Product Description
Chemical Name: (S)-1-Acetylpiperidine-3-carboxylicacid
Synonyms :
(3S)-1-acetylpiperidine-3-carboxylic acid
| (S)-1-acetylpiperidine-3-carboxylic acid
|3-Piperidinecarboxylicacid, 1-acetyl-, (3S)-
|3-Piperidinecarboxylic acid, 1-acetyl-, (3S)- (9CI)
Cas No : 111479-21-1
Purity : 95%
MolecularFormula : C8H13NO3
Molecular Weight :171.2Key Features and BenefitsThis compound offers exceptional chemical purity (>98%) and enantiomeric selectivity, making it a preferred choice for researchers working on advanced organic and pharmaceutical syntheses. Its solid, crystalline form ensures easy handling and accurate measurement for laboratory applications. The product is securely packaged to maintain its stability throughout its shelf life.
Application and Usage(S)-1-Acetylpiperidine-3-carboxylic acid serves as a valuable building block in the preparation of chiral ligands, pharmaceutical intermediates, and drugs. Its enantiomerically pure (S) configuration is critical for stereoselective syntheses, allowing for precise control over product chirality in research and development settings.
Handling and Storage GuidelinesTo maintain optimal quality, store the compound in a cool, dry, and well-ventilated space. Ensure the container remains tightly closed and avoid exposure to moisture and direct sunlight. Provided in sealed HDPE bottles, typical packaging includes 10g or 25g options to suit research scale. The product retains stability for up to two years.
FAQ's of (S)-1-Acetylpiperidine-3-carboxylic acid:
Q: How should (S)-1-Acetylpiperidine-3-carboxylic acid be stored to preserve its quality?
A: Store the compound in a cool, dry, and well-ventilated place. Keep the container tightly closed and away from moisture and direct sunlight to ensure stability and extend shelf life up to two years.
Q: What is the primary application of (S)-1-Acetylpiperidine-3-carboxylic acid in research?
A: It is mainly used as a chiral auxiliary and intermediate in organic synthesis, particularly for preparing chiral ligands and pharmaceutical compounds that require precise stereochemical control.
Q: When should researchers select the (S) enantiomerically pure form of this compound?
A: The (S) form is chosen when stereoselective synthesis is necessary, as it allows researchers to achieve high enantiomeric purity and optimal activity in pharmaceutical and chemical applications.
Q: Where can this product typically be sourced, and how is it packaged?
A: This laboratory-grade compound is available from suppliers and traders in India, usually provided in sealed HDPE bottles with common pack sizes of 10g and 25g to ensure secure and contamination-free storage.
Q: What is the process for utilizing (S)-1-Acetylpiperidine-3-carboxylic acid in chiral synthesis?
A: In stereoselective synthesis, this compound acts as a chiral building block or auxiliary, enabling the production of compounds with desired enantiomeric purity. It is easily dissolved in DMSO or methanol for reaction setups.
Q: Are there any hazardous considerations with handling this compound?
A: Under normal laboratory conditions, (S)-1-Acetylpiperidine-3-carboxylic acid is considered non-hazardous. However, standard laboratory safety practices should be observed during handling and storage.
Q: What benefits does the high chemical purity and enantiomeric selectivity of this compound provide?
A: High purity and enantiomeric selectivity ensure reliable, reproducible results in stereoselective reactions, making it valuable for preparing active pharmaceutical ingredients requiring strict chiral integrity.