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149225

Sigma-Aldrich

Dipropyldisulfid

98%

Synonym(e):

Propyldisulfid

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About This Item

Lineare Formel:
CH3CH2CH2SSCH2CH2CH3
CAS-Nummer:
629-19-6
Molekulargewicht:
150.31
Beilstein:
969200
EG-Nummer:
211-079-8
MDL-Nummer:
MFCD00009378
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24848938
NACRES:
NA.22

Qualitätsniveau

100

Assay

98%

Form

liquid

Brechungsindex

n20/D 1.497 (lit.)

bp

195-196 °C (lit.)

mp (Schmelzpunkt)

−86 °C (lit.)

Dichte

0.96 g/mL at 25 °C (lit.)

Funktionelle Gruppe

disulfide

SMILES String

CCCSSCCC

InChI

1S/C6H14S2/c1-3-5-7-8-6-4-2/h3-6H2,1-2H3

InChIKey

ALVPFGSHPUPROW-UHFFFAOYSA-N

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Allgemeine Beschreibung

Dipropyl disulfide (DPDS) was an efficient scavenger of reactive oxygen species (ROS) at a lower concentration in both HL-60 and HepG2 cells. It prevents the oxidative DNA damage caused by N-nitrosopiperidine (NPIP) and N-nitrosodibutylamine (NDBA).

Piktogramme

Exclamation markEnvironment
GHS07,GHS09

Signalwort

Warning

Gefahreneinstufungen

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

147.2 °F - closed cup

Flammpunkt (°C)

64 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
SHBL5904
422793/1
06819HE
13108EQ
10130PO

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Sigma-Aldrich

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Sigma-Aldrich

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1-Benzothiophene for synthesis

Sigma-Aldrich

8.41538

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Diallyldisulfid ≥98% (HPLC)

Sigma-Aldrich

SMB00378

Diallyldisulfid

Diethylsulfid 98%

Sigma-Aldrich

107247

Diethylsulfid

Opender Koul
Journal of economic entomology, 97(3), 1142-1147 (2004-07-29)
Head space volatiles, including 73% di-n-propyl disulfide, were collected from freshly crushed neem seeds. This compound along with previously reported diallyl disulfide (di-2-propenyl disulfide) were toxic when applied topically or as a fumigant to Tribolium castaneum adults and 8-, 12-
Han-Seung Shin et al.
Journal of agricultural and food chemistry, 50(26), 7684-7690 (2002-12-12)
Organosulfur compounds and sodium bisulfite significantly inhibited (P < 0.05) heterocyclic aromatic amine (HAA) formation in model systems containing phenylalanine, creatinine, and glucose. There was, however, no inhibition by the same compounds in a model system containing only phenylalanine and
C Teyssier et al.
Drug metabolism and disposition: the biological fate of chemicals, 28(6), 648-654 (2000-05-23)
The metabolism of dipropyl disulfide (DPDS), an Allium sulfur compound, was investigated in rat liver cell subfractions and in an isolated perfused rat liver. DPDS is oxidized to dipropyl thiosulfinate (DPDSO) by rat microsomes. The contribution of cytochrome P450 enzymes
C Dwivedi et al.
Anti-cancer drugs, 9(3), 291-294 (1998-06-13)
Clinical efficacy of doxorubicin is compromised due to free radical generation leading to cardiac toxicity. Oil-soluble organosulfur compounds, diallyl sulfide (DAS), diallyl disulfide (DADS), dipropyl sulfide (DPS) and dipropyl disulfide (DPDS), present in garlic were examined for their antiperoxidant effects.
S V Singh et al.
Biochemical and biophysical research communications, 244(3), 917-920 (1998-04-16)
This study was undertaken to elucidate the mechanism of organ specificity and differential efficacy of garlic organosulfides (OSCs) [diallyl sulfide (DAS), diallyl disulfide (DADS), diallyl trisulfide (DATS), dipropyl sulfide (DPS) and dipropyl disulfide (DPDS)] in preventing benzo(a)pyrene (BP)-induced tumorigenesis in
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