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Merck
CN

109630

1-Hydroxy-2-naphthoic acid

≥97.0%

Synonym(s):

α-Hydroxynaphthoic acid

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About This Item

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

General description

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


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pictograms

Exclamation mark

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



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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
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



Global Trade Item Number

SKUGTIN
109630-5G04061838688835
109630-100G04061838688828