Diallyldisulfide CAS#2179-57-9
CAS Number: 2179-57-9
Chemical Formula:C6H10S2
Synonyms:
Disulfide, di-2-propenyl
ALLYL DISULFIDE 80+%
DIALLYL DISULPHIDE 90%(GC)
Appearance:colorless to yellow oil
HS Code: 29309090
MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)
Products Description of Diallyldisulfide CAS#2179-57-9
A colorless to pale yellow liquid with a strong garlic-like odor, it is one of the main components of sulfur-containing compounds in plants of the Liliaceae family such as garlic and onion. Containing sulfide ether bonds (-S-S-), it has reducing properties, is prone to oxidation in the air, and may decompose to produce sulfides at high temperatures.
Parameters
Boiling point | 180-195 °C(lit.) |
density | 1.008 g/mL at 25 °C(lit.) |
vapor density | >5 (vs air) |
vapor pressure | 1 mm Hg ( 20 °C) |
FEMA | 2028 | ALLYL DISULFIDE |
refractive index | n |
Fp | 144 °F |
storage temp. | 2-8°C |
Water Solubility | Insoluble in water |
solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. |
form | oil |
color | colorless to yellow |
Odor | Diallyl disulfide is an essential odor component of garlic oil. |
Odor Threshold | 0.00022ppm |
Odor Type | alliaceous |
biological source | synthetic |
JECFA Number | 572 |
BRN | 1699241 |
InChIKey | PFRGXCVKLLPLIP-UHFFFAOYSA-N |
LogP | 3.26 |
CAS DataBase Reference | 2179-57-9(CAS DataBase Reference) |
NIST Chemistry Reference | Diallyl disulphide(2179-57-9) |
EPA Substance Registry System | Diallyl disulfide (2179-57-9) |
Safety Information
Hazard Codes | Xn,Xi |
Risk Statements | 22-36/37/38-10 |
Safety Statements | 26-36/37/39-37/39-16-36 |
RIDADR | UN 2810 6.1/PG 3 |
WGK Germany | 3 |
RTECS | BB1000000 |
F | 13 |
TSCA | Yes |
HazardClass | 6.1 |
PackingGroup | II |
HS Code | 29309090 |
Hazardous Substances Data | 2179-57-9(Hazardous Substances Data) |
Product Application of Diallyldisulfide CAS#2179-57-9
Diallyldisulfide has a range of uses varying from a Cytocrome P450 inhibitor to vasorelaxant and hypotensive. Being in the class of organosulfur compounds, it carries chemopreventive characteristics .
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