Determine the necessary mass, volume, or concentration for preparing a solution.
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10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
2-Hydroxy-1,4-naphthoquinone is one among the forensic reagents used for fingerprint detection 2-Hydroxy-1,4-naphthoquinone, produced from Lawsonia inermis, is an orange dye. It belongs to the class of naphthoquinone dyes. 2-Hydroxy-1,4-naphthoquinone is used to dye hair and to color textiles. It has antibacterial, antifungal, anti-inflammatory, antiviral and antineoplastic properties. 2-Hydroxy-1,4-naphthoquinone inhibits tumor cell growth. It stimulates the production of reactive oxygen species (ROS).[
An antimicrobial antioxidant dye isolated from Henna.
2-Hydroxy-1,4-naphthoquinone is used for preparing decorative hair and skin dyes. 2-Hydroxy-1,4-naphthoquinone also demonstrates antimicrobial and antioxidant effects. It also suppress the formation of hydrogen peroxide and superoxide radical anion by aldehyde oxidase-catalyzed reactions.
| Canonical Smiles | C1=CC=C2C(=C1)C(=CC(=O)C2=O)O |
|---|---|
| IUPAC Name | 4-hydroxynaphthalene-1,2-dione |
| InChIKey | WVCHIGAIXREVNS-UHFFFAOYSA-N |
| INCHI | 1S/C10H6O3/c11-8-5-9(12)10(13)7-4-2-1-3-6(7)8/h1-5,11H |
| Isomeric SMILES | C1=CC=C2C(=C1)C(=CC(=O)C2=O)O |
| WGK Germany | 3 |
| RTECS | QL8200000 |
| Molecular Weight | 174.15 |
| Beilstein | 1565260 |
| Reaxy-Rn | 2575949 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2575949&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Naphthalenes |
| Subclass | Naphthoquinones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthoquinones |
| Alternative Parents | Naphthols and derivatives Quinones Aryl ketones Vinylogous acids Enols Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Naphthoquinone - 1-naphthol - Aryl ketone - Quinone - Vinylogous acid - Cyclic ketone - Ketone - Enol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as naphthoquinones. These are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone). |
| External Descriptors | Not available |
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| Melt Point(°C) | 193°C |
|---|---|
| Molecular Weight | 174.150 g/mol |
| XLogP3 | 0.900 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 174.032 Da |
| Monoisotopic Mass | 174.032 Da |
| Topological Polar Surface Area | 54.400 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 291.000 |
| 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 |
| 1. Yitao Lv, Yi Zhang, Yunyin Yang, Jingyan Li, Jiacheng Wang, Xilin Xiao, Min Zhang. (2023) Strategy of In Situ Electrochemical Regulation for Highly Enhanced Nonenzymatic Sensing of Carbaryl. ANALYTICAL CHEMISTRY, [PMID:36802553] [10.1021/acs.analchem.2c04373] |
| 2. Meng Li, Dong Wang, Xiaoduo Liu, Jingmei Sun. (2019) Evaluation and correction on quinones’ quantification errors: Derived from the coexistence of different quinone species and pH-sensitive feature. CHEMOSPHERE, [PMID:31102873] [10.1016/j.chemosphere.2019.04.146] |
| 3. Yang Li, Cai Tianming, Ding Dahu, Cai Tianjin, Jiang Canlan, Li Hua, Yang Qian, Chen Liwei. (2017) Biodegradation of 2-hydroxyl-1,4 naphthoquinone (lawsone) by Pseudomonas taiwanensis LH-3 isolated from activated sludge. Scientific Reports, 7 (1): (1-10). [PMID:28754900] [10.1038/s41598-017-06338-1] |
| 4. Lisong Xia, Lei Cheng, Wenni Xi, Xiliang Zhang, Xianyang Shi. (2024) Distinct influence of model electron shuttles on anaerobic mononitrophenols reduction in aquatic environments by Shewanella oneidensis MR-1. JOURNAL OF HAZARDOUS MATERIALS, [PMID:39079298] [10.1016/j.jhazmat.2024.135348] |
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| 6. Yanpeng Huang, Qiong Wu, Jingfan Yan, Fumin Chu, Yuming Xu, Dongmin Li, Hongjia Zhang, Sen Yang. (2024) Efficient removal and recovery of phosphate by biochar loaded with ultrafine MgO nanoparticles. ENVIRONMENTAL RESEARCH, [PMID:39638027] [10.1016/j.envres.2024.120518] |
| 7. Neng Guo, Shuaipeng Li, Dongdong Zhu, Yufan Wu, Dongjin Wang, Yaru Wang, Zhiguo Sun, Shengwen Chen, Jifen Wang. (2025) Preparation and Denitrification Performance of Sodium Humate/TiO₂ Composite Nanoparticles. ChemistrySelect, 10 (22): (e01220). [PMID:] [10.1002/slct.202501220] |
| 8. Jinyang Chen, Xiaoyu Lin, Wei Wang, Li Gan, Zuliang Chen. (2026) Mediated electron transfer in the bio-reduction of graphene oxide by Lysinibacillus sphaericus: Mechanisms and facilitation. JOURNAL OF POWER SOURCES, [PMID:] [10.1016/j.jpowsour.2026.239646] |