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Merck
CN

E4402

Sigma-Aldrich

2-乙氧基苯甲酰胺

97%

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About This Item

线性分子式:
C2H5OC6H4CONH2
CAS号:
分子量:
165.19
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

mp

132-134 °C (lit.)

SMILES字符串

CCOc1ccccc1C(N)=O

InChI

1S/C9H11NO2/c1-2-12-8-6-4-3-5-7(8)9(10)11/h3-6H,2H2,1H3,(H2,10,11)

InChI key

SBNKFTQSBPKMBZ-UHFFFAOYSA-N

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


从最新的版本中选择一种:

分析证书(COA)

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Kunikazu Moribe et al.
Chemical & pharmaceutical bulletin, 52(5), 524-529 (2004-05-11)
We prepared and characterized a grinding-induced equimolar complex of thiourea with ethenzamide. When thiourea and ethenzamide were co-ground at a molar ratio of 3 : 1, new powder X-ray diffraction (PXRD) peaks were observed in addition to PXRD peaks of
Tadashi Fukunaka et al.
Journal of pharmaceutical sciences, 94(5), 1004-1012 (2005-03-29)
Milling is a common procedure to improve bioavailability of many active pharmaceutical ingredients (APIs), which typically have low solubility in water. But such micronization can yield an increase in the cohesiveness of particles. Although particle cohesiveness is desirable for tablet
Y Miyamoto et al.
Chemical & pharmaceutical bulletin, 46(9), 1432-1437 (1998-10-17)
A computer optimization technique based on surface response methodology was applied to optimize the wet granulation process for designing tablets. Physical properties (mean granule size, granule size distribution, compressibility, granule strength) of a model granule formulation containing ethenzamide were accurately
Takuto Mizoe et al.
Journal of controlled release : official journal of the Controlled Release Society, 120(3), 205-210 (2007-06-22)
We studied the use of a 4-fluid nozzle spray drier as a new one-step method for preparing drug-containing microparticles to enhance the dissolution and absorption of poorly water-soluble drugs. We employed ethenzamide (EZ) and flurbiprofen (FP) as poorly water-soluble drugs
H Uehara et al.
Cancer letters, 135(1), 83-90 (1999-03-17)
Six-week-old male F344 rats were given a mixture of 0.01% diethylnitrosamine, 0.05% N-butyl-N-(4-hydroxybutyl)nitrosamine and 0.02% N-methyl-N'-nitro-N-nitrosoguanidine in their drinking water for 1 week. When 0.8%, 0.4%, or 0% of a mixture of non-steroidal anti-inflammatory drugs (NSAIDs) (acetaminophen, aspirin, dipyrone plus

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