9-Vinylcarbazole
ALDRICH/277592 - 98%
Synonym: 9-Vinyl-9H-carbazole; N-Ethenylcarbazole; N-Vinylcarbazole
CAS Number: 1484-13-5
Empirical Formula (Hill Notation): C14H11N
Molecular Weight: 193.24
EC Number: 216-055-0
MDL Number: MFCD00004966
Linear Formula: C14H11N
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 277592-100G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 277592-25G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 277592-5G
| assay | 98% |
| bp | 154-155 °C/3 mmHg (lit.) |
| InChI | 1S/C14H11N/c1-2-15-13-9-5 |
| InChI key | KKFHAJHLJHVUDM-UHFFFAOYSA |
| mp | 60-65 °C (lit.) |
| SMILES string | C=Cn1c2ccccc2c3ccccc13 |
| Application: | 9-Vinylcarbazole can be used:• As a monomer to synthesize electrochromic conductive thin film copolymer with 3,4-ethylenedioxythiophen • As a precursor to prepare a copolymer which is used to fabricate highly efficient polymeric thermally activated delayed fluorescent (TADF) organic light-emitting diode (OLED) with high quantum efficiency. • As a functional monomer to synthesize poly(vinyl carbazole) (p(VC)) microgel particles via surfactant free emulsion polymerization. These microgels find application in the field of drug delivery and tissue engineering. • As a precursor to fabricate hole transport layer for perovskite solar cells. |
| General description: | 9-Vinylcarbazole (9-VC) is a monomer characterized by photochemical properties, thermal stability, and high reactivity due to its vinyl group. It enhances the performance of conducting polymers and thermosetting resins. In drug delivery systems, 9-VC facilitates the encapsulation of therapeutic agents, enabling controlled release and improved efficacy, particularly in cancer therapy. Additionally, its photochemical capabilities allow for advancements in photonic devices. |
| Packaging: | 5, 25, 100 g in glass bottle |
| Symbol |    GHS06,GHS08,GHS09 |
| Signal word | Danger |
| Hazard statements | H300 - H312 - H315 - H317 - H341 - H410 |
| Precautionary statements | P202 - P261 - P273 - P280 - P301 + P310 - P302 + P352 + P312 |
| Hazard Codes | Xn,N |
| Risk Statements | 21/22-38-43-50/53-68 |
| Safety Statements | 22-23-36/37-60-61 |
| RIDADR | UN2811 - class 6.1 - PG 2 - EHS - Toxic solids, organic, n.o.s., |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | 98% |
| bp | 154-155 °C/3 mmHg (lit.) |
| mp | 60-65 °C (lit.) |
| UNSPSC | 12162002 |