≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
3,6-Di-tert-butylcarbazole is a carbazole based material with hole transporting characteristics. The 3,6-Di-tert-butyl component of the carbazole results in an increase in the glass transition temperature (Tg) of the compound. It can be used in combination with another carbazole to form novel electroluminescent materials.
Application
3,6-Di-tert-butylcarbazole is mainly used as a monomeric precursor in the syntheses of new carbazole based materials which consist of ethynylphenyl. These materials include 9-(4-bromophenyl)-3,6-di-tert-butylcarbazol and 2-(4-(2-(4-(3,6-di-tert-butyl-9H-carbazol-9-yl)phenyl)ethynyl)benzylidene)malononitrile (PBM) which can be further be used in organic light emitting diodes (OLEDs) and optical switching devices.
| Pubchem Sid | 504767860 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504767860 |
| Sonrisas canónicas | CC(C)(C)C1=CC2=C(C=C1)NC3=C2C=C(C=C3)C(C)(C)C |
| IUPAC Name | 3,6-ditert-butyl-9H-carbazole |
| InChIKey | OYFFSPILVQLRQA-UHFFFAOYSA-N |
| INCHI | 1S/C20H25N/c1-19(2,3)13-7-9-17-15(11-13)16-12-14(20(4,5)6)8-10-18(16)21-17/h7-12,21H,1-6H3 |
| Isómeros SMILES | CC(C)(C)C1=CC2=C(C=C1)NC3=C2C=C(C=C3)C(C)(C)C |
| WGK Alemania | 3 |
| Peso molecular | 279.42 |
| Beilstein | 20(5)8,188 |
| Reaxy-Rn | 215712 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=215712&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Indoles and derivatives |
| Subclass | Carbazoles |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Carbazoles |
| Alternative Parents | Indoles Benzenoids Pyrroles Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Carbazole - Indole - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as carbazoles. These are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 F2204195 | Certificate of Analysis | Mar 13, 2026 | D293780 |
| F2204233 | Certificate of Analysis | Mar 13, 2026 | D293780 |
| F2204248 | Certificate of Analysis | Mar 13, 2026 | D293780 |
| I2404323 | Certificate of Analysis | Aug 22, 2024 | D293780 |
| I2404325 | Certificate of Analysis | Aug 22, 2024 | D293780 |
| I2404340 | Certificate of Analysis | Aug 22, 2024 | D293780 |
| F2204367 | Certificate of Analysis | Mar 14, 2022 | D293780 |
| G2306098 | Certificate of Analysis | Mar 14, 2022 | D293780 |
| Punto de fusión (°C) | 228-233℃ |
|---|---|
| Peso molecular | 279.400 g/mol |
| XLogP3 | 6.700 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 2 |
| Exact Mass | 279.199 Da |
| Monoisotopic Mass | 279.199 Da |
| Topological Polar Surface Area | 15.800 Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 336.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Can Xu, Shang Gong, Xiang Wu, Yuwei Wu, Qiuyan Liao, Ying Xiong, Zhen Li, Hongding Tang. (2021) High-efficient carbazole-based photo-bleachable dyes as free radical initiators for visible light polymerization. DYES AND PIGMENTS, [PMID:] [10.1016/j.dyepig.2021.110039] |
| 2. Chang Zhang, Xin Zhang, Wei Wang, Hao Xue, Qian He, Fenglin Li, Xiaoli Wang, Qinghui Jin, Kun Zhou, Jiawen Jian. (2025) Enhanced ammonia sensing with the MAPbBr3 perovskite and (R/S)-OBN-tCz: a study on sensitivity and stability improvements. Journal of Materials Chemistry C, [PMID:] [10.1039/D4TC04794J] |
| 3. Chang Zhang, Zhimin Wang, Tongbin Chen, Meng Tang, Junliang Zhang, Jiawen Jian, Yuheng Wang, Kun Zhou, Xin Zhang. (2024) Methylamine Gas Sensor Based on Fluorescent Perovskite Nanocrystal Nanofibers Incorporating Aggregation-Induced Emission Materials. ACS Applied Nano Materials, [PMID:] [10.1021/acsanm.4c02342] |
