|
Category: cosmetic and flavor agents
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
| Appearance: | colorless clear liquid (exp) |
| Assay: | 99.00 to 100.00
|
| Food Chemicals Codex Listed: | Yes |
| Specific Gravity: | 0.77500 to 0.78500 @ 25.00 °C.
|
| Pounds per Gallon - (est).: | 6.449 to 6.532
|
| Specific Gravity: | 0.77600 to 0.78600 @ 20.00 °C.
|
| Pounds per Gallon - est.: | 6.465 to 6.548
|
| Refractive Index: | 1.32300 to 1.33700 @ 20.00 °C.
|
| Melting Point: | -125.00 to -123.00 °C. @ 760.00 mm Hg
|
| Boiling Point: | 20.00 to 21.00 °C. @ 760.00 mm Hg
|
| Boiling Point: | -54.00 to -53.00 °C. @ 15.00 mm Hg
|
| Vapor Pressure: | 902.000000 mmHg @ 25.00 °C. |
| Vapor Density: | 1.5 ( Air = 1 ) |
| Flash Point: | -40.00 °F. TCC ( -40.00 °C. )
|
| logP (o/w): | -0.340 |
| Shelf Life: | 12.00 month(s) or longer if stored properly. |
| Storage: | refrigerate in tightly sealed containers. |
| Soluble in: |
| | acetone | | | alcohol | | | can be salted out of water with calcium chloride | | | ethyl ether | | | water, 1.00E+06 mg/L @ 25 °C (exp) |
Organoleptic Properties:
| Odor Type: ethereal |
Odor Strength:high ,
recommend smelling in a 0.10 % solution or less |
| Substantivity: < 1 hour(s) at 100.00 % |
| pungent ethereal aldehydic fruity |
Odor Description:at 0.10 % in propylene glycol. pungent ethereal aldehydic fruity
Luebke, William tgsc, (2017) |
| pungent ethereal fresh fruity musty |
Odor Description:Pungent, etherial, fresh, lifting, penetrating, fruity and musty
Mosciano, Gerard P&F 22, No. 4, 75, (1997) |
| Flavor Type: pungent |
| pungent fresh aldehydic green |
| Taste Description: pungent fresh aldehydic refreshing green |
| pungent fresh aldehydic green |
Taste Description: at 10.00 ppm. Pungent, fresh, aldehydic, refreshing and green
Mosciano, Gerard P&F 22, No. 4, 75, (1997) |
| Odor and/or flavor descriptions from others (if found). |
Cosmetic Information:
Suppliers:
| Advanced Biotech |
| ACETALDEHYDE 10% IN ETOH NATURAL
Odor: Alcoholic, ethereal |
| Advanced Biotech |
| ACETALDEHYDE 100% SYNTHETIC
98% min. Odor: Ethereal |
| Advanced Biotech |
| ACETALDEHYDE 50% ETOH SYNTHETIC
Odor: Alcoholic ethereal |
| Advanced Biotech |
| ACETALDEHYDE 50% IN 5 FOLD ORANGE OIL SYNTHETIC
|
| Advanced Biotech |
| ACETALDEHYDE 50% IN BENZYL BENZOATE SYNTHETIC
Odor: Acrid, Almond, Aromatic |
| Advanced Biotech |
| ACETALDEHYDE 50% IN D'LIMONENE NATURAL
Odor: Pungent, orange |
| Advanced Biotech |
| ACETALDEHYDE 50% IN ETOH NATURAL
Odor: Alcoholic, ethereal |
| Advanced Biotech |
| ACETALDEHYDE 50% IN ORANGE OIL 5-FOLD NATURAL
Odor: Pungent, orange |
| Advanced Biotech |
| ACETALDEHYDE 50% IN ORANGE OIL NATURAL
Odor: Pungent, orange |
| Advanced Biotech |
| ACETALDEHYDE 50% IN ORANGE OIL SYNTHETIC
Odor: Pungent, orange |
| Advanced Biotech |
| ACETALDEHYDE 50% IN ORANGE TERPENES NATURAL
Odor: Pungent, orange |
| Advanced Biotech |
| ACETALDEHYDE 50% IN TRIACETIN NATURAL
|
| Advanced Biotech |
| ACETALDEHYDE 50% PG NATURAL
|
| Advanced Biotech |
| ACETALDEHYDE NATURAL
98% min. Odor: Pungent, ethereal |
| Alfrebro |
| ACETALDEHYDE 100%
|
| Alfrebro |
| ACETALDEHYDE 50% IN ETHANOL
|
| Alfrebro |
| ACETALDEHYDE NATURAL 10% IN ETHANOL
|
| Alfrebro |
| ACETALDEHYDE NATURAL 100%
Odor: Pungent |
| Alfrebro |
| ACETALDEHYDE NATURAL 50% IN ETHANOL
Odor: Pungent |
| Apple Flavor & Fragrance |
| Acetaldehyde
20% in water |
| Apple Flavor & Fragrance |
| Acetaldehyde
40% in ethanol alcohol |
| Apple Flavor & Fragrance |
| Acetaldehyde
40% in orange oil |
| Apple Flavor & Fragrance |
| Acetaldehyde
40% in PG |
| Astral Extracts |
| 10% Natural Acetaldehyde
|
| Astral Extracts |
| Acetaldehyde 50% In Ethanol
|
| Astral Extracts |
| Acetaldehyde
|
| Augustus Oils |
| Acetaldehyde 50% Solution
|
| Services |
| Augustus Oils |
| Acetaldehyde
|
| Axxence Aromatic |
| ACETALDEHYDE 98%, Natural
Kosher |
| Sustainability |
| Azelis UK |
| Acetaldehyde
|
| CJ Latta & Associates |
| ACETALDEHYDE SOLUTION IN VARIOUS DILUTENT
|
| Diffusions Aromatiques |
| ACETALDEHYDE
|
| Eastman Chemical |
| Acetaldehyde, Kosher
99.7 wt % min. |
| Elan Inc. |
| ALDEFRESH
10%, (natural), Kosher |
| ENNOLYS |
| Acetaldehyde 50% + ethanol 50%
Natural (EU,US), Kosher & Halal Odor: apple, fresh |
| ENNOLYS |
| Acetaldehyde 50% + orange terpenes 50%
Natural (EU,US), Kosher & Halal Odor: apple, orange, fresh |
| ENNOLYS |
| Acetaldehyde 50% + triacetin 50%
Natural (EU,US), Kosher & Halal Odor: sweet, apple, fresh |
| ENNOLYS |
| Acetaldehyde 50% + water 50%
Natural (EU,US), Kosher & Halal Odor: apple, fresh |
| ENNOLYS |
| Acetaldehyde
Natural (EU,US), Kosher & Halal Odor: apple |
| Fleurchem |
| acetaldehyde 50% alcohol natural
|
| Fleurchem |
| acetaldehyde natural
|
| Frutarom |
| ACETALDEHYDE
KOSHER Flavor: Pungent, Ethereal, Aldehydic, Fruity |
| CBD Offering |
| Frutarom |
| Natural Acetaldehyde 50% ex. Orange
KOSHER Flavor: pungent ethereal aldehydic fruity |
| IFF |
| ACETALDEHYDE
KOSHER Flavor: Pungent, Ethereal, Aldehydic, Fruity |
| IFF |
| Natural Acetaldehyde 50% ex. Orange
KOSHER Flavor: pungent ethereal aldehydic fruity |
| Indenta Group |
| Acetaldehyde
|
| Inoue Perfumery |
| ACETALDEHYDE
|
| Jiangyin Healthway |
| Acetaldehyde
|
| New functional food ingredients |
| Lluch Essence |
| ACETALDEHYDE 35% WATER
|
| Lluch Essence |
| ACETALDEHYDE 99%
Odor: ETHEREAL, FRESH, PUNGENT |
| Lluch Essence |
| ACETALDEHYDE NATURAL 50% LIMONENE
|
| Lluch Essence |
| ACETALDEHYDE NATURAL 50% TRIACETIN
|
| Lluch Essence |
| ACETALDEHYDE NATURAL 99%
|
| M&U International |
| NAT.ACETALDEHYDE, Kosher
|
| Natural Advantage |
| Acetaldehyde Nat ex Orange, 10% in Orange Aroma
Flavor: alcoholic, citrus, etherial, nutty |
| Riverside Aromatics LTD.is the exclusive distributor for Europe in UK for any non-US based inquiries |
| Natural Advantage |
| Acetaldehyde Nat, 10% in d-Limonene
Flavor: alcoholic, citrus, etherial, nutty |
| Natural Advantage |
| Acetaldehyde Nat, 50% in OH
Flavor: alcoholic, citrus, etherial, nutty |
| Natural Advantage |
| Acetaldehyde Nat, 50% in PG
Flavor: alcoholic, citrus, etherial, nutty |
