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1-Bromononadecane

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Identification
Molecular formula
C19H39Br
CAS number
6932-07-8
IUPAC name
1-bromononadecane
State
State

At room temperature, 1-bromononadecane is typically a liquid.

Melting point (Celsius)
16.00
Melting point (Kelvin)
289.15
Boiling point (Celsius)
374.00
Boiling point (Kelvin)
647.15
General information
Molecular weight
333.39g/mol
Molar mass
333.3940g/mol
Density
0.8590g/cm3
Appearence

1-Bromononadecane is a colorless to light yellow liquid. It is a long-chain alkyl bromide and appears oily and viscous.

Comment on solubility

Solubility of 1-bromononadecane

1-bromononadecane, with the chemical formula C19H39Br, is characterized by its long hydrocarbon chain, which significantly influences its solubility in different solvents. As a general characteristic of long-chain aliphatic compounds, 1-bromononadecane tends to be:

  • Non-polar: The extensive hydrocarbon portion is predominantly non-polar, which limits its solubility in polar solvents such as water.
  • Soluble in organic solvents: Due to its non-polar characteristics, 1-bromononadecane is typically soluble in organic solvents like hexane, heptane, or chloroform.
  • Limited solubility in aqueous solutions: As is often the case with long-chain halogenoalkanes, its solubility in water is quite low, making it primarily a hydrophobic compound.

In summary, the solubility behavior of 1-bromononadecane can be summarized as follows:

  1. Highly soluble in non-polar organic solvents.
  2. Poorly soluble in polar solvents, particularly water.

As a result, understanding these solubility properties is essential for applications involving 1-bromononadecane in various chemical processes and environmental systems.

Interesting facts

Interesting Facts about 1-Bromononadecane

1-Bromononadecane is a fascinating compound that belongs to the class of organic compounds known as haloalkanes. Below are some intriguing aspects of this compound:

  • Structure and Composition: This compound consists of a long hydrocarbon chain with a bromine atom attached, making it a part of the alkyl halide family. Its structure showcases the importance of bromine in modifying chemical properties and functionalities.
  • Applications: 1-bromononadecane is primarily used in organic synthesis. It serves as a starting material for various chemical reactions including substitution reactions, which are crucial in the development of pharmaceuticals and agrochemicals.
  • Biochemical Relevance: Compounds similar to 1-bromononadecane can play significant roles in biological systems. Alkyl halides are often studied for their reactivity and interaction with biological molecules, making them important in toxicology and pharmacology.
  • Environmental Impact: The brominated compounds can exhibit varying degrees of bioaccumulation. Studying their environmental effects is essential to understanding their role in ecosystems, especially in connection with pollution and human health.
  • Historical Significance: Like many haloalkanes, 1-bromononadecane contributes to the understanding of the development of organic compound synthesis during the 19th century, illustrating the evolution of chemical methodologies.

The study of 1-bromononadecane and its derivatives opens doors to new discoveries in organic chemistry, allowing researchers to explore innovative reactions and applications. As one of many haloalkanes, it exemplifies the versatility of carbon chains and the profound impact of functional group substitutions.

Synonyms
1-BROMONONADECANE
Nonadecane, 1-bromo-
EINECS 224-641-2
NSC 133439
DTXSID4063458
DTXCID7040310
224-641-2
gwesglgummnxdu-uhfffaoysa-n
4434-66-6
Nonadecyl bromide
1-nonadecyl bromide
NSC133439
SCHEMBL5273324
1-Bromononadecane, >=97.0% (GC)
NSC-133439
NS00031417
G78075