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| | DL-3-Aminoisobutyric acid Basic information |
| Product Name: | DL-3-Aminoisobutyric acid | | Synonyms: | DL-BETA-AMINOISOBUTYRIC ACID;2-Methyl-3-aminopropanoic acid;2-Methyl-3-aminopropionic acid;3-azanyl-2-methyl-propanoic acid;3-aminoisobutyric ac;DL-3-AMinoisobutyric acid DL-3-AMinoisobutyric acid;DL-3-AMinoisobutyric acid 98%;2-(aminomethyl)propanoic acid | | CAS: | 144-90-1 | | MF: | C4H9NO2 | | MW: | 103.12 | | EINECS: | 205-644-8 | | Product Categories: | | | Mol File: | 144-90-1.mol |  |
| | DL-3-Aminoisobutyric acid Chemical Properties |
| Melting point | 246.72°C (estimate) | | Boiling point | 223.6±23.0 °C(Predicted) | | density | 1.2300 (estimate) | | refractive index | 1.4650 (estimate) | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | solubility | Methanol (Slightly), Water (Slightly) | | form | powder to crystal | | pka | 3.69±0.16(Predicted) | | color | White | | BRN | 1720958 | | Major Application | peptide synthesis | | InChI | InChI=1S/C4H9NO2/c1-3(2-5)4(6)7/h3H,2,5H2,1H3,(H,6,7) | | InChIKey | QCHPKSFMDHPSNR-UHFFFAOYSA-N | | SMILES | C(O)(=O)C(C)CN |
| WGK Germany | 3 | | RTECS | UA2430000 | | HS Code | 2922.49.4950 | | Storage Class | 11 - Combustible Solids |
| | DL-3-Aminoisobutyric acid Usage And Synthesis |
| Uses | DL-3-Aminoisobutyric Acid Hydrate is a beta-amino acid used for proteomics research. | | Definition | ChEBI: 3-aminoisobutyric acid is a beta-amino-acid that is isobutyric acid in which one of the methyl hydrogens is substituted by an amino group. It has a role as a metabolite. It is functionally related to an isobutyric acid. It is a conjugate acid of a 3-aminoisobutyrate. It is a tautomer of a 3-aminoisobutanoic acid zwitterion. | | General Description | DL-3-Aminoisobutyric acid (for short, 3AIBA), synonymous with α-Methyl-β-alanine, is a β-amino acid occurring naturally in all living organisms. 3AIBA can be formed in humans and animals from the nucleotide thymine and amino acid valine. Since 3AIBA is structurally similar to β-alanine; it can also be called α-methyl-β-alanine having one additional methyl group on α-carbon atom. In their free form, β-alanine and 3AIBA are metabolites in mammals and moieties in several pharmacologically active compounds such as antibiotics, antitumor, and antifungal agents[1]. | | reaction suitability | reaction type: solution phase peptide synthesis | | References |
[1] Shashikala Yalagi, Jayashree Tonannavar, Jagdish Tonannavar. “DL-3-Aminoisobutyric acid: vibrational, NBO and AIM analysis of N-HO bonded-zwitterionic dimer model.” Heliyon 5 6 (2019): e01933.
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| | DL-3-Aminoisobutyric acid Preparation Products And Raw materials |
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