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vapor density
2.9 (vs air)
Quality Level
vapor pressure
40 mmHg ( 12.5 °C)
Assay
≥99%
autoignition temp.
743 °F
expl. lim.
12.5 %
refractive index
n20/D 1.529 (lit.)
bp
84 °C (lit.)
mp
−38 °C (lit.)
density
1.051 g/mL at 25 °C (lit.)
SMILES string
c1ccsc1
InChI
1S/C4H4S/c1-2-4-5-3-1/h1-4H
InChI key
YTPLMLYBLZKORZ-UHFFFAOYSA-N
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Application
Thiophene is an essential precursor to synthesize a wide range of conjugated organosulfur moieties, sulfur-containing polycyclic aromatic hydrocarbons, macrocycles, and pharmaceutical compounds. It has been widely used in the synthesis of polythiophenes and a host of active materials for organic field effect transistors (OFETs) and organic solar cells (OSCs).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
15.8 °F
Flash Point(C)
-9 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Construction of synthetic macrocyclic compounds possessing subheterocyclic rings, specifically pyridine, furan, and thiophene.
Chemical Reviews, 77(4), 513-597 (1977)
Thiophene-based push-pull chromophores for small molecule organic solar cells (SMOSCs)
Royal Society of Chemistry Advances, 5(1), 354-397 (2015)
Scientific reports, 5, 11201-11201 (2015-06-19)
The growth kinetics of polymer thin films prepared by plasma-based deposition method were explored using atomic force microscopy. The growth behavior of the first layer of the polythiophene somewhat differs from that of the other layers because the first layer
Solution-processed and high-performance organic solar cells using small molecules with a benzodithiophene unit.
Journal of the American Chemical Society, 135(23), 8484-8487 (2013)
Thiophene, Benzo [b] thiophene and Dibenzo [b, d] thiophene as Precursors to Highly Conjugated Organosulfur Compounds.
Synlett, 1997(06), 643-649 (1997)
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