D-Valine

98%

  • Product Code: 67175
  Alias:    D-Valine ; D-Isovaleric Acid, D-α-Aminoisovaleric Acid
  CAS:    640-68-6
Molecular Weight: 117.15 g./mol Molecular Formula: C₅H₁₁NO₂
EC Number: 211-368-9 MDL Number: MFCD00064219
Melting Point: >295 °C (subl.)(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: D-Valine is widely used in the pharmaceutical industry as a chiral building block for the synthesis of various drugs and bioactive compounds. It plays a crucial role in the production of antibiotics, such as penicillins and cephalosporins, where it helps enhance their efficacy and stability. Additionally, D-Valine is utilized in the development of peptide-based drugs, contributing to the optimization of their pharmacokinetic properties. In research, it serves as a selective agent in cell culture media to inhibit the growth of fibroblasts, enabling the study of specific cell types like neurons. Its application extends to the field of asymmetric synthesis, where it acts as a chiral auxiliary to produce enantiomerically pure compounds.
Product Specification:
Test Specification
APPEARANCE WHITE CRYSTALS AND/OR CHUNKS OR FLAKES
PURITY 97.5
HCL -30
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days $14.57
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25.000 10-20 days $29.63
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100.000 10-20 days $93.92
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500.000 10-20 days $336.01
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D-Valine
D-Valine is widely used in the pharmaceutical industry as a chiral building block for the synthesis of various drugs and bioactive compounds. It plays a crucial role in the production of antibiotics, such as penicillins and cephalosporins, where it helps enhance their efficacy and stability. Additionally, D-Valine is utilized in the development of peptide-based drugs, contributing to the optimization of their pharmacokinetic properties. In research, it serves as a selective agent in cell culture media to inhibit the growth of fibroblasts, enabling the study of specific cell types like neurons. Its application extends to the field of asymmetric synthesis, where it acts as a chiral auxiliary to produce enantiomerically pure compounds.
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