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Catalog Number:
41676
CAS Number:
2185-03-7
(S)-(-)-α-Amino-γ-butyrolactone hydrochloride
Purity:
≥ 99% (HPLC)
Synonym(s):
(S)-(-)-3-Aminotetrahydrofuran-2-one hydrochloride, L-(-)-Homoserine lactone hydrochloride
Documents
$39.26 /1G
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Product Information

(S)-(-)-a-Amino-g-butyrolactone hydrochloride is a versatile compound widely utilized in the pharmaceutical and biochemical industries. This chiral amino acid derivative is known for its role as a building block in the synthesis of various bioactive molecules, including pharmaceuticals and agrochemicals. Its unique structure allows for specific interactions in biological systems, making it a valuable tool in drug development and research. Researchers often leverage its properties to enhance the efficacy of therapeutic agents, particularly in the fields of neuropharmacology and metabolic studies.

Additionally, (S)-(-)-a-Amino-g-butyrolactone hydrochloride serves as a precursor in the synthesis of other important compounds, contributing to advancements in medicinal chemistry. Its ability to facilitate the development of novel therapeutic agents positions it as a critical component in ongoing research and industrial applications. With its favorable safety profile and effectiveness, this compound is an essential resource for professionals aiming to innovate in drug formulation and development.

Synonyms
(S)-(-)-3-Aminotetrahydrofuran-2-one hydrochloride, L-(-)-Homoserine lactone hydrochloride
CAS Number
2185-03-7
Purity
≥ 99% (HPLC)
Molecular Formula
C4H7NO2·HCl
Molecular Weight
137.56
MDL Number
MFCD00058172
PubChem ID
13071747
Melting Point
217 - 219 °C
Appearance
White powder
Optical Rotation
[a]20D = -25 ± 2 ° (C = 1 in H2O)
Conditions
Store at ≤ -10 °C
General Information
Synonyms
(S)-(-)-3-Aminotetrahydrofuran-2-one hydrochloride, L-(-)-Homoserine lactone hydrochloride
CAS Number
2185-03-7
Purity
≥ 99% (HPLC)
Molecular Formula
C4H7NO2·HCl
Molecular Weight
137.56
MDL Number
MFCD00058172
PubChem ID
13071747
Melting Point
217 - 219 °C
Appearance
White powder
Optical Rotation
[a]20D = -25 ± 2 ° (C = 1 in H2O)
Conditions
Store at ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-(-)-a-Amino-g-butyrolactone hydrochloride 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.
  • Neurotransmitter Research: It is used in studies investigating neurotransmitter systems, aiding researchers in understanding the mechanisms of action for certain drugs and their effects on the central nervous system.
  • Biochemical Assays: The compound is employed in biochemical assays to evaluate enzyme activity and metabolic pathways, providing insights into cellular functions and potential therapeutic targets.
  • Analytical Chemistry: It is utilized as a standard in analytical chemistry for the quantification of amino acids and related compounds, ensuring accuracy in research and quality control processes.
  • Academic Research: This chemical is a valuable tool in academic settings for teaching and conducting experiments related to organic synthesis and medicinal chemistry, enhancing the educational experience for students.

Citations