Weight | 210.28 g/mol |
---|---|
Formula | C14H14N2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 3 |
Rotatable Bonds | 1 |
3-AMINO-9-ETHYLCARBAZOLE (132-32-1)
3-amino-9-ethylcarbazole hydrochloride
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- CYTOCHEMICAL DEMONSTRATION OF PEROXIDASE ACTIVITY WITH 3-AMINO-9-ETHYLCARBAZOLE (Journal of Histochemistry and Cytochemistry, 1965)
- A Sensitive Derivatization Method for the Determination of the Sugar Composition after Pre-column Reductive Amination with 3-Amino-9-ethylcarbazole (AEC) by High-Performance Liquid Chromatography (Chinese Journal of Chemistry, 2007)
- A selective optical sensor for picric acid assay based on photopolymerization of 3-(N-methacryloyl) amino-9-ethylcarbazole (Analytica Chimica Acta, 2006)
- Metal Complexes of Carbazole Derivatives for Optoelectronics: Synthesis, Structures, and UVVisible Absorption Spectra of (3-Amino-9-ethylcarbazole)chromium Tricarbonyl Complexes (Organometallics, 2005)
- Metachromasia of 3-amino-9-ethylcarbazole (AEC) and its prevention in immunoperoxidase techniques (Histochemistry and Cell Biology, 1987)
- Immunocytochemical identification of human chorionic gonadotropin. Comparative study of diaminobenzidine and 3-amino, 9-ethylcarbazole, a nonhazardous chromogen. (Archives of Pathology & Laboratory Medicine, 1979)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H350: May cause cancer
Danger Carcinogenicity - Category 1A, 1B - 3-amino-9-ethylcarbazole hydrochloride
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SMILESCCN1C2=C(C=C(C=C2)N)C3=CC=CC=C31
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InChIKeyOXEUETBFKVCRNP-UHFFFAOYSA-N
- Pubchem - 3-AMINO-9-ETHYLCARBAZOLE
- Wikipedia - 3-amino-9-ethylcarbazole
3-Amino-9-ethylcarbazole (AEC) is a chemical compound commonly used as a chromogenic substrate in immunohistochemistry, specifically for visualizing sections stained with HRP-conjugated secondary antibodies. After the chromogenic oxidation reaction catalyzed by HRP, a red water-insoluble precipitate is formed in situ, visualizing the location of the antigen detected by the HRP-conjugated antibody. The resulting stained section can be destained by organic solvents in which the red precipitate is soluble.
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