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| N-alpha-(tert-Butoxycarbonyl)-L-lysine Basic information |
| N-alpha-(tert-Butoxycarbonyl)-L-lysine Chemical Properties |
| Melting point | ~205 °C (dec.)(lit.) | | alpha | 22 º (c=2, CH3OH) | | Boiling point | 389.3°C (rough estimate) | | density | 1.1313 (rough estimate) | | refractive index | 21.5 ° (C=2, MeOH) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Acetic Acid (Slightly), Methanol (Slightly, Sonicated), Water (Slightly, Heated, | | pka | 3.92±0.21(Predicted) | | form | Powder | | color | White | | optical activity | [α]20/D +4.6±0.5°, c = 2% in H2O | | Water Solubility | Soluble in water. Slightly soluble in methanol. | | BRN | 4252546 | | CAS DataBase Reference | 13734-28-6(CAS DataBase Reference) |
| N-alpha-(tert-Butoxycarbonyl)-L-lysine Usage And Synthesis |
| Chemical Properties | white to off-white powder | | Uses | N-Boc-L-lysine is a protected analogue of a major amino acid participating in the binding of AcH to proteins. N-Boc-L-lysine as well as other t-butoxycarbonyl (Boc) amino acids can be converted to the
ir respective amino acids via cleavage of the urethane bond. | | Uses | N-Boc-L-lysine is a protected analogue of a major amino acid participating in the binding of AcH to proteins. N-Boc-L-lysine as well as other t-butoxycarbonyl (Boc) amino acids can be converted to their respective amino acids via cleavage of the urethane bond. | | Uses | Boc-Lys-OH (Nα-Boc-L-lysine) can be used as a building block to synthesize:- A heterotrifunctional peptide-based linker molecule applicable as a bio-labeling reagent.
- Lysine derivatives of azamacrocycle and anthraquinone.
- Boc-Lys(Bn4-DTPA)-OH, a precursor to synthesize diethylene triamine pentaacetic acid (DTPA) containing peptides.
- A ferrocene-amino acid conjugate which is used in developing chemical warfare agent (CWA) sensor.
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| N-alpha-(tert-Butoxycarbonyl)-L-lysine Preparation Products And Raw materials |
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