• 2-Decyl-7-phenyl[1]benzothieno[3,2-b][1]benzothiophene [for organic electronics] (CAS 1398395-83-9) - TCI D5491 - AMI Scientific
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TCI

CAS 1398395-83-9

2-Decyl-7-phenyl[1]benzothieno[3,2-b][1]benzothiophene [for organic electronics] TCI D5491

2-Decyl-7-phenyl[1]benzothieno[3,2-b][1]benzothiophene [for organic electronics] TCI D5491

Chemical Identity

Other names
Ph-BTBT-10 · Ph-BTBT-C10 · 2-Decyl-7-phenylbenzo[b]benzo[4,5]thieno[2,3-d]thiophene · Ph-BTBT-10
CAS No.
1398395-83-9
PubChem
CID 90049095·SID 468591369
Formula
C30H32S2
Molecular weight
456.71 g/mol
Purity
>99.5%(HPLC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
7-decyl-2-phenyl-[1]benzothiolo[3,2-b][1]benzothiole
SMILES
CCCCCCCCCCC1=CC2=C(C=C1)C3=C(S2)C4=C(S3)C=C(C=C4)C5=CC=CC=C5
InChIKey
ZIQBVBKYAZMQPC-UHFFFAOYSA-N
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2-Decyl-7-phenyl[1]benzothieno[3,2-b][1]benzothiophene is a specialized organic compound used in the field of organic electronics. This material plays a crucial role in laboratories where research into advanced electronic devices is conducted. It is specifically designed for applications in organic light-emitting diodes (OLEDs) and field-effect transistors (FETs), where its unique molecular structure contributes to the performance of these devices. Its presence in research settings helps scientists develop next-generation electronic systems with improved efficiency and functionality.

The compound is valued for its high chemical stability and ability to form uniform thin films, which are essential in the fabrication of electronic components. These properties make it a preferred choice for researchers aiming to achieve consistent and reliable results in their experiments. Additionally, its molecular structure can be tailored to enhance the performance of electronic devices, offering flexibility in material design. This adaptability is particularly important in the development of new technologies and materials for display and sensor applications.

In Indonesian laboratories, this compound is widely used in the study and development of organic semiconductors. It is a key component in research projects focused on advanced electronic technologies and innovations. Many research institutions and universities in Indonesia rely on this material to support their work in creating new electronic devices and materials for various industrial and academic applications.

Advantages (TCI brochure)

  • Practical hole mobility > 10 cm2/Vs (ensured specification by a vapor diffusion method)
  • Also available for solution processable device

TCI brochures (PDF)

Related TCI products

  • Organic Light-Emitting Diodes (OLEDs) benefit from this compound's ability to form stable and conductive thin films, enhancing device performance and longevity.
  • Field-Effect Transistors (FETs) utilize its molecular structure to improve charge transport efficiency, leading to better electronic performance in semiconductor applications.
  • Organic Semiconductor Research leverages its chemical stability and tunable molecular structure to develop new materials for advanced electronic devices.
  • Display Technology Development relies on its properties to create high-quality, energy-efficient display components for next-generation screens.
  • Energy Storage Device Innovation uses its conductive properties to enhance the performance of organic-based energy storage solutions.

From the TCI brochure

  • Organic transistor device

Brand TCI
CAS number 1398395-83-9
Molecular formula —
Purity —
Category Materials Science > Electronic Materials > High-Quality Organic Semiconductors [for Organic Electronics]
Pack sizes Available in various quantities as per standard laboratory supply practices
Physical form Solid (exact form may vary depending on supplier specifications)
Storage Store in a cool, dry place away from direct light and moisture

Data from the TCI brochure

Hole mobility, SAM bare, annealing w/o0.87 - 0.91 cm2/Vs (OFET top contact, by own equipment)
Vth, SAM bare, annealing w/o-24 V (OFET top contact, by own equipment)
Hole mobility, SAM bare, annealing 1204.24 - 4.86 cm2/Vs (Annealing 120°C, 5min, by own equipment)
Vth, SAM bare, annealing 120-8 V (Annealing 120°C, 5min, by own equipment)
Hole mobility, SAM ODTS [O0079], annealing w/o1.40 - 1.42 cm2/Vs (OFET top contact, by own equipment)
Vth, SAM ODTS [O0079], annealing w/o-23 V (OFET top contact, by own equipment)
Hole mobility, SAM ODTS [O0079], annealing 12010.3 - 14.0 cm2/Vs (Annealing 120°C, 5min, by own equipment)
Vth, SAM ODTS [O0079], annealing 120-22 V (Annealing 120°C, 5min, by own equipment)
Channel length50 µm (Top contact OFET structure (Figure 1))
Channel width1.5 mm (Top contact OFET structure (Figure 1))
Organic layer thickness40 nm (Top contact OFET structure (Figure 1))
Source, drain electrodeAu (Top contact OFET structure (Figure 1); printed as 'South, Drain')

Source: TCI brochure FF077 (2025-03-04)

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its performance. In laboratory settings, it should be handled with care to avoid contamination and ensure safe usage. Proper labeling of containers is essential for identification and safety. General laboratory precautions include wearing appropriate personal protective equipment when handling the material to minimize exposure risks. The compound is not classified as hazardous under standard safety classifications, but standard laboratory safety protocols should still be followed.

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