(S)-6-Amino-2-((S)-2-((S)-6-amino-2-palmitamidohexanamido)-3-methylbutanamido)hexanoic acid compound with 2,2,2-trifluoroacetic acid (1:2)
≥98%
- Product Code: 54093
CAS:
623172-56-5
Molecular Weight: | 839.95 g./mol | Molecular Formula: | C₃₇H₆₇F₆N₅O₉ |
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EC Number: | MDL Number: | MFCD16621111 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of peptide synthesis and biochemical research. Its structure, featuring multiple amino acid residues and a palmitoyl group, makes it valuable for studying lipidated peptides, which are crucial in understanding cell signaling and membrane interactions. It is often employed in the development of peptide-based therapeutics, particularly those targeting intracellular pathways or requiring enhanced cellular uptake due to its lipophilic properties. Additionally, the compound’s trifluoroacetic acid component aids in purification and isolation processes during peptide synthesis, ensuring high purity and stability of the final product. Its applications extend to drug delivery systems, where lipidated peptides can improve bioavailability and targeting efficiency.
Product Specification:
Test | Specification |
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APPEARANCE | White to off-white solid |
PURITY | 98-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,650.00 |
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0.250 | 10-20 days | ฿2,500.00 |
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1.000 | 10-20 days | ฿9,870.00 |
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(S)-6-Amino-2-((S)-2-((S)-6-amino-2-palmitamidohexanamido)-3-methylbutanamido)hexanoic acid compound with 2,2,2-trifluoroacetic acid (1:2)
This compound is primarily utilized in the field of peptide synthesis and biochemical research. Its structure, featuring multiple amino acid residues and a palmitoyl group, makes it valuable for studying lipidated peptides, which are crucial in understanding cell signaling and membrane interactions. It is often employed in the development of peptide-based therapeutics, particularly those targeting intracellular pathways or requiring enhanced cellular uptake due to its lipophilic properties. Additionally, the compound’s trifluoroacetic acid component aids in purification and isolation processes during peptide synthesis, ensuring high purity and stability of the final product. Its applications extend to drug delivery systems, where lipidated peptides can improve bioavailability and targeting efficiency.
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