Translation for 'nitrous acid' from English to Swedish

nitrous acid

salpetersyrlighet {u} [HNO2]kemi

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nitrous oxide

lustgas {u} [N2O]kemimed.

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acid

syra {u}kemi

cholic acid

cholsyra {u} [C24H40O5]kemi

boric acid

borsyra {u} [H3BO3] [E-284]kemilivsmed.

isobutyric acid

isosmörsyra {u} [C₄H₈O₂] [C₃H₇COOH]kemi

acid anhydride

syraanhydrid {u}kemi

hydrofluoric acid

fluorvätesyra {u}kemi

lactic acid

mjölksyra {u} [C3H6O3] [C3H4O(OH)2] [acidum lacticum] [E-270]biokemilivsmed.

tannic acid

garvsyra {u}

phosphoric acid

fosforsyra {u} [Acidum phosphoricum] [H3PO4] [E-338]kemilivsmed.

orthophosphoric acid

fosforsyra {u} [Acidum phosphoricum] [H3PO4] [E-338]kemi

phthalic acid

ftalsyra {u} [C8H6O4, C6H4(COOH)2]kemi

fatty acid

fettsyra {u}kemi

stearic acid

stearinsyra {u} [E-570]kemilivsmed.

nitric acid

salpetersyra {u} [HNO3]kemi

amino acid

aminosyra {u}biokemi

acid rain

surt regn {n}miljö

methanoic acid

myrsyra {u} [CH2O2] [HCOOH] [acidum formicum]kemi

formic acid

myrsyra {u} [CH2O2] [HCOOH] [acidum formicum]kemi

washing acid

tvättsyra {u}kemi

• 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.