Record Information |
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Version | 1.0 |
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Creation date | 2015-10-09 22:28:40 UTC |
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Update date | 2017-01-19 02:36:13 UTC |
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FoodComEx ID | PC000124 |
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FoodDB Record | FDB008937 |
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Chemical Information |
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Name | 4-Aminobutyric acid |
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Description | gamma-Aminobutyric acid, also known as GABA or g-amino-butanoate, belongs to the class of organic compounds known as gamma amino acids and derivatives. These are amino acids having a (-NH2) group attached to the gamma carbon atom. gamma-Aminobutyric acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. gamma-Aminobutyric acid exists in all living species, ranging from bacteria to humans. Outside of the human body, gamma-Aminobutyric acid has been detected, but not quantified in, several different foods, such as fox grapes, oxheart cabbages, garden onion (var.), yellow zucchinis, and chinese mustards. This could make gamma-aminobutyric acid a potential biomarker for the consumption of these foods. gamma-Aminobutyric acid is a potentially toxic compound. A gamma-amino acid that is butanoic acid with the amino substituent located at C-4. |
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CAS Number | 56-12-2 |
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Structure | |
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Synonyms | Synonym | Source |
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3-Carboxypropylamine | biospider | 4-amino-butanoic acid | biospider | 4-Amino-n-butyric acid | biospider | 4-Aminobutanoate | biospider | 4-Aminobutanoic acid | biospider | 4-Aminobutylate | biospider | 4-Aminobutyrate | biospider | 4Abu | ChEBI | Aminalon | HMDB | Aminobutanoic acid | biospider | Aminobutyric acid | biospider | Aminobutyric acid,-4-, α | biospider | Butanoic acid, 4-amino- (9CI) | biospider | Butyric acid, 4-amino- | biospider | DL-gamma-amino-n-butyric acid | biospider | g-amino-BUTANOate | Generator | g-amino-BUTANOic acid | Generator | g-amino-N-Butyrate | Generator | g-amino-N-Butyric acid | Generator | g-Aminobutanoate | Generator | g-Aminobutanoic acid | Generator | g-Aminobuttersaeure | Generator | g-Aminobutyrate | Generator | g-aminobutyric acid | biospider | GABA | biospider | Gaballon | biospider | Gamarex | biospider | Gamastan | biospider | Gamma aminobutyrate | biospider | Gamma aminobutyric acid | biospider | Gamma-amino butyric acid | biospider | gamma-amino-BUTANOate | Generator | Gamma-amino-butanoic acid | biospider | gamma-amino-N-Butyrate | Generator | Gamma-amino-n-butyric acid | biospider | gamma-Aminobutanoate | Generator | Gamma-aminobutanoic acid | biospider | Gamma-aminobutryic acid | biospider | gamma-Aminobuttersaeure | ChEBI | Gamma-aminobutyrate | biospider | Gamma-aminobutyric acid | biospider | Gamma(amino)-butyric acid | biospider | Gammagee | biospider | Gammalon | HMDB | Gammalon (TN) | biospider | Gammalone | HMDB | Gammar | biospider | Gammasol | biospider | Gamulin | biospider | Mielogen | biospider | Mielomade | biospider | Omega-aminobutyrate | Generator | Omega-aminobutyric acid | ChEBI | Piperidate | biospider | Piperidic acid | biospider | Piperidinate | biospider | Piperidinic acid | biospider | Reanal | biospider | W-Aminobutyrate | HMDB | W-Aminobutyric acid | HMDB | γ-amino-butanoate | Generator | γ-amino-butanoic acid | Generator | γ-amino-N-butyrate | Generator | γ-amino-N-butyric acid | Generator | γ-aminobutanoate | Generator | γ-aminobutanoic acid | Generator | γ-aminobuttersaeure | Generator | γ-aminobutyrate | Generator | γ-aminobutyric acid | Generator |
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Chemical Formula | C4H9NO2 |
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IUPAC name | 4-aminobutanoic acid |
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InChI Identifier | InChI=1S/C4H9NO2/c5-3-1-2-4(6)7/h1-3,5H2,(H,6,7) |
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InChI Key | BTCSSZJGUNDROE-UHFFFAOYSA-N |
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Isomeric SMILES | NCCCC(O)=O |
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Average Molecular Weight | 103.1198 |
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Monoisotopic Molecular Weight | 103.063328537 |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as gamma amino acids and derivatives. These are amino acids having a (-NH2) group attached to the gamma carbon atom. |
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Kingdom | Organic compounds |
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Super Class | Organic acids and derivatives |
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Class | Carboxylic acids and derivatives |
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Sub Class | Amino acids, peptides, and analogues |
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Direct Parent | Gamma amino acids and derivatives |
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Alternative Parents | |
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Substituents | - Gamma amino acid or derivatives
- Amino fatty acid
- Straight chain fatty acid
- Fatty acid
- Fatty acyl
- Amino acid
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Organic oxide
- Organopnictogen compound
- Primary amine
- Organooxygen compound
- Organonitrogen compound
- Primary aliphatic amine
- Organic oxygen compound
- Carbonyl group
- Organic nitrogen compound
- Amine
- Hydrocarbon derivative
- Aliphatic acyclic compound
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Molecular Framework | Aliphatic acyclic compounds |
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External Descriptors | |
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Physico-Chemical Properties - Experimental |
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Property | Value | Reference |
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Experimental logP | -3.17 | HANSCH,C ET AL. (1995) |
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Experimental Water Solubility | 1300 mg/mL at 25 oC | YALKOWSKY,SH & DANNENFELSER,RM (1992) |
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Melting Point | 203 oC | |
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Foods of Origin |
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Food | Content Range | Average | Reference |
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Food | | | Reference |
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Production Data |
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Production Method | commercial |
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Production Method Reference | Not Available |
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Production Method Reference File | Not Available |
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Quantity Available | Production upon request, up to 2 g |
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Delivery Time | Not Available |
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Storage Form | solid |
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Storage Conditions | -80°C |
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Stability | Not Available |
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Purity | Not Available |
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Spectra |
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Spectral Data Upon Request | Not Available |
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Provider Information |
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Commercial Vendors |
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AKSci | A578 |
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AKSci | J93537 |
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Glentham | GK0362 |
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MetaSci | HMDB0000112 |
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Sigma-Aldrich | HMDB0000112 |
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Toronto Research Chemicals | A602920 |
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