399051
3-Hexylthiophene
≥99%
Synonyme(s) :
3-Hexylthiophene
Se connecter pour consulter les tarifs organisationnels et contractuels.
Sélectionner une taille de conditionnement
Changer de vue
A propos de cet article
Formule empirique (notation de Hill) :
C10H16S
Numéro CAS:
Poids moléculaire :
168.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1617129
Assay:
≥99%
Form:
liquid
Service technique
Besoin d'aide ? Notre équipe de scientifiques expérimentés est là pour vous.
Laissez-nous vous aiderQuality 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
Classe de stockage
3 - Flammable liquids
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Faites votre choix parmi les versions les plus récentes :
Déjà en possession de ce produit ?
Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.
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)