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292370

Sigma-Aldrich

γ-Nonan-Lakton

97%

Synonym(e):

Coconut aldehyde

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About This Item

Empirische Formel (Hill-System):
C9H16O2
CAS-Nummer:
104-61-0
Molekulargewicht:
156.22
EG-Nummer:
203-219-1
MDL-Nummer:
MFCD00005403
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24857580
NACRES:
NA.22

Assay

97%

Brechungsindex

n20/D 1.447 (lit.)

bp

121-122 °C/6 mmHg (lit.)

Dichte

0.976 g/mL at 25 °C (lit.)

SMILES String

CCCCCC1CCC(=O)O1

InChI

1S/C9H16O2/c1-2-3-4-5-8-6-7-9(10)11-8/h8H,2-7H2,1H3

InChIKey

OALYTRUKMRCXNH-UHFFFAOYSA-N

Angaben zum Gen

human ... CYP1A2(1544)

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Verwandte Kategorien

Anwendung

γ-Nonanoic lactone has been used:
  • in quantitative analysis of oak volatile compounds in aged red wine by headspace solid-phase microextraction-GC-MS method
  • as substrate in serum paraoxonase-1 (PON1) enzyme assay
  • in synthesis of 4-hydroxynonanal via reduction of γ-nonanoic lactone by diisobutylaluminum hydride in toluene

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

258.8 °F - closed cup

Flammpunkt (°C)

126 °C - closed cup

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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R L Haynes et al.
Molecular pharmacology, 58(4), 788-794 (2000-09-22)
4-Hydroxy-2-nonenal (HNE) is a highly reactive lipid aldehyde byproduct of the peroxidation of cellular membranes. The structure of HNE features three functional groups, a C1 aldehyde, a C2==C3 double bond, and a C4- hydroxyl group, each of which may contribute
Mira Rosenblat et al.
The Journal of biological chemistry, 281(11), 7657-7665 (2006-01-13)
High density lipoprotein (HDL)-associated paraoxonase-1 (PON1) anti-atherogenic properties in macrophages, i.e. inhibition of cell-mediated oxidation of low density lipoprotein (LDL) and stimulation of cholesterol efflux, were studied using recombinant variants of PON1 and apoA-I expressed in Escherichia coli and reconstituted
José David Carrillo et al.
Journal of chromatography. A, 1102(1-2), 25-36 (2005-11-11)
A headspace solid-phase microextraction (HS-SPME) and gas chromatography (GC) coupled to mass spectrometry (MS) method was developed to identify and quantify 14 volatile oak compounds in aged red wines. The most important HS-SPME variables were optimised by experimental design technique
Laura E Korhonen et al.
Journal of medicinal chemistry, 48(11), 3808-3815 (2005-05-27)
The purpose of this study was to determine the cytochrome P450 1A2 (CYP1A2) inhibition potencies of structurally diverse compounds to create a comprehensive three-dimensional quantitative structure-activity relationship (3D-QSAR) model of CYP1A2 inhibitors and to use this model to predict the

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