Description
3,6-Dioctyl-9H-carbazole (CAS No. 937042-97-2) is a high-purity organic compound with the molecular formula C28H41N. This carbazole derivative features two octyl chains at the 3 and 6 positions, enhancing its solubility in organic solvents while maintaining the robust electronic properties of the carbazole core. Ideal for advanced materials research, this compound is widely used in the development of organic semiconductors, OLEDs, and photovoltaic devices due to its excellent hole-transporting characteristics and thermal stability. Supplied as a crystalline solid, it is rigorously tested for purity (typically >98% by HPLC) and is packaged under inert conditions to ensure long-term stability. Researchers can rely on this product for consistent performance in synthetic chemistry and materials science applications.
Properties
- CAS Number: 937042-97-2
- Complexity: 381
- IUPAC Name: 3,6-dioctyl-9H-carbazole
- InChI: InChI=1S/C28H41N/c1-3-5-7-9-11-13-15-23-17-19-27-25(21-23)26-22-24(18-20-28(26)29-27)16-14-12-10-8-6-4-2/h17-22,29H,3-16H2,1-2H3
- InChI Key: AVWQSRXGFSWNGI-UHFFFAOYSA-N
- Exact Mass: 391.323900312
- Molecular Formula: C28H41N
- Molecular Weight: 391.6
- SMILES: CCCCCCCCC1=CC2=C(C=C1)NC3=C2C=C(C=C3)CCCCCCCC
- Topological: 15.8
- Monoisotopic Mass: 391.323900312
- Synonyms: 3,6-dioctyl-9H-carbazole, SCHEMBL12795553, SCHEMBL28402114, 937042-97-2
Application
3,6-Dioctyl-9H-carbazole is a key building block in the synthesis of organic electronic materials, particularly for hole-transport layers in OLEDs and perovskite solar cells. Its extended alkyl chains improve processability without compromising the conjugated system’s electronic properties. The compound is also investigated for use in organic field-effect transistors (OFETs) and as a dopant in conductive polymers. Its thermal stability makes it suitable for high-temperature device fabrication processes.
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