D(-)Arabinose

98%

Reagent Code: #98018
label
Alias D-(-)-Arabinose; D-(-)-Arabinose, D(-)Arabinose
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CAS Number 10323-20-3

science Other reagents with same CAS 10323-20-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.13 g/mol
Formula C₅H₁₀O₅
badge Registry Numbers
EC Number 233-708-5
MDL Number MFCD00064361
thermostat Physical Properties
Melting Point 156-160 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used in the production of antiviral drugs, particularly in the synthesis of nucleoside analogs such as vidarabine that combat viral infections. It serves as a chiral building block in organic synthesis, enabling the creation of complex molecules with specific stereochemistry. It is employed in microbiological research as a carbon source for studying bacterial metabolism and growth, often in selective media. Its role in the development of diagnostic reagents and biochemical assays is also notable.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white powder
Purity 97.5-100
Solubility in Water Colorless to faint yellow clear, 50 mg/mL H2O
Specific Rotation (20°C, D-line, c=10, H₂O) -106
Melting Point 150-165

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿620.00
inventory 25g
10-20 days ฿980.00
inventory 100g
10-20 days ฿2,480.00
inventory 500g
10-20 days ฿10,560.00
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D(-)Arabinose
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Used in the production of antiviral drugs, particularly in the synthesis of nucleoside analogs such as vidarabine that combat viral infections. It serves as a chiral building block in organic synthesis, enabling the creation of complex molecules with specific stereochemistry. It is employed in microbiological research as a carbon source for studying bacterial metabolism and growth, often in selective media. Its role in the development of diagnostic reagents and biochemical assays is also notable.

Used in the production of antiviral drugs, particularly in the synthesis of nucleoside analogs such as vidarabine that combat viral infections. It serves as a chiral building block in organic synthesis, enabling the creation of complex molecules with specific stereochemistry. It is employed in microbiological research as a carbon source for studying bacterial metabolism and growth, often in selective media. Its role in the development of diagnostic reagents and biochemical assays is also notable.

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