15575-30-1

Basic information

• Product Name: Bis(diethylamino) persulfide
• Synonyms: Bis(diethylamino) persulfide;N,N'-Dithiobis(diethylamine)
• CAS NO: 15575-30-1
• Molecular Formula: C₈H₂₀N₂S₂
• Molecular Weight: 208.39
• Mol File: 15575-30-1.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Bis(diethylamino) persulfide(CAS DataBase Reference)
• NIST Chemistry Reference: Bis(diethylamino) persulfide(15575-30-1)
• EPA Substance Registry System: Bis(diethylamino) persulfide(15575-30-1)

Safety Data

• Hazardous Substances Data: 15575-30-1(Hazardous Substances Data)

Upstream product

• 109-89-7 diethylamine 
• 71-43-2 benzene 
• 10025-67-9 disulfur dichloride 
• 76328-13-7 dibutoxyphosphinothioyl diethylamino trisulfide 
• 42169-95-9 μ-tetrasulfido-1,2-dithio-diphosphoric acid tetra-O-butyl ester 

Downstream Products

• 7783-06-4 hydrogen sulfide 
• 19833-78-4 di-ethylamine hydroiodide 
• 109-89-7 diethylamine 

Relevant articles and documents

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Synthesis and antimicrobial activities of structurally novel S,S′-bis(heterosubstituted) disulfides

The central focus of this study is on the antibacterial and antifungal properties of synthetically produced S,S′-bis(heterosubstituted) disulfides as a means to control the growth of various infection-causing pathogens. Staphylococcus aureus, Francisella tularensis and Candida albicans were each found to be highly susceptible to several of these compounds by agar or broth dilution and Kirby-Bauer diffusion assays. These structurally simple, low molecular weight disulfides have shown promising bioactivities and may serve as leads to the development of effective new antibacterials for pathogenic bacteria such as methicillin-resistant S. aureus and F. tularensis.

Design, synthesis, and insecticidal activities of new N-benzoyl-N'-phenyl- N'-sulfenylureas

Aseries of new N'-alkylaminothio,N'-arylaminothio (or dithio), and N',N'-thio (or dithio) derivatives ofN'-benzoyl-N'-phenylureas were designed and synthesized as insect-growth regulators with sulfur dichloride or disulfur dichloride as the original reactant. The new compounds were identified by 1H nuclear magnetic resonancee (NMR) spectroscopy, elemental analysis [or high-resolution mass spectrometry (HRMS)], and single-crystal X-ray diffraction analysis. The X-ray results demonstrated that there exist N-S-N or N-S-S-N bonds in these new compounds. In comparison to the parent N-benzoyl-N'-phenylureas, these derivatives displayed better solubility. The insecticidal activities of the target compounds were evaluated. The results of bioassays showed that compounds 1-24 retained the larvicidal activities of the corresponding benzoylphenylureas (BPUs) and some compounds exhibited better larvicidal activities against oriental armyworm and mosquitoes than the parent BPUs. The larvicidal activities of the selected target compounds 1 and 24 against diamondback moth were better than that of the corresponding parent compounds E and triflumuron.

Method of treating a disease condition caused or exacerbated by an HPV

The invention provides agents and compounds (see (I) and (II)) for use in the treatment or prophylaxis of disease conditions caused or exacerbated by mammalian papillomaviruses, such as human papillomaviruses, as well as methods for the treatment or prevention thereof. In said formulae, R1–R4 and n are as defined herein.