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品質等級
化驗
99%
形狀
powder
mp
58-60 °C (lit.)
溶解度
xylene: soluble 3%, clear, colorless to yellow
官能基
disulfide
SMILES 字串
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 密鑰
GUUVPOWQJOLRAS-UHFFFAOYSA-N
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一般說明
二苯二硫醚被用作合成苯基硒硫化物(PhS-SePh)的前体,而PhS-SePh在锂离子电池的生产中起着重要的作用。
應用
苯基二硫化物是 dyfonate(杀虫剂)的水解产物 。苯基二硫化物(二苯基二硫化物)通过胺介导的单电子转移机制参与炔烃的加氢硫醚化反应 。
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Identification of hydrolytic metabolites of dyfonate in alkaline aqueous solutions by using high performance liquid chromatography-UV detection and gas chromatography-mass spectrometry.
International Journal of Environmental Analytical Chemistry, 90(12), 948-961 (2010)
Organic letters, 11(15), 3298-3301 (2009-09-02)
Hydrothiolation of alkynes proceeds with diphenyl disulfide and tripropylamine. Amine-mediated single electron transfer to diphenyl disulfide can be proposed for the reaction mechanism. Applications of the method to radical cyclizations of eneyne compounds are also presented.
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
Mutation research, 393(3), 307-316 (1997-12-11)
The suppressive effect of S-methyl methanethiosulfonate (MMTS) on aflatoxin B1 (AFB1)- or methyl methanesulfonate (MMS)-induced chromosome aberrations (CA) in rat bone marrow cells was studied. MMTS significantly suppressed CA induced by both AFB1 (an indirect-acting carcinogen) and MMS (a direct-acting
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
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