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Catalog Number | ACM244633-1 |
CAS Number | 244-63-3 |
Structure | ![]() |
Synonyms | Beta-carboline |
Molecular Weight | 168.19 |
InChI | InChI=1S/C11H8N2/c1-2-4-10-8(3-1)9-5-6-12-7-11(9)13-10/h1-7,13H |
InChI Key | AIFRHYZBTHREPW-UHFFFAOYSA-N |
Melting Point | 199-201 °C |
Purity | 98%+ |
Complexity | 193 |
Covalently-Bonded Unit Count | 1 |
Defined Atom Stereocenter Count | 0 |
Exact Mass | 168.068748264 |
Heavy Atom Count | 13 |
Hydrogen Bond Acceptor Count | 1 |
Hydrogen Bond Donor Count | 1 |
Monoisotopic Mass | 168.068748264 |
PhysicalState | Crystalline |
Rotatable Bond Count | 0 |
Topological Polar Surface Area | 28.7 Ų |
What is the chemical formula of 9H-PYRIDO[3,4-B]INDOLE?
The chemical formula of 9H-PYRIDO[3,4-B]INDOLE is C11H8N2.
What is the molecular weight of 9H-PYRIDO[3,4-B]INDOLE?
The molecular weight of 9H-PYRIDO[3,4-B]INDOLE is 168.19.
At what temperature does 9H-PYRIDO[3,4-B]INDOLE melt?
9H-PYRIDO[3,4-B]INDOLE melts at 199-201 °C.
What is the boiling point of 9H-PYRIDO[3,4-B]INDOLE estimated to be?
The estimated boiling point of 9H-PYRIDO[3,4-B]INDOLE is 287.13°C.
What is the water solubility of 9H-PYRIDO[3,4-B]INDOLE at 17 ºC?
The water solubility of 9H-PYRIDO[3,4-B]INDOLE is 2693g/L at 17 ºC.
What color is 9H-PYRIDO[3,4-B]INDOLE in its crystalline form?
9H-PYRIDO[3,4-B]INDOLE is light yellow in color in its crystalline form.
What are the safety hazard codes associated with 9H-PYRIDO[3,4-B]INDOLE?
The safety hazard code associated with 9H-PYRIDO[3,4-B]INDOLE is Xn.
What is the biological activity of norharmane, a compound related to 9H-PYRIDO[3,4-B]INDOLE?
Norharmane acts as a co-mutagen and is a natural β-carboline found in plants and various sources.
How is 9H-PYRIDO[3,4-B]INDOLE used in chemical analysis?
9H-PYRIDO[3,4-B]INDOLE is used as a matrix for the analysis of cyclodextrins and for sulfated oligosaccharides in combination with DHB as co-matrix.
What is the safety profile of 9H-PYRIDO[3,4-B]INDOLE?
9H-PYRIDO[3,4-B]INDOLE is considered toxic by intravenous route, with some experimental reproductive effects reported.
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