Hydroxylamine Hydrochloride CAS#: 5470-11-1 - ChemicalBook
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| Sodium chloride 1-AdaMantanethylaMine Choline chloride METARAMINOL Ferric chloride Ammonium chloride Diphenhydramine Hydrochloride Sulfuryl chloride N,N-Diethylhydroxylamine Metaraminol bitartrate Ciprofloxacin hydrochloride Calcium chloride Topotecan hydrochloride Potassium chloride HYDROXYLAMINE Polyvinyl chloride Hydroxylamine sulfate Hydroxydiethylphenamine Hydroxylamine Hcl | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Hydroxylamine converts aldehydes and ketones (carbonyls) to their oxime derivative in weak bases, therefore cross‐linkers and other compounds with carbonyl groups are cleavable with Hydroxylamine hydrochloride.SATA and SATP are modification reagents that add a sulfhydryl group to primary amines on biomolecules. The initial modification results in the addition of an acetyl‐protected sulfur enabling storage of the biomolecule. To generate a free sulfhydryl the biomolecule is treated with hydroxylamine to remove the protecting acetyl group (see figure).EGS and sulfo‐EGS are homobifunctional, succinimidyl ester, amine reactive crosslinkers that are resistant to cleavage by denaturants used in SDS‐PAGE conditions, but may be cleaved with hydroxylamine.