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General Material Information

Preferred name benzyl acetate
Trivial Name Benzyl acetate
Short Description acetic acid, phenylmethyl ester
Formula C9 H10 O2
CAS Number 140-11-4
FEMA Number 2135
ECHA Number 205-399-7
FDA UNII 0ECG3V79ZJ
Nikkaji Number J2.950E
Beilstein Number 1908121
MDL MFCD00008712
COE Number 204
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 23 benzyl acetate
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 140-11-4 ; BENZYL ACETATE
Synonyms
  • acetic acid benzyl ester
  • acetic acid benzylester
  • acetic acid phenyl methyl ester
  • acetic acid phenylmethyl ester
  • acetic acid, benzyl ester
  • acetic acid, phenylmethyl ester
  • ( acetoxymethyl)benzene
  • a- acetoxytoluene
  • alpha- acetoxytoluene
  • benteine
  • benzenemethanol acetate
  • benzenemethanol ethanoate
  • nat. benzyl acetate
  • benzyl acetate (natural)
  • benzyl acetate 99%, (naturals)
  • benzyl acetate extra
  • benzyl acetate FCC
  • benzyl acetate natural
  • benzyl acetate natural, comores
  • benzyl acetate puissiume FCC
  • benzyl acetate, natural
  • benzyl alcohol acetate
  • benzyl ethanoate
  • benzylacetate
  • ethanoic acid phenylmethyl ester
  • Benzyl alcohol, acetate
  • α-Acetoxytoluene
  • (Acetoxymethyl)benzene
  • Phenylmethyl acetate
  • NSC 4550
  • Jeffsol AG 1705
  • Jeffsol AG 1700

