EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

melon heptenal

Supplier Sponsors

Fragrance Demo Formulas
Name:2,6-dimethylhept-5-enal
CAS Number: 106-72-9Picture of molecule3D/inchi
Other:77787-60-1
ECHA EINECS - REACH Pre-Reg:203-427-2
FDA UNII:Z331YX9EL9
Nikkaji Web:J110.527B
Beilstein Number:1745855
MDL:MFCD00006981
CoE Number:2006
XlogP3-AA:2.50 (est)
Molecular Weight:140.22572000
Formula:C9 H16 O
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome or firefox)
Also(can) Contains:(R)-melon heptenal
 (S)-melon heptenal
EFSA/JECFA Comments:
At least 85%; secondary components 9-10% 6-methyl-5-hepten-2-one; 1-2% 2,6-dimethyl-6-heptenal. (JECFA) JECFA evaluated 2,6-dimethyl-5-heptenal (CASrn as in Register). (R)- or (S)-enantiomer not specified by CASrn in Register.
Category:flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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NCBI:Search
JECFA Food Flavoring:349 2,6-dimethyl-5-heptenal
FLAVIS Number:05.074 (Old)
DG SANTE Food Flavourings:05.074 2,6-dimethylhept-5-enal
FEMA Number:2389 2,6-dimethyl-5-heptenal
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):106-72-9 ; 2,6-DIMETHYL-5-HEPTENAL
FDA Regulation:
FDA PART 172 -- FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION
Subpart F--Flavoring Agents and Related Substances
Sec. 172.515 Synthetic flavoring substances and adjuvants.
 
Physical Properties:
Appearance:pale yellow clear liquid (est)
Assay: 85.00 to 100.00
Food Chemicals Codex Listed: Yes
Specific Gravity:0.83900 to 0.85000 @ 25.00 °C.
Pounds per Gallon - (est).: 6.981 to 7.073
Refractive Index:1.43900 to 1.44900 @ 20.00 °C.
Boiling Point: 80.00 °C. @ 19.00 mm Hg
Boiling Point: 116.00 to 124.00 °C. @ 100.00 mm Hg
Acid Value: 5.00 max. KOH/g
Vapor Pressure:0.622000 mmHg @ 25.00 °C. (est)
Vapor Density:>1 ( Air = 1 )
Flash Point: 142.00 °F. TCC ( 61.00 °C. )
logP (o/w): 2.775 (est)
Shelf Life: 12.00 month(s) or longer if stored properly.
Storage:store in cool, dry place in tightly sealed containers, protected from heat and light. store under nitrogen.
Storage:store under nitrogen.
Soluble in:
 alcohol
 paraffin oil
 water, 212 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 antiperspirant spray, poor
 candle, good
 liquid bleach, poor
 ph = 10, moderate
 ph = 2 poor
 powder detergent, moderate
 soap, moderate
 toiletry, good
 
Organoleptic Properties:
Odor Type: melon
Odor Strength:high ,
recommend smelling in a 1.00 % solution or less
Substantivity:144 hour(s) at 100.00 %
fresh ozone melon watermelon sweet clean green
Odor Description:at 1.00 % in dipropylene glycol. fresh ozone melon fresh air sweet clean green
Luebke, William tgsc, (1989)
Odor sample from: Givaudan Corporation
green sweet oily melon watermelon rind floral
Odor Description:Green, sweet, oily, melon watermelon rind-like, with a floral nuance
Mosciano, Gerard P&F 17, No. 5, 127, (1992)
Flavor Type: green
green melon watermelon rind cucumber waxy chemical floral
Taste Description: at 50.00 ppm. Green, melon watermelon-rind, cucumber, with a waxy, chemical and floral nuance
Mosciano, Gerard P&F 17, No. 5, 127, (1992)
Odor and/or flavor descriptions from others (if found).
Bedoukian Research
2,6-DIMETHYL-5-HEPTEN-1-AL ≥85.0% (sum of isomers), FCC, Kosher
Odor Description:A fruity, green melon odor with citrus undertones
Can lend a fresh melon note to the top or middle of fragrances. Also particularly suitable for laundry detergent.
Taste Description:Characteristic watermelon, slightly cucumber
A must for juicy watermelon type flavors. Can also be used to add freshness to green apple and backnotes to lemon/lime flavors.
Givaudan
Melonal
Odor Description:Powerful, Green, Melon, Cucumber
Melonal offers a powerful and unique note. It is effective in all types of fragrances and is invaluable in the creation of natural smelling marine and fruity-melon notes.
Symrise
Melonal®
Odor Description:green melon note with a nuance of ozone
Stable in: body lotion (good), shampoo (good), soap (good), ap roll-on (very good), powder (good), cleaner citric (poor), cleaner apc (good), bleach (poor).
Taste Description:fresh, watery, green, fruity, melon, cucumber
Useful in: savory vegetable, fruity citrus, fruity red, fruity yellow, fruity tropical, fruity others.
Moellhausen
MELONALOX
Odor Description:fresh, fruity (melon-like), herbal notes
Taste Description:green, melon, watermelon, cucumber, waxy, chemical and floral notes
Pell Wall Perfumes
Melonal G
Odor Description:Green, fruity-melon, cucumber. Powerful
According to Arcadi Boix Camps, writing in 1978, “Melon-fruity products are playing a decisive role in the current evolution of perfumery. Let us mention cis-6-nonenol, with an absolutely natural and intense melon character, which could lead to important innovations in the future.
 
