-dihydroxy- | 1,4-Doa | Q906609 | 1,4-Dioxyanthraquinone [Russian] | BBL010354 | EN300-6486266 | Macrolex Orange GG | SR-01000637713-1 | 1,4-Dihydroxyanthra-9,10-quinone # | NCGC00160196-02 | Quinizarin; 1,4-Dihydroxyanthraquinone
Storage
Room temperature
Shipped In
Normal
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Size
Estado
Price
Qty
25g
D104680-25g
10

11,90US$

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100g
D104680-100g
9

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32,90US$
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250g
D104680-250g
3

48,90US$

73,90US$
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500g
D104680-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

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103,90US$
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Why this grade

≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

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

📋

Quality documents

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

📚

Literature proof

Cited in 14 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

1,4-Dihydroxyanthraquinone is an organic dye molecule with an aromatic structure. It is a derivative of anthraquinone bearing hydroxyl moieties. They may find uses in pharmacological, biochemical and dye industries. Anthraquinone dye are resistant to degradation.


application:

1,4-Dihydroxyanthraquinone may be used in the synthesis of cyclopentanoids by cyclization of α,β-unsaturated aldehyde with 1, 4 1,4-Dihydroxyanthraquinone. It has been studied as a long range emissive ratiometric fluorescent probe for live cell imaging.

Specifications

Sinónimos
9, 10-Anthracenedione, 1, 4-dihydroxy- | 1, 4-Doa | Q906609 | 1, 4-Dioxyanthraquinone [Russian] | BBL010354 | EN300-6486266 | Macrolex Orange GG | SR-01000637713-1 | 1, 4-Dihydroxyanthra-9, 10-quinone # | NCGC00160196-02 | Quinizarin; 1, 4-Dihydroxyanthraquinone
Especificaciones y pureza
≥96%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥96%
Nombres e identificadores
Pubchem Sid488180130
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180130
Sonrisas canónicasC1=CC=C2C(=C1)C(=O)C3=C(C=CC(=C3C2=O)O)O
IUPAC Name1,4-dihydroxyanthracene-9,10-dione
InChIKeyGUEIZVNYDFNHJU-UHFFFAOYSA-N
INCHI1S/C14H8O4/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6,15-16H
Isómeros SMILES C1=CC=C2C(=C1)C(=O)C3=C(C=CC(=C3C2=O)O)O
WGK Alemania 2
RTECS CB6600000
Peso molecular 240.21
Beilstein 1914036
Reaxy-Rn 1914036
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1914036&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ Certificate of Analysis (COA)

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

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseAnthracenes
SubclassAnthraquinones
Intermediate Tree Nodes Not available
Direct ParentAnthraquinones
Alternative Parents Aryl ketones  1-hydroxy-2-unsubstituted benzenoids  Vinylogous acids  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Anthraquinone - 9,10-anthraquinone - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - Vinylogous acid - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
DescripciónThis 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 dihydroxyanthraquinone
Estructura 3D
Modelo de Estructura Química Interactiva





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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

19 results found

Lot NumberCertificate TypeFechaArticulo
K1819121Certificate of AnalysisJun 11, 2026 D104680
A2627166Certificate of AnalysisFeb 07, 2026 D104680
L2123381Certificate of AnalysisOct 11, 2025 D104680
L2123380Certificate of AnalysisOct 11, 2025 D104680
L2123373Certificate of AnalysisOct 11, 2025 D104680
K2102017Certificate of AnalysisAug 11, 2025 D104680
F1722014Certificate of AnalysisJan 20, 2025 D104680
F2503235Certificate of AnalysisJul 15, 2024 D104680
F2503236Certificate of AnalysisJul 15, 2024 D104680
E2528435Certificate of AnalysisJul 15, 2024 D104680
E2528440Certificate of AnalysisJul 15, 2024 D104680
E2528436Certificate of AnalysisJul 15, 2024 D104680
I2308464Certificate of AnalysisDec 13, 2022 D104680
I2308465Certificate of AnalysisDec 13, 2022 D104680
I2308466Certificate of AnalysisDec 13, 2022 D104680
I2308467Certificate of AnalysisDec 13, 2022 D104680
I2308437Certificate of AnalysisDec 13, 2022 D104680
I2308328Certificate of AnalysisDec 13, 2022 D104680
I2308327Certificate of AnalysisDec 13, 2022 D104680

