推薦產品
等級
SAJ first grade
蒸汽壓力
10 mmHg ( 693 °C)
化驗
98.0-102.0%
形狀
fine crystals
反應適用性
reagent type: catalyst
core: iron
存貨情形
available only in Japan
pH值
2.5 (20 °C, 100 g/L)
SMILES 字串
O.O.O.O.Cl[Fe]Cl
InChI
1S/2ClH.Fe.4H2O/h2*1H;;4*1H2/q;;+2;;;;/p-2
InChI 密鑰
WSSMOXHYUFMBLS-UHFFFAOYSA-L
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訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Eye Dam. 1
儲存類別代碼
8B - Non-combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 1
閃點(°F)
does not flash
閃點(°C)
does not flash
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
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
Journal of bacteriology, 194(22), 6162-6173 (2012-09-11)
Nontypeable Haemophilus influenzae (NTHI), an opportunistic pathogen that is commonly found in the human upper respiratory tract, has only four identified two-component signal transduction systems. One of these, an ortholog to the QseBC (quorum-sensing Escherichia coli) system, was characterized. This
Journal of pharmacological sciences, 120(2), 105-111 (2012-09-29)
Sodium nitroprusside (SNP) is widely used as a potent vasodilator and a nitric oxide (NO) donor, whereas the cytotoxicity of SNP has been well documented. SNP releases several potentially toxic products such as cyanide anion, NO, and iron. We investigated
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
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
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