(S)-3-Amino-2-methylpropan-1-ol

97%

Reagent Code: #233321
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CAS Number 88586-62-3

science Other reagents with same CAS 88586-62-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 89.14 g/mol
Formula C₄H₁₁NO
badge Registry Numbers
MDL Number MFCD19203687
thermostat Physical Properties
Boiling Point 168.3±13.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.927±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its primary amine and hydroxyl functional groups allow for versatile reactivity, enabling use in asymmetric synthesis and the development of enantiomerically pure drugs. Commonly employed in the preparation of beta-adrenergic receptor blockers and other cardiovascular medications. Also utilized in the design of enzyme inhibitors and as an intermediate in the manufacture of agrochemicals and specialty polymers.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,570.00
inventory 250mg
10-20 days ฿28,470.00
(S)-3-Amino-2-methylpropan-1-ol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its primary amine and hydroxyl functional groups allow for versatile reactivity, enabling use in asymmetric synthesis and the development of enantiomerically pure drugs. Commonly employed in the preparation of beta-adrenergic receptor blockers and other cardiovascular medications. Also utilized i

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its primary amine and hydroxyl functional groups allow for versatile reactivity, enabling use in asymmetric synthesis and the development of enantiomerically pure drugs. Commonly employed in the preparation of beta-adrenergic receptor blockers and other cardiovascular medications. Also utilized in the design of enzyme inhibitors and as an intermediate in the manufacture of agrochemicals and specialty polymers.

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