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About This Item
Linear Formula:
CH3CO2C10H7
CAS Number:
Molecular Weight:
186.21
UNSPSC Code:
12352202
NACRES:
NA.77
PubChem Substance ID:
EC Number:
212-599-8
Beilstein/REAXYS Number:
2046403
MDL number:
Product Name
1-Naphthyl acetate, ≥98% (C)
InChI key
VGKONPUVOVVNSU-UHFFFAOYSA-N
InChI
1S/C12H10O2/c1-9(13)14-12-8-4-6-10-5-2-3-7-11(10)12/h2-8H,1H3
SMILES string
CC(=O)Oc1cccc2ccccc12
assay
≥98% (C)
form
crystals
mp
43-46 °C (lit.)
storage temp.
−20°C
Quality Level
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Application
1-Naphthyl acetate may be used in a rapid staining method for identification of macrophages; counts by this method were confirmed by the more complex morphological criteria, by phagocytosis, and by the presence of Fc receptors. It may be employed as substrate to investigate the distribution of non-specific carboxylic esterases (EC 3.1.1) in the digestive tract of perch, Perm fliiviatilis L.
General description
1-Naphthyl acetate is a 1-napthyl ester. Mechanism of photo-Fries rearrangement of 1-naphthyl acetate has been studied using steady state photolysis and laser flash photolysis. Kinetics of photo-Fries rearrangement of 1-napthyl acetate has been studied using steady-state, time-resolved chemically induced dynamic nuclear polarization (CIDNP) and flash photolysis methods.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F
flash_point_c
113 °C
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Non-specific carboxylic esterase activity in the digestive tract of the perch, Perca fluviatilis L.
Hirji KN and Courtney WAM.
Journal of Fish Biology, 22(1), 1-7 (1983)
Magnetic isotope and external magnetic field effects upon the photo-Fries rearrangement of 1-naphthyl acetate.
Nakagaki R, et al.
The Journal of Physical Chemistry, 89(15), 3222-3226 (1985)
Johan M Calderón et al.
Parasites & vectors, 13(1), 163-163 (2020-04-05)
Triatomine bugs are responsible for the vectorial transmission of the parasite Trypanosoma cruzi, etiological agent of Chagas disease, a zoonosis affecting 10 million people and with 25 million at risk of infection. Several triatomine species of the genus Rhodnius have
Purification and kinetic characterisation of juvenile hormone esterase from Drosophila melanogaster.
P M Campbell et al.
Insect biochemistry and molecular biology, 28(7), 501-515 (1998-08-27)
Juvenile hormone esterase (JHE) from the prepupal stage of Drosophila melanogaster was purified about 429-fold to near homogeneity by selective precipitations, isoelectric focussing, anion exchange and gel filtration chromatography. The KM and Vmax of the purified enzyme for juvenile hormone
Hye Kyung Kim et al.
Acta crystallographica. Section D, Biological crystallography, 61(Pt 7), 920-931 (2005-06-29)
The enzyme dienelactone hydrolase (DLH) has undergone directed evolution to produce a series of mutant proteins that have enhanced activity towards the non-physiological substrates alpha-naphthyl acetate and p-nitrophenyl acetate. In terms of steady-state kinetics, the mutations caused a drop in
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