TSTU丨CAS 105832-38-0

TSTU丨CAS 105832-38-0
Product Introduction:
Catalog No.: SS119047
CAS No.: 105832-38-0
Purity(HPLC): 99% min.
Product Name: TSTU
Molecular Formula: C9H16BF4N3O3
Molecular Weight: 301.05
Synonym(s): O-(N-Succinimidyl)-1,1,3,3-tetramethyluronium tetrafluoroborate
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of tstu丨cas 105832-38-0 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 crystalline powder
Purity (HPLC) 99% min
Melting point 196.0 - 205.0 ℃
Clarity Clear and Transparent (1g in 10ml acetonitrile)
Loss on drying 0.5% max

 

Transport Information

 

Parameter

Specification

UN Number

 

Class

 

Packing Group

 

H.S. Code

2928000090309

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature: 2-8℃

Condition to Avoid

 

Package

25kg/drum

 

Manufacturing Information

 

Parameter

Specification

Capacity

50MT/month

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

Production since 2010

Stock

 

 

 

 

Applications

 

TSTU (N,N,N′,N′-Tetramethyl-O-(N-succinimidyl)uronium tetrafluoroborate, CAS 105832-38-0) is a highly efficient coupling reagent widely used in peptide synthesis and organic chemistry. Its primary applications include activating carboxylic acids for amide bond formation, facilitating the synthesis of peptides, proteins, and other amide-containing compounds. TSTU is particularly valued in solid-phase peptide synthesis (SPPS) and solution-phase coupling reactions, where it enables rapid and high-yielding formation of peptide bonds with minimal racemization. Additionally, it is used in the preparation of pharmaceutical intermediates and other bioactive molecules requiring precise amide linkage formation.

 

Benefits

 

The benefits of TSTU stem from its high reactivity, stability, and efficiency. It provides fast and clean activation of carboxyl groups, improving coupling efficiency and reducing by-product formation. Compared to traditional carbodiimide reagents, TSTU minimizes racemization and allows milder reaction conditions, protecting sensitive functional groups. Its solubility in common organic solvents and compatibility with a wide range of amino acids and nucleophiles make it a versatile and reliable reagent for both laboratory-scale and industrial peptide synthesis.

 

Conclusion

 

In conclusion, TSTU is a powerful and versatile coupling reagent essential for peptide synthesis and amide bond formation. Its high reactivity, low racemization risk, and compatibility with diverse substrates make it indispensable in pharmaceutical, biochemical, and organic synthesis. By enabling efficient and high-fidelity peptide and amide formation, TSTU plays a critical role in modern chemical and medicinal research.

 

 

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