Skip to the beginning of the images gallery

1,6-Dihydroxynaphthalene - >99.0%(GC), high purity , CAS No.575-44-0

6 Citations

COA

Grade & Purity:

≥99%(GC)

Cas Number: 575-44-0
Molecular Weight: 160.17
Beilstein Registry Number: 6(3)5279
MDL number: MFCD00003981
PubChem CID: 68463
PubChem SID: 488184147

In stock

Item Number

D154708

Grouped product items
SKU	Size	Availability	Price
D154708-5g	5g	5	$10.90
D154708-10g	10g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$16.90
D154708-25g	25g	3	$32.90
D154708-100g	100g	3	$116.90
D154708-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$317.90

View related series

Diol monomer (70) Polymer / polymer reagent (675)

Basic Description

Synonyms	BDBM36288 \| CI 76630 \| 1,6-DIHYDROXY NAPHTHALENE \| 34C30KW024 \| 1,6-naphthalene diol \| 6-Hydroxy-1-naphthol \| NSC 7201 \| PD005577 \| AKOS000496309 \| FT-0607003 \| C.I. 76630 \| F11438 \| EN300-105164 \| 2,5-Naphthalenediol \| FS-3180 \| Q27096881 \| UNII-34C30KW0
Specifications & Purity	≥99%(GC)
Storage Temp	Argon charged
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Naphthalenes
    - Subclass Naphthols and derivatives

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 - 2-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	naphthalenediol
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)

T-24 (2342 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

IDO1 Tchem Indoleamine 2,3-dioxygenase (6650 Activities)

Discover Target: IDO1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HFL1 (586 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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	488184147
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488184147
IUPAC Name	naphthalene-1,6-diol
INCHI	InChI=1S/C10H8O2/c11-8-4-5-9-7(6-8)2-1-3-10(9)12/h1-6,11-12H
InChIKey	FZZQNEVOYIYFPF-UHFFFAOYSA-N
Smiles	C1=CC2=C(C=CC(=C2)O)C(=C1)O
Isomeric SMILES	C1=CC2=C(C=CC(=C2)O)C(=C1)O
Molecular Weight	160.17
Beilstein	6(3)5279
Reaxy-Rn	1939032
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1939032&ln=

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.

12 results found

Lot Number	Certificate Type	Date	Item
D2007018	Certificate of Analysis	Jan 10, 2024	D154708
K1813015	Certificate of Analysis	Sep 15, 2022	D154708
K2205115	Certificate of Analysis	Jul 21, 2022	D154708
F2328089	Certificate of Analysis	Jul 21, 2022	D154708
B2311421	Certificate of Analysis	Jul 21, 2022	D154708
F2526016	Certificate of Analysis	Jul 21, 2022	D154708
F2328096	Certificate of Analysis	Jul 21, 2022	D154708
K2205112	Certificate of Analysis	Jul 21, 2022	D154708
K2205113	Certificate of Analysis	Jul 21, 2022	D154708
K2205114	Certificate of Analysis	Jul 21, 2022	D154708
D2416032	Certificate of Analysis	Jul 21, 2022	D154708
C2207028	Certificate of Analysis	May 21, 2021	D154708

Show more⌵

Chemical and Physical Properties

Sensitivity	Air sensitive
Melt Point(°C)	135 °C
Molecular Weight	160.170 g/mol
XLogP3	1.900
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 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	158.000
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

How to Cite Aladdin Scientific Products?

1. Minjie Peng, Yufeng Sun, Wen Zang, Changyong Gao, Lijing Miao, Aiguo Wu, Yujie Zhang. (2023) A highly sensitive method for the detection of p-Aminophenol based on Cu–Au nanoparticles and KIO3. ANALYTICA CHIMICA ACTA, 1283 (341954).
2. Anhua Wei, Jingfang OuYang, Yuyang Guo, Suju Jiang, Feifei Chen, Jun Huang, Qi Xiao, Zihua Wu. (2023) Controlled synthesis of monodisperse gold nanorods with a small diameter of around 10 nm and largest plasmon wavelength of 1200 nm. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 25 (31): (20843-20853).
3. Xiao Yang, Yi Zhao, Qiuju Xu, Xiangcheng Yuan, Jinzhang Liu. (2023) Unraveling Factors Affecting Performance of Quinone-based Polymer Cathode in Aqueous Zinc-Ion Battery. Batteries & Supercaps, 6 (3): (e202200480).
4. Yuan Zu, Lishuai Zong, Jinyan Wang, Xigao Jian. (2021) Kinetic analysis of the curing of branched phthalonitrile resin based on dynamic differential scanning calorimetry. POLYMER TESTING, 96 (107062).
5. Shiwei Zhang, Jiurong Li, Xiao Gong. (2024) A Strategy for Rapid Synthesis of Carbon Nanodots with Reversible Photoluminescence Switching for Sensitive Dynamic Anti-Counterfeiting. Advanced Optical Materials, 12 (22): (2400648).
6. Xingzhong Chen, Fang Yan, Jiurong Li, Xiao Gong. (2025) Control Synthesis of Multicolor Emitting Carbonized Polymer Dots Using Different Dihydroxynaphthalene Isomers. JACS Au,

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration