acetaldehyde
ethylaldehyde
 
Notes:
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]
Synonyms   Articles   Notes   Search
    Flavor Demo Formulas
acetaldehyde (Click)
CAS Number: 75-07-0Picture of molecule
ECHA EINECS - REACH Pre-Reg: 200-836-8
FDA UNII: GO1N1ZPR3B
Nikkaji Web: J2.388D
Beilstein Number: 505984
MDL: MFCD00006991
CoE Number: 89
XlogP3-AA: -0.30 (est)
Molecular Weight: 44.05308000
Formula: C2 H4 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: cosmetic and flavor agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
JECFA Food Flavoring: 80  acetaldehyde
Flavis Number: 05.001 (Old)
DG SANTE Food Flavourings: 05.001  acetaldehyde
DG SANTE Food Contact Materials: acetaldehyde
FEMA Number: 2003  acetaldehyde
FDA Regulation:
FDA PART 177 -- INDIRECT FOOD ADDITIVES: POLYMERS
Subpart C--Substances for Use Only as Components of Articles Intended for Repeated Use
Sec. 177.2410 Phenolic resins in molded articles.


FDA PART 182 -- SUBSTANCES GENERALLY RECOGNIZED AS SAFE
Subpart A--General Provisions
Sec. 182.60 Synthetic flavoring substances and adjuvants.
Synonyms   Articles   Notes   Search   Top
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 mm/Hg @ 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)
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
Odor Type: ethereal
Odor Strength: high ,
recommend smelling in a 0.10 % solution or less
 pungent  ethereal  aldehydic  fruity  
Odor Description:
at 0.10 % in propylene glycol. 
pungent ethereal aldehydic fruity
 pungent  ethereal  fresh  fruity  musty  
Odor Description:
Pungent, etherial, fresh, lifting, penetrating, fruity and musty
Mosciano, Gerard P&F 22, No. 4, 75, (1997)
 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)
Substantivity: < 1 hour(s) at 100.00 %
  
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: masking agents
nail conditioning
Synonyms   Articles   Notes   Search   Top
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
Services
Axxence Aromatic
ACETALDEHYDE 98%, Natural
Kosher
Sustainability
Azelis
Acetaldehyde
Services
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 20% (NATURAL)
Frutarom
ACETALDEHYDE 50% (NATURAL)
Frutarom
ACETALDEHYDE 50%
Frutarom
ACETALDEHYDE
≥99.00%, NI, Kosher
Odor: Aldehydic, Apple, Green, Pungent
Use: Suggested Uses: Alcoholic Beverages, Apple, Cheese, Dairy Products, Hard Fruits, Soft Fruits
Hindustan Polyamides & Fibres
Acetaldehyde
Indenta Group
Acetaldehyde
Inoue Perfumery
ACETALDEHYDE
Jiangyin Healthway
Acetaldehyde
New functional food ingredients
Kunshan Sainty
Acetaldehyde, Natural
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 50% in Orange Aroma
Natural Advantage
Acetaldehyde Nat ex Orange, 10% in Orange Aroma
Natural Advantage
Acetaldehyde Nat, 10% in d-Limonene
Natural Advantage
Acetaldehyde Nat, 50% in OH
Natural Advantage
Acetaldehyde Nat, 50% in PG
O'Laughlin Industries
ACETALDEHYDE NATURAL 50% in ORANGE TERPENES
O'Laughlin Industries
ACETALDEHYDE NATURAL 50% in ETHANOL
O'Laughlin Industries
ACETALDEHYDE NATURAL 50% in WATER
Penta International
ACETALDEHYDE 10% IN ETHANOL NATURAL ,Kosher
Penta International
ACETALDEHYDE 100% NATURAL, Kosher
Penta International
ACETALDEHYDE 50% IN ETHANOL NATURAL, Kosher
Penta International
ACETALDEHYDE 50% IN ETHANOL SYNTHETIC, Kosher
Reincke & Fichtner
Acetaldehyde natural
Reincke & Fichtner
Acetaldehyde
Santa Cruz Biotechnology
For experimental / research use only.
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
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
Wujiang CIYUN Flavor & Fragrance
Acetaldehyde ≥99.0%, Natural
Wujiang CIYUN Flavor & Fragrance
Acetaldehyde solution 40%
Synonyms   Articles   Notes   Search   Top
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
 
Pictogramflame.jpghealth-hazard.jpgexclamation-mark.jpg
 
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.

