798312
3-(2-Ethylhexyl)thiophene
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C12H20S
CAS Number:
Molecular Weight:
196.35
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Assay:
97%
Form:
liquid
InChI
1S/C12H20S/c1-3-5-6-11(4-2)9-12-7-8-13-10-12/h7-8,10-11H,3-6,9H2,1-2H3
SMILES string
CCC(CCCC)CC1=CSC=C1
InChI key
HWMQCIZYXLAJKM-UHFFFAOYSA-N
assay
97%
form
liquid
refractive index
n/D 1.494
bp
150-152 °C/7.5 Torr
density
0.915 g/mL at 25 °C
Application
3-(2-Ethylhexyl)thiophene is a 3-alkylthiophene monomer, which can be used in the formation of conjugated highly regio-regular block polymers for applications in organic field effect transistors (OFETs), and organic photovoltaics (OPVs).
Organic semiconducting polymer or small molecule precursor.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Impact of the Alkyl Side Chains on the Optoelectronic Properties of a Series of Photovoltaic Low-?Band-?Gap Copolymers
Biniek, Laure; Fall; Sadiara, Chochos; Christos L., Anokhin; et al.
Macromolecules, 43(23), 9779-9786 (2010)
Influence of intermolecular interactions of electron donating small molecules on their molecular packing and performance in organic electronic devices
Kim, Ki-Hyun; Yu, Hojeong; Kang, Hyunbum; et al.
Journal of Material Chemistry A, 1(46), 14538-14547 (2013)
Influence of the Ethylhexyl Side-Chain Content on the Open-Circuit Voltage in rr-Poly(3-hexylthiophene-co-3-(2-ethylhexyl)thiophene) Copolymers
Burkhart, Beate; Khlyabich, Petr P.; Thompson, Barry C.
Macromolecules, 45(9), 3740-3748 (2012)
Nanostructure formation in poly (3-hexylthiophene-block-3-(2-ethylhexyl) thiophene) s
Zhang Y, et al.
Macromolecules, 42(18), 7008-7015 (2009)
3, 6-Dialkylthieno [3, 2-b] thiophene moiety as a soluble and electron donating unit preserving the coplanarity of photovoltaic low band gap copolymers
Biniek L, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 50(9), 1861-1868 (2012)
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