Taiy Chemical
1-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-proline
Product Name Fmoc-Pro-OH
Synonyms:103668 1,2-pyrrolidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) ester; 1-[(9H-Fluoren-9-ylmethoxy)carbonyl]proline; 1-[(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid; 1-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-proline; (2S)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylate; Fmoc-L-Proline; Fmoc-L-Pro-OH
CAS RN. 71989-31-6
EINECS 276-259-0
Molecular Weight 336.3618
Molecular Formula C20H18NO4
Melting Point(℃) 112-115℃
Boiling Point(℃) 548.6°C at 760 mmHg
Flash Point(℃) 285.6°C
Hazard Symbols Xi Details
Xi
Risk Codes  R36/37/38;    Details
 R36/37/38;     Details
Safety Description  S26;S36;Details
 S26;S36; Details
FAQ
What is 1-(9H-fluoren-9-ylmethoxy)carbonyl-L-proline (FLP)?

1-(9H-fluoren-9-ylmethoxy)carbonyl-L-proline, or FLP, is a solid phase organic reagent commonly used in peptide synthesis. It is often used as a protecting group for the carboxyl functional group of amino acids.

How is FLP used in peptide synthesis?

FLP is typically used as a protecting group for the carboxyl functional group of amino acids during peptide synthesis. By temporarily masking this reactive group, FLP ensures that unwanted side reactions do not occur during peptide bond formation. After the desired peptide sequence has been assembled, the FLP protecting group can be easily removed to reveal the free carboxyl group.

What are the advantages of using FLP in peptide synthesis?

One of the main advantages of using FLP in peptide synthesis is its stability and ease of removal. FLP can be easily cleaved under mild conditions, allowing for efficient deprotection of the carboxyl group without affecting the rest of the peptide sequence. Additionally, FLP is compatible with a wide range of protecting groups commonly used in peptide synthesis, making it a versatile reagent in peptide chemistry.

Are there any specific considerations to keep in mind when using FLP in peptide synthesis?

While FLP is a highly effective protecting group in peptide synthesis, it is important to ensure that the deprotection conditions are carefully optimized to prevent any unwanted side reactions. Additionally, it is recommended to perform a thorough purification of the final peptide product to remove any remaining traces of FLP or other byproducts. Overall, proper handling and usage of FLP can lead to high yields and purity in peptide synthesis.

How can one purchase FLP for peptide synthesis?

FLP can be purchased from various chemical suppliers specializing in reagents for peptide synthesis. It is important to ensure that the FLP reagent is of high quality and purity to achieve optimal results in peptide synthesis. Customers can inquire with their preferred chemical supplier or distributor for availability and pricing of FLP for their specific needs.
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