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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 ppmaverage maximum ppm
baked goods: -12.00000
beverages(nonalcoholic): -3.90000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: 20.00000270.00000
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: --
Synonyms   Articles   Notes   Search   Top
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
NLM Hazardous Substances Data Bank: Search
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
Carcinogenic Potency Database: Search
EPA GENetic TOXicology: Search
Env. Mutagen Info. Center: Search
NLM Developmental and Reproductive Toxicity: 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
Synonyms   Articles   Notes   Search   Top
References:
 acetaldehyde
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 75-07-0
Pubchem (cid): 177
Pubchem (sid): 134970736
Flavornet: 75-07-0
Pherobase: View
Synonyms   Articles   Notes   Search   Top
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 Everything Added to Food in the United States (EAFUS): View
CHEBI: View
CHEMBL: View
UM BBD: Search
KEGG (GenomeNet): C00084
HMDB (The Human Metabolome Database): HMDB00990
FooDB: FDB008297
YMDB (Yeast Metabolome Database): YMDB01369
Export Tariff Code: 2912.12.0000
Haz-Map: View
Household Products: Search
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
RSC Learn Chemistry: View
Read: Under the conditions of intended use - New developments in the FEMA GRAS program and the safety assessment of flavor ingredients
Read: A GRAS assessment program for flavor ingredients
Read: Sensory testing for flavorings with modifying properties. Food Technology
Read: Criteria for the safety evaluation of flavoring substances
Read: A procedure for the safety evaluation of natural flavor complexes used as ingredients in food: essential oils
Read: FEMA Expert Panel: 30 Years of safety evaluation for the flavor industry
Read: Consumption ratio and food predominance of flavoring materials
Formulations/Preparations:
grades: commercially avail as 50% aq soln or 99% cp in small steel cylinders.acetaldehyde is avail in usa with following typical specifications: purity, 99.5% min; acidity (as acetic acid), 0.1% max to meet the requirements of the food chemical codex, acetaldehyde must pass an infrared identification test & meet the following specifications: purity, 99.0% min; acidity (as acetic acid) 0.1% max; non-volatile residue, 0.006% max .grade: technical 99%
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
 satinaldehydeFL/FR
3-hexanolFL/FR
aldehydic
 octanal (aldehyde C-8)FL/FR
isovaleraldehydeFL/FR
animal
 methyl (E)-2-octenoateFL/FR
balsamic
isoamyl benzoateFL/FR
brown
sec-heptyl acetateFL/FR
buttery
 butyl octanoateFL/FR
chemical
isobutyl formateFL/FR
 propyl propionateFL/FR
citrus
 citralFL/FR
 dihydromyrcenolFL/FR
2-heptanolFL/FR
 tetrahydrocitralFL/FR
creamy
3-heptyl dihydro-5-methyl-2(3H)-furanoneFL/FR
earthy
 methyl (E)-3-hexenoateFL/FR
 methyl 3-hexenoateFL/FR
ethereal
 acetalFL/FR
 acetaldehyde dimethyl acetalFL/FR
isoamyl acetoacetateFL/FR
isobutyl alcoholFL/FR
 cyclohexyl formateFL/FR
 decyl propionateFL/FR
 ethyl acetateFL/FR
 ethyl formateFL/FR
 ethyl nitrite 
 ethyl pyruvateFL/FR
1-hexen-3-olFL/FR
 methyl acetateFL/FR
 methyl ethyl ketoneFL/FR
(E)-methyl tiglateFL/FR
2-methyl valeraldehydeFL/FR
3-pentanoneFL/FR
isopropyl acetateFL/FR
isopropyl formateFL/FR
 propyl formateFL/FR
 propyl valerateFL/FR
isovaleraldehyde propylene glycol acetalFL/FR
3-decen-2-oneFL/FR
(E,Z)-2,6-dodecadienalFL/FR
 ethyl undecylenateFL/FR
 methyl (E)-2-hexenoateFL/FR
 methyl 2-hexenoateFL/FR
floral
