Interesting facts
Interesting Facts about 1-Aminobutan-2-ol
1-Aminobutan-2-ol is an intriguing compound that offers a variety of applications and interesting characteristics. Here are some key points regarding this compound:
- Amine Group: The presence of an amine group (-NH2) in its structure categorizes 1-aminobutan-2-ol as an amino alcohol. This makes it a valuable precursor in organic synthesis and pharmaceutical chemistry.
- Synthesis Potential: This compound is often utilized in synthesis reactions, allowing chemists to produce more complex molecules. Its unique chiral center allows the creation of enantiomerically pure compounds, which is vital in drug development.
- Versatile Applications: 1-Aminobutan-2-ol has been studied for its potential use in several areas, including:
- As an intermediate in the synthesis of agrochemicals.
- In the production of surfactants and detergents.
- As a chiral auxiliary in asymmetric synthesis.
- Stereochemistry: The configuration of 1-aminobutan-2-ol introduces interesting stereochemical properties, making it a subject of study in stereochemistry and its applications in enantioselective reactions.
- Biochemical Relevance: Compounds structurally similar to 1-aminobutan-2-ol play roles in biological systems, serving as building blocks for amino acids and various metabolic processes.
In summary, 1-aminobutan-2-ol is not only a fascinating compound for chemists, but it also serves as a vital tool in the development of pharmaceuticals and other industrial applications. As research continues, we can expect to discover even more about this compound's potential.
Synonyms
1-aminobutan-2-ol
1-Amino-2-butanol
13552-21-1
Monobutanolamine
MONO-SEC-BUTANOLAMINE
2-hydroxybutylamine
1-amino-2-hydroxybutane
1-Ethyl-2-aminoethanol
2-hydroxy-n-butylamine
19453GN3YQ
NSC-17695
1-AMINO-SEC-BUTANOL
DTXSID8025676
J81.643D
DTXCID205676
670-502-8
2-Butanol, 1-amino-
MFCD00059196
CCRIS 4675
(s)-1-amino-2-butanol
UNII-19453GN3YQ
1-ethylglycinol
1-azanylbutan-2-ol
1-Amino-butan-2-ol
2-Butanol,1-amino-
dl-1-amino-2-butanol
(r)-1-amino-2-butanol
SCHEMBL24906
(R,S)-1-aminobutan-2-ol
SCHEMBL245364
SCHEMBL988465
SCHEMBL3033085
SCHEMBL3239178
SCHEMBL6014660
SCHEMBL6545795
SCHEMBL10747765
1-Amino-2-butanol, AldrichCPR
KODLUXHSIZOKTG-UHFFFAOYSA-
ALBB-026517
FBA60863
NAA55221
NSC17695
MFCD00079691
NSC 17695
SBB017626
(+/-)-1-AMINO-2-BUTANOL
AKOS009157866
SB83793
LS-09053
SY199885
SY209856
A0823
CS-0109319
EN300-94408
D97409
A806946
Q27252061
Z419084746
InChI=1/C4H11NO/c1-2-4(6)3-5/h4,6H,2-3,5H2,1H3
Solubility of 1-aminobutan-2-ol
1-aminobutan-2-ol, with its molecular formula C4H11NO, exhibits intriguing solubility characteristics. This compound, categorized as an amino alcohol, is known for its ability to interact with water due to the presence of both amine and alcohol functional groups.
Key aspects of its solubility include:
It is noteworthy that compounds like 1-aminobutan-2-ol exhibit varying degrees of solubility depending on temperature and concentration. As the temperature rises, solubility generally increases, enhancing the compound's utility in various applications.
Overall, 1-aminobutan-2-ol’s solubility profile is a fascinating demonstration of how small structural components can profoundly influence chemical behavior: