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About This Item
Empirical Formula (Hill Notation):
C6H13O5P
CAS Number:
Molecular Weight:
196.14
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Product Name
6-Phosphonohexanoic acid, 97%
InChI
1S/C6H13O5P/c7-6(8)4-2-1-3-5-12(9,10)11/h1-5H2,(H,7,8)(H2,9,10,11)
SMILES string
OC(=O)CCCCCP(O)(O)=O
InChI key
SYFTUNQVCGSBOV-UHFFFAOYSA-N
assay
97%
form
solid
mp
98-104 °C
Quality Level
Related Categories
Application
PHA can be used in the surface functionalization of phynox material which can further be utilized in the biomedical applications such as surgical implant and stents. It can also be used in dispersing manganese dioxide (MnO2)-MWCNT for the formation of electrodes for supercapacitors. It may also be coated on indium tin oxide (ITO) as an alternative to silane based SAMs for the fabrication of organic electronic devices such as organic solar cells (OSCs).
General description
6-Phosphonohexanoic acid (PHA) is an alkylphosphonic acid that forms a self-assembled monolayer (SAM) on a variety of surfaces. It has carboxylic groups that facilitate the grafting of the surface atoms while the phosphonic groups allow the surface modification of the substrate material.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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Proceedings of the National Academy of Sciences of the United States of America, 114(41), 10954-10959 (2017-09-07)
There is an urgent and unmet need for humanized in vivo models of type 1 diabetes to study immunopathogenesis and immunotherapy, and in particular antigen-specific therapy. Transfer of patient blood lymphocytes to immunodeficient mice is associated with xenogeneic graft-versus-host reactivity
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Journal of Material Chemistry A, 4(45), 17857-17865 (2016)
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Journal of industrial microbiology & biotechnology, 46(8), 1139-1153 (2019-05-16)
Extreme environments are a unique source of microorganisms encoding metabolic capacities that remain largely unexplored. In this work, we isolated two Antarctic bacterial strains able to produce poly(3-hydroxyalkanoates) (PHAs), which were classified after 16S rRNA analysis as Pseudomonas sp. MPC5
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