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General Material Information

Preferred name delta-decalactone
Trivial Name δ-Decalactone
Short Description decano-1,5-lactone
Formula C10 H18 O2
CAS Number 705-86-2
Deleted CAS Number 35221-79-5
FEMA Number 2361
Flavis Number 10.007
ECHA Number 211-889-1
FDA UNII CNA0S5T234
Nikkaji Number J35.391D
Beilstein Number 0117520
MDL MFCD00006649
COE Number 621
xLogP3-AA 2.50 (est)
NMR Predictor External link
JECFA Food Flavoring 232 delta-decalactone
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 705-86-2 ; DELTA-DECALACTONE
Synonyms
  • 5-amyl-5-hydroxypentanoic acid lactone
  • 5-N- amyl-5-hydroxypentanoic acid lactone
  • amyl-d-valerolactone
  • amyl-delta-valerolactone
  • delta- amyl-delta-valerolactone
  • d- amylvalerolactone
  • delta- deca lactone
  • 5-decalactone
  • d- decalactone
  • delta decalactone
  • nat.delta- decalactone
  • delta- decalactone (natural)
  • decalactone delta
  • decalactone delta natural
  • d- decalactone FCC
  • delta- decalactone FCC
  • d- decalactone natural
  • delta- decalactone natural
  • delta- decalactone R80
  • delta- decalactone S80
  • delta- decalactone synthetic
  • decan-5-olide
  • decano-1,5-lactone
  • d- decanolactone
  • (±)-5-decanolide
  • 5-decanolide
  • decanolide-1,5
  • 5-hydroxydecanoic acid d-lactone
  • 5-hydroxydecanoic acid delta-lactone
  • 6-pentyl tetrahydro-2H-pyran-2-one
  • 6-pentyl-3H-4,5,6-trihydropyran-2-one
  • 5-pentyl-5-pentanolide
  • d- pentyl-d-valerolactone
  • delta- pentyl-delta-valerolactone
  • 6-pentyl-tetrahydro-pyran-2-one
  • 6-pentyloxan-2-one
  • 6-pentyltetrahydro-2H-pyran-2-one
  • 2H- pyran-2-one, tetrahydro-6-pentyl-
  • tetrahydro-6-pentyl-2H-pyran-2-one
  • 6-pentyloxan-2-one
  • 2H-Pyran-2-one, tetrahydro-6-pentyl-
  • Decanoic acid, 5-hydroxy-, δ-lactone
  • Capric acid, δ-hydroxy-, lactone
  • δ-Decalactone
  • 5-Decanolide
  • 5-Hydroxydecanoic acid δ-lactone
  • δ-Amylvalerolactone
  • 5-Pentyl-5-pentanolide
  • δ-Pentyl-δ-valerolactone
  • 6-Pentyltetrahydro-2H-pyran-2-one
  • Dihydrojasmin lactone
  • δ-Decanolactone
  • (±)-5-Hydroxydecanoic acid lactone
  • (±)-δ-Decalactone
  • (RS)-δ-Decalactone
  • (±)-δ-Decanolactone
  • δ-Amyl-δ-valerolactone
  • δ-Decane lactone

US / EU / FDA / JECFA / FEMA / Scholar / Patents

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Perfumer & Flavorists Start search
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NCBI Start search

