(S)-3-Amino-1,2-propanediol

98%

Reagent Code: #234215
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CAS Number 61278-21-5

science Other reagents with same CAS 61278-21-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 91.11 g/mol
Formula H₂NCH₂CH(OH)CH₂OH
badge Registry Numbers
MDL Number MFCD00798260
thermostat Physical Properties
Melting Point 54-56°C
Boiling Point 117-119 °C0.4 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.175 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in antiviral and antibacterial agents. Its hydroxyl and amino groups allow for easy modification, making it valuable in creating biologically active molecules. Commonly employed in the preparation of protease inhibitors and nucleoside analogs. Also utilized in the development of enantioselective catalysts and functionalized polymers. Its structural similarity to glycerol enables integration into lipid-like compounds for drug delivery systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿380.00
inventory 5g
10-20 days ฿1,100.00
inventory 25g
10-20 days ฿4,480.00
(S)-3-Amino-1,2-propanediol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in antiviral and antibacterial agents. Its hydroxyl and amino groups allow for easy modification, making it valuable in creating biologically active molecules. Commonly employed in the preparation of protease inhibitors and nucleoside analogs. Also utilized in the development of enantioselective catalysts and functionalized polymers. Its structural similarity to glycerol enables integration into lipid-like compounds for dru

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in antiviral and antibacterial agents. Its hydroxyl and amino groups allow for easy modification, making it valuable in creating biologically active molecules. Commonly employed in the preparation of protease inhibitors and nucleoside analogs. Also utilized in the development of enantioselective catalysts and functionalized polymers. Its structural similarity to glycerol enables integration into lipid-like compounds for drug delivery systems.

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