alpha-amyl cinnamaldehyde diethyl acetalFR
 boronia absoluteFL/FR
 cilantro herb oil egyptFL/FR
 citronellolFL/FR
 citronellyl acetateFL/FR
 citronellyl formateFL/FR
 cuminyl acetaldehydeFL/FR
beta-damascenoneFL/FR
 dihydrocarvyl acetateFL/FR
(±)-2,3-dihydrofarnesolFL/FR
 geranyl acetoneFL/FR
(E)-geranyl acetoneFL/FR
 geranyl formateFL/FR
 geranyl isobutyrateFL/FR
 hexyl lactateFL/FR
 hexyl nonanoateFL/FR
beta-iononeFL/FR
(Z)-jasmoneFL/FR
isojasmoneFL/FR
isojasmoneFL/FR
 lilac pentanolFL/FR
para-methyl benzyl acetateFL/FR
(Z)-methyl epi-jasmonateFL/FR
 methyl jasmonateFL/FR
 nerolFL/FR
 neryl formateFL/FR
 ocean propanalFL/FR
 papaya isobutyrateFL/FR
clementine petitgrain oilFL/FR
 phenethyl acetateFL/FR
2-phenyl propionaldehyde dimethyl acetalFL/FR
 styralyl propionateFL/FR
fruity
 acetaldehyde diisoamyl acetalFL/FR
 allyl 2-ethyl butyrateFL/FR
 allyl butyrateFL/FR
 amyl acetateFL/FR
isoamyl butyrateFL/FR
 amyl formateFL/FR
 amyl heptanoateFL/FR
isoamyl hexanoateFL/FR
isoamyl isobutyrateFL/FR
isoamyl isovalerateFL/FR
 benzyl methyl etherFL/FR
 berry pentadienoateFL/FR
 bisaboleneFL/FR
 butyl 2-decenoateFL/FR
isobutyl acetateFL/FR
 butyl hexanoateFL/FR
isobutyl isovalerateFL/FR
isobutyl octanoateFL/FR
isobutyl propionateFL/FR
 cherry pentenoateFL/FR
 cinnamyl hexanoateFL/FR
 citronellyl isobutyrateFL/FR
2-cyclopentyl cyclopentanoneFL/FR
 diethyl malonateFL/FR
 dimethyl succinateFL/FR
 ethyl (E)-3-hexenoateFL/FR
 ethyl 2-hexenoateFL/FR
 ethyl 2-octenoateFL/FR
 ethyl 3-hexenoateFL/FR
 ethyl acetoacetateFL/FR
 ethyl bicyclo(2.2.1)-5-heptene-2-carboxylateFL/FR
2-ethyl butyl acetateFL/FR
 ethyl isobutyrateFL/FR
 ethyl levulinateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 ethyl propionateFL/FR
(E,E)-ethyl sorbateFL/FR
(E)-ethyl tiglateFL/FR
 geranyl butyrateFL/FR
 geranyl ethyl etherFL/FR
 geranyl isovalerateFL/FR
 grape butyrateFL/FR
2-heptyl butyrateFL/FR
 heptyl isobutyrateFL/FR
 hexanal propylene glycol acetalFL/FR
2-hexen-1-olFL/FR
(E)-3-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl anthranilateFL/FR
(Z)-3-hexen-1-yl isobutyrateFL/FR
 hexyl (E)-tiglateFL/FR
 hexyl acetateFL/FR
 hexyl isovalerateFL/FR
 hexyl propionateFL/FR
 hexyl valerateFL/FR
 methyl 2-methyl butyrateFL/FR
 methyl dimethyl anthranilateFL/FR
 methyl heptanoateFL/FR
 methyl hexanoateFL/FR
 methyl isobutyrateFL/FR
 methyl octadienoateFL/FR
 methyl valerateFL/FR
3-methyl-2-butenalFL/FR
 neryl propionateFL/FR
2-nonanoneFL/FR
 octen-1-yl cyclopentanoneFL/FR
 octyl butyrateFL/FR
2-pentanoneFL/FR
2-pentyl furanFL/FR
3-phenyl propyl hexanoateFL/FR
4-phenyl-2-butyl acetateFL/FR
 pineapple pentenoateFL/FR
 prenolFL/FR
 prenyl hexanoateFL/FR
isopropenyl acetateFL/FR
isopropyl 2-methyl butyrateFL/FR
 propyl acetateFL/FR
isopropyl butyrateFL/FR
isopropyl propionateFL/FR
 sorbyl butyrateFL/FR
(E,E)-sorbyl butyrateFL/FR
 tetrahydrofurfuryl acetateFL/FR
 tetrahydrofurfuryl butyrateFL/FR
 tropical thiazoleFL/FR
 tropical trithianeFL/FR
(E)-2-undecenalFL/FR
 acetaldehyde benzyl 2-methoxyethyl acetalFL/FR
 actinidia chinensis fruit extractFL/FR
isoamyl formateFL/FR
black currant bud absolute replacerFL/FR
isocyclocitral (IFF)FL/FR
alpha-decalactoneFL/FR
 ethyl (E)-2-hexenoateFL/FR
 ethyl (E)-4-decenoateFL/FR
 green note propionateFL/FR
 hexanal (aldehyde C-6)FL/FR
(E)-3-hexen-1-olFL/FR
(Z)-3-hexen-1-yl (E)-2-hexenoateFL/FR
(Z)-3-hexen-1-yl (Z)-3-hexenoateFL/FR
(Z)-3-hexen-1-yl 2-methyl butyrateFL/FR
(Z)-3-hexen-1-yl acetateFL/FR
(E)-2-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
(Z)-3-hexen-1-yl hexanoateFL/FR
(Z)-3-hexen-1-yl isovalerateFL/FR
(E)-2-hexen-1-yl propionateFL/FR
(Z)-3-hexen-1-yl valerateFL/FR
(E)-2-hexen-1-yl valerateFL/FR
