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O-Phosphorylethanolamine - 10mM in Water, high purity , CAS No.1071-23-4
Basic Description
Synonyms
2-Aminoethyl dihydrogen phosphate | O-Phosphorylethanolamine | 1071-23-4 | O-Phosphoethanolamine | Phosphorylethanolamine | phosphoethanolamine | Colamine phosphate | O-Phosphocolamine | ethanolamine phosphate | Ethanolamine O-phosphate | Phosphonoethanolamine | Phosphorylcola
Specifications & Purity
10mM in Water
Biochemical and Physiological Mechanisms
Phosphorylethanolamine participates in phospholipid metabolism. Its release can be stimulated occasionally by depolarizing stimuli. Reduction of phosphorylethanolamine levels has been observed in Alzheimer′s and Huntington′s disease.
Storage Temp
Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic acids and derivatives
Class
Organic phosphoric acids and derivatives
Subclass
Phosphate esters
Intermediate Tree Nodes
Not available
Direct Parent
Phosphoethanolamines
Alternative Parents
Monoalkyl phosphates Organopnictogen compounds Organooxygen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives
Molecular Framework
Aliphatic acyclic compounds
Substituents
Phosphoethanolamine - Monoalkyl phosphate - Alkyl phosphate - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as phosphoethanolamines. These are compounds containing a phosphate linked to the second carbon of an ethanolamine.
External Descriptors
primary amino compound - phosphoethanolamine
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)
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
2-aminoethyl dihydrogen phosphate
INCHI
InChI=1S/C2H8NO4P/c3-1-2-7-8(4,5)6/h1-3H2,(H2,4,5,6)
InChIKey
SUHOOTKUPISOBE-UHFFFAOYSA-N
Smiles
C(COP(=O)(O)O)N
Isomeric SMILES
C(COP(=O)(O)O)N
RTECS
KJ5830000
Molecular Weight
141.06
Reaxy-Rn
1758916
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1758916&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Melt Point(°C)
242.3℃
Molecular Weight
141.060 g/mol
XLogP3
-4.800
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
5
Rotatable Bond Count
3
Exact Mass
141.019 Da
Monoisotopic Mass
141.019 Da
Topological Polar Surface Area
92.800 Ų
Heavy Atom Count
8
Formal Charge
0
Complexity
98.200
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.
Lei Yang, Yuese Chen, Ting Zhang, Heqing Fu.
(2023)
Superior anti-smudge and flame retardancy of polydimethylsiloxane composite coating with phosphorus modified CO0.5Ni0.5Fe2O4. JOURNAL OF APPLIED POLYMER SCIENCE,
140
(19):
(e53832).
2.
Lin Wu, Yunchao Wu, Liu Jingjin, Suwan Liu, Qianzhe Li, Mengyu Yang, Miaomiao Zhang, Qing Ji, Feimin Zhang, Fengyi Du.
(2022)
Calcium and phosphorus co-doped carbon dots enhance osteogenic differentiation for calvarial defect repair in situ. Biomedical Materials,
17
(5):
(55007).
3.
Weisu Kong, Da Zhu, Rengan Luo, Siqi Yu, Huangxian Ju.
(2022)
Framework-promoted charge transfer for highly selective photoelectrochemical biosensing of dopamine. BIOSENSORS & BIOELECTRONICS,
211
(114369).
4.
Zhongshan Chen, Xuan He, Qian Li, Hui Yang, Yang Liu, Lining Wu, Zhixin Liu, Baowei Hu, Xiangke Wang.
(2022)
Low-temperature plasma induced phosphate groups onto coffee residue-derived porous carbon for efficient U(VI) extraction. Journal of Environmental Sciences,
122
(1).
5.
Liu Wenqian, Wang Qing, Zhang Ruoyan, Liu Mengshuang, Wang Cuicui, Liu Zixi, Xiang Chenggang, Lu Xiaohong, Zhang Xiaojing, Li Xiaojun, Wang Tao, Gao Lihong, Zhang Wenna.
(2022)
Rootstock–scion exchanging mRNAs participate in the pathways of amino acid and fatty acid metabolism in cucumber under early chilling stress. Horticulture Research,
9
6.
Hua-Rui Nan, Yun-Hai Liu, Wen-Juan Gong, Hong-Bo Peng, You-Qun Wang, Zhi-Bin Zhang, Xiao-Hong Cao.
(2022)
An inner-filter-effect based ratiometric fluorescent sensor for the detection of uranyl ions in real samples. Analytical Methods,
14
(5):
(532-540).
7.
Yu Xiao-Feng, Liu Yun-Hai, Zhou Zhi-Wei, Xiong Guo-Xuan, Cao Xiao-Hong, Li Min, Zhang Zhi-Bin.
(2014)
Adsorptive removal of U(VI) from aqueous solution by hydrothermal carbon spheres with phosphate group. JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY,
300
(3):
(1235-1244).
8.
Shuang Shen, Shuli Nong, Xianpeng Zhang, Jiaqi Song, Caiting Meng, Xinling Liu, Liang Shao, Guanying Li, Li Xu.
(2024)
An ALP-responsive, anionic iridium complex for specific recognition of osteosarcoma cells. DALTON TRANSACTIONS,
9.
He Liangrui, Wang Liyang, Yu Xujiang, Tang Yizhang, Jiang Zhao, Yang Guoliang, Liu Zhuang, Li Wanwan.
(2024)
Full-course NIR-II imaging-navigated fractionated photodynamic therapy of bladder tumours with X-ray-activated nanotransducers. Nature Communications,
15
(1):
(1-19).
10.
Xiang-Bo Zeng, Xue-Chen Pei, De-Yang Li, Fa-Wen Yin, Hui-Lin Liu, Meng-Ling Jin, Jiang-Hua Zhang, Da-Yong Zhou.
(2024)
Mechanism of discoloration of Antarctic krill oil upon storage: A study based on model systems. FOOD CHEMISTRY,
(140376).
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10 Citations