Potassium clavulanate CAS#61177-45-5

Potent β-Lactamase Inhibitory Effect: It functions as an efficient β-lactamase inhibitor, which improves the therapeutic effect of antibiotic preparations against drug-resistant bacterial strains.

Core Pharmaceutical Intermediate: It is a critical building block for the fabrication of high-grade antibiotic products, representing an indispensable raw material for pharmaceutical production.

Facilitates Advanced Pharmaceutical Research: It is extensively employed in the synthesis of antibacterial compounds and novel drug formulations developed for the treatment of bacterial infectious diseases.

Adaptable to Mass Industrial Manufacturing: It is produced in compliance with strict quality and performance criteria to satisfy the needs of contemporary pharmaceutical processing and large-scale production.

Product Overview Of Potassium Clavulanate CAS#61177-45-5

Potassium clavulanate, the potassium salt of clavulanic acid (CAS#61177-45-5), is a highly potent β‑lactamase inhibitor. It is broadly applied within the pharmaceutical sector to boost the therapeutic effect of antibiotic regimens for bacterial infections.

It acts as a vital intermediate and active ingredient for formulating high-performance antibiotic combinations. Its production adheres to rigorous quality specifications and performance benchmarks set for modern pharmaceutical manufacturing.

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Potassium Clavulanate Chemical Properties

English Name

Potassium clavulanate

English Synonyms

CLAVULANATE POTASSIUM;CLAVULANIC ACID POTASSIUM;CLAVULANIC ACID POTASSIUM SALT;CLAVULA NTE POTASSIUM;MM 1415;Potassium Clavulanat;Clavulanate;4-Oxa-1-azabicyclo3.2.0heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, monopotassium salt, (2R,3Z,5R)

CAS Number

61177-45-5

Molecular Formula

C8H10KNO5

Molecular Weight

239.27

EINECS Number

262-640-9

Melting point

>1600C (dec)

Specific rotation

+55~+60°

Storage conditions

Inert atmosphere,2-8°C

Solubility

Easily soluble in water, slightly soluble in ethanol (96%), and very slightly soluble in acetone.

Form

Solid

Color

Light brown to brown

Main applications

agriculture
clinical
environmental
forensics and toxicology
pharmaceutical (small molecule)

InChI

InChl=1/C8H9NO5.K.H/c10-2-1-4-7(8(12)13)9-5(11)3-6(9)14-4;/h1,6-7,10H,2-3H2,(H,12,13);/b4-1-/t6-,7 -/s3

InChIKey

ABVRVIZBZKUTMK-JSYANWSFSA-M

SMILES

C([C@H]1/CV/O[C@]2([H])CC(=O)N12)=C/CO)(=O)O.[KH] [&1:1,4,r

Key Features

Boosted Antibacterial Activity

Potassium Clavulanate suppresses bacterial β-lactamase enzymes to shield β-lactam antibiotics from breakdown. This elevates their therapeutic potency and strengthens their action against drug-resistant bacterial strains.

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High Purity and Regulatory Conformity

Synthesized under rigorous quality specifications, our Potassium Clavulanate (CAS#61177-45-5) delivers superior purity, batch uniformity and dependable performance for pharmaceutical use. This product meets global regulatory criteria, enabling seamless incorporation into international supply networks.

Wide Application Flexibility

Potassium Clavulanate finds extensive use across diverse pharmaceutical preparations. It is frequently compounded with antibiotics including amoxicillin to achieve strengthened efficacy against a broad spectrum of bacterial infections.

Application Industries

Pharmaceutical Production

Potassium Clavulanate functions as a core raw material for antibiotic formulation. It generates synergistic effects with other active pharmaceutical ingredients to lift therapeutic outcomes.

Research & Development

Within pharmaceutical R&D, Potassium Clavulanate acts as a critical material for creating novel antibacterial treatments and advanced strategies to tackle antibiotic resistance.

Conclusion

Potassium Clavulanate (CAS#61177-45-5) is far more than a β-lactamase inhibitor; it constitutes an indispensable building block for contemporary antibacterial treatment. Manufactured in accordance with the strict requirements of the pharma sector, it facilitates the creation of safe, potent and stable antibiotic preparations.

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