2-Methyl-2-thiopropylamine Hydrochloride
98%
- Product Code: 39909
Alias:
Dimethylcysteine hydrochloride; Dimethylcysteine hydrochloride; Dimethylcysteine hydrochloride;
CAS:
32047-53-3
Molecular Weight: | 141.66 g./mol | Molecular Formula: | C₄H₁₂ClNS |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 146.2ºC | |
Density: | 0.936 g/cm3 | Storage Condition: | 2-8℃, inert gas environment |
Product Description:
Used primarily in the synthesis of pharmaceuticals, this compound acts as a key intermediate in the production of various drugs. It is particularly valuable in the development of compounds targeting neurological disorders, where its structure facilitates the creation of molecules that interact with specific brain receptors. Additionally, it is employed in organic synthesis to introduce thioether functional groups, which are crucial in the design of molecules with enhanced biological activity. Its role in medicinal chemistry also extends to the creation of prodrugs, improving the bioavailability and stability of active pharmaceutical ingredients.
Product Specification:
Test | Specification |
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APPEARANCE | Light-green to Yellow to Brown Sticky Oil to Solid |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | £45.23 |
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1.000 | 10-20 days | £112.18 |
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5.000 | 10-20 days | £291.76 |
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25.000 | 10-20 days | £456.64 |
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2-Methyl-2-thiopropylamine Hydrochloride
Used primarily in the synthesis of pharmaceuticals, this compound acts as a key intermediate in the production of various drugs. It is particularly valuable in the development of compounds targeting neurological disorders, where its structure facilitates the creation of molecules that interact with specific brain receptors. Additionally, it is employed in organic synthesis to introduce thioether functional groups, which are crucial in the design of molecules with enhanced biological activity. Its role in medicinal chemistry also extends to the creation of prodrugs, improving the bioavailability and stability of active pharmaceutical ingredients.
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