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General Material Information

Preferred name acetic acid
Trivial Name Acetic acid
Short Description ethanoic acid
Formula C2 H4 O2
CAS Number 64-19-7
Deleted CAS Number 1053656-97-5
FEMA Number 2006
Flavis Number 8.002
ECHA Number 200-580-7
FDA UNII Q40Q9N063P
Nikkaji Number J2.355H
Beilstein Number 0506007
MDL MFCD00036152
COE Number 2
xLogP3-AA -0.20 (est)
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 81 acetic acid
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 64-19-7 ; ACETIC ACID
Synonyms
  • acetasol
  • eastapure acetic acid
  • glacial acetic acid
  • nat. acetic acid
  • acetic acid (natural)
  • acetic acid glacial
  • acetic acid natural
  • acetic acid natural FCC
  • acetic acid naturel
  • acetic acid, dry vinegar- essiccum K
  • glacial acetic acid, food grade
  • acetic acid, glacial FCC
  • acetic acid, glacial USP
  • aci-jel
  • acide acétique
  • acido acetico
  • azido azetikoa
  • azijnzuur
  • essiccum and essiccum K - dry vinegar substitutes
  • essigsäure
  • ethanoic acid
  • ethylic acid
  • INCI acetic acid
  • methane carboxylic acid
  • methanecarboxylic acid
  • methyl carboxylic acid
  • orlex
  • otic tridesilon
  • pyroligneous acid
  • vinegar acid
  • vosol
  • Ethanoic acid monomer
  • E 260
  • NSC 111201
  • NSC 112209
  • NSC 115870
  • NSC 127175
  • NSC 132953
  • NSC 406306
  • Munger Horticultural Vinegar Plus
  • Weed Pharm
  • Engage Agro
  • HACP 85
  • Acetic acids
  • Cedrosa
  • Acetic acid HAC
  • HZ 006
  • MeSH ID: D019342
  • HL 385

