24-3800
Polyvinylpyrrolidone
CP, Mw 1200000, K 90, 11.5-12.8% N basis
Synonyme(s) :
PVP, Polyvidone, Povidone
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About This Item
Qualité:
CP
Le tarif et la disponibilité ne sont pas disponibles actuellement.
Produits recommandés
Qualité
CP
Forme
solid
Poids mol.
Mw 1200000
Disponibilité
available only in Japan
Concentration
11.5-12.8% (N)
Chaîne SMILES
C=CN1CCCC1=O
InChI
1S/C6H9NO/c1-2-7-5-3-4-6(7)8/h2H,1,3-5H2
Clé InChI
WHNWPMSKXPGLAX-UHFFFAOYSA-N
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Autres remarques
Le polyvinylpyrrolidone est un constituant de la solution de Denhardt et est inclus à une concentration de 1 % (p/v) dans la solution-mère standard 50X.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Nicole M Sanders et al.
American journal of physiology. Endocrinology and metabolism, 294(5), E853-E860 (2008-03-13)
Selective serotonin reuptake inhibitors (SSRIs) are widely prescribed for patients with comorbid diabetes and depression. Clinical case studies in diabetic patients, however, suggest that SSRI therapy may exacerbate hypoglycemia. We hypothesized that SSRIs might increase the risk of hypoglycemia by
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
Markéta Julinová et al.
Water environment research : a research publication of the Water Environment Federation, 84(12), 2123-2132 (2013-01-25)
Polyvinylpyrrolidone (PVP) is a frequently used polymer in the pharmaceutical and foodstuff industries. Because it is not subject to metabolic changes and is virtually nondegradable, trace concentrations of PVP are often found in community wastewaters. The literature finds that the
Massimiliano di Cagno et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 48(4-5), 775-780 (2013-01-29)
The objective of this study was to investigate if the increase in apparent solubility induced by liposomalization or micellization of the poorly soluble drug hydrocortisone (HC) would lead to an enhancement of its permeability through biological membranes. For this purpose
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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