| O'Laughlin Industries |
| ACETALDEHYDE 50% in ORANGE OIL
|
| O'Laughlin Industries |
| ACETALDEHYDE NAT 25% PCT IN TRIETHYL CITRATE
|
| O'Laughlin Industries |
| ACETALDEHYDE NATURAL 50% in ORANGE TERPENES
|
| O'Laughlin Industries |
| ACETALDEHYDE NATURAL (20% Acetaldehyde 80% Alcohol)
|
| O'Laughlin Industries |
| ACETALDEHYDE NATURAL (50% Acetaldehyde 50% Limonene
|
| O'Laughlin Industries |
| ACETALDEHYDE NATURAL (80% Acetaldehyde 20% Alcohol)
|
| O'Laughlin Industries |
| ACETALDEHYDE NATURAL 50% in ETHANOL
|
| O'Laughlin Industries |
| ACETALDEHYDE NATURAL 50% in WATER
|
| O'Laughlin Industries |
| ACETALDEHYDE SYNTHETIC 25% IN TRIACETIN
|
| Penta International |
| ACETALDEHYDE 10% IN ETHANOL NATURAL
|
| Penta International |
| ACETALDEHYDE 100% NATURAL
|
| Penta International |
| ACETALDEHYDE NATURAL EX- ORANGE 50% IN D'LIMONENE
|
| Penta International |
| ACETALDEHYDE NATURAL 50% IN ETHANOL
|
| Penta International |
| ACETALDEHYDE NATURAL 50% IN PROPYLENE GLYCOL
|
| Penta International |
| ACETALDEHYDE NATURAL 50% IN TRIACETIN
|
| Penta International |
| ACETALDEHYDE NATURAL EX-ORANGE 50% IN ORANGE AROMA
|
| Penta International |
| ACETALDEHYDE SYNTHETIC 50% IN ISOPROPYL MYRISTATE
|
| Penta International |
| ACETALDEHYDE SYNTHETIC 50% IN DIPROPYLENE GLYCOL
|
| Penta International |
| ACETALDEHYDE SYNTHETIC 50% IN ETHYL ALCOHOL
|
| Penta International |
| ACETALDEHYDE SYNTHETIC 50% IN PROPYLENE GLYCOL
|
| Reincke & Fichtner |
| Acetaldehyde natural
|
| Reincke & Fichtner |
| Acetaldehyde
|
| Sigma-Aldrich |
| Acetaldehyde ≥99%, FCC
|
| Certified Food Grade Products |
| Sigma-Aldrich |
| Acetaldehyde ≥99%, meets FCC analytical specification
|
| Sigma-Aldrich |
| Acetaldehyde solution, 40 wt. % in H2O
|
| Sigma-Aldrich |
| Acetaldehyde solution, 40 wt. % in isopropanol
|
| Sigma-Aldrich |
| Acetaldehyde solution, 50 wt. % in ethanol
Odor: ethereal; wine-like; coffee |
| Sigma-Aldrich |
| Acetaldehyde solution, natural, 50 wt. % ethanol, FG
Odor: ethereal; wine-like; coffee |
| Sigma-Aldrich |
| Acetaldehyde, ≥99%, meets FCC analytical specification
Odor: ethereal; wine-like; coffee |
| Sigma-Aldrich |
| Acetaldehyde, natural, ≥99%, FG
Odor: ethereal; wine-like; coffee |
| Silverline Chemicals |
| Acetaldehyde 50% in p.g.
|
| Sunaux International |
| nat.Acetaldehyde
|
| Taytonn ASCC |
| Acetaldehyde
Odor: Pungent, Green, Fruity, Aldehydic/ Aldehyde |
| Ungerer & Company |
| Acetaldehyde 50%
|
| Universal Preserv-A-Chem Inc. |
| ACETALDEHYDE REAGENT
|
| Vigon International |
| Acetaldehyde Natural
50% in Grain Alcohol Odor: Sharp,Citrus,Orange |
Safety Information:
| Preferred SDS: View |
| European information : |
| Most important hazard(s): | | Xn - Harmful. |
R 12 - Extremely flammable.
R 36/37 - Irritating to eyes and respiratory system.
R 40 - Limited evidence of a carcinogenic effect.
S 02 - Keep out of the reach of children.
S 16 - Keep away from sources of ignition - No Smoking.
S 33 - Take precautionary measures against static discharge.
S 36/37 - Wear suitable protective clothing and gloves.
|
| |
| Hazards identification |
| |
| Classification of the substance or mixture |
| GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
Eye irritation (Category 2A), H319
Specific target organ toxicity - single exposure (Category 3), Respiratory system, H335
Carcinogenicity (Category 2), H351
Acute aquatic toxicity (Category 3), H402
|
| GHS Label elements, including precautionary statements |
| |
| Pictogram |    |
| |
| Signal word | Danger |
| Hazard statement(s) |
H224 - Extremely flammable liquid and vapour
H319 - Causes serious eye irritation
H335 - May cause respiratory irritation
H351 - Suspected of causing cancer
H402 - Harmful to aquatic life
|
| Precautionary statement(s) |
P201 - Obtain special instructions before use.
P202 - Do not handle until all safety precautions have been read and understood.
P210 - Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P233 - Keep container tightly closed.
P240 - Ground/bond container and receiving equipment.
P241 - Use explosion-proof electrical/ventilating/lighting/…/equipment.
P242 - Use only non-sparking tools.
P243 - Take precautionary measures against static discharge.
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.
P273 - Avoid release to the environment.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P303 + P361 + P353 - IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
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.
P308 + P313 - IF exposed or concerned: Get medical advice/attention.
P337 + P313 - IF eye irritation persists: Get medical advice/attention.
P370 + P378 - In case of fire: Use dry sand, dry chemical or alcohol-resistant foam for extinction.
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 661 mg/kg
PERIPHERAL NERVE AND SENSATION: SPASTIC PARALYSIS WITH OR WITHOUT SENSORY CHANGE
BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)
LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Agents and Actions, A Swiss Journal of Pharmacology. Vol. 4, Pg. 125, 1974.
intraperitoneal-rat LDLo 500 mg/kg
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Journal of Biological Chemistry. Vol. 152, Pg. 41, 1944.
intravenous-rabbit LDLo 300 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Journal of Pharmacology and Experimental Therapeutics. Vol. 30, Pg. 429, 1927.
oral-mouse LD50 900 mg/kg
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 25(11), Pg. 57, 1981.
intraperitoneal-mouse LD50 500 mg/kg
IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man. Vol. 36, Pg. 101, 1985.
intravenous-frog LDLo 800 mg/kg
CARDIAC: OTHER CHANGES
BEHAVIORAL: GENERAL ANESTHETIC
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Journal of Pharmacology and Experimental Therapeutics. Vol. 30, Pg. 429, 1927.
intratracheal-hamster LD50 96 mg/kg
Progress in Experimental Tumor Research. Vol. 24, Pg. 162, 1979.
|
| Dermal Toxicity: |
skin-rabbit LD50 3540 mg/kg
Union Carbide Data Sheet. Vol. 12/13/1963
subcutaneous-rat LD50 640 mg/kg
BEHAVIORAL: GENERAL ANESTHETIC
Acta Pharmacologica et Toxicologica. Vol. 6, Pg. 299, 1950.