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

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Literature & References

acetic acid
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:64-19-7
Pubchem (cid):176
Pubchem (sid):134971968
Flavornet:64-19-7
Pherobase:View
Publications by Info
Volatile Flavor Components in Bogyojosaeng and Suhong Cultivars of Strawberry (Fragaria ananassa Duch.)
Publications by PubMed
Effect of temperature on chinese rice wine brewing with high concentration presteamed whole sticky rice.
Yeasts are essential for cocoa bean fermentation.
Volatile organic compounds profile during milk fermentation by Lactobacillus pentosus and correlations between volatiles flavor and carbohydrate metabolism.
Acidic Organic Compounds in Beverage, Food, and Feed Production.
Flavor of cold-hardy grapes: impact of berry maturity and environmental conditions.
High-pressure processing decelerates lipolysis and formation of volatile compounds in ovine milk blue-veined cheese.
Exploring microbial succession and diversity during solid-state fermentation of Tianjin duliu mature vinegar.
Role of the microbial population on the flavor of the soft-bodied cheese Torta del Casar.
Effects of buffered vinegar and sodium dodecyl sulfate plus levulinic acid on Salmonella Typhimurium survival, shelf-life, and sensory characteristics of ground beef patties.
Identification of the key odorants in Tahitian cured vanilla beans (Vanilla tahitensis) by GC-MS and an aroma extract dilution analysis.
Characterization of aroma compounds in Chinese bayberry (Myrica rubra Sieb. et Zucc.) by gas chromatography mass spectrometry (GC-MS) and olfactometry (GC-O).
Effect of maturity stage and storage on flavor compounds and sensory description of berrycactus (Myrtillocactus geometrizans).
The effect of cocoa fermentation and weak organic acids on growth and ochratoxin A production by Aspergillus species.
Enzymatic activity and flavor compound production in fermented silver carp fish paste inoculated with douchi starter culture.
Species diversity, community dynamics, and metabolite kinetics of the microbiota associated with traditional ecuadorian spontaneous cocoa bean fermentations.
Influence of pulsed electric field treatments on the volatile compounds of milk in comparison with pasteurized processing.
Key aroma components of a dry-cured sausage with high fat content (sobrassada).
Application of infrared microspectroscopy and multivariate analysis for monitoring the effect of adjunct cultures during Swiss cheese ripening.
Irradiation effects on meat flavor: A review.
Changes in key aroma compounds of Criollo cocoa beans during roasting.
Volatile and color composition of young and model-aged Shiraz wines as affected by diammonium phosphate supplementation before alcoholic fermentation.
Preservation of kombucha tea-effect of temperature on tea components and free radical scavenging properties.
Targeting key aromatic substances on the typical aroma of sherry vinegar.
Aroma components of American country ham.
Assessment of the microbial contribution to the processing of salted salmon roe (Sujiko).
Analysis of volatile compounds in fresh healthy and diseased peppers (Capsicum annuum L.) using solvent free solid injection coupled with gas chromatography-flame ionization detector and confirmation with mass spectrometry.
Application of Fourier transform infrared spectroscopy for monitoring short-chain free fatty acids in Swiss cheese.
Identification of the key aroma compounds in cocoa powder based on molecular sensory correlations.
Comparison of volatiles of cultured and wild sea bream (Sparus aurata) during storage in ice by dynamic headspace analysis/gas chromatography-mass spectrometry.
Descriptive sensory analysis of broiler breast fillets marinated in phosphate, salt, and acid solutions.
Food Prot. 2004 Nov;67(11):2456-64. Control of Listeria monocytogenes on frankfurters with antimicrobials in the formulation and by dipping in organic acid solutions.
The microbiology of cocoa fermentation and its role in chocolate quality.
Investigation of the change in the flavor of a coffee drink during heat processing.
Effects of lactic and acetic acid salts on quality characteristics of enhanced pork during retail display.
Quantitation of odor-active compounds in rye flour and rye sourdough using stable isotope dilution assays.
Chemical composition and flavor of ecuadorian cocoa liquor.
Determination of key aroma compounds in the crumb of a three-stage sourdough rye bread by stable isotope dilution assays and sensory studies.
Lipolytic and proteolytic properties of dry-cured boneless hams ripened in modified atmospheres.
Utilization of bee (Apis mellifera) honey for vinegar production at laboratory scale.
Solid-phase microextraction method development for headspace analysis of volatile flavor compounds.
Identification of impact odorants in Bordeaux red grape juice, in the commercial yeast used for its fermentation, and in the produced wine.
The effect of an acetic acid dip on carcass appearance, microbiological quality, and cooked breast meat texture and flavor.
Characterization of volatile aroma compounds in different brewing barley cultivars.
Exploring microbial succession and diversity during solid-state fermentation of Tianjin duliu mature vinegar.
Identification of the key odorants in Tahitian cured vanilla beans (Vanilla tahitensis) by GC-MS and an aroma extract dilution analysis.
Ultrasound-assisted butyl acetate synthesis catalyzed by Novozym 435: enhanced activity and operational stability.
Development of an effective treatment for A 5-log reduction of Escherichia coli in refrigerated pickle products.
Chemical characterization of commercial liquid smoke products.
[Simultaneous determination of 14 restricted substances in flavor and fragrant by ultra high performance liquid chromatography].
Effect of maturity stage and storage on flavor compounds and sensory description of berrycactus (Myrtillocactus geometrizans).
Production of flavor esters catalyzed by CALB-displaying Pichia pastoris whole-cells in a batch reactor.
Species diversity, community dynamics, and metabolite kinetics of the microbiota associated with traditional ecuadorian spontaneous cocoa bean fermentations.
Wine flavor and aroma.
Key aroma components of a dry-cured sausage with high fat content (sobrassada).
Effects of sodium lactate and acetic acid derivatives on the quality and sensory characteristics of hot-boned pork sausage patties.
Proton transfer reaction time-of-flight mass spectrometry monitoring of the evolution of volatile compounds during lactic acid fermentation of milk.
Flying the fly: long-range flight behavior of Drosophila melanogaster to attractive odors.
[Separation and identification of 5 glycosidic flavor precursors in tobacco by ultra performance liquid chromatography-electrospray ionization tandem mass spectrometry].
Functional analysis of a tomato salicylic acid methyl transferase and its role in synthesis of the flavor volatile methyl salicylate.
The role of transient receptor potential vanilloid-1 on neural responses to acids by the chorda tympani, glossopharyngeal and superior laryngeal nerves in mice.
Application of infrared microspectroscopy and multivariate analysis for monitoring the effect of adjunct cultures during Swiss cheese ripening.
Effect of tenderizers combined with organic acids on Escherichia coli O157:H7 thermal resistance in non-intact beef.
[Food additive hypersenisivity--near myth].
Irradiation effects on meat flavor: A review.
Application of Fourier transform infrared spectroscopy for monitoring short-chain free fatty acids in Swiss cheese.
Production of butyl acetate ester by lipase from novel strain of Rhizopus oryzae.
Specific pretreatments reduce curing period of vanilla (Vanilla planifolia) beans.
Identification of the key aroma compounds in cocoa powder based on molecular sensory correlations.
The nociceptive response of stressed and lithium-treated rats is differently modulated by different flavors.
Production of natural fruity aroma by Geotrichum candidum.
Influence of condensed sweet cream buttermilk on the manufacture, yield, and functionality of pizza cheese.
Control of Listeria monocytogenes on frankfurters with antimicrobials in the formulation and by dipping in organic acid solutions.
The microbiology of cocoa fermentation and its role in chocolate quality.
Quantitation of odor-active compounds in rye flour and rye sourdough using stable isotope dilution assays.
Chemical composition and flavor of ecuadorian cocoa liquor.
Development of a CE method to analyze organic acids in dairy products: application to study the metabolism of heat-shocked spores.
Lipolytic and proteolytic properties of dry-cured boneless hams ripened in modified atmospheres.
Vanillin content in boiled peanuts.
Utilization of bee (Apis mellifera) honey for vinegar production at laboratory scale.
Tyrosine and phenylalanine catabolism by Lactobacillus cheese flavor adjuncts.
Acetaldehyde metabolism by wine lactic acid bacteria.
Solid-phase microextraction method development for headspace analysis of volatile flavor compounds.
Determination of tryptophan and tryptophan metabolites in grape must and wine.
Identification of impact odorants in Bordeaux red grape juice, in the commercial yeast used for its fermentation, and in the produced wine.
Effect of increased yeast alcohol acetyltransferase activity on flavor profiles of wine and distillates.
Propionibacterium cyclohexanicum sp. nov., a new acid-tolerant omega-cyclohexyl fatty acid-containing propionibacterium isolated from spoiled orange juice.
The effect of an acetic acid dip on carcass appearance, microbiological quality, and cooked breast meat texture and flavor.