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

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Literature & References

benzyl acetate
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:140-11-4
Pubchem (cid):8785
Pubchem (sid):134974597
Flavornet:140-11-4
Pherobase:View
Publications by Info
Volatile Flavor Components in Bogyojosaeng and Suhong Cultivars of Strawberry (Fragaria ananassa Duch.)
Publications by PubMed
A comparative analysis of characteristic floral scent compounds in Prunus mume and related species.
Do flower color and floral scent of silene species affect host preference of Hadena bicruris, a seed-eating pollinator, under field conditions?
Attraction of the orange mint moth and false celery leaftier moth (Lepidoptera: Crambidae) to floral chemical lures.
Aroma profiles and preferences of Jasminum sambac L. flowers grown in Thailand.
Volatile constituents of commercial imported and domestic black-ripe table olives (Olea europaea).
Headspace solid-phase microextraction analysis of volatile components in Narcissus tazetta var. chinensis Roem.
Pomegranate juice adulteration by addition of grape or peach juices.
Production of phenolics and the emission of volatile organic compounds by perennial ryegrass (Lolium perenne L.)/Neotyphodium lolii association as a response to infection by Fusarium poae.
Field trials of solid triple lure (trimedlure, methyl eugenol, raspberry ketone, and DDVP) dispensers for detection and male annihilation of Ceratitis capitata, Bactrocera dorsalis, and Bactrocera cucurbitae (Diptera: Tephritidae) in Hawaii.
Essential oils and their compositions as spatial repellents for pestiferous social wasps.
Driving force dependence of charge recombination in reactive and nonreactive solvents.
Liquid CO2 extraction of Jasminum grandiflorum and comparison with conventional processes.
Fragrance material review on benzyl acetate.
Grape contribution to wine aroma: production of hexyl acetate, octyl acetate, and benzyl acetate during yeast fermentation is dependent upon precursors in the must.
The catalytic efficiency of lipase in a novel water-in-[Bmim][PF6] microemulsion stabilized by both AOT and Triton X-100.
Chemotactic effect of odorants and tastants on the ciliate Tetrahymena pyriformis.
Monitoring the emission of volatile organic compounds from flowers of Jasminum sambac using solid-phase micro-extraction fibers and gas chromatography with mass spectrometry detection.
Fusarium infection in maize: volatile induction of infected and neighboring uninfected plants has the potential to attract a pest cereal leaf beetle, Oulema melanopus.
Repellent activity of essential oils and some of their individual constituents against Tribolium castaneum herbst.
A core in vitro genotoxicity battery comprising the Ames test plus the in vitro micronucleus test is sufficient to detect rodent carcinogens and in vivo genotoxins.
Behavioral responses of the leafhopper, Cicadulina storeyi China, a major vector of maize streak virus, to volatile cues from intact and leafhopper-damaged maize.
Structural characterization and substrate specificity of VpAAT1 protein related to ester biosynthesis in mountain papaya fruit.
Selective retardation of perfume oil evaporation from oil-in-water emulsions stabilized by either surfactant or nanoparticles.
Antimutagenic; differentiation-inducing; and antioxidative effects of fragrant ingredients in Katsura-uri (Japanese pickling melon; Cucumis melo var. conomon).
[carbonyl-C]Benzyl acetate: automated radiosynthesis via Pd-mediated [C]carbon monoxide chemistry and PET measurement of brain uptake in monkey.
VpAAT1, a gene encoding an alcohol acyltransferase, is involved in ester biosynthesis during ripening of mountain papaya fruit.
Assessment of genotoxic effects of benzyl derivatives by the comet assay.
Poly[tetra-kis[μ(2)-1,3-bis-(4-pyrid-yl)propane-κN:N']dichloridobis(phenyl-acetato)dimanganese(II)].
Determination of cobalt ions at nano-level based on newly synthesized pendant armed macrocycle by polymeric membrane and coated graphite electrode.
Jasminum flexile flower absolute from India--a detailed comparison with three other jasmine absolutes.
Identification of host attractants for the ethiopian fruit fly, Dacus ciliatus loew.
Evaluation of the glycoside hydrolase activity of a Brettanomyces strain on glycosides from sour cherry (Prunus cerasus L.) used in the production of special fruit beers.
[Composition and seasonality of Euglossina Species (Hymenoptera: Apidae) in forest and dune in the Environmental Protection Area of the Mamanguape River Bar, PB].
Electroanalytical performance of a terbium(III)-selective sensor based on a neutral ionophore in environmental and medicinal samples.
[Activity time of male Euglossina and preference for artificial fragrances in forest and dunes in the Environmental Protection Area of the Mamanguape River Bar, Rio Tinto, Paraíba, Brazil].
Vinegar classification based on feature extraction and selection from headspace solid-phase microextraction/gas chromatography volatile analyses: a feasibility study.
Use of cyclodextrins as a cosmetic delivery system for fragrance materials: linalool and benzyl acetate.
Genotoxicity testing of four benzyl derivatives in the Drosophila wing spot test.
[14C]Benzyl acetate is a potential radiotracer for the measurement of glial metabolism in the rat brain.
Selective electrochemical sensor for copper (II) ion based on chelating ionophores.
Tripodal chelating ligand-based sensor for selective determination of Zn(II) in biological and environmental samples.
Transesterification of primary and secondary alcohols using Pseudomonas aeruginosa lipase.
Chromium(III) selective membrane sensors based on Schiff bases as chelating ionophores.
Antioxidant activities and volatile constituents of various essential oils.
Lipase catalyzed synthesis of benzyl acetate in solvent-free medium using vinyl acetate as acyl donor.
Generation of phenylpropanoid pathway-derived volatiles in transgenic plants: rose alcohol acetyltransferase produces phenylethyl acetate and benzyl acetate in petunia flowers.
Functional characterization of a melon alcohol acyl-transferase gene family involved in the biosynthesis of ester volatiles. Identification of the crucial role of a threonine residue for enzyme activity*.
Floral odor variation in two heterostylous species of Primula.
Floral scent emission and pollinator attraction in two species of Gymnadenia (Orchidaceae).
An Eu(III) sensor based on N,N-diethyl-N-(4-hydroxy-6-methylpyridin-2-yl)guanidine.
Development of highly active and selective novel Pd based acetoxylation catalysts and prevention of catalyst deactivation by Bi modification.
One-step synthesis of benzyl acetate by gas phase acetoxylation of toluene over highly active and selective Pd-Sb-TiO2 catalysts.
