2-Amino-9H-pyrido[2,3-β]indole-15N3
2-Amino-9H-pyrido[2,3-β]indole-15N3 Basic information
- Product Name:
- 2-Amino-9H-pyrido[2,3-β]indole-15N3
- Synonyms:
-
- 1H-Pyrido[2,3-β]indol-2-amine-15N3
- 2-Amino-9H-pyrido[2,3-β]indole-15N3
- 2-Amino-α-carboline-15N3
- 9H-1,9-Diazafluoren-2-amine-15N3
- AaC-15N3
- 1H-Pyrido[2,3-b]indol-2-amine-15N3
- 2-Amino-9H-pyrido[2,3-b]indole-15N3
- 2-Amino-a-carboline-15N3
- CAS:
- 1189920-50-0
- MF:
- C11H8N3
- MW:
- 182.20132
- Product Categories:
-
- Aromatics, Heterocycles, Isotope Labelled Compounds, Mutagenesis Research Chemicals
- Isotope Labeled Compounds
- Mutagenesis Research Chemicals
- Aromatics
- Heterocycles
- Isotope Labelled Compounds
- Mol File:
- 1189920-50-0.mol
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2-Amino-9H-pyrido[2,3-β]indole-15N3 Chemical Properties
- Melting point:
- 198-200°C
- storage temp.
- Refrigerator
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- color
- Blue to Dark Brown
- Stability:
- Light Sensitive
- CAS DataBase Reference
- 1189920-50-0
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2-Amino-9H-pyrido[2,3-β]indole-15N3 Usage And Synthesis
Chemical Properties
Bluish Green Solid
Uses
A pyrolysate that exhibited mutagenic activity toward Salmonella typhimurium TA98 and TA100 from the pyrolytic products of soybean globulin. 2-Amino-9H-pyrido[2,3-b]indole (AαC) and 2-amino-3-methyl-9H-pyrido[2,3-b]indole (MeAαC) are two mutagenic and carcinogenic heterocyclic amines formed during ordinary cooking.
2-Amino-9H-pyrido[2,3-β]indole-15N3Supplier
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