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等级
SAJ first grade
蒸汽压
10 mmHg ( 693 °C)
方案
98.0-102.0%
表单
fine crystals
反应适用性
reagent type: catalyst
core: iron
存货情况
available only in Japan
pH值（酸碱度）
2.5 (20 °C, 100 g/L)
SMILES字符串
O.O.O.O.Cl[Fe]Cl
InChI
1S/2ClH.Fe.4H2O/h2*1H;;4*1H2/q;;+2;;;;/p-2
InChI key
WSSMOXHYUFMBLS-UHFFFAOYSA-L
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警示用语：
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Eye Dam. 1
储存分类代码
8B - Non-combustible corrosive hazardous materials
WGK
WGK 1
闪点(°F)
does not flash
闪点(°C)
does not flash
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Sofia Tresintsi et al.
Water research, 46(16), 5255-5267 (2012-07-25)
Various iron oxy-hydroxides were synthesized in a continuous flow kilogram-scale production reactor through the precipitation of FeSO(4) and FeCl(2) in the pH range 3-12 under intense oxidative conditions to serve as arsenic adsorbents. The selection of the optimum adsorbent and
Qinqin Xia et al.
The Journal of organic chemistry, 77(20), 9366-9373 (2012-10-03)
Iron-catalyzed direct C-N bond formation between azoles and amides is described. The oxidative coupling reactions of sp(3) C-H bonds adjacent to a nitrogen atom in amides and sulfonamides with the N-H bond in azoles proceeded smoothly in the presence of
Jiangfei Meng et al.
Journal of food science, 77(1), C8-14 (2011-12-21)
Wines made from 3 spine grape (Vitis davidii Foex) genotypes-Junzi 1# (JZ 1#), Junzi 2# (JZ 2#), and Liantang (LT)-and Cherokee rose (Rosa laevigata Michx., CR) were evaluated for their phenolics composition and antioxidant activities by several assays, including 2,2'-azino-bis-(3-ethylbenzothiazoline-6-sulfonic
Ju-Suk An et al.
Environmental technology, 35(13-16), 1668-1675 (2014-06-25)
The precipitation reaction between the orthophosphate and Fe2+ ions was studied to describe the optimum condition for the removal of orthophosphate from the aqueous solution. The effects of pH, Fe:P molar ratio, and alkalinity were evaluated for the initial orthophosphate
Chong Qin et al.
Angewandte Chemie (International ed. in English), 51(28), 6971-6975 (2012-06-13)
Ironing it out: an efficient and convenient nitrogenation strategy involving C-C bond cleavage for the straightforward synthesis of versatile arylamines is presented. Various alkyl azides and alkylarenes, including the common industrial by-product cumene, react using this protocol. Moreover, this method
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