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シグナルワード
Danger
危険有害性情報
危険有害性の分類
Eye Dam. 1 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 3
ターゲットの組織
Respiratory system
保管分類コード
4.1B - Flammable solid hazardous materials
WGK
nwg
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
dust mask type N95 (US), Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
適用法令
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Jan Code
263257-VAR:
263257-1G:
263257-5G:
263257-BULK:
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Biochemical Society transactions, 40(6), 1330-1335 (2012-11-28)
Electrochemical communication between micro-organisms and electrodes is the integral and fundamental part of BESs (bioelectrochemical systems). The immobilization of bacterial cells on the electrode and ensuring efficient electron transfer to the electrode via a mediator are decisive features of mediated
Chemical Society reviews, 40(1), 114-128 (2010-11-05)
Numerous synthetic protocols for producing syn-diols from the corresponding alkenes have been developed and published over recent years. It is the intent of the following tutorial review to present a concise summary of the main methods used to prepare syn-diol
Chemical communications (Cambridge, England), 48(82), 10183-10185 (2012-09-13)
Using the well-known exoelectrogen Shewanella oneidensis MR-1, an osmium redox polymer modified anode exhibited ca. 4-fold increase in current generation. Additionally, a significant decrease in the start-up time for electrocatalysis was observed. The findings suggest that the inherent extracellular electron
Chemical communications (Cambridge, England), 48(68), 8559-8561 (2012-07-17)
A modified paullone ligand bearing a TEMPO free-radical unit (HL) and its ruthenium(II) and osmium(II)-arene complexes [M(p-cymene)(HL)Cl]Cl·nH(2)O (M = Ru, Os) exhibit high antiproliferative activity in human cancer cell lines.
Journal of the American Chemical Society, 134(46), 19270-19280 (2012-11-02)
For the synthesis of the 1,2-diols, cis-1,2-dihydroxylation of alkenes catalyzed by osmium(VIII) tetroxide (OsO(4)) is a powerful method. However, OsO(4) is quite toxic due to its highly volatile and sublimable nature. Thus, the development of alternative catalysts for cis-1,2-dihydroxylation of
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