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  • H-Lys(Boc)-OH
H-Lys(Boc)-OH

Amino Acids & Derivatives for Peptide Synthesis

H-Lys(Boc)-OH

H-Lys(Boc)-OH (CAS No. 2418-95-3) is a mono-protected lysine derivative, where the ε-amino group is blocked with a tert-butyloxycarbonyl (Boc) group. This structure allows selective activation of the α-amino group, making it suitable for applications in fragment coupling, solution-phase peptide synthesis, and protecting group strategies. It’s often used in the preparation of GLP-1 and related peptides when ε-amino reactivity needs to be suppressed.

  • CAS No.: 2418-95-3
  • Molecular Formula: C₁₁H₂₂N₂O₄
  • Purity: 99% min
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  • Appearance White powder
  • Molecular Weight 246.30 g/mol
  • Density 1.1313 (estimated)
  • Boiling Point 389.3 °C (estimated)
  • Melting Point 250 °C (decomposition)
  • Flash Point 203.5 ± 27.3 °C
  • Packaging 25 kg / fibre drum
  • Customs Code 29241990
  • Storage Conditions Store sealed at 2–8 °C, in a dry place protected from moisture
  • Product Name
    1. H-Lys(Boc)-OH;
    2. N₆-(tert-butoxycarbonyl)-L-lysine;
    3. Nepsilon-Boc-L-lysine;
    4. N₆-Boc-L-lysine;
    5. Nepsilon-(tert-Butoxycarbonyl)-L-lysine;
    6. Ne-Boc-L-lysine;
    7. (S)-2-Amino-6-((tert-butoxycarbonyl)amino)hexanoic acid
  • Production Capacity 3 ton/month
  • Applications Raw material for GLP-1 peptide synthesis, polypeptides
Amino Acids & Derivatives for Cell Culture
Amino Acids & Derivatives for Cell Culture
Amino Acids & Derivatives for Cell Culture
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Product Name
CAS No.
  • Fmoc-Arg(pbf)-OH 154445-77-9
  • Fmoc-L-His(Trt)-OH 109425-51-6
  • Fmoc-Gly-OH 29022-11-5
  • Fmoc-L-Glu(OtBu)-OH 71989-18-9
  • Fmoc-L-Thr(tBu)-OH 71989-35-0
  • Fmoc-L-Phe-OH 35661-40-6
  • Fmoc-L-Ser(tBu)-OH 71989-33-8
  • Fmoc-L-Asp(OtBu)-OH 71989-14-5
  • Fmoc-L-Leu-OH 35661-60-0
  • Fmoc-L-Lys(Boc)-OH 71989-26-9
  • Fmoc-L-Gln(Trt)-OH 132327-80-1
  • Fmoc-L-Met-OH 71989-28-1
  • Fmoc-L-Ala-OH 35661-39-3
  • Fmoc-L-Val-OH 68858-20-8
  • Fmoc-L-Ile-OH 71989-23-6
  • Fmoc-Gln-OH 71989-20-3
  • Fmoc-Aib-OH 94744-50-0
  • Fmoc-L-Trp(Boc)-OH 143824-78-6
  • Fmoc-L-Asn(Trt)-OH 132388-59-1
  • Fmoc-L-Pro-OH 71989-31-6
  • Fmoc-L-Cys(Trt)-OH 103213-32-7
  • Fmoc-L-Tyr(tBu)-OH 71989-38-3
  • Boc-L-Lys(Z)-OH 2389-45-9
  • Boc-Lys(Ivdde)-OH 862847-44-7
  • H-Lys(Ivdde)-OH 919281-76-8
  • Fmoc-Lys(Ivdde)-OH 204777-78-6
  • Boc-Lys(dde)-OH 444795-66-8
Product Name
CAS No.
  • Fmoc-Lys(dde)-OH 150629-67-7
  • H-Lys(Boc)-OH 2418-95-3
  • BOC-L-Lysine 13734-28-6