subcutaneous-rabbit LDLo 1200 mg/kg
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Journal of Pharmacology and Experimental Therapeutics. Vol. 30, Pg. 429, 1927.
subcutaneous-mouse LD50 560 mg/kg
BEHAVIORAL: GENERAL ANESTHETIC
Acta Pharmacologica et Toxicologica. Vol. 6, Pg. 299, 1950.
|
| Inhalation Toxicity: |
inhalation-hamster LC50 17000 ppm/4H
Progress in Experimental Tumor Research. Vol. 24, Pg. 162, 1979.
inhalation-mammal (species unspecified) LC50 20100 mg/m3
BEHAVIORAL: EXCITEMENT
LUNGS, THORAX, OR RESPIRATION: DYSPNEA
SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 19(7), Pg. 54, 1975.
inhalation-mouse LC50 23000 mg/m3/4H
Current Toxicology. Vol. 1, Pg. 47, 1993.
inhalation-rat LC50 13300 ppm/4H
LUNGS, THORAX, OR RESPIRATION: DYSPNEA
BEHAVIORAL: EXCITEMENT
National Technical Information Service. Vol. OTS0534485
inhalation-human TCLo 134 ppm/30M
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
JAMA, Journal of the American Medical Association. Vol. 165, Pg. 1908, 1957.
|
Safety in Use Information:
| Category: | | cosmetic and flavor agents |
| Recommendation for acetaldehyde usage levels up to: | | | not for fragrance use.
|
| |
| NOEL (No Observed Effect Level): | 125 (mg/kg bw per day) |
| Structure Class: | I |
| 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 |
| Click here to view publication 3 |
| | average usual ppm | average maximum ppm |
| baked goods: | - | 12.00000 |
| beverages(nonalcoholic): | - | 3.90000 |
| beverages(alcoholic): | - | - |
| breakfast cereal: | - | - |
| cheese: | - | - |
| chewing gum: | 20.00000 | 270.00000 |
| condiments / relishes: | - | - |
| confectionery froastings: | - | - |
| egg products: | - | - |
| fats / oils: | - | - |
| fish products: | - | - |
| frozen dairy: | - | 25.00000 |
| fruit ices: | - | 25.00000 |
| gelatins / puddings: | - | 6.80000 |
| granulated sugar: | - | - |
| gravies: | - | - |
| hard candy: | - | 22.00000 |
| 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: | - | - |
| soups: | - | - |
| sugar substitutes: | - | - |
| sweet sauces: | - | - |
Safety References:
European Food Safety Authority (EFSA) reference(s):
|
Flavouring Group Evaluation 3, Revision 1 (FGE.03Rev1): Acetals of branched- and straight-chain aliphatic saturated primary alcohols and branched- and straight-chain saturated or unsaturated aldehydes, an ester of a hemiacetal and an orthoester of formic acid, from chemical groups 1, 2 & 4 Commission Regulation (EC) No 1565/2000 of 18 July 2000) [1] - Scientific Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)on a request from the Commission
View page or View pdf
|
Flavouring Group Evaluation 61 (FGE.61): Consideration of aliphatic acyclic acetals evaluated by JECFA (57th meeting) structurally related to acetals of branched- and straight-chain aliphatic saturated primary alcohols and branched- and straight-chain saturated aldehydes, and an orthoester of formic acid evaluated by EFSA in FGE.03 (2004) (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf
|
Flavouring Group Evaluation 14, Revision 1 (FGE.14Rev1): Phenethyl alcohol, aldehyde, acetals, carboxylic acid and related esters from chemical group 15 and 22 [1] - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
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
|
Flavouring Group Evaluation 20, Revision 1 (FGE.20Rev1): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids and related esters from chemical group 23
View page or View pdf
|
Flavouring Group Evaluation 8 (FGE.08)[1]: Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical group 20
View page or View pdf
|
Flavouring Group Evaluation 8, Revision 1 (FGE.08Rev1): Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30
View page or View pdf
|
Flavouring Group Evaluation 61, Revision 1 (FGE.61Rev1): Consideration of aliphatic acetals evaluated by JECFA (57th meeting) structurally related to acetals of branched- and straight-chain aliphatic saturated primary alcohols and branched- and straight-chain saturated aldehydes and one orthoester of formic acid evaluated
View page or View pdf
|
Scientific Opinion on Flavouring Group Evaluation 8, Revision 3 (FGE.08Rev3): Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30
View page or View pdf
|
Scientific Opinion on the safety and efficacy of straight-chain primary aliphatic alcohols/aldehydes/acids, acetals and esters with esters containing saturated alcohols and acetals containing saturated aldehydes (chemical group 1) when used as flavourings for all animal species
View page or View pdf
|
| EPI System: View |
| EPA-Iris:IRIS |
| ClinicalTrials.gov:search |
| Daily Med:search |
| NIOSH International Chemical Safety Cards:search |
| NIOSH Pocket Guide:search |
| Chemical Carcinogenesis Research Information System:Search |
| AIDS Citations:Search |
| Cancer Citations:Search |
| Toxicology Citations:Search |
| Carcinogenic Potency Database:Search |
| EPA GENetic TOXicology:Search |
| EPA Substance Registry Services (TSCA):75-07-0 |
| EPA ACToR:Toxicology Data |
| EPA Substance Registry Services (SRS):Registry |
| Laboratory Chemical Safety Summary :177 |
| National Institute of Allergy and Infectious Diseases:Data |
| SCCNFP:opinion |
| WISER:UN 1089 |
| WGK Germany:1 |
| acetaldehyde |
| Chemidplus:0000075070 |
| EPA/NOAA CAMEO:hazardous materials |
| RTECS:75-07-0 |
References:
Other Information:
Potential Blenders and core components note
| For Odor |
| No odor group found for these |
ethyl (R)-2-methyl butyrate
FL/FR |
satinaldehyde
FL/FR |
|
carbitol
CS |
| alcoholic |
| alcoholic |
3- hexanol
FL/FR |
| aldehydic |
octanal (aldehyde C-8)
FL/FR |
iso valeraldehyde
FL/FR |
| animal |
methyl (E)-2-octenoate
FL/FR |
| balsamic |
iso amyl benzoate
FL/FR |
hexyl benzoate
FL/FR |
| brown |
sec- heptyl acetate
FL/FR |
| buttery |
butyl octanoate
FL/FR |
| chemical |
iso butyl formate
FL/FR |
propyl propionate
FL/FR |
| citrus |
citral
FL/FR |
dihydromyrcenol
FL/FR |
2- heptanol
FL/FR |
tetrahydrocitral
FL/FR |
| creamy |
3- heptyl dihydro-5-methyl-2(3H)-furanone
FL/FR |
| earthy |
methyl 3-hexenoate
FL/FR |
| ethereal |
acetal
FL/FR |
acetaldehyde dimethyl acetal
FL/FR |
iso amyl acetoacetate
FL/FR |
