(S)-(-)-1,2,4-Butanetriol
95%
- Product Code: 126480
Alias:
1,2,4-trihydroxybutane, butanetriol
CAS:
42890-76-6
| Molecular Weight: | 106.12 g./mol | Molecular Formula: | HOCH₂CH₂CH(OH)CH₂OH |
|---|---|---|---|
| EC Number: | 221-323-5 | MDL Number: | MFCD00002929 |
| Melting Point: | Boiling Point: | 150 °C0.04 mm Hg(lit.) | |
| Density: | 1.19 g/mL at 25 °C(lit.) | Storage Condition: | Room temperature, dry, sealed |
Product Description:
(S)-(-)-1,2,4-Butanetriol is primarily used as a chiral building block in the synthesis of pharmaceuticals and fine chemicals. Its three hydroxyl groups make it a versatile intermediate for creating complex molecules, particularly in the production of antiviral and anticancer agents. It is also employed in the development of biodegradable polymers and as a precursor for specialty chemicals in the agrochemical industry. Additionally, it finds application in the formulation of personal care products, where it acts as a humectant and moisturizer due to its ability to retain water. Its chiral nature is particularly valuable in asymmetric synthesis, enabling the production of enantiomerically pure compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $18.79 |
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| 5.000 | 10-20 days | $84.07 |
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| 25.000 | 10-20 days | $417.51 |
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| 100.000 | 10-20 days | $1,653.60 |
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(S)-(-)-1,2,4-Butanetriol
(S)-(-)-1,2,4-Butanetriol is primarily used as a chiral building block in the synthesis of pharmaceuticals and fine chemicals. Its three hydroxyl groups make it a versatile intermediate for creating complex molecules, particularly in the production of antiviral and anticancer agents. It is also employed in the development of biodegradable polymers and as a precursor for specialty chemicals in the agrochemical industry. Additionally, it finds application in the formulation of personal care products, where it acts as a humectant and moisturizer due to its ability to retain water. Its chiral nature is particularly valuable in asymmetric synthesis, enabling the production of enantiomerically pure compounds.
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