ppt level detection of samarium(III) with a coated graphite sensor based on an antibiotic.
Flavor release and rheology behavior of strawberry fatfree stirred yogurt during storage.
Sulfate-selective PVC membrane electrode based on a strontium Schiff's base complex.
Novel membrane potentiometric sulfate ion sensor based on zinc-phthalocyanine for the quick determination of trace amounts of sulfate.
Use of inverse gas chromatography to characterize cotton fabrics and their interactions with fragrance molecules at controlled relative humidity.
Thresholds of carcinogenicity of flavors.
Improved hardware and software for quick gas chromatography-olfactometry using CHARM and GC-"SNIF" analysis.
Comparative investigation of multiple organs of mice and rats in the comet assay.
Palladium(0)-catalyzed coupling-cyclization reaction of polymer-supported aryl iodides with 1,2-allenyl carboxylic acids. Solid-phase parallel synthesis of butenolides.
Micronucleus formation in human lymphocytes and in the metabolically competent human hepatoma cell line Hep-G2: results with 15 naturally occurring substances.
areCBA is an operon in Acinetobacter sp. strain ADP1 and Is controlled by AreR, a sigma(54)-dependent regulator.
Laboratory evaluation of miticides to control Varroa jacobsoni (Acari: Varroidae), a honey bee (Hymenoptera: Apidae) parasite.
Determination of acetic acid in aqueous samples, by water-phase derivatisation, solid-phase microextraction and gas chromatography.
Subchronic inhalation studies of complex fragrance mixtures in rats and hamsters.
SOS induction of selected naturally occurring substances in Escherichia coli (SOS chromotest).
Effect of Types of Perfume Compounds on the Hydrophile-Lipophile Balance Temperature.
Benzyl acetate.
areABC genes determine the catabolism of aryl esters in Acinetobacter sp. Strain ADP1.
Glycine modulates the toxicity of benzyl acetate in F344 rats.
Deodorants on the European market: quantitative chemical analysis of 21 fragrances.
The thioesterase I of Escherichia coli has arylesterase activity and shows stereospecificity for protease substrates.
Evaluation of certain food additives and contaminants. Forty-sixth report of the Joint FAO/WHO Expert Committee on Food Additives.
Electroantennogram responses ofHyles lineata (Sphingidae: Lepidoptera) to volatile compounds fromClarkia breweri (Onagraceae) and other moth-pollinated flowers.
On-Line Monitoring of the Photolysis of Benzyl Acetate and 3,5-Dimethoxybenzyl Acetate by Membrane Introduction Mass Spectrometry.
Re-evaluation of chromosomal aberration induction on nine mouse lymphoma assay "unique positive' NTP carcinogens.
Acute and long-term effects of nine chemicals on the Japanese medaka (Oryzias latipes).
Effects of gavage versus dosed feed administration on the toxicokinetics of benzyl acetate in rats and mice.
The identification of polar organic compounds found in consumer products and their toxicological properties.
Percutaneous absorption of benzyl acetate through rat skin in vitro. 3. A comparison with human skin.
Benzyl acetate: from mutagenic carcinogen to non-mutagenic non-carcinogenic in 7 years?
[Toxicologic and hygienic evaluation of benzyl acetate as an atmospheric air pollutant].
NTP Toxicology and Carcinogenesis Studies of Benzyl Acetate (CAS No. 140-11-4) in F344/N Rats and B6C3F1 Mice Feed Studies).
Automatic evaluation of antifungal volatile compounds on the basis of the dynamic growth process of a single hypha.
Perspective on the usefulness of the mouse lymphoma assay as an indicator of a genotoxic carcinogen: ten compounds which are positive in the mouse lymphoma assay but are not genotoxic carcinogens.
Percutaneous absorption of benzyl acetate through rat skin in vitro. 2. Effect of vehicle and occlusion.
Lewis cell studies to determine reactor design data for two-liquid-phase bacterial and enzymic reactions.
Evaluation of promotion of pancreatic carcinogenesis in rats by benzyl acetate.
Percutaneous absorption of benzyl acetate through rat skin in vitro. 1. Validation of an in vitro model against in vivo data.
In vivo percutaneous absorption of fragrance ingredients in rhesus monkeys and humans.
Induction of chromosome loss by mixtures of organic solvents including neurotoxins.
Age-related changes in the disposition of benzyl acetate. A model compound for glycine conjugation.
What is the proper experimental unit for long-term rodent studies? An examination of the NTP benzyl acetate study.
Measurement of unscheduled DNA synthesis and S-phase synthesis in rodent hepatocytes following in vivo treatment: testing of 24 compounds.
Responses of the L5178Y tk+/tk- mouse lymphoma cell forward mutation assay: III. 72 coded chemicals.
Perfume interactions with sodium dodecyl sulphate solutions.
[Experimental study of the toxic properties of phenylethyl alcohol and phenylethyl acetate].
Studies on benzyl acetate. III. The percutaneous absorption and disposition of [methylene-14C]benzyl acetate in the rat.
Studies on benzyl acetate. II. Use of specific metabolic inhibitors to define the pathway leading to the formation of benzylmercapturic acid in the rat.
Studies on benzyl acetate. I. Effect of dose size and vehicle on the plasma pharmacokinetics and metabolism of [methylene-14C]benzyl acetate in the rat.
[Use of orthogonal plans for the experimental analysis of the combined effects of harmful substances].
Effects of corn oil and benzyl acetate on number and size of azaserine-induced foci in the pancreas of LEW and F344 rats.
NTP Toxicology and Carcinogenesis Studies of Benzyl Acetate (CAS No. 140-11-4) in F344/N Rats and B6C3F1 Mice (Gavage Studies).
Pancreatic tumors in male rats elicited by corn oil gavage.
Benzyl acetates as attractants for the male oriental fruit fly, Dacus dorsalis, and the male melon fly, Dacus cucurbitae.
Benzyl acetate.
Benzyl acetate carcinogenicity, metabolism, and disposition in Fischer 344 rats and B6C3F1 mice.
[Toxicological and hygienic characteristics of benzyl acetate].
[Gas chromatographic determination of benzyl alcohol, benzaldehyde and benzyl acetate in the air].
Taste agnosia following gustatory neocortex ablation: dissociation from odor and generality across taste qualities.
Substituted benzyl acetates: a new class of compounds that reduce gap junctional conductance by cytoplasmic acidification.
Bioassay of compounds derived from the honeybee sting.
A chemical-modification approach to the olfactory code. Studies with a thiol-specific reagent.
The mode of binding of potential transition-state analogs to acetylcholinesterase.
Acetylcholinesterase substrates: acetoxymethylpyridines and benzyl acetate.
Formation of mercapturic acids in rats after the administration of aralkyl esters.
STUDIES ON ENZYME ACTION : XXXV. LIPASE ACTIONS OF EXTRACTS OF TISSUES OF RABBITS AT DIFFERENT AGES.