iso butyl alcohol
FL/FR |
cyclohexyl formate
FL/FR |
decyl propionate
FL/FR |
ethyl acetate
FL/FR |
ethyl formate
FL/FR |
ethyl pyruvate
FL/FR |
1- hexen-3-ol
FL/FR |
methyl acetate
FL/FR |
methyl ethyl ketone
FL/FR |
(E)- methyl tiglate
FL/FR |
2- methyl valeraldehyde
FL/FR |
3- pentanone
FL/FR |
iso propyl acetate
FL/FR |
propyl formate
FL/FR |
iso propyl formate
FL/FR |
propyl valerate
FL/FR |
iso valeraldehyde propylene glycol acetal
FL/FR |
| fatty |
3- decen-2-one
FL/FR |
(E,Z)-2,6- dodecadienal
FL/FR |
ethyl undecylenate
FL/FR |
methyl (E)-2-hexenoate
FL/FR |
methyl 2-hexenoate
FL/FR |
5- methyl-5-hexen-2-one
FL/FR |
| floral |
alpha- amyl cinnamaldehyde diethyl acetal
FR |
boronia absolute
FL/FR |
boronia absolute replacer
FL/FR |
cilantro herb oil egypt
FL/FR |
citronellol
FL/FR |
citronellyl acetate
FL/FR |
citronellyl formate
FL/FR |
cuminyl acetaldehyde
FL/FR |
beta- damascenone
FL/FR |
dihydrocarvyl acetate
FL/FR |
(±)-2,3- dihydrofarnesol
FL/FR |
geranyl acetone
FL/FR |
(E)- geranyl acetone
FL/FR |
geranyl formate
FL/FR |
geranyl isobutyrate
FL/FR |
hexyl lactate
FL/FR |
hexyl nonanoate
FL/FR |
beta- ionone
FL/FR |
jasminum sambac flower oil CO2 extract
FL/FR |
iso jasmone
FL/FR |
(Z)- jasmone
FL/FR |
iso jasmone
FL/FR |
lilac pentanol
FL/FR |
para- methyl benzyl acetate
FL/FR |
(Z)- methyl epi-jasmonate
FL/FR |
methyl jasmonate
FL/FR |
nerol
FL/FR |
neryl formate
FL/FR |
ocean propanal
FL/FR |
papaya isobutyrate
FL/FR |
clementine petitgrain oil
FL/FR |
phenethyl acetate
FL/FR |
2- phenyl propionaldehyde dimethyl acetal
FL/FR |
styralyl propionate
FL/FR |
| fruity |
acetaldehyde diisoamyl acetal
FL/FR |
allyl 2-ethyl butyrate
FL/FR |
allyl butyrate
FL/FR |
amyl acetate
FL/FR |
iso amyl butyrate
FL/FR |
amyl formate
FL/FR |
amyl heptanoate
FL/FR |
iso amyl hexanoate
FL/FR |
iso amyl isobutyrate
FL/FR |
iso amyl isovalerate
FL/FR |
benzyl methyl ether
FL/FR |
berry pentadienoate
FL/FR |
bisabolene
FL/FR |
butyl 2-decenoate
FL/FR |
iso butyl acetate
FL/FR |
butyl butyrate
FL/FR |
butyl hexanoate
FL/FR |
iso butyl isovalerate
FL/FR |
iso butyl octanoate
FL/FR |
iso butyl propionate
FL/FR |
cherry pentenoate
FL/FR |
cinnamyl hexanoate
FL/FR |
citronellyl isobutyrate
FL/FR |
2- cyclopentyl cyclopentanone
FL/FR |
(E)-beta- damascone
FL/FR |
(Z)-beta- damascone
FL/FR |
(E)-alpha- damascone
FL/FR |
diethyl malonate
FL/FR |
dimethyl succinate
FL/FR |
ethyl (E)-3-hexenoate
FL/FR |
ethyl 2-ethyl acetoacetate
FL/FR |
ethyl 2-hexenoate
FL/FR |
ethyl 2-octenoate
FL/FR |
ethyl 3-hexenoate
FL/FR |
ethyl acetoacetate
FL/FR |
ethyl bicyclo(2.2.1)-5-heptene-2-carboxylate
FL/FR |
2- ethyl butyl acetate
FL/FR |
ethyl isobutyrate
FL/FR |
ethyl levulinate
FL/FR |
ethyl methyl-para-tolyl glycidate
FL/FR |
ethyl propionate
FL/FR |
(E,E)- ethyl sorbate
FL/FR |
(E)- ethyl tiglate
FL/FR |
geranyl butyrate
FL/FR |
geranyl ethyl ether
FL/FR |
geranyl isovalerate
FL/FR |
grape butyrate
FL/FR |
heptyl butyrate
FL/FR |
2- heptyl butyrate
FL/FR |
heptyl isobutyrate
FL/FR |
hexanal propylene glycol acetal
FL/FR |
2- hexen-1-ol
FL/FR |
(E)-3- hexen-1-yl acetate
FL/FR |
(Z)-3- hexen-1-yl anthranilate
FL/FR |
(Z)-3- hexen-1-yl isobutyrate
FL/FR |
hexyl (E)-tiglate
FL/FR |
hexyl acetate
FL/FR |
hexyl isovalerate
FL/FR |
hexyl propionate
FL/FR |
hexyl valerate
FL/FR |
malus sylvestris fruit oil CO2 extract
FL/FR |
methyl 2-methyl butyrate
FL/FR |
methyl 3-nonenoate
FL/FR |
methyl dimethyl anthranilate
FL/FR |
methyl heptanoate
FL/FR |
methyl hexanoate
FL/FR |
methyl isobutyrate
FL/FR |
methyl octadienoate
FL/FR |
methyl propionate
FL/FR |
methyl valerate
FL/FR |
3- methyl-2-butenal
FL/FR |
neryl propionate
FL/FR |
2- nonanone
FL/FR |
octen-1-yl cyclopentanone
FL/FR |
(Z)-3- octen-1-yl propionate
FL/FR |
octyl butyrate
FL/FR |
2- pentanone
FL/FR |
2- pentyl furan
FL/FR |
3- phenyl propyl hexanoate
FL/FR |
2- phenyl propyl tetrahydrofuran
FL/FR |
4- phenyl-2-butyl acetate
FL/FR |
pineapple pentenoate
FL/FR |
prenol
FL/FR |
prenyl hexanoate
FL/FR |
iso propenyl acetate
FL/FR |
iso propyl 2-methyl butyrate
FL/FR |
propyl acetate
FL/FR |
iso propyl butyrate
FL/FR |
iso propyl propionate
FL/FR |
sorbyl butyrate
FL/FR |
(E,E)- sorbyl butyrate
FL/FR |
strawberry furanone butyrate
FL/FR |
tetrahydrofurfuryl acetate
FL/FR |
tetrahydrofurfuryl butyrate
FL/FR |
tropical thiazole
FL/FR |
tropical trithiane
FL/FR |
(E)-2- undecenal
FL/FR |
vanilla carboxylate
FL/FR |
| green |
acetaldehyde benzyl 2-methoxyethyl acetal
FL/FR |
actinidia chinensis fruit extract
FL/FR |
iso amyl formate
FL/FR |
butyl heptanoate
FL/FR |
green cognac oil
FL/FR |
black currant bud absolute replacer
FL/FR |
iso cyclocitral (IFF)
FL/FR |
alpha- decalactone
FL/FR |
ethyl (E)-2-hexenoate
FL/FR |
ethyl (E)-4-decenoate
FL/FR |
green note propionate
FL/FR |
heptanal (aldehyde C-7)
FL/FR |
hexanal (aldehyde C-6)
FL/FR |
(E)-3- hexen-1-ol
FL/FR |
(Z)-3- hexen-1-yl (E)-2-hexenoate
FL/FR |
(Z)-3- hexen-1-yl (Z)-3-hexenoate
FL/FR |
(Z)-3- hexen-1-yl 2-methyl butyrate
FL/FR |
(Z)-3- hexen-1-yl acetate
FL/FR |
(E)-2- hexen-1-yl acetate
FL/FR |
(Z)-3- hexen-1-yl benzoate
FL/FR |
(E)-2- hexen-1-yl butyrate
FL/FR |
(Z)-3- hexen-1-yl hexanoate
FL/FR |
(Z)-3- hexen-1-yl isovalerate
FL/FR |
(Z)-3- hexen-1-yl octanoate
FL/FR |
(E)-2- hexen-1-yl propionate
FL/FR |
(E)-2- hexen-1-yl valerate
FL/FR |
(Z)-3- hexen-1-yl valerate
FL/FR |
(E)-2- hexenal propylene glycol acetal
FL/FR |
3- hexenyl 2-methyl butyrate
FL/FR |
3- hexenyl acetate
FL/FR |
hexyl hexanoate
FL/FR |
hexyl isobutyrate
FL/FR |
hexyl octanoate
FL/FR |
3,5- ivy carbaldehyde
FL/FR |
2,4- ivy carbaldehyde
FL/FR |
3,6- ivy carbaldehyde
FL/FR |
ivy carbaldehyde
FL/FR |
manzanate (Givaudan)
FL/FR |
methyl (E)-3-hexenoate
FL/FR |
methyl octine carbonate
FL/FR |
neryl butyrate
FL/FR |
(E)-2- octen-1-yl acetate
FL/FR |
(Z)-5- octen-1-yl propionate
FL/FR |
3- octyl formate
FL/FR |
olive oil absolute
FL/FR |
(Z)-2- penten-1-ol
FL/FR |
(E)-2- pentenal
FL/FR |
phenoxyethyl isobutyrate
FL/FR |
1- phenyl-2-pentanol
FL/FR |
propylene acetal
FL/FR |
sorbyl isobutyrate
FL/FR |
(E,E)- sorbyl isobutyrate
FL/FR |
terpinyl propionate
FL/FR |
thiogeraniol
FL/FR |
tiglaldehyde
FL/FR |
| herbal |
hexanol
FL/FR |
(1S,5R)- myrtenyl acetate
