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Sodium nitroprusside is often used as a reference compound for the calibration of Mössbauer spectrometers. [54] Sodium nitroprusside crystals are also of interest for optical storage. For this application, sodium nitroprusside can be reversibly promoted to a metastable excited state by blue-green light, and de-excited by heat or red light. [55]
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.
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 .
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.
Hydralazine and Sodium nitroprusside are systemic vasodilators, thereby reducing afterload, however can be found to have reflex tachycardia, making them likely second or third line choices. Sodium nitroprusside was previously the first-line choice due to its rapid onset, although now it is less commonly used due to side effects, drastic drops ...
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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.
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 ...