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化驗
≥98.0% (NT)
形狀
crystals
雜質
≤1% water
mp
~280 °C (dec.)
SMILES 字串
[O-][N+]([O-])=O.CC[N+](CC)(CC)CC
InChI
1S/C8H20N.NO3/c1-5-9(6-2,7-3)8-4;2-1(3)4/h5-8H2,1-4H3;/q+1;-1
InChI 密鑰
JTJKNAJRGLQKDZ-UHFFFAOYSA-N
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應用
Tetraethylammonium nitrate can be used:
- To prepare nitronium triflate by reacting with triflic anhydride for subsequent use as a nitrating agent for benzene.
- To study the dependency of luminescence intensity of Eu3+ complexes on the nitrate anion concentration.
- To prepare the lanthanum(III) complex named (NEt4)[La(ntfa)4] by reacting with La(NO3)3·6H2O, NaOH and 4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedion.
訊號詞
Danger
危險分類
Eye Irrit. 2 - Ox. Sol. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
5.1B - Oxidizing hazardous materials
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
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
其他客户在看
Synthesis and characterization of Lanthanum (III) complexes containing 4, 4, 4-trifluoro-1-(naphthalen-2yl) butane-1, 3-dionate
Polyhedron, 179, 114384-114384 (2020)
Molecules (Basel, Switzerland), 25(1) (2020-01-08)
In the investigation presented here the synthesis of new lariat ether derivative obtained from the modification of tetrapyrrolidinyl-PNP-crown ether macrocycle is described. The polyheterotopic molecular coreceptor consisted of the replacement of chlorine atoms with an optically active (S)-(1-benzylpyrrolidin-2-yl) methanamine. The
New europium (III) complexes containing hybrid ligands with hard and soft complexation centres
New. J. Chem., 27(1), 134-139 (2003)
Electrophilic tetraalkylammonium nitrate nitration. II. Improved anhydrous aromatic and heteroaromatic mononitration with tetramethylammonium nitrate and triflic anhydride, including selected microwave examples
The Journal of Organic Chemistry, 68(2), 267-275 (2003)
Industrial & engineering chemistry research, 58(34), 15628-15636 (2019-10-11)
The separation of metals by liquid-liquid extraction largely relies on the affinity of metals to the extractants, which normally reside in the organic (less polar) phase because of their high hydrophobicity. Following a different route, using aminopoly(carboxylic acid)s (e.g., EDTA)
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