推荐产品
生物来源
synthetic
等级
pharmaceutical primary standard
Agency
USP
API类
famotidine
表单
powder
包装
pkg of 25 mg
制造商/商品名称
USP
储存条件
protect from light
颜色
white
应用
pharmaceutical (small molecule)
包装形式
neat
储存温度
2-8°C
SMILES字符串
[s]1c(nc(c1)CSSCc2nc([s]c2)N=C(N)N)N=C(N)N
InChI
1S/C10H14N8S4/c11-7(12)17-9-15-5(1-19-9)3-21-22-4-6-2-20-10(16-6)18-8(13)14/h1-2H,3-4H2,(H4,11,12,15,17)(H4,13,14,16,18)
InChI key
ZWHJVLVEEDAPHN-UHFFFAOYSA-N
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一般描述
Famotidine Related Compound E (Famotidine Impurity E) is an impurity of famotidine, which is a hydrophilic, cationic, histamine H2 receptor antagonist drug that effectively inhibits gastric acid secretion in humans.
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.
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.
应用
Famotidine Related Compound E can be used as a pharmaceutical primary standard for the determination of the analyte in pharmaceutical formulations by various analytical techniques.
Also, for use with USP monograph such as Famotidine
Also, for use with USP monograph such as Famotidine
分析说明
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.
其他说明
Sales restrictions may apply.
相关产品
产品编号
说明
价格
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Famotidine
United States Pharmacopeia, 39(1)(1-2), 1815-1815 (2020)
RP-HPLC determination of famotidine and its potential impurities in pharmaceuticals
Chromatographia, 60(7-8) (2004)
Photoaffinity labeling of the anionic sites in Caco-2 cells mediating saturable transport of hydrophilic cations ranitidine and famotidine
Journal of medicinal chemistry, 47(11) (2004)
Potentiometric determination of famotidine in pharmaceutical formulations
Journal of Pharmaceutical and Biomedical Analysis, 29(1-2) (2002)
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