Interesting facts
Interesting Facts about 3-Aminopropanoic Acid
3-Aminopropanoic acid, also known as alanine, is a fascinating amino acid that serves as a building block for proteins in living organisms. Here are some interesting facts to explore:
- Biological Importance: Alanine plays a crucial role in the metabolism of nitrogen, assisting in the transamination process where amino groups are transferred between amino acids and keto acids.
- Varieties: It exists in two enantiomeric forms: L-alanine and D-alanine. While L-alanine is prevalent in proteins, D-alanine is an essential component in the cell walls of certain bacteria.
- Energy Source: It is a valuable energy source for muscles, particularly during prolonged exercise, as it can be converted into glucose through gluconeogenesis.
- Sweetness: Interestingly, alanine has a sweet taste, which has led to its exploration as a potential flavor enhancer in food science.
- Supplements: 3-Aminopropanoic acid is popular in dietary supplements, especially among bodybuilders and athletes, due to its role in protein synthesis and muscle recovery.
In summary, 3-aminopropanoic acid is not just a simple amino acid; it holds significant biochemical roles and has various applications in health and nutrition. It’s a prime example of how compounds can contribute to the intricate tapestry of life at the molecular level.
Synonyms
beta-alanine
3-Aminopropanoic acid
107-95-9
3-Aminopropionic acid
Beta Alanine
Abufene
H-beta-Ala-OH
beta-Aminopropionic acid
2-Carboxyethylamine
.beta.-Alanine
Alanine, beta-
beta-Ala
Propanoic acid, 3-amino-
3-Aminopropionsaeure
beta-Aminopropionsaeure
B-ALANINE
omega-Aminopropionic acid
3-Aminopropanoate
FEMA No. 3252
.beta.-Aminopropionic acid
3-amino-propionic acid
NSC 7603
AI3-18470
b-Aminopropanoate
b-Aminopropionate
3-Aminopropionate
b-Ala
EINECS 203-536-5
MFCD00008200
3-amino-Propanoate
beta-Aminopropanoate
beta-Aminopropionate
Abufene (TN)
omega-Aminopropionate
11P2JDE17B
b-Aminopropanoic acid
b-Aminopropionic acid
87867-95-6
CHEBI:16958
3-amino-Propanoic acid
beta-Aminopropanoic acid
NSC-7603
ALANINE, .BETA.-
BETA-ALANINE [VANDF]
.BETA.-ALANINE [MI]
BETA ALANINE [USP-RS]
BETA-ALANINE [WHO-DD]
CHEMBL297569
.BETA.-ALANINE [FHFI]
DTXSID0030823
NSC7603
EC 203-536-5
3-Aminopropanoic Acid (beta-Alanine)
3 Aminopropionic Acid
BETA ALANINE (USP-RS)
beta-ALANINE-13C3-15N
beta-alanin
PAMIDRONATE DISODIUM PENTAHYDRATE IMPURITY A [EP IMPURITY]
beta-Alaine
ALANINE, BETA
UNII-11P2JDE17B
Alanine-beta
PAMIDRONATE DISODIUM PENTAHYDRATE IMPURITY A (EP IMPURITY)
beta -alanine
beta- alanine
beta--alanine
2Carboxyethylamine
beta-Alanine #
aminopropionic acid
3Aminopropionsaeure
Beta Alanine; Pamidronate Disodium Pentahydrate Imp. A (EP); Pamidronate Imp. A (EP); Calcium Pantothenate Impurity A; Pamidronate Disodium Pentahydrate Impurity A; Pamidronate Impurity A
3aminopropanoic acid
3aminopropionic acid
A-Ala
betaAminopropionsaeure
betaaminopropionic acid
beta-Alanine, 99%
Tocris-0206
Propanoic acid, 3amino
Propanoic acid, amino-
|A-Alanine (Standard)
H2NCH2CH2COOH
bmse000159
bmse000967
bmse001019
.omega.-Aminopropionic acid
BETA-ALANINE [INCI]
Oprea1_583450
beta-Alanine, >=98%, FG
GTPL2365
DTXCID8010823
3-aminopropanoic acidbeta-alanine
HY-N0230R
beta-Alanine (6CI,8CI,9CI)
beta-Alanine, analytical standard
HY-N0230
STR03358
BBL037332
BDBM50000102
PDSP1_000144
PDSP2_000143
s5526
STK301638
AKOS000119659
CS-W020126
DB03107
FA10356
NCGC00024495-01
NCGC00024495-02
BP-10083
beta-Alanine, BioXtra, >=99.0% (NT)
beta-Alanine, BioUltra, >=99.0% (NT)
DB-022630
A0180
NS00009116
EN300-18046
C00099
D07561
F86478
Q310919
SR-01000597690
SR-01000597690-1
Z57127544
F2191-0213
7CA041EF-5103-439A-9D84-1761529BA8DA
beta-Alanine, United States Pharmacopeia (USP) Reference Standard
Beta Alanine, Pharmaceutical Secondary Standard; Certified Reference Material
beta-Alanine, BioReagent, suitable for cell culture, suitable for insect cell culture
203-536-5
25513-34-2
Solubility of 3-Aminopropanoic Acid
3-Aminopropanoic acid, with the chemical formula C3H7NO2, exhibits notable solubility characteristics in different solvents due to its unique functional groups. The presence of both an amino group (-NH2) and a carboxylic acid group (-COOH) contributes to its solubility properties:
As a result, it's essential to consider the solvent system when working with this compound. The solubility profile underlines the importance of functional groups in dictating solubility behavior:
In conclusion, 3-aminopropanoic acid’s solubility in water makes it a valuable compound in various chemical and biological applications, while its limited solubility in non-polar solvents can restrict its use in certain formulations.