share

Levomoprolol CAS NO 77164-20-6


Unit Price:

CAS No.:77164-20-6

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Levomoprolol is a high-purity, single-enantiomer pharmaceutical intermediate and active ingredient. This compound is valued for its specific stereochemistry, which is critical for achieving targeted pharmacological activity and minimizing side effects in advanced therapeutic formulations. It is essential for research institutions and manufacturers developing next-generation cardiovascular and ophthalmic medications, where chiral purity directly impacts efficacy and safety profiles.

Application

  • Pharmaceutical Intermediate: Key chiral building block in the synthesis of advanced β-adrenergic blocking agents (β-blockers).
  • Active Pharmaceutical Ingredient (API): Used in the research and development of enantiomerically pure cardiovascular drugs.
  • Ophthalmic Solutions: A potential component in the formulation of eye drops for managing intraocular pressure.
  • Biochemical Research: Serves as a standard or reagent in stereoselective metabolism and receptor-binding studies.
  • Process Development: Utilized in scaling up and optimizing asymmetric synthesis pathways in pilot plants.
  • Reference Standard: Acts as a high-purity calibrant in analytical method development for quality control laboratories.

Basic Information

Product Name Levomoprolol
CAS No. 77164-20-6
Molecular Formula C15H25NO3
Molecular Weight 267.36 g/mol
Synonyms (-)-Moprolol; (S)-Moprolol; Levomoprolol [INN]; L-Moprolol; (2S)-1-(Isopropylamino)-3-(2-methoxyphenoxy)propan-2-ol; (S)-1-(Isopropylamino)-3-(o-methoxyphenoxy)-2-propanol; UNII-6Q8WX6U3QN
EINECS Contact for details

Quality Control

Our Levomoprolol is manufactured under strict quality management systems. Each batch is tested to ensure it meets stringent specifications for identity, purity, and enantiomeric excess, relevant for pharmaceutical development. Certificates of Analysis (COA) detailing comprehensive test results, including chiral HPLC purity, are provided with every shipment to support your regulatory and R&D requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Assay (HPLC) ≥98.5%
Enantiomeric Purity (Chiral HPLC) ≥99.0%
Loss on Drying ≤0.5%
Residue on Ignition ≤0.1%
Heavy Metals ≤20 ppm
Related Substances (HPLC) Individual impurity ≤0.5%; Total impurities ≤1.0%

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.