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General Material Information

Preferred name methyl salicylate
Trivial Name Methyl salicylate
Short Description benzoic acid, 2-hydroxy-, methyl ester
Formula C8 H8 O3
CAS Number 119-36-8
Deleted CAS Number 648434-07-5
FEMA Number 2745
Flavis Number 9.749
ECHA Number 204-317-7
FDA UNII LAV5U5022Y
Nikkaji Number J2.915G
Beilstein Number 0971516
MDL MFCD00002214
COE Number 433
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 899 methyl salicylate
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 119-36-8 ; METHYL SALICYLATE
Synonyms
  • benzoic acid, 2-hydroxy-, methyl ester
  • synthetic sweet birch oil
  • birch-me
  • 2-carbomethoxyphenol
  • hewedolor
  • 2-hydroxybenzoic acid methyl ester
  • o- hydroxybenzoic acid methyl ester
  • ortho- hydroxybenzoic acid methyl ester
  • linsal
  • 2-( methoxycarbonyl) phenol
  • 2-( methoxycarbonyl)phenol
  • methyl 2-hydroxybenzoate
  • methyl o-hydroxybenzoate
  • methyl ortho-hydroxybenzoate
  • methyl salicylate (+)
  • methyl salicylate BP
  • methyl salicylate extra pure
  • methyl salicylate FCC
  • methyl salicylate fractions
  • methyl salicylate low phenol
  • methyl salicylate natural
  • methyl salicylate NF FCC
  • methyl salicylate NF grade
  • methyl salicylate synthetic
  • methyl salicylate synthetic NF/FCC
  • methyl salicylate USP
  • methylsalicylate
  • metsal liniment
  • rheumabal
  • rhodiaflor
  • salicylic acid methyl ester
  • synthetic teaberry oil
  • synthetic wintergreen oil
  • Salicylic acid, methyl ester
  • o-Hydroxybenzoic acid methyl ester
  • 2-Hydroxybenzoic acid methyl ester
  • Analgit
  • Exagien
  • Flucarmit
  • 2-(Methoxycarbonyl)phenol
  • Anthrapole ND
  • Wintergreen oil
  • 2-Carbomethoxyphenol
  • NSC 8204
  • Ben Gay
  • Methyl ester of 2-hydroxy benzoic acid
  • Methyl ester 2-hydroxy benzoic acid
  • PredaLure
  • Holly oil

