(R)-3-Hydroxypyrrolidine hydrochloride

98%

Reagent Code: #229860
label
Alias (R)-3-hydroxypyrrolidine hydrochloride
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CAS Number 104706-47-0

science Other reagents with same CAS 104706-47-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 123.58 g/mol
Formula C₄H₉NO·HCl
badge Registry Numbers
MDL Number MFCD00191570
thermostat Physical Properties
Melting Point 104-107 °C(lit.)
inventory_2 Storage & Handling
Storage 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) requiring stereochemical control. Commonly employed in the preparation of antiviral and antidiabetic drugs due to its ability to enhance metabolic stability and binding selectivity. Also utilized in the production of nootropic agents and neuropharmaceuticals, where the (R)-enantiomer contributes to improved cognitive function and neuroprotective effects. Its hydrochloride salt form enhances solubility and bioavailability in aqueous formulations, making it suitable for oral and injectable dosage forms.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿162.00
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿920.00
inventory 100g
10-20 days ฿3,530.00
inventory 500g
10-20 days ฿17,600.00
(R)-3-Hydroxypyrrolidine 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) requiring stereochemical control. Commonly employed in the preparation of antiviral and antidiabetic drugs due to its ability to enhance metabolic stability and binding selectivity. Also utilized in the production of nootropic agents and neuropharmaceuticals, where the (R)-enantiomer contributes to improved cognitive function and neuroprotective effects. Its hyd

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Commonly employed in the preparation of antiviral and antidiabetic drugs due to its ability to enhance metabolic stability and binding selectivity. Also utilized in the production of nootropic agents and neuropharmaceuticals, where the (R)-enantiomer contributes to improved cognitive function and neuroprotective effects. Its hydrochloride salt form enhances solubility and bioavailability in aqueous formulations, making it suitable for oral and injectable dosage forms.

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