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H45353

Sigma-Aldrich

2-Hydroxy-1-Naphthaldehyd

technical grade

Synonym(e):

1-Formyl-2-hydroxynaphthalene, 1-Formyl-2-naphthol, 2-Hydroxynaphthyl-1-carboxaldehyde

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About This Item

Lineare Formel:
HOC10H6CHO
CAS-Nummer:
708-06-5
Molekulargewicht:
172.18
Beilstein:
742777
EG-Nummer:
211-902-0
MDL-Nummer:
MFCD00004005
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24895523
NACRES:
NA.22

Qualität

technical grade

bp

192 °C/27 mmHg (lit.)

mp (Schmelzpunkt)

76-80 °C (lit.)

SMILES String

[H]C(=O)c1c(O)ccc2ccccc12

InChI

1S/C11H8O2/c12-7-10-9-4-2-1-3-8(9)5-6-11(10)13/h1-7,13H

InChIKey

NTCCNERMXRIPTR-UHFFFAOYSA-N

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Piktogramme

Environment
GHS09

Signalwort

Warning

H-Sätze

H410

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

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6-Methoxy-2-naphthaldehyd 98%

Sigma-Aldrich

533084

6-Methoxy-2-naphthaldehyd

4-Methoxy-1-naphthaldehyd 99%

Sigma-Aldrich

103241

4-Methoxy-1-naphthaldehyd

Zheng Li et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 212, 349-355 (2019-01-23)
A selective diaminomaleonitrile-based fluorescent probe for Al3+(L) has been synthesized and characterized. The sensing behavior of L towards different metal ions was investigated by fluorescent spectra and competition experiment. The results showed that L exhibited a dual channel emission (λem
Rupashree Balia Singh et al.
Journal of photochemistry and photobiology. B, Biology, 91(1), 1-8 (2008-02-26)
In the present work, we have studied the interaction of proton transfer probe 1-hydroxy-2-naphthaldehyde (HN12) with Human Serum Albumin (HSA) and Bovine Serum Albumin (BSA) by steady state absorption and emission spectroscopy combined with time resolved fluorescence measurements. The measured
J Mañes et al.
Journal of pharmaceutical and biomedical analysis, 8(8-12), 795-798 (1990-01-01)
A selective and sensitive high-performance liquid chromatographic method is described for determination of hydralazine and its metabolites in human plasma. The method involves pre-column derivatization with 2-hydroxy-1-naphthaldehyde at pH 1.2. The reaction product and Methyl Red used as internal standard
K Kiran et al.
Journal of hazardous materials, 150(3), 582-586 (2007-06-23)
bis-[2-Hydroxy-1-naphthaldehyde] thiourea was synthesized and preconcentration cloud point extraction (CPE) for speciation determination of chromium(III) and (VI) in various environmental samples with flame atomic absorption spectrometry (FAAS) has been developed. Chromium(III) complexes with bis-[2-hydroxynaphthaldehyde] thiourea is subsequently entrapped in the
A M el-Brashy et al.
The Analyst, 122(2), 147-150 (1997-02-01)
2-Hydroxy-1-naphthaldehyde (HNA) was investigated as a derivatizing reagent for the fluorescence detection of histidine, methionine and tryptophan at 385 and 265 nm. The separation of HNA-derivatized amino acids on a conventional reversed-phase column was achieved in less than 40 min.
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