N8505
1-Naphthyl acetate
≥98% (C)
Synonyme(s) :
α-Naphthyl acetate
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A propos de cet article
Formule linéaire :
CH3CO2C10H7
Numéro CAS:
Poids moléculaire :
186.21
UNSPSC Code:
12352202
NACRES:
NA.77
PubChem Substance ID:
EC Number:
212-599-8
Beilstein/REAXYS Number:
2046403
MDL number:
Assay:
≥98% (C)
Form:
crystals
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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
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F
flash_point_c
113 °C
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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
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)
Laser flash photolysis and CIDNP studies of 1-naphthyl acetate photo-Fries rearrangement.
Gritsan NP, et al.
The Journal of Physical Chemistry, 100(11), 4448-4458 (1996)
Juan C Sanchez-Hernandez et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 150(4), 503-511 (2009-08-05)
Carboxylesterases (CbEs) are key enzymes in pesticide detoxification. These esterases are involved in the biochemical mechanism for pesticide resistance in some pest species, and further they are considered an efficient protective mechanism against acute toxicity by organophosphate (OP) pesticides in
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