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399051

Sigma-Aldrich

3-Hexylthiophene

≥99%

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Empirical Formula (Hill Notation):
C10H16S
CAS Number:
Molecular Weight:
168.30
Beilstein:
1617129
MDL number:
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

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This Item
751871456373900563
3-Hexylthiophene ≥99%

Sigma-Aldrich

399051

3-Hexylthiophene

3,4-Dihexylthiophene 97%

Sigma-Aldrich

751871

3,4-Dihexylthiophene

form

liquid

form

liquid

form

-

form

solid

refractive index

n20/D 1.496 (lit.)

refractive index

n20/D 1.494

refractive index

n20/D 1.557 (lit.)

refractive index

-

bp

65 °C/0.45 mmHg (lit.)

bp

-

bp

-

bp

-

density

0.936 g/mL at 25 °C (lit.)

density

0.925 g/mL at 25 °C

density

1.521 g/mL at 25 °C (lit.)

density

-

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

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Customers Also Viewed

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
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
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
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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