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
CHEBI:View
CHEMBL:View
KEGG (GenomeNet):C15513
HMDB (The Human Metabolome Database):HMDB31310
FooDB:FDB003367
Export Tariff Code:2915.39.1000
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
Formulations/Preparations:
free from chlorine grade which should have ester content of 97% but for which lower grade material is sometimes substituted; technical grade which is not free from chlorine & for which ester content varies considerably; "food chemicals codex".

Suppliers

Advanced Biotech Alfrebro
Allan Chemical Ambles Nature et Chimie
Anhui Haibei Augustus Oils
Aurochemicals Axxence Aromatic
Beijing Lys Chemicals Berjé
BOC Sciences LBB Specialties
Creatingperfume.com De Monchy Aromatics
Diffusions Aromatiques ECSA Chemicals
Elan Inc. EMD Millipore
Ernesto Ventós Excellentia International
ExtraSynthese Fleurchem
Foreverest Resources Fuzhou Farwell
George Uhe Company Global Essence
H. Interdonati, Inc. Hermitage Oils
Indenta Group Indukern F&F
Inoue Perfumery Jiangyin Healthway
John Kellys (London) K.L. Koh Enterprise
Keva Kingchem Laboratories
Lluch Essence M&U International
Moellhausen Naturamole
O'Laughlin Industries OQEMA
Payand Betrand PCW France
Pearlchem Corporation Pell Wall Perfumes
Penta International PerfumersWorld
Perfumery Laboratory Phoenix Aromas & Essential Oils
Primechem Prinova
Prodasynth R C Treatt & Co Ltd
Reincke & Fichtner Robertet
Santa Cruz Biotechnology Sigma-Aldrich
Silverline Chemicals SRS Aromatics
Sunaux International Symrise
TCI AMERICA The John D. Walsh Company
The Lermond Company The Perfumers Apprentice
Ungerer & Company United International
Universal Preserv-A-Chem Inc. Vigon International
Vistachem WEN International
WholeChem Zanos
Alfrebro LLC/ Archer Daniels Midland Company Augustus Oils Ltd
Global Essence Inc. Indukern, S.A. F&F Ingredients Division
Jiangyin Healthway International Trade Co., Ltd M&U International LLC
Penta International Corporation Anhui Primechem Co., Ltd.
SRS Aromatics Ltd Taytonn ASCC
Qingdao Free Trade Zone United International Co Ltd Ernesto Ventós S.A.

