Interesting facts
              Interesting Facts about 5-Hydroxy-7-Methyl-Naphthalene-1,4-Dione
5-Hydroxy-7-methyl-naphthalene-1,4-dione, commonly known as lawsonia, is a fascinating compound primarily derived from the leaves of the henna plant (Lawsonia inermis). This compound has garnered considerable attention due to its distinct properties and applications in various fields. Here are some intriguing aspects of this chemical:
- Natural Dye: Lawsonia is renowned for its natural dyeing properties. It has been used for centuries in textiles, body art, and hair coloring. The rich colors produced are not only aesthetically pleasing but also have cultural significance in many societies.
- Biological Activity: This compound exhibits various biological activities, including antioxidant and anti-inflammatory properties. This has prompted research into its potential therapeutic applications, especially in traditional medicine.
- Cosmetic Use: Due to its ability to bind to keratin, 5-hydroxy-7-methyl-naphthalene-1,4-dione is a popular ingredient in cosmetics and hair products for enhancing color and conditioning effects.
- Research Interest: Scientists are actively investigating its potential effects on skin and hair health. Ongoing studies aim to explore its mechanisms of action and possible benefits in dermatology.
- Historical Significance: The use of henna and its derivatives dates back to ancient civilizations, including the Egyptians and Indus Valley cultures, highlighting its historical and cultural importance.
In summary, 5-hydroxy-7-methyl-naphthalene-1,4-dione is not just a chemical compound; it is a bridge between nature and human tradition, embodying a blend of science, art, and culture. As researchers continue to unravel its mysteries, this compound may hold even more secrets waiting to be discovered.
Synonyms
          7-Methyljuglone
          Ramentaceone
          14787-38-3
          5-hydroxy-7-methylnaphthalene-1,4-dione
          7-Methyljuglon
          JUGLONE, 7-METHYL-
          5-Hydroxy-7-methyl-1,4-naphthoquinone
          5-Hydroxy-7-methyl-1,4-naphthalenedione
          1,4-Naphthalenedione, 5-hydroxy-7-methyl-
          ZS3RW9P6DY
          1,4-NAPHTHOQUINONE, 5-HYDROXY-7-METHYL-
          NSC-208733
          NSC-624625
          4-08-00-02374 (Beilstein Handbook Reference)
          5-hydroxy-7-methyl-naphthalene-1,4-dione
          DTXSID80163824
          DTXCID8086315
          7-METHYL-JUGLONE
          NSC208733
          CHEBI:8773
          CHEMBL430853
          NSC624625
          C11H8O3
          NSC 208733
          NSC 624625
          BRN 2047829
          5-Hydroxy-7-methyl-2,3-dihydronaphthal-ene-1,4-dione
          7-Methyl juglon
          UNII-ZS3RW9P6DY
          1, 5-hydroxy-7-methyl-
          orb1702883
          SCHEMBL5904880
          SCHEMBL30594728
          BDBM50107009
          AKOS006278204
          5-Hydroxy-7-methyl-[1,4]naphthoquinone
          5-Hydroxy-7-methyll-,1,4-naphtoquinone
          NCI60_001745
          NCI60_007460
          DB-063738
          HY-121684
          CS-0083051
          H27850
          Q27108145
              
Solubility of 5-hydroxy-7-methyl-naphthalene-1,4-dione
5-hydroxy-7-methyl-naphthalene-1,4-dione, also known as TMN, exhibits unique solubility characteristics that are influenced by its chemical structure. Understanding its solubility is essential for applications in organic synthesis and medicinal chemistry. Here are some notable points regarding its solubility:
In summary, the solubility of 5-hydroxy-7-methyl-naphthalene-1,4-dione can be summarized as follows:
This intricate balance of solubility is crucial for its reactivity and utility in various chemical reactions, making it an interesting compound for further study.