- Min.Order :100 Gram
- Purity: 99%
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Keywords
BOC-L-LYSINE BOC-L-LYS-OH Boc-Amino acid series
Quick Details
- Appearance:white to off-white powder
- Application: 13734-28-6 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 con
- PackAge:1g;5g;10g;25g;50g;100g;500g;1KG;5KG,25kg,50kg or as customers request
- ProductionCapacity:100|Kilogram|Month
- Storage:2-8, cold storage, to avoid light storage.
- Transportation:BY SEA /BY AIR /BY COURIER
Superiority:
| N-alpha-(tert-Butoxycarbonyl)-L-lysine Basic information |
| Product Name: | N-alpha-(tert-Butoxycarbonyl)-L-lysine |
| Synonyms: | BOC-L-LYSINE;BOC-L-LYSINE-OH;BOC-L-LYS-OH;BOC-LYSINE;BOC-LYS-OH;N-ALPHA-BOC-L-LYSINE;N-ALPHA-T-BUTOXYCARBONYL-L-LYSINE;N-ALPHA-T-BOC-L-LYSINE |
| CAS: | 13734-28-6 |
| MF: | C11H22N2O4 |
| MW: | 246.3 |
| EINECS: | 237-303-4 |
| Product Categories: | Amino Acids;Lysine [Lys, K];Boc-Amino Acids and Derivative;Amino Acids (N-Protected);Biochemistry;Boc-Amino Acids;Boc-Amino acid series |
| Mol File: | 13734-28-6.mol |
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| N-alpha-(tert-Butoxycarbonyl)-L-lysine Chemical Properties |
| mp | ~205 °C (dec.)(lit.) |
| alpha | 22 º (c=2, CH3OH) |
| refractive index | 21.5 ° (C=2, MeOH) |
| storage temp. | 2-8°C |
| BRN | 4252546 |
| CAS DataBase Reference | 13734-28-6(CAS DataBase Reference) |
| Safety Information |
| Hazard Codes | Xn |
| Risk Statements | 20/21/22-36/37/38 |
| Safety Statements | 24/25-36-26 |
| WGK Germany | 3 |
| HazardClass | IRRITANT |
| MSDS Information |
| Provider | Language |
|---|---|
| N-alpha-(tert-Butoxycarbonyl)-L-lysine | English |
| SigmaAldrich | English |
| ACROS | English |
| N-alpha-(tert-Butoxycarbonyl)-L-lysine Usage And Synthesis |
| Chemical Properties | white to off-white powder |
| Usage | 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. |
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