Molecular structure of Hydroxylamine hydrochloride, CAS Number: 5470-11-1
Hydroxylamine hydrochloride (CAS 5470-11-1)
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Alternate Names:
Hydroxylamine HCl; Oxammonium hydrochloride; Oxammonium HCI
Application:
Hydroxylamine hydrochloride is an agent used as a catalyst and copolymerization inhibitor
CAS Number:
5470-11-1
Purity:
≥97%
Molecular Weight:
69.49
Molecular Formula:
NH2OH•HCl
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Description
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SDS & Certificate of Analysis
Hydroxylamine hydrochloride is a compound used as a catalyst, copolymerization inhibitor, and swelling agent that acts as a potent reducing agent, converting aldehydes and ketones to oximes. It also exhibits activity of converting acid chlorides to hydroxamic acids. It is also a MAO inhibitor and inhibits platelet aggregation.
Hydroxylamine hydrochloride (CAS 5470-11-1) References
- Use of hydroxylamine hydrochloride in the titrimetric determination of manganese in pyrolusite. | Chatterjee, BP. and Mukhopadhyay, SK. 1977. Talanta. 24: 180-1. PMID: 18962060
- Detection limits of electron and electron capture negative ionization-mass spectrometry for aldehydes derivatized with o-(2,3,4,5,6-pentafluorobenzyl)-hydroxylamine hydrochloride. | Beránek, J., et al. 2010. J Am Soc Mass Spectrom. 21: 592-602. PMID: 20106680
- Transamidation of primary amides with amines using hydroxylamine hydrochloride as an inorganic catalyst. | Allen, CL., et al. 2012. Angew Chem Int Ed Engl. 51: 1383-6. PMID: 22213128
- Lewis Acid Mediated Tandem Reaction of Propargylic Alcohols with Hydroxylamine Hydrochloride To Give α,β-Unsaturated Amides and Alkenyl Nitriles. | Han, YP., et al. 2015. J Org Chem. 80: 9200-7. PMID: 26317753
- Route to Highly Substituted Pyridines. | Hilf, JA., et al. 2016. J Org Chem. 81: 10376-10382. PMID: 27579766
- Some factors affecting the process of photoinduced hydroxylaminolysis in different bacteriorhodopsin-based media. | Druzhko, AB., et al. 2017. Eur Biophys J. 46: 509-515. PMID: 28474199
- Determination of kinetic parameters of redox reactions using CE-ICP-MS: A case study for the reduction of Np(V) by hydroxylamine hydrochloride. | Willberger, C., et al. 2018. Electrophoresis. 39: 3013-3021. PMID: 30192411
- [Hypobromite oxidation combined with hydroxylamine hydrochloride reduction method for analyzing ammonium nitrogen isotope in atmospheric samples.]. | Xiang, YK., et al. 2019. Ying Yong Sheng Tai Xue Bao. 30: 1847-1853. PMID: 31257755
- Nitrogen isotopic analysis of nitrate in aquatic environment using cadmium-hydroxylamine hydrochloride reduction. | Jin, J., et al. 2020. Rapid Commun Mass Spectrom. 34: e8804. PMID: 32267563
- Reaction of dibenzalacetone with hydroxylamine hydrochloride under phase-transfer conditions. 1 H and 13 C 2D NMR structural elucidation of the products. | Aguilera, JL., et al. 1989. Magn Reson Chem. 27: 823-829. PMID: 34034430
- Vibrational characterization of the pesticide molecule Tebuconazole. | Jurašeková, Z., et al. 2022. Spectrochim Acta A Mol Biomol Spectrosc. 268: 120629. PMID: 34824006
- Paired Derivatization Approach with H/D-Labeled Hydroxylamine Reagents for Sensitive and Accurate Analysis of Monosaccharides by Liquid Chromatography Tandem Mass Spectrometry. | Wang, SL., et al. 2022. Anal Chem. 94: 3590-3599. PMID: 35171578
- Application of hydroxylamine hydrochloride for post-PCR sterilization. | Aslanzadeh, J. 1993. Mol Cell Probes. 7: 145-50. PMID: 8391642
Inhibitor of:
MAO, and TAT1.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Hydroxylamine hydrochloride, 25 g | sc-211616 | 25 g | $50.00 | |||
Hydroxylamine hydrochloride, 100 g | sc-211616A | 100 g | $64.00 |