(S)-()-2-Amino-1-butanol

98%

Reagent Code: #234216
label
Alias (S)-(+)-2-amino-1-butanol
fingerprint
CAS Number 5856-62-2

science Other reagents with same CAS 5856-62-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 89.14 g/mol
Formula C₄H₁₁NO
badge Registry Numbers
EC Number 227-475-9
MDL Number MFCD00064418
thermostat Physical Properties
Melting Point -2 °C(lit.)
Boiling Point 179-183 °C(lit.)
inventory_2 Storage & Handling
Density 0.944 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 the production of antibiotics and antiviral agents. Its stereochemistry makes it valuable in asymmetric synthesis for creating enantiomerically pure compounds. Also employed in the development of catalysts and ligands for enantioselective reactions. Additionally, it finds use in the preparation of biologically active molecules and fine chemicals where specific spatial orientation is critical for activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿150.00
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿350.00
inventory 100g
10-20 days ฿1,270.00
inventory 500g
10-20 days ฿6,150.00
(S)-()-2-Amino-1-butanol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antibiotics and antiviral agents. Its stereochemistry makes it valuable in asymmetric synthesis for creating enantiomerically pure compounds. Also employed in the development of catalysts and ligands for enantioselective reactions. Additionally, it finds use in the preparation of biologically active molecules and fine chemicals where specific spatial orientation is critical for activity.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antibiotics and antiviral agents. Its stereochemistry makes it valuable in asymmetric synthesis for creating enantiomerically pure compounds. Also employed in the development of catalysts and ligands for enantioselective reactions. Additionally, it finds use in the preparation of biologically active molecules and fine chemicals where specific spatial orientation is critical for activity.

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