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109630

Sigma-Aldrich

1-Hydroxy-2-naphthoic acid

≥97.0%

Sinonimo/i:

α-Hydroxynaphthoic acid

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About This Item

Formula condensata:
HOC10H6CO2H
Numero CAS:
86-48-6
Peso molecolare:
188.18
Beilstein:
974438
Numero CE:
201-674-0
Numero MDL:
MFCD00003960
Codice UNSPSC:
12352100
ID PubChem:
24846929
NACRES:
NA.22

Livello qualitativo

200

Saggio

≥97.0%

Punto di fusione

195-200 °C (dec.) (lit.)

Solubilità

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

Gruppo funzionale

carboxylic acid

Stringa SMILE

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)
SJJCQDRGABAVBB-UHFFFAOYSA-N

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Descrizione generale

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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

302.0 °F - closed cup

Punto d’infiammabilità (°C)

150 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCB8098
BCBV5128
BCBR3567V
BCBN3482V
BCBL2949V

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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
Journal of colloid and interface science, 309(2), 419-428 (2007-02-17)
The transport of aromatic carboxylate compounds in the environment can be strongly influenced by adsorption onto certain minerals, such as iron oxides and hydroxides, found in ground water and soils. Batch experiments with five iron oxides were conducted to quantify
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
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
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
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