2-methyl thioacetaldehyde
2-methylthioacetaldehyde
 
Notes:
Flavouring ingredient
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      Product(s):
      23328-62-3 2-Methylthioacetaldehyde
       
  • M&U International
    • M&U International LLC
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      A0308 2-METHYL THIOACETALDEHYDE, Kosher
       
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      13-69350 2-METHYLTHIOACETALDEHYDE
      13-69355 2-METHYLTHIOACETALDEHDYE SYNTHETIC 1% IN ETOH
       
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      W1449 2-methyl thioacetaldehyde
       
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      2-Methylthioacetaldehyde
       
Synonyms   Articles   Notes   Search
CAS Number: 23328-62-3Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 245-587-6
FDA UNII: F0NVN68DIT
Nikkaji Web: J228.930J
MDL: MFCD02824035
CoE Number: 11686
XlogP3-AA: 0.40 (est)
Molecular Weight: 90.14502000
Formula: C3 H6 O S
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: flavoring agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
JECFA Food Flavoring: 465  2-methylthioacetaldehyde
DG SANTE Food Flavourings: 12.040  2-methyl thioacetaldehyde
FEMA Number: 3206 2-methylthioacetaldehyde
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):23328-62-3 ; 2-METHYLTHIOACETALDEHYDE
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Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 99.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.04500 to 1.05500 @  25.00 °C.
Pounds per Gallon - (est).: 8.695 to  8.779
Refractive Index: 1.46600 @  20.00 °C.
Boiling Point: 118.00 to  120.00 °C. @ 760.00 mm Hg
Vapor Pressure: 14.900000 mmHg @ 25.00 °C. (est)
Flash Point: 87.00 °F. TCC ( 30.56 °C. )
logP (o/w): 0.489 (est)
Soluble in:
 alcohol
 water, 1.454e+005 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 alkalis
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Organoleptic Properties:
 
Odor Type: sulfurous
 
 sulfurous  vegetable  onion  garlic  mustard  nutty  potato  
Odor Description:
at 0.10 % in propylene glycol. 
sulfurous vegetable onion garlic mustard nutty potato
 
 sulfurous  vegetable  onion  garlic  mustard  nutty  potato  
Odor Description:
Sulfureous, vegatative, onion, garlic, mustard and nutty with a potato nuance
Mosciano, Gerard P&F 20, No. 5, 49, (1995)
 
 
Flavor Type: alliaceous
 
 alliaceous  vegetable  onion  garlic  potato  bready  
Taste Description:
at 25.00 ppm.  
Alliaceous and vegetative with a good mouthfeel and onion and garlic-like with a potato and bready nuance
Mosciano, Gerard P&F 20, No. 5, 49, (1995)
 
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.
2-Methylthioacetaldehyde
Carbosynth
For experimental / research use only.
2-Methylthioacetaldehyde
DeLong Chemicals America
2-Methylthioacetaldehyde, Kosher
M&U International
2-METHYL THIOACETALDEHYDE, Kosher
Parchem
2-methyl thioacetaldehyde
Penta International
2-METHYLTHIOACETALDEHDYE SYNTHETIC 1% IN ETOH
Penta International
2-METHYLTHIOACETALDEHYDE
Synerzine
2-methyl thioacetaldehyde
Tengzhou Jitian Aroma Chemiclal
2-Methylthio acetaldehyde
WholeChem
2-Methylthioacetaldehyde
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Safety Information:
 
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
Recommendation for 2-methyl thioacetaldehyde usage levels up to:
 not for fragrance use.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): ND (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: 4
Click here to view publication 4
 average usual ppmaverage maximum ppm
baked goods: -0.50000
beverages(nonalcoholic): -0.50000
beverages(alcoholic): --
breakfast cereal: -0.50000
cheese: --
chewing gum: -0.50000
condiments / relishes: -0.50000
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -0.50000
fruit ices: -0.50000
gelatins / puddings: -0.50000
granulated sugar: --
gravies: -0.50000
hard candy: -0.50000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: -0.50000
milk products: -0.50000
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: -0.50000
sugar substitutes: --
sweet sauces: --
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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 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 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
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 23328-62-3
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 10887828
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 2-methylsulfanylacetaldehyde
Chemidplus: 0023328623
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References:
 2-methylsulfanylacetaldehyde
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 23328-62-3
Pubchem (cid): 10887828
Pubchem (sid): 135263575
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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): HMDB31718
FooDB: FDB008381
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
FAO: 2-Methylthioacetaldehyde
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Potential Blenders and core components note
 
