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N,N-Diethylhydroxylamine - 98%, high purity , CAS No.3710-84-7
Basic Description
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 Temp
Argon charged
Shipped In
Normal
Product Description
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.
Taxonomic Classification
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.
Names and Identifiers
IUPAC Name
N,N-diethylhydroxylamine
INCHI
InChI=1S/C4H11NO/c1-3-5(6)4-2/h6H,3-4H2,1-2H3
InChIKey
FVCOIAYSJZGECG-UHFFFAOYSA-N
Smiles
CCN(CC)O
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=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
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
Citations of This Product
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,
49
(18770).
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,
874
(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).
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,
123
(11):
(2558–2566).
5.
Yang Haiquan, Hu Jinyuan, Lu Xiao, Wang Fuxiang, Shen Wei, Hu Wei, Wang Lingling, Chen Xianzhong, Liu Long.
(2019)
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).
6.
Xiangning Han, Daicheng Liu.
(2018)
Di(2-ethylhexyl) adipate (DEHA) detection in Antarctic krill (Euphasia superba Dana). POLAR RESEARCH,
7.
Ye Zhang, Ning Zhou, Keqin Zhang, Feng Yan.
(2017)
Plasmonic copper nanowire@TiO2 nanostructures for improving the performance of dye-sensitized solar cells. JOURNAL OF POWER SOURCES,
342
(292).
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,
266
(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,
222
(106535).
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9 Citations
I2127080