allyl methyl trisulfide
methyl allyl trisulfide
 
Notes:
platelet aggregation inhibitor in garlic. Constit. of Allium sativum (garlic oil) and other Allium spp.
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      34135-85-8 Allyl Methyl Trisulfide
       
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      01-20500 ALLYL METHYL TRISULFIDE
       
  • Taytonn ASCC
    • Taytonn ASCC Pte Ltd
      Supplying Asia Pacific
      We fully understand the demands of the F&F industry and we endeavour to supply quality products, with ready availability and a personalised service.
      Since 2001 TAYTONN has been distributing key ingredients to the Fragrance and Flavor industry in Asia. We work closely with customers, principals and vendors. Together we forecast demand and match it with supply of aroma chemicals, essential oils and natural isolates & extracts. Sourced from around the world, our F&F ingredient inventory in Singapore is ready to ship to any location in Asia and beyond. Time and again, we help our principals introduce new discoveries to the F&F market - stimulating creativity and bringing value added proposition to our customers.
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      Allyl methyl trisulfide
       
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CAS Number: 34135-85-8Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 251-843-8
FDA UNII: 983O8ZL28A
Nikkaji Web: J132.895F
MDL: MFCD00040024
CoE Number: 11867
XlogP3-AA: 2.00 (est)
Molecular Weight: 152.30276000
Formula: C4 H8 S3
NMR Predictor: Predict (works with chrome, Edge or firefox)
Also(can) Contains: dimethyl trisulfide 10.00% to 12.00%
 diallyl trisulfide 6.00% to 8.00%
EFSA/JECFA Comments: Min. 10% dimethyl trisulfide; 68% allyl trisulfide (EFFA, 2017). More than 95% identified components
Category: flavoring agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
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JECFA Food Flavoring: 586  allyl methyl trisulfide
DG SANTE Food Flavourings: 12.045  methyl allyl trisulfide
FEMA Number: 3253 allyl methyl trisulfide
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):34135-85-8 ; ALLYL METHYL TRISULFIDE
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Physical Properties:
Appearance: yellow clear liquid (est)
Assay: 80.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.10000 to 1.16000 @  20.00 °C.
Pounds per Gallon - (est).: 9.164 to  9.664
Specific Gravity: 0.97500 to 0.98500 @  25.00 °C.
Pounds per Gallon - est.: 8.113 to 8.196
Refractive Index: 1.58000 to 1.61000 @  20.00 °C.
Refractive Index: 1.59300 to 1.60300 @  21.00 °C.
Boiling Point: 47.00 °C. @ 0.80 mm Hg
Vapor Pressure: 0.050000 mmHg @ 25.00 °C.
Flash Point: 90.00 °F. TCC ( 32.22 °C. )
logP (o/w): 2.647 (est)
Soluble in:
 alcohol
 water, slightly
 water, 353.1 mg/L @ 25 °C (est)
Insoluble in:
 water
Similar Items: note
allyl methyl tetrasulfide
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Organoleptic Properties:
 
Odor Type: sulfurous
 
 alliaceous  creamy  garlic  onion  
Odor Description:
at 0.10 % in propylene glycol. 
alliaceous creamy garlic onion
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
BOC Sciences
For experimental / research use only.
Allyl Methyl Trisulfide
DeLong Chemicals America
Allyl methyl trisulfide, Kosher
Penta International
ALLYL METHYL TRISULFIDE
Taytonn ASCC
Allyl Methyl Trisulphide
Odor: Alliaceous, Creamy, Garlic, Onion
Tengzhou Jitian Aroma Chemiclal
Methyl allyl trisulfide
WholeChem
Allyl methyl trisulfide
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Safety Information:
European information :
Most important hazard(s):
Xi - Irritant
R 10 - Flammable.
R 36/37 - Irritating to eyes and respiratory system.
S 02 - Keep out of the reach of children.
S 23 - Do not breath vapour.
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)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: flavoring agents
IFRA Purity Specification: < 0.1% free allyl alcohol
Recommendation for allyl methyl trisulfide usage levels up to:
 not for fragrance use.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.001 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.90 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 348 (μg/person/day)
Threshold of Concern:540 (μg/person/day)
Structure Class: II
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: 5
Click here to view publication 5
 average usual ppmaverage maximum ppm
baked goods: -2.00000
beverages(nonalcoholic): --
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: -2.00000
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: --
fruit ices: --
gelatins / puddings: --
granulated sugar: --
gravies: -2.00000
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: -2.00000
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: -2.00000
sugar substitutes: --
sweet sauces: --
 
