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Vitamin K1

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Identification
Molecular formula
C31H46O2
CAS number
84-80-0
IUPAC name
2-methyl-3-(3,7,11,15-tetramethylhexadec-2-enyl)naphthalene-1,4-dione
State
State

At room temperature, Vitamin K1 is in a liquid state. It is an oil that is commonly found in dietary sources such as green leafy vegetables.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
406.00
Boiling point (Kelvin)
679.15
General information
Molecular weight
450.71g/mol
Molar mass
450.7080g/mol
Density
0.9879g/cm3
Appearence

Vitamin K1 is a yellow viscous oil at room temperature. It is light-sensitive and can degrade if exposed to light for prolonged periods. It has a mild odor.

Comment on solubility

Solubility of 2-methyl-3-(3,7,11,15-tetramethylhexadec-2-enyl)naphthalene-1,4-dione

The solubility of the chemical compound 2-methyl-3-(3,7,11,15-tetramethylhexadec-2-enyl)naphthalene-1,4-dione (C31H46O2) is an intriguing topic given its complex structure. Being a large organic molecule, its solubility can be influenced by several factors:

  • Molecular structure: The presence of long aliphatic chains and the naphthalene structure can affect solubility in various solvents.
  • Polarity: The overall polarity of the compound suggests that it may be more soluble in non-polar solvents rather than polar solvents like water.
  • Hydrophobic interactions: The significant hydrophobic character attributed to the large carbon chain likely reduces solubility in aqueous environments.

In summary, it is likely that 2-methyl-3-(3,7,11,15-tetramethylhexadec-2-enyl)naphthalene-1,4-dione displays preferential solubility in organic solvents such as hexane or dichloromethane, while exhibiting limited solubility in water. This soluble behavior aligns with the general principle that "like dissolves like," where similar types of intermolecular forces facilitate solubility.

Interesting facts

Interesting Facts about 2-Methyl-3-(3,7,11,15-tetramethylhexadec-2-enyl)naphthalene-1,4-dione

This fascinating compound, commonly known as a derivative of naphthalene, is part of a family of chemical compounds that exhibit unique structural characteristics and biological activities. Here are some noteworthy facts:

  • Natural Origins: Many naphthoquinones, including this compound, are found in various plants and have been studied for their roles in natural products and potential medicinal applications.
  • Antioxidant Properties: Compounds similar to this one often exhibit strong antioxidant properties, which make them interesting candidates for further research in health and nutrition.
  • Color and Pigmentation: Naphthalene derivatives are known for their vivid colors, which can find use in dyes and pigments.
  • Biological Significance: This compound might display a range of biological activities, including antimicrobial and anticancer properties, which is a vibrant area of research in pharmaceuticals.
  • Structure-Activity Relationship (SAR): The specific structure, with its long hydrocarbon tail and multiple methyl groups, can significantly influence the compound's reactivity and stability, making it a great subject for SAR studies.

As a scientist or chemistry student, you might find it intriguing to explore the synthesis pathways of such complex compounds. The interactions between different functional groups can lead to an array of different properties and potential applications. As the famous chemist Linus Pauling once said, “The best way to have a good idea is to have a lot of ideas.” This compound exemplifies how intricate molecular structures can lead to exciting possibilities in both academia and industry!

Synonyms
DTXSID80859134
2-Methyl-3-(3,7,11,15-tetramethyl-2-hexadecen-1-yl)-1,4-naphthoquinone
2-Methyl-3-(3,7,11,15-tetramethylhexadec-2-enyl)-1,4-naphthoquinone
phylloquinone;2-METHYL-3-PHYTYL-1,4-NAPHTHOQUINONE
SCHEMBL351364
CHEMBL4549212
DTXCID70809643
MBWXNTAXLNYFJB-UHFFFAOYSA-N
HMS3259K20
HMS3372D04
10485-69-5
BCP28241
NC00596
DB-056823
NS00090248
Q27166249
84-80-0 pound>>Phylloquinone; Phytomenadione pound>>Vitamin K 1