(E)-2-hexenal propylene glycol acetalFL/FR
3-hexenyl 2-methyl butyrateFL/FR
3-hexenyl acetateFL/FR
 hexyl hexanoateFL/FR
 hexyl isobutyrateFL/FR
 hexyl octanoateFL/FR
 ivy carbaldehydeFL/FR
2,4-ivy carbaldehydeFL/FR
3,5-ivy carbaldehydeFL/FR
 manzanate (Givaudan)FL/FR
 methyl octine carbonateFL/FR
 neryl butyrateFL/FR
(E)-2-octen-1-yl acetateFL/FR
3-octyl formateFL/FR
 olive oil absoluteFL/FR
(Z)-2-penten-1-olFL/FR
(E)-2-pentenalFL/FR
 phenoxyethyl isobutyrateFL/FR
1-phenyl-2-pentanolFL/FR
 propylene acetalFL/FR
 sorbyl isobutyrateFL/FR
(E,E)-sorbyl isobutyrateFL/FR
 terpinyl propionateFL/FR
 thiogeraniolFL/FR
 tiglaldehydeFL/FR
herbal
 hexanolFL/FR
(1S,5R)-myrtenyl acetateFL/FR
2-pentyl acetateFL/FR
 rue oilFL/FR
 rue oil cubaFL/FR
 tagete oil indiaFL/FR
 viridiflorolFL/FR
minty
 carvyl acetateFL/FR
phenolic
 anisoleFL/FR
spicy
 cinnamyl propionateFL/FR
sulfurous
4-methyl 4-mercaptopentan-2-one 1% solutionFL/FR
terpenic
 cassis bud oilFL/FR
 psidium guajava fruit extractFL/FR
waxy
 decanal diethyl acetalFL/FR
(E)-methyl geranateFL/FR
 methyl octanoateFL/FR
2-nonanolFL/FR
 octyl 2-methyl butyrateFL/FR
winey
 methyl 3-acetoxyoctanoateFL/FR
 
For Flavor
 
No flavor group found for these
 acetaldehyde 1,3-octane diol acetalFL
 acetaldehyde benzyl 2-methoxyethyl acetalFL/FR
 acetaldehyde diisoamyl acetalFL/FR
 acetyl acetaldehyde dimethyl acetalFL
 actinidia chinensis fruit juiceFL
 allyl 2-ethyl butyrateFL/FR
 allyl levulinateFL
 allyl tiglateFL
 anisoleFL/FR
 benzyl methyl etherFL/FR
 butyl methyl ketoneFL
 butyl octanoateFL/FR
isobutyl octanoateFL/FR
 cinnamyl hexanoateFL/FR
isocyclocitral (IFF)FL/FR
2-cyclopentyl cyclopentanoneFL/FR
alpha-decalactoneFL/FR
 decyl propionateFL/FR
 diethyl sulfideFL
2,5-diethyl-4-propyl thiazoleFL
(±)-2,3-dihydrofarnesolFL/FR
 epoxy-2-decenalFL
 ethanolFL
 ethyl (E)-3-hexenoateFL/FR
 ethyl 2-(methyl thio) acetateFL
 ethyl 2-hexenoateFL/FR
 ethyl bicyclo(2.2.1)-5-heptene-2-carboxylateFL/FR
 ethyl nitrite 
 geranyl ethyl etherFL/FR
2-heptenoic acidFL
2-heptyl butyrateFL/FR
(Z)-3-hexen-1-yl (E)-2-hexenoateFL/FR
2-hexenalFL
(E)-3-hexenalFL
2-hexenal diethyl acetalFL
(E)-2-hexenal propylene glycol acetalFL/FR
3-hexenyl acetateFL/FR
 hexyl (E)-2-hexenoateFL
 hexyl nonanoateFL/FR
 hexyl propionateFL/FR
 hexyl valerateFL/FR
 ivy carbaldehydeFL/FR
3,5-ivy carbaldehydeFL/FR
 methyl (E)-2-hexenoateFL/FR
 methyl 2-hexenoateFL/FR
 methyl 3-acetoxyoctanoateFL/FR
 methyl 3-hydroxybutyrateFL
4-methyl 4-mercaptopentan-2-one 1% solutionFL/FR
para-methyl benzyl acetateFL/FR
 methyl dimethyl anthranilateFL/FR
2-methyl furanFL
(E)-methyl geranateFL/FR
 methyl octadienoateFL/FR
S-(methyl thio) hexanoateFL
(E)-methyl tiglateFL/FR
2-methyl-3-heptanoneFL
(E,E)-3,5-octadien-2-oneFL
3-octyl butyrateFL
3-pentanoneFL/FR
4-phenyl-2-butyl acetateFL/FR
 prenyl hexanoateFL/FR
 propyl valerateFL/FR
 propylene acetalFL/FR
 pyrazinyl methyl sulfideFL
(E,E)-sorbyl butyrateFL/FR
(E,E)-sorbyl isobutyrateFL/FR
 tetrahydrocitralFL/FR
 viridiflorolFL/FR
 sorbyl isobutyrateFL/FR
alcoholic
3-hexanolFL/FR
aldehydic
 octanal (aldehyde C-8)FL/FR
alliaceous
 tropical thiazoleFL/FR
berry
 heptyl isobutyrateFL/FR
brown
 tetrahydrofurfuryl acetateFL/FR
caramellic
 pyruvaldehydeFL
cheesy
2-nonanoneFL/FR
chemical
2,5-dimethyl furanFL
 methyl ethyl ketoneFL/FR
citrus
 bisaboleneFL/FR
 citralFL/FR
 nerolFL/FR
2-pentyl acetateFL/FR
clementine petitgrain oilFL/FR
 styralyl propionateFL/FR
coconut
(R)-massoia lactoneFL
cooling
 manzanate (Givaudan)FL/FR
creamy
2,4-heptadienalFL
 massoia lactoneFL
earthy
1-hexen-3-yl acetateFL
estery
 ethyl acetoacetateFL/FR
 propyl acetateFL/FR
ethereal
 acetaldehyde dimethyl acetalFL/FR
