Skip to Content
Merck
All Photos(1)

Documents

399051

Sigma-Aldrich

3-Hexylthiophene

≥99%

Synonym(s):

3-Hexylthiophene

Sign Into View Organizational & Contract Pricing


About This Item

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

Quality Level

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

Looking for similar products? Visit Product Comparison Guide

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

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)

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

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)
A photochemical study of poly (3-hexylthiophene).
Holdcroft S.
Macromolecules, 24(17), 4839-4844 (1991)
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
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
Thien An Phung Hai et al.
Carbohydrate polymers, 179, 221-227 (2017-11-08)
Surface functionalization of cellulose with poly(3-hexylthiophene) (P3HT) was conducted with FeCl

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