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γ-Nonanoic lactone

Name: γ-Nonanoic lactone
Brand: ALDRICH

97%

Synonym(s):

Coconut aldehyde

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About This Item

Empirical Formula (Hill Notation):

C₉H₁₆O₂

CAS Number:

104-61-0

Molecular Weight:

156.22

EC Number:

203-219-1

MDL number:

MFCD00005403

UNSPSC Code:

12352100

PubChem Substance ID:

24857580

NACRES:

NA.22

Assay

97%

refractive index

n20/D 1.447 (lit.)

bp

121-122 °C/6 mmHg (lit.)

density

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

InChI key

OALYTRUKMRCXNH-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

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Related Categories

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Application

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

258.8 °F - closed cup

Flash Point(C)

126 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Structure-activity relationships for growth inhibition and induction of apoptosis by 4-hydroxy-2-nonenal in raw 264.7 cells.

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

The catalytic histidine dyad of high density lipoprotein-associated serum paraoxonase-1 (PON1) is essential for PON1-mediated inhibition of low density lipoprotein oxidation and stimulation of macrophage cholesterol efflux.

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

Determination of volatile oak compounds in wine by headspace solid-phase microextraction and gas chromatography-mass spectrometry.

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

Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors.

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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