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
FDA Indirect Additives used in Food Contact Substances:View
CHEBI:View
CHEMBL:View
Metabolomics Database:Search
UM BBD:Search
KEGG (GenomeNet):C00033
HMDB (The Human Metabolome Database):HMDB00042
FooDB:FDB019725
YMDB (Yeast Metabolome Database):YMDB00056
Export Tariff Code:2915.21.0000
FDA Listing of Food Additive Status:View
MedlinePlusSupp:View
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
Formulations/Preparations:
grades: usp united states pharmacopeia (glacial, 99.4 wt % and dilute, 36-37 wt %), cp chemically pure: a grade designation signifying a minimum of impurities, but not 100% purity; technical (80; 99.5%); commercial (6, 28, 30, 36, 56, 70, 80 & 99.5%); nf national formulary (diluted; 6.0 g100 ml). reagent grade (glacial)-99.7%, usp grade glacial-99.5%; aq acetic acid-28,36,56,70,80,85 and 90%; lab reagent (aq)-36% household vinegar is usually 5% acetic acid

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 60.052280426025
Specific gravity @ 25 °C
Pounds per Gallon 8.712 to 8.812
Refractive Index 1.366 to 1.376 @ 20 °C
Melting Point 16.6 to 16.7°C @ 760 mm Hg
Boiling Point 117 to 118°C @ 760 mm Hg
Boiling Point 48 to 49°C @ 50 mm Hg
Vapor Pressure 15.7 mmHg @ 25 °C
Vapor Density 2.07
Flash Point TCC Value 40 °C TCC
logP (o/w) -0.17
Shelf life 36 months (or longer if stored properly.)
Storage notes Store in cool, dry place in tightly sealed containers, protected from heat and light.
Solubility
alcohol Yes
water, 4.759e+005 mg/L @ 25 °C (est) Yes
water, 1.00E+06 mg/L @ 25 °C (exp) Yes

