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Details

Stereochemistry ACHIRAL
Molecular Formula C14H14S2
Molecular Weight 246.391
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZYL DISULFIDE

SMILES

C(SSCC1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=GVPWHKZIJBODOX-UHFFFAOYSA-N
InChI=1S/C14H14S2/c1-3-7-13(8-4-1)11-15-16-12-14-9-5-2-6-10-14/h1-10H,11-12H2

HIDE SMILES / InChI
Molecular Formula C14H14S2
Molecular Weight 246.391
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Functional groups and sulfur K-edge XANES spectra: divalent sulfur and disulfides.
2010-09-09
Acaricidal activity of extracts from Petiveria alliacea (Phytolaccaceae) against the cattle tick, Rhipicephalus (Boophilus) microplus (Acari: ixodidae).
2010-03-25
A fragment-based approach to probing adenosine recognition sites by using dynamic combinatorial chemistry.
2009-11-23
Antioxidant activity of the new thiosulfinate derivative, S-benzyl phenylmethanethiosulfinate, from Petiveria alliacea L.
2008-03-21
Patch testing with components of water-based metalworking fluids: results of a multicentre study with a second series.
2006-12
Antibacterial and antifungal activity of sulfur-containing compounds from Petiveria alliacea L.
2006-03-08
Aromatic derivatives and tellurium analogues of cyclic seleninate esters and spirodioxyselenuranes that act as glutathione peroxidase mimetics.
2005-11-11
Synthesis of radioiodine labeled dibenzyl disulfide for evaluation of tumor cell uptake.
2004-03-01
Diselenides and allyl selenides as glutathione peroxidase mimetics. Remarkable activity of cyclic seleninates produced in situ by the oxidation of allyl omega-hydroxyalkyl selenides.
2003-11-05
Comparative haemolytic activity of bis(phenylmethyl) disulphide, bis(phenylethyl) disulphide and bis(phenylpropyl) disulphide in rats.
2003-11
Antifungal polysulphides from Petiveria alliacea L.
2001-07
Sulfur compounds reduce potato toxins during extrusion cooking.
2001-06
Fungal cleavage of thioether bond found in Yperite.
1997-07-28
Evaluation of selected chemotypes in coupled cellular and molecular target-based screens identifies novel HIV-1 zinc finger inhibitors.
1996-09-13
Patents

Patents

04720498
1
05708008
8
07691882
5
08507530
5
JPH01180821A
1
JPS5634736A
1
JPS5898398A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:27:24 GMT 2025
Edited
by admin
on Mon Mar 31 19:27:24 GMT 2025
Record UNII
BG7680605N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIBENZYL DISULFIDE
MI  
Preferred Name English
BENZYL DISULFIDE
FHFI   USP-RS  
Systematic Name English
FEMA NO. 3617
Code English
1,4-DIPHENYL-2,3-DITHIABUTANE
Systematic Name English
NSC-6841
Code English
.ALPHA.-(BENZYLDITHIO)TOLUENE
Systematic Name English
BENZYL DISULFIDE [FHFI]
Common Name English
DIBENZYL DISULFIDE [MI]
Common Name English
DISULFIDE, DIBENZYL
Systematic Name English
NSC-677465
Code English
DAILUBE S 700
Common Name English
BENZYL DISULFIDE [USP-RS]
Common Name English
DISULFIDE, BIS(PHENYLMETHYL)
Systematic Name English
DI(PHENYLMETHYL)DISULFIDE
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION BENZYL DISULFIDE
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
Code System Code Type Description
PUBCHEM
9012
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
CAS
150-60-7
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
NSC
6841
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
CHEBI
72752
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
JECFA MONOGRAPH
149
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
NSC
677465
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
MERCK INDEX
m4288
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
205-764-0
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
RS_ITEM_NUM
1062020
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
FDA UNII
BG7680605N
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
EPA CompTox
DTXSID6059738
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
MESH
C492349
Created by admin on Mon Mar 31 19:27:24 GMT 2025 , Edited by admin on Mon Mar 31 19:27:24 GMT 2025
PRIMARY
NIH
NCATS
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