Food categories according to Commission Regulation EC No. 1565/2000 (EC, 2000) in FGE.06 (EFSA, 2002a). According to the Industry the "normal" use is defined as the average of reported usages and "maximum use" is defined as the 95th percentile of reported usages (EFSA, 2002i).
Note: mg/kg = 0.001/1000 = 0.000001 = 1/1000000 = ppm.
 average usage mg/kgmaximum usage mg/kg
Dairy products, excluding products of category 02.0 (01.0): 0.600002.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): 0.040001.00000
Edible ices, including sherbet and sorbet (03.0): 0.500002.00000
Processed fruit (04.1): --
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): 0.200001.50000
Confectionery (05.0): 0.750002.00000
Chewing gum (05.0): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): 0.620001.00000
Bakery wares (07.0): 0.800002.00000
Meat and meat products, including poultry and game (08.0): 0.730001.00000
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): 0.100001.00000
Eggs and egg products (10.0): 0.080001.00000
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): 0.450001.00000
Foodstuffs intended for particular nutritional uses (13.0): --
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 0.500001.00000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 0.100002.00000
Ready-to-eat savouries (15.0): 1.100005.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): --
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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):
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
Scientific Opinion on Flavouring Group Evaluation 74, Revision 1 (FGE.74Rev1): Consideration of Simple Aliphatic Sulphides and Thiols evaluated by the JECFA (53rd and 61st meeting) Structurally related to Aliphatic and Alicyclic Mono-, Di-, Tri-, and Polysulphides with or without Additional Oxygenated Functional Groups from Chemical Group 20 evaluated by EFSA in FGE.08Rev1 (2009)
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 74, Revision 2 (FGE.74Rev2): Consideration of Simple Aliphatic Sulphides and Thiols evaluated by the JECFA (53rd and 61st meeting) Structurally related to Aliphatic and Alicyclic Mono-, Di-, Tri-, and Polysulphides with or without Additional Oxygenated Functional Groups from Chemical Group 20 evaluated by EFSA in FGE.08Rev3 (2011)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 08, Revision 4 (FGE.08Rev4): 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
Statement on List of Representative Substances for Testing. The current Statement lays down a list of substances in sub-groups with representative substances for which additional data are required prior to their evaluation through the Procedure (Regulation (EC) No 1565/2000).
View page or View pdf
EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 74, Revision 4 (FGE.74Rev4): Consideration of aliphatic sulphides and thiols evaluated by JECFA (53rd and 61st meeting) structurally related to aliphatic and alicyclic mono-, di-, tri- and polysulphides with or without additional oxygenated functional groups from chemical group 20 evaluated by EFSA in FGE.08Rev5
View page or View pdf
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Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
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EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 61926
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 1993
 3-methylsulfanyldisulfanylprop-1-ene
Chemidplus: 0034135858
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References:
 3-methylsulfanyldisulfanylprop-1-ene
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 34135-85-8
Pubchem (cid): 61926
Pubchem (sid): 135018356
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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
HMDB (The Human Metabolome Database): HMDB34416
FooDB: FDB012813
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
FAO: Allyl methyl trisulfide
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Potential Blenders and core components note
 
For Odor
alliaceous
 dimethyl trisulfideFL/FR
 dipropyl disulfideFL/FR
 ferula assa-foetida gum oilFL/FR
 garlic oil chinaFL/FR
 methyl furfuryl disulfideFL/FR
spicy
 ethyl vinyl ketoneFL/FR
 ferula assa-foetida absoluteFL/FR
2-methyl 5-(methyl thio) furanFL/FR
 methyl mercaptanFL/FR
2-(methyl thio) phenolFL/FR
 onion oilFL/FR
4-tropical oxathianeFL/FR
 
For Flavor
 
No flavor group found for these
 allyl methyl disulfideFL
 allyl propyl disulfideFL
 allyl propyl trisulfideFL
isoamyl mercaptanFL
 diethyl trisulfideFL
 dimethyl tetrasulfideFL
 dipropyl sulfideFL
 ethyl methyl trisulfideFL
 ethyl propyl disulfideFL
 ethyl propyl trisulfideFL
 furfuryl propyl disulfideFL
4-mercapto-3-methyl-2-butanolFL
 methyl butyl sulfideFL
 methyl propyl sulfideFL
S-methyl thiopropionateFL
isopropyl disulfideFL
 thiopheneFL
alliaceous
 allyl disulfideFL
 allyl mercaptanFL
 allyl thiopropionateFL
 benzyl mercaptanFL
1,3-butane dithiolFL
 cyclopentyl mercaptanFL
 dicyclohexyl disulfideFL
 dimethyl trisulfideFL/FR
 dipropyl disulfideFL/FR
 dipropyl trisulfideFL
 ferula assa-foetida gum oilFL/FR
 garlic oil chinaFL/FR
 leek oilFL
3-mercapto-2-pentanoneFL
 methyl 3-mercaptobutanoateFL
2-methyl thioacetaldehydeFL
 shallot oilFL
3-tetrahydrothiophenoneFL
 truffle sulfideFL
coffee
 methyl furfuryl disulfideFL/FR
eggy
isopropyl mercaptanFL
fruity
4-tropical oxathianeFL/FR
garlic
 allyl methyl sulfideFL
 garlic oleoresinFL
meaty
(R,S)-2-mercapto-3-butanolFL
2-methyl 3-(methyl thio) furanFL
2-(methyl thio) phenolFL/FR
bis(2-methyl-3-furyl) disulfideFL
 phenyl mercaptanFL
ortho-thiocresolFL
musty
2-methyl 5-(methyl thio) furanFL/FR
onion
 methyl propyl disulfideFL
 methyl propyl trisulfideFL
2-methyl-1,3-dithiolaneFL
roasted
 ethyl 3-(furfuryl thio) propionateFL
seafood
1,4-dithianeFL
spicy
 ethyl vinyl ketoneFL/FR
sulfurous
 allyl sulfideFL
 diallyl polysulfidesFL
 diallyl tetrasulfideFL
 diallyl trisulfideFL
S-ethyl thioacetateFL
 ferula assa-foetida absoluteFL/FR
 furfuryl methyl sulfideFL
 furfuryl thiopropionateFL
 methyl 4-(methyl thio) butyrateFL
 methyl mercaptanFL/FR
2-methyl thiopheneFL
 onion oilFL/FR
 onion oleoresinFL
 
