399051
3-Hexylthiophene
≥99%
Synonym(s):
3-Hexylthiophene
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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
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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
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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).
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
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X-ray and electron induced oligomerization of condensed 3-hexylthiophene.
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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
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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
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