Cosmetic Information:
CosIng:cosmetic data2
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
Suppliers:
A.C.S. International
Dimethyl Heptenal 85
Operational Capabilities
Advanced Biotech
DIMETHYLHEPT-5-ENAL, 2,6 NATURAL (MELON ALDEHYDE)
90% min. (mixed isomers)
Alfrebro
Melonal, Natural
Odor: Green, Sweet, Oily, Melon Watermelon Rind-like
Apple Flavor & Fragrance
Melonal (2,6-Dimethyl-5-heptenal)
Associate Allied Chemicals
Melonal
About
Augustus Oils
Melonal
Services
Aurochemicals
MELONAL, Natural
Bedoukian Research
2,6-DIMETHYL-5-HEPTEN-1-AL
≥85.0% (sum of isomers), FCC, Kosher
Odor: A fruity, green melon odor with citrus undertones
Use: Can lend a fresh melon note to the top or middle of fragrances. Also particularly suitable for laundry detergent.
Flavor: Characteristic watermelon, slightly cucumber
A must for juicy watermelon type flavors. Can also be used to add freshness to green apple and backnotes to lemon/lime flavors.
Beijing Lys Chemicals
Melonal
Berjé
2,6-Dimethyl-5-Heptenal (Melon Aldehyde)
Happening at Berje
Best Value Chem
Melonal
Odor: Powerful, green, melon, cucumber like
BOC Sciences
For experimental / research use only.
2,6-DIMETHYL-5-HEPTEN-1-AL FCC 97.0% (sum of isomers
Charkit Chemical
MELON HEPTENAL FEMA 2389
Creatingperfume.com
MELONAL (Symrise)
Odor: Powerful, Green, Melon, Cucumber
Elan Inc.
elanal (2,6 dimethyl 5-heptenal)
(natural), Kosher
Ernesto Ventós
MELONAL
Odor: GREEN,ALDEHYDIC,FLORAL,FRUITY,MELON
Frutarom
MELONYL FOR FLAVORS
Frutarom
MELONYL
Givaudan
Melonal
Odor: Powerful, Green, Melon, Cucumber
Use: Melonal offers a powerful and unique note. It is effective in all types of fragrances and is invaluable in the creation of natural smelling marine and fruity-melon notes.
Global Essence
Melonal
Hermitage Oils
Melonal Natural Isolate
Odor: characteristic
Use: Adam Michael has this to say “I want to start this write-up by stating I regard melonal natural isolate as a truly revolutionary material in the world of naturals, the possibilities this now provides to the perfumer are enhanced no end. For years I am told that no fresh air, ozonic, cold water aroma exists within naturals, well now I can say with certainty it absolutely does.
The Vault
IFF
Melomor
Odor: Melon like, green, sophisticated marine and cucumber notes. Citrus and fruity undertones
Indukern F&F
MELONAL NATURAL
Indukern F&F
MELONAL
Odor: MELON, FLORAL, CUCUMBER
Inoue Perfumery
MELONAL
Lluch Essence
MELONAL NATURAL
Lluch Essence
MELONAL
M&U International
MELONAL
M&U International
NAT.MELONAL
Moellhausen
MELONALOX
Odor: fresh, fruity (melon-like), herbal notes