Organoleptic Properties

Odor Type: Acidic
sharp, pungent, sour, vinegar
Odor strength high , recommend smelling in a 10.00 % solution or less
Substantivity 10 hour(s) at 100.00 %
General comment At 10.00 % in propylene glycol. sharp pungent sour vinegar
Flavor Type: Sour
pungent, sour, fruit overripe fruit, acetic
General comment Pungent sour overripe fruit
Useful in: dairy, savory vegetable, savory meat, savory others, fruity red, fruity yellow, fruity tropical, fruity others, sweet others, alcoholics. Pungent, sour, overripe fruit

Occurrences

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
C - Corrosive.
R 10 - Flammable.
R 35 - Causes severe burns.
S 02 - Keep out of the reach of children.
S 23 - Do not breath fumes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 45 - In case of accident or if you feel unwell seek medical advice immediately.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Flammable liquids (Category 3), H226
Skin corrosion (Category 1B), H314
GHS Label elements, including precautionary statements
Pictogramflame.jpgcorrosion.jpg
Signal word Danger
Hazard statement(s)
H226 - Flammable liquid and vapour
H314 - Causes severe skin burns and eye damage
Precautionary statement(s)
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.
P264 - Wash skin thouroughly after handling.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P301 + P330 + P331 - IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
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.
P310 - Immediately call a POISON CENTER or doctor/physician.
P363 - Wash contaminated clothing before reuse.
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 3310 mg/kg
Delaware State Medical Journal. Vol. 31, Pg. 276, 1959.

intravenous-mouse LD50 525 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Acta Pharmacologica et Toxicologica. Vol. 18, Pg. 141, 1961.

oral-human TDLo 1470 ug/kg
GASTROINTESTINAL: ULCERATION OR BLEEDING FROM SMALL INTESTINE GASTROINTESTINAL: CHANGE IN STRUCTURE OR FUNCTION OF ESOPHAGUS GASTROINTESTINAL: ULCERATION OR BLEEDING FROM LARGE INTESTINE
American Industrial Hygiene Association Journal. Vol. 33, Pg. 624, 1972.

oral-rabbit LDLo 600 mg/kg
Comptes Rendus des Seances de la Societe de Biologie et de Ses Filiales. Vol. 83, Pg. 136, 1920.

Dermal Toxicity:
skin-rabbit LD50 1060 ul/kg
Union Carbide Data Sheet. Vol. 8/7/1963

subcutaneous-rabbit LDLo 600 mg/kg
Comptes Rendus des Seances de la Societe de Biologie et de Ses Filiales. Vol. 83, Pg. 136, 1920.

Inhalation Toxicity:
inhalation-mouse LC50 5620 ppm/1H
American Industrial Hygiene Association Quarterly. Vol. 17, Pg. 129, 1956.

inhalation-human TCLo 816 ppm/3M
SENSE ORGANS AND SPECIAL SENSES: OTHER CHANGES: OLFACTION SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
AMA Archives of Industrial Health. Vol. 21, Pg. 28, 1960.

inhalation-mouse LC50 5620 ppm/1H
BLOOD: OTHER CHANGES SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE SENSE ORGANS AND SPECIAL SENSES: CONJUNCTIVE IRRITATION: EYE
Medicina del Lavoro. Industrial Medicine. Vol. 48, Pg. 559, 1957.

inhalation-rat LCLo 16000 ppm/4H
American Industrial Hygiene Association Quarterly. Vol. 17, Pg. 129, 1956.

