Skip to Content
Merck
CN

109630

1-Hydroxy-2-naphthoic acid

≥97.0%

Synonym(s):

α-Hydroxynaphthoic acid

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
HOC10H6CO2H
CAS Number:
86-48-6
Molecular Weight:
188.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24846929
EC Number:
201-674-0
Beilstein/REAXYS Number:
974438
MDL number:
MFCD00003960
Assay:
≥97.0%

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

SJJCQDRGABAVBB-UHFFFAOYSA-N

InChI

1S/C11H8O3/c12-10-8-4-2-1-3-7(8)5-6-9(10)11(13)14/h1-6,12H,(H,13,14)

SMILES string

OC(=O)c1ccc2ccccc2c1O

assay

≥97.0%

mp

195-200 °C (dec.) (lit.)

solubility

alcohol: freely soluble, benzene: freely soluble, cold water: insoluble, diethyl ether: freely soluble

functional group

carboxylic acid

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

1-Hydroxy-2-naphthoic acid is produced by the transformation of phenanthrene by NCIB 9816 clones.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCB8098
BCBV5128
BCBR3567V
BCBN3482V
BCBL2949V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Marta Ferraroni et al.
The FEBS journal, 280(7), 1643-1652 (2013-02-07)
The salicylate 1,2-dioxygenase (SDO) from the bacterium Pseudaminobacter salicylatoxidans BN12 is a versatile gentisate 1,2-dioxygenase (GDO) that converts both gentisate (2,5-dihydroxybenzoate) and various monohydroxylated substrates. Several variants of this enzyme were rationally designed based on the previously determined enzyme structure
Marta Ferraroni et al.
Journal of structural biology, 177(2), 431-438 (2011-12-14)
The crystallographic structures of the adducts of salicylate 1,2-dioxygenase (SDO) with substrates salicylate, gentisate and 1-hydroxy-2-naphthoate, obtained under anaerobic conditions, have been solved and analyzed. This ring fission dioxygenase from the naphthalenesulfonate-degrading bacterium Pseudaminobacter salicylatoxidans BN12, is a homo-tetrameric class
K Hanna et al.
Chemosphere, 70(2), 178-186 (2007-08-11)
The adsorption of naphthoic acids to iron oxides and hydroxides influences strongly their mobility in soils and sediments. Sorption of 1-hydroxy-2-naphthoic acid (HNA) to three iron oxides was examined over a wide range of conditions (pH, ionic strength, sorbate and
Mario Cazzola et al.
Clinical pharmacokinetics, 41(1), 19-30 (2002-02-05)
Salmeterol is an inhaled long-acting selective beta(2)-adrenoceptor agonist that is commercially available as the xinafoate (1-hydroxy-2-naphthoic acid) salt of the racemic mixture of the two optical isomers, (R)- and (S)-, of salmeterol. It acts locally in the lung through action
N V Balashova et al.
Biodegradation, 12(3), 179-188 (2002-02-06)
1-Hydroxy-2-naphthoate is formed as an intermediate in the bacterial degradation of phenanthrene. A monooxygenase which catalyzed the oxidation of 1-hydroxy-2-naphthoate to 1,2-dihydroxynaphthalene was purified from the phenanthrene- and naphthalene-degrading Pseudomonas putida strain BS202-P1. The purified protein had a molecular weight
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service