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Catalog Number:
41527
CAS Number:
128345-57-3
(S)-(-)-3-Aminopyrrolidine
Purity:
≥ 99% (Chiral purity)
Synonym(s):
(3S)-(-)-3-Aminopyrrolidine
Hazmat
Documents
$180.27 /1G
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Product Information
Synonyms
(3S)-(-)-3-Aminopyrrolidine
CAS Number
128345-57-3
Purity
≥ 99% (Chiral purity)
Molecular Formula
C4H10N2
Molecular Weight
0
MDL Number
MFCD00143193
PubChem ID
164401
Density
0.967 g/mL at 25 °C (Lit.)
Appearance
Colorless to brown liquid or clear colorless liquid
Boiling Point
164 - 165 °C (Lit.)
Refractive Index
n20D 1.48 (Lit.)
Optical Rotation
[á]20/D = −20 ° neat
Conditions
Store at RT
General Information
Synonyms
(3S)-(-)-3-Aminopyrrolidine
CAS Number
128345-57-3
Purity
≥ 99% (Chiral purity)
Molecular Formula
C4H10N2
Molecular Weight
0
MDL Number
MFCD00143193
PubChem ID
164401
Density
0.967 g/mL at 25 °C (Lit.)
Appearance
Colorless to brown liquid or clear colorless liquid
Boiling Point
164 - 165 °C (Lit.)
Refractive Index
n20D 1.48 (Lit.)
Optical Rotation
[á]20/D = −20 ° neat
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-(-)-3-Aminopyrrolidine is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Chiral Catalysis: Its chiral nature makes it an excellent candidate for asymmetric synthesis, enhancing the efficiency of producing enantiomerically pure compounds in the pharmaceutical industry.
  • Neurotransmitter Research: Researchers use this compound to study its effects on neurotransmitter systems, which can lead to advancements in treatments for conditions like depression and anxiety.
  • Material Science: It is applied in the development of new materials, particularly in creating polymers with enhanced properties for use in various industrial applications.
  • Biochemical Assays: The compound is utilized in biochemical assays to investigate enzyme interactions and mechanisms, providing insights into metabolic pathways.

Citations