Safety in use information

Category:
flavoring agents and adjuvants, curing and pickling agents, flavor enhancers, acidity regulators
Recommendation for acetic acid usage levels up to:
not for fragrance use.
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. Update in publication number(s): 29
Click here to view publication 3
average usual ppmaverage maximum ppm
baked goods: 0.1000038.00000
beverages(nonalcoholic): 0.0600039.00000
beverages(alcoholic): 500.000002000.00000
breakfast cereal: --
cheese: --
chewing gum: 400.000005000.00000
condiments / relishes: 136.000005900.00000
confectionery froastings: --
egg products: --
fats / oils: 15.0000031.00000
fish products: --
frozen dairy: 0.0300032.00000
fruit ices: --
gelatins / puddings: 0.0400015.00000
granulated sugar: --
gravies: 2.0000012.00000
hard candy: 0.2000052.00000
imitation dairy: 0.100000.10000
instant coffee / tea: --
jams / jellies: --
meat products: 8.0000016.00000
milk products: 0.800001.00000
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: 2.000002.00000
soft candy: 0.050000.07000
soups: --
sugar substitutes: --
sweet sauces: 0.100000.10000

Safety references

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

Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 22 (FGE.22): Ring-substituted phenolic substances from chemical groups 21 and 25 (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf

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 47, (FGE.47)[1] - Bicyclic secondary alcohols, ketones and related esters from chemical group 8 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf

Flavouring Group Evaluation 23, Revision 1 (FGE.23Rev1): Aliphatic, alicyclic and aromatic ethers including anisole derivatives from chemical groups 15, 16, 26 and 30[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 33 (FGE.33)[1] - Six Tetrahydrofuran Derivatives from Chemical Groups 13, 14, 16 and 26 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf

Flavouring Group Evaluation 9, Revision 1: (FGE.09 Rev1)[1] - Secondary alicyclic saturated and unsaturated alcohols, ketones and esters containing secondary alicyclic alcohols from chemical groups 8 and 30, and an ester of a phenol carboxylic acid from chemical group 25 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf

Flavouring Group Evaluation 04 - 2-Ethylhexyl derivatives from chemical group 2 - 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 18, Revision 1 (FGE. 18 Rev1)[1] : Aliphatic, alicyclic and aromatic saturated and unsaturated tertiary alcohols, aromatic tertiary alcohols and their esters from chemical groups 6 and 8
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 7, Revision 2 (FGE.07Rev2) : Saturated and unsaturated aliphatic secondary alcohols, ketones and esters of secondary alcohols and saturated linear or branched-chain carboxylic acids from chemical group 5
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

Scientific Report of EFSA on the risk assessment of salts of authorised acids, phenols or alcohols for use in food contact materials [1]
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 20, Revision 2 (FGE.20Rev2): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters from chemical groups 23 and 30
View page or View pdf

Flavouring Group Evaluation 9, Revision 2 (FGE.09Rev2): Secondary alicyclic saturated and unsaturated alcohols, ketones and esters containing secondary alicyclic alcohols from chemical group 8 and 30, and an ester of a phenol derivative from chemical group 25
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 22, Revision 1 (FGE.22Rev1): Ring-substituted phenolic substances from chemical groups 21 and 25
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 Flavouring Group Evaluation 20, Revision 3(FGE.20Rev3): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters from chemical groups 23 and 30
View page or View pdf

Scientific Opinion on the safety and efficacy of acetic acid, sodium diacetate and calcium acetate as preservatives for feed for all animal species
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

Scientific Opinion on the evaluation of the safety and efficacy of peroxyacetic acid solutions for reduction of pathogens on poultry carcasses and meat
View page or View pdf

Retrospective analysis of the immunotoxic effects of plant protection products as reported in the Draft Assessment Reports for their peer review at EU level
View page or View pdf

Outcome of the consultation with Member States, the applicant and EFSA on the pesticide risk assessment for acetic acid in light of confirmatory data
View page or View pdf

Evaluation of the safety and efficacy of the organic acids lactic and acetic acids to reduce microbiological surface contamination on pork carcasses and pork cuts
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Re-evaluation of acetic acid, lactic acid, citric acid, tartaric acid, mono- and diacetyltartaric acid, mixed acetic and tartaric acid esters of mono- and diglycerides of fatty acids (E 472a-f) as food additives
View page or View pdf

Safety and efficacy of a feed additive consisting of acetic acid for all animal species
View page or View pdf

EPI System: View
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
EPA GENetic TOXicology:Search
EPA Substance Registry Services (TSCA):64-19-7
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :176
National Institute of Allergy and Infectious Diseases:Data
WISER:UN 2789
WGK Germany:1
acetic acid
Chemidplus:0000064197
EPA/NOAA CAMEO:hazardous materials
RTECS:64-19-7