O-Benzyl-L-serine

99%

  • Product Code: 59235
  Alias:    O-Benzyl-L-serine
  CAS:    4726-96-9
Molecular Weight: 195.22 g./mol Molecular Formula: C₁₀H₁₃NO₃
EC Number: 225-220-6 MDL Number: MFCD00065937
Melting Point: ~227 °C (dec.) Boiling Point: 359℃
Density: 1.217 Storage Condition: room temperature
Product Description: O-Benzyl-L-serine is widely used in the synthesis of peptides and proteins, serving as a protected form of serine. Its benzyl group acts as a protective moiety, preventing unwanted reactions during peptide bond formation. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection is required to build complex peptide structures. It is also employed in the development of pharmaceutical compounds, especially in the creation of serine-based drugs or enzyme inhibitors. Additionally, O-Benzyl-L-serine is utilized in biochemical research to study enzyme mechanisms and protein interactions, owing to its ability to mimic natural serine in controlled environments. Its stability and reactivity make it a key intermediate in organic and medicinal chemistry applications.
Product Specification:
Test Specification
PURITYNONAQUEOUS TIERATION 99 100%
HCL 6.5-8
APPEARANCE White to off-white powder or solid or chunks
INFRARED SPECTROMETRY Conforms to Structure
SOLUBILITY IN HOT WATER almost transparency
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿450.00
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5.000 10-20 days ฿1,460.00
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25.000 10-20 days ฿6,610.00
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O-Benzyl-L-serine
O-Benzyl-L-serine is widely used in the synthesis of peptides and proteins, serving as a protected form of serine. Its benzyl group acts as a protective moiety, preventing unwanted reactions during peptide bond formation. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection is required to build complex peptide structures. It is also employed in the development of pharmaceutical compounds, especially in the creation of serine-based drugs or enzyme inhibitors. Additionally, O-Benzyl-L-serine is utilized in biochemical research to study enzyme mechanisms and protein interactions, owing to its ability to mimic natural serine in controlled environments. Its stability and reactivity make it a key intermediate in organic and medicinal chemistry applications.
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