(2R,3S,4R,5S)-2,3,4,5,6-pentahydroxyhexanal

95%

Reagent Code: #123615
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CAS Number 5934-56-5

science Other reagents with same CAS 5934-56-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.16 g/mol
Formula C₆H₁₂O₆
badge Registry Numbers
MDL Number MFCD00069825
thermostat Physical Properties
Boiling Point 527.1±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.581±0.06 g/cm3(Predicted)
Storage room temperature, dry

description Product Description

This L-aldose compound is primarily utilized in biochemical research and pharmaceutical development due to its unique stereochemistry, serving as a valuable intermediate for stereospecific syntheses. It is employed in the creation of complex carbohydrates, glycoconjugates, and enantiomerically pure compounds essential for studying cell signaling, immune responses, and chiral interactions. As a non-metabolizable sugar in humans, it shows promise as a precursor in the production of certain antibiotics and antiviral agents. In the food industry, its sugar-like properties are leveraged as a potential low-calorie sweetener that does not impact blood glucose levels, suitable for diabetic and weight management applications. Furthermore, it functions as a humectant in cosmetics and personal care products to retain moisture, with ongoing studies exploring its antioxidant potential.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿52,398.00
inventory 100mg
10-20 days ฿41,400.00

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(2R,3S,4R,5S)-2,3,4,5,6-pentahydroxyhexanal
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This L-aldose compound is primarily utilized in biochemical research and pharmaceutical development due to its unique stereochemistry, serving as a valuable intermediate for stereospecific syntheses. It is employed in the creation of complex carbohydrates, glycoconjugates, and enantiomerically pure compounds essential for studying cell signaling, immune responses, and chiral interactions. As a non-metabolizable sugar in humans, it shows promise as a precursor in the production of certain antibiotics and

This L-aldose compound is primarily utilized in biochemical research and pharmaceutical development due to its unique stereochemistry, serving as a valuable intermediate for stereospecific syntheses. It is employed in the creation of complex carbohydrates, glycoconjugates, and enantiomerically pure compounds essential for studying cell signaling, immune responses, and chiral interactions. As a non-metabolizable sugar in humans, it shows promise as a precursor in the production of certain antibiotics and antiviral agents. In the food industry, its sugar-like properties are leveraged as a potential low-calorie sweetener that does not impact blood glucose levels, suitable for diabetic and weight management applications. Furthermore, it functions as a humectant in cosmetics and personal care products to retain moisture, with ongoing studies exploring its antioxidant potential.

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