Polyvinylpyrrolidon...

Polyvinylpyrrolidone K30
Polyvinylpyrrolidone K30

Polyvinylpyrrolidone K30

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  • Min.Order :0
  • Purity: 99%?
  • Payment Terms : L/C,T/T,Other

Keywords

2-Pyrrolidinone,1-vinyl-, polymers (8CI) 1-Vinyl-2-pyrrolidinone polymer 1-Vinyl-2-pyrrolidone homopolymer

Quick Details

  • Appearance:white or slightly yellow powder
  • Application:
  • PackAge:25kg/fiber drum
  • ProductionCapacity:6000|Kilogram|Month
  • Storage:
  • Transportation:By sea

Superiority:

 PVP K30

1. Superior Product Quality

  • High Purity & Purity Consistency: Manufactured under strict GMP standards, PVP K30 features ultra-low impurity levels (e.g., residual monomers, heavy metals), ensuring compliance with international pharmacopoeias (USP, EP, CP, JP).
  • Uniform Molecular Weight Distribution: Precise control over polymerization processes guarantees consistent molecular weight (K-value 28–32), leading to stable viscosity and binding performance in pharmaceutical formulations.
  • Excellent Stability: Resistant to thermal degradation and chemical interference, making it suitable for heat-sensitive drugs and long-term storage.
  • Biocompatibility & Safety: Non-toxic, non-irritating, and low-allergenic, with a proven safety profile for oral, topical, and parenteral applications.

2. Advanced Manufacturing Technology

  • Proprietary Polymerization Processes: Adopts innovative solution polymerization or bulk polymerization techniques to optimize molecular structure and reduce production impurities.
  • High-Precision Control Systems: Automated production lines with real-time monitoring of temperature, pressure, and reaction kinetics ensure batch-to-batch consistency.
  • Green Production Practices: Employs environmentally friendly solvents and energy-efficient processes, aligning with global sustainability standards.
  • R&D Capabilities: Backed by a team of polymer chemistry experts, capable of customizing PVP K30 for specific application needs (e.g., modified surface activity for targeted drug delivery).

3. Competitive Pricing Strategy

  • Economies of Scale: Large-scale production facilities enable cost-efficient manufacturing, offering competitive prices without compromising quality.
  • Transparent Cost Structure: Clear pricing models based on order volume, supporting flexible procurement for both small-scale R&D and large-scale commercial production.
  • Long-Term Partnership Discounts: Exclusive pricing agreements for long-term clients, reducing total cost of ownership for pharmaceutical manufacturers.
  • Value-Added Cost Efficiency: High binding efficiency minimizes usage rates, lowering formulation costs compared to alternative excipients.

4. Comprehensive Service Support

  • Technical Expertise & Consultation: Dedicated technical teams provide formulation guidance, troubleshooting, and compatibility testing for clients.
  • Rapid Response & Customization: 24/7 customer service for urgent inquiries, plus tailored solutions for special requirements (e.g., sterile-grade PVP K30 for injectables).
  • Regulatory Compliance Assistance: Support in preparing DMFs, CE certifications, and local regulatory filings to facilitate global market access.
  • Reliable Supply Chain: Robust logistics networks ensure on-time delivery, with contingency plans to prevent supply disruptions (e.g., redundant raw material sources).
  • After-Sales Support: Post-installation training, performance tracking, and continuous process optimization to enhance client operational efficiency.

Details:

Polyvinylpyrrolidone K30 (PVP K30) Product Introduction

1. COA Information (Certificate of Analysis)

Chemical Name: Polyvinylpyrrolidone K30

Molecular Formula: (C?H?NO)

CAS No. : 9003-39-8

Molecular Weight: ~38,000 Da

Appearance: White to off-white free-flowing powder with hygroscopic property

Key Quality Indicators:

  • K-Value: 27.0–32.0 (indicates molecular weight consistency)
  • pH (1% Aqueous Solution): 3.0–7.0
  • Moisture Content: ≤5.0%
  • Residual Monomer (N-vinylpyrrolidone): ≤0.1%
  • Heavy Metals: ≤10 ppm
  • Nitrogen Content: 11.5%–12.8% (anhydrous basis)
  • Aldehydes (as acetaldehyde): ≤0.05%
  • Sulfated Ash: ≤0.1%

Standards Compliance:

Comply with USP, EP, CP, and JP pharmacopoeias, manufactured under GMP-certified facilities

2. Product Applications

PVP K30 serves as a versatile excipient and functional additive across multiple industries:

Pharmaceutical Industry

  • Binder for Tablets & Granules: Enhances particle aggregation and tablet hardness, suitable for direct compression or wet granulation
  • Solubilizer for Injectables: Improves solubility of poorly water-soluble drugs via complexation
  • Stabilizer for Sensitive Formulations: Protects enzymes and heat-labile drugs from degradation
  • Film Former in Ophthalmic Solutions: Forms a protective layer on ocular surfaces with excellent biocompatibility
  • Disinfectant Component: Combined with iodine to form PVP-I, a broad-spectrum antiseptic

Other Industries

  • Cosmetics: Thickener and film former in shampoos, toothpastes, and contact lens solutions
  • Food & Beverage: Fining agent for white wine and beer, binder in food coatings
  • Technical Applications: Additive for batteries, ceramics, inks, and inkjet paper to improve processability

3. Supply Capacity & Manufacturing Advantages

Supply Capability

  • Annual Production: 20,000 metric tons, supported by large-scale reactors and automated production lines
  • Lead Time: 1–3 weeks for standard orders, with flexible batch sizes from 1 kg (sample) to bulk shipments
  • Packaging Options: 25 kg drums, custom packaging available (e.g., sterile-grade bags for pharmaceutical use)

Process Advantages

  • Proprietary Polymerization Technology:

Adopts solution polymerization with precise temperature (±0.5°C) and pressure control, minimizing residual monomers and ensuring narrow molecular weight distribution

  • Green Manufacturing:

Employs eco-friendly solvents and energy-efficient processes, reducing carbon footprint by 30% compared to conventional methods

  • Quality Control System:

Real-time monitoring of key process parameters (e.g., reaction kinetics, viscosity) via HPLC and FTIR, ensuring batch-to-batch consistency

  • Regulatory Support:

Pre-certified DMF files, assistance with local registrations (e.g., CE, FDA), and annual GMP audits

4. Visual Assets for Company Presentation

  • Sample & Packaging Images:

Showcases white powder samples in 25 kg drums (with tamper-evident seals) and 1 kg aluminum foil bags for R&D purposes

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