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

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Literature & References

methyl 2-hydroxybenzoate
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:119-36-8
Pubchem (cid):4133
Pubchem (sid):134974376
Flavornet:119-36-8
Pherobase:View
Publications by PubMed
Postharvest biology and technology of pomegranate.
Fractionation and identification of minor and aroma-active constituents in Kangra orthodox black tea.
Role of internal atmosphere on fruit ripening and storability-a review.
Inoculation of the nonlegume Capsicum annuum L. with Rhizobium strains. 2. Changes in sterols, triterpenes, fatty acids, and volatile compounds.
Efficient scavenging of β-carotene radical cations by antiinflammatory salicylates.
New chemical constituents from Oryza sativa straw and their algicidal activities against blue-green algae.
Static liquid permeation cell method for determining the migration parameters of low molecular weight organic compounds in polyethylene terephthalate.
Apple volatiles synergize the response of codling moth to pear ester.
Assessment of potential causes of falsely positive Mycobacterium tuberculosis breath test.
Profiling of volatile compounds of Phyllostachys pubescens shoots in Taiwan.
What happens if people start drinking mouthwash as surrogate alcohol? A quantitative risk assessment.
Volatiles from apple trees infested with light brown apple moth larvae attract the parasitoid Dolichogenidia tasmanica.
Hull split and damaged almond volatiles attract male and female navel orangeworm moths.
Sequence comparisons of odorant receptors among tortricid moths reveal different rates of molecular evolution among family members.
The estrogenic potential of salicylate esters and their possible risks in foods and cosmetics.
Methyl salicylate-induced arginine catabolism is associated with up-regulation of polyamine and nitric oxide levels and improves chilling tolerance in cherry tomato fruit.
Vicia faba Hypersensitivity and ASA Intolerance in a Farmer: A Case Report.
Methyl salicylate attracts natural enemies and reduces populations of soybean aphids (Hemiptera: Aphididae) in soybean agroecosystems.
Evaluation of genotype and environment effects on taste and aroma flavor components of Spanish fresh tomato varieties.
Leaf volatile emissions of Betula pendula during autumn coloration and leaf fall.
Effect of methyl salicylate-based lures on beneficial and pest arthropods in strawberry.
Efficacy and safety profile of a topical methyl salicylate and menthol patch in adult patients with mild to moderate muscle strain: a randomized, double-blind, parallel-group, placebo-controlled, multicenter study.
Levels of mint and wintergreen flavorants: smokeless tobacco products vs. confectionery products.
Elicitation of pharmacologically active substances in an intact medical plant.
Odorant receptors from the light brown apple moth (Epiphyas postvittana) recognize important volatile compounds produced by plants.
Oriented responses of grapevine moth larvae Lobesia botrana to volatiles from host plants and an artificial diet on a locomotion compensator.
Field-testing of synthetic herbivore-induced plant volatiles as attractants for beneficial insects.
Repellency of an over-the-counter essential oil product in China against workers of red imported fire ants.
The use of a semiochemical bait to enhance exposure of Amblyomma variegatum (Acari: Ixodidae) to Metarhizium anisopliae (Ascomycota: Hypocreales).
Floral attractants for the female soybean looper, Thysanoplusia orichalcea (Lepidoptera: Noctuidae).
Predatory mite attraction to herbivore-induced plant odors is not a consequence of attraction to individual herbivore-induced plant volatiles.
Fragrance material review on methyl salicylate.
First report of an attractant for a tumbling flower beetle (Coleoptera: Mordellidae).
Influence of the application of three different elicitors on soybean plants on the concentrations of several isoflavones in soybean seeds.
Antifungal activities of major tea leaf volatile constituents toward Colletorichum camelliae Massea.
Salicylate activity. 2. Potentiation of atrazine.
Salicylate activity. 1. Protection of plants from paraquat injury.
Stable isotope characterization of the ortho-oxygenated phenylpropanoids: coumarin and melilotol.
Effects of cyclamen mite (Phytonemus pallidus) and leaf beetle (Galerucella tenella) damage on volatile emission from strawberry (Fragaria x ananassa Duch.) plants and orientation of predatory mites (Neoseiulus cucumeris, N. californicus, and Euseius finlandicus).
The involvement of volatile infochemicals from spider mites and from food-plants in prey location of the generalist predatory mite Neoseiulus californicus.
Natural abundance 2H-ERETIC-NMR authentication of the origin of methyl salicylate.
Effect of volatile constituents from Securidaca longepedunculata on insect pests of stored grain.
Hydrolysis of glycosidically bound volatiles from apple leaves (Cv. Anna) by Aspergillus niger beta-glucosidase affects the behavior of codling moth (Cydia pomonella L.).
Contaminants and levels of occurrence in washed and shredded poly(ethylene terephthalate) from curbside collection. Part 1: Extraction conditions.
Ovicidal and adulticidal effects of Eugenia caryophyllata bud and leaf oil compounds on Pediculus capitis.
Aerosolized essential oils and individual natural product compounds as brown treesnake repellents.
Composition of the volatiles from intact and mechanically pierced tea aphid-tea shoot complexes and their attraction to natural enemies of the tea aphid.
Plant odor analysis of apple: antennal response of codling moth females to apple volatiles during phenological development.
Analysis of glycosidically bound aroma precursors in tea leaves. 1. Qualitative and quantitative analyses of glycosides with aglycons as aroma compounds.
(Z)-3-hexenyl and trans-linalool 3,7-oxide beta-primeverosides isolated as aroma precursors from leaves of a green tea cultivar.
Airway morphology and function of rats following dermal sensitization and respiratory challenge with low molecular weight chemicals.
Local lymph node activation and IgE responses in brown Norway and Wistar rats after dermal application of sensitizing and non-sensitizing chemicals.
Characterization of esterase and alcohol dehydrogenase activity in skin. Metabolism of retinyl palmitate to retinol (vitamin A) during percutaneous absorption.
Drugs in the food supply.
Evaluation of safety for food additives: An illustration involving the influence of methyl salicylate on rat reproduction.

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
KEGG (GenomeNet):C12305
HMDB (The Human Metabolome Database):HMDB34172
FooDB:FDB012459
YMDB (Yeast Metabolome Database):YMDB01370
Export Tariff Code:2918.23.0000
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
Formulations/Preparations:
•usp: liniment, compound: menthol 4.5 g, camphor oil rectified 25 ml, olive or peanut oil 30 ml, methyl salicylate to make 100 ml. ointment, compound: methyl salicylate 10 ml, menthol 10 g, white wax 5 g, hydrous wool fat to make 100 g. •usp: spirit, phenolated (podiatry): liquefied phenol 1 ml, methyl salicylate 3 ml, compound myrcia spirit 25 ml, alcohol rubbing compound to make 100 ml. •grades: technical; usp; fcc.

