Determine the necessary mass, volume, or concentration for preparing a solution.
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≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships FedEx DG Service Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 12 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product introduction:
2-(Dibutylamino)ethanol is a tertiary amine.Dibutylethanolamine belongs to the class of N-alkylated aminoalcohols.
Application:
2-(Dibutylamino)ethanol (DBAE) may be used as a coreactant to enhance the electrochemiluminescence (ECL) of tris(2,2′-bipyridyl)ruthenium(II) [Ru(bpy)32+], employed in the ECL immunoassays and DNA probe assays. DBAE may also be used as a catalyst during the synthesis of protected D-erythro-(2S,3R)-sphingosine.
Dibutylethanolamine belongs to the class of N-alkylated aminoalcohols. Dibutylethanolamine (DBEOA) serves as a specialty additive in a variety of industries.
| Pubchem Sid | 528765704 |
|---|---|
| Sorrisi canonici | CCCCN(CCCC)CCO |
| IUPAC Name | 2-(dibutylamino)ethanol |
| InChIKey | IWSZDQRGNFLMJS-UHFFFAOYSA-N |
| INCHI | 1S/C10H23NO/c1-3-5-7-11(9-10-12)8-6-4-2/h12H,3-10H2,1-2H3 |
| Isomeri SMILES | CCCCN(CCCC)CCO |
| WGK Germania | 1 |
| RTECS | KK3850000 |
| Numero UN | 2873 |
| Gruppo di imballaggio | III |
| Peso molecolare | 173.3 |
| Beilstein | 1738441 |
| Reaxy-Rn | 1738441 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1738441&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Classe | Organonitrogen compounds |
| Subclass | Amines |
| Intermediate Tree Nodes | Alkanolamines |
| Direct Parent | 1,2-aminoalcohols |
| Alternative Parents | Trialkylamines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Tertiary aliphatic amine - Tertiary amine - 1,2-aminoalcohol - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom. |
| External Descriptors | Not available |
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| Indice di rifrazione | 1.44 |
|---|---|
| Punto di infiammabilità (°F) | 203 °F |
| Punto di infiammabilità (°C) | 90 °C |
| Punto di ebollizione (°C) | 229-230 °C(lit.) |
| Punto di fusione (°C) | -70 °C |
| Peso molecolare | 173.300 g/mol |
| XLogP3 | 2.100 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 8 |
| Exact Mass | 173.178 Da |
| Monoisotopic Mass | 173.178 Da |
| Topological Polar Surface Area | 23.500 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 77.900 |
| 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 |
| 1. Yitian Huang, Dandan Zhao, Yanjie Chen, Shupei Zhang, Feng Lin, Hong Dai. (2022) Ratiometric electrochemiluminescence biosensor for hepatitis C virus E2 protein based on block copolymers-solubilized Ir(ppy)3 with high electrochemiluminescence efficiency. ELECTROCHIMICA ACTA, [PMID:] [10.1016/j.electacta.2022.141028] |
| 2. Xianda Han, Zhigang Yu, Yangkejia Xiang, Fengqin Li, Xiaoping Tan, Lan Xu, Guiling Zhang. (2022) Electrochemical fabrication of Ru[bpy]32+@Cu-MOF(-SH)/Au photo/electrochemical coupling interface and its DNA-based biosensing performance. APPLIED SURFACE SCIENCE, [PMID:] [10.1016/j.apsusc.2022.153697] |
| 3. Tingting Han, Jinling Yang, Yan Wang, Yue Cao, Yuanyuan Wang, Hong-Yuan Chen, Jun-Jie Zhu. (2021) Boosted anodic electrochemiluminescence from blue-emissive sulfur quantum dots and its bioanalysis of glutathione. ELECTROCHIMICA ACTA, [PMID:] [10.1016/j.electacta.2021.138281] |
| 4. Yue Lin, Jinpeng Jia, Rui Yang, Daozhen Chen, Jian Wang, Fang Luo, Longhua Guo, Bin Qiu, Zhenyu Lin. (2019) Ratiometric Immunosensor for GP73 Detection Based on the Ratios of Electrochemiluminescence and Electrochemical Signal Using DNA Tetrahedral Nanostructure as the Carrier of Stable Reference Signal. ANALYTICAL CHEMISTRY, [PMID:30742421] [10.1021/acs.analchem.9b00013] |
| 5. Dandan Fang, Mian Pan, Huan Yi, Hong Dai, Zhensheng Hong, Xiangqin Zheng, Yanyu Lin. (2019) Enhanced electrochemiluminescence of luminol-DBAE system based on self-assembled mesocrystalline hybrid for the detection of ovarian cancer marker. SENSORS AND ACTUATORS B-CHEMICAL, [PMID:] [10.1016/j.snb.2019.01.151] |
| 6. Jialian Ding, Bin Su. (2024) Dual-Coreactants Enhanced Electrochemiluminescence. CHEMISTRY-A EUROPEAN JOURNAL, [PMID:39560166] [10.1002/chem.202403804] |
| 7. Zhigang Yu, Yangkejia Xiang, Xianda Han, Yi Guang, Fengqin Li. (2024) Study on the photo/electrochemical bi-functional properties of a coupling interface of Ru[dcbpy]32+-AMT/Au by SECM imaging-based joint analytical method. TALANTA, [PMID:38897005] [10.1016/j.talanta.2024.126423] |
| 8. Qian Qu, Yan Hu, Jiahao Xiong, Yu Ding, Yuqi Tang, Lingrui Chen, Yajun Zhao, Yuanzhu Mi. (2024) Two-step synthesis of ionic liquid demulsifiers for demulsification of water-in-oil emulsion. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2024.130210] |
| 9. Li Fu, Pengjie Dong, Zerui Liu, Qi Li, Yingshu Guo. (2024) Unary Au Nanocrystal with Prestored Electrons and Intrinsic Low Hole-Injected Potential for Low-Triggering Potential Electrochemiluminescence. ANALYTICAL CHEMISTRY, [PMID:39480793] [10.1021/acs.analchem.4c04594] |
| 10. Qinghai Long, Yutao Bai, Anteng Dai, Huajie Qiu, Xuanang Fu, Xiaoyun Chen, Chao Liu, Waseem Hayat, Bihong Lv, Guohua Jing, Zuoming Zhou. (2025) Energy-efficient CO₂ capture using a biphasic tertiary-amine ionic liquid with reversible phase behavior. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2025.167326] |
| 11. Jian-Dong Wang, Qi Gu, Zi-Hui Cai, Guo-Sheng Liu, Quan Zhou, Li-Na Fu, Shi-Liang Yang, Su Zhang, Yujie Fu. (2023) Efficient Extraction and Mechanism Analysis of Different Polarity Phytochemicals from Rosa roxburghii by a Green CO2-Responsive Switchable Solvent Combined with Ultrasound. ACS Sustainable Chemistry & Engineering, [PMID:] [10.1021/acssuschemeng.3c06085] |
| 12. Jielong Zhou, Bo Wang, Xiandong Hao, Zhiyong Xu, Wenbo Zhao. (2025) A systematic mathematical model to accurately predict SO2 absorption performance of binary mixture of alkanolamine and ionic liquid. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2025.133087] |