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292370

Sigma-Aldrich

γ-Nonanoic lactone

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

Quality Level

100

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.)

functional group

ester

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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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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

292370-VAR:
292370-500ML:
292370-100ML:
292370-5ML:
292370-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
SHBL6910
MKBR8939V
MKBK5232V
04714DE
04112PC

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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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