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Merck
CN

1614669

USP

羧甲基淀粉钠 A 型

United States Pharmacopeia (USP) Reference Standard

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关于此项目

线性分子式:
(C2H4O3)x · (Na)x
化学文摘社编号:
MDL number:
NACRES:
NA.24
UNSPSC Code:
41116107
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产品名称

羧甲基淀粉钠 A 型, United States Pharmacopeia (USP) Reference Standard

grade

pharmaceutical primary standard

API family

starch

manufacturer/tradename

USP

application(s)

pharmaceutical (small molecule)

format

neat

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Analysis Note

这些产品仅供测试和化验使用。它们不适用于人类或动物,也不能用于诊断、治疗或治愈任何类型的疾病。

Application

A 型淀粉甘醇酸钠USP参考标准品,预期用途是美国药典规定的指定质量测试和检测。也用于USP各论,例如:粉甘醇酸钠

General description

本品按现行药典规定交付。所有为支持本产品而提供的信息,包括SDS和任何产品信息单均由药典颁发机构制定并发布。如需进一步信息和支持,请访问现行药典网站。

Other Notes

可能适用相应的销售限制。

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Balasubramaniam Jagadish et al.
Chemical & pharmaceutical bulletin, 58(3), 293-300 (2010-03-02)
The present study investigated the effect of co-grinding raloxifene HCL (RHCL) with different superdisintegrants, namely crospovidone (CP), croscarmellose sodium (CCS) and sodium starch glycolate (SSG), using a ball mill, in order to determine the potential effect on dissolution rate and
Sagarika Bose et al.
International journal of pharmaceutics, 393(1-2), 32-40 (2010-02-09)
Film coating is generally accomplished by spraying polymers dissolved in solvents onto a cascading bed of tablets. The limitations associated with the use of solvents (both aqueous and organic) can be overcome by the use of solventless coating technologies. In
Aiman A Obaidat et al.
Acta pharmaceutica (Zagreb, Croatia), 61(1), 83-91 (2011-03-17)
The aim of this study was to prepare fast-dissolving tablets of meloxicam after its complexation with β-cyclodextrin (β-CD) and to investigate the effect of using different superdisintegrants on the disintegration and release of meloxicam from the tablets. A complex of
Ramji Anil Kumar Arza et al.
AAPS PharmSciTech, 10(1), 220-226 (2009-03-12)
Drugs that have narrow absorption window in the gastrointestinal tract (GIT) will have poor absorption. For these drugs, gastroretentive drug delivery systems offer the advantage in prolonging the gastric emptying time. Swellable, floating, and sustained release tablets are developed by
M Maghsoodi et al.
Pharmaceutical development and technology, 16(3), 243-249 (2010-02-24)
Spherical crystallization (SC) of carbamazepine (CBZ) was carried out for preparation of the agglomerates using the solvent change method. The potential of the intraagglomerate addition of sodium starch glycolate (SSG) as a disintegrant agent and povidone (PVP) as a hydrophilic

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