isobutyl alcoholFL/FR
 ethyl acetateFL/FR
 ethyl formateFL/FR
 ethyl isobutyrateFL/FR
4-hexen-3-oneFL
 methyl acetateFL/FR
 methyl isobutyrateFL/FR
isopropenyl acetateFL/FR
isopropyl acetateFL/FR
fatty
(E,E)-2,4-decadienalFL
 ethyl (E)-4-decenoateFL/FR
 ethyl undecylenateFL/FR
sec-heptyl acetateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
floral
 cinnamyl propionateFL/FR
 citronellolFL/FR
 citronellyl acetateFL/FR
 dihydrocarvyl acetateFL/FR
 geranyl acetoneFL/FR
(E)-geranyl acetoneFL/FR
 geranyl isobutyrateFL/FR
(Z)-3-hexen-1-yl anthranilateFL/FR
(Z)-methyl epi-jasmonateFL/FR
 methyl jasmonateFL/FR
 ocean propanalFL/FR
 satinaldehydeFL/FR
fruity
 amyl acetateFL/FR
isoamyl acetoacetateFL/FR
isoamyl benzoateFL/FR
 amyl formateFL/FR
 amyl heptanoateFL/FR
isoamyl hexanoateFL/FR
isoamyl isobutyrateFL/FR
 berry pentadienoateFL/FR
 boronia absoluteFL/FR
 butyl 2-decenoateFL/FR
isobutyl acetateFL/FR
 butyl hexanoateFL/FR
isobutyl propionateFL/FR
 cassis bud oilFL/FR
 cherry pentenoateFL/FR
 citronellyl formateFL/FR
 citronellyl isobutyrateFL/FR
black currant bud absolute replacerFL/FR
 diethyl malonateFL/FR
 dimethyl succinateFL/FR
 ethyl (E)-2-hexenoateFL/FR
 ethyl (E)-2-octenoateFL
 ethyl 2-octenoateFL/FR
 ethyl 3-hexenoateFL/FR
2-ethyl butyl acetateFL/FR
 ethyl levulinateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 ethyl propionateFL/FR
(E,E)-ethyl sorbateFL/FR
(E)-ethyl tiglateFL/FR
2-furyl pentyl ketoneFL
 geranyl butyrateFL/FR
2-heptanolFL/FR
3-heptyl dihydro-5-methyl-2(3H)-furanoneFL/FR
 hexanal propylene glycol acetalFL/FR
2-hexen-1-olFL/FR
(Z)-3-hexen-1-yl (Z)-3-hexenoateFL/FR
(E)-3-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl isobutyrateFL/FR
 hexyl acetateFL/FR
 hexyl hexanoateFL/FR
 hexyl lactateFL/FR
 kiwi distillatesFL
 lilac pentanolFL/FR
 methyl (E)-2-octenoateFL/FR
 methyl 2-methyl butyrateFL/FR
 methyl 3-hexenoateFL/FR
2-methyl allyl butyrateFL
 methyl heptanoateFL/FR
 methyl hexanoateFL/FR
 methyl valerateFL/FR
3-methyl-2-butenalFL/FR
 neryl formateFL/FR
(Z)-3-nonen-1-yl acetateFL
(Z)-5-octen-1-yl acetateFL
 octen-1-yl cyclopentanoneFL/FR
2-pentanoneFL/FR
2-phenyl propionaldehyde dimethyl acetalFL/FR
3-phenyl propyl hexanoateFL/FR
1-phenyl-2-pentanolFL/FR
 pineapple pentenoateFL/FR
 prenolFL/FR
isopropyl 2-methyl butyrateFL/FR
isopropyl butyrateFL/FR
 propyl formateFL/FR
isopropyl formateFL/FR
isopropyl propionateFL/FR
 sorbyl butyrateFL/FR
 tetrahydrofurfuryl butyrateFL/FR
 tiglaldehydeFL/FR
 tropical trithianeFL/FR
isovaleraldehydeFL/FR
isovaleraldehyde propylene glycol acetalFL/FR
green
 actinidia chinensis fruit extractFL/FR
 allyl butyrateFL/FR
isoamyl formateFL/FR
isoamyl isovalerateFL/FR
isobutyl isovalerateFL/FR
 cuminyl acetaldehydeFL/FR
 cyclohexyl formateFL/FR
3-decen-2-oneFL/FR
 dihydromyrcenolFL/FR
(E,Z)-2,6-dodecadienalFL/FR
2-ethyl butyraldehydeFL
 geranyl formateFL/FR
 geranyl isovalerateFL/FR
 grape butyrateFL/FR
 green note propionateFL/FR
(E,E)-2,4-hexadienalFL
2,4-hexadienalFL
 hexanal (aldehyde C-6)FL/FR
 hexanolFL/FR
(E)-3-hexen-1-olFL/FR
(Z)-3-hexen-1-yl 2-methyl butyrateFL/FR
(Z)-3-hexen-1-yl acetateFL/FR
(E)-2-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl hexanoateFL/FR
(Z)-3-hexen-1-yl isovalerateFL/FR
(E)-2-hexen-1-yl propionateFL/FR
(E)-2-hexen-1-yl valerateFL/FR
(Z)-3-hexen-1-yl valerateFL/FR
1-hexen-3-olFL/FR
3-hexenyl 2-methyl butyrateFL/FR
 hexyl (E)-tiglateFL/FR
 hexyl isobutyrateFL/FR
 hexyl isovalerateFL/FR
 hexyl octanoateFL/FR
2,4-ivy carbaldehydeFL/FR
isojasmoneFL/FR
isojasmoneFL/FR
 methyl (E)-3-hexenoateFL/FR
 methyl 2-undecynoateFL
 methyl octanoateFL/FR
 methyl octine carbonateFL/FR
3-(5-methyl-2-furyl) butanalFL
