おすすめの製品
品質水準
アッセイ
97%
mp
132-134 °C (lit.)
SMILES記法
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
関連するカテゴリー
保管分類コード
11 - Combustible Solids
WGK
WGK 2
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
Eyeshields, Gloves, type N95 (US)
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
E4402-5G:
E4402-VAR:
E4402-BULK:
E4402-100G:
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
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
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
Tadashi Fukunaka et al.
International journal of pharmaceutics, 310(1-2), 146-153 (2006-01-18)
In this paper, dissolution characteristics of primary-particles and compressed tablets were investigated by experiments using a mathematical model. For the primary-particle, it was found that the dissolution rate increased with a decrease in the particle size. Assuming that primary-particles of
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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