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Merck

197637

Imidazole sodium derivative

technical grade

Synonym(s):

Imidazolylsodium, Sodium imidazolide

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R$1,277.00

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About This Item

Empirical Formula (Hill Notation):
C3H3N2Na
CAS Number:
Molecular Weight:
90.06
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39161001
UNSPSC Code:
12352005
EC Number:
226-988-5
MDL number:
Beilstein/REAXYS Number:
3569312

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Product Name

Imidazole sodium derivative, technical grade

InChI key

ITAWMPSVROAMOE-UHFFFAOYSA-N

InChI

1S/C3H3N2.Na/c1-2-5-3-4-1;/h1-3H;/q-1;+1

SMILES string

[Na]n1ccnc1

grade

technical grade

mp

284 °C (dec.) (lit.)

Quality Level

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56760307815206288
Quality Level

100

Quality Level

100

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200

Quality Level

100

mp

284 °C (dec.) (lit.)

mp

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grade

technical grade

grade

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Application

Imidazole sodium derivative (Imidazolylsodium) was used in the synthesis of arylazidoamorphigenin[1].

pictograms

CorrosionExclamation mark

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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F G Earley et al.
The Biochemical journal, 224(2), 525-534 (1984-12-01)
A photoaffinity-labelling analogue of the respiratory inhibitor rotenone was synthesized from the naturally occurring rotenoid amorphigenin. The analogue inhibits NADH-ubiquinone oxidoreductase activity at concentrations comparable with those of rotenone. Photolysis of the radiolabelled analogue bound to isolated NADH-ubiquinone oxidoreductase resulted
Yun Dai et al.
Electrophoresis, 34(6), 833-840 (2013-01-22)
The first member of the single-isomer, dicationic cyclodextrin (CD) family, 6(A)-ammonium-6(C)-butylimidazolium-β-cyclodextrin chlorides (AMBIMCD), has been synthesized, analytically characterized, and used to separate a variety of acidic enantiomers and amino acids by CE. Starting from mono-6(A)-azido-β-cyclodextrin, the cationic imidazolium and ammonium
Kushal Sengupta et al.
Inorganic chemistry, 52(4), 2000-2014 (2013-01-30)
Electrodes bearing thiolate and imidazole coordinated iron porphyrin catalysts are constructed and characterized using resonance Raman spectroscopy, absorption spectroscopy, and electrochemistry. The cyclic voltammetry data and their pH dependences are used to establish the nature of the exchangeable trans ligands
Lizhen Qiao et al.
Journal of chromatography. A, 1286, 137-145 (2013-03-16)
Hydrophilic interaction liquid chromatography (HILIC) has been widely used for separating polar compounds as a complement mode to reversed-phase liquid chromatography. The development of new stationary phases for HILIC is significant to improve the coverage of various polar and hydrophilic
Vijay Satam et al.
Bioorganic & medicinal chemistry letters, 23(6), 1699-1702 (2013-02-12)
Hx-amides are fluorescent hybrids of imidazole (I)- and pyrrole (P)-containing polyamides and Hoechst 33258, and they bind in the minor groove of specific DNA sequences. Synthesis and DNA binding studies of HxII (5) complete our studies on the first set

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