Category: flavor and fragrance agents
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
Appearance: | pale yellow clear oily liquid (est) |
Assay: | 97.00 to 100.00 %
|
Food Chemicals Codex Listed: | No |
Specific Gravity: | 1.19500 to 1.21000 @ 25.00 °C.
|
Pounds per Gallon - (est).: | 9.944 to 10.068
|
Refractive Index: | 1.59500 to 1.60500 @ 20.00 °C.
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Melting Point: | -68.00 °C. @ 760.00 mm Hg
|
Boiling Point: | 165.00 to 170.00 °C. @ 760.00 mm Hg
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Boiling Point: | 41.00 °C. @ 6.00 mm Hg
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Vapor Pressure: | 1.068000 mmHg @ 25.00 °C. (est) |
Vapor Density: | 4.3 ( Air = 1 ) |
Flash Point: | 125.00 °F. TCC ( 51.67 °C. )
|
logP (o/w): | 1.926 (est) |
Soluble in: |
| alcohol | | oils | | propylene glycol | | water, 2390 mg/L @ 25 °C (est) |
Insoluble in: |
| water |
Organoleptic Properties:
|
Odor Type: alliaceous |
|
| sulfurous onion cooked onion savory meaty |
Odor Description: at 0.10 % in propylene glycol. | sulfurous cooked onion savory meaty |
|
| sulfurous alliaceous cooked savory meaty eggy vegetable fresh onion green onion |
Odor Description:
| Sulfureous, alliaceous, cooked, savory, meaty, eggy and vegetative with a fresh, green, onion topnote Mosciano, Gerard P&F 20, No. 5, 49, (1995) |
|
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Flavor Type: alliaceous |
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| sulfurous alliaceous gassy savory meaty fresh vegetable |
Taste Description: at 2.00 ppm. | Sulfureous, alliaceous, gassy, savory and meaty with a fresh, vegetative nuance Mosciano, Gerard P&F 20, No. 5, 49, (1995) |
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Odor and/or flavor descriptions from others (if found). |
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Cosmetic Information:
Suppliers:
Ambles Nature et Chimie |
DIMETHYL TRISULFIDE
|
Beijing Lys Chemicals |
Dimethyl trisulfide
|
BOC Sciences |
For experimental / research use only. |
Dimethyltrisulfide 98%
|
Charkit Chemical |
DIMETHYL TRISULPHIDE FEMA 3275
|
DeLong Chemicals America |
Dimethyl trisulfide, Kosher
|
Endeavour Specialty Chemicals |
Dimethyl trisulphide 98% F&F
|
Speciality Chemical Product Groups |
Frutarom |
DIMETHYL TRISULPHIDE
KOSHER Flavor: Alliaceous, Onion, Savory, Meaty |
H. Interdonati, Inc. |
Dimethyl trisulfide Kosher
|
Featured Products |
IFF |
DIMETHYL TRISULPHIDE
KOSHER Flavor: Alliaceous, Onion, Savory, Meaty |
Jinan Enlighten Chemical Technology(Wutong Aroma ) |
Dimethyl trisulfide, Kosherk
|
Lluch Essence |
DIMETHYL TRISULFIDE
|
M&U International |
DIMETHYL TRISULFIDE, Kosher
|
Natural Advantage |
Dimethyl Trisulfide Nat
Flavor: alliaceous, garlic, meaty |
Riverside Aromatics LTD.is the exclusive distributor for Europe in UK for any non-US based inquiries |
Penta International |
DIMETHYL TRISULFIDE NATURAL 1% IN PROPYLENE GLYCOL
|
Penta International |
DIMETHYL TRISULFIDE NATURAL
|
Penta International |
DIMETHYL TRISULFIDE
|
R C Treatt & Co Ltd |
Dimethyl trisulphide
Halal, Kosher |
Riverside Aromatics |
DIMETHYL TRISULPHIDE NATURAL
|
Robinson Brothers |
Dimethyl trisulphide F&F
|
https://www.robinsonbrothers.uk/chemistry-competences |
Santa Cruz Biotechnology |
For experimental / research use only. |
Dimethyl Trisulfide
|
Shijiazhuang Donglian Nankai Aroma Chemicals |
Dimethyl Trisulfide
Odor: Meat, onion and vegetables |
Sigma-Aldrich |
Dimethyl trisulfide, ≥98%, FG
Odor: meaty; alliaceous (onion, garlic). |
Certified Food Grade Products |
Sunaux International |
Dimethyl Trisulfide
|
TCI AMERICA |
For experimental / research use only. |
Dimethyl Trisulfide >98.0%(GC)
|
Tengzhou Jitian Aroma Chemiclal |
Dimethyl Trisulfide
|
Tianjin Danjun International |
Dimethyl trisulfide
|
United International |
Dimethyl Trisulfide
|
WholeChem |
Dimethyl trisulfide
|
Safety Information:
Preferred SDS: View |
European information : |
Most important hazard(s): | Xi - Irritant |
R 10 - Flammable. 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.
