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Sigma-Aldrich

2-Hexadecanone

98%

Synonyme(s) :

Methyl tetradecyl ketone

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About This Item

Formule linéaire :
CH3(CH2)13COCH3
Numéro CAS:
18787-63-8
Poids moléculaire :
240.42
Numéro Beilstein :
1769889
Numéro CE :
242-571-0
Numéro MDL:
MFCD00042873
Code UNSPSC :
12352100
ID de substance PubChem :
24863286
Nomenclature NACRES :
NA.22

Pureté

98%

Point d'ébullition

138-140 °C/2 mmHg (lit.)

Pf

43-45 °C (lit.)

Chaîne 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

Clé InChI

XCXKZBWAKKPFCJ-UHFFFAOYSA-N

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Description générale

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.
2-Hexadecanone is reported to inhibit the fatty acid synthetase activity of Holtzman male rat liver. It is reported to reduce the serum cholesterol levels significantly without altering serum triglyceride levels in rats. It is reported as lipophilic compound, found in femoral secretions of male Schreiber′s green lizards, Lacerta schreiberi.

Application

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. 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.
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.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

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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
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
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
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