42960
Diphenyl disulfide
technical, ≥97.0% (HPLC)
Synonym(s):
Phenyl disulfide
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About This Item
Linear Formula:
C6H5SSC6H5
CAS Number:
Molecular Weight:
218.34
Beilstein:
639794
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
grade
technical
Assay
≥97.0% (HPLC)
mp
58-60 °C
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
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Other Notes
Reagent for the α-phenylsulfenylation of carbonyl compounds
This product has been replaced by 169021-ALDRICH | Phenyl disulfide 99%
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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J I Rossato et al.
Neurochemical research, 27(4), 297-303 (2002-04-18)
Ebselen (2-phenyl- 1,2-benzisoselenazole-3 (2H)-one) is a seleno-organic compound with antioxidant properties, and anti-inflammatory actions. Recently, ebselen improved the outcome of acute ischemic stroke in humans. In the present study, the potential antioxidant capacity of organochalcogenide compounds diphenyl diselenide (PhSe)2, diphenyl
Molecular modeling and enzyme kinetics indicate a novel mechanism for mammalian 5-lipoxygenase.
R W Egan et al.
Advances in prostaglandin, thromboxane, and leukotriene research, 17A, 69-74 (1987-01-01)
C W Nogueira et al.
Toxicology, 191(2-3), 169-178 (2003-09-11)
Organochalcogens are important intermediates and useful reagents in organic synthesis, which can increase human exposure risk to these chemicals in the workplace. As well, there are a number of reported cases of acute toxicity following organochalcogen ingestion of vitamins and
Y K Nakamura et al.
Mutation research, 385(1), 41-46 (1997-12-31)
S-Methyl methanethiosulfonate (MMTS) and diphenyl disulfide (DPDS) are temporary enzyme-sulfhydryl blocking agents. They are naturally occurring phytoalexin-like and synthetic substances known to be very potent bio-antimutagens in Escherichia coli B/r WP2. In the present paper, the suppressing effects of MMTS
J M Young et al.
Agents and actions, 21(3-4), 314-315 (1987-08-01)
Indomethacin was administered subcutaneously to rats, 4 mg/kg/day for 4 consecutive days in order to produce erosions of the small intestine which were scored at necropsy on day 5. Orally administered phenidone (up to 250 mg/kg/day), a mixed cycloocygenase-lipoxygenase inhibitor
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