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1,5-Dihydroxynaphthalene - 98%, high purity , CAS No.83-56-7
Basic Description
Synonyms
1,5-DIHYDROXYNAPHTHALENE | 1,5-dihydroxy-naphthalene | AC-11727 | BIDD:GT0202 | C.I. 76625 | 1.5-naphthalenediol | D72512 | NCGC00357051-01 | 1,5-Naphthalenediol | AKOS005287408 | BDBM36287 | Durafur Developer E | P25HC23VH6 | BRN 2044951 | A19217 | napht
Specifications & Purity
≥98%
Storage Temp
Argon charged
Shipped In
Normal
Product Description
application：
1,5-Dihydroxynaphthalene is an intermediate of synthetic mordant azo dyes. It is an intermediate used in organic synthesis, pharmaceuticals, dyestuff fields and photograph industry.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Naphthalenes
Subclass
Naphthols and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Naphthols and derivatives
Alternative Parents
1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Organooxygen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
1-naphthol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as naphthols and derivatives. These are naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position.
External Descriptors
Not available
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.
Associated Targets(Human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
488180147
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488180147
IUPAC Name
naphthalene-1,5-diol
INCHI
InChI=1S/C10H8O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1-6,11-12H
InChIKey
BOKGTLAJQHTOKE-UHFFFAOYSA-N
Smiles
C1=CC2=C(C=CC=C2O)C(=C1)O
Isomeric SMILES
C1=CC2=C(C=CC=C2O)C(=C1)O
WGK Germany
2
RTECS
QJ4740000
Molecular Weight
160.17
Beilstein
2044951
Reaxy-Rn
2044951
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2044951&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Solubility in water: 0.6 g/l in water (20°C) Solubility in other solvents: soluble in methanol
Sensitivity
Air Sensitive
Flash Point(°F)
486°F
Flash Point(°C)
252°C
Melt Point(°C)
265°C
Molecular Weight
160.170 g/mol
XLogP3
1.800
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
0
Exact Mass
160.052 Da
Monoisotopic Mass
160.052 Da
Topological Polar Surface Area
40.500 Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
140.000
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
Citations of This Product
1.
Junhua Chen, Shiting Li, Xuan Wang, Lili Fang, Dingding Huang, Lin Ke, Jinlian Chen, Qingwei Wang, He Zhang, Yinping Wu, Dongyu Zhu, Chunsheng Li, Xiangying Hao.
(2023)
Synthesis and Characterization of Pressure-Sensitive Adhesives Based on a Naphthyl Curing Agent. Polymers,
15
(23):
(4516).
2.
Jintao An, Qianrui Lv, Yuchao Wang, Wenbo Yang, Shengyang Tao, Lijing Zhang, Alexander A. Miskevich, Valery A. Loiko.
(2023)
Study of the Coupling Effect of Multiple Factors on the Photoreaction Process Based on a Standard Photoreactor. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,
62
(26):
(10266–10276).
3.
Yu Caili, Lu Guangjie, Yan Chengfei, Xu Jianben, Zhang Faai.
(2023)
Preparation and pH Detection Performance of Rosin-Based Fluorescent Polyurethane Microspheres. JOURNAL OF FLUORESCENCE,
33
(4):
(1593-1602).
4.
Zheng Yin, Zou Bo, Yuan Liangjie.
(2013)
Structure and properties of novel epoxy resins containing naphthalene units and aliphatic chains. IRANIAN POLYMER JOURNAL,
22
(5):
(325-334).
5.
Shan Wu, Yuhan Duan, Wenru Kuang, Wenyue Dong, Xu Cui, Xiaodong Zhang, Qian Duan.
(2024)
Homogeneous catalysis and heterogeneous recovery: Thermo-responsive copolymer visible light catalyst with phthalocyanine as side groups. REACTIVE & FUNCTIONAL POLYMERS,
197
(105857).
6.
Yifei Ma, Lijie Zhang, Hong Yang, Shanshan Zhu, Jinhua Liu.
(2025)
Imidazole-triggered in situ fluorescence reaction system for quantitatively determination of dopamine from multiple sources. TALANTA,
(127975).
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6 Citations
F2428001