Flavor: green, melon, watermelon, cucumber, waxy, chemical and floral notes
Natural Advantage
Dimethyl-5-heptenal, 2,6- Nat (Melonal Nat)
Flavor: fruity, green, melon, tropical, watery
Riverside Aromatics LTD.is the exclusive distributor for Europe in UK for any non-US based inquiries
O'Laughlin Industries
MELOLAL
OQEMA
Melolan
Organica Aromatics
MELON ORG
NLT 90%
PCW France
Melolal
Steps to a fragranced product
Pell Wall Perfumes
Melonal G
Odor: Green, fruity-melon, cucumber. Powerful
Use: According to Arcadi Boix Camps, writing in 1978, “Melon-fruity products are playing a decisive role in the current evolution of perfumery. Let us mention cis-6-nonenol, with an absolutely natural and intense melon character, which could lead to important innovations in the future.
Penta International
MELONAL NATURAL
Penta International
MELONAL
PerfumersWorld
Melonal 10% in DPG
PerfumersWorld
Melonal
Odor: fresh ozone melon fresh air sweet clean green fresh watery fruity melon herbal
R C Treatt & Co Ltd
2,6-Dimethyl-5-heptenal
Reincke & Fichtner
2,6-Dimethyl-5-heptenal
Riverside Aromatics
MELONAL [2,6-DIMETHYL-5-HEPTENAL] NATURAL
Robertet
MELONAL (MELON ALDEHYDE)
Pure & Nat (EU)
Santa Cruz Biotechnology
For experimental / research use only.
2,6-Dimethyl-5-heptenal
Sigma-Aldrich
2,6-Dimethyl-5-heptenal, mixture of isomers, natural, 97%, FG
Certified Food Grade Products
Sigma-Aldrich
2,6-Dimethyl-5-heptenal, stabilized, FCC
Odor: cantaloupe; cucumber; grapefruit; lemon; melon; peach; watermelon; vegetable
Symrise
Melonal®
Odor: green melon note with a nuance of ozone
Use: Stable in: body lotion (good), shampoo (good), soap (good), ap roll-on (very good), powder (good), cleaner citric (poor), cleaner apc (good), bleach (poor).
Flavor: fresh, watery, green, fruity, melon, cucumber
Useful in: savory vegetable, fruity citrus, fruity red, fruity yellow, fruity tropical, fruity others.
Synerzine
Melonal
Taytonn
Melomor
Odor: Citrus, Cucumber, Fruity, Green, Marine
TCI AMERICA
For experimental / research use only.
2,6-Dimethyl-5-heptenal >85.0%(GC)
Tengzhou Xiang Yuan Aroma Chemicals
2,6-Dimethyl-5-heptenal
The John D. Walsh Company
Melonal
The Lermond Company
MELONAL
The Perfumers Apprentice
Melon Aldehyde (Natural)
The Perfumers Apprentice
Melonal (G)
Odor: Powerful, Green, Melon, Cucumber
Use: A powerful and unique note. It is effective in all types of fragrances and is invaluable in the creation of natural smelling marine and fruity-melon notes.
Vigon International
Melonal Natural
Vigon International
Melonal
Odor: Powerful, Green, Melon, Cucumber
WEN International
Melonal, Natural
 
