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| 2-Oxobutyric acid Basic information |
| 2-Oxobutyric acid Chemical Properties |
Melting point | 30-34 °C(lit.) | Boiling point | 84 °C20 mm Hg(lit.) | density | 1.2000 | FEMA | 3723 | 2-OXOBUTYRIC ACID | refractive index | 1.3972 (estimate) | Fp | 179 °F | storage temp. | Store at +2°C to +8°C. | solubility | H2O: soluble0.1g/mL, clear | pka | 2.5(at 25℃) | form | liquid | color | White to Almost white | Specific Gravity | 1.3972 (20/4℃) | PH | 3.11(1 mM solution);2.38(10 mM solution);1.79(100 mM solution); | Odor | at 1.00 % in propylene glycol. sweet brown caramel creamy lactonic | Odor Type | caramellic | JECFA Number | 589 | BRN | 1700514 | InChIKey | TYEYBOSBBBHJIV-UHFFFAOYSA-N | LogP | -0.75 | CAS DataBase Reference | 600-18-0(CAS DataBase Reference) | NIST Chemistry Reference | Butanoic acid, 2-oxo-(600-18-0) | EPA Substance Registry System | 2-Oxobutyric acid (600-18-0) |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-36/37/39-36 | RIDADR | 1759 | WGK Germany | 3 | HazardClass | 8 | PackingGroup | III | HS Code | 29183000 |
| 2-Oxobutyric acid Usage And Synthesis |
Chemical Properties | COLOURLESS TO ALMOST COLOURLESS CRYSTALS | Chemical Properties | 2-Oxobutyric acid has a sweet, brown, caramel, creamy odor. | Occurrence | Reported found in beer and black tea. | Uses | A substrate for the determination of lactate dehydrogenase isoenzymes.This compound is suitable for lactate dehydrogenase (LDH) related research. | Uses | 2-Oxobutyric acid (α-ketobutyric acid) may be used as an analytical reference standard for the determination of the analyte in K562 cells by high-performance liquid chromatography with fluorescence detection and in drinking water at low microgram per liter concentrations by ion chromatography technique. | Definition | ChEBI: A 2-oxo monocarboxylic acid that is the 2-oxo derivative of butanoic acid. | Taste threshold values | Taste characteristics at 25 ppm: sweet, brown, creamy, caramellic with a fatty nuance. | General Description | 2-Oxobutyric acid is mainly found in the hydrolysates of proteins, reportedly being formed by the degradation of threonine. |
| 2-Oxobutyric acid Preparation Products And Raw materials |
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