L-Valinol

97%

Reagent Code: #202199
label
Alias L-valine;(S)-2-amino-3-methyl-1-butanol
fingerprint
CAS Number 2026-48-4

science Other reagents with same CAS 2026-48-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 103.16 g/mol
Formula C₅H₁₃NO
badge Registry Numbers
EC Number 217-975-5
MDL Number MFCD00064296
thermostat Physical Properties
Melting Point 30-34 °C
Boiling Point 81 °C8 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.926 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

L-Valinol is widely used in the synthesis of pharmaceuticals, particularly as a chiral building block in the development of active pharmaceutical ingredients (APIs). Its chiral nature makes it valuable in asymmetric synthesis, where it helps control the stereochemistry of complex molecules. It is commonly employed in the preparation of protease inhibitors and other biologically active compounds that require specific stereoconfiguration for efficacy. Additionally, L-Valinol serves as a ligand or auxiliary in catalytic reactions, enhancing enantioselectivity in organic transformations. It is also utilized in the production of agrochemicals and specialty chemicals where chirality plays a critical role in function and performance.

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 ฿950.00
inventory 100g
10-20 days ฿3,600.00
inventory 500g
10-20 days ฿17,800.00
L-Valinol
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L-Valinol is widely used in the synthesis of pharmaceuticals, particularly as a chiral building block in the development of active pharmaceutical ingredients (APIs). Its chiral nature makes it valuable in asymmetric synthesis, where it helps control the stereochemistry of complex molecules. It is commonly employed in the preparation of protease inhibitors and other biologically active compounds that require specific stereoconfiguration for efficacy. Additionally, L-Valinol serves as a ligand or auxiliary in catalytic reactions, enhancing enantioselectivity in organic transformations. It is also utilized in the production of agrochemicals and specialty chemicals where chirality plays a critical role in function and performance.
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