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Juvenile Hormone III

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Identification
Molecular formula
C16H28O3
CAS number
1222-78-8
IUPAC name
11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid
State
State

At room temperature, Juvenile Hormone III is typically found in a liquid state.

Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.00
Boiling point (Celsius)
83.00
Boiling point (Kelvin)
356.00
General information
Molecular weight
250.38g/mol
Molar mass
250.3820g/mol
Density
1.0036g/cm3
Appearence

Juvenile Hormone III is a colorless or pale yellow liquid. It is typically clear and has a distinctly sharp odor.

Comment on solubility

Solubility of 11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid

11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid (C16H28O3) exhibits interesting solubility characteristics that can be influenced by various factors:

  • Polar vs. Nonpolar Solvents: The presence of the methoxy group and carboxylic acid functional group suggests that this compound is more soluble in polar solvents like ethanol and water compared to nonpolar solvents.
  • Temperature Effects: As with many organic compounds, increasing temperature can often enhance solubility, allowing for better interaction with solvent molecules.
  • pH Influence: The acidic nature of the carboxyl group means that solubility may change significantly with changes in pH. In a highly alkaline environment, this compound could become more soluble due to deprotonation.
  • Concentration Dependency: While this compound can dissolve to a certain extent, its solubility may be limited, leading to potential precipitation at higher concentrations.

In conclusion, the solubility of 11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid is primarily characterized by its interaction with solvent polarity, temperature variations, pH levels, and concentration limits. Understanding these factors can aid in predicting its behavior in different environments and applications.

Interesting facts

Interesting Facts about 11-Methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic Acid

11-Methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid, often referred to by its systematic name, is a fascinating compound with a multitude of applications and properties that make it stand out in the world of chemistry. Here are some intriguing points to consider:

  • Natural Occurrence: This compound is a type of carboxylic acid that can be found in various natural products, particularly in certain essential oils. Its presence contributes to the aromatic profiles that many essential oils are celebrated for, making it relevant in the field of natural product chemistry.
  • Biological Importance: The role of 11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid in biological systems is noteworthy. It is involved in metabolic pathways and has been studied for its potential effects in various biological activities, including antibacterial and antifungal properties.
  • Synthesis: The synthesis of this compound can involve intricate organic reactions, and its structure allows for interesting synthetic routes. Chemists often explore its reactions with other compounds to discover novel derivatives and explore their respective properties.
  • Medicinal Chemistry: Research has shown that compounds with similar structures may have therapeutic applications. Studying 11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid could lead to the development of new pharmaceuticals or natural health products.
  • Flavor and Fragrance: With its unique structure, this acid might also find its applications in the flavor and fragrance industry, contributing to the complexity of flavors and scents. The use of such compounds in food and cosmetic products often hinges on their stability and sensory properties.

As we continue to explore this class of compounds, the significance of 11-methoxy-3,7,11-trimethyl-dodeca-2,4-dienoic acid in science and industry cannot be overstated. Understanding its properties not only furthers our knowledge of organic chemistry but also expands potential uses in various fields.

In the words of chemist Robert H. Grubbs, "The important point in any organic synthesis is to identify the key intermediates." For compounds like this, identifying and manipulating those intermediates could lead to groundbreaking discoveries!

Synonyms
11-methoxy-3,7,11-trimethyldodeca-2,4-dienoic acid
CBiol_001854
KBioGR_000136
KBioSS_000136
(2E,4E)-11-METHOXY-3,7,11-TRIMETHYLDODECA-2,4-DIENOIC ACID
KBio2_000136
KBio2_002704
KBio2_005272
KBio3_000271
KBio3_000272
Bio1_000140
Bio1_000629
Bio1_001118
Bio2_000136
Bio2_000616
NS00057267
Q27163507