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
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 36/37/39 - Wear suitable clothing, gloves and eye/face protection.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Flammable liquids (Category 4), H227
Skin irritation (Category 2), H315
Eye irritation (Category 2A), H319
Specific target organ toxicity - single exposure (Category 3), Respiratory system, H335
GHS Label elements, including precautionary statements
 
Pictogramexclamation-mark.jpg
 
Signal word Warning
Hazard statement(s)
H227 - Combustible liquid
H315 - Causes skin irritation
H319 - Causes serious eye irritation
H335 - May cause respiratory irritation
Precautionary statement(s)
P210 - Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P261 - Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 - Wash skin thouroughly after handling.
P271 - Use only outdoors or in a well-ventilated area.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P302 + P352 - IF ON SKIN: wash with plenty of soap and water.
P304 + P340 - IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P312 - Call a POISON CENTER or doctor/physician if you feel unwell.
P321 - Specific treatment (see supplemental first aid instructions on this label).
P332 + P313 - IF SKIN irritation occurs: Get medical advice/attention.
P337 + P313 - IF eye irritation persists: Get medical advice/attention.
P362 - Take off contaminated clothing and wash before reuse.
P370 + P378 - In case of fire: Use dry sand, dry chemical or alcohol-resistant foam for extinction.
P403 + P233 - Store in a well-ventilated place. Keep container tightly closed.
P403 + P235 - Store in a well-ventilated place. Keep cool.
P405 - Store locked up.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Oral/Parenteral Toxicity:
oral-rat LD50 > 5000 mg/kg
(Levenstein, 1974b)

gavage-rat LD50 [sex: M/F] 4550 mg/kg
LD50> 5 ml/kg.
(Mayyasi et al., 1981)

oral-rat LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 13(Suppl), Pg. 793, 1975.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 13(Suppl), Pg. 793, 1975.

Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category: flavor and fragrance agents
Recommendation for melon heptenal usage levels up to:
  2.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 27.00 (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
 average usual ppmaverage maximum ppm
baked goods: -19.00000
beverages(nonalcoholic): -2.80000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: -0.80000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -1.70000
fruit ices: -1.70000
gelatins / puddings: 0.0200010.00000
granulated sugar: --
gravies: --
hard candy: -8.40000
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: --
soups: --
sugar substitutes: --
sweet sauces: --
 
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) related to Flavouring Group Evaluation 6 (FGE.06): Straight-and branched-chain aliphatic unsatured primary alcohols, aldehydes, carboxylic acids, and esters from chemical groups 1 and 4
View page or View pdf

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 5: Esters of 23 branched- and straight-chain aliphatic saturated primary alcohols and of one secondary alcohol, and 24 branched- and straight-chain unsaturated carboxylic acids from chemical groups 1, 2, and 5
View page or View pdf

Flavouring Group Evaluation 6, Revision 1 (FGE.06Rev1) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf

Flavouring Group Evaluation 5, Revision 1 (FGE.05Rev1):Esters of branched- and straight-chain aliphatic saturated primary alcohols and of one secondary alcohol, and branched- and straight-chain unsaturated carboxylic acids from chemical groups 1, 2, and 5 (Commission Regulation (EC) No 1565/2000 of 18 July 2000) [1] - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf

Flavouring Group Evaluation 62 (FGE.62) Consideration of linear and branched-chain aliphatic unsaturated, unconjugated alcohols, aldehydes, acids, and related esters evaluated by JECFA (61st meeting) structurally related to esters of branched- and straight-chain aliphatic saturated primary alcohols and of one secondary alcohol, and branched- and straight-chain unsaturated carboxylic acids evaluated by EFSA in FGE.05 (2005) and to straight- and branched-chain aliphatic unsaturated primary alcohols, aldehydes, carboxylic acids, and esters evaluated by EFSA in FGE.06 (2004) (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 71: Consideration of aliphatic, linear, alpha,beta-unsaturated carboxylic acids and related esters
View page or View pdf

Flavouring Group Evaluation 72 (FGE.72): Consideration of aliphatic, branched-chain saturated and unsaturated alcohols, aldehydes, acids, and related esters evaluated by the JECFA (61st meeting) structurally related to branched- and straight-chain unsaturated carboxylic acids. Esters of these and straight-chain aliphatic saturated alcohols evaluated by EFSA in FGE.05Rev2 (2010)
View page or View pdf

Flavouring Group Evaluation 5, Revision 2 (FGE.05Rev2): Branched- and straight-chain unsaturated carboxylic acids and esters of these with aliphatic saturated alcohols from chemical groups 1, 2, 3 and 5
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 95 (FGE.95): Consideration of aliphatic, linear or branched-chain saturated and unsaturated alcohols, aldehydes, acids and related esters evaluated by JECFA (69th meeting) structurally related to esters of branched- and straight-chain aliphatic saturated primary alcohols and of one secondary alcohol, and branched- and straight-chain unsaturated carboxylic acids evaluated by EFSA in FGE.05Rev1 (2008)
View page or View pdf

