L-2-Amino-3-guanidinopropionic acid hydrochloride

98%

  • Product Code: 105219
  Alias:    L-3-guanidinoalanine hydrochloride
  CAS:    1482-99-1
Molecular Weight: 182.61 g./mol Molecular Formula: C₄H₁₀N₄O₂HCl
EC Number: 216-044-0 MDL Number: MFCD00036989
Melting Point: ~220 °C (dec.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: L-2-Amino-3-guanidinopropionic acid hydrochloride is primarily used in biochemical research and pharmaceutical development. It serves as a precursor or intermediate in the synthesis of more complex organic compounds, particularly those with potential therapeutic applications. The compound is often utilized in studies related to amino acid metabolism and protein synthesis due to its structural similarity to naturally occurring amino acids. Additionally, it finds application in the development of peptide-based drugs, where it can be incorporated into peptide chains to modify their biological activity or stability. Its guanidinium group also makes it useful in research involving enzyme inhibition and receptor binding studies, as it can interact with various biological targets.
Product Specification:
Test Specification
Purity (Tlc) 98-100
Specific Rotation 16-18
A20D50MGMLWATER
Appearance White To Light Yellow Powder
Infrared Spectrum Conforms To Structure
Solubility In Water Colorless And Transparent Solution
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $80.41
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0.500 10-20 days $281.73
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1.000 10-20 days $480.65
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L-2-Amino-3-guanidinopropionic acid hydrochloride
L-2-Amino-3-guanidinopropionic acid hydrochloride is primarily used in biochemical research and pharmaceutical development. It serves as a precursor or intermediate in the synthesis of more complex organic compounds, particularly those with potential therapeutic applications. The compound is often utilized in studies related to amino acid metabolism and protein synthesis due to its structural similarity to naturally occurring amino acids. Additionally, it finds application in the development of peptide-based drugs, where it can be incorporated into peptide chains to modify their biological activity or stability. Its guanidinium group also makes it useful in research involving enzyme inhibition and receptor binding studies, as it can interact with various biological targets.
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