Tetradecylphosphonic Acid - ≥98%(T) , CAS No.4671-75-4

CAS: 4671-75-4 Cat. No.: T162675 Peso molecular: 278.37 Número EC: 225-118-1 PubChem CID: 78401

GRADE & PURITY ≥98%(T)

Synonyms

n-Tetradecylphosphonic acid | Tetradecylphosphonic acid | Tetradecyl-phosphonic acid | Tetradecanephosphonic acid | Phosphonic acid, tetradecyl- | 1-Tetradecanephosphonic acid | Tetradecyl Phosphonate | CHEMBL190999 | N-TETRADECYLPHOSPHONICACID

Storage

Store at 2-8°C

Shipped In

Wet ice

Descripción general

Tetradecylphosphonic acid forms a self-assembled monolayer (SAM) to functionalize a variety of nanoparticles.

TDPA can be used to cap copper nanoparticles to protect them from oxidation.It may also be used in the synthesis of cadmium sulfate (CdS) core, which can be used in the fabrication of cadmium selenium (CdSe)/CdS core quantum dots (QDs).It may also be coated on caesium lead bromide (CsPbBr3) perovskite quantum dots for the development of white light emitting diodes (wLED).

Specifications

Sinónimos

n-Tetradecylphosphonic acid | Tetradecylphosphonic acid | Tetradecyl-phosphonic acid | Tetradecanephosphonic acid | Phosphonic acid, tetradecyl- | 1-Tetradecanephosphonic acid | Tetradecyl Phosphonate | CHEMBL190999 | N-TETRADECYLPHOSPHONICACID

Especificaciones y pureza

≥98%(T)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%(T)

Nombres e identificadores

• Pubchem Sid: 504755281
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755281
• Sonrisas canónicas: CCCCCCCCCCCCCCP(=O)(O)O
• IUPAC Name: tetradecylphosphonic acid
• InChIKey: BVQJQTMSTANITJ-UHFFFAOYSA-N
• INCHI: 1S/C14H31O3P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18(15,16)17/h2-14H2,1H3,(H2,15,16,17)
• Isómeros SMILES: CCCCCCCCCCCCCCP(=O)(O)O
• RTECS: TA0460000
• PubChem CID: 78401
• Peso molecular: 278.37
• Reaxy-Rn: 1784271

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Organic phosphonic acids and derivatives
      • Subclass Organic phosphonic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Organic phosphonic acids and derivatives
• Subclass: Organic phosphonic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic phosphonic acids
• Alternative Parents: Organopnictogen compounds Organophosphorus compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organophosphonic acid - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organophosphorus compound - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as organic phosphonic acids. These are organic compounds containing phosphonic acid.
• 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.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

LPAR1 Tchem Lysophosphatidic acid receptor Edg-2 (779 Activities)

Discover Target: LPAR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

LPAR2 Tchem Lysophosphatidic acid receptor Edg-4 (418 Activities)

Discover Target: LPAR2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

LPAR3 Tchem Lysophosphatidic acid receptor Edg-7 (471 Activities)

Discover Target: LPAR3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in ethanol, dimethyl sulfoxide and dimethyl formamide. Partially soluble in water.
• Punto de fusión (°C): 95.0 - 99.0 °C
• Peso molecular: 278.370 g/mol
• XLogP3: 5.100
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 13
• Exact Mass: 278.201 Da
• Monoisotopic Mass: 278.201 Da
• Topological Polar Surface Area: 57.500 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 213.000
• 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

Referencias

1. Hao Wu, Xiaoyu Cheng, Songjun Xie, Yan Huang, Raheel Ahmed Janjua, Xinzi Liu, Sailing He.  (2023)  Aluminum Quantum Dots with Surface Controlled Blue-UV Photoluminescence.  Journal of Physical Chemistry C,      [PMID:] [10.1021/acs.jpcc.2c08441]

