(S)-()-2-Amino-3-methylbutane

98%,ee 99%

Reagent Code: #234207
label
Alias (S)-(+)-3-methyl-2-butylamine; (S)-(+)-2-amino-3-methylbutane
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CAS Number 22526-46-1

science Other reagents with same CAS 22526-46-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 87.16 g/mol
Formula C₅H₁₃N
badge Registry Numbers
MDL Number MFCD01075732
thermostat Physical Properties
Boiling Point 85-87°C
inventory_2 Storage & Handling
Density 0.746 g/mL at 20 °C(lit.)
Storage Room temperature, stored in inert gas

description Product Description

Used primarily as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its stereochemistry makes it valuable in the development of enantioselective drugs, particularly in the production of certain central nervous system agents and enzyme inhibitors. It also serves as an intermediate in the preparation of specialty amino acids and peptides. Due to its amine functionality and branched alkyl chain, it can be employed in asymmetric synthesis and catalysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿27,000.00
inventory 5g
10-20 days ฿70,700.00
(S)-()-2-Amino-3-methylbutane
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Used primarily as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its stereochemistry makes it valuable in the development of enantioselective drugs, particularly in the production of certain central nervous system agents and enzyme inhibitors. It also serves as an intermediate in the preparation of specialty amino acids and peptides. Due to its amine functionality and branched alkyl chain, it can be employed in asymmetric synthesis and catalysis.

Used primarily as a chiral building block in the synthesis of pharmaceuticals and biologically active compounds. Its stereochemistry makes it valuable in the development of enantioselective drugs, particularly in the production of certain central nervous system agents and enzyme inhibitors. It also serves as an intermediate in the preparation of specialty amino acids and peptides. Due to its amine functionality and branched alkyl chain, it can be employed in asymmetric synthesis and catalysis.

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