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About This Item
Empirical Formula (Hill Notation):
C12H20S
CAS Number:
Molecular Weight:
196.35
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
liquid
Quality Level
assay
97%
form
liquid
refractive index
n20/D 1.492 (lit.)
bp
106-107 °C/3 mmHg (lit.)
density
0.92 g/mL at 25 °C (lit.)
SMILES string
CCCCCCCCc1ccsc1
InChI
1S/C12H20S/c1-2-3-4-5-6-7-8-12-9-10-13-11-12/h9-11H,2-8H2,1H3
InChI key
WQYWXQCOYRZFAV-UHFFFAOYSA-N
General description
3-Octylthiophene is an alkyl thiophene derivative. It has been synthesized by the reaction of 3-bromothiophene with octylmagnesium bromide.
Application
3-Octylthiophene may be used as a starting material in the synthesis of the following:
- 2,5-dibromo-3-octylthiophene
- poly(3-butylthiophene)-b-poly(3-octylthiophene), a diblock copoly(3-alkylthiophene)
- regioregular poly(3-octylthiophene) (POT)
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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New convenient synthesis of highly regioregular poly (3-octylthiophene) based on the Suzuki coupling reaction.
Guillerez S and Bidan G.
Synthetic Metals, 93(2), 123-126 (1998)
Soluble Phenanthrenyl-Imidazole-Presenting Regioregular Poly (3-octylthiophene) Copolymers Having Tunable Bandgaps for Solar Cell Applications.
Chang YT, et al.
Advances in Functional Materials, 17(16), 3326-3331 (2007)
Crystalline diblock conjugated copolymers: Synthesis, self-assembly, and microphase separation of poly (3-butylthiophene)-b-poly (3-octylthiophene).
Wu PT, et al.
Macromolecules, 42(7), 2317-2320 (2009)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 424285-5G | 04061837843907 |
