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Home ProductsBOC-Amino Acids

Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0

Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0

Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0
Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0

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Product Details:
Place of Origin: CHINA
Brand Name: Enlai Biotech
Certification: ISO 9001 COA HPLC NMR
Payment & Shipping Terms:
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Inside: double PE bag Outside: paper drum
Delivery Time: In Stock
Payment Terms: T/T
Supply Ability: 100 kilograms per month
Detailed Product Description
Product Name: Boc-Ala-Pro-OH CAS No: 33300-72-0
M.W: 286.32 Appearance: White Powder
HPLC: 99+ Storage: Room Temp
Highlight:

Boc-Ala-Pro-OH

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Boc-Ala-Pro-OH CAS NO. 33300-72-0

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Tirzepatide Intermediate Boc-Ala-Pro-OH

 

Product Description

 

Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0

 

NameBoc-Ala-Pro-OH

CAS NO: 33300-72-0

M.W: 286.32

Appearance: White Powder

Purity: 99+   

Synonyms: BOC-ALA-PRO-OH

 

Application

 

As a Synthetic Intermediate in Peptide Synthesis: BOC-ALA-GLY-PRO-OH serves as an intermediate in the synthesis of more complex peptides. By incorporating this fragment, researchers can streamline the synthesis process, improve efficiency, and potentially reduce costs. It allows for the formation of longer peptide chains through coupling reactions with other amino acid fragments.

 

Role of the BOC Protecting Group: The BOC group acts as a protecting group for the amino functionality of alanine, ensuring that it remains unreactive during synthetic steps where other functionalities are being manipulated. This allows for controlled and sequential addition of amino acids during peptide synthesis.

 

Solid-Phase Peptide Synthesis (SPPS): BOC-ALA-GLY-PRO-OH can be utilized in solid-phase peptide synthesis, where it is attached to a solid support via its carboxyl group. This attachment facilitates the sequential addition of amino acids, forming the desired peptide sequence step-by-step. The BOC group is typically removed under acidic conditions, such as with trifluoroacetic acid (TFA), to expose the free amino group for further coupling reactions.

 

Drug Discovery and Development: In the realm of drug discovery, BOC-ALA-GLY-PRO-OH may serve as a building block for the synthesis of peptide-based drugs. By modifying this fragment with additional functional groups or incorporating it into larger peptide structures, researchers can create novel compounds with specific biological activities. These compounds may have therapeutic potential in treating various diseases, including but not limited to cancer, infectious diseases, and metabolic disorders.

 

Package

 

 Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0 0     Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0 1 

Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0 2Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0 3

Transportation

 

Small package(1g, 25g, 1Kg, 25Kg) can be shipped by Express. (DHL, FedEx, EMS, etc.)
Large package(100kg and more than100Kg) can be transported by Air or Sea.

All transportation is in accordance with the customer's needs.

 

Company Profile

 

Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0 4Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0 5

Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0 6Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0 7

Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0 8Tirzepatide Intermediate Boc-Ala-Pro-OH CAS NO. 33300-72-0 9

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