|
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Hazards identification |
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Classification of the substance or mixture |
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
None found. |
GHS Label elements, including precautionary statements |
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Pictogram | |
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Hazard statement(s) |
None found. |
Precautionary statement(s) |
None found. |
Oral/Parenteral Toxicity: |
Not determined
|
Dermal Toxicity: |
Not determined
|
Inhalation Toxicity: |
Not determined
|
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 |
|
Maximised Survey-derived Daily Intakes (MSDI-EU): | 7.83 (μg/capita/day) |
Maximised Survey-derived Daily Intakes (MSDI-USA): | 0.02 (μg/capita/day) |
Modified Theoretical Added Maximum Daily Intake (mTAMDI): | 348 (μg/person/day) |
Threshold of Concern: | 1800 (μg/person/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: 5 |
Click here to view publication 5 |
| average usual ppm | average maximum ppm |
baked goods: | - | 1.00000 |
beverages(nonalcoholic): | - | - |
beverages(alcoholic): | - | - |
breakfast cereal: | - | - |
cheese: | - | - |
chewing gum: | - | - |
condiments / relishes: | - | 1.00000 |
confectionery froastings: | - | - |
egg products: | - | - |
fats / oils: | - | - |
fish products: | - | - |
frozen dairy: | - | - |
fruit ices: | - | - |
gelatins / puddings: | - | - |
granulated sugar: | - | - |
gravies: | - | 1.00000 |
hard candy: | - | - |
imitation dairy: | - | - |
instant coffee / tea: | - | - |
jams / jellies: | - | - |
meat products: | - | 1.00000 |
milk products: | - | - |
nut products: | - | - |
other grains: | - | - |
poultry: | - | - |
processed fruits: | - | - |
processed vegetables: | - | - |
reconstituted vegetables: | - | - |
seasonings / flavors: | - | - |
snack foods: | - | - |
soft candy: | - | - |
soups: | - | 1.00000 |
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/kg | maximum usage mg/kg |
Dairy products, excluding products of category 02.0 (01.0): | 0.60000 | 2.00000 |
Fats and oils, and fat emulsions (type water-in-oil) (02.0): | 0.04000 | 1.00000 |
Edible ices, including sherbet and sorbet (03.0): | 0.50000 | 2.00000 |
Processed fruit (04.1): | - | - |
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): | 0.20000 | 1.50000 |
Confectionery (05.0): | 0.75000 | 2.00000 |
Chewing gum (05.0): | - | - |
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): | 0.62000 | 1.00000 |
Bakery wares (07.0): | 0.80000 | 2.00000 |
Meat and meat products, including poultry and game (08.0): | 0.73000 | 1.00000 |
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): | 0.10000 | 1.00000 |
Eggs and egg products (10.0): | 0.08000 | 1.00000 |
Sweeteners, including honey (11.0): | - | - |
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): | 0.45000 | 1.00000 |
Foodstuffs intended for particular nutritional uses (13.0): | - | - |
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): | 0.50000 | 1.00000 |
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): | 0.10000 | 2.00000 |
Ready-to-eat savouries (15.0): | 1.10000 | 5.00000 |
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): | - | - |
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 |
