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  • Fmoc-L-Pro-OH
Fmoc-L-Pro-OH

Amino Acids & Derivatives for Peptide Synthesis

Fmoc-L-Pro-OH

Fmoc-L-Pro-OH (CAS No. 71989-31-6) is a widely used derivative of L-proline for Fmoc-based solid-phase peptide synthesis. Its cyclic structure plays a role in inducing turns and rigidity within peptide chains, making it a key component in the development of GLP-1 analogs such as Semaglutide and Tirzepatide. This compound offers high purity and predictable reactivity in automated synthesis workflows.

  • CAS No.: 71989-31-6
  • Molecular Formula: C₂₀H₁₉NO₄
  • Purity: 99% min
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  • Appearance White to off-white crystalline powder
  • Molecular Weight 337.4 g/mol
  • Density 1.3 ± 0.1 g/cm³
  • Boiling Point 548.6 ± 43.0 °C at 760 mmHg
  • Melting Point 112–115 °C
  • Flash Point 285.6 ± 28.2 °C
  • Packaging 25 kg / fibre drum
  • Customs Code 29339980
  • Storage Conditions Keep sealed in a dry place away from heat and light to preserve structural integrity
  • Product Name
    1. Fmoc-Pro-OH;
    2. Fmoc-L-proline;
    3. N-(9-Fluorenylmethoxycarbonyl)-L-proline;
    4. Fmoc-L-Pro-OH;
    5. N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-proline;
    6. L-Proline-N-Fmoc;
    7. (2S)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid
  • Production Capacity 5 ton/month
  • Applications Raw material for GLP-1 peptide synthesis, polypeptides, Semaglutide, and Tirzepatide
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
Boc-His(Trt)-Aib-GIn(Trt)-Gly-OH
Boc-His(Trt)-Aib-GIn(Trt)-Gly-OH CAS No.: N/A
Boc-His(Trt)-Ala-Glu(OtBu)-Gly-OH
Boc-His(Trt)-Ala-Glu(OtBu)-Gly-OH CAS No.: 1418291-58-3
Fmoc-Thr(tBu)-Phe-OH
Fmoc-Thr(tBu)-Phe-OH CAS No.: 1962160-86-6
Fmoc-Gly-Ser[PSI(Me,Me)pro]-OH
Fmoc-Gly-Ser[PSI(Me,Me)pro]-OH CAS No.: 1095952-22-9
Fmoc-Tyr(tBu)-Ser(MeMe)pro-OH
Fmoc-Tyr(tBu)-Ser(MeMe)pro-OH CAS No.: 878797-09-2
Fmoc-N(HMB)-Gly-OH
Fmoc-N(HMB)-Gly-OH CAS No.: 148515-78-0
Fmoc-Ser(tBu)-Ser[Psi(Me,Me)Pro]-OH
Fmoc-Ser(tBu)-Ser[Psi(Me,Me)Pro]-OH CAS No.: 1000164-43-1
H-Gly-Pro-Hyp-OH
H-Gly-Pro-Hyp-OH CAS No.: 2239-67-0
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What are some medical applications of peptide-based drugs?

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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Amino Acids & Derivatives for Peptide Synthesis
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  • General Protected Amino Acids
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