Name | D(-)-2-Aminobutyric acid |
Synonyms | H-D-Abu-OH D-ETHYLGLYCINE R-AMINOBUTYRIC ACID D-2-Aminobutyric acid D-2-AMINO-BUTANOIC ACID (R) 2-AMINOBUTYRIC ACID (R)-2-Aminobutyric acid -(-)-2-Aminobutyric acid D(-)-2-Aminobutyric acid D-A-AMINO-N-BUTYRIC ACID D-(-)-2-AMINOBUTYRIC ACID D-ALPHA-AMINO-BUTYRIC ACID (R)-(-)-2-Aminobutyric acid (R)-(-)-2-AMINOBUTYRIC ACID D-alpha-Amino-n-butyric Acid D-(-)-2-AMINO-N-BUTYRIC ACID D-ALPHA-AMINO-N-BUTYRIC ACID (R)-(-)-2-AMINO-N-BUTYRIC ACID |
CAS | 2623-91-8 |
EINECS | 220-084-4 |
InChI | InChI=1/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7) |
InChIKey | QWCKQJZIFLGMSD-GSVOUGTGSA-N |
Molecular Formula | C4H9NO2 |
Molar Mass | 103.12 |
Density | 1.2300 (estimate) |
Melting Point | >300 °C (lit.) |
Boling Point | 215.2±23.0 °C(Predicted) |
Specific Rotation(α) | -21.2 º (c=2, 6N HCl) |
Water Solubility | soluble |
Solubility | soluble |
Appearance | White crystal |
Color | White |
BRN | 1720934 |
pKa | 2.34±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Refractive Index | 1.4650 (estimate) |
MDL | MFCD00064414 |
Use | Used as a drug Intermediate |
In vitro study | D(-)-2-Aminobutyric acid (D-α-aminobutyric acid) is a substrate of D-amino acid oxidase. |
Hazard Symbols | Xi - Irritant |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
WGK Germany | 3 |
HS Code | 29224999 |
Hazard Note | Irritant |
Reference Show more | 1. Wang Jian, Sun Yu, Chen Lili, Han Zhenzhen, Sun proficient. Evaluation of different metabolites in processed products of Polygonum multiflorum Thunb based on ~ 1H-NMR metabolomics [J]. Modern medicine and clinic, 2020,35(08):1537-1543. |
introduction | D-2-aminobutyric acid is an amino acid derivative and can be used as a biochemical reagent. |
application | D-2-aminobutyric acid is a key intermediate of chiral drugs, chiral pesticides and chiral food additives, and is widely used in the fields of medicine, pesticides and food. D-2-aminobutyric acid is an important unnatural chiral α-amino acid. It is an important chemical raw material and chiral intermediate, and is widely used in drug synthesis. |
synthesis method | at present, the literature reports on the synthesis of D-2-aminobutyric acid, such as using methionine in d configuration as raw material to synthesize D-2-aminobutyric acid through desulfurization and other steps. Ammonia hydrolysis reaction method, chemical separation method, etc. First, the racemic 2-aminobutyric acid is acetylated to obtain N-acetyl-2-aminobutyric acid, and then the amino acylase extracted from the pig kidney is used to selectively hydrolyze the (S)-configuration N-Acetyl-2-aminobutyric acid, thereby obtaining (S)-2-aminobutyric acid, the unhydrolyzed (R)-N-acetyl -2-aminobutyric acid was racemized by an appropriate method to obtain racemic 2-aminobutyric acid, thus realizing its dynamic kinetic resolution and its final yield reaching 71.9%. |
biological activity | D(-)-2-Aminobutyric acid is a pharmaceutical intermediate. |
Use | Used as a pharmaceutical intermediate |