L-Threonine tert-Butyl Ester Hydrochloride

95%

  • Product Code: 76451
  CAS:    69320-90-7
Molecular Weight: 211.69 g./mol Molecular Formula: C₈H₁₇NO₃HCl
EC Number: MDL Number: MFCD00672361
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, sealed, dry
Product Description: L-Threonine tert-Butyl Ester Hydrochloride is primarily used in the synthesis of peptides and proteins, serving as a protected form of L-threonine. It is particularly valuable in solid-phase peptide synthesis (SPPS), where the tert-butyl group acts as a protective group for the hydroxyl side chain, preventing unwanted reactions during the peptide assembly process. This compound ensures the selective deprotection and coupling of amino acids, enabling the efficient production of complex peptides. Additionally, it is employed in the preparation of modified peptides and peptidomimetics for pharmaceutical research, aiding in the development of therapeutic agents targeting various diseases. Its stability and compatibility with common peptide synthesis protocols make it a reliable reagent in organic and medicinal chemistry.
Product Specification:
Test Specification
APPEARANCE White to Orange to Green powder to crystal
PURITY 94.5-100
SPECIFIC ROTATION A20DC1 CH3OH -13.0--9.0
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿1,160.00
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L-Threonine tert-Butyl Ester Hydrochloride
L-Threonine tert-Butyl Ester Hydrochloride is primarily used in the synthesis of peptides and proteins, serving as a protected form of L-threonine. It is particularly valuable in solid-phase peptide synthesis (SPPS), where the tert-butyl group acts as a protective group for the hydroxyl side chain, preventing unwanted reactions during the peptide assembly process. This compound ensures the selective deprotection and coupling of amino acids, enabling the efficient production of complex peptides. Additionally, it is employed in the preparation of modified peptides and peptidomimetics for pharmaceutical research, aiding in the development of therapeutic agents targeting various diseases. Its stability and compatibility with common peptide synthesis protocols make it a reliable reagent in organic and medicinal chemistry.
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