(R)-2-Aminohexan-1-ol hydrochloride

95%

Reagent Code: #230512
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CAS Number 158741-04-9

science Other reagents with same CAS 158741-04-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.65 g/mol
Formula C₆H₁₆ClNO
badge Registry Numbers
MDL Number MFCD28986146
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its functional groups—amine and alcohol—allow for versatile chemical modifications, making it valuable in creating intermediates for drugs targeting the central nervous system and cardiovascular diseases. Commonly employed in asymmetric synthesis to introduce chirality, which can enhance drug efficacy and reduce side effects. Also utilized in the preparation of enzyme inhibitors and receptor agonists/antagonists. Its hydrochloride salt form improves stability and solubility, facilitating handling and purification during manufacturing processes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,040.00
5g
10-20 days ฿5,170.00
(R)-2-Aminohexan-1-ol hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its functional groups—amine and alcohol—allow for versatile chemical modifications, making it valuable in creating intermediates for drugs targeting the central nervous system and cardiovascular diseases. Commonly employed in asymmetric synthesis to introduce chirality, which can enhance drug ef

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its functional groups—amine and alcohol—allow for versatile chemical modifications, making it valuable in creating intermediates for drugs targeting the central nervous system and cardiovascular diseases. Commonly employed in asymmetric synthesis to introduce chirality, which can enhance drug efficacy and reduce side effects. Also utilized in the preparation of enzyme inhibitors and receptor agonists/antagonists. Its hydrochloride salt form improves stability and solubility, facilitating handling and purification during manufacturing processes.

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