CAS 1492-24-6
:(+)-α-Aminobutyric acid
Description:
(+)-α-Aminobutyric acid, commonly known as L-α-aminobutyric acid or simply L-AB, is an amino acid characterized by its aliphatic structure and the presence of both an amino group (-NH2) and a carboxylic acid group (-COOH). It is a chiral compound, with the (+) designation indicating its specific optical activity. This amino acid plays a role in various biological processes and is involved in the synthesis of neurotransmitters. L-AB is soluble in water, which facilitates its biological functions and interactions in physiological environments. It is typically found in its zwitterionic form at physiological pH, where it carries both a positive and a negative charge. The compound is utilized in research and has potential applications in pharmaceuticals and nutrition. Its CAS number, 1492-24-6, is a unique identifier that helps in the cataloging and regulation of chemical substances. Overall, (+)-α-Aminobutyric acid is significant in both biochemical research and potential therapeutic applications.
Formula:C4H9NO2
InChI:InChI=1/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m1/s1
InChI key:InChIKey=QWCKQJZIFLGMSD-VKHMYHEASA-N
SMILES:[C@@H](C(O)=O)(CC)N
Synonyms:- (+)-2-Aminobutyric acid
- (+)-α-Aminobutyric acid
- (2R)-2-aminobutanoic acid
- (2S)-2-aminobutanoic acid
- (S)-(+)-2-Aminobutyric acid
- (S)-(+)-α-Aminobutyric acid
- (S)-2-Aminobutanoate
- (S)-2-Aminobutanoic acid
- (S)-2-amino butyric acid
- 2-Aminobutanoic Acid
- <span class="text-smallcaps">L</span>-2-Amino-n-butyric acid
- <span class="text-smallcaps">L</span>-2-Aminobutanoic acid
- <span class="text-smallcaps">L</span>-2-Aminobutyric acid
- <span class="text-smallcaps">L</span>-Butyrine
- <span class="text-smallcaps">L</span>-Ethylglycine
- <span class="text-smallcaps">L</span>-Homoalanine
- <span class="text-smallcaps">L</span>-α-Amino-n-butyric acid
- <span class="text-smallcaps">L</span>-α-Aminobutyric acid
- Aminobutyric acid, 2-
- Butanoic acid, 2-amino-, (2S)-
- Butanoic acid, 2-amino-, (S)-
- Butyric acid, 2-amino-, <span class="text-smallcaps">L</span>-
- H-Abu-OH
- L-2-Amino butyric acid
- L-2-Aminobutanoic acid
- L-Amino butanoic acid
- L-alpha-amino-n-butyrate
- NSC 97060
- S-Butyrine
- Butyric acid, 2-amino-, L-
- L-α-Amino-n-butyric acid
- L(+)-2-Aminobutyric Acid
- L(+)-2-Aminobutyric acid
- L-(+)-2-Aminobutyric acid
- L-2-AMINO-N-BUTYRIC ACID
- H-L-NHCH(CH2CH3)-COOH
- L-ALPHA-AMINO-N-BUTYRIC ACID
- H-L-ABU-OH
- (S)-(+)-α-aminobutyricacid
- (S)-(+)-2-AMINO-N-BUTYRIC ACID
- H-2-ABU-OH
- L-ABU
- H-ABU(2)-OH
- H-ABU(ALPHA)-OH
- L-ALPHA-AMINOBUTYRIC ACID
- 2-AMINO-BUTYRIC ACID
- See more synonyms
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Found 15 products.
(S)-(+)-2-Aminobutyric Acid
CAS:Formula:C4H9NO2Purity:>99.0%(T)Color and Shape:White powder to crystalMolecular weight:103.12L-(+)-2-Aminobutyric acid, 98+%
CAS:<p>L-(+)-2-Aminobutyric acid is used in the biosynthesis of nonribosomal peptides. It acts as a receptor antagonist. It is also used as a chiral reagent. Further, it is used in the determination of substrate of glutamyl cysteine acid synthase. In addition to this, it is also utilized as a drug intermed</p>Formula:C4H9NO2Purity:98+%Color and Shape:Crystals or powder or crystalline powder or flakes, White to pale cream to pale brownMolecular weight:103.12H-Abu-OH
CAS:<p>Bachem ID: 4030313.</p>Formula:C4H9NO2Purity:> 99%Color and Shape:WhiteMolecular weight:103.12Butanoic acid, 2-amino-, (2S)-
CAS:Formula:C4H9NO2Purity:95%Color and Shape:SolidMolecular weight:103.1198Ref: IN-DA001LG6
5gTo inquire10gTo inquire25g22.00€100g26.00€200g37.00€500g38.00€1000g68.00€100kgTo inquire(2S)-2-Aminobutanoic acid
CAS:<p>(2S)-2-Aminobutanoic acid</p>Formula:C4H9NO2Purity:≥95%Color and Shape: white crystalline powderMolecular weight:103.12g/molL-2-Aminobutyric acid
CAS:Formula:C4H9NO2Purity:≥ 98.0%Color and Shape:White powderMolecular weight:103.12H-Abu-OH
CAS:<p>H-Abu-OH, or (S)-2-aminobutanoic acid, is a non-proteogenic L-alpha-amino acid found in human kidneys, liver, and bodily fluids.</p>Formula:C4H9NO2Purity:99.96%Color and Shape:SolidMolecular weight:103.12L-2-Aminobutyric Acid 3,3,4,4,4-d5
CAS:Controlled Product<p>Applications Isotope labelled L-2-Aminobutyric Acid (A602930) Receptor antagonist.<br>References Porter, D.J.T., et al.: Biochem. Pharmacol., 50, 1475 (1995),<br></p>Formula:C4D5H4NO2Color and Shape:NeatMolecular weight:108.151L-Aminobutyric Acid
CAS:<p>Applications Receptor antagonist.<br>References Porter, D.J.T., et al.: Biochem. Pharmacol., 50, 1475 (1995),<br></p>Formula:C4H9NO2Color and Shape:NeatMolecular weight:103.12L-2-Aminobutyric acid
CAS:<p>L-2-Aminobutyric acid is a nonessential amino acid that serves as a substrate for enzymes that catalyze the alpha-elimination of hydroxyl groups. This process is used in the synthesis of proteins and other biological molecules. The L-2-Aminobutyric acid is also an analog to 2-aminoethanol, which has been shown to inhibit amyloid protein production in human serum. A synthetic route for the preparation of L-2-Aminobutyric acid has been developed using anhydrous sodium hydroxide and blood sampling from a bacterial strain. L-2-Aminobutyric acid inhibits protease activity and has been shown to have antibacterial properties. The optimum pH for this compound is 5.5, with an approximate intramolecular hydrogen bond distance of 3.1 angstroms.</p>Formula:C4H9NO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:103.12 g/mol(S)-(+)-2-Aminobutyric acid
CAS:Formula:C4H9NO2Purity:95%Color and Shape:Solid, Crystalline Powder or FlakesMolecular weight:103.121
