Molecular structure of N,N-Diethylhydroxylamine, CAS Number: 3710-84-7
N,N-Diethylhydroxylamine (CAS 3710-84-7)
CAS Number:
3710-84-7
Molecular Weight:
89.14
Molecular Formula:
C4H11NO
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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N,N-Diethylhydroxylamine serves as a reagent extensively employed in organic synthesis processes, particularly in the creation of peptides and nucleic acids. It plays a pivotal role in exploring enzyme and protein properties and investigating chemical reaction mechanisms. Moreover, this compound has proven instrumental in developing methodologies for detecting trace elements in biological samples. Due to its high reactivity as a nucleophile, N,N-Diethylhydroxylamine readily forms covalent bonds with electrophiles, such as carbonyl compounds and aromatic rings. This unique reactivity allows it to engage with diverse substrates, including proteins, nucleic acids, and various organic molecules.
N,N-Diethylhydroxylamine (CAS 3710-84-7) References
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- Theoretical and spectroscopic study of the reaction of diethylhydroxylamine on silicon(100)-2 x 1. | DiLabio, GA., et al. 2007. Phys Chem Chem Phys. 9: 1629-34. PMID: 17429556
- Enhancement of photochemical smog by n,n'-diethylhydroxylamine in polluted ambient air. | Pitts, JN., et al. 1977. Science. 197: 255-7. PMID: 17750455
- Mixed unsymmetric oxadiazoline and/or imine platinum(II) complexes. | Lasri, J., et al. 2007. Dalton Trans. 3259-66. PMID: 17893771
- N,N-diethylhydroxylamine: a new electron donor to photosystem II. | Sabat, SC., et al. 1991. Biochem Biophys Res Commun. 179: 1127-33. PMID: 1898394
- Dramatic synergistic effects between hydroquinone and resorcinol derivatives for the organocatalyzed reduction of dioxygen by diethylhydroxylamine. | Lebeuf, R., et al. 2014. Chem Commun (Camb). 50: 866-8. PMID: 24296880
- A mild hydration of nitriles catalysed by copper(ii) acetate. | Marcé, P., et al. 2016. Chem Commun (Camb). 52: 1436-8. PMID: 26645321
- The formation and inhibition of photochemical smog. | Heicklen, J. 1987. Ann N Y Acad Sci. 502: 145-59. PMID: 3310800
- Spectroscopic and quantum mechanical study of a scavenger molecule: N,N-diethylhydroxylamine. | Salvitti, G., et al. 2022. Spectrochim Acta A Mol Biomol Spectrosc. 281: 121555. PMID: 35926273
- How Water Interacts with the NOH Group: The Rotational Spectrum of the 1:1 N,N-diethylhydroxylamine·Water Complex. | Salvitti, G., et al. 2022. Molecules. 27: PMID: 36500289
- Increase in life expectancy for mice fed diethylhydroxylamine (DEHA). | Heicklen, J. and Brown, E. 1987. J Gerontol. 42: 674-80. PMID: 3680886
- Effects of diethylhydroxylamine on hepatic microsomal lipid peroxidation and glutathione S-transferases. | Reddy, CC., et al. 1985. J Toxicol Environ Health. 15: 467-75. PMID: 4032493
- The effect of diethylhydroxylamine on the incidence of tumors induced by benzo(a)pyrene in the mouse. | Heicklen, J., et al. 1984. Drug Chem Toxicol. 7: 315-27. PMID: 6489187
- Toxicological testing of rats subjected to inhalation of diethylhydroxylamine, nitroethane, and diethylamine hydrogen sulfite. | Heicklen, J., et al. 1981. Environ Res. 26: 258-73. PMID: 7318784
- The photooxidation of diethylhydroxylamine by rose bengal in micellar and nonmicellar aqueous solutions. | Bilski, P., et al. 1993. Photochem Photobiol. 58: 11-8. PMID: 8378429
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
N,N-Diethylhydroxylamine, 100 ml | sc-250507 | 100 ml | $27.00 | |||
N,N-Diethylhydroxylamine, 500 ml | sc-250507A | 500 ml | $88.00 |