Literature & References

6-pentyloxan-2-one
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:705-86-2
Pubchem (cid):12810
Pubchem (sid):134977157
Flavornet:705-86-2
Pherobase:View
Publications by Info
Volatile Flavor Components in Bogyojosaeng and Suhong Cultivars of Strawberry (Fragaria ananassa Duch.)
Publications by PubMed
Effects of alpha-tocopherol on lactones in beef headspace during storage.
Odor-active compounds in cardboard.
Characterization and quantification of odor-active compounds in unsaturated fatty acid/conjugated linoleic acid (UFA/CLA)-enriched butter and in conventional butter during storage and induced oxidation.
Comparison of sugar, acids, and volatile composition in raspberry bushy dwarf virus-resistant transgenic raspberries and the wild type 'meeker' (rubus idaeus L.).
Optimization of headspace solid-phase microextraction for the analysis of specific flavors in enzyme modified and natural Cheddar cheese using factorial design and response surface methodology.
Sensory-directed identification of creaminess-enhancing volatiles and semivolatiles in full-fat cream.
Effect of cold storage and packaging material on the major aroma components of sweet cream butter.
Characterization of the key aroma compounds in apricots (Prunus armeniaca) by application of the molecular sensory science concept.
Aroma-active components of nonfat dry milk.
Evidence of starch inclusion complexation with lactones.
Differences in key odorants of handmade juice of yellow-flesh peaches (Prunus persica L.) induced by the workup procedure.
Characterization of odor-active compounds in extracts obtained by simultaneous extraction/distillation from moroccan black olives.
6-Pentyl-2H-pyran-2-one: a potent peach-derived kairomone for New Zealand flower thrips, Thrips obscuratus.
Two lactones in the androconial scent of the lycaenid butterfly Celastrina argiolus ladonides.
The molecular receptive range of a lactone receptor in Anopheles gambiae.
Effects of bagging on volatiles and polyphenols in "Wanmi" peaches during endocarp hardening and final fruit rapid growth stages.
Expression of genes associated with aroma formation derived from the fatty acid pathway during peach fruit ripening.
Analysis of volatile compounds in beef fat by dynamic-headspace solid-phase microextraction combined with gas chromatography-mass spectrometry.
Volatile composition in raspberry cultivars grown in the Pacific Northwest determined by stir bar sorptive extraction-gas chromatography-mass spectrometry.
Comparative chemical analysis of the essential oil constituents in the bark, heartwood and fruits of Cryptocarya massoy (Oken) Kosterm. (Lauraceae) from Papua New Guinea.
Identification of novel decenoic acids in heated butter.
Authenticity assessment of gamma- and delta-decalactone from prunus fruits by gas chromatography combustion/pyrolysis isotope ratio mass spectrometry (GC-C/P-IRMS).
Investigation of bound aroma constituents of yellow-fleshed nectarines (Prunus persica L. Cv. Springbright). changes in bound aroma profile during maturation.
Gas chromatographic-olfactometric characterization of aroma compounds in two types of cashew apple nectar.
Characterization of Volatiles in Rambutan Fruit (Nephelium lappaceum L.).
Similarities in the aroma chemistry of Gewürztraminer variety wines and lychee (Litchi chinesis sonn.) fruit.
Publications by J-Stage
Identification of Novel Decenoic Acids in Heated Butter

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
CHEBI:View
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB37116
FooDB:FDB016109
YMDB (Yeast Metabolome Database):YMDB01579
Export Tariff Code:2932.20.5050
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View

Suppliers

ACS International Advanced Biotech
Ambles Nature et Chimie Anhui Haibei
Artiste Augustus Oils
Aurochemicals Axxence Aromatic
Bedoukian Research Beijing Lys Chemicals
Bell Flavors & Fragrances Berjé
BOC Sciences Charkit Chemical
Citrus and Allied Essences CJ Latta & Associates
Creatingperfume.com De Monchy Aromatics
Diffusions Aromatiques Ernesto Ventós
Excellentia International FCI SAS
Fine Fragrances Pvt Ltd Firmenich
Fleurchem Foreverest Resources
H. Interdonati, Inc. Indenta Group
Indukern F&F Inoue Perfumery
Jiangyin Healthway K.L. Koh Enterprise
Kingchem Laboratories Kun Shan P&A
Lluch Essence M&U International
Mane Moellhausen
Natural Advantage Oamic Ingredients
Odowell Co.,ltd Omega Ingredients
OQEMA Pearlchem Corporation
Pell Wall Perfumes Penta International
Perfumer Supply House PerfumersWorld
Phoenix Aromas & Essential Oils Primechem
Prodasynth Quimdis
R C Treatt & Co Ltd Reincke & Fichtner
Riverside Aromatics Robertet
Sigma-Aldrich Soda Aromatic
SRS Aromatics Stort Chemicals
Sunaux International Synerzine
TCI AMERICA The Lermond Company
Tianjin Danjun International United International
Vigon International WEN International
WholeChem ZEON Corporation
ACS International GmbH Advanced Biotech. Inc.
Augustus Oils Ltd Axxence Aromatic GmbH
Bedoukian Research, Inc. Beijing Lys Chemicals Co, LTD.
Berje Inc. Charkit Chemical Corporation
CJ Latta & Associates, LLC Firmenich Inc.
Fleurchem, Inc. Foreverest Resources Ltd.
Indukern, S.A. F&F Ingredients Division Jiangyin Healthway International Trade Co., Ltd
Lluch Essence S.L. M&U International LLC
Moellhausen S.P.A. Penta International Corporation
PerfumersWorld Ltd. Anhui Primechem Co., Ltd.
Riverside Aromatics Ltd. Robertet, Inc.
Soda Aromatic Co., Ltd. SRS Aromatics Ltd
Synerzine, Inc. Tianjin Danjun International Trade Co., LTD.
R C Treatt and Co Ltd Qingdao Free Trade Zone United International Co Ltd
Ernesto Ventós S.A. WholeChem, LLC

