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Amyl methyl sulfide

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Identification
Molecular formula
C9H20S
CAS number
4033-80-3
IUPAC name
1-isopentylsulfanyl-3-methyl-butane
State
State

At room temperature, amyl methyl sulfide is in a liquid state.

Melting point (Celsius)
-81.00
Melting point (Kelvin)
192.15
Boiling point (Celsius)
182.00
Boiling point (Kelvin)
455.15
General information
Molecular weight
146.29g/mol
Molar mass
146.2900g/mol
Density
0.8199g/cm3
Appearence

Amyl methyl sulfide is a clear, colorless liquid with a distinctive and strong odor commonly associated with sulfur compounds. It has a slightly oily texture.

Comment on solubility

Solubility of 1-isopentylsulfanyl-3-methyl-butane

The solubility of 1-isopentylsulfanyl-3-methyl-butane can be quite intriguing due to its unique structural features. Generally, the solubility of organic compounds is influenced by factors such as polarity, molecular weight, and the presence of functional groups. Here are some key points to consider:

  • Polarity: 1-isopentylsulfanyl-3-methyl-butane is likely to exhibit low polarity because of the hydrocarbons in its structure. This property suggests that it may be more soluble in nonpolar solvents.
  • Molecular Weight: With a relatively higher molecular weight, this compound could demonstrate limited solubility in water. Larger hydrocarbon chains typically interfere with solvation processes in polar solvents.
  • Functional Groups: The presence of a sulfanyl (-S-) group may slightly enhance solubility in some polar organic solvents, although it is not as polarizing as hydroxyl or carboxyl groups.

In conclusion, 1-isopentylsulfanyl-3-methyl-butane likely exhibits low solubility in water, aligning with many similar alkane and sulfanyl compounds. However, it may find favorable solubility in nonpolar organic solvents, such as hexane or ether. As always, experimental measurements provide the most accurate insights into specific solubility behavior.

Interesting facts

Exploring 1-Isopentylsulfanyl-3-methyl-butane

1-Isopentylsulfanyl-3-methyl-butane is a fascinating compound that showcases the complexity and diversity of organic chemistry. Here are some intriguing facts about this chemical:

  • Structure and Composition: This compound contains multiple functional groups, predominantly featuring a sulfanyl (thiol) group. The presence of sulfur in its structure enriches its chemical reactivity and properties.
  • Applications: 1-Isopentylsulfanyl-3-methyl-butane, due to its unique structural features, can be used in various applications, including:
    • As a potential intermediate in organic synthesis.
    • In the development of novel materials that require specific electronic or optical properties.
    • In the study of biochemical pathways and mechanisms involving sulfur-containing metabolites.
  • Odor Profile: Compounds containing sulfur often have distinct and sometimes pungent odors, which can be utilized in perfumery and flavoring.
  • Natural Occurrence: Sulfur-containing compounds frequently occur in nature, contributing to the scent of garlic and onions, and may also play roles in biological systems.
  • Research Significance: Scientists are drawn to study compounds like 1-isopentylsulfanyl-3-methyl-butane due to their potential applications in medicinal chemistry, especially in developing drugs with enhanced efficacy and reduced side effects.

In conclusion, 1-isopentylsulfanyl-3-methyl-butane is more than just a chemical; it represents a wealth of opportunities for research and application in various fields. As the understanding of its properties and reactivity deepens, the potential for innovative uses will likely expand, cementing its place in the annals of chemical exploration.

Synonyms
Butane, 1,1'-thiobis[3-methyl-
Butane, 1,1'-thiobis(3-methyl-
AI3-18864
DTXSID6060264
DTXCID2041703
Diisopentyl sulfide
544-02-5
Isoamyl sulfide
DIISOAMYL SULFIDE
Isopentyl sulfide
3-methyl-1-(3-methylbutylsulfanyl)butane
1-(Isopentylsulfanyl)-3-methylbutane
3-methyl-1-(3-methylbutylthio)butane
Diisoamylsulfid
3-methyl-1-[(3-methylbutyl)sulfanyl]butane
Diisopentyl sulphide
Di(3-methylbutyl) sulfide
2,8-Dimethyl-5-thianonane
U52GC8XA4C
SCHEMBL1114588
1,1'-Thiobis[3-methylbutane]
STL453664
AKOS015897537
DB-254476