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About This Item
Empirical Formula (Hill Notation):
C4H4S
CAS Number:
Molecular Weight:
84.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-729-4
Beilstein/REAXYS Number:
103222
MDL number:
Product Name
Thiophene, ≥99%
InChI
1S/C4H4S/c1-2-4-5-3-1/h1-4H
InChI key
YTPLMLYBLZKORZ-UHFFFAOYSA-N
SMILES string
c1ccsc1
vapor density
2.9 (vs air)
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.)
Quality Level
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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).
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
15.8 °F
flash_point_c
-9 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Solution-processed and high-performance organic solar cells using small molecules with a benzodithiophene unit.
Zhou J, et al.
Journal of the American Chemical Society, 135(23), 8484-8487 (2013)
Sukyoung Hwang et al.
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
Thiophene-based push-pull chromophores for small molecule organic solar cells (SMOSCs)
Malytskyi V, et al.
Royal Society of Chemistry Advances, 5(1), 354-397 (2015)
Construction of synthetic macrocyclic compounds possessing subheterocyclic rings, specifically pyridine, furan, and thiophene.
Newkome GR, et al.
Chemical Reviews, 77(4), 513-597 (1977)
Yanzhong Zhen et al.
Nanomaterials (Basel, Switzerland), 9(7) (2019-07-26)
The novel ternary-component Ag/AgI/α-MoO3 (AAM) photocatalyst was successfully fabricated by a facile hydrothermal method combined with a charge-induced physical adsorption and photo-reduced deposition technique. X-ray diffraction, scanning/transmission electron microscope, X-ray photoelectron, UV-vis diffuse reflectance, photoluminescence and electrochemical impedance spectroscopy were
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