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| (2R,3R)-2-Amino-3-methylpentanoic acid Basic information |
| (2R,3R)-2-Amino-3-methylpentanoic acid Chemical Properties |
Melting point | 272-274 °C | alpha | -37 º (c=5, 1 N HCl 24 ºC) | Boiling point | 225.8±23.0 °C(Predicted) | density | 1.1720 (estimate) | refractive index | -40.5 ° (C=4, 6mol/L HCl) | storage temp. | Sealed in dry,Room Temperature | solubility | Aqueous Acid (Slightly), Water (Slightly) | pka | 2.57±0.24(Predicted) | form | Solid | color | White to Off-White | CAS DataBase Reference | 319-78-8(CAS DataBase Reference) | EPA Substance Registry System | D-Isoleucine (319-78-8) |
Hazard Codes | Xn | Risk Statements | 40 | Safety Statements | 24/25-36-22 | WGK Germany | 3 | RTECS | NR4700000 | HS Code | 29224995 | Toxicity | rat,LD50,intraperitoneal,6822mg/kg (6822mg/kg),BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)LUNGS, THORAX, OR RESPIRATION: DYSPNEA,Archives of Biochemistry and Biophysics. Vol. 64, Pg. 319, 1956. |
| (2R,3R)-2-Amino-3-methylpentanoic acid Usage And Synthesis |
Chemical Properties | white to very slightly yellow powder | Uses | May contain up to 10% allo-isomer. | Uses | D-Isoleucine is not biosynthesized in the human body and is therefore categorized as an essential amino acid that must be obtained through diet. It is also an important building block that is used in the formation of hemoglobin in humans. | Definition | ChEBI: The D-enantiomer of isoleucine. |
| (2R,3R)-2-Amino-3-methylpentanoic acid Preparation Products And Raw materials |
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