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 150.17709350586
Specific gravity @ 25 °C
Pounds per Gallon 8.729 to 8.812
Specific gravity @ 15 °C
Pounds per Gallon 8.83 to 8.855
Refractive Index 1.5 to 1.504 @ 20 °C
Melting Point -51 to -50°C @ 760 mm Hg
Boiling Point 212 to 215°C @ 760 mm Hg
Boiling Point 128 to 129°C @ 50 mm Hg
Acid Value 1 max KOH/g
Vapor Pressure 0.177 mmHg @ 25 °C
Flash Point TCC Value 95 °C TCC
logP (o/w) 1.96
Shelf life 24 months (or longer if stored properly.)
Storage notes Store in cool, dry place in tightly sealed containers, protected from heat and light.
Solubility
ethyl alcohol, 5 vol. of 60% alcohol Yes
fixed oils Yes
kerosene Yes
paraffin oil Yes
propylene glycol Yes
water-alcohol mixtures: 30% 1:200, 35% 1:120 40% 1:70 50% 1:20 60% 1:5 Yes
water, 3100 mg/L @ 25 °C (exp) Yes
glycerin No
Stability
non-discoloring in most media Unspecified

Organoleptic Properties

Odor Type: Floral
sweet, floral, fruity, jasmin, fresh
Odor strength medium
Substantivity 4 hour(s) at 100.00 %
Luebke, William tgsc, (1981) At 100.00 %. sweet floral fruity jasmin fresh
Mosciano, Gerard P&F 15, No. 4, 59, (1990) Sweet, fruity and floral
Flavor Type: Fruity
fruity, sweet, balsamic, jasmin, floral
Mosciano, Gerard P&F 15, No. 4, 59, (1990) At 30.00 ppm. Fruity, sweet, with balsamic and jasmin floral undernotes
Useful in: brown nuts, vanilla, fruity citrus, fruity red, fruity yellow, fruity tropical, fruity others, sweet others. Green, dry-powdery, fruity somewhat milky and estery
General comment Fruity, sweet, milk

Occurrences

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
S 02 - Keep out of the reach of children.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36/37/39 - Wear suitable clothing, gloves and eye/face protection.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Skin irritation (Category 2), H315
Eye irritation (Category 2A), H319
Specific target organ toxicity - single exposure (Category 3), Respiratory system, H335
Chronic aquatic toxicity (Category 2), H411
GHS Label elements, including precautionary statements
Pictogramexclamation-mark.jpgenvironment.jpg
Signal word Warning
Hazard statement(s)
H315 - Causes skin irritation
H319 - Causes serious eye irritation
H335 - May cause respiratory irritation
H411 - Toxic to aquatic life with long lasting effects
Precautionary statement(s)
P261 - Avoid breathing dust/fume/gas/mist/vapours/spray.
P264 - Wash hands thoroughly 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.
P302 + P352 - IF ON SKIN: wash with plenty of soap and water.
P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P312 - Call a POISON CENTER or doctor/physician if you feel unwell.
P321 - Specific treatment (see supplemental first aid instructions on this msds).
P332 + P313 - IF SKIN irritation occurs: Get medical advice/attention.
P337 + P313 - IF eye irritation persists: Get medical advice/attention.
P362 - Take off contaminated clothing and wash before reuse.
P391 - Collect spillage. Hazardous to the aquatic environment
P403 + P233 - Store in a well-ventilated place. Keep container tightly closed.
P405 - Store locked up.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Human Experience:
32 % solution: no skin irritation.
Oral/Parenteral Toxicity:
oral-rabbit LD50 2640 mg/kg
(Graham & Kuizenga, 1945)

