Frequently Asked
Common questions about L-2-Aminobutanamide hydrochloride
What is L-2-Aminobutanamide hydrochloride used for?
L-2-Aminobutanamide hydrochloride is an amine-functionalized compound with nucleophilic nitrogen reactivity used primarily in the pharmaceutical and polymer industries. Key applications include buchwald–hartwig amination for aryl c–n bond construction and peptide bond mimetic for peptidomimetic drug design.
Where can I buy L-2-Aminobutanamide hydrochloride in the USA?
ChemContract Research is a trusted USA-based supplier of L-2-Aminobutanamide hydrochloride. We offer competitive pricing, fast domestic shipping from our Huntington Beach, California facility, and full quality documentation including Certificates of Analysis (CoA). Request a quote at chemistry@chem-contract.com or call +1 (714) 732-8549.
What purity levels are available for L-2-Aminobutanamide hydrochloride?
ChemContract Research supplies L-2-Aminobutanamide hydrochloride in multiple purity grades: ≥95% standard grade, ≥97% high-purity grade, and ≥99% ultra-high-purity grade depending on application requirements. We can also provide custom purity grades through our synthesis capabilities. Contact us for specific purity information and CoA documentation.
Can ChemContract synthesize L-2-Aminobutanamide hydrochloride in custom quantities?
Yes. ChemContract Research offers custom synthesis services for L-2-Aminobutanamide hydrochloride from milligram to multi-kilogram scale. Our cGMP-compliant facilities and experienced chemists can accommodate custom specifications, packaging requirements, and delivery timelines. Contact our team to discuss your project.
What is the stereochemical purity of L-2-Aminobutanamide hydrochloride?
ChemContract Research supplies L-2-Aminobutanamide hydrochloride with verified enantiomeric or diastereomeric purity as documented in our Certificate of Analysis (CoA). Chiral HPLC analysis is standard for stereodefined compounds. We can provide material with ≥98% ee/de for demanding applications. Contact us for specific optical purity requirements.
What reactions can I perform with the amine group in L-2-Aminobutanamide hydrochloride?
The amine functionality in L-2-Aminobutanamide hydrochloride enables diverse transformations: reductive amination with aldehydes/ketones, acylation to form amides, sulfonylation to form sulfonamides, Buchwald–Hartwig coupling with aryl halides, urea and carbamate formation, and salt generation for improved drug properties. The nucleophilicity of the nitrogen makes it one of the most versatile handles in synthetic chemistry.
How should I store L-2-Aminobutanamide hydrochloride?
Store in a cool, well-ventilated area away from acids and oxidizing agents. Keep containers tightly sealed as many amines are hygroscopic. Store at room temperature or as specified. Keep tightly sealed and protect from moisture. Store at room temperature in a tightly sealed container. Protect from humidity. Store under recommended conditions. Some chiral compounds may racemize at elevated temperatures or in the presence of base. Always consult the compound-specific Safety Data Sheet (SDS) provided with your order for detailed storage requirements. ChemContract Research includes handling and storage documentation with every shipment.
What is the CAS number of L-2-Aminobutanamide hydrochloride?
The CAS Registry Number for L-2-Aminobutanamide hydrochloride is 7682-20-4. This unique identifier is used worldwide to reference this specific compound in chemical databases, regulatory filings, and scientific literature. ChemContract Research supplies this compound with full quality documentation. Contact us at chemistry@chem-contract.com for availability and pricing.