Scientific Opinion on the safety and efficacy of aliphatic and aromatic mono- and di-thiols and mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups (chemical group 20) when used as flavourings for all animal species 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 |
EPI System: | View |
AIDS Citations: | Search |
Cancer Citations: | Search |
Toxicology Citations: | Search |
EPA Substance Registry Services (TSCA): | 3658-80-8 |
EPA ACToR: | Toxicology Data |
EPA Substance Registry Services (SRS): | Registry |
Laboratory Chemical Safety Summary : | 19310 |
National Institute of Allergy and Infectious Diseases: | Data |
WISER: | UN 1993 |
WGK Germany: | 3 |
| methylsulfanyldisulfanylmethane |
Chemidplus: | 0003658808 |
References:
Other Information:
Potential Blenders and core components note
|
For Odor |
No odor group found for these |
| satinaldehyde | FL/FR |
| dipropyl disulfide | FL/FR |
| ferula assa-foetida gum oil | FL/FR |
| methyl furfuryl disulfide | FL/FR |
citrus |
| grapefruit mercaptan | FL/FR |
coffee |
| coffee difuran | FL/FR |
2- | methyl-3-,5 or 6-(furfuryl thio) pyrazine | FL/FR |
ethereal |
| propylene glycol dibenzoate | CS |
floral |
| cyclamen aldehyde | FL/FR |
| cyclamen propanal | FR |
6,8- | dimethyl-2-nonanol | FR |
| hyacinth acetals | FL/FR |
| leerall | FR |
| ocean propanal | FL/FR |
herbal |
2- | cyclohexyl cyclohexanone | FR |
meaty |
| meaty dithiane | FL/FR |
4- | methyl nonanoic acid | FL/FR |
moldy |
| strawberry furanone methyl ether | FL/FR |
savory |
laevo- | methionyl glycine | |
sulfurous |
| allium fistulosum oil | |
| allium ursinum extract | CS |
| benzothiazole | FL/FR |
| buchu mercaptan | FL/FR |
| dimethyl sulfide | FL/FR |
| fish thiol | FL/FR |
| furfuryl thioacetate | FL/FR |
2- | mercaptopropionic acid | FL/FR |
2- | methyl 5-(methyl thio) furan | FL/FR |
| methyl mercaptan | FL/FR |
3-( | methyl thio) hexanol | FL/FR |
4- | methyl-1,3-dithiolane | |
| onion oil | FL/FR |
|
For Flavor |
|
No flavor group found for these |
| allium fistulosum oil | |
| allyl methyl disulfide | FL |
| allyl methyl trisulfide | FL |
| allyl propyl trisulfide | FL |
| benzyl methyl sulfide | FL |
| ethyl propyl trisulfide | FL |
| furfuryl propyl disulfide | FL |
| heptyl mercaptan | FL |
4- | mercapto-3-methyl-2-butanol | FL |
laevo- | methionyl glycine | |
| methyl dihydrofuran thiol | FL |
2-( | methyl thio) methyl-2-butenal | FL |
S- | methyl thiopropionate | FL |
2- | methyl-3-,5 or 6-(furfuryl thio) pyrazine | FL/FR |
1,9- | nonane dithiol | FL |
1,1- | propane dithiol | FL |
iso | propyl disulfide | FL |
| thiophene | FL |
2,3,5- | trithiahexane | FL |
alliaceous |
| allyl mercaptan | FL |
| allyl thiopropionate | FL |
1,3- | butane dithiol | FL |
| cyclopentyl mercaptan | FL |
| dicyclohexyl disulfide | FL |
| dipropyl disulfide | FL/FR |
| dipropyl trisulfide | FL |
| ferula assa-foetida gum oil | FL/FR |
| leek oil | FL |
3- | mercapto-2-methyl pentanol | FL |
3- | mercapto-2-pentanone | FL |
| shallot oil | FL |
3- | tetrahydrothiophenone | FL |
| truffle sulfide | FL |
ammoniacal |
| pyrrolidine | FL |
aromatic |
| hyacinth acetals | FL/FR |
citrus |
| grapefruit mercaptan | FL/FR |
coffee |
| coffee difuran | FL/FR |
| methyl furfuryl disulfide | FL/FR |
corn chip |
2- | acetyl-2-thiazoline | FL |
