Interesting facts
Interesting Facts about Pentane-1,5-Diamine
Pentane-1,5-diamine, also known as 1,5-diaminopentane, is a fascinating compound that falls under the category of alkylene diamines. This organic compound is notable for its unique molecular structure, consisting of a five-carbon straight chain with amino groups at each end. Here are some intriguing insights about pentane-1,5-diamine:
- Biological Relevance: Pentane-1,5-diamine plays a crucial role in biological systems. Its structure is similar to that of certain amino acids, making it a candidate for studying metabolic pathways and biological reactions involving amines.
- Synthesis Pathways: The synthesis of pentane-1,5-diamine can involve various methods, including the reduction of appropriate nitriles or the amination of pentanes. This versatility makes it an appealing target for synthetic chemists.
- Industrial Applications: Due to its properties as a diamine, pentane-1,5-diamine is utilized in the production of polyamides, which are essential for creating durable plastics and fibers. This contributes to its importance in the materials science field.
- Toxicity and Safety: As with many amines, it's essential to handle pentane-1,5-diamine with care. It may cause irritation upon contact with skin or eyes, and appropriate safety measures should always be taken when working with it in the laboratory.
- Role in Research: Pentane-1,5-diamine is often used in research settings to explore the properties of polymerization and the behavior of polyamines. It aids researchers in understanding amine reactivity and functionality.
In summary, pentane-1,5-diamine is a compound that bridges organic chemistry and practical applications, making it a valuable substance in both academic research and industrial production. Its unique characteristics and biological significance continue to inspire further study and exploration.
Synonyms
Pentane-1,5-diamine
1,5-Diaminopentane
cadaverine
462-94-2
1,5-pentanediamine
pentamethylenediamine
Cadaverin
1,5-Pentamethylenediamine
Animal coniine
AI3-26937
1,5-Diamino-n-pentane
BRN 1697256
UNII-L90BEN6OLL
L90BEN6OLL
EINECS 207-329-0
CHEBI:18127
HSDB 7866
CHEMBL119296
DTXSID5075448
EC 207-329-0
4-04-00-01310 (Beilstein Handbook Reference)
MFCD00008239
pentane, 1,5-diamino-
1-BioDex
N2P
1,5 Pentanediamine
Cadaverine, 95%
1,5-diamino-pentane
BioDex 1-
1,5-Amylene diamine
CADAVERINE [MI]
5-azaniumylpentylammonium
alpha,omega-Pentanediamine
bmse000072
SCHEMBL21367
Cadaverine, analytical standard
H2N(CH2)5NH2
SCHEMBL5495920
DTXCID9040479
BBL027704
BDBM50323741
GEO-00925
MSK000515
STL372961
AKOS005169829
Cadaverine, purum, >=97.0% (GC)
CCG-266036
DB03854
FD00335
NCGC00166285-01
AS-30673
1ST000515
DB-051367
NS00007504
EN300-84224
C01672
A827022
Q161555
InChI=1/C5H14N2/c6-4-2-1-3-5-7/h1-7H
Z951173830
1948270A-6D1B-4F40-BC13-9B680ED17B17
207-329-0
LB9
Solubility of Pentane-1,5-diamine (C5H14N2)
Pentane-1,5-diamine, also known as 1,5-diaminopentane, exhibits interesting solubility characteristics due to its chemical structure. Being an aliphatic diamine with both amine functional groups and a hydrocarbon chain, its solubility can be influenced by both polarity and chain length.
Generally, the solubility of pentane-1,5-diamine in various solvents can be summarized as follows:
Furthermore, temperature significantly affects solubility: as the temperature increases, the solubility of pentane-1,5-diamine in water tends to improve due to enhanced molecular motion and solvation processes. As a result, one can expect varying degrees of solubility based on specific conditions.
In summary, pentane-1,5-diamine displays:
This unique solubility profile makes pentane-1,5-diamine a versatile compound in various chemical applications.