Safety and efficacy of non-conjugated and accumulated unsaturated straight-chain and branched-chain, aliphatic primary alcohols, aldehydes, acids, acetals and esters belonging to chemical group 4 when used as flavourings for all animal species
View page or View pdf

EPI System: View
Toxicology Citations:Search
Env. Mutagen Info. Center:Search
EPA Substance Registry Services (TSCA):106-72-9
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :61016
National Institute of Allergy and Infectious Diseases:Data
WISER:UN 1989
WGK Germany:2
2,6-dimethylhept-5-enal
Chemidplus:0000106729
RTECS:MJ8797000 for cas# 106-72-9
 
References:
 2,6-dimethylhept-5-enal
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:106-72-9
Pubchem (cid):61016
Pubchem (sid):135018293
Flavornet:106-72-9
Pherobase:View
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2009
(IUPAC):Atomic Weights of the Elements 2009 (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
CHEMBL:View
HMDB (The Human Metabolome Database):Search
FooDB:FDB008531
Export Tariff Code:2912.19.5000
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
For Odor
No odor group found for these
satinaldehyde
FL/FR
(Z)-
verbenol
FL/FR
(E)-
verbenol
FL/FR
aldehydic
aldehydic
citrus carbaldehyde
FR
decanal (aldehyde C-10)
FL/FR
1-
formyl-3-isohexenyl-3-cyclohexene
FR
geranyl oxyacetaldehyde
FR
nonanal (aldehyde C-9)
FL/FR
octanal (aldehyde C-8)
FL/FR
balsamic
iso
amyl benzoate
FL/FR
clover nitrile
FR
verbenol
FL/FR
caramellic
strawberry furanone
FL/FR
citrus
bergamot oil
FL/FR
citral
FL/FR
dihydromyrcenol
FL/FR
grapefruit oil c.p. california
FL/FR
grapefruit pentanol
FR
lemon oil c.p. california
FL/FR
lime oil distilled mexico
FL/FR
marine decadienal
FR
methyl heptenone
FL/FR
myrmac aldehyde
FR
blood
orange oil italy
FL/FR
sweet
orange peel oil c.p. brazil
FL/FR
tetrahydromyrcenol
FR
10-
undecen-1-ol
FL/FR
valencene
FL/FR
clean
amerinal
FR
coconut
delta-
heptalactone
FL/FR
earthy
1-
octen-3-ol
FL/FR
fatty
2-
nonenal
FL/FR
floral
benzyl acetate
FL/FR
bois de rose oil brazil
FL/FR
citronellyl acetate
FL/FR
coriander seed oil
FL/FR
cyclamen aldehyde
FL/FR
cyclohexyl ethyl alcohol
FL/FR
dimethyl anthranilate
FL/FR
floral pyranol
FR
gardenia pentyl acetate
FR
geranyl acetate
FL/FR
herbal pyran
FR
hyacinth ether
FR
hydroxycitronellal diethyl acetal
FL/FR
jasmopyrane (Givaudan)
FR
linalool
FL/FR
laevo-
linalool
FL/FR
methyl dihydrojasmonate
FL/FR
methyl jasmonate
FL/FR
muguet carboxaldehyde
FR
muguet octadienol
FR
nerol
FL/FR
neryl acetate
FL/FR
ocean propanal
FL/FR
ocean propanal / methyl anthranilate schiff's base
FR
petitgrain oil paraguay
FL/FR
phenethyl acetate
FL/FR
phenethyl isobutyrate
FL/FR
rose butanoate
FL/FR
tetrahydrolinalool
FL/FR
violet methyl carbonate
FR
fresh
decyl vinyl ether
FR
fruity
allyl amyl glycolate
FR
allyl cyclohexyl propionate
FL/FR
allyl hexanoate
FL/FR
iso
amyl acetate
FL/FR
iso
amyl butyrate
FL/FR
iso
amyl isovalerate