Suppliers

Achiewell Acme-Hardesty
Advanced Biotech Alfa Biotechnology
Ambles Nature et Chimie Augustus Oils
Aurochemicals Axxence Aromatic
Beijing Lys Chemicals Bell Flavors & Fragrances
Berjé BOC Sciences
Charkit Chemical Citrus and Allied Essences
Creatingperfume.com De Monchy Aromatics
ECSA Chemicals Ernesto Ventós
Excellentia International ExtraSynthese
Fleurchem Foodchem International
Foreverest Resources Frey + Lau
Fuzhou Farwell George Uhe Company
Global Essence Graham Chemical
Indenta Group Indukern F&F
John Kellys (London) K.L. Koh Enterprise
Keva Kraft Chemical
Lluch Essence M&U International
Moellhausen Northwestern Extract
OQEMA Pearlchem Corporation
Pell Wall Perfumes Penta International
PerfumersWorld Perfumery Laboratory
Phoenix Aromas & Essential Oils Prinova
Prodasynth R C Treatt & Co Ltd
Reincke & Fichtner Robertet
Sigma-Aldrich SRS Aromatics
Sunaux International SysKem Chemie
TCI AMERICA The John D. Walsh Company
The Lermond Company The Perfumers Apprentice
Ungerer & Company United International
Vigon International WEN International
Advanced Biotech. Inc. Augustus Oils Ltd
Axxence Aromatic GmbH Beijing Lys Chemicals Co, LTD.
Berje Inc. Charkit Chemical Corporation
Fleurchem, Inc. Foreverest Resources Ltd.
Global Essence Inc. Indukern, S.A. F&F Ingredients Division
Lluch Essence S.L. M&U International LLC
Moellhausen S.P.A. Penta International Corporation
PerfumersWorld Ltd. Robertet, Inc.
SRS Aromatics Ltd The John D. Walsh Company, Inc
R C Treatt and Co Ltd Qingdao Free Trade Zone United International Co Ltd
Ernesto Ventós S.A.

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 152.14935302734
Specific gravity @ 25 °C
Pounds per Gallon 9.819 to 9.86
Refractive Index 1.535 to 1.538 @ 20 °C
Melting Point -8 to -7°C @ 760 mm Hg
Boiling Point 222 to 224°C @ 760 mm Hg
Boiling Point 132 to 133°C @ 50 mm Hg
Acid Value 1 max KOH/g
Vapor Pressure 0.0343 mmHg @ 25 °C
Vapor Density 5.26
Flash Point TCC Value 96 °C TCC
logP (o/w) 2.55
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
alcohol Yes
dipropylene glycol Yes
kerosene Yes
paraffin oil Yes
water, 700 mg/L @ 30 °C (exp) Yes
water No
Stability
non-discoloring in most media Unspecified

Organoleptic Properties

Odor Type: Minty
wintergreen, minty, sweet, root beer, aromatic, phenolic, camphoreous
Odor strength medium , recommend smelling in a 10.00 % solution or less
Substantivity 8 hour(s) at 100.00 %
Luebke, William tgsc, (1983) At 10.00 % in dipropylene glycol. wintergreen mint
Mosciano, Gerard P&F 20, No. 6, 49, (1995) Sweet, salicylate, root beer, wintergreen, aromatic, slightly phenolic and camphoreous
Flavor Type: Minty
sweet, wintergreen, root beer, aromatic, balsamic
Mosciano, Gerard P&F 20, No. 6, 49, (1995) At 10.00 ppm. Sweet, salicylate and root beer with aromatic and balsamic nuances
General comment Sweet, wintergreen

Occurrences

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 22 - Harmful if swallowed.
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 37/39 - Wear suitable gloves and eye/face protection.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Acute toxicity, Oral (Category 4), H302
Acute aquatic toxicity (Category 3), H402
GHS Label elements, including precautionary statements
Pictogramexclamation-mark.jpg
Signal word Warning
Hazard statement(s)
H302 - Harmful if swallowed
H402 - Harmful to aquatic life
Precautionary statement(s)
P264 - Wash skin thouroughly after handling.
P270 - Do not eat, drink or smoke when using this product.
P273 - Avoid release to the environment.
P301 + P312 - IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P330 - Rinse mouth.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Human Experience:
8 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
gavage-mouse LD50 [sex: M] 1390 mg/kg
(Ohsumi et al., 1984)

gavage-rat LD50 1250 mg/kg
(Giroux et al., 1954b)

oral-rat LD50 [sex: M,F] M:3049.00 F:2642 mg/kg
(Givaudan Corporation, 1982)

gavage-rat LD50 [sex: M,F] 887 mg/kg
(Jenner et al., 1964)

oral-rat LD50 1220 mg/kg
(Nivikov et al., 1994)

oral-mouse LD50 [sex: M] 1110 mg/kg
(Davison et al., 1961)

gavage-guinea pig LD50 [sex: M,F] 1060 mg/kg
(Jenner et al., 1964)

gavage-mouse LD50 [sex: M,F] 1440 mg/kg
(NTP, 1984a)

oral-woman LDLo 355 mg/kg
LUNGS, THORAX, OR RESPIRATION: RESPIRATORY STIMULATION GASTROINTESTINAL: NAUSEA OR VOMITING BEHAVIORAL: COMA
American Journal of the Medical Sciences. Vol. 193, Pg. 772, 1937.

