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1,3-Dibromopropane

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Identification
Molecular formula
C3H6Br2
CAS number
109-64-8
IUPAC name
1,3-dibromopropane;N,N,N',N'-tetramethylhexane-1,6-diamine
State
State

At room temperature, 1,3-dibromopropane is a liquid.

Melting point (Celsius)
-34.00
Melting point (Kelvin)
239.15
Boiling point (Celsius)
167.00
Boiling point (Kelvin)
440.15
General information
Molecular weight
201.95g/mol
Molar mass
201.9530g/mol
Density
2.0270g/cm3
Appearence

1,3-Dibromopropane is a clear, colorless to light yellow liquid. It is often described as having a faint, sweet odor. It is relatively dense and viscous, making it distinguishable from water-like compounds in terms of texture and flow.

Comment on solubility

Solubility of 1,3-dibromopropane and N,N,N',N'-tetramethylhexane-1,6-diamine

When examining the solubility of the compounds 1,3-dibromopropane and N,N,N',N'-tetramethylhexane-1,6-diamine, we encounter intriguing characteristics that highlight their unique behaviors in various solvents.

1,3-dibromopropane

This compound is a halogenated alkane, and as is often the case with such compounds, its solubility is influenced by several factors:

  • The presence of the bromine atoms makes 1,3-dibromopropane more polar than its non-brominated counterparts, which affects its interactions with solvents.
  • It is generally soluble in organic solvents such as alcohols, ethers, and aromatic hydrocarbons.
  • However, it exhibits poor solubility in water due to its hydrophobic nature and the relatively large size of the bromine substituents.

N,N,N',N'-tetramethylhexane-1,6-diamine

This compound acts as a diamine with four methyl groups, contributing to its solubility profile:

  • The amine functional groups are capable of forming hydrogen bonds, which can enhance solubility in polar solvents such as water.
  • Despite this, the large hydrophobic carbon chain and bulky methyl groups may lead to lower solubility in very polar solvents.
  • It typically shows good solubility in organic solvents, potentially making it useful in various applications.

In summary, the solubility of these compounds illustrates the intricate balance between polarity and hydrophobic interactions. As we navigate through complex mixtures and various solvents, it becomes clear that understanding these characteristics is crucial for applications in chemical synthesis and product formulation. As the old saying goes, "Like dissolves like," and these compounds serve as excellent examples of this principle in action.

Interesting facts

1,3-Dibromopropane

1,3-Dibromopropane is an interesting chemical compound with unique properties and applications. Here are some intriguing facts about it:

  • Versatile Building Block: This compound serves as a vital intermediate in organic synthesis. It is often used for constructing more complex molecules, especially in the creation of pharmaceuticals and agrochemicals.
  • Halogenated Hydrocarbon: As a dihalide, 1,3-dibromopropane's halogen atoms give rise to distinct reactivity patterns, making it a subject of study for many chemical reactions, such as nucleophilic substitutions.
  • Solvent Properties: Due to its structure, this compound is also used as a solvent in various chemical reactions, enabling chemists to dissolve polar and non-polar substances effectively.
  • Safety Considerations: Handling this compound requires caution. Its bromine substituents can pose health risks, and proper safety measures should always be in place.

In summary, 1,3-dibromopropane is not just a simple molecule; its role in chemical synthesis and its distinct properties make it an essential compound for chemists working in multiple fields.

N,N,N',N'-Tetramethylhexane-1,6-diamine

N,N,N',N'-Tetramethylhexane-1,6-diamine is a fascinating compound notable for its unique structural characteristics and applications. Here are some exciting facts:

  • Polymer Precursor: This diamine is commonly used as a precursor in the synthesis of polyamides and polyurethanes, which are integral to the production of various materials, including plastics and fibers.
  • Hydrogen Bonding: The presence of multiple amine groups allows for potential hydrogen bonding, enhancing solubility and interaction with other compounds, making it a vital player in formulations.
  • Reactivity: The amine functional groups contribute to its reactivity, enabling it to participate in a variety of chemical reactions, including alkylation and acylation.
  • Influence on Chemical Properties: The steric hindrance provided by the tetramethyl groups affects the compound's overall behavior, making it more selective in certain reactions compared to other similar amines.

N,N,N',N'-Tetramethylhexane-1,6-diamine exemplifies how a molecular structure can significantly influence reactivity and applications in the chemical world. Its role in polymer chemistry marks it as an important compound in both industrial and research settings.

Synonyms
Hexadimethrine Bromide
9011-04-5
1,3-dibromopropane;N,N,N',N'-tetramethylhexane-1,6-diamine
HEXADIMETHRIN BROMIDE FOR PROTEIN
6,3-Ionene bromide
6,3-Ionene
NCGC00090921-01
NSC 25133
UNII-4C905MSK4W
Hexadimethrine bromide [INN]
DSSTox_CID_17684
DSSTox_RID_79354
DSSTox_GSID_37684
4C905MSK4W
CHEBI:5699
SCHEMBL1650408
CHEMBL3186282
KZKAYEGOIJEWQB-UHFFFAOYSA-N
Tox21_111041
NSC118096
AKOS040740806
NSC-118096
DA-74105
FH165280
LS-14259
WLN: 1N1&6N1&1 &E3E/
CAS-28728-55-4