Molecular structure of Hydroxylamine-O-sulfonic acid, CAS Number: 2950-43-8
Hydroxylamine-O-sulfonic acid (CAS 2950-43-8)
CAS Number:
2950-43-8
Purity:
≥97%
Molecular Weight:
113.09
Molecular Formula:
H3NO4S
Supplemental Information:
This is 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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Hydroxylamine-O-sulfonic acid is a compound that is in biochemistry. It is a derivative of hydroxylamine and is utilized as a reagent in various chemical reactions. Hydroxylamine-O-Sulfonic Acid is for its ability to act as a reducing agent, particularly in the conversion of nitro compounds to amines. It is also in the preparation of oximes from carbonyl compounds. Hydroxylamine-O-sulfonic acid is particularly useful in the synthesis of agrochemicals. Its unique properties make it important in the field of biochemistry, allowing for the efficient and selective transformation of various functional groups in organic molecules. Hydroxylamine-O-sulfonic acid plays a role in the development and production of a wide range of chemical products.
Hydroxylamine-O-sulfonic acid (CAS 2950-43-8) References
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- Direct and Stereospecific Synthesis of N-H and N-Alkyl Aziridines from Unactivated Olefins Using Hydroxylamine-O-Sulfonic Acids. | Ma, Z., et al. 2017. Angew Chem Int Ed Engl. 56: 9886-9890. PMID: 28614619
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- Chemiluminescence assay for Listeria monocytogenes based on Cu/Co/Ni ternary nanocatalyst coupled with penicillin as generic capturing agent. | Zhang, Y., et al. 2021. Luminescence. 36: 11-19. PMID: 32602594
- Cu(OTf)2-catalyzed Beckmann Rearrangement of Ketones Using Hydroxylamine-O-sulfonic Acid (HOSA). | Munnuri, S., et al. 2019. Synthesis (Stuttg). 51: 3709-3714. PMID: 32684655
- Rapid 'on-column' preparation of hydrogen [11C]cyanide from [11C]methyl iodide via [11C]formaldehyde. | Kikuchi, T., et al. 2022. Chem Sci. 13: 3556-3562. PMID: 35432866
- Aminations of guanosine and deoxyguanosine with hydroxylamine-O-sulfonic acid and 2,4-dinitrophenoxyamine. Dependence on the reaction medium. | Kohda, K., et al. 1986. Nucleic Acids Symp Ser. 145-8. PMID: 3562259
- Site-selective amination and/or nitrilation via metal-free C(sp2)-C(sp3) cleavage of benzylic and allylic alcohols. | Anugu, RR. and Falck, JR. 2022. Chem Sci. 13: 4821-4827. PMID: 35655896
- Cu-α-diimine Compounds Encapsulated in Porous Materials as Catalysts for Electrophilic Amination of Aromatic C-H Bonds. | Van Emelen, L., et al. 2022. ACS Appl Mater Interfaces. 14: 51867-51880. PMID: 36349551
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- Direct C-amination of guanosine with hydroxylamine-O-sulfonic acid. Simplest model reaction possible involved in DNA damage leading to carcinogenesis by N-arylhydroxylamines. | Kawazoe, Y. and Huang, GF. 1972. Chem Pharm Bull (Tokyo). 20: 2073-4. PMID: 4645225
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Hydroxylamine-O-sulfonic acid, 5 g | sc-250138 | 5 g | $32.00 | |||
Hydroxylamine-O-sulfonic acid, 25 g | sc-250138A | 25 g | $72.00 |