  • Fmoc-Ala-Gly-OH 116747-54-7
  • Boc-Gly-Pro-OH 14296-92-5
  • Fmoc-Val-Gly-OH 142810-19-3
  • Fmoc-Pro-Pro-OH 129223-22-9
  • Fmoc-Glu(OtBu)-Phe-OH 1122076-55-4
  • H-Lys(Z)-OBzL.HCl 6366-70-7
  • Fmoc-D-Arg(Pbf) 187618-60-0
  • H-Gln(Trt)-OH 102747-84-2
  • N₆-Cbz-L-Lysine 1155-64-2
  • H-Ser(tBu)-OH 18822-58-7
  • H-Glu(OtBu)-OH 2419-56-9
  • H-Tyr(tBu)-OH 18822-59-8
  • H-Asp(OtBu)-OH 3057-74-7
  • H-Thr(tBu)-OH 4378-13-6
  • Boc-Glycine 4530-20-5
  • Boc-D-Arg HCl 35897-34-8
  • Boc-D-Arg HCl.H2O 113712-06-4
  • Boc-L-Leu.H2O 131139-15-6
  • Boc-Glycine tert-butyl ester 111652-20-1
  • Z-Gln(Trt)-OH 132388-60-4
  • Boc-beta-Alanine 3303-84-2
  • Boc-L-Pyroglutamic acid ethyl ester/Boc-Pyr-Oet 144978-12-1
  • Boc-L-Pyroglutamic acid methyl ester 108963-96-8
  • Boc-Arg(NO₂)-OH 2188-18-3
Fmoc-L-Lys[Oct-(otBu)-γ-Glu-(otBu)-AEEA-AEEA]-OH
Fmoc-L-Lys[Oct-(otBu)-γ-Glu-(otBu)-AEEA-AEEA]-OH CAS No.: 1662688-20-1
Ste-γ-Glu-AEEA-AEEA-OSU
Ste-γ-Glu-AEEA-AEEA-OSU CAS No.: 1169630-40-3
tBuO-C₁₈-γ-Glu(AEEA-AEEA-OSu)-OtBu
tBuO-C₁₈-γ-Glu(AEEA-AEEA-OSu)-OtBu CAS No.: 166108-71-0
tBuO-Ste-γ-Glu(AEEA-AEEA-OH)-OtBu
tBuO-Ste-γ-Glu(AEEA-AEEA-OH)-OtBu CAS No.: 1118767-16-0
Boc-L-His(Trt)-Aib-OH
Boc-L-His(Trt)-Aib-OH CAS No.: 2061897-68-3
Fmoc-His(Trt)-Aib-OH
Fmoc-His(Trt)-Aib-OH CAS No.: 1446013-13-3
Boc-His(Trt)-Aib-Glu(OtBu)-Gly-OH
Boc-His(Trt)-Aib-Glu(OtBu)-Gly-OH CAS No.: 1890228-73-5
Fmoc-His-Aib-OH TFA
Fmoc-His-Aib-OH TFA CAS No.: 1446013-08-6
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Peptides are used in treating viral infections such as hepatitis, HIV, and SARS. Some can target cancer cells by binding to specific tumor markers or mimicking signaling molecules. Others are derived from natural sources to address cardiovascular conditions, offering a wide range of therapeutic potential.

How do researchers select amino acids when designing peptides?

Longer peptides tend to be more difficult to purify and synthesize due to lower yield and stability. In these cases, auxiliary amino acids may be added at the ends to improve solubility and handling. For shorter peptides, typically under five residues, adding hydrophobic amino acids can enhance structural integrity and functionality.

What role do bioactive peptides play in the food industry?

Bioactive peptides are gaining popularity in functional food and nutrition sectors. These peptides can help regulate physiological processes, support immune health, and delay the onset of chronic diseases. Common sources include dairy proteins, plant extracts, collagen, and marine or animal-derived peptides.

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