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317691

Sigma-Aldrich

Allyl disulfide

technical grade, 80%

Sinônimo(s):

Diallyl disulfide

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About This Item

Fórmula linear:
CH2=CHCH2SSCH2CH=CH2
Número CAS:
2179-57-9
Peso molecular:
146.27
Beilstein:
1699241
Número CE:
218-548-6
Número MDL:
MFCD00008656
Código UNSPSC:
12352100
ID de substância PubChem:
24859096
NACRES:
NA.22

grau

technical grade

Nível de qualidade

100

densidade de vapor

>5 (vs air)

pressão de vapor

1 mmHg ( 20 °C)

Ensaio

80%

Formulário

liquid

índice de refração

n20/D 1.541 (lit.)

p.e.

180-195 °C (lit.)

densidade

1.008 g/mL at 25 °C (lit.)

grupo funcional

disulfide

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

C=CCSSCC=C

InChI

1S/C6H10S2/c1-3-5-7-8-6-4-2/h3-4H,1-2,5-6H2

chave InChI

PFRGXCVKLLPLIP-UHFFFAOYSA-N

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Ações bioquímicas/fisiológicas

Organosulfur compound that is naturally found in garlic. Contributes to the pungent odor of crushed garlic. Anticancer agent and may provide protection against cardiovascular disease.

Outras notas

Remainder other allyl sulfides

Pictogramas

Skull and crossbones
GHS06

Palavra indicadora

Danger

Frases de perigo

H301,H315,H319,H335

Classificações de perigo

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

143.6 °F - closed cup

Ponto de fulgor (°C)

62 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
SHBL9118
SHBL9119
MKCF8258
MKCB4951
MKBW2934V

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Nathaniel Edward Bennett Saidu et al.
Bioorganic & medicinal chemistry, 20(4), 1584-1593 (2012-01-24)
Coumarins and coumarin derivatives as well as diallyl polysulfides are well known as anticancer drugs. In order to find new drugs with anticancer activities, we combined coumarins with polysulfides in the form of di-coumarin polysulfides. These novel compounds were tested
Hailin Tang et al.
Cancer letters, 340(1), 72-81 (2013-07-16)
The purpose of this study was to identify a mechanism related to miRNA pathway which plays a role in the anti-tumor effects of Diallyl disulfide. Alterations in miRNA expression were observed in Diallyl disulfide-treated MGC-803 cells, including up-regulation of miR-200b
Hye Young Park et al.
Toxicology and applied pharmacology, 262(2), 177-184 (2012-05-09)
Diallyl disulfide (DADS), a main organosulfur component responsible for the diverse biological effects of garlic, displays a wide variety of internal biological activities. However, the cellular and molecular mechanisms underlying DADS' anti-inflammatory activity remain poorly understood. In this study, therefore
R Arunkumar et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 19(10), 912-923 (2012-06-29)
Diallyl Disulfide (DADS) is one of the major components of garlic, which inhibits the proliferation of various cancer cells. Our previous studies showed that DADS inhibits cell growth and induces apoptosis on prostate cancer cells. Insulin like growth factor signaling
Fenja Klevenhusena et al.
Archives of animal nutrition, 65(4), 255-266 (2011-09-06)
Currently research on feed supplementation with natural compounds to improve energy and protein utilisation and to mitigate the greenhouse gas methane in ruminants is intensively pursued. Two compounds, diallyl disulphide (DADS), an important component of garlic oil, and lovastatin, an
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