Diallyl trisulfide
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Diallyl trisulfide
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CAS No:
2050-87-5
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Formula:
C6H10S3
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Chemical Name:
Diallyl trisulfide
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Synonyms:
Trisulfide,di-2-propen-1-yl;Allyl trisulfide;Trisulfide,di-2-propenyl;Di-2-propen-1-yl trisulfide;Diallyl trisulfide;Allitridin;Allitridum;Di(2-propenyl) trisulfide;NSC 651936;Allitride;DATS
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CAS No:
Description
Diallyl Trisulfide is isolated from Garlic. Diallyl Trisulfide suppresses the growth of Penicillium expansum (MFC99 value: ≤ 90 μg/mL) and promotes apoptosis via production of reactive oxygen species (ROS) and disintegration of cellular ultrastructure. Anticancer effect[1].
Liquid|yellow liquid with disagreeable odour
Diallyl trisulfide is an organic trisulfide that is trisulfane in which both of the hydrogens are replaced by allyl groups. A component of the essential oil of garlic and a major component of the traditional Chinese medicine allitridium, it exhibits antifungal, antitumour and antioxidant activity It has a role as an apoptosis inducer, an estrogen receptor antagonist, an antineoplastic agent, a vasodilator agent, an antioxidant, an anti-inflammatory agent, an insecticide, an antiprotozoal drug, a platelet aggregation inhibitor and an antilipemic drug.
Diallyl trisulfide Basic Attributes
178.34
178.34
218-107-8
0ZO1U5A3XX
651936
DTXSID9045972
2930909090
Characteristics
75.90000
4.59
Liquid
1.1±0.1 g/cm3
60-95 °C @ Press: 12 Torr
87.8±25.2 °C
1.582
insoluble in water; slightly soluble in alcohol; miscible in oil
0.105mmHg at 25°C
Oral-Mouse LD50: 100 mg/kg
Combustible; the fire breaks down toxic sulfur oxide fumes
126.9 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]
Safety Information
III
6.1(b)
2810
3
BC6168000
Storeroom low temperature, ventilated, dry; fireproof; stored separately from oxidants
P301 + P310
H301
|Danger|H226 (98.27%): Flammable liquid and vapor [Warning Flammable liquids]|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, and P501|Aggregated GHS information provided by 1469 companies from 16 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|Warning|H302 (97.48%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 1590 companies from 2 notifications to the ECHA C&L Inventory.
Drug Information
Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues. (See all compounds classified as Antifungal Agents.)|Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)|Pesticides designed to control insects that are harmful to man. The insects may be directly harmful, as those acting as disease vectors, or indirectly harmful, as destroyers of crops, food products, or textile fabrics. (See all compounds classified as Insecticides.)|Substances that are destructive to protozoans. (See all compounds classified as Antiprotozoal Agents.)|Drugs or agents which antagonize or impair any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system. (See all compounds classified as Platelet Aggregation Inhibitors.)|Chemical substances that are destructive to spermatozoa used as topically administered vaginal contraceptives. (See all compounds classified as Spermatocidal Agents.)|Substances that lower the levels of certain LIPIDS in the BLOOD. They are used to treat HYPERLIPIDEMIAS. (See all compounds classified as Hypolipidemic Agents.)
allitridi
Diallyl trisulfide Use and Manufacturing
Diallyl Trisulfide, is an organosulfur garlic compound that induces neovasculogenesis and has preventive effects against ischemic injuries. Antiarrythmic effect.
Food additives -> Flavoring Agents|Cosmetics -> Antimicrobial
Flavoring Agents
Computed Properties
Molecular Weight:178.3
XLogP3:2.6
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:177.99446384
Monoisotopic Mass:177.99446384
Topological Polar Surface Area:75.9
Heavy Atom Count:9
Complexity:70.4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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DIALLYL MALATE Formula
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2-PROPENYL PROPYL TRISULFIDE Structure
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