hydroxylamine , auch: hydroxylapatite

A variety of hydroxylamine derivatives have been used for this purpose.

However, hydroxylamine is almost always provided and used as an aqueous solution.

At least two factories dealing in hydroxylamine have been destroyed since 1999 with loss of life.

Hydrazines and hydroxylamine can be used in place of amines.

It is a salt derived from hydroxylamine and nitric acid.

Further reduction of the hydroxylamine leads to the amine.

The reaction involved the use of hydroxylamine to convert benzophenone into an oxime.

Aliphatic nitro compounds are more difficult to reduce, often remaining as the hydroxylamine.

It is primarily used as an easily-handled form of hydroxylamine, which is explosive when pure.

The company manufactures hydroxylamine which can be used for cleaning computer chips or etching integrated circuits.

The reaction of iron powder upon o-nitrocinnamic acid first yields a substituted hydroxylamine.

Oximes are usually generated by the reaction of hydroxylamine and aldehydes or ketones.

Hydroxylammonium chloride is the hydrochloric acid salt of hydroxylamine.

The resulting intermediate is a hydroxylamine.

Hydroxylamine may explode on heating.

Substituted derivatives of hydroxylamine are known.

In 2013, astrophysicists reported that the signature of hydroxylamine may have been detected in a star-forming field 1000 light years from earth.

Semicarbazide inhibits the enzyme, in addition to other hydrazines, hydroxylamine and propargylamine.

The intermediate hydroxylamine then condenses with the 2nd carbon on the 1-position to yield indole-2-carboxylic acid, giving off HO in the process.

Oximes can be synthesized by condensation of an aldehyde or a ketone with hydroxylamine.

BAIB may then oxidize the resulting hydroxylamine to an oxoammonium salt.

The sulfonamide can be prepared by reaction of hydroxylamine and benzenesulfonyl chloride in ethanol with potassium metal.

The compound behaves like a ketone in its reaction with hydroxylamine, forming the tris(oxime).

The syntheses of 1,2,4-oxadiazole systems all rely on hydroxylamine for providing a preformed N-O linkage.

Examples of compounds containing a hydroxylamine functional group are N-tert-butyl-hydroxylamine or the glycosidic bond in calicheamicin.