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Catalog Number:
19565
CAS Number:
258530-57-3
Acide 3-hydroxy-pyrrolidin-1-yl)acétique
Purity:
≥ 97 % (HPLC)
Documents
$86.23 /250 mg
Taille
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Product Information

(3-Hydroxy-pyrrolidin-1-yl)acetic acid is a versatile compound with significant potential in pharmaceutical and biochemical research. This compound, also known as 3-Hydroxy-1-pyrrolidineacetic acid, features a unique pyrrolidine ring structure that enhances its solubility and bioavailability, making it an attractive candidate for drug formulation. Its hydroxyl group contributes to its reactivity, allowing for various modifications that can lead to the development of novel therapeutic agents.

Researchers have explored the applications of (3-Hydroxy-pyrrolidin-1-yl)acetic acid in the synthesis of amino acid derivatives and as a building block in the design of bioactive molecules. Its potential use in neuropharmacology is particularly noteworthy, as it may play a role in modulating neurotransmitter systems. The compound's favorable properties, including its stability and compatibility with various solvents, make it suitable for a range of laboratory applications, including drug discovery and development.

CAS Number
258530-57-3
Purity
≥ 97 % (HPLC)
Molecular Formula
C 6 H 11 NON 3
Molecular Weight
145.16
MDL Number
MFCD06796154
PubChem ID
19817652
Appearance
Solide brun pâle ou blanc cassé
Conditions
Conserver à 0-8 °C
General Information
CAS Number
258530-57-3
Purity
≥ 97 % (HPLC)
Molecular Formula
C 6 H 11 NON 3
Molecular Weight
145.16
MDL Number
MFCD06796154
PubChem ID
19817652
Appearance
Solide brun pâle ou blanc cassé
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(3-Hydroxy-pyrrolidin-1-yl)acetic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is explored for its potential in drug formulation, particularly in creating novel therapies for neurological disorders due to its ability to cross the blood-brain barrier.
  • Biochemical Research: It serves as a valuable tool in studying metabolic pathways, helping researchers understand amino acid metabolism and its implications in various diseases.
  • Neuroscience Applications: The compound is investigated for its neuroprotective properties, making it a candidate for treatments aimed at neurodegenerative conditions like Alzheimer's disease.
  • Analytical Chemistry: Used as a standard in chromatographic techniques, it aids in the accurate quantification of related compounds in complex biological samples.
  • Cosmetic Formulations: Its hydrophilic nature allows it to be incorporated into skincare products, enhancing moisture retention and skin barrier function.

Citations