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About This Item
Linear Formula:
(C2H5)4N(NO3)
CAS Number:
Molecular Weight:
192.26
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
EC Number:
217-725-5
MDL number:
Beilstein/REAXYS Number:
3918466
Product Name
Tetraethylammonium nitrate, ≥98.0% (NT)
InChI key
JTJKNAJRGLQKDZ-UHFFFAOYSA-N
InChI
1S/C8H20N.NO3/c1-5-9(6-2,7-3)8-4;2-1(3)4/h5-8H2,1-4H3;/q+1;-1
SMILES string
[O-][N+]([O-])=O.CC[N+](CC)(CC)CC
assay
≥98.0% (NT)
form
crystals
impurities
≤1% water
mp
~280 °C (dec.)
Quality Level
Application
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.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Ox. Sol. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
5.1B - Oxidizing hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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New europium (III) complexes containing hybrid ligands with hard and soft complexation centres
Prodi L, et al.
New. J. Chem., 27(1), 134-139 (2003)
Synthesis and characterization of Lanthanum (III) complexes containing 4, 4, 4-trifluoro-1-(naphthalen-2yl) butane-1, 3-dionate
Mautner FA, et al.
Polyhedron, 179, 114384-114384 (2020)
Electrophilic tetraalkylammonium nitrate nitration. II. Improved anhydrous aromatic and heteroaromatic mononitration with tetramethylammonium nitrate and triflic anhydride, including selected microwave examples
Shackelford SA, et al.
The Journal of Organic Chemistry, 68(2), 267-275 (2003)
Natalia Gutowska et al.
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
Zheng Li et al.
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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