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Postion:Product Catalog >API>Digestive system drugs>Appetite suppressants and other diet pills>Orlistat
Orlistat
  • Orlistat
  • Orlistat
  • Orlistat
  • Orlistat
  • Orlistat

Orlistat NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-06-18

Product Details

Product Name: Orlistat CAS No.: 96829-58-2
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/06/18

Orlistat; 96829-58-2

Article illustration


  • Product Information

  • Product Code:O020000

  • English Name:Orlistat

  • English Alias:(S)-(S)-1-((2S,3S)-3-hexyl-4-oxooxetan-2-yl)tridecan-2-yl 2-formamido-4-methylpentanoate

  • CAS No.:96829-58-2

  • Molecular Formula:C??H??NO?

  • Molecular Weight:495.73

  • Advantages

  • Pharmaceutical-Grade Purity:Complies with USP, EP pharmacopoeia standards, HPLC purity ≥99.0%, suitable for oral formulation raw material requirements.

  • Stability Profile:Shelf life of 36 months under 2-8℃ light-protected storage; melting point ~50-52℃, prone to ester bond hydrolysis at high temperatures, requiring production environment temperature control.

  • Applications

  • Obesity Treatment:As a gastrointestinal lipase inhibitor, it reduces dietary fat absorption by 30% via pancreatic lipase inhibition, clinically used for obese patients with BMI ≥30 or BMI ≥27 with comorbidities.

  • Formulation Development:Available in oral dosage forms (capsules, tablets), often combined with low-calorie diets; co-administration with vitamins A, D, E, K is recommended to prevent fat-soluble vitamin deficiency.

  • Background Description

  • Orlistat is the first non-central obesity treatment drug approved by FDA, developed by Roche and launched in 1999. Its mechanism relies on selective inhibition of gastrointestinal lipases without entering the bloodstream, leading to minimal systemic adverse reactions. With rising global obesity rates, Orlistat has become a WHO-recommended first-line weight loss drug, marketed as an over-the-counter medication in multiple countries since 2010.
  • Research Status

  • Dosage Form Optimization:Novel microencapsulated formulations reduce gastrointestinal discomfort (e.g., diarrhea, oily stools) and increase bioavailability by 15%; topical fat-reducing gels are in Phase II clinical trials for local adipose tissue treatment.

  • Combination Therapy:Phase III trials of Orlistat + GLP-1 receptor agonists (e.g., semaglutide) show 22% greater weight loss than monotherapy, but hepatobiliary function monitoring is required.

  • Safety Research:Long-term use (≥5 years) may increase gallstone risk (incidence ~5-8%), with FDA-mandated labeling warnings; recent studies suggest its modulation of gut microbiota may affect weight loss efficacy.

  • 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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