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Fórmula empírica (notación de Hill):
C10H16S
Número CAS:
Peso molecular:
168.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1617129
Assay:
≥99%
Form:
liquid
Servicio técnico
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Permítanos ayudarleQuality 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
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).
signalword
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
Clase de almacenamiento
3 - Flammable liquids
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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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
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

