D-Alanine benzyl ester p-toluenesulfonate salt

98%

  • Product Code: 104915
  Alias:    D-Alanine Benzyl Ester p-Toluenesulfonate
  CAS:    41036-32-2
Molecular Weight: 351.42 g./mol Molecular Formula: C₁₇H₂₁NO₅S
EC Number: 255-185-2 MDL Number: MFCD00039092
Melting Point: 115 °C Boiling Point:
Density: Storage Condition: -20°C
Product Description: D-Alanine benzyl ester p-toluenesulfonate salt is primarily used in peptide synthesis as a protecting group for the carboxyl group of D-alanine. This compound helps in the selective formation of peptide bonds by preventing unwanted reactions at the carboxyl site during the synthesis process. It is particularly valuable in the production of complex peptides and proteins, where precise control over the sequence and structure is essential. Additionally, it finds application in the preparation of chiral compounds and in pharmaceutical research for developing drugs with specific stereochemical properties. Its stability and ease of removal make it a preferred choice in organic synthesis and biochemical studies.
Product Specification:
Test Specification
Melting Point 113-116
Purity (HPLC) 98-100
Specific Rotation 3.5-6.5
Appearance White To Off-White Powder
Infrared Spectrum Conforms To Structure
Solubility In Alcohol Pass
SOLUBILITY IN ALCOHOL PASS
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿560.00
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-
5.000 10-20 days ฿1,060.00
+
-
25.000 10-20 days ฿3,200.00
+
-
D-Alanine benzyl ester p-toluenesulfonate salt
D-Alanine benzyl ester p-toluenesulfonate salt is primarily used in peptide synthesis as a protecting group for the carboxyl group of D-alanine. This compound helps in the selective formation of peptide bonds by preventing unwanted reactions at the carboxyl site during the synthesis process. It is particularly valuable in the production of complex peptides and proteins, where precise control over the sequence and structure is essential. Additionally, it finds application in the preparation of chiral compounds and in pharmaceutical research for developing drugs with specific stereochemical properties. Its stability and ease of removal make it a preferred choice in organic synthesis and biochemical studies.
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