Home » Products » Pharmaceuticals » Pharmaceutical Intermediates » 3,4-O-ISOPROPYLIDENE-D-MANNITOL
Purity:98%
Appearance: White or yellowish-white Crystalline powder
| Product name | 3,4-O-ISOPROPYLIDENE-D-MANNITOL |
| Synonym |
(1R,1’R)-1,1′-((4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-diyl)bis(ethane-1,2-diol);3,4-ISOPROPYLIDENE-D-MANNITOL;3,4-Isopropylidene-D-mannitol,98%;3,4-O-ISOPROChemicalbookPYLIDENE-D-MANNITOL;3,4-O-Isopropylidene-D-mannitol,98%;3,4-O-Isopropylidene-D-maitol;D-Mannitol,3,4-O-(1-Methylethylidene)-;3,4-O-Isopropylidene-D-mannitol |
| CAS NO. | 3969-84-4 |
| Appearance | White or yellowish-white Crystalline powder |
| Purity | 98% |
| MF | C9H18O6 |
| MW | 222.24 |
| Related categories | Pharmaceutical Intermediates |
| Storage | Keep in dark place,sealed in dry,room temperature |
| Transport Information | Non-dangerous goods |
| HS Code(in China) | 2905430000 |
| Contact information | Name:Echo Liu E-mail:echo@coreychem.com |
3,4-O-Isopropylidene-D-Mannitol is a chemically protected derivative of D-mannitol that provides stability and selectivity in complex chemical reactions. This crystalline sugar derivative is widely used in organic synthesis, carbohydrate chemistry, and pharmaceutical research. Its unique structure protects the hydroxyl groups at the 3,4-position, allowing chemists to carry out precise and controlled chemical transformations while preventing unwanted side reactions.
🧪 Applications in Research & Synthesis
Organic Synthesis: Acts as a crucial building block for the preparation of glycosides, sugar derivatives, and other bioactive molecules. Its protective group allows selective reactions on other parts of the molecule without compromising the sugar backbone.
Pharmaceutical Intermediates: Used extensively in the preparation of stereochemically defined drug precursors. It ensures that sensitive functional groups remain intact during multi-step synthesis, improving yield and reaction predictability.
Laboratory Research: Serves as a protected sugar in multi-step syntheses, enabling selective reactions that are essential for complex carbohydrate chemistry. It also facilitates the study of sugar-based enzymatic reactions and mechanistic investigations.
Carbohydrate Derivative Studies: This compound is often used in research focused on novel sugar-based materials, polymers, and glyco-conjugates. Its structural stability provides a reliable platform for experimentation.
🌟 Advantages & Properties
Stable crystalline form ensures easy handling, weighing, and storage over extended periods.
Protects hydroxyl groups for selective reactions at other positions, increasing synthetic flexibility.
Compatible with a wide range of organic reactions, including acylation, oxidation, substitution, and cyclization.
Supports medicinal chemistry, carbohydrate research, and synthetic organic chemistry due to its versatility.
Non-volatile, odorless, and thermally stable, making it ideal for laboratory and industrial environments.
⚠️ Storage & Handling
Store in airtight containers in a cool, dry place away from moisture and direct sunlight.
Follow standard laboratory safety precautions, including gloves, goggles, and lab coats.
Avoid prolonged exposure to heat or incompatible chemicals to maintain compound integrity.
💡 Summary
It is a highly versatile sugar derivative that enables chemists to perform precise and selective chemical transformations. Its protective properties make it an essential intermediate in pharmaceutical research, carbohydrate chemistry, and advanced synthetic applications. The combination of stability, selectivity, and chemical compatibility ensures that it remains a cornerstone reagent for synthetic and medicinal chemists seeking reliable and efficient outcomes.
●Product Manager Email: Echo@coreychem.com
Packaging:
Sample: 10g/bottle
Bulk: 250g/bag
Customized packaging available upon request.