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Diallyl disulfide information


Diallyl disulfide
Diallyl disulfide
Names
Preferred IUPAC name
3-[(Prop-2-en-1-yl)disulfanyl]prop-1-ene
Other names
Diallyl disulfide
Garlicin
1,2-Diallyldisulfane (not recommended)
4,5-Dithia-1,7-octadiene
Identifiers
CAS Number
  • 2179-57-9 checkY
3D model (JSmol)
  • Interactive image
Beilstein Reference
1699241
ChEBI
  • CHEBI:4488 checkY
ChEMBL
  • ChEMBL366603 checkY
ChemSpider
  • 15730 checkY
ECHA InfoCard 100.016.862 Edit this at Wikidata
EC Number
  • 218-548-6
Gmelin Reference
217847
KEGG
  • C08369 checkY
PubChem CID
  • 16590
UNII
  • 5HI47O6OA7 checkY
CompTox Dashboard (EPA)
  • DTXSID9035206 Edit this at Wikidata
InChI
  • InChI=1S/C6H10S2/c1-3-5-7-8-6-4-2/h3-4H,1-2,5-6H2 checkY
    Key: PFRGXCVKLLPLIP-UHFFFAOYSA-N checkY
  • InChI=1/C6H10S2/c1-3-5-7-8-6-4-2/h3-4H,1-2,5-6H2
    Key: PFRGXCVKLLPLIP-UHFFFAOYAX
SMILES
  • S(SC\C=C)C\C=C
Properties
Chemical formula
C6H10S2
Molar mass 146.28 g/mol
Appearance yellowish clear liquid with an intense garlic smell[1]
Density 1.01 g/cm3[2]
Boiling point 180 °C (356 °F; 453 K)
Solubility in water
soluble in ethanol and oils[1]
Hazards
GHS labelling:
Pictograms
GHS02: FlammableGHS06: ToxicGHS07: Exclamation mark
Signal word
Danger
Hazard statements
H226, H301, H315, H317, H319
Precautionary statements
P210, P233, P240, P241, P242, P243, P261, P264, P270, P272, P280, P301+P310, P302+P352, P303+P361+P353, P305+P351+P338, P321, P330, P332+P313, P333+P313, P337+P313, P362, P363, P370+P378, P403+P235, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Diallyl disulfide (DADS or 4,5-dithia-1,7-octadiene) is an organosulfur compound derived from garlic and a few other genus Allium plants.[3] Along with diallyl trisulfide and diallyl tetrasulfide, it is one of the principal components of the distilled oil of garlic. It is a yellowish liquid which is insoluble in water and has a strong garlic odour. It is produced during the decomposition of allicin, which is released upon crushing garlic and other plants of the family Alliaceae. Diallyl disulfide has many of the health benefits of garlic, but it is also an allergen causing garlic allergy. Highly diluted, it is used as a flavoring in food. It decomposes in the human body into other compounds such as allyl methyl sulfide.

  1. ^ a b allyl disulfide
  2. ^ Diallyl disulfide at Sigma Aldrich
  3. ^ Block, Eric (2010). Garlic and Other Alliums: The Lore and the Science. Royal Society of Chemistry. ISBN 9780854041909.[page needed]

and 29 Related for: Diallyl disulfide information

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Diallyl disulfide

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Diallyl disulfide (DADS or 4,5-dithia-1,7-octadiene) is an organosulfur compound derived from garlic and a few other genus Allium plants. Along with diallyl...

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Diallyl trisulfide

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several compounds produced by hydrolysis of allicin, including diallyl disulfide and diallyl tetrasulfide; DATS is one of the most potent.[clarification...

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Allicin

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changes into a series of other sulfur-containing compounds such as diallyl disulfide. Allicin is an antifeedant, i.e. the defense mechanism against attacks...

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Alliin

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and form a number of other compounds, such as diallyl sulfide (DAS), diallyl disulfide (DADS) and diallyl trisulfide (DAT), dithiins and ajoene. Garlic...

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Capsaicin

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Cuminaldehyde (cumin) Curcumin (turmeric) Dehydroligustilide (celery) Diallyl disulfide Dicentrine (Lindera spp.) Farnesyl thiosalicylic acid Formalin Gingerols...

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Garlic oil

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containing the oil. Garlic oil contains volatile sulfur compounds such as diallyl disulfide, a 60% constituent of the oil. Steam-distilled garlic oil typically...

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Garlic

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its spiciness. Allicin, along with its decomposition products diallyl disulfide and diallyl trisulfide, are major contributors to the characteristic odor...

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Nicotinamide

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Belinostat Butyric acid (butyrate) Capsaicin Citarinostat Curcumin Diallyl disulfide Entinostat Fimepinostat Givinostat Indole-3-carbinol Kevetrin Martinostat...

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Curcumin

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Rosemary

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Phytochemical

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Isothiocyanate Nitriles Thiocyanates Organosulfides Sulfides Polysulfides Diallyl disulfide Indoles Indole-3-carbinol 3,3'-Diindolylmethane Allicin Alliin Allyl...

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Thyme

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Turmeric

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List of phytochemicals in food

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methyl trisulfide garlic, onions, leeks, chives, shallots. Sulfides Diallyl disulfide garlic, onions, leeks, chives, shallots. Allicin garlic. Alliin garlic...

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Garlic allergy

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cause of the latter is the chemical diallyl disulfide (DADS), together with related compounds allyl propyl disulfide and allicin. These chemicals occur...

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Stevia rebaudiana

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Clove

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Mustard plant

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Clotrimazole

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Mentha

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Paracetamol

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Wasabi

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Sulfur

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syn-propanethial-S-oxide responsible of lacrymal irritation (onions), or diallyl disulfide and allicin (garlic). Sulfates, commonly found in soils and groundwaters...

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Ketone bodies

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Belinostat Butyric acid (butyrate) Capsaicin Citarinostat Curcumin Diallyl disulfide Entinostat Fimepinostat Givinostat Indole-3-carbinol Kevetrin Martinostat...

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Nicotine

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Cannabidiol

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Hydrogen peroxide

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indicative of particularly strong hydrogen bonding. Diphosphane and hydrogen disulfide exhibit only weak hydrogen bonding and have little chemical similarity...

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Steviol glycoside

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Cannabis

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