JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Chemistry & Biochemicals
Building Blocks
Organic Building Blocks
1-Naphthoic acid - 98%, high purity , CAS No.86-55-5

Skip to the end of the images gallery

Skip to the beginning of the images gallery

1-Naphthoic acid - 98%, high purity , CAS No.86-55-5

4 Citations

COA

Grade & Purity:

≥98%

Cas Number: 86-55-5
Molecular Weight: 172.18
Beilstein Registry Number: 1908896
EC Number: 201-681-9
MDL number: MFCD00004007
PubChem CID: 6847
PubChem SID: 488180175

In stock

Item Number

N106387

Grouped product items
SKU	Size	Availability	Price
N106387-10g	10g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$12.90
N106387-25g	25g	7	$24.90
N106387-100g	100g	3	$88.90
N106387-250g	250g	3	$199.90
N106387-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$358.90

View related series

carboxylic acid (2098) Non heterocyclic block (8163)

Basic Description

Synonyms	MFCD00004007 \| AE-508/40217755 \| HY-Y0236 \| .alpha.-Naphthoic acid \| bmse000178 \| SY005963 \| AC-4952 \| Naphthalenecarboxylic acid \| naphthalene mono carboxylic acid \| SCHEMBL17258 \| UNII-2NIV4O66BH \| CCG-208689 \| naphthalene carboxylic acid \| 1-Naphthoica
Specifications & Purity	≥98%
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Naphthalenes
    - Subclass Naphthalenecarboxylic acids and derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Naphthalenes
Subclass	Naphthalenecarboxylic acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Naphthalenecarboxylic acids
Alternative Parents	Monocarboxylic acids and derivatives Carboxylic acids Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homopolycyclic compounds
Substituents	1-naphthalenecarboxylic acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as naphthalenecarboxylic acids. These are compounds containing a naphthalene moiety, which bears a carboxylic acid group one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
External Descriptors	naphthoic acid
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

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	488180175
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488180175
IUPAC Name	naphthalene-1-carboxylic acid
INCHI	InChI=1S/C11H8O2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,(H,12,13)
InChIKey	LNETULKMXZVUST-UHFFFAOYSA-N
Smiles	C1=CC=C2C(=C1)C=CC=C2C(=O)O
Isomeric SMILES	C1=CC=C2C(=C1)C=CC=C2C(=O)O
WGK Germany	2
RTECS	QL0960000
Molecular Weight	172.18
Beilstein	1908896
Reaxy-Rn	1908896
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1908896&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.

8 results found

Lot Number	Certificate Type	Date	Item
I1820098	Certificate of Analysis	Jul 21, 2022	N106387
K2308183	Certificate of Analysis	Jul 19, 2022	N106387
I2219095	Certificate of Analysis	Jul 19, 2022	N106387
I2219093	Certificate of Analysis	Jul 19, 2022	N106387
G2419023	Certificate of Analysis	Jul 19, 2022	N106387
I2219094	Certificate of Analysis	Jul 19, 2022	N106387
I2219096	Certificate of Analysis	Jul 19, 2022	N106387
D2321420	Certificate of Analysis	Sep 19, 2021	N106387

Chemical and Physical Properties

Solubility	Freely soluble in hot alcohol and ether. Slightly soluble in hot water.
Boil Point(°C)	300°C
Melt Point(°C)	158-162°C
Molecular Weight	172.180 g/mol
XLogP3	3.100
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	1
Exact Mass	172.052 Da
Monoisotopic Mass	172.052 Da
Topological Polar Surface Area	37.300 Å²
Heavy Atom Count	13
Formal Charge	0
Complexity	200.000
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. Shishi Shao, Jiaqiang Zhao, Wei Wang, Hanbing Nie, Yan Jie Li, Xuepeng Zhang, Cheng Zhi Huang, Peng Fei Gao. (2024) Ratiometric room-temperature phosphorescence platform for visual and spectral analysis of naphthalene. SENSORS AND ACTUATORS B-CHEMICAL, 402 (135047).
2. Zhen Chi, Jia Xu, Shida Luo, Xia Ran, Xiaojuan Wang, Pingan Liu, Yulu He, Yanmin Kuang, Lijun Guo. (2023) Triplet generation at the CdTe quantum dot/anthracene interface mediated by hot and thermalized electron exchange for enhanced production of singlet oxygen. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 25 (12): (8913-8920).
3. Kui Li, Miao Sun, Wei-De Zhang. (2018) Polycyclic aromatic compounds-modified graphitic carbon nitride for efficient visible-light-driven hydrogen evolution. CARBON, 134 (134).
4. Liu Hongmei, Chang Hong, Lv Jia, Jiang Cong, Li Zhenxi, Wang Fei, Wang Hui, Wang Mingming, Liu Chongyi, Wang Xinyu, Shao Naimin, He Bingwei, Shen Wanwan, Zhang Qiang, Cheng Yiyun. (2016) Screening of efficient siRNA carriers in a library of surface-engineered dendrimers. Scientific Reports, 6 (1): (1-11).

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

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.