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 170.25186157227
Specific gravity @ 25 °C
Pounds per Gallon 7.972 to 8.121
Refractive Index 1.456 to 1.459 @ 20 °C
Boiling Point 117 to 120°C @ 0.02 mm Hg
Acid Value 5 max KOH/g
Vapor Pressure 0.001 mmHg @ 20 °C
Flash Point TCC Value 110 °C TCC
logP (o/w) 2.469 est
Shelf life 12 months (or longer if stored properly.)
Storage notes Store in cool, dry place in tightly sealed containers, protected from heat and light.
Solubility
alcohol Yes
fixed oils Yes
propylene glycol Yes
water, very slightly Yes
water, 393.8 mg/L @ 25 °C (est) Yes

Organoleptic Properties

Odor Type: Coconut
fresh, sweet, oily, coconut, fruity, peach, creamy, dairy, lactonic, fatty, milky
Odor strength medium
Substantivity 336 hour(s) at 100.00 %
Luebke, William tgsc, (1997) At 100.00 %. fresh sweet oily coconut fruity peach creamy dairy
Mosciano, Gerard P&F 21, No. 3, 51, (1996) Sweet, creamy, lactonic, fatly, coconut, milky
Flavor Type: Coconut
coconut, creamy, fatty, buttery, milky, nutty, fruity
Mosciano, Gerard P&F 21, No. 3, 51, (1996) Coconut, creamy, fatty, buttery, milky and nutty with a slightly fruity nuance
Lactone notes for all creamy, dairy, and coconut flavors. Also imparts creamy, dairy notes for peach, mango, and other fruit flavors. Characteristic fresh butter, full mouthfeel for all dairy flavors
General comment Fruity peach note, creamy, nutty
Useful in: brown nuts, brown others, dairy, vanilla, savory meat, fruity red, fruity yellow, fruity tropical. Lactone, peach, coconut
DECALACTONE DELTA is an indispensable lactone with the typical creamy, coconut profile and slightly fruity nuance. It is widely used in coconut, butter, cream, vanilla, peach and other fruit flavors. Milky creamy buttery coconut very tenacious

Occurrences

Potential Uses

Applications
Odor purposes Apricot, Butter, Coconut, Cream, Mango, Peach, Pina colada, Raspberry, Strawberry
Flavoring purposes Dairy, Necterine, Nut, Pecan, Tropical
Cosmetic purposes Fragrance, Perfuming agents

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Pictogram
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Human Experience:
1 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50 > 5000 mg/kg
(Levenstein, 1975c)

oral-rat LD > 4300 mg/kg
National Technical Information Service. Vol. AD-A053-896

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
FCTXAV
National Technical Information Service. Vol. AD-A053-896

Inhalation Toxicity:
Not determined

Safety in use information

Category:
flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for delta-decalactone usage levels up to:
8.0000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU): 7200.00 (μg/capita/day)
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3. Update in publication number(s): 29
Click here to view publication 3
average usual ppmaverage maximum ppm
baked goods: 14.0000026.00000
beverages(nonalcoholic): 5.0000014.00000
beverages(alcoholic): 15.0000020.00000
breakfast cereal: --
cheese: --
chewing gum: 15.00000100.00000
condiments / relishes: --
confectionery froastings: 0.500005.00000
egg products: --
fats / oils: 9.0000020.00000
fish products: --
frozen dairy: 19.0000037.00000
fruit ices: --
gelatins / puddings: 15.0000030.00000
granulated sugar: --
gravies: 4.000008.00000
hard candy: 0.300005.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: 13.0000026.00000
soups: --
sugar substitutes: --
sweet sauces: 0.100000.10000

Safety references

European Food Safety Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...

European Food Safety Authority (EFSA) reference(s):

Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC) on a request from the Commission related to - Flavouring Group Evaluation 10: Aliphatic primary and secondary saturated and unsaturated alcohols, aldehydes, acetals, carboxylic acids and esters containing an additional oxygenated functional group and lactones from chemical groups 9, 13 and 30 - (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf

Flavouring Group Evaluation 10, Revision 1 (FGE10 Rev1)[1] - Aliphatic primary and secondary saturated and unsaturated alcohols, aldehydes, acetals, carboxylic acids and esters containing an additional oxygenated functional group and lactones from chemical groups 9, 13 and 30 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food (AFC)
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 10, Revision 2 (FGE.10Rev2): Aliphatic primary and secondary saturated and unsaturated alcohols, aldehydes, acetals, carboxylic acids and esters containing an additional oxygenated functional group and lactones from chemical groups 9, 13 and 30
View page or View pdf

EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):705-86-2
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :12810
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:1
6-pentyloxan-2-one
Chemidplus:0000705862
RTECS:UQ1355000 for cas# 705-86-2