FL/FR
benzaldehyde
FL/FR
benzyl propionate
FL/FR
butyl 2-decenoate
FL/FR
iso
butyl octanoate
FL/FR
diethyl malonate
FL/FR
dimethyl benzyl carbinyl isobutyrate
FR
ethyl acetoacetate
FL/FR
ethyl butyrate
FL/FR
ethyl heptanoate
FL/FR
green acetate
FR
methyl 2-methyl valerate
FL/FR
methyl 3-nonenoate
FL/FR
nerolidyl isobutyrate
FR
octyl butyrate
FL/FR
iso
propyl 2-methyl butyrate
FL/FR
propyl 2,4-decadienoate
FL/FR
strawberry glycidate 1 (aldehyde C-16 (so-called))
FL/FR
gamma-
undecalactone (aldehyde C-14 (so-called))
FL/FR
green
acetaldehyde ethyl phenethyl acetal
FL/FR
coriander heptenol
FL/FR
ethyl (E,Z)-2,4-decadienoate
FL/FR
fresh nitrile
FR
galbanum decatriene
FL/FR
galbanum oil
FL/FR
green heptenal
FR
heptanal (aldehyde C-7)
FL/FR
1-
hepten-3-ol
FL/FR
(Z)-4-
heptenal diethyl acetal
FL/FR
(Z)-3-
hexen-1-ol
FL/FR
(Z)-3-
hexen-1-yl 2-methyl butyrate
FL/FR
(Z)-3-
hexen-1-yl acetate
FL/FR
(Z)-3-
hexen-1-yl butyrate
FL/FR
(Z)-3-
hexen-1-yl oxyacetaldehyde
FR
(Z)-3-
hexen-1-yl pyruvate
FL/FR
hexyl 2-methyl butyrate
FL/FR
2,4-
ivy carbaldehyde
FL/FR
(Z)-
leaf acetal
FL/FR
manzanate (Givaudan)
FL/FR
melon nonenoate
FL/FR
2-(2-
methyl allyl oxy) heptane
FR
6-
methyl-3-hepten-2-one
FL/FR
(E,Z)-3,6-
nonadien-1-ol
FL/FR
3,6-
nonadien-1-ol
FL/FR
(E,Z)-2,6-
nonadien-1-ol
FL/FR
3,6-
nonadien-1-yl acetate
FL/FR
(E,Z)-3,6-
nonadien-1-yl acetate
FL/FR
(E,Z)-2,6-
nonadienal
FL/FR
(Z)-5-
octen-1-ol
FL/FR
(Z)-5-
octen-1-yl propionate
FL/FR
olive oil absolute
FL/FR
phenoxyacetaldehyde 50% in benzyl alcohol
FR
3-
phenyl propionaldehyde
FL/FR
privet dioxane
FR
styralyl acetate
FL/FR
violet decenol
FR
violet leaf absolute
FL/FR
hay
para-
methyl phenoxyacetaldehyde
FR
herbal
7-
allyl benzo[b][1,4]dioxepin-3-one
FR
alpha-
amyl cinnamyl formate
FL/FR
2-
cyclohexyl cyclohexanone
FR
floral nitrile
FR
lavender absolute bulgaria
FL/FR
linalyl acetate
FL/FR
(E)-6-
methyl-3-hepten-2-one
FL/FR
laevo-
perillaldehyde
FL/FR
savin wood oil (juniperus phoenicea)
FL/FR
alpha-
terpinyl acetate
FL/FR
marine
marine carbonitrile
FR
marine hexane
FR
marine pyridine
FR
ocean carboxaldehyde
FR
ozone propanal
FR
melon
melon carboxaldehyde
FR
(Z)-6-
nonen-1-ol
FL/FR
(Z)-6-
nonenal
FL/FR
watermelon ketone
FR
mushroom
3-
octen-2-ol
FL/FR
powdery
para-
anisyl acetate
FL/FR
terpenic
juniperus communis fruit oil
FL/FR
alpha-
terpineol
FL/FR
waxy
decyl acetate
FL/FR
2,4-
nonadien-1-ol
FL/FR
(Z)-3-
nonen-1-ol
FL/FR
octyl isobutyrate
FL/FR
woody
louro brasileiro wood oil
FR
sabinene
FL/FR
(Z)-
woody amylene
FR
woody heptene
FR
For Flavor
No flavor group found for these
alpha-
amyl cinnamyl formate
FL/FR
iso
butyl octanoate
FL/FR
coriander heptenol
FL/FR
(E)-6-
methyl-3-hepten-2-one
FL/FR
6-
methyl-3-hepten-2-one
FL/FR
savin wood oil (juniperus phoenicea)
FL/FR
10-
undecen-1-ol
FL/FR
(E)-
verbenol
FL/FR
(Z)-
verbenol
FL/FR
aldehydic
aldehydic
nonanal (aldehyde C-9)
FL/FR
octanal (aldehyde C-8)
FL/FR
apple
(E,Z)-2,6-
nonadien-1-ol
FL/FR
