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Details

Stereochemistry ACHIRAL
Molecular Formula C6H14S2
Molecular Weight 150.305
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROPYL DISULFIDE

SMILES

CCCSSCCC

InChI

InChIKey=ALVPFGSHPUPROW-UHFFFAOYSA-N
InChI=1S/C6H14S2/c1-3-5-7-8-6-4-2/h3-6H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C6H14S2
Molecular Weight 150.305
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Antimutagenic activity of organosulfur compounds from Allium is associated with phase II enzyme induction.
2001 Aug 22
Antifungal polysulphides from Petiveria alliacea L.
2001 Jul
Inhibition of heterocyclic aromatic amine formation in fried ground beef patties by garlic and selected garlic-related sulfur compounds.
2002 Nov
Design of heterogeneous catalysts via multiple active site positioning in organic-inorganic hybrid materials.
2003 Aug 6
Formation of aroma compounds and lipoxygenase (EC 1.13.11.12) activity in unblanched leek (Allium ampeloprasum Var. Bulga) slices during long-term frozen storage.
2003 Mar 26
Factors accounting for the variability in the behavioral response of the onion fly (Delia antiqua) to n-dipropyl disulfide.
2003 Sep
Biological activity of volatile di-n-propyl disulfide from seeds of neem, Azadirachta indica (Meliaceae), to two species of stored grain pests, Sitophilus oryzae (L.) and Tribolium castaneum (Herbst).
2004 Jun
Determination of odor active aroma compounds in freshly cut leek (Allium ampeloprasum Var. bulga) and in long-term stored frozen unblanched and blanched leek slices by gas chromatography olfactometry analysis.
2004 Mar 24
Ultrasonic cleavage of thioethers.
2005 Apr 28
Modulation of cytochrome P450 enzymes by organosulfur compounds from garlic.
2005 Dec
Antioxidative activity and ameliorative effects of memory impairment of sulfur-containing compounds in Allium species.
2006
Selective effects of diallyl disulfide, a sulfane sulfur precursor, in the liver and Ehrlich ascites tumor cells.
2007 Aug 13
Chemoprevention of aberrant crypt foci in the colon of rats by dietary onion.
2007 Jan
Protective effects of organosulfur compounds towards N-nitrosamine-induced DNA damage in the single-cell gel electrophoresis (SCGE)/HepG2 assay.
2007 Sep
Allium compounds, dipropyl and dimethyl thiosulfinates as antiproliferative and differentiating agents of human acute myeloid leukemia cell lines.
2008 Dec
Disposition and metabolism of dipropyl disulphide in vivo in rat.
2008 Jan
Organosulfur compounds alone or in combination with vitamin C protect towards N-nitrosopiperidine- and N-nitrosodibutylamine-induced oxidative DNA damage in HepG2 cells.
2008 May 9
Effects of selected organo-sulfur compounds on melanin formation.
2009 Aug 12
Antiapoptotic effects of dietary antioxidants towards N-nitrosopiperidine and N-nitrosodibutylamine-induced apoptosis in HL-60 and HepG2 cells.
2009 Jul
Chicken manure increased concentration of organic sulfur compounds in field-grown onions.
2009 Jun
Some food toxic for pets.
2009 Sep
Toxicity mechanisms of onion (Allium cepa) extracts and compounds in multidrug resistant erythroleukemic cell line.
2010
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:16:51 GMT 2023
Edited
by admin
on Fri Dec 15 19:16:51 GMT 2023
Record UNII
I7K169J70F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROPYL DISULFIDE
FHFI  
Systematic Name English
DI-N-PROPYL DISULFIDE
Common Name English
FEMA NO. 4577, DIPROPYL-
Code English
NSC-75122
Code English
N-PROPYL DISULFIDE
Common Name English
DISULFIDE, DIPROPYL
Systematic Name English
FEMA NO. 3228
Code English
PROPYL DISULFIDE [FHFI]
Common Name English
DIPROPYL DISULFIDE
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
JECFA EVALUATION PROPYL DISULFIDE
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
EPA PESTICIDE CODE 129088
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
Code System Code Type Description
MESH
C041288
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
PRIMARY
NSC
75122
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
PRIMARY
FDA UNII
I7K169J70F
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
PRIMARY
CAS
629-19-6
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
PRIMARY
ECHA (EC/EINECS)
211-079-8
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
PRIMARY
CHEBI
45758
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
PRIMARY
JECFA MONOGRAPH
1107
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
PRIMARY
PUBCHEM
12377
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
PRIMARY
EPA CompTox
DTXSID2022096
Created by admin on Fri Dec 15 19:16:51 GMT 2023 , Edited by admin on Fri Dec 15 19:16:51 GMT 2023
PRIMARY