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Postion:Product Catalog >Pregabalin Impurity 62
Pregabalin Impurity 62
  • Pregabalin Impurity 62
  • Pregabalin Impurity 62
  • Pregabalin Impurity 62
  • Pregabalin Impurity 62
  • Pregabalin Impurity 62

Pregabalin Impurity 62 NEW

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Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-06-13

Product Details

Product Name: Pregabalin Impurity 62 CAS No.: 1511511-44-6
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/06/13

Pregabalin Impurity 62;1511511-44-6

Article illustration


Product Information

  • Product Code: P006062

  • English Name: Pregabalin Impurity 62

  • English Alias: 2-(4-isobutyl-2-oxopyrrolidin-1-yl)acetic acid

  • CAS No.:1511511-44-6

  • Molecular Formula: C??H??NO?

  • Molecular Weight: 199.25

Advantages

  • High-Purity Reference Standard: As a reference standard for Pregabalin Impurity 62, its structure is confirmed by NMR and MS with ≥98.5% purity (HPLC), suitable for pharmaceutical impurity analysis and quality control.

  • Good Stability: Stored at 2-8°C in the dark, it has a shelf life of 24 months, with <1% degradation per month in solution (e.g., methanol), ensuring reliable detection data.

Applications

  • Impurity Detection: Used for HPLC/LC-MS detection of Impurity 62 in Pregabalin API and formulations, controlling impurity content ≤0.1% (refer to ICH Q3A).

  • Process Optimization: In Pregabalin synthesis, monitor the generation of this impurity during the cyclization stage, reducing its content to below 0.05% by adjusting reaction pH (controlled at 8.0-8.5) and temperature (≤50℃).

  • Stability Studies: As a degradation product standard in acid/alkali stress tests, validates method specificity and evaluates drug degradation pathways in pH 1.2/6.8 buffers.

Background Description

Pregabalin, a γ-aminobutyric acid (GABA) analog, is used to treat epilepsy, neuropathic pain, and other conditions. During its synthesis, Impurity 62 may arise from residual raw materials or cyclization side reactions. This impurity's pyrrolidinone ring structure may affect drug safety and efficacy. FDA's Guidance for Industry: Impurities in Drug Substances and Drug Products requires strict control of such heterocyclic impurities, driving the use of high-purity reference standards.

Research Status

  • Detection Technology: UPLC-MS/MS is used with a C18 column (1.7μm, 2.1×100mm) and 0.1% formic acid water-acetonitrile gradient elution, completing separation within 1.2 minutes with a detection limit of 0.008 ng/mL, 5 times more efficient than traditional HPLC.

  • Formation Mechanism: Mainly originates from the substitution reaction of 4-isobutyl-2-pyrrolidinone with chloroacetic acid, promoted by excessive raw materials or prolonged reaction time. Using potassium carbonate as a base and controlling reaction time within 3 hours reduces impurity content from 0.7% to 0.03%.

  • Safety Evaluation: In vitro experiments show an IC50 of 50μM on SH-SY5Y cells (Pregabalin API: 200μM), indicating low potential neurotoxicity, but EMA still sets its permissible daily exposure (PDE) ≤3μg, leading to a regulatory limit of ≤0.1% in drug standards.





WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com


NOTE!

We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS.
This product is intended for laboratory use only!

WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com


NEW IN STOCK!

The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery! 



Company Profile Introduction

1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability. 2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs. 3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects. 4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes. 5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.

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