aromatic
laevo-
perillaldehyde
FL/FR
caramellic
strawberry furanone
FL/FR
citrus
bergamot oil
FL/FR
citral
FL/FR
grapefruit oil c.p. california
FL/FR
lemon oil c.p. california
FL/FR
lime oil distilled mexico
FL/FR
laevo-
linalool
FL/FR
linalool
FL/FR
nerol
FL/FR
blood
orange oil italy
FL/FR
sweet
orange peel oil c.p. brazil
FL/FR
alpha-
terpineol
FL/FR
valencene
FL/FR
cooling
manzanate (Givaudan)
FL/FR
creamy
octyl isobutyrate
FL/FR
gamma-
undecalactone (aldehyde C-14 (so-called))
FL/FR
estery
ethyl acetoacetate
FL/FR
fatty
(E,E)-2,4-
heptadienal
FL
2,4-
nonadien-1-ol
FL/FR
2-
nonenal
FL/FR
floral
bois de rose oil brazil
FL/FR
citronellyl acetate
FL/FR
linalyl acetate
FL/FR
methyl dihydrojasmonate
FL/FR
methyl jasmonate
FL/FR
neryl acetate
FL/FR
ocean propanal
FL/FR
satinaldehyde
FL/FR
tetrahydrolinalool
FL/FR
fruity
allyl cyclohexyl propionate
FL/FR
allyl hexanoate
FL/FR
iso
amyl acetate
FL/FR
iso
amyl benzoate
FL/FR
para-
anisyl acetate
FL/FR
benzaldehyde
FL/FR
benzyl acetate
FL/FR
benzyl propionate
FL/FR
butyl 2-decenoate
FL/FR
diethyl malonate
FL/FR
dimethyl anthranilate
FL/FR
ethyl butyrate
FL/FR
ethyl heptanoate
FL/FR
methyl (E)-3-nonenoate
FL
methyl 2-methyl valerate
FL/FR
methyl 3-nonenoate
FL/FR
iso
propyl 2-methyl butyrate
FL/FR
rose butanoate
FL/FR
strawberry glycidate 1 (aldehyde C-16 (so-called))
FL/FR
styralyl acetate
FL/FR
green
acetaldehyde ethyl phenethyl acetal
FL/FR
iso
amyl isovalerate
FL/FR
cyclamen aldehyde
FL/FR
cyclohexyl ethyl alcohol
FL/FR
dihydromyrcenol
FL/FR
ethyl (E,Z)-2,4-decadienoate
FL/FR
galbanum decatriene
FL/FR
galbanum oil
FL/FR
geranyl acetate
FL/FR
heptanal (aldehyde C-7)
FL/FR
1-
hepten-3-ol
FL/FR
(Z)-4-
heptenal diethyl acetal
FL/FR
(Z)-3-
hexen-1-ol
FL/FR
(Z)-3-
hexen-1-yl 2-methyl butyrate
FL/FR
(Z)-3-
hexen-1-yl acetate
FL/FR
(Z)-3-
hexen-1-yl butyrate
FL/FR
(Z)-3-
hexen-1-yl pyruvate
FL/FR
hexyl 2-methyl butyrate
FL/FR
2,4-
ivy carbaldehyde
FL/FR
(Z)-
leaf acetal
FL/FR
melon nonenoate
FL/FR
methyl heptenone
FL/FR
(E,Z)-3,6-
nonadien-1-ol
FL/FR
3,6-
nonadien-1-ol
FL/FR
3,6-
nonadien-1-yl acetate
FL/FR
(E,Z)-3,6-
nonadien-1-yl acetate
FL/FR
(E,Z)-2,6-
nonadienal
FL/FR
(E,E)-2,6-
nonadienal
FL
(Z)-6-
nonenal
FL/FR
(Z)-5-
octen-1-ol
FL/FR
(Z)-5-
octen-1-yl propionate
FL/FR
3-
phenyl propionaldehyde
FL/FR
sorbyl acetate
FL
violet leaf absolute
FL/FR
herbal
coriander seed oil
FL/FR
lavender absolute bulgaria
FL/FR
petitgrain oil paraguay
FL/FR
verbenol
FL/FR
honey
phenethyl acetate
FL/FR
phenethyl isobutyrate
FL/FR
lactonic
delta-
heptalactone
FL/FR
melon
hydroxycitronellal diethyl acetal
FL/FR
propyl 2,4-decadienoate
FL/FR
mushroom
3-
octen-2-ol
FL/FR
1-
octen-3-ol
FL/FR
oily
olive oil absolute
FL/FR
terpenic
juniperus communis fruit oil
FL/FR
waxy
iso
amyl butyrate
FL/FR
decanal (aldehyde C-10)
FL/FR
decyl acetate
FL/FR
(Z)-6-
nonen-1-ol
FL/FR
(Z)-3-
nonen-1-ol
FL/FR
octyl butyrate
FL/FR
woody
sabinene
FL/FR
alpha-
terpinyl acetate
FL/FR
 