FL/FR |
2- pentyl acetate
FL/FR |
rue oil
FL/FR |
rue oil cuba
FL/FR |
tagete oil india
FL/FR |
tagete oil south africa
FL/FR |
viridiflorol
FL/FR |
| melon |
2- octenyl acetate
FL/FR |
| minty |
carvyl acetate
FL/FR |
| mushroom |
1- octen-3-yl butyrate
FL/FR |
| phenolic |
anisole
FL/FR |
| rummy |
rum extract
FL/FR |
| soapy |
benzyl laurate
FL/FR |
| spicy |
cinnamyl propionate
FL/FR |
cumin seed oil
FL/FR |
| sulfurous |
4- methyl 4-mercaptopentan-2-one 1% solution
FL/FR |
| terpenic |
cassis bud oil
FL/FR |
| tropical |
psidium guajava fruit extract
FL/FR |
| waxy |
decanal diethyl acetal
FL/FR |
(E)- methyl geranate
FL/FR |
methyl octanoate
FL/FR |
2- nonanol
FL/FR |
octyl 2-methyl butyrate
FL/FR |
| winey |
methyl 3-acetoxyoctanoate
FL/FR |
| For Flavor |
| No flavor group found for these |
acetaldehyde 1,3-octane diol acetal
FL |
acetaldehyde benzyl 2-methoxyethyl acetal
FL/FR |
acetaldehyde diisoamyl acetal
FL/FR |
acetyl acetaldehyde dimethyl acetal
FL |
actinidia chinensis fruit juice
FL |
allyl levulinate
FL |
allyl tiglate
FL |
boronia absolute replacer
FL/FR |
butyl methyl ketone
FL |
iso butyl octanoate
FL/FR |
butyl octanoate
FL/FR |
cinnamyl hexanoate
FL/FR |
2- cyclopentyl cyclopentanone
FL/FR |
alpha- decalactone
FL/FR |
decyl propionate
FL/FR |
diethyl sulfide
FL |
2,5- diethyl-4-propyl thiazole
FL |
epoxy-2-decenal
FL |
ethanol
FL |
ethyl (R)-2-methyl butyrate
FL/FR |
ethyl 2-(methyl thio) acetate
FL |
ethyl 2-hexenoate
FL/FR |
ethyl bicyclo(2.2.1)-5-heptene-2-carboxylate
FL/FR |
geranyl ethyl ether
FL/FR |
2- heptenoic acid
FL |
2- heptyl butyrate
FL/FR |
2- hexenal
FL |
(E)-3- hexenal
FL |
2- hexenal diethyl acetal
FL |
(E)-2- hexenal propylene glycol acetal
FL/FR |
3- hexenyl acetate
FL/FR |
hexyl (E)-2-hexenoate
FL |
hexyl nonanoate
FL/FR |
hexyl propionate
FL/FR |
hexyl valerate
FL/FR |
3,5- ivy carbaldehyde
FL/FR |
ivy carbaldehyde
FL/FR |
malus sylvestris fruit oil CO2 extract
FL/FR |
methyl (E)-2-hexenoate
FL/FR |
methyl 2-hexenoate
FL/FR |
methyl 3-acetoxyoctanoate
FL/FR |
methyl 3-hydroxybutyrate
FL |
4- methyl 4-mercaptopentan-2-one 1% solution
FL/FR |
methyl dimethyl anthranilate
FL/FR |
(E)- methyl geranate
FL/FR |
methyl octadienoate
FL/FR |
S-( methyl thio) hexanoate
FL |
(E)- methyl tiglate
FL/FR |
2- methyl-3-heptanone
FL |
(E,E)-3,5- octadien-2-one
FL |
3- octyl butyrate
FL |
3- pentanone
FL/FR |
4- phenyl-2-butyl acetate
FL/FR |
prenyl hexanoate
FL/FR |
propyl valerate
FL/FR |
propylene acetal
FL/FR |
pyrazinyl methyl sulfide
FL |
(E,E)- sorbyl butyrate
FL/FR |
(E,E)- sorbyl isobutyrate
FL/FR |
tetrahydrocitral
FL/FR |
viridiflorol
FL/FR |
|
sorbyl isobutyrate
FL/FR |
| alcoholic |
| alcoholic |
3- hexanol
FL/FR |
| aldehydic |
octanal (aldehyde C-8)
FL/FR |
| alliaceous |
tropical thiazole
FL/FR |
| apple |
green apple concentrate
FL |
| aromatic |
anisole
FL/FR |
| berry |
heptyl isobutyrate
FL/FR |
| brown |
tetrahydrofurfuryl acetate
FL/FR |
| caramellic |
pyruvaldehyde
FL |
| cheesy |
2- nonanone
FL/FR |
| chemical |
2,5- dimethyl furan
FL |
methyl ethyl ketone
FL/FR |
| citrus |
bisabolene
FL/FR |
citral
FL/FR |
nerol
FL/FR |
clementine petitgrain oil
FL/FR |
styralyl propionate
FL/FR |
| cocoa |
2- methyl furan
FL |
| coconut |
(R)- massoia lactone
FL |
| cooling |
manzanate (Givaudan)
FL/FR |
| creamy |
2,4- heptadienal
FL |
massoia lactone
FL |
| dairy |
2- pentyl acetate
FL/FR |
| earthy |
1- hexen-3-yl acetate
FL |
| estery |
ethyl acetoacetate
FL/FR |
propyl acetate
FL/FR |
| ethereal |
acetaldehyde dimethyl acetal
FL/FR |
allyl 2-ethyl butyrate
FL/FR |
benzyl laurate
FL/FR |
iso butyl alcohol
FL/FR |
ethyl acetate
FL/FR |
ethyl formate
FL/FR |
ethyl isobutyrate
FL/FR |
4- hexen-3-one
FL |
methyl acetate
FL/FR |
methyl isobutyrate
FL/FR |
5- methyl-5-hexen-2-one
FL/FR |
iso propenyl acetate
FL/FR |
iso propyl acetate
FL/FR |
| fatty |
(E,E)-2,4- decadienal
FL |
ethyl (E)-4-decenoate
FL/FR |
ethyl undecylenate
FL/FR |
sec- heptyl acetate
FL/FR |
(Z)-3- hexen-1-yl benzoate
FL/FR |
2- phenyl propyl tetrahydrofuran
FL/FR |
| floral |
cinnamyl propionate
FL/FR |
citronellol
FL/FR |
citronellyl acetate
FL/FR |
dihydrocarvyl acetate
FL/FR |
(±)-2,3- dihydrofarnesol
FL/FR |
geranyl acetone
FL/FR |
(E)- geranyl acetone
FL/FR |
geranyl isobutyrate
FL/FR |
(Z)-3- hexen-1-yl anthranilate
FL/FR |
jasminum sambac flower oil CO2 extract
FL/FR |
(Z)- methyl epi-jasmonate
FL/FR |
methyl jasmonate
FL/FR |
ocean propanal
FL/FR |
satinaldehyde
FL/FR |
| fruity |
amyl acetate
FL/FR |
iso amyl acetoacetate
FL/FR |
iso amyl benzoate
FL/FR |
amyl formate
FL/FR |
amyl heptanoate
FL/FR |
iso amyl hexanoate
FL/FR |
iso amyl isobutyrate
FL/FR |
green apple flavor
FL |
apple grape flavor
FL |
benzyl methyl ether
FL/FR |
berry pentadienoate
FL/FR |
boronia absolute
FL/FR |
butyl 2-decenoate
FL/FR |
iso butyl acetate
FL/FR |
butyl butyrate
FL/FR |
butyl heptanoate
FL/FR |
butyl hexanoate
FL/FR |
iso butyl propionate
FL/FR |
cassis bud oil
FL/FR |
cherry pentenoate
FL/FR |
citronellyl formate
FL/FR |
citronellyl isobutyrate
FL/FR |
black currant bud absolute replacer
FL/FR |
(Z)-beta- damascone
FL/FR |
(E)-beta- damascone
FL/FR |
(E)-alpha- damascone
FL/FR |
diethyl malonate
FL/FR |
dimethyl succinate
FL/FR |
2,6- dipropyl-5,6-dihydro-2H-thiopyran-3-carboxaldehyde
FL |
ethyl (E)-2-hexenoate
FL/FR |
ethyl (E)-2-octenoate
FL |
ethyl (E)-3-hexenoate
FL/FR |
ethyl 2-ethyl acetoacetate
FL/FR |
ethyl 2-octenoate
FL/FR |
ethyl 3-hexenoate
FL/FR |
2- ethyl butyl acetate
FL/FR |
ethyl levulinate
FL/FR |
ethyl methyl-para-tolyl glycidate
FL/FR |
ethyl propionate
FL/FR |
(E,E)- ethyl sorbate
FL/FR |
(E)- ethyl tiglate
FL/FR |
furfuryl propionate
FL |
2- furyl pentyl ketone
FL |
geranyl butyrate
FL/FR |
2- heptanol
FL/FR |
3- heptyl dihydro-5-methyl-2(3H)-furanone
FL/FR |
hexanal propylene glycol acetal
FL/FR |
2- hexen-1-ol
FL/FR |
(Z)-3- hexen-1-yl (E)-2-hexenoate
FL/FR |
(E)-3- hexen-1-yl acetate
FL/FR |
(Z)-3- hexen-1-yl isobutyrate
FL/FR |
hexyl acetate
FL/FR |
hexyl hexanoate
FL/FR |
hexyl lactate
FL/FR |
kiwi distillates
FL |
lilac pentanol
FL/FR |
methyl (E)-2-octenoate
FL/FR |
methyl 2-methyl butyrate
FL/FR |
methyl 3-hexenoate
FL/FR |
methyl 3-nonenoate
