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Sigma-Aldrich

Octylphosphonic acid

97%

Synonym(s):

n-Octylphosphonic acid, OPA

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About This Item

Empirical Formula (Hill Notation):
C8H19O3P
CAS Number:
4724-48-5
Molecular Weight:
194.21
EC Number:
225-218-5
MDL number:
MFCD00015841
UNSPSC Code:
12352300
PubChem Substance ID:
329765066
NACRES:
NA.23

Assay

97%

form

solid

mp

93-98 °C

SMILES string

CCCCCCCCP(O)(O)=O

InChI

1S/C8H19O3P/c1-2-3-4-5-6-7-8-12(9,10)11/h2-8H2,1H3,(H2,9,10,11)

InChI key

NJGCRMAPOWGWMW-UHFFFAOYSA-N

Related Categories

General description

Octylphosphonic acid (OPA) forms a self-assembled monolayer (SAM), which serves as a protective anti-corrosive phosphonate layer on a variety of surfaces.

Application

OPA can be used as a surfactant that may be added to silver (Ag)/titanium oxide (TiO2) for uniform dispersion into the polymeric matrix. It may be coated on indium-tin oxide (ITO) substrates, which can be used for super-resolution microscopy. OPA based charge blocking layer may be used to prevent leakage of current in a hybrid dielectric film.

Signal Word

Danger

Hazard Statements

H302 - H314 - H373

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B - STOT RE 2 Oral

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Characterization of functionalized glass and indium tin oxide surfaces as substrates for super-resolution microscopy
Nicovich PR, et al.
Journal of Physics D: Applied Physics, 52(3), 034003-034003 (2018)
Surface modification of passive iron by alkyl-phosphonic acid layers
Paszternak A, et al.
Electrochimica Acta, 53(2), 337-345 (2007)
High-energy-density hybrid sol-gel dielectric film capacitors with a polymeric charge blocking layer
Kim Y, et al.
Journal of Material Chemistry A, 5(48), 25522-25528 (2017)
Rickdeb Sen et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(53), 13015-13022 (2017-07-14)
Rapid and quantitative click functionalization of surfaces remains an interesting challenge in surface chemistry. In this regard, inverse electron demand Diels-Alder (IEDDA) reactions represent a promising metal-free candidate. Herein, we reveal quantitative surface functionalization within 15 min. Furthermore, we report the
Alasdair A M Brown et al.
Nanoscale, 11(25), 12370-12380 (2019-06-20)
We report the self-assembly of an extensive inter-ligand hydrogen-bonding network of octylphosphonates on the surface of cesium lead bromide nanocrystals (CsPbBr3 NCs). The post-synthetic addition of octylphosphonic acid to oleic acid/oleylamine-capped CsPbBr3 NCs promoted the attachment of octylphosphonate to the
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