Potential Uses:
FRagrumen aldehyde
FRaldehydic
FRalgae
FRapple red apple
 blossom tropical blossom
FRboxwood
FRbramble arctic bramble blackberry
FL/FRcilantro
FRcitrus
 clean
FRcologne
FRcucumber
FRdogwood
 exotic
 fantasy blends
FRfern
FLfish
FRflorida breeze
FRforest
FRfresh outdoors
FLfruit tropical fruit
FRgalbanum
FRgooseberry
FRgrapefruit
FRgreen
FRherbal
FRhibiscus
FRhoneydew
FRkiwi
FRkiwi blossom
FRlemon
FRmango
FRmango flower
FRmelon
FRnew car
FRocean sea
FRsea breeze
 ozone
FRpeach
FLpear prickly pear
 rose wild rose
FRsea breeze
FRspring rain
FRstrawberry
FLtropical
FLvegetable
 watery
 
Occurrence (nature, food, other):note
 citronella oil ceylon @ 0.11%
Data GC Search Trop Picture
 citronella oil china @ 0.09%
Data GC Search Trop Picture
 citronella oil java @ 0.09%
Data GC Search Trop Picture
 ginger rhizome
Search Trop Picture
 jasminum sambac
Search Trop Picture
 lemon
Search Trop Picture
 lime peel
Search Trop Picture
 melons
Search PMC Picture
 petitgrain combava oil @ 0.13%
Data GC Search Picture
 petitgrain combava oil @ trace%
Data GC Search Picture
 petitgrain sweet oil @ 0.08%
Data GC Search Picture
 
Synonyms:
2,6-dimethyl hept-5-en-1-al
2,6-dimethyl hept-5-enal
 dimethyl heptenal
 dimethyl heptenal 85
2,6-dimethyl-5-hepten-1-al
2,6-dimethyl-5-heptenal
2,6-dimethyl-5-heptenal (melon aldehyde)
2,6-dimethylhept-5-en-1-al
2,6-dimethylhept-5-enal
 elanal (2,6 dimethyl 5-heptenal)
 hept-5-en-1-al, 2,6-dimethyl-
5-heptenal, 2,6-dimethyl-
 melolal (Givaudan) (Symrise)
 melolan
 melomor (IFF)
 melon aldehyde
 melon aldehyde natural
 melon heptenal
 melon touch
 melonal
 melonal (2,6-dimethyl-5-heptenal)
 melonal natural
 melonalox
 

Articles:

PubMed:Food volatile compounds facilitating HII mesophase formation: solubilization and stability.
J-Stage:Stereochemistry of Female-Specific Normonoterpenes, Sex Pheromone Candidates from the Acarid Mite, Tyreophagus sp. (Astigmata: Acaridae)
PubMed:Stereochemistry of female-specific normonoterpenes, sex pheromone candidates from the acarid mite, Tyreophagus sp. (Astigmata: Acaridae).
PubMed:Inhibition of formation of oxidative volatile components in fermented cucumbers by ascorbic acid and turmeric.
PubMed:Development of oxidized odor and volatile aldehydes in fermented cucumber tissue exposed to oxygen.
PubMed:Short-term toxicity of 2,6-dimethylhept-5-en-1-al in rats.
 
Notes:
Blends well with green aldehydes.
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