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Merck

399051

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24864785
MDL number:
MFCD00143181
Beilstein/REAXYS Number:
1617129

Key Documents

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Product Name

3-Hexylthiophene, ≥99%

InChI

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

SMILES string

CCCCCCc1ccsc1

InChI key

JEDHEMYZURJGRQ-UHFFFAOYSA-N

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.)

Quality Level

100

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Application

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

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).

pictograms

FlameExclamation mark
GHS02,GHS07

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

Storage Class

3 - Flammable liquids

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SHBS7196
SHBK0797
SHBF0792V
SHBC1591V
SHBB2960V

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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
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
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
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)
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