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Tetrabutylammonium phosphate monobasic - 0.5mol/L in water, for Ion-pair chromatography, high purity , CAS No.5574-97-0
Basic Description
Synonyms
1-Butanaminium, N,N,N-tributyl-, phosphate (1:1) | H11293 | AS-15201 | DTXSID4063951 | FT-0635772 | tetra-n-butylammonium phosphate | Tetrabutylammonium dihydrogen phosphate | tetrabutyl-ammonium dihydrogen phosphate | CRD3CJW5P4 | tetrabutylammonium dihy
Specifications & Purity
for ion pair chromatography, 0.5mol/L in water
Storage Temp
Argon charged,Desiccated
Shipped In
Normal
Grade
for ion pair chromatography
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic acids and derivatives
Class
Organic phosphoric acids and derivatives
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Organic phosphoric acids and derivatives
Alternative Parents
Tetraalkylammonium salts Organopnictogen compounds Organic salts Organic oxides Hydrocarbon derivatives Amines
Molecular Framework
Aliphatic acyclic compounds
Substituents
Organic phosphoric acid derivative - Tetraalkylammonium salt - Quaternary ammonium salt - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organonitrogen compound - Amine - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as organic phosphoric acids and derivatives. These are organic compounds containing phosphoric acid or a derivative thereof.
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(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
dihydrogen phosphate;tetrabutylazanium
INCHI
InChI=1S/C16H36N.H3O4P/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-5(2,3)4/h5-16H2,1-4H3;(H3,1,2,3,4)/q+1;/p-1
InChIKey
ARRNBPCNZJXHRJ-UHFFFAOYSA-M
Smiles
CCCC[N+](CCCC)(CCCC)CCCC.OP(=O)(O)[O-]
Isomeric SMILES
CCCC[N+](CCCC)(CCCC)CCCC.OP(=O)(O)[O-]
WGK Germany
3
PubChem CID
2735142
Molecular Weight
339.45
Beilstein
5196532
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Hygroscopic.light & air sensitive
Melt Point(°C)
151-154 °C
Molecular Weight
339.450 g/mol
XLogP3
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
12
Exact Mass
339.254 Da
Monoisotopic Mass
339.254 Da
Topological Polar Surface Area
80.600 Ų
Heavy Atom Count
22
Formal Charge
0
Complexity
166.000
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
2
Citations of This Product
1.
Dongyang Shen, Zhenwei Ren, Qinyi Li, Chengzhao Luo, Wenlin Xia, Zhishuai Zheng, Wenchen Ma, Jie Li, Yu Chen.
(2022)
Highly Emissive Quasi-2D Perovskites Enabled by a Multifunctional Molecule for Bright Light-Emitting Diodes. ACS Applied Materials & Interfaces,
14
(18):
(21636–21644).
2.
Yu Ding, Qiaochu Wang, Guangqu Liu, Yaqian Feng, Wei Zhou.
(2020)
Cholesterol moieties as building blocks for assembling nanoparticles to achieve effective oral delivery of insulin. Biomaterials Science,
8
(14):
(3979-3993).
3.
Aiqing Feng, Yongmei Jia, Liping Huang, Lin Wang, Guohua Zhou, Sheng Wang, Peilian Liu.
(2019)
1,6-Elimination reaction induced detection of fluoride ions in vitro and in vivo based on a NIR fluorescent probe. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,
220
(117108).
4.
Xuefang Shang, Xuejing Yue, Yanmei Chen, Congshu Li, Hongli Chen, Tianyun Wang.
(2019)
Design, synthesis, crystal structure and cytotoxicity studies of colorimetric fluorescent “OFF-ON” probes for rapid detection of hydrogen sulfide based on Cu(II) complex. INORGANIC CHEMISTRY COMMUNICATIONS,
99
(1).
5.
Chen Yanmei, Shang Xuefang, Li Congshu, Xue Zhenzhen, Chen Hongli, Wu Hongwei, Wang Tianyun.
(2018)
The synthesis, crystal, hydrogen sulfide detection and cell assement of novel chemsensors based on coumarin derivatives. Scientific Reports,
8
(1):
(1-9).
6.
Shang Xuefang, Li Jie, Feng Yaqian, Chen Hongli, Guo Wei, Zhang Jinlian, Wang Tianyun, Xu Xiufang.
(2018)
Low-Cytotoxicity Fluorescent Probes Based on Anthracene Derivatives for Hydrogen Sulfide Detection. Frontiers in Chemistry,
6
7.
Yanmei Chen, Xuefang Shang, Xing Zhao, Jie Li, Jianmei Yuan, Hongli Chen, Jinlian Zhang, Tianyun Wang.
(2018)
Highly selective probes of copper(II) complexes for sulfide detection and cytotoxicity assay. Journal of Sulfur Chemistry,
8.
Kui Ren, Xuefang Shang, Yanmei Chen, Xueli Zhang, Jiajia Fu, Peipei Zhao, Jinlian Zhang.
(2016)
Synthesis and crystal structure of a highly selective colorimetric and fluorometric sensor for hydrogen sulfide. LUMINESCENCE,
32
(5):
(765-771).
9.
Kui Ren, Xuefang Shang, Jiajia Fu, Peipei Zhao, Jinlian Zhang.
(2016)
Copper complex based on 2-(phenylimino-methyl)-phenol as a high selective fluoresencent probe for hydrogen sulfide. POLYHEDRON,
104
(99).
10.
Xuefang Shang, Wanli Li, Yaqian Feng, Xin Li, Xiufang Xu.
(2015)
Double Properties of Novel Acylhydrazone Nanomaterials Based on a Conjugated System: Anion Binding Ability and Antibacterial Activity. Applied Sciences-Basel,
5
(4):
(910-925).
11.
Xuefang Shang, Wanli Li, Xiaofang Wei, Huanle Zhang, Zhiyuan Fu, Jinlian Zhang, Xiufang Xu.
(2014)
Synthesis, Bioactivity, and the Anion-Binding Property of 2-Sulfydryl-1,3,4-thiodiazole Derivatives. HETEROATOM CHEMISTRY,
26
(2):
(142-149).
12.
Wei Lu, Jinting Zhou, Keyuan Liu, Dan Chen, Liming Jiang, Zhiquan Shen.
(2013)
A polymeric film probe with a turn-on fluorescence response to hydrogen sulfate ions in aqueous media. Journal of Materials Chemistry B,
1
(38):
(5014-5020).
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12 Citations
L2304354