N-Methyl-4-(dimethylamino)benzylamine Hydrochloride
≥97%
- Product Code: 69651
CAS:
1158441-78-1
| Molecular Weight: | 200.71 g./mol | Molecular Formula: | C₁₀H₁₇ClN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07106762 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceuticals and specialty chemicals. Its structure, featuring both amine and aromatic groups, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological and psychiatric disorders. Additionally, it serves as a reagent in the synthesis of dyes and pigments due to its ability to form stable intermediates. In research settings, it is employed in the study of amine chemistry and as a building block for designing novel compounds with potential therapeutic applications. Its hydrochloride form enhances solubility, facilitating its use in aqueous reaction environments.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to brown solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿4,200.00 |
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| 5.000 | 10-20 days | ฿12,290.00 |
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N-Methyl-4-(dimethylamino)benzylamine Hydrochloride
This compound is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceuticals and specialty chemicals. Its structure, featuring both amine and aromatic groups, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting neurological and psychiatric disorders. Additionally, it serves as a reagent in the synthesis of dyes and pigments due to its ability to form stable intermediates. In research settings, it is employed in the study of amine chemistry and as a building block for designing novel compounds with potential therapeutic applications. Its hydrochloride form enhances solubility, facilitating its use in aqueous reaction environments.
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