Skip to Content
Merck
All Photos(1)

Key Documents

W369608

Sigma-Aldrich

6-Amyl-α-pyrone

≥96%, FG

Synonym(s):

5-Hydroxy-2,4-decadienoic acid γ-lactone

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H14O2
CAS Number:
Molecular Weight:
166.22
FEMA Number:
3696
EC Number:
Council of Europe no.:
10967
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
10.031
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

FG
Halal
Kosher

reg. compliance

EU Regulation 1334/2008 & 178/2002

Assay

≥96%

refractive index

n20/D 1.505 (lit.)

density

1.004 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

coconut; creamy; fatty; waxy

SMILES string

CCCCCC1=CC=CC(=O)O1

InChI

1S/C10H14O2/c1-2-3-4-6-9-7-5-8-10(11)12-9/h5,7-8H,2-4,6H2,1H3

InChI key

MAUFTTLGOUBZNA-UHFFFAOYSA-N

General description

6-Amyl-α-pyrone occurs naturally in peaches. It is also the main volatile organic compound produced by Trichoderma species.

Application


  • Demonstrating the Applicability of Proton Transfer Reaction Mass Spectrometry to Quantify Volatiles Emitted by the Mycoparasitic Fungus Trichoderma atroviride in Real Time: Monitoring of Trichoderma-Based Biopesticides.: This study showcases how Proton Transfer Reaction Mass Spectrometry can be used to monitor volatile organic compounds such as 6-Amyl-alpha-pyrone emitted by Trichoderma atroviride. The findings have significant implications for real-time monitoring and efficacy assessment of biopesticides, contributing to sustainable agriculture practices and biocontrol agent development (Ruzsanyi V et al., 2024).

  • Chemotropism Assays for Plant Symbiosis and Mycoparasitism Related Compound Screening in Trichoderma atroviride.: 6-Amyl-alpha-pyrone is used as a standard in chemotropism assays, which are critical for screening compounds that facilitate plant symbiosis and mycoparasitism. This research is vital for identifying new bioactive compounds that can improve the interactions between beneficial fungi and host plants, advancing both agricultural and ecological research (Zeilinger S et al., 2020).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Comparison of the volatile compounds from several commercial peach cultivars.
Horvat RJ, et al.
Journal of Agricultural and Food Chemistry, 38(1), 234-237 (1990)
Xin Jin et al.
Pesticide biochemistry and physiology, 170, 104683-104683 (2020-09-28)
Root rot caused by Cylindrocarpon destructans is one of the most devastating diseases of Panax notoginseng, and Trichoderma species are potential agents for the biocontrol of fungal diseases. Thus, we screened a total of 10 Trichoderma isolates against C. destructans
David Maxwell Suckling et al.
Insects, 11(9) (2020-09-17)
This project investigated how kairomone lures, camera traps, and counting software could together contribute to pest management. Images of cumulative daily catch of New Zealand Flower Thrips (NZFT) attracted to a ripe peach lactone (6-pentyl-2H-pyran-2-one; 6-PAP) were automatically loaded to
Nematicidal effect of volatiles produced by Trichoderma sp.
Yang Z, et al.
Journal of Asia-Pacific Entomology, 15(4), 647-650 (2012)
6-Pentyl-2H-pyran-2-one: a potent peach-derived kairomone for New Zealand flower thrips, Thrips obscuratus.
El-Sayed AM, et al.
Journal of Chemical Ecology, 40(1), 50-55 (2014)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service