(R)-2-Methyl-1-phenylpropan-1-amine hydrochloride
≥95%
- Product Code: 113527
CAS:
51600-25-0
| Molecular Weight: | 185.69 g./mol | Molecular Formula: | C₁₀H₁₆ClN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12068520 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily used in the pharmaceutical industry as a chiral building block in the synthesis of various active pharmaceutical ingredients (APIs). Its enantiomeric purity makes it valuable in producing drugs that require specific stereochemistry for efficacy, particularly in central nervous system (CNS) medications. It is also employed in research and development for studying receptor interactions and pharmacological activities due to its structural similarity to certain neurotransmitters. Additionally, it serves as a precursor in the preparation of compounds with potential therapeutic effects, such as stimulants or appetite suppressants. Its applications extend to asymmetric synthesis, where it acts as a chiral auxiliary or resolving agent in organic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £219.38 |
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| 0.250 | 10-20 days | £274.12 |
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| 1.000 | 10-20 days | £701.13 |
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(R)-2-Methyl-1-phenylpropan-1-amine hydrochloride
This compound is primarily used in the pharmaceutical industry as a chiral building block in the synthesis of various active pharmaceutical ingredients (APIs). Its enantiomeric purity makes it valuable in producing drugs that require specific stereochemistry for efficacy, particularly in central nervous system (CNS) medications. It is also employed in research and development for studying receptor interactions and pharmacological activities due to its structural similarity to certain neurotransmitters. Additionally, it serves as a precursor in the preparation of compounds with potential therapeutic effects, such as stimulants or appetite suppressants. Its applications extend to asymmetric synthesis, where it acts as a chiral auxiliary or resolving agent in organic chemistry.
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