L-Glutamic acid dimethyl ester hydrochloride
98%
- Product Code: 105387
Alias:
Dimethyl L-glutamate hydrochloride
CAS:
23150-65-4
Molecular Weight: | 211.64 g./mol | Molecular Formula: | C₇H₁₃NO₄HCl |
---|---|---|---|
EC Number: | 245-461-0 | MDL Number: | MFCD00038879 |
Melting Point: | 89-90°C | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
L-Glutamic acid dimethyl ester hydrochloride is widely used in biochemical research as a precursor or intermediate in the synthesis of more complex molecules, particularly peptides and proteins. It plays a role in studying enzyme mechanisms and receptor interactions due to its structural similarity to glutamate, a key neurotransmitter in the central nervous system. This compound is also utilized in the development of prodrugs, where its ester groups can be hydrolyzed to release the active form of the drug. Additionally, it serves as a building block in organic synthesis, contributing to the creation of various bioactive compounds and pharmaceuticals. Its applications extend to neuroscience research, where it helps in understanding glutamate-mediated processes and their implications in neurological disorders.
Product Specification:
Test | Specification |
---|---|
Melting Point | 90-101 |
Purity (%) | 97.5-102.5 |
Specific Rotation [A]20/D(C=5,H2O) | 24-28 |
Appearance | White To Off-White Solid |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | ฿290.00 |
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25.000 | 10-20 days | ฿980.00 |
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100.000 | 10-20 days | ฿2,540.00 |
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500.000 | 10-20 days | ฿12,280.00 |
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L-Glutamic acid dimethyl ester hydrochloride
L-Glutamic acid dimethyl ester hydrochloride is widely used in biochemical research as a precursor or intermediate in the synthesis of more complex molecules, particularly peptides and proteins. It plays a role in studying enzyme mechanisms and receptor interactions due to its structural similarity to glutamate, a key neurotransmitter in the central nervous system. This compound is also utilized in the development of prodrugs, where its ester groups can be hydrolyzed to release the active form of the drug. Additionally, it serves as a building block in organic synthesis, contributing to the creation of various bioactive compounds and pharmaceuticals. Its applications extend to neuroscience research, where it helps in understanding glutamate-mediated processes and their implications in neurological disorders.
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