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149225

Sigma-Aldrich

Dipropyl disulfide

98%

Sinônimo(s):

Propyl disulfide

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About This Item

Fórmula linear:
CH3CH2CH2SSCH2CH2CH3
Número CAS:
629-19-6
Peso molecular:
150.31
Beilstein:
969200
Número CE:
211-079-8
Número MDL:
MFCD00009378
Código UNSPSC:
12352100
ID de substância PubChem:
24848938
NACRES:
NA.22

Ensaio

98%

forma

liquid

índice de refração

n20/D 1.497 (lit.)

pb

195-196 °C (lit.)

pf

−86 °C (lit.)

densidade

0.96 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCCSSCCC

InChI

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

chave InChI

ALVPFGSHPUPROW-UHFFFAOYSA-N

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Descrição geral

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).

Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335,H411

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

147.2 °F - closed cup

Ponto de fulgor (°C)

64 °C - closed cup

Equipamento de proteção individual

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

Certificados de análise (COA)

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sec-Butyl sulfide 98%

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124311

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1-Benzothiophene for synthesis

Sigma-Aldrich

8.41538

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Diallyl disulfide ≥98% (HPLC)

Sigma-Aldrich

SMB00378

Diallyl disulfide

Diethyl sulfide 98%

Sigma-Aldrich

107247

Diethyl sulfide

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
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
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
D Guyonnet et al.
Mutation research, 495(1-2), 135-145 (2001-07-13)
In a previous study, we showed that naturally occurring organosulfur compounds (OSCs) from garlic and onion modulated the activation of carcinogen via the alteration of cytochromes P450. The present study was undertaken to determine the incidence of the in vivo
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