1614669
USP
Sodium Starch Glycolate Type A
United States Pharmacopeia (USP) Reference Standard
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About This Item
Formule linéaire :
(C2H4O3)x · (Na)x
Numéro CAS:
Numéro MDL:
Code UNSPSC :
41116107
Nomenclature NACRES :
NA.24
Produits recommandés
Qualité
pharmaceutical primary standard
Famille d'API
starch
Fabricant/nom de marque
USP
Application(s)
pharmaceutical (small molecule)
Format
neat
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Description générale
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia. For further information and support please go to the website of the issuing Pharmacopoeia.
Application
Sodium Starch Glycolate Type A USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia. Also, for use with USP monograph such as Sodium Starch Glycolate
Remarque sur l'analyse
These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.
Autres remarques
Sales restrictions may apply.
Produit(s) apparenté(s)
Réf. du produit
Description
Tarif
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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Certificats d'analyse (COA)
Lot/Batch Number
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Les clients ont également consulté
G Szakonyi et al.
Journal of pharmaceutical and biomedical analysis, 63, 106-111 (2012-03-01)
Water contents of superdisintegrant pharmaceutical excipients were determined by attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy using simple linear regression. Water contents of the investigated three common superdisintegrants (crospovidone, croscarmellose sodium, sodium starch glycolate) varied over a wide range
Solventless visible light-curable coating: II. Drug release, mechanical strength and photostability.
Sagarika Bose et al.
International journal of pharmaceutics, 393(1-2), 41-47 (2010-04-08)
Solventless photocurable film coating was used to obtain modified release coatings. Different pore-forming agents were used to achieve immediate and sustained release of a blue dye contained in the coated pellets (non-pareil beads). A super-disintegrant, sodium starch glycolate, was used
Samata Mehta et al.
International journal of pharmaceutics, 422(1-2), 310-317 (2011-11-22)
A design of experiments (DOE) approach (2-level full factorial design) was used to investigate the effect of several formulation and process variables on the properties of fast disintegrating tablets comprising starch-based pellets and excipient granules and to optimize and validate
R C A Schellekens et al.
Journal of controlled release : official journal of the Controlled Release Society, 132(2), 91-98 (2008-09-09)
Conventional pH-responsive coatings used for oral drug delivery to the lower parts of the gastro-intestinal tract often show a poor performance. A new system for site-specific pulsatile delivery in the ileo-colonic regions is described. The system is based on the
Bytul M Rahman et al.
Pakistan journal of pharmaceutical sciences, 21(4), 455-459 (2008-10-22)
High shear wet granulation is a preferred manufacturing method of tablets. It allowed for rapid production of compressible granulations. The resultant granulation characteristics depend on a combination of formulation properties and processing parameters. Fully pregelatinized starches are currently being used
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