All Photos(2)
About This Item
Linear Formula:
C10H7CH2OH
CAS Number:
Molecular Weight:
158.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
98%
form
solid
bp
301 °C/715 mmHg (lit.)
mp
61-63 °C (lit.)
SMILES string
OCc1cccc2ccccc12
InChI
1S/C11H10O/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7,12H,8H2
InChI key
PBLNHHSDYFYZNC-UHFFFAOYSA-N
Related Categories
General description
3′-Phosphoadenylyl sulfate dependent sulfation of 1-naphthalenemethanol catalyzed by isoenzyme of arylsulfotransferase has been studied. 1-Naphthalenemethanol is an intermediate photolysis product of 1-napthaleneacetic acid.
Application
1-Naphthalenemethanol was used to investigate UV photooxidation of 1-methylnaphthalene in the presence of dry or humid air.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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UV Light Induced Transformation of 1-Methylnaphthalene in the Presence of Air and Its Implications for Contaminants Research.
Feng Y-L, et al.
Journal of Environmental Protection, 3(11), 1519-1531 (2012)
Photodecomposition of 1-naphthaleneacetic acid.
Crosby DG and Tang C-S.
Journal of Agricultural and Food Chemistry, 17(6), 1291-1293 (1969)
M W Duffel et al.
Analytical biochemistry, 183(2), 320-324 (1989-12-01)
An assay procedure for purified aryl sulfotransferase is described. The method utilizes isocratic paired-ion reverse-phase HPLC analysis of adenosine-3',5'-diphosphate formed in the reaction. Evaluation of the assay procedure was carried out with 1-naphthalene-methanol as a model substrate for purified rat
Arylsulfotransferase IV catalyzed sulfation of 1-naphthalenemethanol.
M W Duffel et al.
Advances in experimental medicine and biology, 197, 415-422 (1986-01-01)
Tsunehisa Hirose et al.
Molecules (Basel, Switzerland), 24(13) (2019-07-05)
The retention behavior of a wide variety of stationary phases was compared in supercritical fluid chromatography (SFC) and normal-phase high-performance liquid chromatography (NP-HPLC). We also attempted to elucidate the retention behavior in SFC by investigating the selectivity of the different
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