Boc-L-Leucine丨CAS 13139-15-6

Boc-L-Leucine丨CAS 13139-15-6
Product Introduction:
Catalog No.: SS122619
CAS No.: 13139-15-6
Purity (HPLC): 98% min
Product Name: Boc-L-Leucine
Molecular Formula: C11H21NO4
Molecular Weight: 231.29
Synonym(s): N-tert-Butoxycarbonyl-L-leucine; Boc-L-Leu-OH
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of boc-l-leucine丨cas 13139-15-6 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications

 

Appearance: White to off-white powder
Purity (HPLC): 98% min
Solubility: 1 mmol should be clear and transparent after dissolution in 5 mL DMF
IR: Consistent with structure
Water (KF): 8.0% max
Specific rotation: -26° to -22° (c=2, in AcOH)

 

Transport Information

 

Parameter

Specification

UN Number

 

Class

 

Packing Group

 

H.S. Code

2924199090305

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

Sealed in dry, 2-8°C

Condition to Avoid

 

Package

 

 

Manufacturing Information

 

Parameter

Specification

Capacity

1MT/month

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

Production since 2015

Stock

 

 

 

 

Applications

 

1. Peptide Synthesis

Boc-L-Leucine is a fundamental protected amino acid used in the assembly of peptides and proteins.

The Boc group protects the amino group, preventing undesired side reactions during coupling steps.

Used in Boc-based peptide synthesis strategies, often in solution-phase or solid-phase protocols.

2. Organic Synthesis

Acts as a chiral building block or intermediate in the synthesis of chiral auxiliaries, catalysts, or bioactive molecules.

Employed in the preparation of non-natural amino acids or derivatives with modified properties.

3. Pharmaceutical Research

Used in the development of peptide-based drugs, enzyme inhibitors, and ligands.

Helps explore structure-activity relationships (SAR) in medicinal chemistry.

 

Benefits

✅ Protection of Amino Group

The Boc group is stable under neutral and basic conditions but can be selectively removed under acidic conditions (e.g., trifluoroacetic acid), facilitating stepwise synthesis.

✅ Chiral Purity

Derived from natural L-leucine, ensuring correct stereochemistry in peptide chains.

✅ Commercial Availability

Available in high purity and bulk quantities for both research and industrial peptide synthesis.

✅ Compatibility

Compatible with a wide range of coupling reagents and deprotection protocols.

 

Conclusion

 

Boc-L-Leucine (CAS 13139-15-6) is an indispensable reagent in peptide synthesis and organic chemistry, providing amino group protection with a readily removable Boc group. Its use allows for precise and efficient construction of peptides and complex bioactive molecules, making it a staple in synthetic and medicinal chemistry laboratories.

 

 

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