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N,N-Diethylaniline - Analytical Reagent, high purity , CAS No.91-66-7
Basic Description
Synonyms
N,N-DIETHYLANILINE | 91-66-7 | Diethylaniline | Benzenamine, N,N-diethyl- | N,N-Diethylanilin | Diethylphenylamine | N,N-Diethyl aniline | Diaethylanilin | Aniline, N,N-diethyl- | Phenyldiethylamine | N,N-Diethylbenzenamine | N,N-Diethylaminobenzene | N,N-Diethylaniline-4-D | N-Ph
Specifications & Purity
AR
Storage Temp
Protected from light
Shipped In
Normal
Grade
AR
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic nitrogen compounds
Class
Organonitrogen compounds
Subclass
Amines
Intermediate Tree Nodes
Tertiary amines - Tertiary alkylarylamines
Direct Parent
Dialkylarylamines
Alternative Parents
Aniline and substituted anilines Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Aniline or substituted anilines - Dialkylarylamine - Benzenoid - Monocyclic benzene moiety - Organopnictogen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as dialkylarylamines. These are aliphatic aromatic amines in which the amino group is linked to two aliphatic chains and one aromatic group.
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.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
N,N-diethylaniline
INCHI
InChI=1S/C10H15N/c1-3-11(4-2)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3
InChIKey
GGSUCNLOZRCGPQ-UHFFFAOYSA-N
Smiles
CCN(CC)C1=CC=CC=C1
Isomeric SMILES
CCN(CC)C1=CC=CC=C1
WGK Germany
2
RTECS
BX3400000
UN Number
2432
Packing Group
III
Molecular Weight
149.23
Beilstein
742483
Reaxy-Rn
742483
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=742483&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Light sensitive.
Refractive Index
1.542
Flash Point(°F)
190.4 °F
Flash Point(°C)
92 °C
Boil Point(°C)
217°C
Melt Point(°C)
-38°C
Molecular Weight
149.230 g/mol
XLogP3
3.300
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
3
Exact Mass
149.12 Da
Monoisotopic Mass
149.12 Da
Topological Polar Surface Area
3.200 Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
91.000
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.
Zhengyu Wang, Yufeng Hu, Zhiduo Ding, Hao Zhou, Jianye Zhang, Jingjing Zhan, Minghuo Wu.
(2023)
Determination of Organic Nitrogen Compounds in Gasoline by Water-Assisted Dispersive Solid-Phase Extraction (DSPE) and High-Performance Liquid Chromatography-High-Resolution Mass Spectrometry (HPLC-HRMS). ANALYTICAL LETTERS,
2.
Rui Yuan, Zheng Chu, Xiaolian Wu, Fanmin Kong, Guodong Jiang, Yucai Shen, Dong Zhao.
(2022)
Surface modification of UHMWPE fibers with chlorination and polydopamine for enhancing the mechanical properties of composites. JOURNAL OF APPLIED POLYMER SCIENCE,
139
(41):
(e52988).
3.
Shaoyun Chen, Yalu Duan, Wenqiang Hua, Qilang Lin, Bo Qu, Rui Wang, Yanyu Zheng, Xiaoying Liu, Wenjie Li, Dongxian Zhuo.
(2022)
Synthesis of novel acrylic liquid-crystal resin and its in-situ enhancement in light-curing 3D printing performance. Journal of Materials Research and Technology-JMR&T,
17
(2158).
4.
Qi Zhao, Xudong Li, Zishang Tian, Hui Ma, Xianglin Hou, Yingxiong Wang, Yuqi Wang.
(2022)
Controlling degradation and recycling of carbon fiber reinforced bismaleimide resin composites via selective cleavage of imide bonds. COMPOSITES PART B-ENGINEERING,
231
(109595).
5.
Yangjie Fu, Kejie Zhang, Yi Zhang, Yanqing Cong, Qi Wang.
(2021)
Fabrication of visible-light-active MR/NH2-MIL-125(Ti) homojunction with boosted photocatalytic performance. CHEMICAL ENGINEERING JOURNAL,
412
(128722).
6.
Pengcheng Hu, Ruimin Chai, Quanyou Liu, Junlin Wang, Shu-Feng Zhou.
(2019)
A novel dissolution-precipitation method for high-efficiency separation of oil-wetted oil sands. CANADIAN JOURNAL OF CHEMICAL ENGINEERING,
98
(5):
(1157-1163).
7.
Zhan Yi-zhen, Zhao Xue, Wang Wei.
(2017)
Synthesis and application of phthalimide disperse dyes. FIBERS AND POLYMERS,
18
(12):
(2278-2286).
8.
Yi-zhen Zhan, Xue Zhao, Bi-jia Wang, Wei Wang.
(2017)
Computational modelling of the influence of substituent effects on phthalimidylazo disperse dye hydrolysis and interaction energy. COLORATION TECHNOLOGY,
134
(1):
(24-32).
9.
Yizhen Zhan, Xue Zhao, Wei Wang.
(2017)
Synthesis of phthalimide disperse dyes and study on the interaction energy. DYES AND PIGMENTS,
146
(240).
10.
Huiying Li, Honghao Zheng, Weijun Tong, Changyou Gao.
(2017)
Non-covalent assembly of poly(allylamine hydrochloride)/triethylamine microcapsules with ionic strength-responsiveness and auto-fluorescence. JOURNAL OF COLLOID AND INTERFACE SCIENCE,
496
(228).
11.
Mingming Liu, Xin Zhou, Yingyi Chen, Hanlan Liu, Xionghan Feng, Guohong Qiu, Fan Liu, Zhaorui Zeng.
(2010)
Innovative chemically bonded ionic liquids-based sol–gel coatings as highly porous, stable and selective stationary phases for solid phase microextraction. ANALYTICA CHIMICA ACTA,
683
(96).
12.
Weijie Ren, Ning Li, Qing Chang, Jie Wu, Jinlong Yang, Shengliang Hu, Zhenhui Kang.
(2024)
Abstracting photogenerated holes from covalent triazine frameworks through carbon dots for overall hydrogen peroxide photosynthesis. CHINESE JOURNAL OF CATALYSIS,
62
(178).
13.
Zongbo Zhang, Shiliang Song, Yan Ding, Jianhai Yu, Wenting Wu, Jin Li, Xin Wang, Yong Guo, Liang Gong.
(2024)
Ultrasonic enhanced liquid-liquid interfacial reaction for improving the synthesis of Iron-doped carbon dots (Fe-CDs) for achieving superior photocatalytic performance. JOURNAL OF COLLOID AND INTERFACE SCIENCE,
669
(816).
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13 Citations
H2202058