For Odor
alliaceous
 dibutyl sulfideFL/FR
 methyl furfuryl disulfideFL/FR
citrus
 grapefruit mercaptanFL/FR
fermented
 ethyl (E)-2-crotonateFL/FR
spicy
 ethyl vinyl ketoneFL/FR
 dimethyl disulfideFL/FR
 dimethyl sulfideFL/FR
 ethyl 2-mercaptopropionateFL/FR
 ethyl methyl mercaptopropionateFL/FR
 ferula assa-foetida absoluteFL/FR
 methyl 3-(methyl thio) propionateFL/FR
2-methyl 5-(methyl thio) furanFL/FR
3-(methyl thio) hexanolFL/FR
2-(methyl thio) phenolFL/FR
 onion oilFL/FR
4-tropical oxathianeFL/FR
vegetable
1-furfuryl pyrroleFL/FR
 methionalFL/FR
 
For Flavor
 
No flavor group found for these
 allyl methyl trisulfideFL
 allyl propyl trisulfideFL
isobutyl mercaptanFL
 diethyl trisulfideFL
 diisopropyl sulfideFL
 diisopropyl trisulfideFL
 dipropyl sulfideFL
 ethyl isothiocyanateFL
3-ethyl thiopropanolFL
2-heptane thiolFL
 heptyl mercaptanFL
 methyl butyl sulfideFL
 methyl isothiocyanateFL
3-methyl mercaptopropyl amineFL
4-(methyl thio) butanolFL
2-methyl-5-methoxythiazoleFL
4-pentenyl isothiocyanateFL
2,3,5-trithiahexaneFL
alliaceous
 allyl disulfideFL
 allyl mercaptanFL
 allyl thiopropionateFL
 benzyl mercaptanFL
1,3-butane dithiolFL
 cyclopentyl mercaptanFL
 diethyl disulfideFL
3-mercapto-2-methyl pentanolFL
isopropyl isothiocyanateFL
3-tetrahydrothiophenoneFL
 truffle sulfideFL
buttery
 butter onion garlic flavorFL
citrus
 grapefruit mercaptanFL/FR
coffee
 methyl furfuryl disulfideFL/FR
fruity
4-tropical oxathianeFL/FR
garlic
 allyl methyl sulfideFL
 garlic oleoresinFL
green
 dibutyl sulfideFL/FR
 horseradish oilFL
malty
 yeast thiazolineFL
meaty
(R,S)-2-mercapto-3-butanolFL
2-(methyl thio) phenolFL/FR
bis(2-methyl-3-furyl) disulfideFL
ortho-thiocresolFL
metallic
3-(methyl thio) hexanolFL/FR
musty
 ethyl (E)-2-crotonateFL/FR
2-methyl 5-(methyl thio) furanFL/FR
onion
 ethyl 2-mercaptopropionateFL/FR
 methionolFL
 methyl propyl disulfideFL
 methyl propyl trisulfideFL
 propyl thioacetateFL
roasted
 ethyl 3-(furfuryl thio) propionateFL
seafood
1,4-dithianeFL
spicy
 ethyl vinyl ketoneFL/FR
sulfurous
 allyl sulfideFL
 butyl mercaptanFL
 diallyl polysulfidesFL
 diallyl tetrasulfideFL
 dimethyl disulfideFL/FR
 dimethyl sulfideFL/FR
 ethyl methyl mercaptopropionateFL/FR
 ethyl methyl sulfideFL
S-ethyl thioacetateFL
 ferula assa-foetida absoluteFL/FR
 furfuryl methyl sulfideFL
 furfuryl thiopropionateFL
3-mercapto-2-methyl pentanalFL
 methyl 2-(methyl thio) butyrateFL
 methyl 2-methyl-3-furyl disulfideFL
 methyl 4-(methyl thio) butyrateFL
 methyl thiomethyl butyrateFL
 onion oilFL/FR
 potato butanoneFL
tomato
 methionalFL/FR
vegetable
1-furfuryl pyrroleFL/FR
 methyl 3-(methyl thio) propionateFL/FR
 radish isothiocyanateFL
 
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Potential Uses:
 breadFL
 coffeeFL
 horseradishFL
 mustardFL
 nutFL
 potatoFL
 radishFL
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Occurrence (nature, food, other): note
 bean
Search  PMC Picture
 coffee
Search  PMC Picture
 potato chip
Search  PMC Picture
 tomato
Search Trop  Picture
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Synonyms:
 acetaldehyde, 2-(methylthio)-
(methyl mercapto) acetaldehyde
2-(methyl mercapto) acetaldehyde
 methyl mercaptoacetaldehyde
(methyl thio) acetaldehyde
2-(methyl thio) acetaldehyde
(methylmercapto)acetaldehyde
2-(methylmercapto)acetaldehyde
(methylsulfanyl)acetaldehyde
2-methylsulfanylacetaldehyde
(methylthio)acetaldehyde
2-(methylthio)acetaldehyde
2-methylthioacetaldehyde
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