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Potential Uses:
 coffeeFL
 fruit tropical fruitFL
 garlicFL
 onionFL
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Occurrence (nature, food, other): note
 allium rictorialis
Search Trop  Picture
 chive chinese chive
Search Trop  Picture
 garlic bulb
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 garlic fruit juice
Search Trop  Picture
 garlic oil
Search Trop  Picture
 onion victory onion
Search Trop  Picture
 rakkyo
Search Trop  PMC Picture
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Synonyms:
 allyl methyl trisulphide
1-allyl-3-methyltrisulfane
 methyl 2-propenyl trisulfide
 methyl allyl trisulfide
 methyl-2-propenyltrisulfide
1-methyl-3-(prop-2-en-1-yl)trisulfane
3-methylsulfanyldisulfanylprop-1-ene
 trisulfane, 1-methyl-3-(2-propen-1-yl)-
 trisulfide, allyl methyl
 trisulfide, methyl 2-propenyl
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Articles:
PubMed: Allyl methyl trisulfide protected against acetaminophen (paracetamol)-induced hepatotoxicity by suppressing CYP2E1 and activating Nrf2 in mouse liver
PubMed: Effects of allyl methyl trisulfide on glutathione S-transferase activity and BP-induced neoplasia in the mouse
PubMed: Characterization of Key Aroma-Active Compounds in Black Garlic by Sensory-Directed Flavor Analysis
PubMed: Antithrombotic and anticancer effects of garlic-derived sulfur compounds: a review
PubMed: Composition and immunotoxicity activity of major essential oils from stems of Allium victorialis L. var. platyphyllum Makino against Aedes aegypti L
PubMed: Identification of characteristic aroma components of Thai fried chili paste
PubMed: Diallyl trisulfide protects rats from carbon tetrachloride-induced liver injury
PubMed: Scientific Opinion on Flavouring Group Evaluation 74, Revision 4 (FGE.74Rev4): Consideration of aliphatic sulphides and thiols evaluated by JECFA (53rd and 61st meeting) structurally related to aliphatic and alicycli
PubMed: Effects of organosulfur compounds from garlic and onions on benzo[a]pyrene-induced neoplasia and glutathione S-transferase activity in the mouse
PubMed: Alkenyl group is responsible for the disruption of microtubule network formation in human colon cancer cell line HT-29 cells
PubMed: Laboratory Evaluation of Larvicidal Activity of the Essential oil of Allium tuberosum Roots and its Selected Major Constituent Compounds Against Aedes albopictus (Diptera: Culicidae)
PubMed: Laboratory Evaluation of Acute Toxicity of the Essential Oil of Allium tuberosum Leaves and Its Selected Major Constituents Against Apolygus lucorum (Hemiptera: Miridae)
PubMed: Cancer prevention by organosulfur compounds from garlic and onion
PubMed: Chemical composition, in vitro antioxidant and anti-inflammatory properties of essential oils of four dietary and medicinal plants from Cameroon
PubMed: Evaluation of acute toxicity of essential oil of garlic (Allium sativum) and its selected major constituent compounds against overwintering Cacopsylla chinensis (Hemiptera: Psyllidae)
PubMed: Thermochemical transformation of sulfur compounds in Japanese domestic Allium, Allium victorialis L
PubMed: Inhibition of carcinogenesis by some minor dietary constituents
PubMed: Enhancement by organosulfur compounds from garlic and onions of diethylnitrosamine-induced glutathione S-transferase positive foci in the rat liver
PubMed: Significant inhibition of garlic essential oilon benzo[a]pyrene formation in charcoal-grilled pork sausagesrelates to sulfide compounds
PubMed: Acaricidal effect of essential oils from Lippia graveolens (Lamiales: Verbenaceae), Rosmarinus officinalis (Lamiales: Lamiaceae), and Allium sativum (Liliales: Liliaceae) against Rhipicephalus (Boophilus) microplus (
PubMed: Inhibition of soybean lipoxygenase and mouse skin tumor promotion by onion and garlic components
PubMed: Supercritical Carbon Dioxide Extraction of Allium ursinum: Impact of Temperature and Pressure on the Extracts Chemical Profile
PubMed: Inhibitory effect of sulfur-containing compounds in Scorodocarpus borneensis Becc. on the aggregation of rabbit platelets
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