Vinyl Pyrrolidone Crosslinking9003-39-8

Vinyl Pyrrolidone Crosslinking9003-39-8

PVPP is cross-linked polyvinylpyrrolidone, also known as cross-linked povidone. It is white or nearly white, hygroscopic and easy to flow powder, odorless or slightly odor, insoluble in water, alkali, acid and common organic solvents, and has strong swelling performance and complex ability with many types of substances.
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Product Introduction
What is vinyl pyrrolidone crosslinking?

 

PVPP is cross-linked polyvinylpyrrolidone, also known as cross-linked povidone. It is white or nearly white, hygroscopic and easy to flow powder, odorless or slightly odor, insoluble in water, alkali, acid and common organic solvents, and has strong swelling performance and complex ability with many types of substances.

Due to the high molecular weight and cross-linked structure of PVPP, it is insoluble in water but can quickly introduce water in contact with water, which promotes the expansion of its network structure to produce disintegration, so PVPP is a widely used tablet disintegrant in medicine.

Because the molecules have amide bonds and adsorb the hydroxyl groups on the polyphenol molecules to form hydrogen bonds, they can adsorb polyphenols and improve the non-biological stability of the wine. Therefore, it can be used as a stabilizer for beer, fruit wine, and beverage wine, extending its shelf life up to 300 days, and improving its transparency, color and taste.

Industrial Applications
 

Instant-release tablets

Disintegration <30 seconds (5% w/w)

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ODT formulations

Orodispersible tech without effervescence

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Sorbent media

Hemoperfusion cartridges for toxins

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Wound dressings

Exudate-absorbing hydrocolloids

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Beverage clarification

Colloidal stabilizer in brewing

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comparison of product parameters

Parameter

Specification

CAS No

9003-39-8

Crosslinking Agent

Divinylbenzene (DVB)

Swelling Capacity

550–650% (0.1N HCl, 10 min)

Residual NVP

≤100 ppm (HPLC)

Particle Size

50/100/200μm sieved cuts

Water Uptake

≥5.0 ml/g
 

Processing Protocol

 

1. Tableting: 2–8% w/w in direct compression

2. Hydration: Pre-swell in ethanol for hydrogel production

3. Incompatibilities: Avoid peroxides/alkaline binders (pH>9)

4. Reactivity: Exothermic gelation above 30% water content
 

Performance Validation
product-309-309

For Pharmaceuticals

▼ Disintegration time: 28±3 sec (USP <701>)

▼ Friability reduction: ≤0.1% in high-API formulations

▼ Dissolution variance: RSD <2% (n=12)

For Industrial Use

▼ Phenol adsorption: ≥120 mg/g

▼ Brewing turbidity: ≤0.5 NTU after treatment

▼ Hydrogel swelling: 40x dry weight in saline

product-309-309
 
 


 

Failure Prevention
 

Capping

Max compression force 12 kN

Gel Syneresis

Maintain ionic strength >0.5M

Dissolution Failure

Control RH <55% during blending

Color Shift

Limit UV exposure during storage

 

 

 

Property:

 

This product is white or milky white powder, odorless or slightly characteristic odor, basically tasteless, insoluble in water, alkali, acid and organic solvents. It has hygroscopicity and water absorption. It swells after absorbing water, but does not form a gel; after absorbing water, the molecular chain stretches and the volume increases rapidly, and the expansion force can cause the tablet to disintegrate quickly.

 

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