2-(3-(Benzyloxy)propyl)propane-1,3-diol

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Reagent Code: #152346
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CAS Number 132970-27-5

science Other reagents with same CAS 132970-27-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.30 g/mol
Formula C₁₃H₂₀O₃
badge Registry Numbers
MDL Number MFCD31635054
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized polymers. Its hydroxyl groups allow for easy modification, making it suitable for crosslinking agents or building blocks in specialty chemicals. Commonly employed in the development of surfactants and emulsifiers due to its amphiphilic structure. Also finds use in the synthesis of prodrugs where controlled release is required, leveraging the benzyl-protected alcohol group that can be deprotected under mild conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,080.00
inventory 250mg
10-20 days ฿1,670.00
inventory 1g
10-20 days ฿4,320.00
inventory 5g
10-20 days ฿15,300.00
inventory 25g
10-20 days ฿55,800.00
inventory 100g
10-20 days ฿156,240.00

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2-(3-(Benzyloxy)propyl)propane-1,3-diol
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized polymers. Its hydroxyl groups allow for easy modification, making it suitable for crosslinking agents or building blocks in specialty chemicals. Commonly employed in the development of surfactants and emulsifiers due to its amphiphilic structure. Also finds use in the synthesis of prodrugs where controlled release is required, leveraging the benzyl-protected alcohol group that can be deprotect
Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and functionalized polymers. Its hydroxyl groups allow for easy modification, making it suitable for crosslinking agents or building blocks in specialty chemicals. Commonly employed in the development of surfactants and emulsifiers due to its amphiphilic structure. Also finds use in the synthesis of prodrugs where controlled release is required, leveraging the benzyl-protected alcohol group that can be deprotected under mild conditions.
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