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1,3-Dihydroxynaphthalene - ≥98.0% (HPLC), high purity , CAS No.132-86-5

7 Citations

COA

Grade & Purity:

≥98%(HPLC)

Cas Number: 132-86-5
Molecular Weight: 160.17
Beilstein Registry Number: 2044002
EC Number: 205-079-7
MDL number: MFCD00003965
PubChem CID: 8601
PubChem SID: 504751706

In stock

Item Number

D106385

Grouped product items
SKU	Size	Availability	Price
D106385-200mg	200mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$9.90
D106385-1g	1g	2	$12.90
D106385-5g	5g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$39.90
D106385-25g	25g	1	$169.90
D106385-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$599.90

View related series

Naphthalenes (9) Oxygenated compounds (806) Pharmaceutical ingredients (367)

Basic Description

Synonyms	1,3-Naphthalenediol \| Naphthoresoucinol \| A806508 \| EINECS 205-079-7 \| 1,3-Naphthalindiol \| HY-D0165 \| InChI=1/C10H8O2/c11-8-5-7-3-1-2-4-9(7)10(12)6-8/h1-6,11-12 \| SY010964 \| AI3-08780 \| LCZC2960 \| FT-0631769 \| UNII-5X457YEW8Y \| Naphthoresorcin \| 1,3-Naph
Specifications & Purity	≥98%(HPLC)
Storage Temp	Argon charged
Shipped In	Normal
Product Description	1,3-Dihydroxynaphthalene is used in the naphthoresorcinol test for uronic acids of Tollens and Rorive. After heating of uronic acids with naphthoresorcinol in hydrochloric acid, a blue color can be extracted with ethanol. A reagent for the naphthoresorcinol test of Tollens and Rorive.

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	Not available
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)

NQO2 Tchem Quinone reductase 2 (885 Activities)

Discover Target: NQO2

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

T-24 (2342 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	504751706
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504751706
IUPAC Name	naphthalene-1,3-diol
INCHI	InChI=1S/C10H8O2/c11-8-5-7-3-1-2-4-9(7)10(12)6-8/h1-6,11-12H
InChIKey	XOOMNEFVDUTJPP-UHFFFAOYSA-N
Smiles	C1=CC=C2C(=C1)C=C(C=C2O)O
Isomeric SMILES	C1=CC=C2C(=C1)C=C(C=C2O)O
WGK Germany	3
RTECS	QJ4725000
Molecular Weight	160.17
Beilstein	2044002
Reaxy-Rn	2044002
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2044002&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.

17 results found

Lot Number	Certificate Type	Date	Item
G2425199	Certificate of Analysis	Aug 02, 2024	D106385
D2508066	Certificate of Analysis	May 21, 2024	D106385
E2413217	Certificate of Analysis	May 21, 2024	D106385
E2413232	Certificate of Analysis	May 21, 2024	D106385
E2413340	Certificate of Analysis	May 21, 2024	D106385
E2413341	Certificate of Analysis	May 21, 2024	D106385
E2413216	Certificate of Analysis	May 21, 2024	D106385
E2413233	Certificate of Analysis	May 21, 2024	D106385
B2511023	Certificate of Analysis	May 21, 2024	D106385
K2414113	Certificate of Analysis	May 21, 2024	D106385
K2316192	Certificate of Analysis	Nov 23, 2023	D106385
K2316410	Certificate of Analysis	Nov 23, 2023	D106385
K2316194	Certificate of Analysis	Nov 23, 2023	D106385
K2316193	Certificate of Analysis	Nov 23, 2023	D106385
E2231458	Certificate of Analysis	Jun 23, 2022	D106385
E2231462	Certificate of Analysis	Jun 23, 2022	D106385
E2231471	Certificate of Analysis	Jun 23, 2022	D106385

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Chemical and Physical Properties

Solubility	Soluble in ethanol (50 mg/ml), and water.
Sensitivity	Light & Air sensitive
Melt Point(°C)	123-126°C
Molecular Weight	160.170 g/mol
XLogP3	2.000
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. Shokir Khojiev, Gulmira Hojiyeva, Oybek Tursunkulov, Dan Chen, Hemdan S. H. Mohamed, Abduvali Kholikov, Khamdam Akbarov, Jing Liu, Yu Li. (2023) Red Emissive Upconversion Carbon Quantum Dots Modifying TiO2 for Enhanced Photocatalytic Performance. ACS Applied Nano Materials, 6 (16): (14669–14679).
2. Zhixin Chen, Jiaying Yu, Kai Sun, Jia Song, Lucheng Chen, Yong Jiang, Zhifei Wang. (2023) Rational design of a turn-on near-infrared fluorescence probe for the highly sensitive and selective monitoring of carboxylesterase 2 in living systems. ANALYST, 148 (4): (876-887).
3. Wu Wang, Hua Lai, Zhongjun Cheng, Zhimin Fan, Dongjie Zhang, Jingfeng Wang, Songji Yu, Zhimin Xie, Yuyan Liu. (2020) Superhydrophobic Shape Memory Polymer Microarrays with Switchable Directional/Antidirectional Droplet Sliding and Optical Performance. ACS Applied Materials & Interfaces, 12 (43): (49219–49226).
4. Shuyan Zang,Bin Lian,Juan Wang,Yanjie Yang. (2010-07-09) Biodegradation of 2-naphthol and its metabolites by coupling Aspergillus niger with Bacillus subtilis.. Journal of environmental sciences (China), 22 ((5)): (669-674).
5. Hong Yang, Shanshan Zhu, Lihua Pang, Yifei Ma, Xiaoxue Liu, Jinhua Liu. (2024) Cu2+-triggered wavelength-tunable real-time in situ fluorogenic immunoassay for detection of cTnI in human serum. SENSORS AND ACTUATORS B-CHEMICAL, (135388).
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).
7. Shokir Khojiev, Gulmira Khojieva, Dan Chen, Jun Chen, Hemdan S.H. Mohamed, Jing Liu, Yu Li. (2024) Synthesis and characterization of red emissive carbon quantum dots for MB degradation. CHEMICAL PHYSICS LETTERS, 856 (141652).

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