Interesting facts
Exploring 3-Aminopropan-1-ol
3-Aminopropan-1-ol, often referred to as propylamine, is a fascinating organic compound with a variety of applications in both industry and research. This molecule features an amine and an alcohol group, which grants it unique properties and the ability to participate in diverse chemical reactions.
Key Features and Applications:
- Versatility: 3-Aminopropan-1-ol is a versatile building block in organic synthesis, making it valuable for the production of pharmaceuticals, agrochemicals, and surfactants.
- Biochemical Significance: The presence of both an amine and an alcohol in its structure means it can mimic certain biological molecules, aiding in studies of enzymatic reactions and biological pathways.
- Safety and Handling: It is essential to handle this compound with care. Proper safety protocols should always be followed given its potential to cause irritation upon contact.
- Special Properties: Properties such as its ability to act as a stabilizing agent in chemical formulations highlight its importance across various industries.
Interesting Facts:
- Dual Functionality: With both amine and alcohol characteristics, 3-aminopropan-1-ol can be used as a nucleophile, participating in various substitution reactions.
- Research Applications: In biochemistry, it serves as a crucial compound for studying amino acid interactions and enzymatic catalysis.
- Hyphenated Naming: The systematic name "3-aminopropan-1-ol" gives insight into the compound's structure, where the numbers indicate the positions of the amine and alcohol functional groups.
As a compound with such multi-faceted applications, 3-aminopropan-1-ol continues to intrigue scientists and contribute to advancements in various fields. Its balance of simplicity and functionality makes it a staple in both the laboratory and manufacturing sectors.
Synonyms
3-Aminopropan-1-ol
3-Aminopropanol
3-Amino-1-propanol
156-87-6
1-Propanol, 3-amino-
PROPANOLAMINE
3-Propanolamine
3-Aminopropyl alcohol
1-Amino-3-propanol
1,3-Propanolamine
3-Hydroxypropylamine
1-Amino-3-hydroxypropane
beta-Alaninol
n-Propanolamine
.beta.-Alaninol
gamma-Aminopropanol
3-Hydroxy-1-propylamine
.gamma.-Aminopropanol
gamma-Hydroxy-1-propylamine
NSC 7766
3-hydroxypropan-1-amine
HSDB 5161
3-Hydroxy-1-aminopropane
YMA7C44XGY
EINECS 205-864-4
MFCD00008223
BRN 0741855
AI3-25439
NSC-7766
n-(3-hydroxypropyl)amine
NSC 7766; Propanolamine
PROPANOLAMINE [HSDB]
PROPANOLAMINE [USP-RS]
3-Aminopropanol (Propanolamine)
DTXSID0059746
CHEBI:143408
EC 205-864-4
.GAMMA.-HYDROXY-1-PROPYLAMINE
propane, 1-amino-3-hydroxy-
PROPANOLAMINE (USP-RS)
3-Aminopropanol; 3-Amino-1-propanol
3-Amino-propan-1-ol
3-Aminopropanol-(1)
UNII-YMA7C44XGY
betaAlaninol
nPropanolamine
3aminopropanol
3Propanolamine
1Amino3propanol
3Amino1propanol
3Aminopropan1ol
gammaAminopropanol
3- aminopropanol
3-amino-propanol
aminopropan-3-ol
1,3Propanolamine
3hydroxypropylamine
3-hydroxypropyamine
3-amino-1propanol
3amino-1-propanol
1Propanol, 3amino
3-amino-l-propanol
3Aminopropyl alcohol
3Hydroxy1propylamine
1Amino3hydroxypropane
3-Hydroxylpropylamine
3-aminopropane-1-ol
3-hydroxy-propylamine
1-amino-propan-3-ol
1-propanol, 3-amino
3-amino -1-propanol
3-hydroxy-propyl amine
gammaHydroxy1propylamine
0D8
1-amino-3-propyl alcohol
WLN: Z3Q
3-Amino-1-propanol, 99%
H2N(CH2)3OH
NH2(CH2)3OH
CHEMBL115530
DTXCID1035024
H2N-(CH2)3-OH
CHEBI:35533
3-Amino-1-propanol, >=99%
NSC7766
JCA72007
STR03558
YGA54744
STL194299
AKOS000119899
CS-W020089
SB83761
3-Amino-1-propanol, analytical standard
BP-31041
A0438
DEXPANTHENOL IMPURITY A [EP IMPURITY]
NS00001059
EN300-16772
D77871
Q223042
Z56771034
F2190-0368
Propanolamine, United States Pharmacopeia (USP) Reference Standard
3-Amino-1-propanol, Pharmaceutical Secondary Standard; Certified Reference Material
205-864-4
Solubility of 3-aminopropan-1-ol
3-aminopropan-1-ol, known for its functional amine group, exhibits interesting solubility characteristics that are crucial for various applications.
When considering its solubility, it is essential to note the following:
The ability of 3-aminopropan-1-ol to dissolve well in aqueous solutions is pivotal in biochemical contexts, allowing it to participate in numerous metabolic pathways. As one can see, the compound's interactive hydrogen bonds significantly enhance its solubility profile.
In conclusion, 3-aminopropan-1-ol's solubility is not only a fundamental characteristic of the compound but also a valuable aspect influencing its behavior in various chemical environments.