FL/FR |
2- methyl allyl butyrate
FL |
para- methyl benzyl acetate
FL/FR |
methyl heptanoate
FL/FR |
methyl hexanoate
FL/FR |
methyl propionate
FL/FR |
methyl valerate
FL/FR |
3- methyl-2-butenal
FL/FR |
neryl formate
FL/FR |
(Z)-3- nonen-1-yl acetate
FL |
(Z)-5- octen-1-yl acetate
FL |
octen-1-yl cyclopentanone
FL/FR |
(Z)-3- octen-1-yl propionate
FL/FR |
2- pentanone
FL/FR |
2- phenyl propionaldehyde dimethyl acetal
FL/FR |
3- phenyl propyl hexanoate
FL/FR |
1- phenyl-2-pentanol
FL/FR |
pineapple pentenoate
FL/FR |
prenol
FL/FR |
iso propyl 2-methyl butyrate
FL/FR |
iso propyl butyrate
FL/FR |
propyl formate
FL/FR |
iso propyl formate
FL/FR |
iso propyl propionate
FL/FR |
sorbyl butyrate
FL/FR |
strawberry furanone butyrate
FL/FR |
tagete oil south africa
FL/FR |
tetrahydrofurfuryl butyrate
FL/FR |
tiglaldehyde
FL/FR |
tropical trithiane
FL/FR |
iso valeraldehyde
FL/FR |
iso valeraldehyde propylene glycol acetal
FL/FR |
vanilla carboxylate
FL/FR |
| fusel |
green cognac oil
FL/FR |
| green |
actinidia chinensis fruit extract
FL/FR |
alfalfa distillates
FL |
allyl butyrate
FL/FR |
iso amyl formate
FL/FR |
iso amyl isovalerate
FL/FR |
iso butyl isovalerate
FL/FR |
cuminyl acetaldehyde
FL/FR |
iso cyclocitral (IFF)
FL/FR |
cyclohexyl formate
FL/FR |
3- decen-2-one
FL/FR |
dihydromyrcenol
FL/FR |
3,4- dimethoxystyrene
FL |
(E,Z)-2,6- dodecadienal
FL/FR |
2- ethyl butyraldehyde
FL |
geranyl formate
FL/FR |
geranyl isovalerate
FL/FR |
grape butyrate
FL/FR |
green note propionate
FL/FR |
heptanal (aldehyde C-7)
FL/FR |
heptanal 2,3-butane diol acetal
FL |
heptyl butyrate
FL/FR |
(E,E)-2,4- hexadienal
FL |
2,4- hexadienal
FL |
hexanal (aldehyde C-6)
FL/FR |
hexanol
FL/FR |
(E)-3- hexen-1-ol
FL/FR |
(Z)-3- hexen-1-yl (Z)-3-hexenoate
FL/FR |
(Z)-3- hexen-1-yl 2-methyl butyrate
FL/FR |
(E)-2- hexen-1-yl acetate
FL/FR |
(Z)-3- hexen-1-yl acetate
FL/FR |
(E)-2- hexen-1-yl butyrate
FL/FR |
(Z)-3- hexen-1-yl hexanoate
FL/FR |
(Z)-3- hexen-1-yl isovalerate
FL/FR |
(Z)-3- hexen-1-yl octanoate
FL/FR |
(E)-2- hexen-1-yl propionate
FL/FR |
(Z)-3- hexen-1-yl valerate
FL/FR |
(E)-2- hexen-1-yl valerate
FL/FR |
1- hexen-3-ol
FL/FR |
3- hexenyl 2-methyl butyrate
FL/FR |
hexyl (E)-tiglate
FL/FR |
hexyl benzoate
FL/FR |
hexyl isobutyrate
FL/FR |
hexyl isovalerate
FL/FR |
hexyl octanoate
FL/FR |
2,4- ivy carbaldehyde
FL/FR |
3,6- ivy carbaldehyde
FL/FR |
iso jasmone
FL/FR |
iso jasmone
FL/FR |
methyl (E)-3-hexenoate
FL/FR |
methyl 2-undecynoate
FL |
methyl octanoate
FL/FR |
methyl octine carbonate
FL/FR |
3-(5- methyl-2-furyl) butanal
FL |
4- methyl-2-pentenal
FL |
neryl butyrate
FL/FR |
neryl propionate
FL/FR |
(E,E)-2,4- octadienal
FL |
2,4- octadienal
FL |
(E)-2- octen-1-yl acetate
FL/FR |
(Z)-5- octen-1-yl propionate
FL/FR |
2- octenyl acetate
FL/FR |
papaya isobutyrate
FL/FR |
(Z)-2- penten-1-ol
FL/FR |
(E)-2- pentenal
FL/FR |
2- pentyl furan
FL/FR |
phenoxyethyl isobutyrate
FL/FR |
terpinyl propionate
FL/FR |
thiogeraniol
FL/FR |
| herbal |
cilantro flavor
FL |
cilantro herb oil egypt
FL/FR |
rue oil
FL/FR |
rue oil cuba
FL/FR |
tagete oil india
FL/FR |
| honey |
phenethyl acetate
FL/FR |
| milky |
6-(5(6)- decenoyl oxy) decanoic acid
FL |
| minty |
carvyl acetate
FL/FR |
| mushroom |
1- octen-3-yl butyrate
FL/FR |
| nutty |
acetal
FL/FR |
| oily |
olive oil absolute
FL/FR |
| rummy |
iso butyl formate
FL/FR |
ethyl pyruvate
FL/FR |
rum extract
FL/FR |
rum flavor
FL |
| sour |
3- methyl valeric acid
FL |
| spicy |
cumin flavor
FL |
cumin seed oil
FL/FR |
| tomato |
tomato distillates
FL |
tomato flavor
FL |
| tropical |
guava distillates
FL |
propyl propionate
FL/FR |
psidium guajava fruit
FL |
psidium guajava fruit extract
FL/FR |
| vegetable |
2- methyl valeraldehyde
FL/FR |
| waxy |
iso amyl butyrate
FL/FR |
decanal diethyl acetal
FL/FR |
2- nonanol
FL/FR |
octyl 2-methyl butyrate
FL/FR |
octyl butyrate
FL/FR |
3- octyl formate
FL/FR |
(E)-2- undecenal
FL/FR |
| woody |
beta- damascenone
FL/FR |
beta- ionone
FL/FR |
(Z)- jasmone
FL/FR |
(1S,5R)- myrtenyl acetate
FL/FR |
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
| nat. | acetaldehyde | | | acetaldehyde (natural) | | | acetaldehyde 10% in ethanol natural | | | acetaldehyde 10% in ETOH natural | | | acetaldehyde 100% natural | | | acetaldehyde 20% (natural) | | | acetaldehyde 50% alcohol natural | | | acetaldehyde 50% (natural) | | | acetaldehyde 50% + ethanol 50% | | | acetaldehyde 50% + orange terpenes 50% | | | acetaldehyde 50% + triacetin 50% | | | acetaldehyde 50% + water 50% | | | acetaldehyde 50% ETOH synthetic | | | acetaldehyde 50% in 5 fold orange oil synthetic | | | acetaldehyde 50% in benzyl benzoate synthetic | | | acetaldehyde 50% in D'limonene natural | | | acetaldehyde 50% in ethanol | | | acetaldehyde 50% in ethanol natural | | | acetaldehyde 50% in ethanol synthetic | | | acetaldehyde 50% in ETOH natural | | | acetaldehyde 50% in orange oil 5-fold natural | | | acetaldehyde 50% in orange oil natural | | | acetaldehyde 50% in orange oil synthetic | | | acetaldehyde 50% in orange terpenes natural | | | acetaldehyde 50% PG natural | | | acetaldehyde natural | | | acetaldehyde natural 50% in orange terpenes | | | acetaldehyde natural 50% in ethanol | | | acetaldehyde natural 50% in water | | | acetaldehyde solution | | | acetaldehyde synthetic | | | acetic aldehyde | | | acetic ethanol | | | aceticaldehyde | | | acetyl aldehyde | | | aldefresh (Elan) | | | ethaldehyde | | | ethanal | | | ethanone | | | ethyl aldehyde | | | ethylaldehyde | | | INCI acetaldehyde | | | NCI-C56326 | | | octowy aldehyd |
Articles:
| Info:Volatile Flavor Components in Bogyojosaeng and Suhong Cultivars of Strawberry (Fragaria ananassa Duch.) |
| PubMed:Characterization of aroma compounds of Chinese famous liquors by gas chromatography-mass spectrometry and flash GC electronic-nose. |
| PubMed:Characterization of the key aroma compounds in two bavarian wheat beers by means of the sensomics approach. |
| PubMed:Relating sensory and chemical properties of sour cream to consumer acceptance. |
| PubMed:Development of industrial brewing yeast with low acetaldehyde production and improved flavor stability. |
| PubMed:Multiple automated headspace in-tube extraction for the accurate analysis of relevant wine aroma compounds and for the estimation of their relative liquid-gas transfer rates. |
| PubMed:Characterization of the major odor-active compounds in Thai durian ( Durio zibethinus L. 'Monthong') by aroma extract dilution analysis and headspace gas chromatography-olfactometry. |
| PubMed:In vitro and in vivo flavor release from intact and fresh-cut apple in relation with genetic, textural, and physicochemical parameters. |
| PubMed:Rapid tomato volatile profiling by using proton-transfer reaction mass spectrometry (PTR-MS). |
| PubMed:Diacetyl levels and volatile profiles of commercial starter distillates and selected dairy foods. |
| PubMed:Automated and quantitative headspace in-tube extraction for the accurate determination of highly volatile compounds from wines and beers. |
| PubMed:Main odorants in Jura flor-sherry wines. Relative contributions of sotolon, abhexon, and theaspirane-derived compounds. |
| PubMed:Elucidating the roles of ethanol fermentation metabolism in causing off-flavors in mandarins. |
| PubMed:Wine flavor and aroma. |
| PubMed:Reconstitution of the flavor signature of Dornfelder red wine on the basis of the natural concentrations of its key aroma and taste compounds. |
| PubMed:Monitoring of cocoa volatiles produced during roasting by selected ion flow tube-mass spectrometry (SIFT-MS). |
| PubMed:Beer volatile analysis: optimization of HS/SPME coupled to GC/MS/FID. |
| PubMed:Thermal generation of 3-amino-4,5-dimethylfuran-2(5H)-one, the postulated precursor of sotolone, from amino acid model systems containing glyoxylic and pyruvic acids. |
| PubMed:Volatile flavor compounds in yogurt: a review. |
| PubMed:Proton transfer reaction time-of-flight mass spectrometry monitoring of the evolution of volatile compounds during lactic acid fermentation of milk. |
| PubMed:Identification of a sotolon pathway in dry white wines. |
| PubMed:Chemical and biochemical study of industrially produced San Simón da Costa smoked semi-hard cow's milk cheeses: Effects of storage under vacuum and different modified atmospheres. |
| PubMed:Comparison of two methods to explore consumer preferences for cottage cheese. |
| PubMed:A liquid chromatographic method optimization for the assessment of low and high molar mass carbonyl compounds in wines. |
| PubMed:Decoding the key aroma compounds of a Hungarian-type salami by molecular sensory science approaches. |
| PubMed:Characterization of the key aroma compounds in pink guava (Psidium guajava L.) by means of aroma re-engineering experiments and omission tests. |
| PubMed:Evolution of selected volatiles in chitosan-coated strawberries ( Fragaria x ananassa ) during refrigerated storage. |
| PubMed:Effect of mesophilic lactobacilli and enterococci adjunct cultures on the final characteristics of a microfiltered milk Swiss-type cheese. |
| PubMed:Net effect of wort osmotic pressure on fermentation course, yeast vitality, beer flavor, and haze. |
| PubMed:Fatty acid effect on hydroxypropyl methylcellulose-beeswax edible film properties and postharvest quality of coated 'Ortanique' mandarins. |
| PubMed:Analysis of selected carbonyl oxidation products in wine by liquid chromatography with diode array detection. |
| PubMed:Characterization of kinetic parameters and the formation of volatile compounds during the tequila fermentation by wild yeasts isolated from agave juice. |
| PubMed:The chemical characterization of the aroma of dessert and sparkling white wines (Pedro Ximénez, Fino, Sauternes, and Cava) by gas chromatography-olfactometry and chemical quantitative analysis. |
| PubMed:[Gene regulation to lactic acid bacteria for increasing production of flavor metabolite]. |
| PubMed:Kluyveromyces lactis but not Pichia fermentans used as adjunct culture modifies the olfactory profiles of Cantalet cheese. |
| PubMed:Characterization of the key aroma compounds in apricots (Prunus armeniaca) by application of the molecular sensory science concept. |
| PubMed:Influence of starter culture on flavor and headspace volatile profiles of fermented whey and whey produced from fermented milk. |
| PubMed:Identification based on quantitative measurements and aroma recombination of the character impact odorants in a Bavarian Pilsner-type beer. |
| PubMed:Feeding encapsulated ground full-fat soybeans to increase polyunsaturated fat concentrations and effects on flavor volatiles in fresh lamb. |
| PubMed:Role of pulp in flavor release and sensory perception in orange juice. |
| PubMed:Effect of irradiation on the quality of turkey ham during storage. |
| PubMed:The effect of SO2 on the production of ethanol, acetaldehyde, organic acids, and flavor volatiles during industrial cider fermentation. |
| PubMed:Gas chromatography-olfactometry (GC-O) and proton transfer reaction-mass spectrometry (PTR-MS) analysis of the flavor profile of grana padano, parmigiano reggiano, and grana trentino cheeses. |
| PubMed:Quality characteristics of irradiated ready-to-eat breast rolls from turkeys fed conjugated linoleic acid. |
| PubMed:Sensory and chemical changes in tomato sauces during storage. |
| PubMed:Heterocyclic acetals from glycerol and acetaldehyde in Port wines: evolution with aging. |
| PubMed:Identification of malodorous, a wild species allele affecting tomato aroma that was aelected against during domestication. |
| PubMed:Simple and rapid analysis for quantitation of the most important volatile flavor compounds in yogurt by headspace gas chromatography-mass spectrometry. |
| PubMed:Flavor threshold for acetaldehyde in milk, chocolate milk, and spring water using solid phase microextraction gas chromatography for quantification. |
| PubMed:Evaluation of key aroma compounds in hand-squeezed grapefruit juice (Citrus paradisi Macfayden) by quantitation and flavor reconstitution experiments. |
| PubMed:Acetaldehyde metabolism by wine lactic acid bacteria. |
| PubMed:Formation of volatile compounds during heating of spice paprika (Capsicum annuum) powder. |
| PubMed:Aroma comparisons of traditional and mild yogurts: headspace gas chromatography quantification of volatiles and origin of alpha-diketones. |
