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6α-[(1-Oxopentyl)Amino]Penicillanic Acid CAS NO 4704-53-4


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CAS No.:4704-53-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

6α-[(1-Oxopentyl)Amino]Penicillanic Acid CAS NO 4704-53-4 is a key semi-synthetic penicillin derivative, primarily utilized as a crucial intermediate in the synthesis of advanced β-lactam antibiotics. Its value lies in providing a versatile chemical backbone for developing potent antimicrobial agents with targeted activity. This compound is essential for pharmaceutical manufacturers and research institutions focused on antibiotic development, chemical synthesis, and pharmacological studies.

Application

  • Pharmaceutical Intermediate: A critical building block in the synthesis of novel penicillin and cephalosporin-based antibiotics.
  • Antibiotic Research & Development: Used in medicinal chemistry for creating and testing new antimicrobial compounds with improved efficacy and spectrum.
  • Chemical Synthesis: Serves as a precursor for modifying the β-lactam core structure to develop derivatives with specific pharmacological properties.
  • Bulk API Manufacturing: Employed in the large-scale production of active pharmaceutical ingredients (APIs) for finished antibiotic formulations.
  • Biochemical Studies: Utilized in research to study the structure-activity relationships (SAR) of β-lactam compounds and their interaction with bacterial enzymes.

Basic Information

Product Name 6α-[(1-Oxopentyl)Amino]Penicillanic Acid
CAS No. 4704-53-4
Molecular Formula C14H21N3O4S
Molecular Weight 327.40 g/mol
Synonyms 6-APA Valeramide; 6-(1-Oxopentylamino)penicillanic Acid; 6-(Valerylamino)penicillanic Acid; 6-[(1-Oxopentyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid; N-Valeryl-6-aminopenicillanic Acid; 6-(Pentanamido)penicillanic Acid; 6-APA Pentanamide Derivative
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Quality Control

Our 6α-[(1-Oxopentyl)Amino]Penicillanic Acid is produced under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure high purity and consistency, meeting the stringent requirements for pharmaceutical intermediates. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed to prevent degradation from atmospheric moisture.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to structure
Assay (HPLC) ≥ 98.0%
Water Content (KF) ≤ 1.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Residual Solvents (GC) Complies with ICH guidelines

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

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