eggy |
iso | propyl mercaptan | FL |
fatty |
4- | methyl nonanoic acid | FL/FR |
2,4- | octadien-1-ol | FL |
fishy |
4,5- | dimethyl thiazole | FL |
floral |
| ocean propanal | FL/FR |
| satinaldehyde | FL/FR |
garlic |
| allyl methyl sulfide | FL |
green |
| cyclamen aldehyde | FL/FR |
4- | methyl thiazole | FL |
meaty |
| benzothiazole | FL/FR |
2,6- | dimethyl thiophenol | FL |
| meaty dithiane | FL/FR |
3- | mercapto-2-butanone | FL |
(R,S)-2- | mercapto-3-butanol | FL |
2- | mercaptopropionic acid | FL/FR |
2- | methyl 3-(methyl thio) furan | FL |
bis(2- | methyl-3-furyl) disulfide | FL |
2- | methyl-3-tetrahydrofuran thiol | FL |
| pyrazinyl ethane thiol | FL |
ortho- | thiocresol | FL |
metallic |
2,5- | dihydroxy-1,4-dithiane | FL |
3-( | methyl thio) hexanol | FL/FR |
moldy |
| strawberry furanone methyl ether | FL/FR |
musty |
2- | methyl 5-(methyl thio) furan | FL/FR |
nutty |
| nutty thiazole | FL |
onion |
| furfuryl isopropyl sulfide | FL |
| methionol | FL |
| methyl propyl disulfide | FL |
| methyl propyl trisulfide | FL |
4- | methyl-1,3-dithiolane | |
2- | methyl-1,3-dithiolane | FL |
| propyl thioacetate | FL |
roasted |
| ethyl 3-(furfuryl thio) propionate | FL |
| furfuryl thioacetate | FL/FR |
sulfurous |
| allyl sulfide | FL |
| buchu mercaptan | FL/FR |
| butyl mercaptan | FL |
| dimethyl sulfide | FL/FR |
| fish thiol | FL/FR |
| furfuryl thiopropionate | FL |
3- | mercapto-2-methyl pentanal | FL |
| methyl 2-methyl-3-furyl disulfide | FL |
| methyl mercaptan | FL/FR |
2- | methyl thiophene | FL |
3- | methyl-2-butane thiol | FL |
| onion oil | FL/FR |
|
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
1,3- | dimethyl trisulfane | | dimethyl trisulfide natural | | dimethyl trisulphide | | dimethyltrisulfane | | methyl trisulfide | | methyl trithiomethane | | methylsulfanyldisulfanylmethane | | methyltrithiomethane | | trisulfane, 1,3-dimethyl- | | trisulfane, dimethyl- | | trisulfide, dimethyl | 2,3,4- | trithiapentane |
Articles:
Info: | DIMETHYL DISULFIDE |
PubMed: | Characteristic Odorants from Bailingu Oyster Mushroom (Pleurotus eryngii var. tuoliensis) and Summer Oyster Mushroom (Pleurotus cystidiosus). |
PubMed: | The effect of acidification of liquid whey protein concentrate on the flavor of spray-dried powder. |
PubMed: | Statistical analysis of sake-preparation conditions and dimethyl trisulfide formation. |
PubMed: | Characterization of odor-active compounds in sweet-type Chinese rice wine by aroma extract dilution analysis with special emphasis on sotolon. |
PubMed: | Off-flavor compounds from decaying cyanobacterial blooms of Lake Taihu. |
PubMed: | Characterization of the key aroma compounds in rape honey by means of the molecular sensory science concept. |
PubMed: | Analysis of organic volatile flavor compounds in fermented stinky tofu using SPME with different fiber coatings. |
PubMed: | Effect of liquid retentate storage on flavor of spray-dried whey protein concentrate and isolate. |
PubMed: | Identification of odorous compounds in reclaimed water using FPA combined with sensory GC-MS. |
PubMed: | Heterologous production of methionine-gamma-lyase from Brevibacterium linens in Lactococcus lactis and formation of volatile sulfur compounds. |
PubMed: | Effect of cold storage and packaging material on the major aroma components of sweet cream butter. |
