L-2,4-Diaminobutyric acid hydrochloride

98%

  • Product Code: 105210
  Alias:    L-2,4-diaminobutyric acid dihydrochloride
  CAS:    1883-09-6
Molecular Weight: 191.06 g./mol Molecular Formula: C₄H₁₀N₂O₂₂HCl
EC Number: 217-542-0 MDL Number: MFCD00064561
Melting Point: 197-200 °C (dec.) Boiling Point:
Density: Storage Condition: Room temperature, dry, sealed
Product Description: L-2,4-Diaminobutyric acid hydrochloride is primarily used in biochemical research and pharmaceutical development. It serves as a precursor or intermediate in the synthesis of various biologically active compounds, including peptides and amino acid derivatives. Its role in studying metabolic pathways, particularly those involving amino acid metabolism, is significant. Additionally, it is utilized in the development of drugs targeting specific enzymes or receptors due to its structural similarity to naturally occurring amino acids. In some cases, it is also employed in the preparation of chiral catalysts for asymmetric synthesis, enhancing the efficiency and selectivity of chemical reactions.
Product Specification:
Test Specification
Purity (HPLC) 98-100
Purity (Titration With AgNO3) 97.5-102.5
Specific Rotation [A]20/D(C=3.6, H2O) 13-16
Sulfated Ash 0-0.1
Water By Karl Fischer 0-2.5
Appearance White To Off-White To Light Yellow Powder Or Crystals
Infrared Spectrum Conforms To Structure
Solubility In Water Very Faint Turbidity
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $21.13
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5.000 10-20 days $88.76
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25.000 10-20 days $386.04
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L-2,4-Diaminobutyric acid hydrochloride
L-2,4-Diaminobutyric acid hydrochloride is primarily used in biochemical research and pharmaceutical development. It serves as a precursor or intermediate in the synthesis of various biologically active compounds, including peptides and amino acid derivatives. Its role in studying metabolic pathways, particularly those involving amino acid metabolism, is significant. Additionally, it is utilized in the development of drugs targeting specific enzymes or receptors due to its structural similarity to naturally occurring amino acids. In some cases, it is also employed in the preparation of chiral catalysts for asymmetric synthesis, enhancing the efficiency and selectivity of chemical reactions.
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