Skip to Content
Merck
All Photos(1)

Key Documents

456365

Sigma-Aldrich

3-Dodecylthiophene

97%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C16H28S
CAS Number:
Molecular Weight:
252.46
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Assay

97%

refractive index

n20/D 1.488 (lit.)

bp

290 °C (lit.)

density

0.902 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCCCCCCCCCCCc1ccsc1

InChI

1S/C16H28S/c1-2-3-4-5-6-7-8-9-10-11-12-16-13-14-17-15-16/h13-15H,2-12H2,1H3

InChI key

RFKWIEFTBMACPZ-UHFFFAOYSA-N

General description

3-Dodecylthiophene (3-DT) is a conjugating monomer that can be used as an active layer on semiconductors. It has good electronic properties and can be used in the development of p-type semiconducting polymers. It is mainly used in the formation of poly(3-dodecylthiophene) (P3DT) through electrochemical polymerization. P3DT can further be utilized for a variety of organic electronic based applications.

Application

Conducting polymer precursor.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

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

Visit the Document Library

Subthreshold characteristics of field effect transistors based on poly (3-dodecylthiophene) and an organic insulator
Scheinert S, et al.
Journal of Applied Physics, 92(1), 330-337 (2002)
Nuclear magnetic resonance studies on electrochemically prepared poly (3-dodecylthiophene)
Sato M and Morii H
Macromolecules, 24(5), 1196-1200 (1991)
Controlled charge transport by polymer blend dielectrics in top-gate organic field-effect transistors for low-voltage-operating complementary circuits
Baeg K, et al.
ACS Applied Materials & Interfaces, 4(11), 6176-6184 (2012)
Hiro Minamimoto et al.
Nanoscale, 13(3), 1784-1790 (2021-01-13)
Plasmon-induced chemical reactions triggered by near-infrared light illumination might enable efficient photo energy conversion. Here, electrochemical oxidative polymerization of a conductive polymer was conducted on plasmonic photoconversion electrodes. The absolute electrochemical potential of the generated holes was estimated from the
Journal of the American Chemical Society, 117, 233-233 (1995)

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