Interesting facts
Interesting Facts about N,N'-bis(3-aminopropyl)butane-1,4-diamine
N,N'-bis(3-aminopropyl)butane-1,4-diamine is a fascinating compound with a distinct structure and numerous applications. Here are some intriguing aspects to consider:
- Unique Structure: This compound possesses a unique bis(aminopropyl) structure that contributes to its properties. Its long-chain aliphatic nature is essential in many interactions within biological systems.
- Versatile Applications: N,N'-bis(3-aminopropyl)butane-1,4-diamine is often used as a building block in the synthesis of various polymers and surfactants, offering versatility in both industrial and research settings.
- Biological Significance: The presence of amino groups in the compound can facilitate interactions with biomolecules, making it an interesting candidate for further biological studies and potential pharmaceutical applications.
- Functionalization Potential: Due to its amine groups, this compound can be easily modified or functionalized, allowing researchers to tailor its properties for specific uses.
- Synthetic Pathways: Understanding the synthesis of this compound provides insight into how organic chemists design complex molecules, showcasing techniques like amination and chain elongation.
As a scientist or a chemistry student, delving into N,N'-bis(3-aminopropyl)butane-1,4-diamine opens up an array of possibilities for research and application. Its multifaceted nature and the role it plays in different chemical reactions underscore the complexity and beauty of chemical compounds.
Synonyms
spermine
71-44-3
musculamine
neuridine
gerontine
Spermin
4,9-Diaza-1,12-dodecanediamine
N,N'-Bis(3-aminopropyl)-1,4-butanediamine
Spermine, puriss
Diaminopropyltetramethylenediamine
N,N'-Bis(3-aminopropyl)butane-1,4-diamine
1,4-Butanediamine, N,N'-bis(3-aminopropyl)-
4,9-Diazadodecamethylenediamine
Gerotine
1,4-Bis(aminopropyl)butanediamine
Spermina
4,9-Diazadodecane-1,12-diamine
Actilip sp-91
1,4-Bis(aminopropyl) butanediamine
N1,N1'-(Butane-1,4-diyl)bis(propane-1,3-diamine)
NSC 268508
1,4-Diaminobutane, N,N'-bis(3-aminopropyl)-
BRN 1750791
1,5,10,14-Tetraazatetradecane
UNII-2FZ7Y3VOQX
2FZ7Y3VOQX
AI3-26633
EINECS 200-754-2
Spermine free base
MFCD00008215
NSC-268508
CHEBI:15746
NSC 268508; Neuridine
CHEMBL23194
DTXSID9058781
N,N'-Bis(3-aminopropyl)-1,4-diaminobutane
N1,N4-bis(3-aminopropyl)-1,4-butanediamine
diaminopropyl-tetramethylenediamine
4-04-00-01301 (Beilstein Handbook Reference)
NSC268508
71-44-3 (FREE BASE)
(3-aminopropyl)({4-[(3-aminopropyl)amino]butyl})amine
spermidine 3HCl
1,4-Butanediamine, N1,N4-bis(3-aminopropyl)-
71052-31-8
SPM
MLS002472980
C10H26N4
Spermina [Italian]
SMR001397086
Spermine puriss
EINECS 273-309-3
Spermine (Standard)
4,12-diamine
Spermine, >=97%
Tocris-0958
SPERMINE [MI]
Lopac-S-2876
Biomol-NT_000213
bmse000117
EC 273-309-3
NCIMech_000206
Spermine, min. 98.0%
Lopac0_001077
SCHEMBL14965
WLN: Z3M4M3Z
GTPL710
Spermine, analytical standard
BPBio1_001086
DTXCID8046872
BDBM79403
cid_5351186
HY-B1777R
1, N,N'-bis(3-aminopropyl)-
Spermine, >=99.0% (GC)
HY-B1777
CCG-35276
HB0588
HSCI1_000212
s3948
AKOS024258603
DB00127
FS09798
SB38410
SDCCGSBI-0051047.P003
N1,N4-bis(3-aminopropyl)-butanediamine
NCGC00015941-01
NCGC00015941-02
NCGC00015941-03
NCGC00015941-04
NCGC00015941-05
NCGC00015941-10
NCGC00024902-01
NCGC00024902-02
NCGC00024902-03
AS-35114
BP-21388
NCI60_035280
DB-055526
CS-0013806
N,Na?Bis(3-aminopropyl)-1,4-diaminobutane
NS00014922
Spermine, Vetec(TM) reagent grade, >=97%
N,N''-bis(3-aminopropyl)butane-1,4-diamine
N1,N4-Bis(3-aminopropyl)butane-1,4-diamine
C00750
EN300-175597
L001114
n1,n1'-(butane-1,4-diyl)dipropane-1,3-diamine
Q424597
N,N'-Bis(3-aminopropyl)-1,4-tetramethylenediamine
BRD-K18375018-376-02-3
Z1269219211
2B445AED-6284-43E4-82FE-39598858D67F
3-aminopropyl-[4-(3-aminopropylamino)butyl]amine;hydrochloride
N,N''''-bis(3-aminopropyl)butane-1,4-diamine;hydrochloride
N,N''''-bis(3-azanylpropyl)butane-1,4-diamine;hydrochloride
N,N'-Bis(3-aminopropyl)-1,4-diaminobutane;Gerontine;Musculamine
Spermine, BioReagent, amorphous semi-solid, suitable for cell culture
200-754-2
Solubility of N,N'-bis(3-aminopropyl)butane-1,4-diamine
N,N'-bis(3-aminopropyl)butane-1,4-diamine, with the chemical formula C7H19N3, exhibits notable solubility characteristics due to its specific molecular structure. This compound contains multiple amine functional groups that significantly influence its interactions with solvents.
Factors Influencing Solubility
Several factors contribute to the solubility of this compound:
Solubility Behavior
Generally, one may expect the following:
In summary, it can be said that the solubility of N,N'-bis(3-aminopropyl)butane-1,4-diamine is largely governed by its functional groups and the resulting polarity, making it an intriguing compound for various chemical applications. Understanding its solubility is critical for predicting its behavior in different environments and formulations.