2. Weinan Xue, Xin Zhang, Wei Zhu, Xue Zhang, Wei Wang, Linwei Peng, Xiang Ma, Yan Li.  (2022)  Large-scale heterogeneous synthesis of monodisperse high performance colloidal CsPbBr3 nanocrystals.  Fundamental Research,      [PMID:] [10.1016/j.fmre.2022.05.030]

3. Yingping Zheng, Weidong Bao, Guoning Liu, Shaopeng Qi, Dehua Yu, Kaili Ma, Zhenrong Chen, Xiangting Hu, Yongbing Lou.  (2021)  Cu/Ni-NiOx Nanoparticles Distributed on Graphene as Catalysts for the Methanolysis of Ammonia Borane to Produce Hydrogen.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.1c03706]

4. Wu Hao, Cheng Xiaoyu, Dong Hongguang, Xie Songjun, He Sailing.  (2021)  Aluminum nanocrystals evolving from cluster to metallic state: Size tunability and spectral evidence.  Nano Research,  15  (2): (838-844).  [PMID:] [10.1007/s12274-021-3486-9]

5. Yangen Xie, Chunsheng Wang, Zhijie Yang, Huiying Wei, Jingjing Wei.  (2020)  Dimensionality-controlled self-assembly of CdSe nanorods into discrete suprastructures within emulsion droplets.  NEW JOURNAL OF CHEMISTRY,  44  (48): (21112-21118).  [PMID:] [10.1039/D0NJ05059H]

6. Yang Yuehua, Zhao Baofeng, Gao Yuping, Liu Han, Tian Yiyao, Qin Donghuan, Wu Hongbin, Huang Wenbo, Hou Lintao.  (2015)  Novel Hybrid Ligands for Passivating PbS Colloidal Quantum Dots to Enhance the Performance of Solar Cells.  Nano-Micro Letters,  7  (4): (325-331).  [PMID:30464978] [10.1007/s40820-015-0046-4]

7. Yuwen Wang, Xuan Zhang, Yajuan Wei, Jingbo Zhang.  (2025)  Boosting C2+ Selectivity in CO₂ Electroreduction on Cu Nanoparticles via Molecular Dispersion of Cobalt Phthalocyanine.  ChemCatChem,      [PMID:] [10.1002/cctc.202500056]

8. Hassanien Gomaa, Cuihua An, Penggang Jiao, Wenliu Wu, Hassan A.H. Alzahrani, Mohamed A. Shenashen, Qibo Deng, Ning Hu.  (2024)  Controllable synthesis of a hybrid mesoporous sheets-like Fe0.5NiS2@ P, N-doped carbon electrocatalyst for alkaline oxygen evolution reaction.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:38636218] [10.1016/j.jcis.2024.04.079]

9. Xue Zhang, Linwei Peng, Siyuan Ye, Zhuohan Lin, Yan Li.  (2024)  Efficiently green-emitting and ultra-stable CsPbBr3@SiO2 nanocomposites for white light-emitting diodes.  MATERIALS RESEARCH BULLETIN,      [PMID:] [10.1016/j.materresbull.2024.112833]

10. Siyuan Ye, Fei Lin, Linwei Peng, Jiaxin Li, Qiaohui Ruan, Zhuohan Lin, Wang Xu, Yan Li.  (2024)  Highly Stable Mixed Halide Perovskite Nanocrystals for High Performance Pure-Red Light-Emitting Diodes.  Advanced Optical Materials,      [PMID:] [10.1002/adom.202402396]

11. Xue-Hui Shi, Zhendong Zhu, Changlin Shen, Ya Li, Zhuang Qian, Yonghao Wu, Huifeng Chen, Qing-Qing Ye, Chaojie Hu, Yifan Song, Lei Wang, Zhimou Yang, Wenjie Ren.  (2025)  A facile and universal ligand exchange strategy enables sequential surface functionalization of quantum dots for high quality in vivo imaging.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.169650]