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399051

Sigma-Aldrich

3-Hexylthiophene

≥99%

Synonym(s):

3-Hexylthiophene

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About This Item

Empirical Formula (Hill Notation):
C10H16S
CAS Number:
1693-86-3
Molecular Weight:
168.30
Beilstein:
1617129
MDL number:
MFCD00143181
UNSPSC Code:
12352100
PubChem Substance ID:
24864785
NACRES:
NA.22

Assay

≥99%

form

liquid

refractive index

n20/D 1.496 (lit.)

bp

65 °C/0.45 mmHg (lit.)

density

0.936 g/mL at 25 °C (lit.)

SMILES string

CCCCCCc1ccsc1

InChI

1S/C10H16S/c1-2-3-4-5-6-10-7-8-11-9-10/h7-9H,2-6H2,1H3

InChI key

JEDHEMYZURJGRQ-UHFFFAOYSA-N

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General description

3-Hexylthiophene, a sulfur containing heterocyclic building block, is a thiophene derivative. Poly(3-hexylthiophene) (P3HT) nanofibres have been used for the preparation of organic phototransistors (OPTs).

Application

3-Hexylthiophene may be used as starting reagent in the synthesis of poly(3-hexylthiophene) (P3HT).

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Karolina Gebka et al.
Polymers, 11(2) (2019-04-10)
Electrochemical polymerisation is reported to be a method for readily producing copolymers of various conjugated molecules. We employed this method for mixtures of indole, carbazole or fluorene with 3-hexylthiophene (HT), in order to obtain their soluble copolymers. Although polymer films
X-ray and electron induced oligomerization of condensed 3-hexylthiophene.
Hernandez JE, et al.
The Journal of Physical Chemistry B, 105(35), 8339-8344 (2001)
Fangwen Zha et al.
Soft matter, 16(28), 6591-6598 (2020-07-01)
The fabrication of scaffolds with suitable chemical, physical, and electrical properties is critical for nerve cell adhesion and proliferation. Recently, electrical stimulation on conductive polymers has been applied to construct functional nerve cell scaffolds. Herein, we prepared natural polymer (cellulose)/conductive
Wouter Dierckx et al.
Nanotechnology, 26(6), 065201-065201 (2015-01-20)
Here we report the fabrication of nanofibre-based organic phototransistors (OPTs) using preformed poly(3-hexylthiophene) (P3HT) nanofibres. OPT performance is analysed based on two important parameters: photoresponsivity R and photosensitivity P. Before testing the devices as OPTs, the normal organic field-effect transistor
Alexandru Oprea et al.
Analytical and bioanalytical chemistry, 412(25), 6707-6776 (2020-08-02)
Within the framework outlined in the first part of the review, the second part addresses attempts to increase receptor material performance through the use of sensor systems and chemometric methods, in conjunction with receptor preparation methods and sensor-specific tasks. Conclusions
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