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Key Documents

E4402

Sigma-Aldrich

2-Ethoxybenzamide

97%

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About This Item

Linear Formula:
C2H5OC6H4CONH2
CAS Number:
Molecular Weight:
165.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

mp

132-134 °C (lit.)

SMILES string

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Yoshihiro Hayashi et al.
Pharmaceutics, 12(7) (2020-07-02)
We previously reported a novel method for the precise prediction of tablet properties (e.g., tensile strength (TS)) using a small number of experimental data. The key technique of this method is to compensate for the lack of experimental data by
N Hirasawa et al.
Chemical & pharmaceutical bulletin, 47(3), 417-420 (1999-04-23)
Solid dispersions of carbamazepine or ethenzamide were prepared by melting and rapid cooling with liquid nitrogen using lactose as a carrier. The physical characteristics of these solid dispersions were investigated by powder X-ray diffraction, differential scanning calorimetry, and dissolution rate
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
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

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