L-tyrosine-2,3,5,6-D4
≥98 atom % D, ≥99% (Pharmaceutical Grade)
- Product Code: 92495
CAS:
62595-14-6
Molecular Weight: | 185.21 g./mol | Molecular Formula: | C₉H₇D₄NO₃ |
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EC Number: | MDL Number: | MFCD00079605 | |
Melting Point: | >300°C (lit.) | Boiling Point: | |
Density: | Storage Condition: | 2-8°C |
Product Description:
L-tyrosine-2,3,5,6-D4 is widely used as a stable isotope-labeled compound in biomedical research. It serves as an internal standard in mass spectrometry and nuclear magnetic resonance (NMR) studies, enabling precise quantification and tracing of tyrosine metabolism in biological systems. This compound is particularly valuable in metabolic pathway analysis, helping researchers understand the role of tyrosine in protein synthesis, neurotransmitter production, and hormone regulation. Additionally, it is employed in pharmacokinetic studies to track the absorption, distribution, metabolism, and excretion of tyrosine and its derivatives in vivo. Its deuterium labeling ensures minimal interference with natural biochemical processes, making it a reliable tool for advanced scientific investigations.
Product Specification:
Test | Specification |
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APPEARANCE | solid |
PURITY | 98.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿26,790.00 |
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L-tyrosine-2,3,5,6-D4
L-tyrosine-2,3,5,6-D4 is widely used as a stable isotope-labeled compound in biomedical research. It serves as an internal standard in mass spectrometry and nuclear magnetic resonance (NMR) studies, enabling precise quantification and tracing of tyrosine metabolism in biological systems. This compound is particularly valuable in metabolic pathway analysis, helping researchers understand the role of tyrosine in protein synthesis, neurotransmitter production, and hormone regulation. Additionally, it is employed in pharmacokinetic studies to track the absorption, distribution, metabolism, and excretion of tyrosine and its derivatives in vivo. Its deuterium labeling ensures minimal interference with natural biochemical processes, making it a reliable tool for advanced scientific investigations.
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