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Sigma-Aldrich

Polyvinylpyrrolidone solution

K 60, 45% in H2O

Synonym(s):

Polyvidone, Povidone

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About This Item

CAS Number:
9003-39-8
MDL number:
MFCD01076626
UNSPSC Code:
12162002
NACRES:
NA.23

Quality Level

200

form

solution

concentration

45% in H2O

InChI

1S/C6H9NO/c1-2-7-5-3-4-6(7)8/h2H,1,3-5H2

InChI key

WHNWPMSKXPGLAX-UHFFFAOYSA-N

Application

Polyvinylpyrrolidone solution (PVP) is also known as K60 and can be used in a variety of applications such as biomedical, tissue engineering, and medical materials.

Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H360D

Hazard Classifications

Repr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Zebrafish embryo xenograft and metastasis assay
Paatero I, et al.
Bio-protocol, 8(18) (2018)
How polysulfone dialysis membranes containing polyvinylpyrrolidone achieve excellent biocompatibility?
Hayama M, et al.
Journal of Membrane Science , 234(1-2), 41-49 (2004)
A pictorial representation of endogenous brain ATP by a bioluminescent method
Kogure K and Alonso OF
Brain Research, 154(2), 273-284 (1978)
Chun-Mei Zhao et al.
Environmental toxicology and chemistry, 32(4), 913-919 (2013-01-25)
The toxicity of manufactured silver nanoparticles (AgNPs) has been widely studied, but the influence of AgNPs on the major ions (such as sodium [Na] and calcium [Ca]) regulations are unknown. In the present study, a freshwater cladoceran Daphnia magna was
Liandong Hu et al.
Pakistan journal of pharmaceutical sciences, 26(3), 629-636 (2013-04-30)
Solid dispersion technique has been developed many years for improving solubility of water-insoluble drugs, aiming to achieve a better oral bioavailability. However, this technique exhibits many inconveniences when used for large-scale tableting procedures. The objective of current research work was
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