Allyl α-D-mannopyranoside
Allyl α-D-mannopyranoside (CAS: 41308-76-3; Formula: C9H16O6) is a carbohydrate derivative with a molecular weight of 220.22 g/mol. This compound serves as a valuable building block in organic synthesis and carbohydrate chemistry. It is typically employed in research and development settings for the creation of more complex molecules and for investigating glycosidic linkages and carbohydrate-based structures. Its primary applications lie within chemical synthesis and related biochemical research.
- IUPAC
- 2-Propenyl α-D-mannopyranoside
- Synonyms
- 2-Propenyl α-D-mannopyranoside

Chemical Synthesis
Allyl α-D-mannopyranoside is utilised as a precursor or intermediate in the synthesis of various organic compounds. Its functional groups allow for diverse chemical transformations, making it a useful reagent for constructing complex molecular architectures.
Carbohydrate Chemistry
This compound is employed in studies focused on carbohydrate structure, function, and modification. It aids researchers in understanding glycosylation processes and developing novel carbohydrate-based materials or drugs.
Biochemical Research
Allyl α-D-mannopyranoside can be used in biochemical investigations, particularly in areas concerning glyco-conjugates and enzyme activity related to mannose residues. It assists in probing biological pathways involving carbohydrates.
| Molecular weight | 220.22 |
|---|---|
| Empirical formula | C9H16O6 |
| Assay | 95% |
| Storage temperature | 2-8°C |
| Melting point | 94-100 °C |
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Allyl α-D-mannopyranoside used for?
+
Allyl α-D-mannopyranoside is used in chemical synthesis, carbohydrate chemistry, and biochemical research as a building block for more complex molecules and for studying glycosidic linkages.
What are the CAS number and formula for Allyl α-D-mannopyranoside?
+
The CAS number for Allyl α-D-mannopyranoside is 41308-76-3, and its empirical formula is C9H16O6.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Allyl α-D-mannopyranoside with an assay of 95%. This product is suitable for research and laboratory use. TSS does not represent this product as USP, BP, or EP grade.
How should Allyl α-D-mannopyranoside be handled and stored?
+
Allyl α-D-mannopyranoside is classified under Water Hazard Class 3 (WGK 3) in Germany, indicating it is hazardous to water. It should be stored at refrigerated temperatures between 2-8°C.
Is Allyl α-D-mannopyranoside a controlled substance?
+
The provided data does not indicate that Allyl α-D-mannopyranoside is a controlled substance.
How can I request a sample or quote for Allyl α-D-mannopyranoside?
+
To request a sample or quote for Allyl α-D-mannopyranoside, please contact our sales department through the website or via the provided contact details.
How is Allyl α-D-mannopyranoside packed, shipped, and exported?
+
Allyl α-D-mannopyranoside is carefully packaged to ensure stability during transport and is available for export globally by Tech Serve Solutions, adhering to all relevant shipping regulations.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis