76265-69-5
Fmoc-Lys(Tfa)-OH
CAS: 76265-69-5
Molecular Formula: C23H23F3N2O5
76265-69-5 - Names and Identifiers
| Name | Fmoc-Lys(Tfa)-OH |
| Synonyms | FMOC-LYS(TFA)-OH Fmoc-Lys(Tfa)-OH FMOC-L-LYS(TFA)-OH FMOC-N-EPSILON-TFA-L-LYSINE NA-FMOC-NE-TRIFLUOROACETYL-L-LYSINE N-α-Fmoc-N-ε-tritfluoroacetyl-L-lysine Fmoc-N-Epsilon-Trifluoroacetyl-L-Lysine FMOC-N-EPSILON-TRIFLUOROACETYL-L-LYSINE Fmoc-N-epsilon-trifluoroacetyl-L-lysine N-ALPHA-FMOC-N-EPSILON-TRIFLUOROACETYL-L-LYSINE N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-EPSILON-TRIFLUOROACETYL-L-LYSINE N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-TRIFLUORACETYL-L-LYSINE |
| CAS | 76265-69-5 |
| InChI | InChI=1/C23H23F3N2O5/c24-23(25,26)21(31)27-12-6-5-11-19(20(29)30)28-22(32)33-13-18-16-9-3-1-7-14(16)15-8-2-4-10-17(15)18/h1-4,7-10,18-19H,5-6,11-13H2,(H,27,31)(H,28,32)(H,29,30)/t19-/m0/s1 |
76265-69-5 - Physico-chemical Properties
| Molecular Formula | C23H23F3N2O5 |
| Molar Mass | 464.43 |
| Density | 1.336g/cm3 |
| Melting Point | 170-174℃ |
| Boling Point | 668.3°C at 760 mmHg |
| Flash Point | 358°C |
| Vapor Presure | 9.06E-19mmHg at 25°C |
| Appearance | Solid |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.552 |
| MDL | MFCD00153360 |
| Use | A hetero-protected lysine derivative with Fmoc on the α amino group. |
76265-69-5 - Risk and Safety
| WGK Germany | 3 |
| HS Code | 29242990 |
76265-69-5 - Introduction
Fmoc-Lys(Tfa)-OH(Fmoc-Lys(Tfa)-OH) is a commonly used protected amino acid that is commonly used in peptide synthesis. The following is a description of its nature, use, formulation and safety information:
Nature:
1. Chemical formula: C27H32F3N3O5
2. molecular weight: 547.56g/mol
3. Appearance: white or white solid
Use:
Fmoc-Lys(Tfa)-OH, a protected amino acid, is commonly used in the synthesis of peptides with lysine residues. It can be assembled into a target peptide chain together with other amino acid residues by methods such as solid phase synthesis or liquid phase synthesis. It has a wide range of applications in biomedical research, drug development and preparation.
Preparation Method:
The synthesis of Fmoc-Lys(Tfa)-OH is usually obtained by certain chemical reactions. Specific steps include the introduction of an Fmoc protecting group onto a lysine molecule, followed by reaction with a trifluoroacetic acylating agent to produce Fmoc-Lys(Tfa)-OH.
Safety Information:
1. Fmoc-Lys(Tfa)-OH has low toxicity under general use conditions.
2. when operating, should follow the laboratory safety procedures, and wear appropriate personal protective equipment.
3. Avoid contact with skin and eyes. If contact occurs, rinse immediately with plenty of water and seek medical help.
4. When storing and handling, it should be stored in a dry, well-ventilated place, and away from fire and oxidant.
5. For further safety information on this compound, please refer to the relevant Safety Data Sheet (SDS).
Nature:
1. Chemical formula: C27H32F3N3O5
2. molecular weight: 547.56g/mol
3. Appearance: white or white solid
Use:
Fmoc-Lys(Tfa)-OH, a protected amino acid, is commonly used in the synthesis of peptides with lysine residues. It can be assembled into a target peptide chain together with other amino acid residues by methods such as solid phase synthesis or liquid phase synthesis. It has a wide range of applications in biomedical research, drug development and preparation.
Preparation Method:
The synthesis of Fmoc-Lys(Tfa)-OH is usually obtained by certain chemical reactions. Specific steps include the introduction of an Fmoc protecting group onto a lysine molecule, followed by reaction with a trifluoroacetic acylating agent to produce Fmoc-Lys(Tfa)-OH.
Safety Information:
1. Fmoc-Lys(Tfa)-OH has low toxicity under general use conditions.
2. when operating, should follow the laboratory safety procedures, and wear appropriate personal protective equipment.
3. Avoid contact with skin and eyes. If contact occurs, rinse immediately with plenty of water and seek medical help.
4. When storing and handling, it should be stored in a dry, well-ventilated place, and away from fire and oxidant.
5. For further safety information on this compound, please refer to the relevant Safety Data Sheet (SDS).
Last Update：2024-04-09 20:02:46
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