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N8505

Sigma-Aldrich

1-Naphthyl acetate

≥98% (C)

Sinónimos:

α-Naphthyl acetate

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About This Item

Fórmula lineal:
CH3CO2C10H7
Número de CAS:
830-81-9
Peso molecular:
186.21
Beilstein/REAXYS Number:
2046403
EC Number:
212-599-8
MDL number:
MFCD00003922
UNSPSC Code:
12352202
PubChem Substance ID:
24897679
NACRES:
NA.77

Quality Level

200

assay

≥98% (C)

form

crystals

mp

43-46 °C (lit.)

storage temp.

−20°C

SMILES string

CC(=O)Oc1cccc2ccccc12

InChI

1S/C12H10O2/c1-9(13)14-12-8-4-6-10-5-2-3-7-11(10)12/h2-8H,1H3

InChI key

VGKONPUVOVVNSU-UHFFFAOYSA-N

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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.

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.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F

flash_point_c

113 °C

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Certificados de análisis (COA)

Lot/Batch Number
BCCL6366
BCCL0275
BCCM5910
BCCJ5357
BCCC2673

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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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