4-methyl-2-pentenalFL
 neryl butyrateFL/FR
 neryl propionateFL/FR
(E,E)-2,4-octadienalFL
2,4-octadienalFL
(E)-2-octen-1-yl acetateFL/FR
 papaya isobutyrateFL/FR
(Z)-2-penten-1-olFL/FR
(E)-2-pentenalFL/FR
2-pentyl furanFL/FR
 phenoxyethyl isobutyrateFL/FR
 terpinyl propionateFL/FR
herbal
 cilantro herb oil egyptFL/FR
 rue oilFL/FR
 rue oil cubaFL/FR
 tagete oil indiaFL/FR
honey
 phenethyl acetateFL/FR
minty
 carvyl acetateFL/FR
 thiogeraniolFL/FR
nutty
 acetalFL/FR
oily
 olive oil absoluteFL/FR
rummy
isobutyl formateFL/FR
 ethyl pyruvateFL/FR
sour
3-methyl valeric acidFL
tropical
 guava distillatesFL
 propyl propionateFL/FR
 psidium guajava fruitFL
 psidium guajava fruit extractFL/FR
vegetable
2-methyl valeraldehydeFL/FR
waxy
isoamyl butyrateFL/FR
 decanal diethyl acetalFL/FR
2-nonanolFL/FR
 octyl 2-methyl butyrateFL/FR
 octyl butyrateFL/FR
3-octyl formateFL/FR
(E)-2-undecenalFL/FR
woody
beta-damascenoneFL/FR
beta-iononeFL/FR
(Z)-jasmoneFL/FR
(1S,5R)-myrtenyl acetateFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 appleFL
 apricotFL
 beerFL
 bread white bread 
 butterFL
 cheese cheddarFL
 cheese swissFL
 cornFL
 cucumberFL
 currant 
 fishFL
 gooseberryFL
 grapeFL
 lemonFL
 melon watermelon muskmelon cantaloupe 
 nail conditioning 
 orangeFL
 pea green pea 
 peachFL
 pearFL
 pineappleFL
 plumFL
 raspberryFL
 strawberryFL
 tomatoFL
 whiskeyFL
 witch hazel 
 yogurtFL
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 angelica
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 anise seed
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 apple fruit
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 apple fruit 755 ppm
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 apple fruit juice
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 apple juice 3643 ppm
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 artemisia brevifloria
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 balm
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 beer 265926 ppm
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 bread
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 bread white bread 40221 ppm
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 butter 109 ppm
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 cabbage leaf
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 cantaloupe petiole
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 caraway seed
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 carrot root
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 carrot root 8533 ppm
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 celery leaf
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 celery shoot
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 cheese cheddar cheese 3409 ppm
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 cheese swiss cheese 924 ppm
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 chenopodium
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 coffee arabica coffee bean
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 coffee bean
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 cornmint
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 cucumber 1088 ppm
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 cumin
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 currant black currant fruit
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 daffodil
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 date palm fruit
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 elder black elder flower oil
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 elder black elder leaf oil
