InChI
1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H
SMILES string
c1ccc2c(c1)[nH]c3ccccc23
InChI key
UJOBWOGCFQCDNV-UHFFFAOYSA-N
grade
certified reference material, TraceCERT®
packaging
ampule of 1 mL
concentration
2000 μg/mL in methylene chloride
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
agriculture
format
single component solution
storage temp.
2-8°C
Quality Level
General description
Carbazole is a cheap kind of raw material, obtained from the distillation process of coal tar, which can be used to prepare carbazole based polymers, which can find a broad array of applications in electrophotographic materials, photorefractive materials and photovoltaic devices.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.
Legal Information
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Central nervous system
存储类别
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
危险化学品
此项目有
Carbazole-containing polymers: synthesis, properties and applications
Grazulevicius.V.J, et al.
Progress in Polymer Science, 28, 1297-1353 (2003)
Xiaorui Liu et al.
Journal of bacteriology, 194(20), 5701-5702 (2012-09-27)
Pseudomonas luteola XLDN4-9 and Pseudomonas stutzeri XLDN-R are two efficient carbazole-degrading pseudomonad strains. Here we present 4.63- and 4.70-Mb assemblies of their genomes. Their annotated key genes for carbazole catabolism are similar, which may provide further insights into the molecular
Lena Arnold et al.
Chemical communications (Cambridge, England), 48(77), 9640-9642 (2012-08-22)
Carbazole-containing porphyrinoid was synthesised for the first time via Suzuki-Miyaura cross-coupling reaction. Oxidation with MnO(2) yielded its porphyrin-state featuring macrocyclic aromaticity in exchange for the loss of the resonance energies of the benzene rings.
Wenzheng Gao et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 98, 215-221 (2012-09-11)
Two new blue luminescent hole transporting materials (HTM) containing triphenylamine, carbazole units and olefinic linkers (TM1 and TM2) were synthesized via Wittig reaction and characterized by (1)H NMR, FT-IR, and HRMS. The compounds show good solubility in common organic solvents
Zahra Farajzadeh et al.
World journal of microbiology & biotechnology, 28(10), 3075-3080 (2012-07-19)
In this work, a bacterial strain with suitable capability to metabolize carbazole (CAR) as a main nitrogen containing compound of petroleum was isolated and characterized. 16S rDNA gene analysis and morphological characteristics of the strain showed that the isolate belonged
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持