Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

109630

Sigma-Aldrich

1-Hydroxy-2-naphthoic acid

≥97.0%

Synonym(s):

α-Hydroxynaphthoic acid

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

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

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

SMILES string

OC(=O)c1ccc2ccccc2c1O

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)

InChI key

SJJCQDRGABAVBB-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

302.0 °F - closed cup

Flash Point(C)

150 °C - closed cup

Personal Protective Equipment

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

Jonathan M Miller et al.
Journal of controlled release : official journal of the Controlled Release Society, 137(1), 31-37 (2009-03-07)
The aim of this research was to gain a mechanistic understanding of ion-pair mediated membrane transport of low-permeability drugs. Quasi-equilibrium mass transport analyses were developed to describe the ion-pair mediated octanol-buffer partitioning and hydrophobic membrane permeation of the model basic
Sanjai J Parikh et al.
Journal of contaminant hydrology, 72(1-4), 1-22 (2004-07-09)
Experiments were conducted to compare the sorption and desorption of phenanthrene and its primary degradation product, 1-hydroxy-2-naphthoic acid (HNA), in estuarine sediment, humic acid (HA) and humin. Ionic composition, ionic strength (0.4 M) and pH (7.6) were employed to mimic
Y Yang et al.
Journal of bacteriology, 176(8), 2158-2164 (1994-04-01)
A modified cloning procedure was used to obtain large DNA insertions (20 to 30 kb) from Pseudomonas putida NCIB 9816 that expressed polycyclic aromatic hydrocarbon (PAH) transformation activity in Escherichia coli HB101. Four subclones (16 [in both orientations], 12, and
Elpiniki Vandera et al.
Applied and environmental microbiology, 78(3), 621-627 (2011-11-22)
A protein fraction exhibiting 1-hydroxy-2-naphthoic acid (1-H2NA) dioxygenase activity was purified via ion exchange, hydrophobic interactions, and gel filtration chromatography from Arthrobacter phenanthrenivorans sp. nov. strain Sphe3 isolated from a Greek creosote-oil-polluted site. Matrix-assisted laser desorption ionization-time of flight mass
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
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