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Catalog Number:
41665
CAS Number:
104347-13-9
(R)-(+)-α-Amino-γ-butyrolactone hydrochloride
Purity:
≥ 97% (HPLC)
Synonym(s):
(R)-(+)-3-Aminotetrahydrofuran-2-one hydrochloride, D-(+)-Homoserine lactone hydrochloride
Documents
$45.77 /1G
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Product Information

(R)-(+)-a-Amino-g-butyrolactone hydrochloride is a versatile compound widely utilized in pharmaceutical and biochemical research. This chiral amino acid derivative is recognized for its role as a building block in the synthesis of various bioactive molecules, particularly in the development of pharmaceuticals targeting neurological disorders. Its unique structure allows for selective interactions in biological systems, making it a valuable tool for researchers focused on drug discovery and development.

In addition to its applications in medicinal chemistry, (R)-(+)-a-Amino-g-butyrolactone hydrochloride is also employed in the synthesis of polymers and as a chiral auxiliary in asymmetric synthesis. Its ability to enhance the efficacy of certain compounds while minimizing side effects positions it as a preferred choice among industry professionals. With its proven track record in enhancing drug formulation and delivery, this compound stands out for its reliability and effectiveness in various applications.

Synonyms
(R)-(+)-3-Aminotetrahydrofuran-2-one hydrochloride, D-(+)-Homoserine lactone hydrochloride
CAS Number
104347-13-9
Purity
≥ 97% (HPLC)
Molecular Formula
C4H7NO2·HCl
Molecular Weight
137.56
MDL Number
MFCD00674071
PubChem ID
13071747
Melting Point
218 - 221 °C
Appearance
White powder
Optical Rotation
[a]20D = 28 ± 2 ° (C = 1 in H2O)
Conditions
Store at 0-8 °C
General Information
Synonyms
(R)-(+)-3-Aminotetrahydrofuran-2-one hydrochloride, D-(+)-Homoserine lactone hydrochloride
CAS Number
104347-13-9
Purity
≥ 97% (HPLC)
Molecular Formula
C4H7NO2·HCl
Molecular Weight
137.56
MDL Number
MFCD00674071
PubChem ID
13071747
Melting Point
218 - 221 °C
Appearance
White powder
Optical Rotation
[a]20D = 28 ± 2 ° (C = 1 in H2O)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R)-(+)-a-Amino-g-butyrolactone hydrochloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a precursor in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting the central nervous system.
  • Neuroscience Research: It is used in studies investigating neurotransmitter systems, helping researchers understand conditions like anxiety and depression.
  • Biochemical Assays: The compound is employed in biochemical assays to evaluate enzyme activity, providing insights into metabolic pathways.
  • Chiral Synthesis: Its chiral nature makes it valuable in asymmetric synthesis, allowing for the production of enantiomerically pure compounds, which are crucial in drug formulation.
  • Educational Purposes: It is often used in academic settings for teaching organic chemistry and pharmacology, providing students with hands-on experience in compound synthesis and analysis.

Citations