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- Nitrous acid can be used to chemically depolymerize heparin/HS.
- The sodium nitrite is first converted to nitrous acid which then forms the electrophilic intermediate dinitrogen trioxide.
- Acyl azides are also obtained from treating acylhydrazines with nitrous acid.
- The nitrosonium group forms from nitrous acid (HNO2) under acidic conditions present in the tobacco curing process.
- Synonyms include "1-butyl nitrite", n"-butyl nitrite" and "nitrous acid butyl ester".
- Alpha-acceptor-substituted primary aliphatic amines R-CH2-NH2 (R = COOR, CN, CHO, COR) react with nitrous acid to generate the diazo compound.
- Similar multicomplex survival curves (without shoulders) were also obtained for the DNA damaging agents P32 decay, psoralen plus near-UV irradiation (PUVA), N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), methyl methane sulfonate (MMS) and nitrous acid.
- Anilines (aryl amines) are converted to their diazonium salts using nitrous acid.
- Deaminative cleavage with nitrous acid results in the formation of an unnatural anhydromannose residue at the reducing terminal of the oligosaccharides produced.
- The method exploits the reactivity of nitrous acid derived from acidification of nitrite.
- Aniline and its ring-substituted derivatives react with nitrous acid to form diazonium salts.
- Nitrous acid (molecular formula [...]) is a weak and monoprotic acid known only in solution, in the gas phase and in the form of nitrite (...) salts.
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Contains translations by TU Chemnitz and Mr Honey's Business Dictionary (German-English only).
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