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Postion:Product Catalog >Pitavastatin(Phenylethylamine Salt)
Pitavastatin(Phenylethylamine Salt)
  • Pitavastatin(Phenylethylamine Salt)
  • Pitavastatin(Phenylethylamine Salt)
  • Pitavastatin(Phenylethylamine Salt)
  • Pitavastatin(Phenylethylamine Salt)

Pitavastatin(Phenylethylamine Salt) NEW

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

Product Details

Product Name: Pitavastatin(Phenylethylamine Salt) Min. Order: 10mg
Purity: 99%+ HPLC Supply Ability: 1000
Release date: 2025/06/13

NEW IN STOCK!

Article illustration

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

Pitavastatin(Phenylethylamine Salt) Product Introduction

Product Number: P001000A
English Name: Pitavastatin(Phenylethylamine Salt)
English Alias: (R)-1-phenylethanamine (3R,5S,E)-7-(2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl)-3,5-dihydroxyhept-6-enoate
CAS Number: 147511-70-4
Molecular Formula: C25H24FNO4.C8H11N 
Molecular Weight: Approximately 542.64 


Pitavastatin is a statin drug commonly used to lower cholesterol levels in the blood to prevent and treat cardiovascular diseases. Its mechanism of action is mainly to inhibit hydroxymethylglutaryl coenzyme A (HMG-CoA) reductase and reduce the biosynthesis of cholesterol. Pitavastatin (Phenylethylamine Salt), as a salt form of Pitavastatin, is of great significance in pharmaceutical preparations. The choice of salt form can affect key properties of the drug such as solubility, stability, and bioavailability.


In terms of the current research status, the research on Pitavastatin (Phenylethylamine Salt) involves multiple fields. In the field of medicinal chemistry, researchers are committed to developing more efficient and safer synthetic routes to improve the yield and purity of this compound while reducing production costs. By improving reaction conditions, optimizing catalysts and reaction solvents, etc., they are constantly exploring greener synthetic methods. In the field of pharmacology research, further exploration of the mechanism of action of Pitavastatin (Phenylethylamine Salt) in the body, including its regulation of the expression of genes related to cholesterol metabolism and its interactions with other drugs, to gain a more comprehensive understanding of its efficacy and safety. In the field of pharmaceutical preparations, research on how to improve the dissolution characteristics and bioavailability of the drug through appropriate dosage form design, such as tablets and capsules, to improve patients' medication compliance. In addition, in clinical research, evaluating its efficacy and safety in different populations and exploring new clinical application areas, such as its therapeutic effect in specific subgroups of cardiovascular diseases.



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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