DL-1-Amino-2-propanol

>99.0%(GC)

Reagent Code: #169149
label
Alias (±)-1-amino-2-propanol, (±)-isopropanolamine, DL-1-amino-2-propanol, DL-isopropanolamine, 1-amino-2-propanol
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CAS Number 78-96-6

science Other reagents with same CAS 78-96-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 75.11 g/mol
Formula C₃H₉NO
badge Registry Numbers
EC Number 201-162-7
MDL Number MFCD00008139
inventory_2 Storage & Handling
Density 0.973 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antibiotics and antiviral agents. Serves as a building block in chiral synthesis due to its functional groups. Employed in the preparation of agrochemicals and fine chemicals. Also utilized in the formulation of surfactants and emulsifiers for industrial applications. Its amino alcohol structure makes it suitable for catalysis and ligand design in asymmetric reactions.

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Size Availability Unit Price Quantity
inventory 100ml
10-20 days ฿460.00
inventory 500ml
10-20 days ฿990.00
inventory 2.5L
10-20 days ฿3,980.00
inventory 12X500ml
10-20 days ฿11,650.00

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DL-1-Amino-2-propanol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antibiotics and antiviral agents. Serves as a building block in chiral synthesis due to its functional groups. Employed in the preparation of agrochemicals and fine chemicals. Also utilized in the formulation of surfactants and emulsifiers for industrial applications. Its amino alcohol structure makes it suitable for catalysis and ligand design in asymmetric reactions.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antibiotics and antiviral agents. Serves as a building block in chiral synthesis due to its functional groups. Employed in the preparation of agrochemicals and fine chemicals. Also utilized in the formulation of surfactants and emulsifiers for industrial applications. Its amino alcohol structure makes it suitable for catalysis and ligand design in asymmetric reactions.

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