Search results
Results from the WOW.Com Content Network
Structure of sodium nitroprusside in the solid state, obtained by neutron diffraction Space filling model of sodium nitroprusside Nitroprusside is an inorganic compound with the chemical formula Na 2 [Fe(CN) 5 NO], usually encountered as the dihydrate , Na 2 [Fe(CN) 5 NO]·2H 2 O. [ 47 ] This red-colored sodium salt dissolves in water or ...
Nitroprusside changes from pink to purple in the presence of acetoacetate, the conjugate base of acetoacetic acid, and the colour change is graded by eye. The test does not measure β-hydroxybutyrate, the most abundant ketone in the body; during treatment of ketoacidosis β-hydroxybutyrate is converted to acetoacetate so the test is not useful ...
Sodium nitroprusside, a medicinally significant metal nitrosyl-pentacyanoferrate (Fe-III) compound, used to treat hypertension. [1] Metal nitrosyl complexes are complexes that contain nitric oxide, NO, bonded to a transition metal. [2] Many kinds of nitrosyl complexes are known, which vary both in structure and coligand.
Mössbauer spectrum of sodium nitroprusside, exhibiting quadruple splitting. Quadrupole splitting is an example of a hyperfine interaction found in gamma-ray spectroscopy, in the circumstance where nuclei with a non-radially-symmetric shape (that is, with a spin quantum number greater than 1/2) are found immersed in an external electric field gradient.
A solution of 2% sodium carbonate in water (solution B) [4] Separate storage of the aldehyde and base are necessary to prevent aldol polymerisation of the aldehyde. When exposed to an amine, reaction with acetaldehyde produces the enamine , which subsequently reacts with sodium nitroprusside to the imine .
Nitrosation is typically performed with nitrous acid, formed from acidification of a sodium nitrite solution. Nitrous acid is unstable, and high yields require a rapid reaction rate. NO + synthon transfer is catalyzed by a strong nucleophile, such as (in order of increasing efficacy) chloride, bromide, thiocyanate, or thiourea.
Structural formula of nitroso group. In organic chemistry, nitroso refers to a functional group in which the nitric oxide (−N=O) group is attached to an organic moiety.As such, various nitroso groups can be categorized as C-nitroso compounds (e.g., nitrosoalkanes; R−N=O), S-nitroso compounds (nitrosothiols; RS−N=O), N-nitroso compounds (e.g., nitrosamines, RN(−R’)−N=O), and O ...
Whether a specific drug is useful or harmful under heart failure and myocardial infarction depends on its speed of action: Fast acting substances such as glyceryl trinitrate and nitroprusside can be helpful for controlling blood pressure and consequently the amount of blood the heart has to pump, if the application is monitored continuously.