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Propiedades químicas y físicas
SolubilidadSoluble in Benzene
Punto de inflamación (°C)222°C
Punto de ebullición (°C)450°C
Punto de fusión (°C)195-200 °C
Peso molecular240.210 g/mol
XLogP33.700
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass240.042 Da
Monoisotopic Mass240.042 Da
Topological Polar Surface Area74.600 Ų
Heavy Atom Count18
Formal Charge0
Complexity342.000
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
Citations of This Product
Referencias
1. Rui Gao, Zihao Jiang, Xiuyu Wu, Zhihong Cai, Nan Sang.  (2023)  Metabolic regulation of tumor cells exposed to different oxygenated polycyclic aromatic hydrocarbons.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:37839476] [10.1016/j.scitotenv.2023.167833]
2. Xu Liu, Xiao Han, Yushuang Shang, Lijuan Wang, Jian Shen, Jiang Yuan.  (2023)  Hydrogen sulfide releasing poly(γ-glutamic acid) biocomposite hydrogel with monitoring, antioxidant, and antibacterial properties for diabetic wound healing.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:37774813] [10.1016/j.ijbiomac.2023.127053]
3. Yunxiao Wang, Chang Liu, Shanshan Tang, Jing Tian, Yi Wang, Yi Yang.  (2023)  Thermodynamics, kinetics and structure-activity relationship of hydroxyanthraquinones scavenging free radicals.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2023.102705]
4. Peiyuan Su, Jianing Yue, Qingyu Kong, Wenkai Zhang.  (2022)  Excited state intramolecular proton transfer in 1,4-dihydroxyanthraquinone.  CHEMICAL PHYSICS,      [PMID:] [10.1016/j.chemphys.2022.111783]
5. Yuanyuan Song, Ziqi Wang, Yijing Long, Yang Mao, Feng Jiang, Yuanyuan Lu.  (2022)  2-Alkyl-anthraquinones inhibit Candida albicans biofilm via inhibiting the formation of matrix and hyphae.  RESEARCH IN MICROBIOLOGY,      [PMID:35550403] [10.1016/j.resmic.2022.103955]
6. Leiqian Zhang, Lingfeng Ge, Guanjie He, Zhihong Tian, Jiajia Huang, Jingtao Wang, Dan J.L. Brett, Johan Hofkens, Feili Lai, Tianxi Liu.  (2021)  Tuning the Linkers in Polymer-Based Cathodes to Realize High Sulfur Content and High-Performance Potassium–Sulfur Batteries.  Journal of Physical Chemistry C,      [PMID:] [10.1021/acs.jpcc.1c05283]
7. Wei Ji, Wenmei Ao, Mengqiu Sun, Chunlai Feng, Yun Wang.  (2020)  Separation and purification of horseradish peroxidase from horseradish roots using a novel integrated method.  NEW JOURNAL OF CHEMISTRY,  45  (4): (1959-1966).  [PMID:] [10.1039/D0NJ04614K]
8. Shuai Li, Changbing Zhou, Yingying He, Hongxia Liu, Li Zhou, Chuanbai Yu, Chun Wei, Chaoyang Wang.  (2020)  Novel Nanocellulose/Polymer Composite Aerogel as Solid-State Fluorescence Probe by Pickering Emulsion Route.  MACROMOLECULAR MATERIALS AND ENGINEERING,  305  (11): (2000467).  [PMID:] [10.1002/mame.202000467]
9. Wei Zhang, Peipei Zhou, Wei Liu, Huili Wang, Xuedong Wang.  (2020)  Enhanced adsorption/extraction of five typical polycyclic aromatic hydrocarbons from meat samples using magnetic effervescent tablets composed of dicationic ionic liquids and NiFe2O4 nanoparticles.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2020.113682]
10. Lixia Lin, Huizhi Du.  (2018)  An anthraquinone compound and its protective effects against homocysteine-induced cytotoxicity and oxidative stress.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:29800895] [10.1016/j.saa.2018.05.058]
11. Jing Li, Qingxiang Zhou, Yongli Liu, Man Lei.  (2017)  Recyclable nanoscale zero-valent iron-based magnetic polydopamine coated nanomaterials for the adsorption and removal of phenanthrene and anthracene.  SCIENCE AND TECHNOLOGY OF ADVANCED MATERIALS,      [PMID:28179954] [10.1080/14686996.2016.1246941]
12. Jing Yang, Yun Yuan, Ruxin Zhang, Chao Liu, Deyi Zhu, Dandan Ji.  (2024)  Rapid detection of Cu2+ and Cr3+ ions in industrial wastewater using gelatin-poly-ε-caprolactone nanofiber fluorescent sensors.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2024.126718]
13. Xin-Yue Wang, Yue Fan, Jia-Jie Long.  (2024)  Synthesis of an anthraquinonoid blue dye based on one-pot amination reactions and its coloration in SCF-CO2.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2024.112029]
14. Jiaxing Zhang, Wen Wang, Zubiyan Yibula, Xin Peng, Rongxin Su, Wei Qi.  (2026)  Anthraquinones Inhibit Insulin Amyloidosis in Crowded Environments.  MOLECULES,  31  (7): (1092).  [PMID:] [10.3390/molecules31071092]
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