374180
2-Hexadecanone
98%
Sinónimos:
Methyl tetradecyl ketone
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About This Item
Fórmula lineal:
CH3(CH2)13COCH3
Número de CAS:
Peso molecular:
240.42
Beilstein:
1769889
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
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Nivel de calidad
Ensayo
98%
bp
138-140 °C/2 mmHg (lit.)
mp
43-45 °C (lit.)
cadena SMILES
CCCCCCCCCCCCCCC(C)=O
InChI
1S/C16H32O/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16(2)17/h3-15H2,1-2H3
Clave InChI
XCXKZBWAKKPFCJ-UHFFFAOYSA-N
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Descripción general
2-Hexadecanone (Methyl tetradecyl ketone) is a long chain aliphatic ketone. It has been identified as one of the air borne volatile electroantennographic active compound released from the Hoplia equina females (scarab beetle). The analysis was obtained by gas chromatographic analysis.[1]
2-Hexadecanone is reported to inhibit the fatty acid synthetase activity of Holtzman male rat liver.[2] It is reported to reduce the serum cholesterol levels significantly without altering serum triglyceride levels in rats.[3] It is reported as lipophilic compound, found in femoral secretions of male Schreiber′s green lizards, Lacerta schreiberi.[4]
Aplicación
2-Hexadecanone (Methyl tetradecyl ketone) may be used to compose the graphite suspension required for the fabrication of thick-cover spray-printed electrodes by spray-printing process.[5] It may be used for the preparation of solid binding matrix (SBM)-based composite electrodes for the construction of simple amperometric biosensor for sensitive detection of various pH-sensitive redox-active compounds.[6]
2-Hexadecanone is suitable for use in the preparation of solid binding matrix (SBM)-based composite electrodes, for constructing a biosensor for amperometric pH-sensing.[6]
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves, type N95 (US)
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Amperometric pH-sensing biosensors for urea, penicillin, and oxalacetate.
Stred'ansky M, et al.
Analytica Chimica Acta, 415(1), 151-157 (2000)
Pilar López et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 61(9-10), 763-768 (2006-12-02)
In spite of the importance of chemoreception and chemical signals in social organization of lizards, only a few studies have examined the chemical composition of secretions that lizards use for intraspecific communication. The secretion of the femoral glands of male
I H Hall et al.
Journal of medicinal chemistry, 19(10), 1257-1261 (1976-10-01)
A number of 2,8-dibenzylcyclooctanone analogues inhibited the HMG-CoA reductases activity of Holtzman male rat liver, whereas only 2-octanone, 2-hexadecanone, 2,8-dibenzylcyclooctanone derivatives, and 2-bis(4-chlorophenyl)-3,5-dimethyltetrahydro-4-pyrone inhibited fatty acid synthetase activity. 2-Octanone significantly lowered serum cholesterol, triglycerides, and glycerol levels in Holtzman male
A Pizzariello et al.
Bioelectrochemistry (Amsterdam, Netherlands), 56(1-2), 99-105 (2002-05-16)
An improved composite bulk-modified bioelectrode setup based on a solid binding matrix (SBM) has been used to develop a glucose/hydrogen peroxide biofuel cell. Fuel is combined through a catalytically promoted reaction with oxygen into and oxidized species and electricity. The
Aijun Zhang et al.
Journal of chemical ecology, 29(7), 1635-1642 (2003-08-19)
Hoplia equina LeConte (Coleoptera Scarabaeidae: Melolonthinae) is a beetle pest of cranberry beds in Massachusetts. Larvae feed on the roots of the cranberry plant, reducing yield as well as vine density. The female sex pheromone was identified as 2-tetradecanone. There
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