| PubMed:Organic acids and volatile flavor components evolved during refrigerated storage of kefir. |
| PubMed:Sensory investigation of yogurt flavor perception: mutual influence of volatiles and acidity. |
| PubMed:Sensory study on the character impact odorants of roasted arabica coffee. |
| PubMed:Manufacture of nonfat yogurt from a high milk protein powder. |
| PubMed:Changes in chemical composition and sensory qualities of peanut milk fermented with lactic acid bacteria. |
| PubMed:Identification of the volatile compounds produced in sterile fish muscle (Sebastes melanops) by Pseudomonas fragi. |
| PubMed:Flavoring exposure in food manufacturing. |
| PubMed:Secretion expression of SOD1 and its overlapping function with GSH in brewing yeast strain for better flavor and anti-aging ability. |
| PubMed:Characterization of volatile aroma compounds in different brewing barley cultivars. |
| PubMed:Characterization of the key aroma compounds in two bavarian wheat beers by means of the sensomics approach. |
| PubMed:Relating sensory and chemical properties of sour cream to consumer acceptance. |
| PubMed:In vitro and in vivo flavor release from intact and fresh-cut apple in relation with genetic, textural, and physicochemical parameters. |
| PubMed:Integrated expression of the α-amylase, dextranase and glutathione gene in an industrial brewer's yeast strain. |
| PubMed:Beer volatile analysis: optimization of HS/SPME coupled to GC/MS/FID. |
| PubMed:Effect of antifungal hydroxypropyl methylcellulose-lipid edible composite coatings on Penicillium decay development and postharvest quality of cold-stored "Ortanique" mandarins. |
| PubMed:Thermal generation of 3-amino-4,5-dimethylfuran-2(5H)-one, the postulated precursor of sotolone, from amino acid model systems containing glyoxylic and pyruvic acids. |
| PubMed:Preharvest calcium sprays improve volatile emission at commercial harvest of 'Fuji Kiku-8' apples. |
| PubMed:Identification of a sotolon pathway in dry white wines. |
| PubMed:A liquid chromatographic method optimization for the assessment of low and high molar mass carbonyl compounds in wines. |
| PubMed:Decoding the key aroma compounds of a Hungarian-type salami by molecular sensory science approaches. |
| PubMed:Genome-scale model of Streptococcus thermophilus LMG18311 for metabolic comparison of lactic acid bacteria. |
| PubMed:Fatty acid effect on hydroxypropyl methylcellulose-beeswax edible film properties and postharvest quality of coated 'Ortanique' mandarins. |
| PubMed:Characterization of kinetic parameters and the formation of volatile compounds during the tequila fermentation by wild yeasts isolated from agave juice. |
| PubMed:Kluyveromyces lactis but not Pichia fermentans used as adjunct culture modifies the olfactory profiles of Cantalet cheese. |
| PubMed:Characterization of the key aroma compounds in apricots (Prunus armeniaca) by application of the molecular sensory science concept. |
| PubMed:Silylating reagents: a powerful tool for the construction of isosteric analogs of highly branched odorants. |
| PubMed:Chemical conversion of alpha-amino acids into alpha-keto acids by 4,5-epoxy-2-decenal. |
| PubMed:Tomato aromatic amino acid decarboxylases participate in synthesis of the flavor volatiles 2-phenylethanol and 2-phenylacetaldehyde. |
| PubMed:Influence of starter culture on flavor and headspace volatile profiles of fermented whey and whey produced from fermented milk. |
| PubMed:Identification based on quantitative measurements and aroma recombination of the character impact odorants in a Bavarian Pilsner-type beer. |
| PubMed:Toxicological evaluation of glycerin as a cigarette ingredient. |
| PubMed:The FEMA GRAS assessment of phenethyl alcohol, aldehyde, acid, and related acetals and esters used as flavor ingredients. |
| PubMed:Toxicologic evaluation of licorice extract as a cigarette ingredient. |
| PubMed:Characterization of aroma compounds responsible for the rosy/floral flavor in Cheddar cheese. |
| PubMed:Gas chromatography-olfactometry (GC-O) and proton transfer reaction-mass spectrometry (PTR-MS) analysis of the flavor profile of grana padano, parmigiano reggiano, and grana trentino cheeses. |
| PubMed:Quality characteristics of irradiated ready-to-eat breast rolls from turkeys fed conjugated linoleic acid. |
| PubMed:Simple and rapid analysis for quantitation of the most important volatile flavor compounds in yogurt by headspace gas chromatography-mass spectrometry. |
| PubMed:Evaluation of key aroma compounds in hand-squeezed grapefruit juice (Citrus paradisi Macfayden) by quantitation and flavor reconstitution experiments. |
| PubMed:Acetaldehyde metabolism by wine lactic acid bacteria. |
| PubMed:[Biosynthesis of congeners during alcohol fermentation]. |
| PubMed:Sensory study on the character impact odorants of roasted arabica coffee. |
| PubMed:Changes in chemical composition and sensory qualities of peanut milk fermented with lactic acid bacteria. |
| PubMed:Identification of the volatile compounds produced in sterile fish muscle (Sebastes melanops) by Pseudomonas fragi. |
| PubMed:[Flavor enhancement in rye bread by pre-baking]. |
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A colorless, flammable liquid used in the manufacture of acetic acid, perfumes, and flavors. it is also an intermediate in the metabolism of alcohol. it has a general narcotic action and also causes irritation of mucous membranes. large doses may cause death from respiratory paralysis. Flavouring agent and adjuvant used to impart orange, apple and butter flavours; component of food flavourings added to milk products, baked goods, fruit juices, candy, desserts and soft drinks [DFC]
Acetaldehyde occurs naturally in ripe fruit, coffee, and bread, and is produced by plants as part of their normal metabolism. [Wikipedia]
A colorless, flammable liquid used in the manufacture of acetic acid, perfumes, and flavors. It is also an intermediate in the metabolism of alcohol. It has a general narcotic action and also causes irritation of mucous membranes. Large doses may cause death from respiratory paralysis. [Pubchem]
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3D/inchi