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149225

Sigma-Aldrich

Dipropyl disulfide

98%

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Synonym(s):
Propyl disulfide
Linear Formula:
CH3CH2CH2SSCH2CH2CH3
CAS Number:
Molecular Weight:
150.31
Beilstein/REAXYS Number:
969200
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.497 (lit.)

bp

195-196 °C (lit.)

mp

−86 °C (lit.)

density

0.96 g/mL at 25 °C (lit.)

SMILES string

CCCSSCCC

InChI

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

InChI key

ALVPFGSHPUPROW-UHFFFAOYSA-N

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1 of 4

This Item
W322806SMB00289SMB00378
vibrant-m

149225

Dipropyl disulfide

vibrant-m

W322806

Propyl disulfide

vibrant-m

SMB00289

Diallyl trisulfide

vibrant-m

SMB00378

Diallyl disulfide

Quality Level

100

Quality Level

400

Quality Level

200

Quality Level

200

bp

195-196 °C (lit.)

bp

195-196 °C (lit.)

bp

-

bp

180-195 °C (lit.)

form

liquid

form

-

form

oil

form

oil

refractive index

n20/D 1.497 (lit.)

refractive index

n20/D 1.497 (lit.)

refractive index

-

refractive index

n20/D 1.541 (lit.)

mp

−86 °C (lit.)

mp

−86 °C (lit.)

mp

-

mp

-

General description

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).

Pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

147.2 °F

flash_point_c

64 °C

ppe

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


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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
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
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-
D Guyonnet et al.
Toxicology and applied pharmacology, 154(1), 50-58 (1999-01-12)
The naturally occurring organosulfur compounds (OSCs) diallyl sulfide (DAS), diallyl disulfide (DADS), dipropyl sulfide (DPS), and dipropyl disulfide (DPDS) were studied with respect to their effects on hepatic, intestinal, renal, and pulmonary phase II drug metabolizing enzymes, i.e., glutathione S-transferase
S K Srivastava et al.
Cancer letters, 118(1), 61-67 (1997-10-06)
The mechanism of differential efficacies of diallyl sulfide (DAS), diallyl disulfide (DADS), diallyl trisulfide (DATS), dipropyl sulfide (DPS) and dipropyl disulfide (DPDS) in preventing benzo(a)pyrene (BP)-induced cancer in mice has been investigated by determining their effects on the enzymes of

Protocols

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