gavage-rat LD50 [sex: M,F] 2490 mg/kg
(Jenner et al., 1964)

oral-rat LD50 3690 mg/kg
(Graham & Kuizenga, 1945)

oral-guinea pig LD50 2200 mg/kg
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 50(7), Pg. 17, 1985.

oral-rat LD50 2490 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
Food and Cosmetics Toxicology. Vol. 2, Pg. 327, 1964.

oral-rabbit LD50 2200 mg/kg
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 50(7), Pg. 17, 1985.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 11, Pg. 875, 1973.

skin-cat LDLo 10000 mg/kg
GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS BEHAVIORAL: MUSCLE WEAKNESS BEHAVIORAL: TREMOR
Journal of Pharmacology and Experimental Therapeutics. Vol. 84, Pg. 358, 1945.

subcutaneous-guinea pig LDLo 3000 mg/kg
Archiv fuer Gewerbepathologie und Gewerbehygiene. Vol. 5, Pg. 1, 1933.

subcutaneous-rabbit LDLo 4000 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Archiv fuer Gewerbepathologie und Gewerbehygiene. Vol. 5, Pg. 1, 1933.

Inhalation Toxicity:
inhalation-cat LC50 245 ppm/8H
AMA Archives of Industrial Health. Vol. 21, Pg. 28, 1960.

inhalation-human TCLo 50 ppm
BEHAVIORAL: ANTIPSYCHOTIC LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES KIDNEY, URETER, AND BLADDER: OTHER CHANGES
"Handbook of Organic Industrial Solvents," 2nd ed., Chicago, National Assoc. of Mutual Casualty Companies, 1961Vol. 2, Pg. 31, 1961.

inhalation-mouse TCLo 1300 mg/m3/22
BEHAVIORAL: GENERAL ANESTHETIC
Archiv fuer Gewerbepathologie und Gewerbehygiene. Vol. 5, Pg. 1, 1933.

Safety in use information

Category:
flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for benzyl acetate usage levels up to:
30.0000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU): 1200.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 850.00 (μg/capita/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: -22.00000
beverages(nonalcoholic): -7.80000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: -760.00000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -14.00000
fruit ices: -14.00000
gelatins / puddings: -23.00000
granulated sugar: --
gravies: --
hard candy: -34.00000
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 Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...

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

Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) on a request from the Commission related to Flavouring Group Evaluation 20 (FGE.20): Benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters from chemical group 23
View page or View pdf

Flavouring Group Evaluation 52 (FGE.52): Consideration of hydroxy- and alkoxy-substituted benzyl derivatives evaluated by JECFA (57th meeting) structurally related to benzyl alcohols, benzaldehydes, a related acetal, benzoic acids, and related esters evaluated by EFSA in FGE.20 (2005) (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf

Flavouring Group Evaluation 54 (FGE.54)[1] - Consideration of benzyl derivatives evaluated by JECFA (57th meeting) structurally related to benzyl alcohols, benzaldehydes, a related acetal, benzoic acids and related esters evaluated by EFSA in FGE.20 (2005) - 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 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 54, Revision 1 (FGE.54Rev1): Consideration of benzyl derivatives evaluated by JECFA (57th meeting) structurally related to benzyl alcohols, benzaldehydes, a related acetal, benzoic acids and related esters evaluated by EFSA in FGE.20Rev1 (2009)
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

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

EPI System: View
ClinicalTrials.gov:search
NIOSH International Chemical Safety Cards:search
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
Carcinogenic Potency Database:Search
EPA Substance Registry Services (TSCA):140-11-4
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :8785
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:1
benzyl acetate
Chemidplus:0000140114
EPA/NOAA CAMEO:hazardous materials
RTECS:140-11-4