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n-dodecylphosphocholine - >99%, high purity
Basic Description
Synonyms
DPC | Fos-Choline-12 | FOS12 | FC-12 | dodecyl 2-(trimethylammonio)ethyl phosphate | dodecyl phosphocholine | DDPPC | M5CF6282DD | dodecyl 2-(trimethylazaniumyl)ethyl phosphate | 2-(Trimethylammonio)ethyl dodecyl phosphate
Specifications & Purity
≥99%
Biochemical and Physiological Mechanisms
n-dodecylphosphocholine in combination with 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) is used for membrane-mimetic bicelle system for orientation based studies in membrane proteins. It provides a zwitterionic surface in the membrane micelle struc
Storage Temp
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
Dodecylphosphocholine is a structural analog of lauroyl lysophosphatidylcholine that is more stable to hydrolytic degradation.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic nitrogen compounds
Class
Organonitrogen compounds
Subclass
Quaternary ammonium salts
Intermediate Tree Nodes
Cholines
Direct Parent
Phosphocholines
Alternative Parents
Dialkyl phosphates Tetraalkylammonium salts Organopnictogen compounds Organooxygen compounds Organic salts Organic oxides Hydrocarbon derivatives Amines
Molecular Framework
Aliphatic acyclic compounds
Substituents
Phosphocholine - Dialkyl phosphate - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - Tetraalkylammonium salt - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Amine - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as phosphocholines. These are compounds containing a [2-(trimethylazaniumyl)ethoxy]phosphonic acid or derivative.
External Descriptors
phosphocholines
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
Pubchem Sid
504759768
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504759768
IUPAC Name
dodecyl 2-(trimethylazaniumyl)ethyl phosphate
INCHI
InChI=1S/C17H38NO4P/c1-5-6-7-8-9-10-11-12-13-14-16-21-23(19,20)22-17-15-18(2,3)4/h5-17H2,1-4H3
InChIKey
QBHFVMDLPTZDOI-UHFFFAOYSA-N
Smiles
CCCCCCCCCCCCOP(=O)([O-])OCC[N+](C)(C)C
Isomeric SMILES
CCCCCCCCCCCCOP(=O)([O-])OCC[N+](C)(C)C
Molecular Weight
351.46
Reaxy-Rn
3980150
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3980150&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Hygroscopic
Molecular Weight
351.500 g/mol
XLogP3
4.500
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
16
Exact Mass
351.254 Da
Monoisotopic Mass
351.254 Da
Topological Polar Surface Area
58.600 Ų
Heavy Atom Count
23
Formal Charge
0
Complexity
310.000
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.
Xian Sun, Xiaochuan Zhang, Xiaohong Ren, Hongyu Sun, Li Wu, Caifen Wang, Xiaohui Ye, Peter York, Zhaobing Gao, Hualiang Jiang, Jiwen Zhang, Xianzhen Yin.
(2021)
Multiscale Co-reconstruction of Lung Architectures and Inhalable Materials Spatial Distribution. Advanced Science,
8
(8):
(2003941).
2.
Yan Xiong, Jie Chen, Ming Duan, Xiang Li, Jun Li, Can Zhang, Shenwen Fang, Rui Liu, Run Zhang.
(2019)
Insight into the Adsorption-Interaction Mechanism of Cr(VI) at the Silica Adsorbent Surface by Evanescent Wave Measurement. LANGMUIR,
35
(45):
(14414–14427).
3.
Shailendra Shakya, Yaping He, Xiaohong Ren, Tao Guo, Abi Maharjan, Ting Luo, Tingting Wang, Ramesh Dhakhwa, Balmukunda Regmi, Haiyan Li, Ruxandra Gref, Jiwen Zhang.
(2019)
Ultrafine Silver Nanoparticles Embedded in Cyclodextrin Metal-Organic Frameworks with GRGDS Functionalization to Promote Antibacterial and Wound Healing Application. Small,
15
(27):
(1901065).
4.
Yaping He, Jian Xu, Xian Sun, Xiaohong Ren, Abi Maharjan, Peter York, Yong Su, Haiyan Li, Jiwen Zhang.
(2019)
Cuboidal tethered cyclodextrin frameworks tailored for hemostasis and injured vessel targeting. Theranostics,
9
(9):
( 2489–2504).
5.
Ling Tan, Yufei Huang, Wei Mao, Xiayi Hu, Yangqiang Huang, Hao Chen, Xiao Luo.
(2024)
Anatase-Layered TiO2 for Selective Transesterification for Diphenyl Carbonate: A Study of the Active Site and Deactivation Mechanism. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,
63
(38):
(16347-16355).
6.
Wen Li, Jintao He, Qijue Chen, Feng Bao, Yinqiang Huo, Jing Deng, Qinlu Lin, Feijun Luo.
(2025)
Enhancement of Oryzanol application by constructing modified β-CD inclusion complex and polycaprolactone-chitosan electrospun fiber membranes: Perspectives on wound dressings and grape preservation. FOOD CHEMISTRY,
473
(143025).
7.
Zhencai Zhang, Zifeng Yang, Ming Jiang, Wenjuan Fang, Heng Wang, Chenhao Li, Xin Yao, Zengxi Li, Fei Xu.
(2024)
Green and Efficient Synthesis of Biobased Polycarbonates with Tunable Performance via Functionalized Ionic Liquid Catalysts Enhanced by Cation–π Interactions. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,
63
(24):
(10512-10523).
8.
Yanfang Huang, Meimei Wang, Bingbing Liu, Shengpeng Su, Hu Sun, Shuzhen Yang, Guihong Han.
(2024)
Highly selective ion precipitation flotation for ternary Co–Zn–Mn separation: Stepwise chelation capture of Co and Zn from simulated zinc hydrometallurgy wastewater. CHEMOSPHERE,
353
(141533).
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8 Citations
L2423091