Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

Safety Information

446653

Sigma-Aldrich

Copper(II) 1,2,3,4,8,9,10,11,15,16,17,18,22,23,24,25-hexadecafluoro-29H,31H-phthalocyanine

Dye content 80 %

Synonym(s):

F16CuPc

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C32CuF16N8
CAS Number:
14916-87-1
Molecular Weight:
863.92
MDL number:
MFCD00274642
UNSPSC Code:
12352103
PubChem Substance ID:
24868290
NACRES:
NA.23

form

powder

composition

Dye content, 80%

mp

>300 °C (lit.)

λmax

689 nm

SMILES string

Fc1c(F)c(F)c2c3nc(nc4n5[Cu]n6c(n3)c7c(F)c(F)c(F)c(F)c7c6nc8nc(nc5c9c(F)c(F)c(F)c(F)c49)c%10c(F)c(F)c(F)c(F)c8%10)c2c1F

InChI

1S/C32F16N8.Cu/c33-9-1-2(10(34)18(42)17(9)41)26-49-25(1)53-27-3-4(12(36)20(44)19(43)11(3)35)29(50-27)55-31-7-8(16(40)24(48)23(47)15(7)39)32(52-31)56-30-6-5(28(51-30)54-26)13(37)21(45)22(46)14(6)38;/q-2;+2

InChI key

FJAOBQORBYMRNO-UHFFFAOYSA-N

Related Categories

General description

Copper(II) 1,2,3,4,8,9,10,11,15,16,17,18,22,23,24,25-hexadecafluoro-29H,31H-phthalocyanine(F16CuPc) is an organic molecule that can be used as an electron transporting material with good air-stability and an electron mobility of 0.11 cm2/Vs . It is majorly used in a variety of energy conservation based applications.

Application

F16CuPc can be used as an electron transporting layer for semiconducting applications such as an electron accepting material for organic photovoltaic cells and as a catalyst in biomimetic sensors. It may also be used in the fabrication of organic thin film transistors(OTFTs) and quartz crystal microbalance(QCM) based sensors.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

446653-VAR:
446653-BULK:
446653-1G:4548173941240
446653-250MG:

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKBS8025V
MKBG1222V
MKBB6450
09698KJ
45996KH

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Agata Sabik et al.
The Journal of chemical physics, 149(14), 144702-144702 (2018-10-15)
We have utilized scanning tunneling microscopy (STM) and low energy electron diffraction to determine the structural properties of two types of metal-phthalocyanines (MPcs), i.e., cobalt-phthalocyanine (CoPc) and hexadecafluorinated copper-phthalocyanine (F16CuPc) on the Ag(100) surface. For coverage close to one monolayer
Fabrication of highly air-stable ambipolar thin-film transistors with organic heterostructure of F16CuPc and DH-alpha 6T.
Ye R, et al.
Solid-State Electron, 52(1), 60-62 (2008)
Thickness-dependent structural transitions in fluorinated copper-phthalocyanine (F16CuPc) films.
de Oteyza DG, et al.
Journal of the American Chemical Society, 128(47), 15052-15053 (2006)
Tetra-tert-butyl copper phthalocyanine-based QCM sensor for toluene detection in air at room temperature.
Kumar A, et al.
Sensors and Actuators B, Chemical, 210(1), 398-407 (2015)
Electroanalytical determination of bumetanide employing a biomimetic sensor for detection of doping in sports.
dos SR, et al.
Analytical Methods : Advancing Methods and Applications, 6(15), 5792-5798 (2014)
View All Related Papers

Articles

Self-Assembly in Organic Thin Film Transistors for Flexible Electronic Devices

Flexible electronic circuits and displays based on organic active materials are future generations of products that may eventually enter mainstream electronics market.

Organic Materials for Thin Film Transistors
Self-Assembled Nanodielectrics (SANDs) for Unconventional Electronics

Self-Assembled Nanodielectrics (SANDs) for Unconventional Electronics

Soluble Pentacene Precursors

Fabrication procedure of organic field effect transistor device using a soluble pentacene precursor.

See All

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service