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Merck
CN

70440

1-Naphthol

puriss., ≥99.0% (GC)

Synonym(s):

α-Naphthol, 1-Hydroxynaphthalene

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About This Item

Linear Formula:
C10H7OH
CAS Number:
90-15-3
Molecular Weight:
144.17
EC Number:
201-969-4
UNSPSC Code:
12352100
PubChem Substance ID:
329762449
Beilstein/REAXYS Number:
1817321
MDL number:
MFCD00003930

Key Documents

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InChI key

KJCVRFUGPWSIIH-UHFFFAOYSA-N

InChI

1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H

SMILES string

Oc1cccc2ccccc12

vapor density

4.5 (120 °C, vs air)

vapor pressure

1 mmHg ( 94 °C)

grade

puriss.

assay

≥99.0% (GC)

autoignition temp.

1007 °F

expl. lim.

5 %

ign. residue

≤0.05%

bp

278-280 °C (lit.)

mp

95-97 °C

suitability

suitable for fluorescence

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General description

1-Naphthol is the hydroxyl derivative of naphthalene. It forms hydrogen bonded complexes with H2O, CH3OH, NH3 and ND3 in gas phase. Hydrogen-bond dissociation energy of these complexes has been evaluated. Its sorption by biochars (obtained from orange peels, having pyrolytic temperatures in the range of 150-700°C and designated as OP150-OP700) has been studied. It has been identified as an impurity in the active pharmaceutical ingredient (API) of duloxetine hydrochloride.

Application

1-Naphthol (Naphthalen-1-ol) may be used as a standard for the NMR, FT-IR and mass spectrometric characterization of impurities present in the Duloxetine Hydrochloride active pharmaceutical ingredient (API).3

wgk

WGK 1

flash_point_f

257.0 °F - closed cup

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1A - STOT SE 2 Oral - STOT SE 3

target_organs

Kidney, Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

flash_point_c

125 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

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Characterization of duloxetine HCL API and its process related impurities
Karagiannidou E, et al.
International Journal of Analytical, Pharmaceutical and Biomedical Sciences, 3(2) (2014)
Baoliang Chen et al.
Chemosphere, 76(1), 127-133 (2009-03-14)
Biochars, derived from biomass, are increasingly recognized as an environmental-friendly sorbent to abate organic pollutants. Sorption variations of biochars with their pyrolytic temperatures are evaluated. Nine biochars of orange peels with different pyrolytic temperatures (150-700 degrees C, referred as OP150-OP700)
Hongbo Zhang et al.
Toxicology in vitro : an international journal published in association with BIBRA, 26(8), 1286-1293 (2012-01-24)
In vitro glucuronidation assays of diclofenac and indomethacin at pH 7.4 are biased by the instability of the glucuronides due to acyl migration. The extent of this acyl migration may be reduced significantly by performing the glucuronidation reaction at pH
Shitong Yang et al.
The Science of the total environment, 420, 214-221 (2012-02-15)
The increasing exploitation of multi-walled carbon nanotubes (MWCNTs) into many industrial processes has raised considerable concerns as they are likely to be released into the environment. The interactions of the pollutants in water with discharged MWNCTs will further influence the
Nenad Manevski et al.
Drug metabolism and disposition: the biological fate of chemicals, 40(11), 2192-2203 (2012-08-23)
The presence of bovine serum albumin (BSA) largely modulates the enzyme kinetics parameters of the human UDP-glucuronosyltransferase (UGT) 1A9, increasing both the apparent aglycone substrate affinity of the enzyme and its limiting reaction velocity (Drug Metab Dispos 39:2117-2129, 2011). For
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