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About This Item
Linear Formula:
C6H5SSC6H5
CAS Number:
Molecular Weight:
218.34
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-926-4
Beilstein/REAXYS Number:
639794
MDL number:
Assay:
99%
Form:
powder
Quality Level
assay
99%
form
powder
mp
58-60 °C (lit.)
solubility
xylene: soluble 3%, clear, colorless to yellow
functional group
disulfide
SMILES string
S(Sc1ccccc1)c2ccccc2
InChI
1S/C12H10S2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H
InChI key
GUUVPOWQJOLRAS-UHFFFAOYSA-N
General description
Phenyl disulfide is used as a precursor for the synthesis of phenyl selenosulfide (PhS-SePh), which is vital in Li-ion battery production.
Application
Phenyl disulfide is the hydrolysis product of dyfonate( insecticide). Phenyl disulfide (diphenyl disulphide) participates in hydrothiolation of alkynes via amine-mediated single electron transfer mechanism.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Articles
Explore Nicewicz Photoredox catalysts—photoexcitable acridinium salts for efficient, metal-free anti-Markovnikov hydrofunctionalizations.
Mixture is better: enhanced electrochemical performance of phenyl selenosulfide in rechargeable lithium batteries
Guo, Wei and Bhargav
Journal of the Chemical Society. Chemical Communications, 54, 8873-8876 (2018)
Identification of hydrolytic metabolites of dyfonate in alkaline aqueous solutions by using high performance liquid chromatography-UV detection and gas chromatography-mass spectrometry.
Wang T, et al.
International Journal of Environmental Analytical Chemistry, 90(12), 948-961 (2010)
S C Mitchell et al.
Drug metabolism and drug interactions, 16(3), 191-206 (2000-12-16)
Radiolabelled [UL-14C]-diphenyl sulphide, [UL-14C]-diphenyl sulphoxide and [UL-14C]-diphenyl sulphone were administered by gavage (1.0 mmol/kg body weight) to adult male Wistar rats following an overnight fast. For all compounds, faeces were the major route of excretion of radioactivity (50%). Urinary elimination
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 169021-10G | 04061838750112 |
| 169021-250G | 04061838750129 |
| 169021-50G | 04061838750136 |

