(R)-3-Dimethylaminopyrrolidine

≥95%(GC)

Reagent Code: #229854
label
Alias N-dimethyl-3-pyrrolidinamine; (3R)-N,N-dimethyl-3-pyrrolidinamine
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CAS Number 132958-72-6

science Other reagents with same CAS 132958-72-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 114.19 g/mol
Formula C₆H₁₄N₂
badge Registry Numbers
MDL Number MFCD00191347
thermostat Physical Properties
Boiling Point 166 °C760 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.899 g/mL at 25 °C(lit.)
Storage 2-8°C, light-proof, inert gas, sealed

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Serves as a ligand or intermediate in asymmetric catalysis, enabling selective formation of chiral centers. Commonly applied in the development of central nervous system agents and protease inhibitors due to its favorable stereochemistry and amine functionality. Also utilized in agrochemicals and specialty chemicals where stereo-selectivity is critical.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿620.00
5g
10-20 days ฿5,304.00
25g
10-20 days ฿29,770.00
1g
10-20 days ฿1,880.00
(R)-3-Dimethylaminopyrrolidine
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Used as a chiral building block in pharmaceutical synthesis, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Serves as a ligand or intermediate in asymmetric catalysis, enabling selective formation of chiral centers. Commonly applied in the development of central nervous system agents and protease inhibitors due to its favorable stereochemistry and amine functionality. Also utilized in agrochemicals and specialty chemicals where stereo-selectivity i

Used as a chiral building block in pharmaceutical synthesis, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Serves as a ligand or intermediate in asymmetric catalysis, enabling selective formation of chiral centers. Commonly applied in the development of central nervous system agents and protease inhibitors due to its favorable stereochemistry and amine functionality. Also utilized in agrochemicals and specialty chemicals where stereo-selectivity is critical.

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