Determine the necessary mass, volume, or concentration for preparing a solution.
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PharmPure™, USP PharmPure™,USP for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 33 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Gene Information
human ... NQO1(1728)
Menadione (Vitamin K3) is the synthetic form of vitamin K. It has the structure similar to vitamin K1 and K2. Vitamin K1, K2 and K3 are biologically active. Water soluble forms of menadiones are used in swine and poultry diets.
Application
Menadione has been used: to treat HL-60 cells as positive control for apoptosis for flow cytometry as an oxidative stress inducer in transgenic embryos after 24 h of post fertilization to treat HaCaT cell line, for quantifying total and oxidised glutathione
| Sorrisos canónicos | CC1=CC(=O)C2=CC=CC=C2C1=O |
|---|---|
| IUPAC Name | 2-methylnaphthalene-1,4-dione |
| InChIKey | MJVAVZPDRWSRRC-UHFFFAOYSA-N |
| INCHI | 1S/C11H8O2/c1-7-6-10(12)8-4-2-3-5-9(8)11(7)13/h2-6H,1H3 |
| SMILES isoméricas | CC1=CC(=O)C2=CC=CC=C2C1=O |
| WGK Alemanha | 3 |
| RTECS | QL9100000 |
| Número UN | 1325 |
| Peso molecular | 172.18 |
| Beilstein | 1908453 |
| Reaxy-Rn | 1908453 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1908453&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Classe | Naphthalenes |
| Subclass | Naphthoquinones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthoquinones |
| Alternative Parents | Quinones Aryl ketones Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Naphthoquinone - Aryl ketone - Quinone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound |
| Descrição | This compound belongs to the class of organic compounds known as naphthoquinones. These are compounds containing a naphthohydroquinone moiety, which consists of a benzene ring linearly fused to a bezene-1,4-dione (quinone). |
| External Descriptors | a vitamin K |
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| Sensibilidade | light sensitive |
|---|---|
| Ponto de fusão (°C) | 105-108°C |
| Peso molecular | 172.180 g/mol |
| XLogP3 | 2.200 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 172.052 Da |
| Monoisotopic Mass | 172.052 Da |
| Topological Polar Surface Area | 34.100 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 288.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
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