oral-rat LD50 887 mg/kg
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
Food and Cosmetics Toxicology. Vol. 2, Pg. 327, 1964.

oral-rabbit LD50 1300 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 821, 1978.

oral-mouse LD50 1110 mg/kg
Journal of Pharmacology and Experimental Therapeutics. Vol. 132, Pg. 207, 1961.

unreported-man LDLo 522 mg/kg
"Poisoning; Toxicology, Symptoms, Treatments," 2nd ed., Arena, J.M., Springfield, IL, C.C. Thomas, 1970Vol. 2, Pg. 73, 1970.

oral-man LDLo 1329 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: COMA BLOOD: HEMORRHAGE
Clinical Toxicology. Vol. 6, Pg. 189, 1973.

oral-man LDLo 101 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD GASTROINTESTINAL: NAUSEA OR VOMITING
American Journal of the Medical Sciences. Vol. 193, Pg. 772, 1937.

oral-human LDLo 506 mg/kg
"Merck Index; an Encyclopedia of Chemicals, Drugs, and Biologicals", 11th ed., Rahway, NJ 07065, Merck & Co., Inc. 1989Vol. 11, Pg. 961, 1989.

oral-guinea pig LD50 700 mg/kg
"Industrial Hygiene and Toxicology," 2nd ed., Patty, F.A., ed., New York, John Wiley & Sons, Inc., 1958-63Vol. 2, Pg. 1897, 1963.

oral-dog LD50 2100 mg/kg
GASTROINTESTINAL: NAUSEA OR VOMITING GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA" LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES
Food and Cosmetics Toxicology. Vol. 16, Pg. 821, 1978.

oral-child LDLo 700 mg/kg
BEHAVIORAL: GENERAL ANESTHETIC PERIPHERAL NERVE AND SENSATION: FLACCID PARALYSIS WITHOUT ANESTHESIA (USUALLY NEUROMUSCULAR BLOCKAGE) LUNGS, THORAX, OR RESPIRATION: DYSPNEA
Archives of Disease in Childhood. Vol. 28, Pg. 475, 1953.

oral-child LDLo 228 mg/kg
GASTROINTESTINAL: NAUSEA OR VOMITING LUNGS, THORAX, OR RESPIRATION: DYSPNEA
American Journal of Diseases of Children. Vol. 69, Pg. 37, 1945.

Dermal Toxicity:
subcutaneous-dog LDLo 2250 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 821, 1978.

subcutaneous-guinea pig LDLo 1500 mg/kg
FAO Nutrition Meetings Report Series. Vol. 44A, Pg. 63, 1967.

subcutaneous-rabbit LDLo 4250 mg/kg
Food and Cosmetics Toxicology. Vol. 16, Pg. 821, 1978.

Inhalation Toxicity:
Not determined

Safety in use information

Category:
cosmetic, 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
maximum skin levels for fine fragrances:
0.2900 % and are based on the assumption that the fragrance mixture is used at 20% in a consumer product (IFRA Use Level Survey).(IFRA, 2002)
Recommendation for methyl salicylate usage levels up to:
10.0000 % in the fragrance concentrate.
use level in formulae for use in cosmetics:
0.1300 %
Dermal Systemic Exposure in Cosmetic Products:
0.0034 mg/kg/day (IFRA, 2002)
Maximised Survey-derived Daily Intakes (MSDI-EU): 410.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 44000.00 (μg/capita/day)
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3
Click here to view publication 3
average usual ppmaverage maximum ppm
baked goods: -54.00000
beverages(nonalcoholic): -59.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: -8400.00000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -27.00000
fruit ices: -27.00000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -840.00000
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 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

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
Daily Med:search
NIOSH International Chemical Safety Cards:search
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):119-36-8
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :4133
National Institute of Allergy and Infectious Diseases:Data
WISER:UN 3082
WGK Germany:1
methyl 2-hydroxybenzoate
Chemidplus:0000119368
EPA/NOAA CAMEO:hazardous materials
RTECS:119-36-8