PubMed: | Identification of sulfur volatiles in canned orange juices lacking orange flavor. |
PubMed: | Short communication: empirical and mechanistic evidence for the role of pyridoxal-5'-phosphate in the generation of methanethiol from methionine. |
PubMed: | Identification of the key aroma compounds in cocoa powder based on molecular sensory correlations. |
PubMed: | YtjE from Lactococcus lactis IL1403 Is a C-S lyase with alpha, gamma-elimination activity toward methionine. |
PubMed: | Sensitivity to allyl isothiocyanate, dimethyl trisulfide, sinigrin, and cooked cauliflower consumption. |
PubMed: | Comparison of volatiles of cultured and wild sea bream (Sparus aurata) during storage in ice by dynamic headspace analysis/gas chromatography-mass spectrometry. |
PubMed: | Production of volatile organic sulfur compounds (VOSCs) by basidiomycetous yeasts. |
PubMed: | Aroma extract dilution analysis of Cv. Marion (Rubus spp. hyb) and Cv. Evergreen (R. laciniatus L.) blackberries. |
PubMed: | Flavor-active compounds potentially implicated in cooked cauliflower acceptance. |
PubMed: | Effect of cultivar and storage time on the volatile flavor components of baked potato. |
PubMed: | How low pH can intensify beta-damascenone and dimethyl trisulfide production through beer aging. |
PubMed: | Volatile flavor components of stored nonfat dry milk. |
PubMed: | Volatile components of the cyanobacterium Oscillatoria perornata (Skuja). |
PubMed: | Change in the flavor of black tea drink during heat processing. |
PubMed: | Effect of various dairy packaging materials on the headspace analysis of ultrapasteurized milk. |
PubMed: | 3-methylthiopropionaldehyde as precursor of dimethyl trisulfide in aged beers. |
PubMed: | Diversity of sulfur compound production in lactic acid bacteria. |
PubMed: | Volatile flavor components of rice cakes. |
PubMed: | The effect of acidification of liquid whey protein concentrate on the flavor of spray-dried powder. |
PubMed: | Generation of aroma compounds in a fermented sausage meat model system by Debaryomyces hansenii strains. |
PubMed: | Evaluation of the volatile composition and sensory properties of five species of microalgae. |
PubMed: | Characterization of odor-active compounds in sweet-type Chinese rice wine by aroma extract dilution analysis with special emphasis on sotolon. |
PubMed: | Determination of compounds responsible for tempeh aroma. |
PubMed: | Salt reduction in slow fermented sausages affects the generation of aroma active compounds. |
PubMed: | Novel approach for the determination of volatile compounds in processed onion by headspace gas chromatography-mass spectrometry (HS GC-MS). |
PubMed: | Decaying mouse volatiles perceived by Calliphora vicina Rob.-Desv. |
PubMed: | Characterization of the key odorants in raw Italian hazelnuts ( Corylus avellana L. var. Tonda Romana) and roasted hazelnut paste by means of molecular sensory science. |
PubMed: | Analysis of organic volatile flavor compounds in fermented stinky tofu using SPME with different fiber coatings. |
PubMed: | Effect of liquid retentate storage on flavor of spray-dried whey protein concentrate and isolate. |
PubMed: | Headspace volatiles along with other instrumental and sensory analyses as indices of maturation of horse mackerel miso. |
