N,N-Diethylhydroxylamine - ≥98% , CAS No.3710-84-7

CAS: 3710-84-7 Cat. No.: D109383 Molecular Weight: 89.14 Beilstein Registry Number: 1731349 EC Number: 223-055-4

GRADE & PURITY ≥98%

Synonyms

DEHA | DTXSID2027543 | N,N-Diethyl hydroxylamine | UNII-314I05EDVH | BRN 1731349 | N,N-Diethylhydroxylamine | DTXCID107543 | EC 223-055-4 | AKOS015903887 | N,N-Diethylhydroxyamine | NCGC00257818-01 | AI3-28026 | AMY25658 | N,N-Diethylhydroxylamine (ca. 85

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview

N,N-Diethylhydroxylamine (diethylhydroxylamine, DEHA, (C2H5)2NOH) is a N,N-dialkylhydroxylamine. Its interaction with the surface of clean silicon(100)-2x1 has been studied by various theoretical and spectroscopic methods.H2O2 along with superoxide and diethylnitroxide radicals have been reported to be formed during the photochemical oxidation of DEHA.

Specifications

Synonyms

DEHA | DTXSID2027543 | N, N-Diethyl hydroxylamine | UNII-314I05EDVH | BRN 1731349 | N, N-Diethylhydroxylamine | DTXCID107543 | EC 223-055-4 | AKOS015903887 | N, N-Diethylhydroxyamine | NCGC00257818-01 | AI3-28026 | AMY25658 | N, N-Diethylhydroxylamine (ca. 85

Specifications & Purity

≥98%

Storage

Room temperature, Argon charged

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Canonical Smiles: CCN(CC)O
• IUPAC Name: N,N-diethylhydroxylamine
• InChIKey: FVCOIAYSJZGECG-UHFFFAOYSA-N
• INCHI: 1S/C4H11NO/c1-3-5(6)4-2/h6H,3-4H2,1-2H3
• Isomeric SMILES: CCN(CC)O
• WGK Germany: 1
• RTECS: NC3500000
• UN Number: 1993
• Molecular Weight: 89.14
• Beilstein: 1731349
• Reaxy-Rn: 1731349
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1731349&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass N-organohydroxylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: N-organohydroxylamines
• Intermediate Tree Nodes: Not available
• Direct Parent: N-organohydroxylamines
• Alternative Parents: Organopnictogen compounds Organic oxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: N-organohydroxylamine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as n-organohydroxylamines. These are organic compounds comprising the hydroxylamine functional group, with the general structure R1ON(R2)R3 (R1,R3=H, organyl; R2 = organyl).
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Soluble in water; Degree of Solubility in water: 89 g/l 25 °C
• Sensitivity: Hygroscopic,Air sensitive
• Refractive Index: 1.42
• Flash Point(°F): 113 °F
• Flash Point(°C): 45℃
• Boil Point(°C): 125-130°C
• Melt Point(°C): -26--25°C
• Molecular Weight: 89.140 g/mol
• XLogP3: 0.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 89.0841 Da
• Monoisotopic Mass: 89.0841 Da
• Topological Polar Surface Area: 23.500 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 26.700
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Yixing Cai, Yangyang Zhang, Shuaibing Gao, Jian Chen, Meilin Wan, Yongming Hu, Yunbin He, Qingfeng Zhang.  (2023)  High-sensitivity and high-stability near-ultraviolet self-powered photodetectors enabled by depolarization electric field and core-shell structured Cu@benzotriazole nanowire electrode.  CERAMICS INTERNATIONAL,      [PMID:] [10.1016/j.ceramint.2023.02.257]

2. Yingcai Wang, Xue Dong, Yunhai Liu, Yuhui Liu, Xiaohong Cao, Jing Chen, Chao Xu.  (2020)  Electrochemical and spectrochemical analysis of U(VI) reduction in nitric acid solutions.  JOURNAL OF ELECTROANALYTICAL CHEMISTRY,      [PMID:] [10.1016/j.jelechem.2020.114482]

3. Ping Li, Cheng Du, Xiaohui Gao, Zhihua Zhuang, Dong Xiang, Chunmei Zhang, Wei Chen.  (2020)  Insights into the morphology and composition effects of one-dimensional CuPt nanostructures on the electrocatalytic activities and methanol oxidation mechanism by in situ FTIR.  Nanoscale,  12  (25): (13688-13696).  [PMID:32573577] [10.1039/D0NR01095B]

4. Shanshan Dai, Peiyao Zhu, Yuxin Suo, Hongsheng Lu.  (2019)  Controllable CO2-Responsiveness of an Oil-in-Water Emulsion by Varying the Number of Tertiary Amine Groups or the Position of the Hydroxyl Group of Tertiary Amine.  JOURNAL OF PHYSICAL CHEMISTRY B,      [PMID:30802057] [10.1021/acs.jpcb.8b11344]

5. Yang Haiquan, Hu Jinyuan, Lu Xiao, Wang Fuxiang, Shen Wei, Hu Wei, Wang Lingling, Chen Xianzhong, Liu Long.  (2018)  Improving extracellular protein production in Escherichia coli by overexpressing D,D-carboxypeptidase to perturb peptidoglycan network synthesis and structure.  APPLIED MICROBIOLOGY AND BIOTECHNOLOGY,  103  (2): (793-806).  [PMID:30417310] [10.1007/s00253-018-9510-7]

6. Xiangning Han, Daicheng Liu.  (2018)  Di(2-ethylhexyl) adipate (DEHA) detection in Antarctic krill (Euphasia superba Dana).  POLAR RESEARCH,      [PMID:] [10.1080/17518369.2018.1457395]

7. Ye Zhang, Ning Zhou, Keqin Zhang, Feng Yan.  (2016)  Plasmonic copper nanowire@TiO2 nanostructures for improving the performance of dye-sensitized solar cells.  JOURNAL OF POWER SOURCES,      [PMID:] [10.1016/j.jpowsour.2016.12.068]

8. Andi Suo, Gongjian Fan, Caie Wu, Tingting Li, Xiaojing Li, Dandan Zhou, Kaiping Cong, Xin Cheng, Wenjuan Sun.  (2024)  Efficient degradation and enhanced α-glucosidase inhibitory activity of apricot polysaccharides through non-thermal plasma assisted non-metallic Fenton reaction.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:38522683] [10.1016/j.ijbiomac.2024.131103]

9. Chengli Zhao, Wenrui Huang, Jiayi Su, Xinshuang Zhang, Jingli Xue, Cailiang Zhang, Juan Han, Yang Zhou, Yun Wang.  (2024)  Purification and characterization of recombinant human superoxide dismutase integrated with resilin-like polypeptide.  PROTEIN EXPRESSION AND PURIFICATION,      [PMID:38901714] [10.1016/j.pep.2024.106535]

10. Qi Liu, Yihan Yin, Hongxia Gao, Lianbo Liu, Shisen Xu, Teerawat Sema, Min Xiao, Zhiwu Liang.  (2025)  The synergetic effect on oxidative degradation inhibition of 1-amino-2-propanol for post-combustion CO2 capture.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2025.122051]

11. Pengzhao Lv, Yu Jiang, Jialin Wang, Yige Shi, Zhengda Lin, Duo Wei, Wei Zuo, Jun Zhang.  (2025)  Selective eradication of pathogenic bacteria using amine-modified corn-straw carbon dots.  Environmental Science and Ecotechnology,      [PMID:41567746] [10.1016/j.ese.2025.100651]