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3-Chloro-DL-alanine

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Identification
Molecular formula
C3H6ClNO2
CAS number
70-61-7
IUPAC name
2-amino-3-chloro-propanoic acid
State
State

At room temperature, 3-Chloro-DL-alanine is typically found as a solid. It has a crystalline structure, which is common for amino acids and their derivatives.

Melting point (Celsius)
211.00
Melting point (Kelvin)
484.15
Boiling point (Celsius)
194.00
Boiling point (Kelvin)
467.15
General information
Molecular weight
123.55g/mol
Molar mass
123.5480g/mol
Density
1.4886g/cm3
Appearence

3-Chloro-DL-alanine is a colorless crystalline solid. It may appear as white or off-white needles or powder, depending on its form and purity.

Comment on solubility

Solubility of 2-amino-3-chloro-propanoic acid

The compound 2-amino-3-chloro-propanoic acid (C3H6ClNO2) exhibits interesting solubility characteristics that are crucial for its applications. Generally, the solubility of amino acids is influenced by both their ionic properties and the presence of functional groups.

Key Points on Solubility:

  • Water Solubility: 2-amino-3-chloro-propanoic acid is expected to be soluble in water due to the presence of the carboxylic acid (-COOH) functional group, which can form strong hydrogen bonds with water molecules.
  • Ionic Form: In a solution, this compound can exist in an ionic form (zwitterionic), enhancing its solubility further due to increased interaction with water.
  • Organic Solvents: The solubility in organic solvents is relatively lower compared to that in water. The presence of polar structures can limit its solubility in non-polar solvents.

As a general rule, compounds that can form ionic bonds or hydrogen bonds tend to have higher solubility in polar solvents like water. Therefore, it can be said that:

"The more polar the solvent, the better the solubility for polar molecules."

In summary, 2-amino-3-chloro-propanoic acid showcases significant solubility in aqueous environments, while it is less soluble in non-polar organic solvents, demonstrating its polar characteristics and potential for various biochemical interactions.

Interesting facts

Interesting Facts about 2-Amino-3-chloro-propanoic Acid

2-Amino-3-chloro-propanoic acid, commonly referred to as chloramino acid, is a fascinating compound with a number of noteworthy attributes and applications. Below are some interesting insights into this unique chemical:

  • Biochemical Importance: This compound is a derivative of the amino acid alanine and plays a crucial role in biochemical pathways, particularly in the synthesis of various proteins.
  • Pharmaceutical Applications: It has garnered attention in medicinal chemistry for its potential use in drug development. As a chlorinated amino acid, it offers unique properties that can enhance therapeutic effects.
  • Antimicrobial Properties: Research suggests that 2-amino-3-chloro-propanoic acid exhibits antimicrobial activity, making it a candidate for further studies in the fight against bacterial infections.
  • Synthetic Utility: In organic chemistry, it serves as a building block for the synthesis of other complex molecules, showcasing its versatility for synthetic chemists.
  • Research Potential: Ongoing studies on this compound may reveal additional functions and uses, creating opportunities for innovation in both biochemistry and pharmacology.

In summary, 2-amino-3-chloro-propanoic acid is much more than just a simple chlorinated amino acid; it is a compound that bridges various scientific fields, from biochemistry to medicinal applications. As researchers continue to explore its properties, the potential for new discoveries remains vast.

Synonyms
2-amino-3-chloropropanoic acid
3-Chloroalanine
3981-36-0
beta-Chloroalanine
13215-35-5
N-Chloroalanine
DL-3-Chloroalanine
Alanine, 3-chloro-
3-CHLORO-DL-ALANINE
beta-chloro-DL-alanine
CHEBI:88164
DTXSID70927558
L-??Chloroalanine
H-beta-Chloro-Ala-OH
MFCD00046536
MFCD01632068
(S)-2-Amino-3-chloropropionic Acid
b-Chloro-L-alanine
.beta.-Chloro-D-alanine
2-amino-3-chloropropanoicacid
SCHEMBL890419
ASBJGPTTYPEMLP-UHFFFAOYSA-N
alanine, 3-chloro-, hydrochloride
DTXCID901008153
HMS3749A15
alpha-Amino-beta-chlor-propionsaure
ALBB-018637
(2S)-2-amino-3-chloropropanoicacid
NSC337715
AKOS006228265
SY034145
SY034148
EN300-195277
G50301
Q27160094
634-355-3