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USP

Sodium Starch Glycolate Type A

United States Pharmacopeia (USP) Reference Standard

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About This Item

Fórmula lineal:
(C2H4O3)x · (Na)x
Número de CAS:
UNSPSC Code:
41116107
NACRES:
NA.24

grade

pharmaceutical primary standard

API family

starch

manufacturer/tradename

USP

application(s)

pharmaceutical (small molecule)

format

neat

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General description

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

Analysis Note

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.  ​

Other Notes

Sales restrictions may apply.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

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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
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
Randa Latif
Pharmaceutical development and technology, 18(6), 1372-1378 (2012-09-12)
This report describes zero-order approximation for metoclopramide hydrochloride sublingual tablet formulation. Effects of type and concentration of excipients on release were investigated. Study revealed that highest rate of dissolution was attained with crosspovidone and decreased in the order crosspovidone >
Mayur M Patel et al.
Pharmaceutical development and technology, 14(1), 62-69 (2008-09-20)
The aim of present study was to develop a time- and pH-dependent system for delivering mesalamine to the colon. The system consists of the core tablet of mesalamine which is compression coated with hydroxypropyl methylcellulose (HPMC K4M) (time-dependent factor). This
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

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