Diacetone-D-galactose
97%
- Product Code: 98129
Alias:
Diacetone-D-Galactose
CAS:
4064-06-6
Molecular Weight: | 260.28 g./mol | Molecular Formula: | C₁₂H₂₀O₆ |
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EC Number: | 223-771-7 | MDL Number: | MFCD00063225 |
Melting Point: | 120-122 °C | Boiling Point: | 117 °C0.015 mm Hg(lit.) |
Density: | 1.143 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
Diacetone-D-galactose is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the production of various galactose derivatives, which are essential in biochemical research and pharmaceutical development. This compound is particularly valuable in the preparation of glycosides, oligosaccharides, and other bioactive molecules that play a role in cell signaling and immune response modulation. Additionally, it is utilized in the study of enzyme mechanisms and carbohydrate metabolism, aiding in the understanding of diseases related to glycosylation disorders. Its stability and reactivity make it a preferred choice for controlled glycosylation reactions in organic synthesis.
Product Specification:
Test | Specification |
---|---|
PURITYGC | 97-100 |
APPEARANCE | Colorless to yellow liquid |
INFRARED SPECTRUM | Conforms to Structure |
REFRACTIVE INDEX N20D | 1.467-1.469 |
SPECIFIC ROTATION A20DC3CHCL3 | -60 -56 |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿940.00 |
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5.000 | 10-20 days | ฿3,960.00 |
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25.000 | 10-20 days | ฿15,520.00 |
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Diacetone-D-galactose
Diacetone-D-galactose is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the production of various galactose derivatives, which are essential in biochemical research and pharmaceutical development. This compound is particularly valuable in the preparation of glycosides, oligosaccharides, and other bioactive molecules that play a role in cell signaling and immune response modulation. Additionally, it is utilized in the study of enzyme mechanisms and carbohydrate metabolism, aiding in the understanding of diseases related to glycosylation disorders. Its stability and reactivity make it a preferred choice for controlled glycosylation reactions in organic synthesis.
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