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 fennel
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 fig fruit
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 fish 3393 ppm
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 garlic bulb
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 ginger oil
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 ginger rhizome
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 ginger rhizome oil
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 guava fruit
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 litsea cubeba
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 magnolia southern magnolia
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 maize 5965 ppm
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 mandarin fruit
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 monarda punctata
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 mushroom giant puffball mushroom
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 mustard
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 oak leaf
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 olive
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 orange bitter orange
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 orange fruit juice
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 orange fruit juice 11040 ppm
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 orris root
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 paprika
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 peach plant
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 pear fruit
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 peas 1049 ppm
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 peppermint plant
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 pineapple fruit
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 pineapple fruit 483 ppm
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 plum fruit
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 potato plant
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 rape
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 raspberry red raspberry fruit
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 rice cooked rice 46 ppm
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 rice plant
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 rosemary
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 rugula herb
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 rum
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 sage clary sage
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 soursop plant
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 soybean plant
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 spearmint oil
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 strawberry wild strawberry fruit
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 strawberry wild strawberry fruit 1288 ppm
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 tea leaf
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 tobacco leaf
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 tomato fruit
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 tomato fruit 32586 ppm
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 yogurt 10585 ppm
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Synonyms   Articles   Notes   Search   Top
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
Synonyms   Articles   Notes   Search   Top
Articles:
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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