ChemicalBook--->CAS DataBase List--->132814-91-6

132814-91-6

132814-91-6 Structure

132814-91-6 Structure
IdentificationBack Directory
[Name]

α,ω-Dihexylquaterthiophene, 5,5μ-Bis(3-hexyl-2-thienyl)-2,2μ-bithiophene, DH-4T
[CAS]

132814-91-6
[Synonyms]

4T6
DH-4T
α,ω-Dihexylquaterthiophene
alpha,omega-Dihexylquaterthiophene
3,3'-dihexyl-2,2':5',2:5,2'-quarterthiophene
5,5'-Bis(3-hexyl-2-thienyl)-2,2'-bithiophene
3,3μμμ-Dihexyl-2,2μ:5μ,2μμ:5μμ,2μμμ-quaterthiophene
2,2':5',2'':5'',2'''-Quaterthiophene, 3,3'''-dihexyl-
3,3'''-Dihexyl-2,2':5',2'':5'',2'''-quaterthiophene 95%
2-(3-hexylthiophen-2-yl)-5-[5-(3-hexylthiophen-2-yl)thiophen-2-yl]thiophene
α,ω-Dihexylquaterthiophene, 5,5μ-Bis(3-hexyl-2-thienyl)-2,2μ-bithiophene, DH-4T
3,3'''-Dihexyl-2,2':5',2'':5'',2'''-quaterthiophene (contains 3% Dichloromethane at maximum)
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C28H34S4
[MDL Number]

MFCD10567045
[MOL File]

132814-91-6.mol
[Molecular Weight]

498.83
Chemical PropertiesBack Directory
[Melting point ]

25-29 °C
[Boiling point ]

592.0±50.0 °C(Predicted)
[density ]

1.131±0.06 g/cm3(Predicted)
[Fp ]

110 °C
[storage temp. ]

2-8°C(protect from light)
[form ]

clear liquid to cloudy liquid
[color ]

Light yellow to Brown
[InChI]

1S/C28H34S4/c1-3-5-7-9-11-21-17-19-29-27(21)25-15-13-23(31-25)24-14-16-26(32-24)28-22(18-20-30-28)12-10-8-6-4-2/h13-20H,3-12H2,1-2H3
[InChIKey]

MLDVGCCQHBDHDR-UHFFFAOYSA-N
[SMILES]

CCCCCCc1ccsc1-c2ccc(s2)-c3ccc(s3)-c4sccc4CCCCCC
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[RIDADR ]

UN 3335
[WGK Germany ]

3
[HS Code ]

2934.99.4400
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Hazard InformationBack Directory
[Uses]

D4HT can be used a conjugating polymer in the fabrication of devices such as organic field effect transistor (OFET), organic thin film transistor (OTFT) and organic photovoltaics (OPV).
[General Description]

3,3′′′-Dihexyl-2,2′:5′,2′′:5′′,2′′′-quaterthiophene (D4HT) is a dihexyl quarterthiophene derivative that can be used as a donor-acceptor molecule in organic electronic devices. It has a field mobility of 0.23 cm2/Vs and acts as an active layer in semiconductors.
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