PubMed: | Chemical characterization of commercial Sherry vinegar aroma by headspace solid-phase microextraction and gas chromatography-olfactometry. |
PubMed: | Impact of the synbiotic combination of Lactobacillus casei shirota and oligofructose-enriched inulin on the fecal volatile metabolite profile in healthy subjects. |
PubMed: | Contribution of 1,2-dihydroxy-5-(methylsulfinyl)pentan-3-one (DMTS-P1) to the formation of dimethyl trisulfide (DMTS) during the storage of Japanese sake. |
PubMed: | Heterologous production of methionine-gamma-lyase from Brevibacterium linens in Lactococcus lactis and formation of volatile sulfur compounds. |
PubMed: | Screening and identification of precursor compounds of dimethyl trisulfide (DMTS) in Japanese sake. |
PubMed: | Effect of electron-beam irradiation before and after cooking on the chemical properties of beef, pork, and chicken. |
PubMed: | Sulfur volatiles in guava (Psidium guajava L.) leaves: possible defense mechanism. |
PubMed: | Coffee roasting and aroma formation: application of different time-temperature conditions. |
PubMed: | The effect of cysteine on production of volatile sulphur compounds by cheese-ripening bacteria. |
PubMed: | Effect of cold storage and packaging material on the major aroma components of sweet cream butter. |
PubMed: | Identification of sulfur volatiles in canned orange juices lacking orange flavor. |
PubMed: | Identification of the key aroma compounds in cocoa powder based on molecular sensory correlations. |
PubMed: | Sensitivity to allyl isothiocyanate, dimethyl trisulfide, sinigrin, and cooked cauliflower consumption. |
PubMed: | Sensitive quantification of sulfur compounds in wine by headspace solid-phase microextraction technique. |
PubMed: | Changes in the aroma compounds of sake during aging. |
PubMed: | Comparison of volatiles of cultured and wild sea bream (Sparus aurata) during storage in ice by dynamic headspace analysis/gas chromatography-mass spectrometry. |
PubMed: | Volatile sulfur compounds in Cheddar cheese determined by headspace solid-phase microextraction and gas chromatograph-pulsed flame photometric detection. |
PubMed: | Inhibitory activity of essential oils of garlic and onion against bacteria and yeasts. |
PubMed: | Automated dynamic headspace/GC-MS analyses affect the repeatability of volatiles in irradiated Turkey. |
PubMed: | Influence of temperature, modified atmosphere packaging, and heat treatment on aroma compounds in broccoli. |
PubMed: | Aroma extract dilution analysis of Cv. Marion (Rubus spp. hyb) and Cv. Evergreen (R. laciniatus L.) blackberries. |
PubMed: | How low pH can intensify beta-damascenone and dimethyl trisulfide production through beer aging. |
PubMed: | Identification of distinctive volatile compounds in fish sauce. |
PubMed: | Volatile components of the cyanobacterium Oscillatoria perornata (Skuja). |
PubMed: | Diversity of sulfur compound production in lactic acid bacteria. |
PubMed: | Volatile flavor components of rice cakes. |
PubMed: | Antimicrobial activity of sulfur compounds derived from cabbage. |
PubMed: | Volatile compounds produced in sterile fish muscle (Sebastes melanops) by Pseudomonas putrefaciens, Pseudomonas fluorescens, and an Achromobacter species. |
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