Description

Pentanamide, 3-Amino-N,N,4-Trimethyl-, (3R)- (9Ci) is a chiral, non-racemic amide derivative with a specific stereochemical configuration at the 3-position. This compound serves as a valuable advanced pharmaceutical intermediate (API intermediate) and a versatile chiral building block for the synthesis of complex organic molecules. It is primarily required by pharmaceutical R&D and fine chemical synthesis sectors for developing new active ingredients and specialty chemicals.

Application

• Pharmaceutical Intermediate: Key chiral synthon in the research and production of novel active pharmaceutical ingredients (APIs), particularly for central nervous system (CNS) and metabolic disorder targets.
• Asymmetric Synthesis: Employed as a chiral auxiliary or precursor in stereoselective chemical reactions to induce desired optical activity in final products.
• Agrochemical Research: Used in the development of new, enantiomerically pure pesticides and herbicides where specific stereochemistry impacts biological activity.
• Ligand and Catalyst Development: Serves as a precursor for synthesizing specialized ligands used in homogeneous catalysis and metal-organic frameworks (MOFs).
• Fine Chemical Manufacturing: Building block for high-value specialty chemicals, including flavors, fragrances, and advanced materials.
• Academic and Industrial R&D: Utilized in chemical research laboratories for methodological studies and exploring new synthetic pathways.

Basic Information

Product Name	Pentanamide, 3-Amino-N,N,4-Trimethyl-, (3R)- (9Ci)
CAS No.	750548-51-7
Molecular Formula	C8H18N2O
Molecular Weight	158.24 g/mol
Synonyms	(3R)-3-Amino-N,N,4-trimethylpentanamide; (R)-3-Amino-N,N,4-trimethylpentanamide; 3-Amino-N,N,4-trimethylpentanamide, (3R)-; 750548-51-7; (R)-3-Amino-4-methyl-N,N-dimethylvaleramide; (3R)-3-Amino-4-methyl-N,N-dimethylpentanamide; (R)-3-Amino-4-methyl-N,N-dimethylpentanamide; (R)-3-Amino-N,N,4-trimethylvaleramide
EINECS	Contact for details

Quality Control

Our production of this chiral intermediate adheres to strict quality management systems. Every batch is characterized and tested to ensure identity, purity, and enantiomeric excess meet the required specifications for advanced synthetic applications. Certificates of Analysis (COA) are provided with each shipment, detailing key parameters such as assay, chiral purity (enantiomeric excess), and impurity profiles. We support cGMP standards for pharmaceutical-grade material upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); keep the container tightly sealed under an inert atmosphere (e.g., nitrogen) for long-term storage to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Enantiomeric Excess (Chiral HPLC)	≥ 99.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Single Unknown Impurity (HPLC)	≤ 0.5%
Total Impurities (HPLC)	≤ 1.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.