Interesting facts
Exploring 2-amino-2-ethyl-propane-1,3-diol
2-amino-2-ethyl-propane-1,3-diol, often referred to as a diol or amino alcohol, carries several intriguing characteristics that make it noteworthy in the realm of chemistry and various applications. Here are some captivating insights:
Key Properties and Applications
- Functional Versatility: This compound serves as a valuable intermediate in the production of pharmaceuticals, agricultural chemicals, and polymers due to its functional groups that enable a range of chemical reactions.
- Biological Importance: The presence of amino and hydroxyl groups lends 2-amino-2-ethyl-propane-1,3-diol the ability to interact with biological systems, paving the way for its use in biochemistry and medicinal chemistry.
- Solvent Applications: It can act as a solvent or a co-solvent in various chemical reactions and formulations, which is beneficial in enhancing the solubility of other compounds.
Interesting Facts
- Synthetic Pathways: The synthesis of this compound often involves straightforward reactions that can be accomplished in the laboratory, making it a staple for educational purposes in organic chemistry courses.
- Research Interest: Ongoing research is exploring its potential as a *stabilizer* in formulations, particularly in areas that require increased stability of the active ingredients.
- Environmental Perspective: With a growing emphasis on green chemistry, compounds like 2-amino-2-ethyl-propane-1,3-diol can offer a more *eco-friendly* alternative to less sustainable chemicals.
In conclusion, 2-amino-2-ethyl-propane-1,3-diol not only illustrates the intricate world of organic compounds, but also highlights the intersection of chemistry with real-world applications. Its diversity in usage and potential for innovation make it a fascinating subject of study for chemists and students alike.
Synonyms
115-70-8
2-AMINO-2-ETHYL-1,3-PROPANEDIOL
2-amino-2-ethylpropane-1,3-diol
1,3-Propanediol, 2-amino-2-ethyl-
Aminoethyl propanediol
AEPD
2-Amino-2-ethylpropanediol
2-Ethyl-2-aminopropanediol
NSC 8803
EINECS 204-101-2
AEPD-85
UNII-0ADF1987D4
2-Amino-1,3-dihydroxy-2-ethylpropane
DTXSID3029150
AI3-03358
0ADF1987D4
NSC-8803
2-Amino-2-ethyl-propane-1,3-diol
MFCD00004680
DTXCID609150
EC 204-101-2
2-AMINO-2-ETHYL-1,3-PROPANEDIOL [MI]
1, 2-amino-2-ethyl-
SCHEMBL45629
CHEMBL119482
NSC8803
BCP30894
Tox21_200845
AMINOETHYL PROPANEDIOL [INCI]
BBL027474
STL372708
AKOS000120518
NCGC00248849-01
NCGC00258399-01
CAS-115-70-8
SY036815
VS-08546
A0620
butane, 2-amino-1-hydroxy-2-hydroxymethyl-
CS-0089934
NS00001265
D71113
2-amino-2-ethyl-;2-amino-2-ethyl-3-propanediol
2-AMINO-2-ETHYL-1,3-PROPANEDIOL, TECH.
Q27236537
1,3-Propanediol, 2-amino-2-ethyl- ; 2-amino-2-ethyl-3-propanediol
Solubility of 2-amino-2-ethyl-propane-1,3-diol
2-amino-2-ethyl-propane-1,3-diol, commonly referred to as TAE (Triamino Ethanol), demonstrates interesting solubility characteristics that can influence its application in various chemical processes. This compound generally exhibits the following solubility behaviors:
Given these properties, TAE’s solubility plays a crucial role in its functionality as a chemical intermediary. As stated, “The solubility of a substance often dictates its applications and reactivity,” further emphasizing the importance of understanding solubility in chemical science.