(2R,3S)-3-Aminobutan-2-ol hydrochloride

95%

Reagent Code: #229335
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CAS Number 126307-45-7

science Other reagents with same CAS 126307-45-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 125.6 g/mol
Formula C₄H₁₂ClNO
badge Registry Numbers
MDL Number MFCD32062591
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the production of bioactive molecules and active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its amino alcohol functionality makes it valuable in asymmetric synthesis and catalysis. Commonly employed in the development of antibiotics, antivirals, and central nervous system agents due to its structural compatibility with biologically active compounds. Also utilized in the preparation of intermediates for agrochemicals and specialty chemicals where stereochemistry plays a critical role in activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿36,200.00
250mg
10-20 days ฿54,230.00
1g
10-20 days ฿135,340.00
(2R,3S)-3-Aminobutan-2-ol hydrochloride
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Used as a chiral building block in pharmaceutical synthesis, particularly in the production of bioactive molecules and active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its amino alcohol functionality makes it valuable in asymmetric synthesis and catalysis. Commonly employed in the development of antibiotics, antivirals, and central nervous system agents due to its structural compatibility with biologically active compounds. Also utilized in the preparation of intermediates for

Used as a chiral building block in pharmaceutical synthesis, particularly in the production of bioactive molecules and active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its amino alcohol functionality makes it valuable in asymmetric synthesis and catalysis. Commonly employed in the development of antibiotics, antivirals, and central nervous system agents due to its structural compatibility with biologically active compounds. Also utilized in the preparation of intermediates for agrochemicals and specialty chemicals where stereochemistry plays a critical role in activity.

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