N,N-Diethylhydroxylamine solution - 85% in H2O , CAS No.3710-84-7

CAS: 3710-84-7 Cat. No.: N432573 Peso molecular: 89.14 Beilstein Registry Number: 1731349 Número EC: 223-055-4
Disponible para pedir
GRADE & PURITY 85% in H2O
Synonyms
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% in Wa
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
250g
N432573-250g
4

90,90US$

118,90US$
Guardar 28,00 US$ (23.55%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

85% in H2O for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

General Description

The product is 85wt.% solution of N,N -diethylhydroxylamine. The reaction of N,N -diethylhydroxylamine with tert -butylhydroperoxide has been studied. It participates in the preparation of symmetrical and an isomeric mixture of unsymmetrical phthalocyanines. It undergoes degradation on exposure to radiation and affords light hydrocarbons. Qualitative and quantitative analyses of the produced hydrocarbons have been reported. It also participates in the conversion of quinones and quinonemonosulfonimide to the corresponding hydroquinones and sulfonylaminophenols, respectively.

Specifications

Sinónimos
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% in Wa
Especificaciones y pureza
85% in H2O
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Nombres e identificadores
Pubchem Sid488182542
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488182542
Sonrisas canónicasCCN(CC)O
IUPAC NameN,N-diethylhydroxylamine
InChIKeyFVCOIAYSJZGECG-UHFFFAOYSA-N
INCHI1S/C4H11NO/c1-3-5(6)4-2/h6H,3-4H2,1-2H3
Isómeros SMILES CCN(CC)O
WGK Alemania 1
RTECS NC3500000
Número ONU 1993
Peso molecular 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=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClaseOrganonitrogen compounds
SubclassN-organohydroxylamines
Intermediate Tree Nodes Not available
Direct ParentN-organohydroxylamines
Alternative Parents Organopnictogen compounds  Organic oxygen compounds  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents N-organohydroxylamine - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeFechaArticulo
D2313931Certificate of AnalysisJan 21, 2026 N432573
D2313953Certificate of AnalysisJan 21, 2026 N432573
D2313954Certificate of AnalysisJan 21, 2026 N432573
D2313963Certificate of AnalysisJan 21, 2026 N432573
Propiedades químicas y físicas
SensibilidadMoisture sensitive
Índice de refracción1.42
Punto de inflamación (°F)113 °F
Punto de inflamación (°C) 45℃
Punto de ebullición (°C)125-130°C
Punto de fusión (°C)-26--25°C
Peso molecular89.140 g/mol
XLogP30.500
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass89.0841 Da
Monoisotopic Mass89.0841 Da
Topological Polar Surface Area23.500 Ų
Heavy Atom Count6
Formal Charge0
Complexity26.700
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
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]
Calculadoras de soluciones
Reseñas

Reseñas de cliente

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.